Advancing Cancer Treatment: Enhanced Combination Therapy through Functionalized Porous Nanoparticles
Round 1
Reviewer 1 Report
Comments and Suggestions for Authors
The manuscript introduces the ongoing challenge of cancer and the need for innovative treatment strategies, then focuses on the promising approach of using functionalized porous nanoparticles for combination therapy. Key details are provided on how combination therapy can enhance efficacy and mitigate the limitations of individual treatments. The unique properties of various porous nanoparticles are also highlighted along with how recent advances in functionalization can aid targeted delivery, controlled release, and overall efficacy of combination therapies. Recent advances in functionalization are also touched upon regarding how ligands, biomaterials, and polymers can tailor nanoparticles for effective combination therapy.
Overall, the manuscript orients the reader well to the purpose and focus of the review article. Relevant background and motivation set the stage for diving deeper into the synthesis, functionalization methods, and therapeutic applications of these porous nanoparticles across the remaining sections.
However, the writing style and organization for aided comprehension and information flow should be minorly checked by native speakers.
Moreover, expanding briefly on the specific limitations of current single-treatment methods may further strengthen the manuscript. But otherwise, all sections present the material clearly for the intended audience. Therefore, I would recommend this manuscript for publication after minor corrections.
Author Response
Comments to the Author
The manuscript introduces the ongoing challenge of cancer and the need for innovative treatment strategies, then focuses on the promising approach of using functionalized porous nanoparticles for combination therapy. Key details are provided on how combination therapy can enhance efficacy and mitigate the limitations of individual treatments. The unique properties of various porous nanoparticles are also highlighted along with how recent advances in functionalization can aid targeted delivery, controlled release, and overall efficacy of combination therapies. Recent advances in functionalization are also touched upon regarding how ligands, biomaterials, and polymers can tailor nanoparticles for effective combination therapy.
Overall, the manuscript orients the reader well to the purpose and focus of the review article. Relevant background and motivation set the stage for diving deeper into the synthesis, functionalization methods, and therapeutic applications of these porous nanoparticles across the remaining sections.
However, the writing style and organization for aided comprehension and information flow should be minorly checked by native speakers.
Moreover, expanding briefly on the specific limitations of current single-treatment methods may further strengthen the manuscript. But otherwise, all sections present the material clearly for the intended audience. Therefore, I would recommend this manuscript for publication after minor corrections.
Comment:
1) The writing style and organization for aided comprehension and information flow should be minorly checked by native speakers.
Answer: Thank you for your valuable comment. This manuscript was edited through an english editing service before submission. The certification was attached to the final page.
2) Expanding briefly on the specific limitations of current single-treatment methods may further strengthen the manuscript.
Answer: Thank you for the valuable comment. Limitation of single-treatment methods was added to manuscript as follow.
“For example, CHT induced multidrug resistance (MDR) which is one of the major causes of cancer treatment failure. CDT has the challenge of limited H2O2 content in the tumor microenvironment (TME). PDT has the challenge of low photosensitizer stability and high dependence on O2. PTT has limitations in treating cancer in deep tissues because light has difficulty penetrating deeply into tissues. The immune system activated by IMT can attack normal tissues, causing immune-related complications.” (Line 35-41)
Reviewer 2 Report
Comments and Suggestions for Authors
Since only one reference is from the year 2023, I presume the years 2018 to 2022 are included. Although there are 161 references, some works that I am aware of have not been included (for example, Bing Xia et al. from Nanjing Forestry University, China). A combination therapy is any therapy in which two or more treatments are applied. With respect to mesoporous silica nanoparticles, the key step in the possibility of their post-functionalization. Therefore I think that a review on functionalization of porous nanoparticles can be useful to a number of researchers. However, as written in Conclusion, " ... Various methods utilizing MSN, NP@MSN, MOF, mesoPt, CDs, COF, and MPPD 545 have been explored to facilitate combination therapy. ... ", not only MNP are discussed and therefore it might be wise to change the title of the review emphasizing the concept of combination therapy.
Table 1 is important part of the review because it offers a quick and concise glance of the the subject reviewed, but to be fully useful it should be accompanied with the explanation of all acronyms, no matter they have already been defined in the main text.
Author Response
Comments to the Author
Since only one reference is from the year 2023, I presume the years 2018 to 2022 are included. Although there are 161 references, some works that I am aware of have not been included (for example, Bing Xia et al. from Nanjing Forestry University, China). A combination therapy is any therapy in which two or more treatments are applied. With respect to mesoporous silica nanoparticles, the key step in the possibility of their post-functionalization. Therefore, I think that a review on functionalization of porous nanoparticles can be useful to a number of researchers.
However, as written in Conclusion, " ... Various methods utilizing MSN, NP@MSN, MOF, mesoPt, CDs, COF, and MPPD 545 have been explored to facilitate combination therapy. ... ", not only MNP are discussed and therefore it might be wise to change the title of the review emphasizing the concept of combination therapy.
Table 1 is important part of the review because it offers a quick and concise glance of the the subject reviewed, but to be fully useful it should be accompanied with the explanation of all acronyms, no matter they have already been defined in the main text.
Comment:
1) Since only one reference is from the year 2023, I presume the years 2018 to 2022 are included. Although there are 161 references, some works that I am aware of have not been included (for example, Bing Xia et al. from Nanjing Forestry University, China). A combination therapy is any therapy in which two or more treatments are applied. With respect to mesoporous silica nanoparticles, the key step in the possibility of their post-functionalization. Therefore, I think that a review on functionalization of porous nanoparticles can be useful to a number of researchers.
Answer: Thank you for the valuable comment. Reference paper (ACS Nano 2023,17,1036-1053.) was added as follow.
“Therefore, research efforts have also been directed towards overcoming these issues by uti-lizing mesoporous nanoparticles [79-84].” (Line 79-84)
- Li, J.; Fan, J.; Gao, Y.; Huang, S.; Huang, D.; Li, J.; Wang, X.; Santos, H.A.; Shen, P. ; Xia, B.,Porous Silicon Nanocarriers Boost the Immunomodulation of Mitochondria-Targeted Bovine Serum Albumins on Macrophage Polarization. ACS Nano 2023,17,1036-1053. (Line 770-772)
2) It might be wise to change the title of the review emphasizing the concept of combination therapy.
Answer: Thank you for your valuable comment. Title was changed as follow.
“Advancing cancer treatment: Enhanced combination therapy through functionalized porous nanoparticles” (Line 2-3)
3) Table 1 is important part of the review because it offers a quick and concise glance of the the subject reviewed, but to be fully useful it should be accompanied with the explanation of all acronyms, no matter they have already been defined in the main text.
Answer: Thank you for the valuable comment. Explanation of all acronyms was added as follow.
Table 1. Summarization of research on combination therapy using mesoporous nanoparticles.
Nanoparticle |
Therapy |
Functionalized material |
Functionalized method |
Drug |
Ref |
HMSN |
CHT PDT PTT |
GPTMS CS FA |
Siloxy bond Amide bond Epoxy-amine reaction |
Dox PA |
[103] |
MSN |
CHT PTT |
MPTMS 3-mercaptopropionic acid PDA |
Siloxy bonds Disulfide bond Self-polymerization |
Dox |
[105] |
MSN |
PDT PTT |
PDA FA-PEG-SH |
Self-polymerization Michael addition π−π stacking |
ICG |
[106] |
XL-MSN |
PTT IMT |
APTMS GNP PEG-SH |
Siloxy bonds Electrostatic interaction Au-thiol bond |
CpG-ODN |
[107] |
HMSN |
CHT PDT |
APTMS HA |
Siloxy bonds Schiff base bonds |
Dox Rose bengal |
[159] |
HMSN |
PTT RT |
APTMS GNP HA-Dopamine |
Siloxy bonds Electrostatic interaction Au–catechol bonds Amide bond |
MnOx |
[160] |
PDA@MS |
PTT IMT |
1-Tetradecanol |
Phase change |
Gardi |
[113] |
AgNP@MS |
CHT CST |
GOx |
Amide bond |
TPZ |
[114] |
GNR@MS |
PTT IMT |
VVP (97-mer peptide) |
Amide bond |
BMS1166 |
[115] |
GNR@MS |
PTT TDT |
PEG Lauric acid |
Physical adsorption. Phase change |
AIPH |
[116] |
INP@MS |
CHT MTT |
CS FA |
Disulfide bond Amide bond |
Dox |
[161] |
CDs@MS |
CHT PTT |
Polyethyleneimine Trastuzumab |
Amide bond |
gemcitabine |
[162] |
PCN-224 |
CHT PDT |
HA |
Coordination bond |
Dox |
[128] |
hMIL-88B(Fe)@ZIF-8 |
CHT CDT |
FA MnOx |
Coordination bond |
Dox |
[129] |
MOF-235 |
PTT CDT |
PDA IR820 |
Self-polymerization π−π stacking hydrophobic interaction |
PL |
[130] |
PCN-224 (Fe) |
CHT CDT |
PEG-SH C12-SH |
Au-thiol bond π−π stacking, Coordination bond |
CPT |
[131] |
mesoPt |
CHT PTT |
PEG |
Pt-thiol bond |
Dox |
[136] |
CDs |
PTT PDT |
TPP |
Amide bond Electro static interaction |
ALA |
[145] |
COF-366 |
PTT PDT |
TAPP terephthaldehyde |
Imine bond |
N/A |
[153] |
MPPD |
PTT PDT |
FA-PEG-SH |
Michael addition |
IR820 PFO |
[158] |
mesoPt |
CHT PTT |
Adamantane β-cyclodextrin |
Pt-thiol bond Host-Guest interaction |
Dox |
[163] |
MPPD |
CHT PTT |
PEG-NH2 |
Michael addition Schiff base reactions |
Dox |
[164] |
(HMSN, hollow mesoporous silica nanoparticles; CHT, chemotherapy; PDT, photodynamic therapy; PTT, photothermal therapy; CS, chitosan; FA, folic acid; Dox, doxorubicin; PA, pheophorbide a; MSN, Mesoporous silica nanoparticles; PDA, polydopamine; ICG, indocyanine green; XL-MSN, extra-large pore mesoporous silica nanoparticles; IMT, immunotherapy; GNP, gold nanoparticle; CpG-ODN, oligodeoxynucleotides containing unmethylated cytosine phosphorothioate-guanine motifs; HA, hyaluronic acid; RT, radiotherapy; MnOx, manganese oxide nanoparticles; Gardi, gardiquimod; AgNP, silver nanoparticle; CST, cancer starvation therapy; GOx, glucose oxidase; TPZ, tirapazamine; GNR, gold nanorod; TDT, thermodynamic therapy PEG, poly ethylene glycol; AIPH, 2,2′-azobis[2-(2-imidazolin-2-yl)propane]-dihydrochloride; INP, iron nanoparticle; MTT, magnetothermal therapy; CDs, carbon dots; CDT, chemodynamic therapy; PL, piperlongumine; CPT, camptothecin; mesoPt, mesoporous platinum nanoparticles; TPP, triphenylphosphonium; ALA, 5-aminolevulinic acid; COF, covalent organic frameworks; TAPP, tetra (p-amino-phenyl) porphyrin; MPPD, mesoporous polydopamine; PFO, perfluorooctane)
(Line 570-582)