Next Article in Journal
Effect of the Esterification of Starch with a Mixture of Carboxylic Acids from Yarrowia lipolitica Fermentation Broth on Its Selected Properties
Next Article in Special Issue
Synthesis and Characterization of Stiff, Self-Crosslinked Thermoresponsive DMAA Hydrogels
Previous Article in Journal
A Study of the Reinforcement Effect of MWCNTs onto Polyimide Flat Sheet Membranes
Previous Article in Special Issue
Thermoresponsive Polymer Gating System on Mesoporous Shells of Silica Particles Serving as Smart Nanocontainers
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Polymers
Volume 12
Issue 6
10.3390/polym12061382
polymers-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effects of Chemical Modifications on the Thermoresponsive Behavior of a PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer

by
Despoina Giaouzi
and
Stergios Pispas
*
Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, 11635 Athens, Greece
*
Author to whom correspondence should be addressed.
Polymers 2020, 12(6), 1382; https://doi.org/10.3390/polym12061382
Submission received: 27 May 2020 / Revised: 16 June 2020 / Accepted: 17 June 2020 / Published: 19 June 2020
(This article belongs to the Special Issue Thermoresponsive Polymers)
Browse Figures
Versions Notes

Abstract

:
In this work, the synthesis, selective chemical modifications, and self-assembly behavior in aqueous media of a novel poly(2-(dimethylamino)ethyl acrylate)20-b-poly(N-isopropylacrylamide)11-b-poly(oligo ethylene glycol methyl ether acrylate)18 (PDMAEA20-b-PNIPAM11-b-POEGA18) dual-responsive (pH and temperature) and triply hydrophilic amino-based triblock terpolymer are reported. The amine functional triblock terpolymer was synthesized by sequential reversible addition fragmentation chain transfer polymerization (RAFT) polymerization and molecularly characterized by size exclusion chromatography (SEC) and 1H-NMR spectroscopy that evidenced the success of the three-step polymerization scheme. The tertiary amine pendant groups of the PDMAEA block were chemically modified in order to produce the Q1PDMAEA20-b-PNIPAM11-b-POEGA18 as well as the Q6PDMAEA20-b-PNIPAM11-b-POEGA18 quaternized triblock terpolymers (Q1 and Q6 prefixes show the number of carbon atoms (C1 and C6) attached on the PDMAEA groups) using methyl iodide (CH3I) and 1-iodohexane (C6H13I) as the quaternizing agents and the SPDMAEA20-b-PNIPAM11-b-POEGA18 sulfobetainized triblock terpolymer using 1,3 propanesultone (C3H6O3S) as the sulfobetainization agent. The self-assembly properties of the triblock terpolymers in aqueous solutions upon varying temperature and solution pH were studied by light scattering and fluorescence spectroscopy experiments. The novel triblock terpolymers self-assemble into nanosized aggregates upon solution temperature rise above the nominal lower critical solution temperature (LCST) of the temperature-responsive PNIPAM block. The remarkable stimuli-responsive self-assembly behavior of the novel triblock terpolymers in aqueous media make them interesting candidates for biomedical applications in the fields of drug and gene delivery.

Graphical Abstract

1. Introduction

Diblock copolymers have garnered the ever-increasing scientific interest over the past decades regarding the design and synthesis of novel copolymer systems by implementing facile polymerization techniques as well as the in-depth comprehension of behavioral motifs intending to their utilization in a wide range of applications [1,2,3,4,5]. Controlled/living polymerization procedures of all types have been followed for the synthesis of diblock copolymers of the AB type (A and B represent the different blocks) [6,7], which have been researched extensively as synthetic materials for various applications in the fields of nanotechnology [8]. Nevertheless, the addition of one more stimuli-responsive block to the AB type diblock copolymers can provide novel linear stimuli-responsive triblock terpolymers of the ABC type with ameliorated functionality and structural complexity at the molecular and supramolecular level in comparison to the diblock copolymer precursors [9,10]. Controlled radical polymerization methodologies such as nitroxide-mediated radical polymerization (NMP) [11], atom transfer radical polymerization (ATRP) [12,13] and reversible addition fragmentation chain transfer polymerization (RAFT) [14,15] have been utilized for the synthesis of linear triblock terpolymers. However, RAFT polymerization demonstrates some significant advantages, which include the synthesis of well-defined polymers with controlled molecular characteristics and complex architectures, under less strict experimental conditions, the compatibility with a wide variety of functional and biocompatible monomers, as well as the absence of non-biocompatible inorganic catalysts [16,17,18,19,20]. Based on the above-mentioned features, RAFT polymerization has been used widely for the synthesis of several stimuli-responsive triblock terpolymers [21,22,23,24] that can be utilized for advanced biomedical applications, such as drug and/or gene delivery [25,26].
Stimuli-responsive polymers are a class of synthetic materials that have attracted considerable interest recently because of their unique ability to form self-assembled nanostructures in aqueous media in response to a range of physicochemical stimuli, demonstrating a wide range of supramolecular morphologies such as spherical or worm-like micelles and vesicles [27,28]. In particular, stimuli-responsive triblock terpolymers of the ABC type containing two different stimuli-responsive blocks and a third one that is a non-responsive hydrophobic or hydrophilic block have gained increased interest on account of their unique macromolecular architecture and fascinating aqueous solution properties, as well as of their potential applications in the fields of nanomedicine [29,30,31,32,33,34]. The amphiphilicity of stimuli-responsive triply hydrophilic triblock terpolymers, and thus their capability of self-assembling in aqueous media, can be manipulated after being exposed to one or more external stimuli such as temperature [35], pH [36,37,38], and ionic strength [39]. Thermo- and pH-responsive polymers are two of the most significant classes of stimuli-responsive polymers owing to their valuable applications as nanosized carriers for the triggered and targeted delivery of therapeutic molecules, including hydrophobic drugs or genes, in the human body [40,41,42,43]. Thermoresponsive polymers are classified in two main subcategories based on their temperature-dependent solubility properties in aqueous media. The first subcategory includes polymers that become dehydrated/hydrophobic upon heating over a lower critical solution temperature (LCST) and the second one includes polymers that become hydrated/hydrophilic upon heating over a UCST value (upper critical solution temperature value) [44,45]. Among various thermoresponsive polymers, PNIPAM (poly(N-isopropylacrylamide))-based polymers have received great interest due to its phase transition temperature being very close to human body temperature (LCST of 32 °C) and thus render it a prominent candidate for biomedical applications [46,47,48,49,50,51,52,53]. Moreover, pH-responsive polymers are of outstanding significance owing to their cationic nature and their pH swelling/deswelling properties in aqueous media, which are properties that make them valuable candidates in the field of gene therapy [54,55,56,57,58,59]. The poly(2-(dimethylamino)ethyl acrylate-based (PDMAEA) polymers, the acrylate version of poly(2-(dimethylamino)ethyl methacrylate (PDMAEMA), respond to pH variations since PDMAEA presents a pKa = 8.41) [60], and they are gaining extensive scientific attention because of their potential utilization as non-viral synthetic carriers for gene delivery. The PDMAEA polymer exhibits several advantages including low cytotoxicity in cultured cells, pH-independent self-catalyzed degradation in aqueous environment, sufficient loading capacity, as well as an absence of immunogenicity, which are features that emerge it an alternative carrier to viral gene delivery systems for nucleic acids or proteins delivery [60,61,62].
In the current work, the synthesis of a novel doubly responsive poly(2-(dimethylamino)ethyl acrylate)-b-poly(N-isopropylacrylamide)-b-poly(oligo ethylene glycol methyl ether acrylate) (PDMAEA-b-PNIPAM-b-POEGA) triblock terpolymer by utilizing sequential three-step RAFT polymerization methodologies is presented. In addition, the chemical modifications of the tertiary amine groups of the PDMAEA block, as well as the stimuli-responsive self-assembly behavior of all the obtained triblock terpolymers, are studied in aqueous media. The selection of these kinds of monomers in the same triblock terpolymer was made due to the stimuli-responsive properties of the PNIPAM and PDMAEA blocks, as well as the high hydrophilicity and biocompatible character of the POEGA block. The obtained triblock terpolymer was molecularly characterized by SEC and 1H-NMR spectroscopy in order to confirm the success of the three-step synthetic scheme. Post-polymerization chemical modification reactions of the tertiary side groups of PDMAEA block were accomplished by using methyl iodide (CH3I) and 1-iodohexane (C6H13) as the quaternizing agents and 1,3-propanesultone (C3H6O3S) as the sulfobetainization agent. In this way, the PDMAEA block transformed into a strong cationic polyelectrolyte, resulting in novel Q1PDMAEA-b-PNIPAM-b-POEGA and Q6PDMAEA-b-PNIPAM-b-POEGA triblock terpolymers, with increased hydrophobicity in the latter case, and a block with zwitterionic character in the SPDMAEA-b-PNIPAM-b-POEGA sulfobetainized triblock terpolymer. In this study, the synthesis of a triple hydrophilic triblock terpolymer consisting of two stimuli-responsive blocks (PDMAEA and PNIPAM blocks) and one invariable hydrophilic block (POEGA), as well as the chemical modifications of the amine PDMAEA block in the amino-based triblock terpolymer are reported for the first time. Furthermore, the chemical modifications of the tertiary amine side groups of PDMAEA-based polymers have obtained rather limited scientific attention compared to the PDMAEMA-based polymers, in which the quaternization reactions have been studied extensively. In the present systems, the self-assembly properties of all obtained triblock terpolymers can be manipulated by varying the solution conditions such pH (pH-dependent PDMAEA block) and temperature (temperature-dependent PNIPAM block) in the case of the amino-based triblock terpolymer and by changing the solution temperature in the cases of chemically modified triblock terpolymers, taking into consideration also their strong polyelectrolyte properties. The triblock terpolymers (amine and chemically modified) self-assembling properties in aqueous media were investigated by conducting light scattering and fluorescence spectroscopy measurements. As the temperature rises above the LCST value of PNIPAM block, all obtained triblock terpolymers display thermoresponsive character and thus self-assemble into nanostructures in aqueous media even though they possess a rather low amount of the thermoresponsive PNIPAM block, in comparison with other two constituting blocks.

2. Materials and Methods

2.1. Materials

The used monomers, N-isopropyl acrylamide (NIPAM, ≥99%), 2-(dimethylamino) ethyl acrylate (DMAEA, 98%) and poly(oligo ethylene glycol methyl ether acrylate) (OEGA, average Mn = 480 g/mol) were obtained from Sigma-Aldrich. The purification of the monomers was achieved as follows: NIPAM monomer was recrystallized from n-hexane/benzene (4:1), while DMAEA and OEGA monomers were passed through an inhibitor-removing column. 1,4-Dioxane (99.8%), acquired from Sigma-Aldrich, was placed over molecular sieves before use in order to remove moisture. 2,2 Azobisisobutyronitrile (AIBN) was recrystallized from ethanol. 2-(Dodecylthiocarbonothioylthio)-2-methylpropionionic acid (DDMAT), Tetrahydrofuran (THF, 99.9%), methyl iodide (CH3I), 1-iodohexane (C6H13I), 1,3-propanesultone (C3H6O3S), pyrene, and other reagents were purchased from Sigma-Aldrich and utilized as received without further purification.

2.2. Synthesis of PDMAEA Homopolymer

The PDMAEA homopolymer was synthesized via RAFT polymerization utilizing 2-(dodecyltiocarbonothioylthio)-2-methylpropionionic acid (DDMAT) as the chain transfer agent (CTA). DMAEA (2 g), DDMAT (0.1458 g, 0.4 mmol), AIBN (0.0064 g, 0.04 as a solution in 1,4-dioxane) (moles DDMAT: moles AIBN = 10:1) were dissolved in 10 mL of 1,4-dioxane, and the solution was placed in a round-bottom flask (25 mL) equipped with a magnetic stirrer and fitted with a rubber septum. Then, the solution was degassed by passing through pure N2 gas bubbling for 15 min and immersed in a thermostated oil bath at 65 °C for 7 h. The polymerization reaction was terminated by placing the flask in a refrigerator (−20 °C) for 10 min and by subsequent exposure to air. The PDMAEA homopolymer was isolated by precipitation in excess of n-hexane, and the yellow product was dried for 48 h in a vacuum oven at ambient temperature. After that period, the PDMAEA macro-CTA (yield: 60%) was collected before being utilized for the polymerization of NIPAM monomer. Size exclusion chromatography (SEC) measurement displays that the weight average molecular weight (Mw) is 2800 g mol−1 and the molecular weight dispersity index (Mw/Mn) is 1.17.

2.3. Synthesis of PDMAEA-b-PNIPAM Block Copolymer

The synthetic procedure of the intermediate PDMAEA-b-PNIPAM block copolymer is described in the following: PDMAEA macro-CTA (0.7 g, 0.259 mmol), NIPAM (0.3 g, 2.65 mmol), and AIBN (0.00426 g, 0.0259 mmol) were dissolved in 5 mL of 1,4-dioxane. The polymerization solution was placed in a 25 mL round-bottom flask with a magnetic stirrer and fitted with a septum. After 15 min degassing by pure N2 gas bubbling, the flask was immersed in a thermostated oil bath at 70 °C for 6 h. After the termination of the reaction, by freezing the polymerization solution at –20 °C and by exposure to air, the PDMAEA-b-PNIPAM block copolymer was isolated by precipitation in excess of n-hexane. After drying in a vacuum oven for 48 h, the block copolymer was collected (yield: 97%) and stored before being utilized as macro-CTA for the polymerization of OEGA monomer. The weight average molecular weight (Mw) determined by SEC is 4100 g mol−1 and the molecular weight dispersity index (Mw/Mn) is 1.28.

2.4. Synthesis of PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer

The synthetic route for the preparation of the PDMAEA-b-PNIPAM-b-POEGA triblock terpolymer is described in the following: the PDMAEA-b-PNIPAM diblock copolymer was used as the macro-CTA, AIBN as the radical initiator, and 1,4-dioxane as the polymerization solvent. PDMAEA-b-PNIPAM (0.3 g, 0.0779 mmol), OEGA (0.7 g, 1.458 mmol), AIBN (0.002558 g, 0.01558 mmol), and 5 mL of 1.4-dioxane were added in a 25 mL round-bottom flask equipped with a magnetic stirrer and a rubber septum. Then, the solution was degassed by passing through pure nitrogen gas bubbling for 15 min, and the round bottom flask was put in an oil bath at 70 °C for 24 h. Subsequently, the polymerization reaction was quenched by cooling the solution in refrigerator at −20 °C and by exposure to air. The triblock terpolymer was isolated by precipitation in excess of n-hexane and dried in a vacuum oven for 48 h. The dry PDMAEA-b-PNIPAM-b-POEGA was collected (yield: 68%) and stored in a fridge for further utilization. The weight average molecular weight (Mw) is 12,800 g mol−1 and the molecular weight dispersity index (Mw/Mn) is 1.57; both values were determined by size exclusion chromatography (SEC).

2.5. Chemical Modifications of Triblock Terpolymer

2.5.1. Synthesis of Q1PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer

The pH-dependent PDMAEA block of the triblock terpolymer was quaternized by using iodomethane (CH3I) so as to produce the Q1PDMAEA-b-PNIPAM-b-POEGA triblock terpolymer. The quaternization reaction procedure for the terpolymer is as follows: in a round-bottom flask, the PDMAEA-b-PNIPAM-b-POEGA terpolymer was dissolved in THF solvent (2% w/v) and subsequently an excess of CH3I quaternizing agent was added to the solution (moles CH3I: moles amine = 2). The reaction was left for 24 h under stirring at room temperature. After this period of time, the solvent was evaporated using a rotary evaporator and the almost dry product was collected and placed in a vacuum oven for 24 h in order to ensure complete drying of the material.

2.5.2. Synthesis of Q6PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer

The PDMAEA block of the triblock terpolymer was modified by 1-iodohexane (C6H13I) to yield the quaternized Q6PDMAEA-b-PNIPAM-b-POEGA triblock terpolymer. The quaternization reaction is described in the following: the triblock terpolymer was dissolved in THF (2% w/v) in a round-bottom flask, an excess of 1-iodohexane was added to the polymer solution (moles CH3I: moles amine = 2), and the quaternization reaction was left under stirring for 72 h at room temperature. After that period, a rotary evaporator was utilized in order to remove the solvent and subsequently the hydrophobically modified quaternized triblock terpolymer was collected and dried further in a vacuum oven for 24 h.

2.5.3. Synthesis of SPDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer

The PDMAEA block of triblock terpolymer was sulfobetainized utilizing 1,3-propanesultone (C3H6O3S) in order to give an SPDMAEA-b-PNIPAM-b-POEGA zwitterionic triblock terpolymer. The functionalization procedure is described in the following: in a round-bottom flask, the triblock terpolymer was dissolved in THF (2% w/v), and then 1,3-propanesultone as the sulfobetainizing agent (moles C3H6O3S/moles amine = 1.5) was added to the solution. The reaction was allowed to stir for 72 h at room temperature. After this period, the solvent was evaporated with a rotary evaporator, and the sulfobetainized triblock terpolymer was dried in a vacuum oven for 24 h.

2.6. Self-Assembly of Triblock Terpolymer and Its Derivatives in Aqueous Solutions

The stock solutions of triblock terpolymer and its derivatives were prepared as follows: a weighted quantity of terpolymer was dissolved directly in the appropriate volume of distilled water. The solutions were allowed overnight at ambient temperature in order to ensure the complete dissolution of the triblock terpolymers. The PDMAEA-b-PNIPAM-b-POEGA triblock terpolymer stock solutions were prepared at three different pHs—3, 7, and 10—and the sample was measured fresh in order to avoid self-catalyzed hydrolysis of the PDMAEA block. The solution pH was regulated by the addition of proper amounts of 0.1 M solutions of HCl or NaOH. The concentration of all solutions measured was 1 × 10−3 g/mL.

2.7. Characterization Methods

Size exclusion chromatography (SEC) was utilized in order to determine the molecular weights and the molecular weight distributions of the synthesized polymers. The SEC system was equipped with a Waters 1515 isocratic pump, a set of three μ-Styragel mixed bed columns (porosity size from 102 to 106Å), a Waters 2414 refractive index detector (at 40 °C), and controlled via Breeze software. Tetrahydrofuran (THF) solvent (containing 5% v/v triethylamine) was the mobile phase, at a flow rate of 1 ml/min and at 30 °C. Linear polystyrene standards with narrow molecular weight distributions and average molecular weights in the range of 1200–152,000 g/mol were used for calibration of the set-up. The concentrations of all the polymers analyzed were in the range of 2–4 mg/mL.
1H-NMR spectra of the triblock terpolymers in deuterated solvents (CDCl3 and D2O) were recorded on a Varian 300MHz spectrometer and analyzed by Vjnmr software. Tetramethylsilane (TMS) was utilized as the internal standard, and the chemical shifts are reported in ppm.
PDMAEA-b-PNIPAM-b-POEGA: 1H-NMR (CDCl3, ppm): 3.63(36H, -(CH2CH2O)9, 3.36 (3H, -(CH2CH2O)9CH3-), 2.53 (6H, -N(CH3)2, 1.13 (6H, -NHCH(CH3)2.
Q1PDMAEA-b-PNIPAM-b-POEGA: 1H-NMR (D2O, ppm): 3.63(36H, -(CH2CH2O)9, 3.36 (3H, -(CH2CH2O)9CH3-), 1.13 (6H, -NHCH(CH3)2.
Q6PDMAEA-b-PNIPAM-b-POEGA: 1H-NMR (D2O, ppm): 3.63(36H, -(CH2CH2O)9, 3.36 (3H, -(CH2CH2O)9CH3-), 1.13 (6H, -NHCH(CH3)2
SPDMAEA-b-PNIPAM-b-POEGA: 1H-NMR (D2O, ppm): 3.63(36H, -(CH2CH2O)9, 3.36 (3H, -(CH2CH2O)9CH3-), 1.13 (6H, -NHCH(CH3).
Dynamic light scattering studies, in the angular range 30° to 150°, were carried out on an AVL/CGS-3 compact goniometer instrument (AVL GmbH, Germany), equipped with an ALV/LSE-5003 light scattering electronics unit for stepper motor drive and limit switch control, as well as an ALV-5000/EPP multi-tau digital correlator with 288 channels. The light source was a JDS Uniphase 22 mW He-Ne laser with a wavelength of 632.8 nm. Moreover, the temperature control of the measurement cell was achieved through a Polyscience 9102A12E water bath circulator. The autocorrelation functions were analyzed using the cumulants method and the CONTIN software. All solutions were filtered carefully through hydrophilic PVDF (polyvinyl difluoride) syringe filters (Membrane Solutions) in order to eliminate dust particles before measurements. Thereafter, the polymer solutions were transfered into standard cylindrical quartz cuvettes and left to equilibrate for 15 min. For temperature-dependent measurements, the polymer solutions were measured in the range from 25 to 55 °C in steps of 5 °C. Furthermore, the amine triblock terpolymer was studied at different solution pHs by directly dissolving the polymer in aqueous solution of three different pHs (pH = 3, 7, and 10). Before the dissolution of triblock terpolymers, the pH adjustment was achieved by the addition of 0.1 M HCl or NaOH solutions in distilled water. Static light scattering (SLS) measurements were performed on the same instrument and at the same temperature and angular range as in dynamic light scattering (DLS) measurements. Toluene was the calibration standard. The SLS results were determined using Zimm plots. The concentration for all samples was 1 × 10−3 g mL−1.
Electrophoretic light scattering measurements were carried out using a Nano Zeta Sizer (Malvern Instrument Ltd., Malvern, UK) equipped with a 4 mW solid-state laser at a wavelength of 633 nm and at 173° fixed backscattering angle. The ζ-potential values were obtained as the average of 50 runs, and the Henry correction of Smoluchowski equation was used to extract the data, after equilibration of the polymer solutions at 25 °C and 45 °C, respectively.
Fluorescence spectroscopy experiments were conducted on a Fluorolog-3 Jobin Yvon-Spex spectrofluometer (model GL3-21) so as to examine the internal polarity of triblock terpolymers (amine and quaternized) in aqueous media at 25 °C and 45 °C, respectively, using pyrene as the fluorescence probe. The excitation wavelength utilized for the experiments was 335 nm, and the obtained emission spectra were recorded in the region 355–500 nm. The preparation of stock solutions for the fluorescence spectroscopy (FS) experiments is described in the following: 1 μL of pyrene stock solution (1 mM) in acetone was transfered into the vial containing 1 mL of aqueous terpolymer solution using a microsyringe. The solutions were allowed for acetone to evaporate overnight before being measured. Excimer formation was not observed for any of the triblock terpolymer solutions studied.

3. Results and Discussion

3.1. PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer Synthesis, Chemical Modifications and Molecular Characterization

The doubly stimuli-responsive PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer (where the subscripts state the monomeric units in each block of the triblock terpolymer) was successfully synthesized via a sequential RAFT polymerization procedure, as depicted in Scheme 1.
The PDMAEA homopolymer and PDMAEA-b-PNIPAM diblock copolymer were used as the precursors for the synthesis of the PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer. The chosen CTA was the DDMAT, because it is known from other studies [63,64] that it is reactive for these kinds of monomers, resulting in well-defined polymers with controlled molecular weights, as well as rather narrow and symmetrical molecular weight distributions.
SEC measurements were conducted after each polymerization step in order to indicate the successful formation of each resulting block. It can be observed that after the polymerization of each monomer, the molecular distributions shift to higher molecular weights (Figure 1). SEC chromatographs confirmed the success of the above depicted synthetic route and revealed that the three-step RAFT polymerization methodology followed resulted in a well-defined PDMAEA20-b-PNIPAM11-POEGA18 triblock terpolymer with narrow and almost symmetrical weight distribution with a small amount of tail, indicating an almost integrated reinitiation of each polymerization step and definite extension of the sequential macromolecular chain generated. After three sequential polymerization steps, the molecular weight polydispersities are within the range ordinarily mentioned for RAFT polymerization methodologies.
Moreover, chemical modifications of the PDMAEA block were carried out via post-polymerization quaternization or sulfobetainization reactions so as to convert the tertiary amine groups of DMAEA units to their quaternary amine analogues and thus to produce strong cationic triblock polyelectrolytes or zwitterionic triblock polyampholyte, consisting of PNIPAM as the temperature-responsive block. It should be noted that the targeted composition of the amino-based triblock terpolymer and especially the higher amount of the POEGA block was designed in order to overcome solubilization barriers in aqueous media of chemically converted triblock terpolymers. Two alkyl halides with different alkyl chain length, i.e., iodomethane (CH3I) and 1-iodohexane (C6H13I), were used as the quaternizing agents in order to produce Q1PDMAEA20-b-PNIPAM11-b-POEGA18 and Q6PDMAEA20-b-PNIPAM11-b-POEGA18 quaternized triblock terpolymers of variable hydrophobicity. Additionally, 1,3 propanesultone (C3H6O3S) was utilized as the sulfobetainization agent to give SPDMAEA20-b-PNIPAM11-b-POEGA18 zwitterionic triblock terpolymers. The post-polymerization modifications taking place on the tertiary amine group of the PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer are illustrated in Scheme 2. Proper stoichiometric calculations were performed such that the amino-based PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymers were modified at 100% utilizing quaternizing and zwitterionic agents. Three different chemical modification reactions of PDMAEA block were carried out in order to investigate the effect of quaternization agents on the thermoresponsive behavior of the terpolymers originating from the PNIPAM block and on the overall self-assembling properties of chemically modified triblock terpolymers in aqueous media. After the chemical modifications, the solubility of the PDMAEA block in water increases in the case of quaternization with iodomethane due to the presence of permanent cationic charges on the amine group, and thus the PDMAEA block converts to strong cationic polyelectrolyte. Its hydrophilicity decreases in the case of quaternization with iodohexane because of the existence of hydrophobic alkyl side chains on the Q6PDMAEA block [64]. Upon sulfobetainization reaction with 1,3-propanesultone, the solubility of the PDMAEA block in aqueous media decreases, as it is known from the literature that polyampholytes are less soluble in water [65]. Nevertheless, in all types of functionalization, the solubility of PDMAEA block is independent of solution pH.
The determination of composition for the precursor PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer, as well as the verification of the chemical structure of all synthesized (amine and quaternized) triblock terpolymer analogues, were accomplished by 1H-NMR measurements. In Figure 2a, the 1H-NMR spectrum of the PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer in CDCl3 is presented. It is worth noting that the composition of the amino-based triblock terpolymer calculated from the characteristic peaks of each block are close to stoichiometric calculations, after taking into account the yields of each synthesis step, as well as the quantity of each monomer utilized. In particular, the spectral peaks of terpolymer used for the calculations of composition are described in the following: the characteristic peak of PDMAEA block is at 2.26 ppm (b) [60,64], which corresponds to the –CH3 protons of the tertiary amine group and the corresponding peaks for the PNIPAM and POEGA blocks are at 1.2 ppm (a, methyl protons of N-isopropyl group of NIPAM) and at 3.63 ppm (d, methylene protons of oligo ethylene glycol side chains of OEGA) respectively [63,66].
Figure 2b–d shows the 1H-NMR spectra of the chemically modified triblock terpolymers. For all modified terpolymers, it can be observed that the peak b of the –CH3 proton attached to the tertiary amino group disappeared, evidencing the formation of quaternary ammonium group in all cases, as also reported in the literature [60,66,67]. Indeed, as observed in other studies [62,67], the characteristic peak of the methyl protons attached to the quaternary ammonium groups appears in the range of 3.1–3.5 ppm, depending on the quaternizing agent. However, in the above spectra, the characteristic peaks of the protons of the quaternary ammonium groups are not visible due to the presence of the POEGA block in the terpolymers (overlap with the corresponding peaks of methyl and methylene protons of the POEGA side chains appears in the range of 3.1–3.6 ppm).
It has been reported in the literature [62,65,67] that the quaternization reactions utilized here are quantitative, and the tertiary amine groups convert to the quaternary amine group at almost 100% yields, as confirmed after conducting 1H-NMR measurements. Consequently, the successful chemical modifications of the amine group on the side chain of PDMAEA block with quaternizing or sulfobetanizing agents were confirmed by the above-mentioned 1H-NMR experiments. The composition and the molecular weights of all quaternized triblock terpolymers were estimated utilizing the obtained molecular characteristics of the amino-based PDMAEA20-b-PNIPAM11-b-POEGA18 tribock terpolymer, as determined by SEC and 1H-NMR measurements. All calculations were made after taking into account that the reactions are almost quantitative. The obtained molecular characteristics for all synthesized triblock terpolymers are listed in Table 1.

3.2. Aqueous Solution Properties of Triblock Terpolymers

Studies on the self-assembly behavior of the novel triblock terpolymers (amino and chemically modified analogs) in the aqueous medium were conducted utilizing light scattering techniques and fluorescence spectroscopy. Taking into account the sequence and the nature of the blocks, it is expected that the amino-based triblock terpolymer should form nanoassembled structures in aqueous solutions responding to temperature changes due to variations in the solvation/conformational state of the thermoresponsive PNIPAM block and to solution pH alterations because of variations in the hydration/conformational state of the pH-responsive PDMAEA block (pKa = 8.41), due to protonation at neutral and low pH and deprotonation at basic pH. The block sequence indicates that as the temperature increases above the nominal LCST of the PNIPAM block, which gradually obtains a less hydrophilic character [47] (not utterly hydrophobic due to interactions with water molecules even at higher temperatures), the triblock terpolymer should self-assemble into nanostructures where the PNIPAM middle block should occupy the core domains, and the PDMAEA as well as POEGA blocks should constitute the mixed hydrophilic shell of the aggregates formed. It is anticipated also that the chemically modified triblock terpolymers should form nanostructures in aqueous media where the PNIPAM middle blocks should constitute the inner part and the chemically modified PDMAEA and POEGA blocks should constitute the outer part as solution temperature increases above the nominal LCST of PNIPAM. Some deviations from this general picture are expected in the case of the Q6PDMAEA20-b-PNIPAM11-b-POEGA18 terpolymer, since in this case, the C6 side chains connected to a positively charged nitrogen confer hydrophobicity in the otherwise hydrophilic cell of the nanostructures. The triblock terpolymers were readily soluble in aqueous media at room temperature.
Light-scattering techniques are a powerful tool in order to get information about the size and morphology of the formed aggregates. Dynamic (DLS) and static (SLS) light scattering measurements for all synthesized triblock terpolymers were conducted so as to determine the weight average apparent molecular weights (Mw, app), the aggregation number (Nagg), and the apparent hydrodynamic radius (Rh) of the formed polymeric nanoassemblies in aqueous solutions as a function of temperature. Moreover, the morphology of the self-assembled nanostructures can be determined using the Rg/Rh ratio extracted by the combination of static and dynamic light scattering. The obtained results from light scattering measurements at 25 °C and 45 °C (above the LCST) are listed in Table 2.
As it can be observed in Table 2, the obtained Mw, app values are much higher than the molecular weight of single chains (Mw) determined by SEC for the PDMAEA20-b-PNIPAM11-b-POEGA18 amino-based terpolymer and the theoretical Mw calculated assuming 100% conversion for chemically modified terpolymers, indicating the presence of aggregation phenomena even at ambient temperature. Bearing in mind that the overall molecular weights of the triblock terpolymers are relatively low, the formation of aggregates even at room temperatures may be attributed to the intramolecular hydrogen bonding between the NIPAM units and the comonomers, and interactions between the carboxylate terminal groups contained in CTA and the segments of triblock terpolymers. This latter behavior is also supported by the aggregation numbers (Nagg) calculated as the Mw, app/Mw ratio, which are in the range of 9–47 at 25 °C (temperature below the nominal LCST of the PNIPAM block). It is worth noting that similar observations are also mentioned in other studies [48,63] for PNIPAM-based block copolymers’ self-assembling behavior in water at room temperatures where the hydrogen bond interactions between the monomeric NIPAM units as well as the influence of terminal end group at the polymer chains are reported as the possible reason for this behavior. At 45 °C (temperature above the nominal LCST of the PNIPAM block), the Nagg values range from 115 to 429, showing that the overall aggregation tendency is considerably higher on account of the thermoresponsiveness of the PNIPAM block that gets a less hydrophilic character above the LCST value, which is due to intramolecular hydrophobic interactions between the isopropyl groups attached to the NIPAM units. However, it could be noticed that the aggregation numbers at both temperatures (25 °C and 45 °C) for Q1PDMAEA20-b-PNIPAM11-b-POEGA18 are significantly lower that the amine-based triblock terpolymer, and this fact should be associated with the permanent positive charges on the triblock terpolymer chains contributing to the increased solubility and therefore to the decreased aggregation tendency in aqueous media. On the contrary, the Q6PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer displays a rather different aggregation behavior at both temperatures (comparatively higher Mw, app and Nagg values at both 25 °C and 45 °C, Table 2) compared to the Q1PDMAEA20-b-PNIPAM11-b-POEGA18, which is most probably due to the existence of hydrophobic alkyl (C6H13) side chains attached to the DMAEA units, leading to secondary aggregation phenomena via hydrophobic interactions between the coronas of the formed aggregates even at room temperature, as also reported in the literature [62]. In the case of SPDMAEA20-b-PNIPAM11-b-POEGA18, the aggregation tendency also may be enhanced by the formation of intramolecular and intermolecular electrostatic interactions between the zwitterionic sulfobetaine groups attached to the DMAEA segments [68].

3.2.1. Effects of Temperature and pH on the Self-Assembly Behavior of PDMAEA-b-PNIPAM-b-POEGA Terpolymers

Taking into consideration the nature of the blocks in the triblock terpolymer and in particular the combination of PDMAEA (pH-responsive block), PNIPAM (thermoresponsive block), and POEGA (hydrophilic block) in the same macromolecule, the investigation of the aqueous solution properties of such a terpolymer is quite appealing. The effects of temperature and pH on the self-assembly process in water of the triblock terpolymer were examined by varying one of these stimuli simultaneously or individually. For this purpose, light scattering (DLS and SLS) measurements were performed at three different solution pHs (acidic, neutral, and basic) and conducting measurements by increasing solution temperature from 25 to 55 °C, by steps of 5 °C.
Figure 3 depicts DLS results for the dependence of scattered intensity and Rh on temperature at acidic (a,b), neutral (c,d), and basic (e,f) pH solutions. It can be observed that the self-assembly behavior of the PDMAEA20-b-PNIPAM11-POEGA18 triblock terpolymer is affected by variations in pH and temperature. For both acidic and neutral solutions, the scattering intensity and the hydrodynamic radius (Rh) values increase as the temperature solution increases, indicating an increase in both mass and size of the formed aggregates. However, it can be noticed that in acidic solution, the LCST is moved to higher temperatures. The latter can be explained by the fact that at pH = 3, the PDMAEA chains are considerably hydrophilic, because their tertiary amine groups are fully protonated and therefore the overall hydrophilicity of the system increases, displacing the LCST phase transition at higher temperatures. At neutral pH, the PDMAEA block is quite hydrophilic because it is partially protonated, and therefore, the thermoresponsiveness of the PNIPAM block has a stronger effect on the self-assembly process. Furthermore, it is worth noting that the almost linear increase in the hydrodynamic radius of the formed aggregates is a consequence of the thermoresponsive nature of low-molecular weight PNIPAM block, as also reported in other studies [63,69]. In contrast, at basic pH, the terpolymer displays a rather different self-assembly behavior where both the scattered intensity and Rh values decrease as the solution temperature increases. At basic pH, the deprotonation of the PDMAEA block renders it less hydrophilic; this feature dictates the self-organization in the system, and the formation of larger aggregates is taking place (judging from the intensity and hydrodynamic radius values). The decrease in hydrodynamic radius of the formed aggregates by increasing temperature can be correlated with the shrinking of PNIPAM chains enhanced by the hydrophobic collapse of PDMAEA chains, which apparently leads to a partial dissociation of the initial aggregates. It can be concluded that at basic pH due to the deprotonation of the PDMAEA block, the thermoresponsiveness of the PNIPAM block affects the self-assembly procedure in a more acute way.
The hydrodynamic radius distributions from Contin analysis extracted by DLS measurements for the PDMAEA-b-PNIPAM-b-POEGA triblock terpolymer at pH = 7 and at three different temperatures are presented in Figure 4.
As observed in Figure 4, the obtained DLS results revealed the formation of monodisperse aggregates by elevation of the temperature above the LCST of the PNIPAM block. At 25 °C, there is a broad peak with an Rh value around 26 nm, indicating the formation of aggregates even at ambient temperature, due to the overall low-molecular weight of terpolymer, the hydrogen bonding interactions between the NIPAM units, as well as hydrogen bonding interactions between the terminal carboxylate groups contained in the chain transfer agent, with the segments of the blocks. The aforementioned behavior at room temperature is consistent with previous findings for low-molecular weight PNIPAM-based copolymers [63]. Increasing the solution temperature, narrow and symmetrical peaks can be observed, pointing out the participation of all polymeric chains in the formation of one type of nanostructure in the solution due to the thermally induced aggregation phenomena driven by the thermoresponsive character of the PNIPAM block. Above the phase-transition temperature, the PNIPAM block experiences conformational variations and changes in the solvation state. As a result, it becomes less hydrophilic (lessened hydrogen bonding interactions with water molecules), leading to the formation of more compact aggregates. Moreover, it should be noted that at 25 °C, the obtained Rh value is rather similar compared to the calculated length (L = 12) of the completely extended macromolecular chain (L = the number of the monomeric units of each block multiplied by 0.254, which corresponds to nearly the half micellar diameter for spherical core–shell micelles) [65], indicating that the formed aggregates may have micellar-like core–shell structures. Above the phase transition temperature, the formation of vesicular-like structures is a possible scenario since the hydrodynamic radius (at 45 °C the Rh is 73 nm and at 50 °C the Rh is 127 nm) is much higher than the block terpolymer counter length, and also, the very low size polydispersity indices (PDI < 0.1) obtained for the aggregates indicates further the formation of vesicular-like morphologies.
Additionally, at both pH = 3 (Figure S1) and pH = 10 (Figure S2), the hydrodynamic size distributions become symmetric and narrower as the temperature increases. It is worth mentioning that the obtained peaks for the acidic pH are broader compared to the hydrodynamic size distributions at basic pH, which is most probably due to the negatively charged PDMAEA block that becomes less hydrophilic, leading to the formation of more compact aggregates.
From SLS/DLS measurements, the Rg/Rho ratio values extracted are in the range of 0.7–1.35 for the triblock terpolymer aqueous solutions at three different pH solutions as a function of temperature (Figure 5).
The Rg/Rho ratio values can give significant details about the morphology/structure of the formed nanostructures. As it is reported in the literature, the corresponding Rg/Rho ratio values for spherical micellar structures (core–shell morphology) are in the range of 0.7–0.9, and for vesicular structures, they are in the range of 0.9–1.9 [70]. Therefore, the formed nanosized particles are expected to have spherical structures in the cases that the determined Rg/Rho ratio values are close to 0.8 and maybe vesicular structures in the cases that the determined Rg/Rho ratio values are above 0.9. However, it should be mentioned that unambiguous conclusions about the morphology of the formed aggregates cannot be made from SLS measurements alone. For acidic pH, the Rg/Rho ratio values are in the range of 1.15–1.35, and there are no important variations with increasing the temperature, which is presumably due to the high hydrophilicity of the fully protonated PDMAEA block. For neutral and basic pH, there are significant changes in the Rg/Rho ratio values, which are in the range of 0.7–1.25. This may be correlated with the fact that at neutral pH solution, the PDMAEA blocks are partially protonated, and at basic pH solution, they are fully deprotonated, which is a feature that seems to have an intense effect on the structure/morphology of the aggregates that are self-assembled in the corresponding aqueous solutions by increasing temperature. However, other morphologies cannot be evaluated by SLS data, and the above-mentioned results are only an indication about the morphology of the nanostructures due to the absence of confirming evidence from imaging techniques.
From the aforementioned results, it can be deduced that the PDMAEA20-PNIPAM11-POEGA18 triblock terpolymer forms well-defined aggregates in response to pH changes due to the pH-responsive PDMAEA block and temperature variations, even though the length of the thermoresponsive PNIPAM block is rather low.

3.2.2. Self-Assembly Properties of Chemically Modified PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymers in Aqueous Media as a Function of Temperature

The self-assembly behavior of chemically modified triblock terpolymers was also investigated using light scattering techniques. In Figure 5, the dependence of scattering intensity and hydrodynamic radius on temperature for chemically modified triblock terpolymers in aqueous media is depicted.
For the Q1PDMAEA20-b-PNIPAM11-b-POEGA18 (Figure 6a) and Q6PDMAEA20-b-PNIPAM11-b-POEGA18 (Figure 6b) cationic triblock terpolymers, the scattering intensity values increase and Rh values decrease as the solution temperature increases above the LCST-like phase-transition temperature. However, it can be observed that the LSCT-like transition of the Q1PDMAEA20-b-PNIPAM11-b-POEGA18 cationic terpolymer is at a higher temperature compared to the LCST-like transition of the Q6PDMAEA20-b-PNIPAM11-b-POEGA18 cationic terpolymer. The existence of long hydrophobic side chains (C6H13) attached to the PDMAEA block of the Q6PDMAEA20-b-PNIPAM11-b-POEGA18 terpolymer decrease the overall hydrophilicity of the system, which explains the shift of the LSCT at lower temperatures. Moreover, it can be noticed that the Q6PDMAEA20-b-PNIPAM11-b-POEGA18 aggregates exhibit an Rh plateau above 40 °C, indicating a rather small diminution in the size compared to the hydrodynamic radius of Q1PDMAEA20-b-PNIPAM11-b-POEGA18 aggregates, which continuously decrease in the whole temperature range. This may be explained by the fact that in the case of the Q6PDMAEA20-b-PNIPAM11-b-POEGA18 terpolymer, secondary aggregation phenomena may take place due to the amphiphilic character of the formed aggregates shell. On the other hand, the SPDMAEA20-b-PNIPAM11-b-POEGA18 zwitterionic terpolymer (Figure 6c) displays a different self-assembly behavior as a function of temperature compared to its cationic counterparts. It should be mentioned that the hydrodynamic radius values in the whole temperature range are the average values extracted from the cumulants method. By increasing temperature, both scattered intensity and hydrodynamic radius increase, showing that the initially formed nanoassemblies increase in mass and size. Increasing the temperature, this behavior may be attributed not only to the shrinking of thermoresponsive PNIPAM blocks but also to the intramolecular and intermolecular electrostatic interactions between the zwitterionic groups attached to the PDMAEA blocks, leading to the formation of larger aggregates. In addition, it should be noted that the obtained hydrodynamic radius values for chemically modified triblock terpolymers are much higher compared to the amine-based triblock terpolymer. It is probable that the existence of positive or zwitterionic charges on the PDMAEA blocks results in the formation of larger nanoaggregates due to electrostatic repulsions of the modified amine groups and thus the extension of the PDMAEA blocks. This is especially true in the case of the zwitterionic terpolymer due to the low solubility of polyzwitterions in aqueous media of low ionic strength.
The hydrodynamic radius distributions for the chemically modified triblock terpolymers at selected temperatures are presented in Figure 7.
By increasing the temperature, the Q1PDMAEA20-b-PNIPAM11-b-POEGA18 cationic triblock terpolymer seems to self-assemble into well-defined aggregates (narrow and symmetric size distributions) in aqueous media, mainly due to conformational variations in the thermoresponsive PNIPAM block. On the contrary, the size distributions for the Q6PDMAEA20-b-PNIPAM11-b-POEGA18 quaternized triblock terpolymer are broader, and the mean size of the formed aggregates are relatively larger, when the solution temperature rises above the LCST-like value, which is most probably because of the existence of hydrophobic alkyl side chains in the PDMAEA block. This is the dominant chemical difference compared to the Q1PDMAEA20-b-PNIPAM11-b-POEGA18 cationic triblock terpolymer that dictates the observed behavior. Hydrophobic interactions between the shells of the formed aggregates lead to secondary aggregation phenomena and result in the formation of less well-defined nanostructures in terms of hydrodynamic radius distributions, as a result of conformational restrictions imposed on the terpolymer chains within the aggregates. In the case of the SPDMAEA20-b-PNIPAM11-b-POEGA18 zwitterionic triblock terpolymer, at 25 °C, two peaks can be obviously observed, showing the presence of two distinct aggregate structures in the aqueous solution. The first peak with Rh = 3 nm presumably refers to non-interacting isolated terpolymer chains and the second one with Rh = 98 nm refers to supramolecular aggregates, which can be formed due to hydrogen bonding interactions between the NIPAM units, as well as electrostatic interactions between the zwitterionic groups attached to the PDMAEA blocks. By increasing temperature, the first peak becomes small in the terms of intensity, the second peak becomes extremely narrow and symmetrical, indicating the participation of nearly all polymer chains in the formation of well-defined nanostructures, which is driven by the collapse of PNIPAM chains and enhanced by the intermolecular and intramolecular electrostatic interactions between the zwitterionic groups in the PDMAEA blocks.
Moreover, it is worth mentioning that the Rg/Rho ratio values extracted by SLS/DLS measurements are in the range of 0.98–1.45 for all the chemically modified triblocks and the temperature ranges studied, which indicate that the formed aggregates probably have spherical or vesicular-like morphologies based on the results extracted from SLS measurements.
A schematic illustration of triblock terpolymers (amino and chemically modified) self-assembly behavior in aqueous media is depicted in Scheme 3.
It can be concluded that as the temperature rises, the triblock terpolymers formed aggregates with probably spherical morphology where the PNIPAM block constitute the core domain and the PDMAEA/POEGA blocks form the mixed hydrophilic shell. In the case of the PDMAEA-b-PNIPAM-b-POEGA triblock terpolymer, the variations in solution pH affect the self-assembly procedure due to the presence of the pH-responsive PDMAEA block, which is protonated at low pH values and deprotonated at high pH values. At elevated temperatures, the Q1PDMAEA-b-PNIPAM-b-POEGA quaternized terpolymer and SPDMAEA-b-PNIPAM-b-POEGA sulfobetainized terpolymer self-assemble into well-defined nanostructured aggregates. In contrast, the hydrophobically modified Q6PDMAEA-b-PNIPAM-b-POEGA terpolymer displays less well-defined aggregates, which is presumably due to hydrophobic interactions in the shell that are derived by the hydrophobic alkyl side chains on the tertiary amine groups of the PDMAEA block.

3.2.3. Surface Charge and Micropolarity of the Formed Aggregates

The surface charge of the formed aggregates from amine-based and chemically modified triblock terpolymers was investigated by utilizing electrophoretic light scattering measurements, and the obtained results are listed in Table 2. As it can be noticed, at room temperature, the ζpot values for all samples are positive, since the PDMAEA blocks are partially protonated in the amine-based triblock terpolymer and fully protonated in the chemically converted triblock terpolymers. Upon the increasing temperature, the surface charges of the amine and quaternized triblock terpolymers aggregates increase. This increase should be attributed to the increased number of positive charges on the surface of the formed aggregates, which is enhanced by the increased aggregation number. However, in the case of the zwitterionic triblock terpolymer, at 45 °C, the ζpot value slightly decreases as the solution temperature rises, which is presumably due to the existence of SO3− groups in the SPDMAEA blocks located in the shell of the aggregates. In addition, it can be observed that at 45 °C, the ζpot value of the Q6PDMAEA20-b-PNIPAM11-POEGA18 quaternized terpolymer presents a less positive surface charge than the Q1PDMAEA20-b-PNIPAM11-POEGA18 quaternized triblock terpolymer, which is most probably because of the presence of hydrophophic alkyl side chains (C6H13) on the Q6PDMAEA blocks, which may partially shield the positively charged amine groups.
Fluorescence spectroscopy (FS) experiments were performed in order to study the internal micropolarity of the formed polymeric aggregates in aqueous solutions using pyrene as the fluorescence probe. Pyrene is commonly utilized to investigate the internal micropolarity, since the I1/I3 ratio (the ratio of the first to the third vibronic peaks in the pyrene emission spectrum) is sensitive to the micropolarity variations, and particularly in less polar media, the I1/I3 ratio values decrease. In our study, the evaluation of the aggregate internal micropolarity was achieved by determining the I1/I3 ratio values at 25 °C and 45 °C, i.e., for comparison below and above LCST-like.
In Figure 8, the fluorescence spectra for amine and quaternized triblock terpolymers are presented. For PDMAEA20-b-PNIPAM11-b-POEGA18, Q1PDMAEA20-b-PNIPAM11-b-POEGA18, and SPDMAEA20-b-PNIPAM11-b-POEGA18 terpolymers aggregates, the I1/I3 values are relatively high even at 45 °C (although lower compared to those at 25 °C). It is known that the PNIPAM does not display an absolutely hydrophobic character because of the existence of hydrogen bonding interactions with water molecules, even at temperatures above the LCST values. This feature of PNIPAM blocks in conjunction with the partially protonated PDMAEA block in the PDMAEA20-b-PNIPAM11-b-POEGA18 terpolymer, the fully protonated PDMAEA block in the Q1PDMAEA20-b-PNIPAM11-b-POEGA18 terpolymer, and the zwitterionic charges on the PDMAEA block in the SPDMAEA20-b-PNIPAM11-b-POEGA18 result in the relatively high I1/I3 values. However, for the Q6PDMAEA20-b-PNIPAM11-b-POEGA18 aggregates, the determined I1/I3 values at 45 °C are lower than that of aggregates at 25 °C, indicating the formation of less hydrophilic nanodomains detected by the pyrene within the aggregates. The presence of hydrophobic alkyl side chains on the PDMAEA block seems to affect the thermoresponsive behavior of the PNIPAM block and reduces the overall hydrophilicity of the system upon temperature rise above the LCST.

4. Conclusions

A dual-responsive PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer was successfully synthesized via sequential RAFT polymerization. The tertiary amine groups attached to the PDMAEA block were chemically modified via quaternization and sulfobetainization reactions in order to produce Q1PDMAEA20-b-PNIPAM11-b-POEGA18 and Q6PDMAEA20-b-PNIPAM11-b-POEGA18 cationic polyelectrolytes utilizing methyl iodide and 1-iodohexane as the quaternizing agents and SPDMAEA20-b-PNIPAM11-b-POEGA18 zwitterionic polyampholyte utilizing 1,3-propanesultone as the surfobetainization agent. Molecular characterization results evidenced the synthesis of a triblock terpolymer with well-controlled molecular weights and close to targeted compositions, as well as the successful chemical modifications of the PDMAEA block.
Self-assembly studies in aqueous solutions as a function of pH and temperature revealed that the amine-based triblock terpolymer displays thermoresponsive behavior, even though the amount of PNIPAM block is considerably lower than the other constituting blocks. As indicated by compiled DLS/SLS measurements, the amine triblock terpolymer self-assembles into nanostructures in solutions of different pH while the temperature increases above the LCST-like transition, where the temperature-responsive PNIPAM block should compose the inner part, and the pH-responsive PDMAEA and hydrophilic POEGA blocks should occupy the outer part of the self-assembled nanostructures. Moreover, light scattering results on all chemically modified triblock terpolymers showed evidence of the formation of nanoassembled structures by increasing the solution temperature above the LCST. The chemically modified triblock terpolymers self-assemble into larger aggregates in the whole temperature range compared to the amine functionalized triblock terpolymer as a result of electrostatic repulsions of the permanently charged quaternary amine groups of the modified PDMAEA block. The chemical functionalization reactions of the PDMAEA block affect the thermoresponsiveness of the PNIPAM block, causing the formation of spherical and more compact nanostructures upon temperature rise. The light scattering and FS results have shown that the carboxylate functional group placed at the end of the terpolymer chain, the variations in pH solution, the functionalization of the PDMAEA block and the overall macromolecular architecture of the synthesized triblock terpolymer have a significant effect on the temperature-responsive self-assembly of the terpolymers in aqueous solutions and on the structure of the formed aggregates. Based on the physicochemical data on the amine-based triblock terpolymer and its quaternized counterparts, especially their capability of self-assembling into aggregates in response to temperature variations, the terpolymers may be considered potential candidates as components of non-viral gene delivery and protein vectors or/and as thermoresponsive nanocarriers for the encapsulation of hydrophobic drugs.

Supplementary Materials

The following are available online at https://www.mdpi.com/2073-4360/12/6/1382/s1, Figure S1: Hydrodynamic radius distributions from Contin analysis for PDMAEA20-b-PNIPAM11-b-POEGA18 at acidic pH and at 25 °C, 45 °C, and 55 °C. Figure S2: Hydrodynamic radius distributions from Contin analysis for PDMAEA20-b-PNIPAM11-b-POEGA18 at acidic pH and at 25 °C, 45 °C, and 55 °C.

Author Contributions

S.P. and D.G. designed the experiments. D.G. conducted the experiments. S.P. contributed the materials/reagents and instrumentation and supervised the project. D.G. and S.P. analyzed the experimental data and wrote the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research is co-financed by Greece and the European Union (European Social Fund- ESF) through the Operational Programme “Human Resources Development, Education and Lifelong Learning” in the context of the project “Strengthening Human Resources Research Potential via Doctorate Research—2nd Call’’ (MIS-5000432), implemented by the State Scholarships Foundation (ΙΚΥ).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Cölfen, H. Double-hydrophilic block copolymers: Synthesis and application as novel surfactants and crystal growth modifiers. Macromol. Rapid Commun. 2001, 22, 219–252. [Google Scholar] [CrossRef]
  2. Mahajan, S.; Renker, S.; Simon, P.F.; Gutmann, J.S.; Jain, A.; Gruner, S.M.; Fetters, L.J.; Coates, G.W.; Wiesner, U. Synthesis and Characterization of Amphiphilic Poly(ethylene oxide)-block-poly(hexyl methacrylate) Copolymers. Macromol. Chem. Phys. 2003, 204, 1047–1055. [Google Scholar] [CrossRef]
  3. Schmidt, B.V. Double Hydrophilic Block Copolymer Self-Assembly in Aqueous Solution. Macromol. Chem. Phys. 2018, 219, 1700494. [Google Scholar] [CrossRef]
  4. Ge, Z.; Liu, S. Supramolecular self-assembly of nonlinear amphiphilic and double hydrophilic block copolymers in aqueous solutions. Macromol. Rapid Commun. 2009, 30, 1523–1532. [Google Scholar] [CrossRef] [PubMed]
  5. Bates, C.M.; Bates, F.S. 50th Anniversary Perspective: Block Polymers Pure Potential. Macromolecules 2017, 50, 3–22. [Google Scholar] [CrossRef]
  6. Mai, Y.; Eisenberg, A. Self-assembly of block copolymers. Chem. Soc. Rev. 2012, 41, 5969–5985. [Google Scholar] [CrossRef] [PubMed]
  7. Hadjichristidis, N.; Pispas, S.; Floudas, G. Block Copolymers: Synthetic Strategies, Physical Properties, and Applications; John Wiley & Sons: Hoboken, NJ, USA, 2003; Chapter 1,3. [Google Scholar]
  8. Cabral, H.; Miyata, K.; Osada, K.; Kataoka, K. Block copolymer micelles in nanomedicine applications. Chem. Rev. 2018, 118, 6844–6892. [Google Scholar] [CrossRef] [Green Version]
  9. Hadjichristidis, N.; Pitsikalis, M.; Iatrou, H. Synthesis of block copolymers. In Block Copolymers I; Springer: New York, NY, USA, 2005; pp. 1–124. [Google Scholar]
  10. Hadjichristidis, N.; Iatrou, H.; Pitsikalis, M.; Pispas, S.; Avgeropoulos, A. Linear and non-linear triblock terpolymers. Synthesis, self-assembly in selective solvents and in bulk. Prog. Polym. Sci. 2005, 30, 725–782. [Google Scholar] [CrossRef]
  11. Grubbs, R.B. Nitroxide-mediated radical polymerization: Limitations and versatility. Polym. Rev. 2011, 51, 104–137. [Google Scholar] [CrossRef]
  12. Shunmugam, R.; Smith, C.E.; Tew, G.N. Atrp synthesis of abc lipophilic hydrophilic–fluorophilic triblock copolymers. J. Polym. Sci. Part A Polym. Chem. 2007, 45, 2601–2608. [Google Scholar] [CrossRef]
  13. Davis, K.A.; Matyjaszewski, K. ABC triblock copolymers prepared using atom transfer radical polymerization techniques. Macromolecules 2001, 34, 2101–2107. [Google Scholar] [CrossRef]
  14. Huang, Y.; Yong, P.; Chen, Y.; Gao, Y.; Xu, W.; Lv, Y.; Yang, L.; Reis, R.L.; Pirraco, R.P.; Chen, J. Micellization and gelatinization in aqueous media of pH-and thermo-responsive amphiphilic ABC (PMMA 82-b-PDMAEMA 150-b-PNIPAM 65) triblock copolymer synthesized by consecutive RAFT polymerization. RSC Adv. 2017, 7, 28711–28722. [Google Scholar] [CrossRef] [Green Version]
  15. Laaser, J.E.; Lohmann, E.; Jiang, Y.; Reineke, T.M.; Lodge, T.P. Architecture-Dependent Stabilization of Polyelectrolyte Complexes between Polyanions and Cationic Triblock Terpolymer Micelles. Macromolecules 2016, 49, 6644–6654. [Google Scholar] [CrossRef]
  16. Perrier, S.B. 50th Anniversary Perspective: RAFT Polymerization: A User Guide. Macromolecules 2017, 50, 7433–7447. [Google Scholar] [CrossRef]
  17. Moad, G.; Rizzardo, E.; Thang, S.H. Living radical polymerization by the RAFT process. Aust. J. Chem. 2005, 58, 379–410. [Google Scholar] [CrossRef]
  18. Moad, G.; Rizzardo, E.; Thang, S.H. Living radical polymerization by the RAFT process—A first update. Aust. J. Chem. 2006, 59, 669–692. [Google Scholar] [CrossRef]
  19. Moad, G.; Rizzardo, E.; Thang, S.H. Toward living radical polymerization. Acc. Chem. Res. 2008, 41, 1133–1142. [Google Scholar] [CrossRef]
  20. Moad, G.; Rizzardo, E.; Thang, S.H. Living radical polymerization by the RAFT process—A second update. Aust. J. Chem. 2009, 62, 1402–1472. [Google Scholar] [CrossRef]
  21. Moad, G. RAFT polymerization to form stimuli-responsive polymers. Polym. Chem. 2017, 8, 177–219. [Google Scholar] [CrossRef]
  22. Smith, A.E.; Xu, X.; McCormick, C.L. Stimuli-responsive amphiphilic (co)polymers via RAFT polymerization. Prog. Polym. Sci. 2010, 35, 45–93. [Google Scholar] [CrossRef]
  23. Mertoglu, M.; Garnier, S.; Laschewsky, A.; Skrabania, K.; Storsberg, J. Stimuli responsive amphiphilic block copolymers for aqueous media synthesised via reversible addition fragmentation chain transfer polymerisation (RAFT). Polymer 2005, 46, 7726–7740. [Google Scholar] [CrossRef]
  24. McCormick, C.L.; Sumerlin, B.S.; Lokitz, B.S.; Stempka, J.E. RAFT-synthesized diblock and triblock copolymers: Thermally-induced supramolecular assembly in aqueous media. Soft Matter 2008, 4, 1760–1773. [Google Scholar] [CrossRef]
  25. Boyer, C.; Bulmus, V.; Davis, T.P.; Ladmiral, V.; Liu, J.; Perrier, S. Bioapplications of RAFT polymerization. Chem. Rev. 2009, 109, 5402–5436. [Google Scholar] [CrossRef] [PubMed]
  26. Fairbanks, B.D.; Gunatillake, P.A.; Meagher, L. Biomedical applications of polymers derived by reversible addition–fragmentation chain-transfer (RAFT). Adv. Drug Deliv. Rev. 2015, 91, 141–152. [Google Scholar] [CrossRef] [Green Version]
  27. Tian, Q.; Fei, C.; Yin, H.; Feng, Y. Stimuli-responsive polymer wormlike micelles. Prog. Polym. Sci. 2019, 89, 108–132. [Google Scholar] [CrossRef]
  28. Li, M.-H.; Keller, P. Stimuli-responsive polymer vesicles. Soft Matter 2009, 5, 927–937. [Google Scholar] [CrossRef]
  29. Wyman, I.W.; Liu, G. Micellar structures of linear triblock terpolymers: Three blocks but many possibilities. Polymer 2013, 54, 1950–1978. [Google Scholar] [CrossRef] [Green Version]
  30. Ye, Z.; Li, Y.; An, Z.; Wu, P. Exploration of doubly thermal phase transition process of PDEGA-b-PDMA-b-PVCL in water. Langmuir 2016, 32, 6691–6700. [Google Scholar] [CrossRef]
  31. Mäkinen, L.; Varadharajan, D.; Tenhu, H.; Hietala, S. Triple hydrophilic UCST–LCST block copolymers. Macromolecules 2016, 49, 986–993. [Google Scholar]
  32. Guan, C.M.; Luo, Z.H.; Qiu, J.J.; Tang, P.P. Novel fluorosilicone triblock copolymers prepared by two-step RAFT polymerization: Synthesis, characterization, and surface properties. Eur. Polym. J. 2010, 46, 1582–1593. [Google Scholar] [CrossRef]
  33. Huang, J.; Xu, J.; Chen, K.; Wang, T.; Cui, C.; Wei, X.; Zhang, R.; Li, L.; Guo, X. Synthesis of triblock copolymers via RAFT polymerization and their application as surfactants for crude oil-in-water emulsion. Ind. Eng. Chem. Res. 2015, 54, 1564–1575. [Google Scholar] [CrossRef]
  34. Vasquez, D.; Einfalt, T.; Meier, W.; Palivan, C.G. Asymmetric Triblock Copolymer Nanocarriers for Controlled Localization and pH-Sensitive Release of Proteins. Langmuir 2016, 32, 10235–10243. [Google Scholar] [CrossRef] [PubMed]
  35. Zhao, J.; Zhang, G.; Pispas, S. Morphological transitions in aggregates of thermosensitive poly (ethylene oxide)-b-poly(N-isopropylacrylamide) block copolymers prepared via RAFT polymerization. J. Polym. Sci. Part A Polym. Chem. 2009, 47, 4099–4110. [Google Scholar] [CrossRef]
  36. Han, X.; Zhang, X.; Zhu, H.; Yin, Q.; Liu, H.; Hu, Y. Effect of composition of PDMAEMA-b-PAA block copolymers on their pH-and temperature-responsive behaviors. Langmuir 2013, 29, 1024–1034. [Google Scholar] [CrossRef]
  37. Atanase, L.I.; Reiss, G. Micellization of pH-stimulable poly(2-vinylpyridine)-b-poly(ethylene oxide) copolymers and their complexation with anionic surfactants. J. Colloid Interface Sci. 2013, 395, 190–197. [Google Scholar] [CrossRef]
  38. Atanase, L.I.; Lerch, J.P.; Caprarescu, S.; Iurciuc, C.E.; Riess, G. Micellization of pH-sensitive poly(butadiene)-block-poly(2-vinylpyridine)-block-poly(ethylene oxide) triblock copolymers: Complex formation with anionic surfactants. J. Appl. Polym. Sci. 2017, 134, 45313. [Google Scholar] [CrossRef]
  39. Stuart, M.A.C.; Huck, W.T.; Genzer, J.; Müller, M.; Ober, C.; Stamm, M.; Sukhorukov, G.B.; Szleifer, I.; Tsukruk, V.V.; Urban, M.; et al. Emerging applications of stimuli-responsive polymer materials. Nat. Mat. 2010, 9, 101–113. [Google Scholar] [CrossRef]
  40. Ganta, S.; Devalapally, H.; Shahiwala, A.; Amiji, M. A review of stimuli-responsive nanocarriers for drug and gene delivery. J. Control. Release 2008, 126, 187–204. [Google Scholar] [CrossRef]
  41. Cabane, E.; Zhang, X.; Langowska, K.; Palivan, C.G.; Meier, W. Stimuli-responsive polymers and their applications in nanomedicine. Biointerphases 2012, 7, 1. [Google Scholar] [CrossRef] [Green Version]
  42. York, A.W.; Kirkland, S.E.; McCormick, C.L. Advances in the synthesis of amphiphilic block copolymers via RAFT polymerization: Stimuli-responsive drug and gene delivery. Adv. Drug Deliv. Rev. 2008, 60, 1018–1036. [Google Scholar] [CrossRef]
  43. Schmaljohann, D. Thermo-and pH-responsive polymers in drug delivery. Adv. Drug Deliv. Rev. 2006, 58, 1655–1670. [Google Scholar] [CrossRef] [PubMed]
  44. Roy, D.; Brooks, W.L.; Sumerlin, B.S. New directions in thermoresponsive polymers. Chem. Soc. Rev. 2013, 42, 7214–7243. [Google Scholar] [CrossRef] [PubMed]
  45. Ward, M.A.; Georgiou, T.K. Thermoresponsive polymers for biomedical applications. Polymers 2011, 3, 1215–1242. [Google Scholar] [CrossRef] [Green Version]
  46. Halperin, A.; Kröger, M.; Winnik, F.M. Poly(N-isopropylacrylamide) phase diagrams: Fifty years of research. Angew. Chem. Int. Ed. 2015, 54, 15342–15367. [Google Scholar] [CrossRef]
  47. Pelton, R. Poly(N-isopropylacrylamide) (PNIPAM) is never hydrophobic. J. Colloid Interface Sci. 2010, 348, 673–674. [Google Scholar] [CrossRef]
  48. Virtanen, J.; Holappa, S.; Lemmetyinen, H.; Tenhu, H. Aggregation in aqueous poly(N-isopropylacrylamide)-block-poly (ethylene oxide) solutions studied by fluorescence spectroscopy and light scattering. Macromolecules 2002, 35, 4763–4769. [Google Scholar] [CrossRef]
  49. Umapathi, R.; Reddy, P.M.; Kumar, A.; Venkatesu, P.; Chang, C.J. The biological stimuli for governing the phase transition temperature of the “smart” polymer PNIPAM in water. Colloids Surf. B 2015, 135, 588–595. [Google Scholar] [CrossRef]
  50. Liu, S.Q.; Tong, Y.W.; Yang, Y.Y. Incorporation and in vitro release of doxorubicin in thermally sensitive micelles made from poly(N-isopropylacrylamide-co-N,N-dimethylacrylamide)-b-poly (D, L-lactide-co-glycolide) with varying compositions. Biomaterials 2005, 26, 5064–5074. [Google Scholar] [CrossRef]
  51. Li, Y.Y.; Zhang, X.Z.; Zhu, J.L.; Cheng, H.; Cheng, S.X.; Zhuo, R.X. Self-assembled, thermoresponsive micelles based on triblock PMMA-b-PNIPAAm-b-PMMA copolymer for drug delivery. Nanotechnology 2007, 18, 215605. [Google Scholar] [CrossRef]
  52. Chung, J.E.; Yokoyama, M.; Yamato, M.; Aoyagi, T.; Sakurai, Y.; Okano, T. Thermo-responsive drug delivery from polymeric micelles constructed using block copolymers of poly(N-isopropylacrylamide) and poly (butylmethacrylate). J. Control. Release 1999, 62, 115–127. [Google Scholar] [CrossRef]
  53. Liu, R.; Fraylich, M.; Saunders, B.R. Thermoresponsive copolymers: From fundamental studies to applications. Colloid Polym. Sci. 2009, 287, 627–643. [Google Scholar] [CrossRef]
  54. Donini, C.; Robinson, D.N.; Colombo, P.; Giordano, F.; Peppas, N.A. Preparation of poly (methacrylic acid-g-poly (ethylene glycol)) nanospheres from methacrylic monomers for pharmaceutical applications. Int. J. Pharm. 2002, 24, 83–91. [Google Scholar] [CrossRef]
  55. Kyriakides, T.R.; Cheung, C.Y.; Murthy, N.; Bornstein, P.; Stayton, P.S.; Hoffman, A.S. pH-sensitive polymers that enhance intracellular drug delivery in vivo. J. Control. Release 2002, 78, 295–303. [Google Scholar] [CrossRef]
  56. De las Heras Alarcón, C.; Pennadam, S.; Alexander, C. Stimuli responsive polymers for biomedical applications. Chem. Soc. Rev. 2005, 34, 276–285. [Google Scholar] [CrossRef] [PubMed]
  57. Kamada, H.; Tsutsumi, Y.; Yoshioka, Y.; Yamamoto, Y.; Kodaira, H.; Tsunoda, S.I.; Okamoto, T.; Mukai, Y.; Shibata, H.; Nakagawa, S.; et al. Design of a pH-sensitive polymeric carrier for drug release and its application in cancer therapy. Clin. Cancer Res. 2004, 10, 2545–2550. [Google Scholar] [CrossRef] [Green Version]
  58. Cho, S.K.; Dang, C.; Wang, X.; Ragan, R.; Kwon, Y.J. Mixing-sequence-dependent nucleic acid complexation and gene transfer efficiency by polyethylenimine. Biomater. Sci. 2015, 3, 1124–1133. [Google Scholar] [CrossRef] [Green Version]
  59. Liao, X.; Walden, G.; Falcon, N.D.; Donell, S.; Raxworthy, M.J.; Wormstone, M.; Riley, G.P.; Saeed, A. A direct comparison of linear and star-shaped poly (dimethylaminoethyl acrylate) polymers for polyplexation with DNA and cytotoxicity in cultured cell lines. Eur. Polym. J. 2017, 87, 458–467. [Google Scholar] [CrossRef] [Green Version]
  60. Truong, N.P.; Jia, Z.; Burges, M.; McMillan, N.A.; Monteiro, M.J. Self-catalyzed degradation of linear cationic poly (2-dimethylaminoethyl acrylate) in water. Biomacromolecules 2011, 12, 1876–1882. [Google Scholar] [CrossRef]
  61. Sun, F.; Feng, C.; Liu, H.; Huang, X. PHEA-g-PDMAEA well-defined graft copolymers: SET-LRP synthesis, self-catalyzed hydrolysis, and quaternization. Polym. Chem. 2016, 7, 6973–6979. [Google Scholar] [CrossRef]
  62. Chroni, A.; Pispas, S. Hydrophilic/hydrophobic modifications of a PnBA-b-PDMAEA copolymer and complexation behaviour with short DNA. Eur. Polym. J. 2020, 2020, 109636. [Google Scholar] [CrossRef]
  63. Giaouzi, D.; Pispas, S. Synthesis and self-assembly of thermoresponsive poly(N-isopropylacrylamide)-b-poly (oligo ethylene glycol methyl ether acrylate) double hydrophilic block copolymers. J. Polym. Sci. Part A Polym. Chem. 2019, 57, 1467–1477. [Google Scholar] [CrossRef]
  64. Chroni, A.; Pispas, S.; Forys, A.; Trzebicka, B. pH-Driven Morphological Diversity in Poly [n-Butyl Acrylate-block-(2-(Dimethylamino) Ethyl Acrylate)] Amphiphilic Copolymer Solutions. Macromol. Rapid Commun. 2019, 40, 1900477. [Google Scholar] [CrossRef] [PubMed]
  65. Chrysostomou, V.; Pispas, S. Stimuli-responsive amphiphilic PDMAEMA-b-PLMA copolymers and their cationic and zwitterionic analogs. J. Polym. Sci. Part A Polym. Chem. 2018, 56, 598–610. [Google Scholar] [CrossRef]
  66. Škvarla, J.; Zedník, J.; Šlouf, M.; Pispas, S.; Štěpánek, M. Poly(N-isopropyl acrylamide)-block-poly(N-butyl acrylate) thermoresponsive amphiphilic copolymers: Synthesis, characterization and self-assembly behavior in aqueous solutions. Eur. Polym. J. 2014, 61, 124–132. [Google Scholar] [CrossRef]
  67. Zhao, W.; Fonsny, P.; FitzGerald, P.; Warr, G.G.; Perrier, S. Unexpected behavior of polydimethylsiloxane/poly (2-(dimethylamino) ethyl acrylate) (charged) amphiphilic block copolymers in aqueous solution. Polym. Chem. 2013, 4, 2140–2150. [Google Scholar] [CrossRef]
  68. Doncom, K.E.; Willcock, H.; O’Reilly, R.K. The direct synthesis of sulfobetaine-containing amphiphilic block copolymers and their self-assembly behavior. Eur. Polym. J. 2017, 87, 497–507. [Google Scholar] [CrossRef] [Green Version]
  69. Qin, S.; Geng, Y.; Discher, D.E.; Yang, S. Temperature-Controlled Assembly and Release from Polymer Vesicles of Poly (ethylene oxide)-block-poly(N-isopropylacrylamide). Adv. Mater. 2006, 18, 2905–2909. [Google Scholar] [CrossRef]
  70. Liu, G.; Hu, X.; Chen, C.; Jin, Q.; Ji, J. Self-assembly and degradation of poly [(2-methacryloyloxyethyl phosphorylcholine)-block-(D, L-lactide)] diblock copolymers: Large compound micelles to vesicles. Polym. Int. 2011, 60, 578–583. [Google Scholar] [CrossRef]
Polymers 12 01382 sch001 550
Scheme 1. Synthesis route for poly(2-(dimethylamino)ethyl acrylate)20-b-poly(N-isopropylacrylamide)11-b-poly(oligo ethylene glycol methyl ether acrylate)18 (PDMAEA-b-PNIPAM-b-POEGA) triblock terpolymer preparation via sequential reversible addition fragmentation chain transfer polymerization (RAFT) polymerization.
Scheme 1. Synthesis route for poly(2-(dimethylamino)ethyl acrylate)20-b-poly(N-isopropylacrylamide)11-b-poly(oligo ethylene glycol methyl ether acrylate)18 (PDMAEA-b-PNIPAM-b-POEGA) triblock terpolymer preparation via sequential reversible addition fragmentation chain transfer polymerization (RAFT) polymerization.
Polymers 12 01382 sch001
Polymers 12 01382 g001 550
Figure 1. Size exclusion chromatography (SEC) traces of PDMAEA20 homopolymer, PDMAEA20-b-PNIPAM11 diblock copolymer, and PDMAEA20-b-PNIPAM11-POEGA18 triblock terpolymer in tetrahydrofuran (THF, containing 5% Et3N).
Figure 1. Size exclusion chromatography (SEC) traces of PDMAEA20 homopolymer, PDMAEA20-b-PNIPAM11 diblock copolymer, and PDMAEA20-b-PNIPAM11-POEGA18 triblock terpolymer in tetrahydrofuran (THF, containing 5% Et3N).
Polymers 12 01382 g001
Polymers 12 01382 sch002 550
Scheme 2. Chemical modification reactions of the amino-based PDMAEA-b-PNIPAM-b-POEGA triblock terpolymer.
Scheme 2. Chemical modification reactions of the amino-based PDMAEA-b-PNIPAM-b-POEGA triblock terpolymer.
Polymers 12 01382 sch002
Polymers 12 01382 g002 550
Figure 2. 1H-NMR spectra for (a) PDMAEA20-b-PNIPAM11-b-POEGA18 (in CDCl3), (b) QPDMAEA20-b-PNIPAM11-b-POEGA18 (in D2O), (c) Q6PDMAEA20-b-PNIPAM11-b-POEGA18 (in D2O), and (d) SPDMAEA20-b-PNIPAM11-b-POEGA18 (in D2O).
Figure 2. 1H-NMR spectra for (a) PDMAEA20-b-PNIPAM11-b-POEGA18 (in CDCl3), (b) QPDMAEA20-b-PNIPAM11-b-POEGA18 (in D2O), (c) Q6PDMAEA20-b-PNIPAM11-b-POEGA18 (in D2O), and (d) SPDMAEA20-b-PNIPAM11-b-POEGA18 (in D2O).
Polymers 12 01382 g002
Polymers 12 01382 g003a 550Polymers 12 01382 g003b 550
Figure 3. The dependence of scattering intensity and Rh on temperature at pH = 3 (a,b), pH = 7 (c,d), and pH = 10 (e,f) for the PDMAEA20-b-PNIPAM11-POEGA18 triblock terpolymer in aqueous media (at an angle of 90°).
Figure 3. The dependence of scattering intensity and Rh on temperature at pH = 3 (a,b), pH = 7 (c,d), and pH = 10 (e,f) for the PDMAEA20-b-PNIPAM11-POEGA18 triblock terpolymer in aqueous media (at an angle of 90°).
Polymers 12 01382 g003aPolymers 12 01382 g003b
Polymers 12 01382 g004 550
Figure 4. Hydrodynamic radius distributions from Contin analysis for the PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer in aqueous solutions at neutral pH and at selected temperatures (at an angle of 90°).
Figure 4. Hydrodynamic radius distributions from Contin analysis for the PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer in aqueous solutions at neutral pH and at selected temperatures (at an angle of 90°).
Polymers 12 01382 g004
Polymers 12 01382 g005 550
Figure 5. Rg/Rho ratio values at acidic, neutral, and basic pH solution as a function of temperature for the PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer.
Figure 5. Rg/Rho ratio values at acidic, neutral, and basic pH solution as a function of temperature for the PDMAEA20-b-PNIPAM11-b-POEGA18 triblock terpolymer.
Polymers 12 01382 g005
Polymers 12 01382 g006a 550Polymers 12 01382 g006b 550
Figure 6. The dependence of scattered intensity and hydrodynamic radius on temperature for Q1PDMAEA20-b-PNIPAM11-b-POEGA18 (a), Q6PDMAEA-b-PNIPAM11-b-POEGA18 (b), and SPDMAEA20-b-PNIPAM11-b-POEGA18 (c) in aqueous solutions at pH = 7 and c = 1 × 10−3g/mL. (measurements obtained at a 90° angle). The hydrodynamic radius of SPDMAEA20-b-PNIPAM11-b-POEGA18 is the average values extracted from the cumulants method.
Figure 6. The dependence of scattered intensity and hydrodynamic radius on temperature for Q1PDMAEA20-b-PNIPAM11-b-POEGA18 (a), Q6PDMAEA-b-PNIPAM11-b-POEGA18 (b), and SPDMAEA20-b-PNIPAM11-b-POEGA18 (c) in aqueous solutions at pH = 7 and c = 1 × 10−3g/mL. (measurements obtained at a 90° angle). The hydrodynamic radius of SPDMAEA20-b-PNIPAM11-b-POEGA18 is the average values extracted from the cumulants method.
Polymers 12 01382 g006aPolymers 12 01382 g006b
Polymers 12 01382 g007 550
Figure 7. Hydrodynamic radius distributions for Q1PDMAEA20-b-PNIPAM11-b-POEGA18 (a), Q6PDMAEA20-b-PNIPAM11-b-POEGA18 (b), and SPDMAEA20-b-PNIPAM11-b-POEGA18 (c) modified triblock terpolymers at 25 °C, 45 °C, and 55 °C. (angle of 90°).
Figure 7. Hydrodynamic radius distributions for Q1PDMAEA20-b-PNIPAM11-b-POEGA18 (a), Q6PDMAEA20-b-PNIPAM11-b-POEGA18 (b), and SPDMAEA20-b-PNIPAM11-b-POEGA18 (c) modified triblock terpolymers at 25 °C, 45 °C, and 55 °C. (angle of 90°).
Polymers 12 01382 g007
Polymers 12 01382 sch003 550
Scheme 3. Graphical illustration of PDMAEA-b-PNIPAM-b-POEGA (a), Q1PDMAEA-b-PNIPAM-b-POEGA (b), Q6PDMAEA-b-PNIPAM-b-POEGA (c), and SPDMAEA-b-PNIPAM-b-POEGA (d) triblock terpolymers self-assembly behavior in water upon increasing the solution temperature.
Scheme 3. Graphical illustration of PDMAEA-b-PNIPAM-b-POEGA (a), Q1PDMAEA-b-PNIPAM-b-POEGA (b), Q6PDMAEA-b-PNIPAM-b-POEGA (c), and SPDMAEA-b-PNIPAM-b-POEGA (d) triblock terpolymers self-assembly behavior in water upon increasing the solution temperature.
Polymers 12 01382 sch003
Polymers 12 01382 g008 550
Figure 8. Fluorescence spectra for PDMAEA20-b-PNIPAM11-b-POEGA18 (a), Q1PDMAEA20-b-PNIPAM11-b-POEGA18 (b), Q6PDMAEA20-b-PNIPAM11-b-POEGA18 (c), and SPDMAEA20-b-PNIPAM11-b-POEGA18 (d) triblock terpolymers in aqueous solutions media at 25 °C and 45 °C.
Figure 8. Fluorescence spectra for PDMAEA20-b-PNIPAM11-b-POEGA18 (a), Q1PDMAEA20-b-PNIPAM11-b-POEGA18 (b), Q6PDMAEA20-b-PNIPAM11-b-POEGA18 (c), and SPDMAEA20-b-PNIPAM11-b-POEGA18 (d) triblock terpolymers in aqueous solutions media at 25 °C and 45 °C.
Polymers 12 01382 g008
Table
Table 1. Molecular characteristics of all synthesized triblock terpolymers.
Table 1. Molecular characteristics of all synthesized triblock terpolymers.
SAMPLEMw a (×104)
(g/mol)		Mw/Mna%wt PDMAEA%wt PNIPAM%wt POEGA
PDMAEA0.281.17-
PDMAEA-b-PNIPAM0.411.2869 b31 b
PDMAEA20-b-PNIPAM11-b-POEGA181.281.5722 b10 b68 b
QPDMAEA20-b-PNIPAM11-b-POEGA181.56 c-36 c8 c55 c
Q6PDMAEA20-b-PNIPAM11-b-POEGA181.70 c-41 c8 c51 c
SPDMAEA20-b-PNIPAM11-b-POEGA181.52 c-34 c8 c58 c
a Measured by SEC in THF containing 5% Et3N, Mw values refer to the apparent molecular weights since the SEC instrument is calibrated with PS standards. b Determined by 1H-NMR. c Mw and composition values are calculated assuming 100% conversion.
Table
Table 2. Light scattering results for triblock amine terpolymers and their chemically modified analogues at neutral pH and at selected temperatures.
Table 2. Light scattering results for triblock amine terpolymers and their chemically modified analogues at neutral pH and at selected temperatures.
SAMPLET (°C)Mw, app (×106) (g/mol) aNagg aRh (nm) bζ-Potential (mV) c
PDMAEA20-b-PNIPAM11-b-POEGA18250.32326+2.27
454.232873+4.60
Q1PDMAEA20-b-PNIPAM11-b-POEGA18250.159126+22.1
451.8115105+42.7
Q6PDMAEA20-b-PNIPAM11-b-POEGA18250.847169+19.2
457.3429137+25.7
SPDMAEA20-b-PNIPAM11-b-POEGA18250.42698+12.1
455.2342160+2.7
a Determined by static light scattering (SLS), b Determined by dynamic light scattering (DLS, at an angle of 90°), c Determined by electrophoretic light scattering (ELS).

Share and Cite

MDPI and ACS Style

Giaouzi, D.; Pispas, S. Effects of Chemical Modifications on the Thermoresponsive Behavior of a PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer. Polymers 2020, 12, 1382. https://doi.org/10.3390/polym12061382

AMA Style

Giaouzi D, Pispas S. Effects of Chemical Modifications on the Thermoresponsive Behavior of a PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer. Polymers. 2020; 12(6):1382. https://doi.org/10.3390/polym12061382

Chicago/Turabian Style

Giaouzi, Despoina, and Stergios Pispas. 2020. "Effects of Chemical Modifications on the Thermoresponsive Behavior of a PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer" Polymers 12, no. 6: 1382. https://doi.org/10.3390/polym12061382

APA Style

Giaouzi, D., & Pispas, S. (2020). Effects of Chemical Modifications on the Thermoresponsive Behavior of a PDMAEA-b-PNIPAM-b-POEGA Triblock Terpolymer. Polymers, 12(6), 1382. https://doi.org/10.3390/polym12061382

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop