Bioprospecting the Efficacy and Safety of Natural Products from Plants

A special issue of Plants (ISSN 2223-7747). This special issue belongs to the section "Phytochemistry".

Deadline for manuscript submissions: 30 April 2025 | Viewed by 3934

Special Issue Editors


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Guest Editor
Laboratory of Experimental Pathology (LAPATEX), Federal University of São João del-Rei, Midwest Campus (Dona Lindu), St. Sebastião Gonçalves Coelho, 400-Chanadour, Divinópolis 35501-296, MG, Brazil
Interests: drug delivery; antioxidants; nutraceuticals; phytotherapics; phytochemicals; cell biology; pathology experimental; natural products; programmed cell death; autophagy

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Guest Editor
Laboratory of Pharmaceutical Development (LADEF), Federal University of São João del-Rei, Midwest Campus (Dona Lindu), St. Sebastião Gonçalves Coelho, 400-Chanadour, Divinópolis 35501-296, MG, Brazil
Interests: drug delivery; antioxidants; nutraceuticals; phytotherapics; multivariate statistical analysis; quality-by-design; phytochemicals; cell biology; autophagy; programmed cell death; plant anatomy
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Special Issue Information

Dear Colleagues,

Plants have been widely studied for their metabolic richness and ability to produce bioactive substances of health interest. These substances are from complex biochemical machinery and are evaluated for their ability to alter pathways that may be related to the cell survival of pathogens (antimicrobials and antivirals), pathways associated with the sequestration of free radicals (antioxidants), or cell toxicity (antitumors), among others. In general, phytotherapy is correlated with a low cytotoxic profile for normal cells, in addition to the fact that many extracts contain metabolites involved in cell detoxification.

Secondary metabolites derived from plants have an extensive history in traditional and modern societies. The discovery of new chemotherapeutic agents from natural products has stimulated the search for new bioactives that can modulate pathways related to the progression of various acute and chronic diseases. One of the most important plant explorations was the isolation of the alkaloids vinblastine and vincristine from Catharanthus roseus (L.) G. Don (Apocynaceae), popularly known as vinca. This plant was initially used to treat diabetes mellitus, and currently, the isolated alkaloids are widely used commercially in therapy against various types of tumors.

As a result, research into different plants, which are powerful sources of bioactive secondary metabolites, has taken up a lot of space in the search for new drugs, especially against cancer, which are as effective as existing chemotherapy drugs and less aggressive toward normal cells.

In this Special Issue, we invite scientists who are dedicated to the bioprospecting of natural products derived from plants. The topics of interest are i) the isolation, identification, and semi-synthesis of bioactive phytochemicals; ii) pre-clinical (in vitro and in vivo) and clinical evaluation of efficacy and safety for pharmacological and toxicological validation of phytocomplexes; iii) studies of unit operations and analytical standardization of plant extracts; and iv) the development of release systems for phytochemicals of medical, biomedical, and veterinary interest. Scientific contributions on subjects relevant to phytotherapy, e.g., metabolomics, experimental pathology, the effect of seasonality on bioactivities, and pharmacometrics are very welcome.

Full original and review articles will be considered for publication. Contributions must contain information on the botanical identification of the species under study, including the deposit of voucher specimens in herbaria, and the phytochemical characterization of plant extracts. Only systematic reviews prepared following the recommendations of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA 2020- https://www.bmj.com/content/372/bmj.n71) will be considered.

Prof. Dr. Rosy Iara Maciel de Azambuja Ribeiro
Prof. Dr. Renê Oliveira Do Couto
Guest Editors

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Keywords

  • in vitro techniques
  • phytochemicals
  • antioxidants
  • medicinal plant
  • toxic plants
  • drug delivery systems
  • animal disease models
  • drug screening
  • pharmacognosy
  • plant extracts

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Published Papers (4 papers)

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10 pages, 927 KiB  
Communication
Anticonvulsant, Anticholinesterase and Cytoprotective Effects of the Aqueous Extract of Lippia sidoides Cham
by Cicera Janaine Camilo, Débora Odília Duarte Leite, Natália Kelly Gomes de Carvalho, José Walber Gonçalves Castro, Jane Eire Silva Alencar de Menezes, Helcio Silva dos Santos, Joanda Paolla Raimundo Silva, Daniela Ribeiro Alves, Selene Maia de Morais, Fabíola Fernandes Galvão Rodrigues and José Galberto Martins da Costa
Plants 2024, 13(21), 3034; https://doi.org/10.3390/plants13213034 - 30 Oct 2024
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Abstract
(1) Background: Lippia sidoides Cham is a Brazilian aromatic plant rich in phenolic compounds. In traditional medicine, its leaves are used to treat diseases of the Central Nervous System such as stress and anxiety. This study evaluates the capacity of the aqueous extract [...] Read more.
(1) Background: Lippia sidoides Cham is a Brazilian aromatic plant rich in phenolic compounds. In traditional medicine, its leaves are used to treat diseases of the Central Nervous System such as stress and anxiety. This study evaluates the capacity of the aqueous extract of L. sidoides as an anticonvulsant, anticholinesterase and antihemolytic agent. (2) Methods: The extract was obtained from the leaves using water as a solvent, then dried in a spray dryer. The anticonvulsant effect was evaluated in zebrafish models using the pentylenetetrazol (PTZ) method. The anticholinesterase effect was determined using the acetylcholinesterase enzyme and physostigmine as a positive control. The antihemolytic action was evaluated by exposing erythrocytes to different concentrations of NaCl in the presence and absence of the extract. (3) Results: The anticonvulsant effect was observed at a concentration of 400 mg/kg, delaying convulsive crises. In the anticholinesterase assay, a dose-dependent action and variation in the effect over time were observed, demonstrating a reversible effect of the extract. For the osmotic fragility test, the extract showed satisfactory results, providing cellular protection across all variations of NaCl concentration. (4) Conclusions: These results demonstrate the promising potential of L. sidoides extract for the development of drugs that act in the treatment of diseases that affect the Central Nervous System. Full article
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13 pages, 2453 KiB  
Article
Design and Optimization of 3D-Printed Tablets Containing Mucuna Extracts for Erectile Dysfunction Management: A DoE-Guided Study
by Ratchapoom Wattanawiggan, Sunee Chansakaow, Pensak Jantrawut, Pattaraporn Panraksa, Jutamas Jiaranaikulwanitch, Suruk Udomsom, Patnarin Worajittiphon and Pratchaya Tipduangta
Plants 2024, 13(16), 2294; https://doi.org/10.3390/plants13162294 - 18 Aug 2024
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Abstract
Erectile dysfunction (ED) refers to the inability of the penis to maintain a firm erection during sexual activity. Mucuna, or M. pruriens, contains levodopa, a compound showing promise in ED treatment. However, formulating Mucuna extract into tablet dosage forms is challenging due [...] Read more.
Erectile dysfunction (ED) refers to the inability of the penis to maintain a firm erection during sexual activity. Mucuna, or M. pruriens, contains levodopa, a compound showing promise in ED treatment. However, formulating Mucuna extract into tablet dosage forms is challenging due to its semisolid nature. This study aimed to develop sustained-release tablets containing Mucuna extract via semisolid extrusion 3D printing. Eudragit RS PO (Eudragit) served as a sustained-release polymer, with poly (vinyl alcohol) (PVA) as a co-polymer for forming the tablet matrices. This study had the following two main phases: screening, which identified the factors affecting the printability, and optimization, which focused on the factors influencing the levodopa release and its consistency. The results showed that both the polymeric solid percentage content (PSPC) in the semisolid slurry and the Eudragit-PVA ratio significantly affected the printability. All of the formulations were printable, and the PSPC and Eudragit-PVA ratios were incorporated into the optimized model. The desired formulation, achieving targeted levodopa release and consistency, had a PSPC of 58.8% and a Eudragit-PVA ratio of 2.87:1. In conclusion, semisolid extrusion 3D printing guided by the design of experiments (DoE) proved feasible for producing reliable 3D-printed tablets with consistent active ingredients and desired release rates. Full article
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10 pages, 1058 KiB  
Article
Phenolic Monoterpenes Conversion of Conobea scoparioides Essential Oil by Hydrotalcite Synthesized from Blast-Furnace Slag
by Monaliza M. Rebelo, Eloisa Helena A. Andrade, José Augusto M. Corrêa and José Guilherme S. Maia
Plants 2024, 13(9), 1199; https://doi.org/10.3390/plants13091199 - 25 Apr 2024
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Abstract
Conobea scoparioides (Plantaginaceae) is an herbaceous plant known as “pataqueira” that grows wild in seasonally wet areas of the Amazon region. It is used for aromatic baths and anti-protozoan remedies by the Brazilian Amazon native people. The main volatile compounds identified in the [...] Read more.
Conobea scoparioides (Plantaginaceae) is an herbaceous plant known as “pataqueira” that grows wild in seasonally wet areas of the Amazon region. It is used for aromatic baths and anti-protozoan remedies by the Brazilian Amazon native people. The main volatile compounds identified in the essential oil of “Pataqueira” were the phenolic monoterpenes thymol and thymol methyl ether and their precursors, the monoterpene hydrocarbons α-phellandrene and p-cymene. A hydrotalcite synthesized from blast-furnace slag exhibited a 3:2 (Mg/Al) molar ratio, and this layered double hydroxide (LDH) was evaluated as a catalyst in converting the main monoterpenes of the “Pataqueira” oil. This action significantly increased the thymol content, from 41% to 95%, associated with the percentual reduction in other main components, such as thymol methyl ether, α-phellandrene, and p-cymene. The LDH reaction showed a strong tendency towards producing hydroxylated derivatives, and its behavior was similar to the hypothetical plant biosynthetic pathway, which leads to the production of the monoterpenes of “Pataqueira” oil. Thymol and its derivatives are potent antiseptics applied in pharmaceutical and hygienic products as antibacterial, antifungal, and antioxidant properties, among others. The present work reports a natural source with a high thymol content in aromatic plants from the Amazon, with evident economic value. Full article
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9 pages, 924 KiB  
Brief Report
Antioxidant and Anti-Melanogenesis Effects of Teucrium chamaedrys L. Cell Suspension Extract and Its Main Phenylethanoid Glycoside in B16-F10 Cells
by Letizia Pruccoli, Benedetta Nicolini, Mariacaterina Lianza, Gabriella Teti, Mirella Falconi, Andrea Tarozzi and Fabiana Antognoni
Plants 2024, 13(6), 808; https://doi.org/10.3390/plants13060808 - 12 Mar 2024
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Abstract
Teucrium chamaedrys L. is a typical European–Mediterranean species of the genus Teucrium. Among the phenolic compounds belonging to phenylethanoid glycosides (PGs), teucrioside (TS) is only found in this species, and it was previously demonstrated to be produced by in vitro-elicited cell cultures at [...] Read more.
Teucrium chamaedrys L. is a typical European–Mediterranean species of the genus Teucrium. Among the phenolic compounds belonging to phenylethanoid glycosides (PGs), teucrioside (TS) is only found in this species, and it was previously demonstrated to be produced by in vitro-elicited cell cultures at levels higher than those found in leaves. However, T. chamaedrys cell suspension extracts (Cell-Ex) and pure TS have not been investigated yet for any biological effects. In this study, we evaluated the antioxidant and anti-melanogenesis activity of both Cell-Ex and TS in B16-F10 mouse melanoma cells. The results showed that Cell-Ex inhibited the reactive oxygen species formation evoked in B16-F10 cells by tert-butyl hydroperoxide and 5 J/cm2 of UVA, as well as the melanin increase stimulated by α-MSH or 20 J/cm2 of UVA. In parallel, a TS concentration equivalent to that present in Cell-Ex recorded the same biological effect profile, suggesting the main contribution of TS to the antioxidant and anti-melanogenic properties of Cell-Ex. Both Cell-Ex and TS also modulated the melanogenesis pathway through their ability to inhibit the tyrosinase activity both in a cell-free system and in B16-F10 cells stimulated by α-MSH. These results support the potential cosmeceutical use of Cell-Ex for protection against photooxidative damage and hyperpigmentation. Full article
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