Stimuli-Responsive Poly(Disulfide)s: A Versatile Platform for Intelligent Drug Delivery Systems

Yuechen He , Qiuhong Ouyang , Xinglv Chen , Qian Zhong , Xunhuan Song , Yujie Sun , Bingran Yu , Meng Qin

MEDCOMM - Biomaterials and Applications ›› 2026, Vol. 5 ›› Issue (2) : e70046

PDF (5207KB)
MEDCOMM - Biomaterials and Applications ›› 2026, Vol. 5 ›› Issue (2) :e70046 DOI: 10.1002/mba2.70046
REVIEW ARTICLE
Stimuli-Responsive Poly(Disulfide)s: A Versatile Platform for Intelligent Drug Delivery Systems
Author information +
History +
PDF (5207KB)

Abstract

Poly(disulfide)s represent a class of dynamic polymers whose synthesis is facilitated by the reversible exchange and recombination of disulfide bonds. This unique polymerization mechanism, combined with the structural flexibility of cyclic disulfide monomers and the diversity of ring-opening polymerization (ROP) methods, enables precise control over polymer architecture and functionality. The resulting materials exhibit remarkable characteristics including reversible redox-responsiveness, tunable degradation kinetics, self-healing capabilities, and enhanced cellular uptake efficiency. This review systematically examines the fundamental aspects of poly(disulfide)s, beginning with the design principles of monomer structures and progressing through various ROP strategies such as thermal, photo-initiated, and catalyst-mediated approaches. We critically analyze how these synthetic parameters influence key polymer properties including molecular weight distribution, stimulus responsiveness, and biocompatibility. The application potential of poly(disulfide)s in drug delivery is comprehensively explored, with particular focus on their performance in nucleic acid delivery systems for gene therapy, protein and peptide delivery for biotherapeutic applications, and small molecule drug carriers for enhanced therapeutic efficacy. By integrating recent advances in polymer chemistry with biomedical engineering perspectives, this review aims to provide valuable insights for the rational design of poly(disulfide)-based delivery platforms and their translation into clinical applications.

Keywords

drug delivery system / dynamic covalent bond / poly(disulfide)s / reduction response

Cite this article

Download citation ▾
Yuechen He, Qiuhong Ouyang, Xinglv Chen, Qian Zhong, Xunhuan Song, Yujie Sun, Bingran Yu, Meng Qin. Stimuli-Responsive Poly(Disulfide)s: A Versatile Platform for Intelligent Drug Delivery Systems. MEDCOMM - Biomaterials and Applications, 2026, 5 (2) : e70046 DOI:10.1002/mba2.70046

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Y. Arun, R. Ghosh, and A. J. Domb, “Biodegradable Hydrophobic Injectable Polymers for Drug Delivery and Regenerative Medicine,” Advanced Functional Materials 31, no. 44 (2021): 2010284.

[2]

N. Kamaly, B. Yameen, J. Wu, and O. C. Farokhzad, “Degradable Controlled-Release Polymers and Polymeric Nanoparticles: Mechanisms of Controlling Drug Release,” Chemical Reviews 116, no. 4 (2016): 2602–2663.

[3]

R. Zhao, C. Fu, Z. Wang, et al., “A pH-Responsive Nanoparticle Library With Precise pH Tunability by Co-Polymerization With Non-Ionizable Monomers,” Angewandte Chemie International Edition 61, no. 19 (2022): e202200152.

[4]

R. Xiao, G. Zhou, Y. Wen, J. Ye, X. Li, and X. Wang, “Recent Advances on Stimuli-Responsive Biopolymer-Based Nanocomposites for Drug Delivery,” Composites, Part B: Engineering 266 (2023): 111018.

[5]

L. Wang, C. Dai, Y. Fang, X. You, and J. Wu, “A Drug/Carrier Dual Redox-Responsive System Based on 6-Mercaptopurine Dimer-Loaded Cysteine Polymer Nanoparticles for Enhanced Lymphoma Therapy,” Nano Research 15, no. 5 (2022): 4544–4551.

[6]

D. Wei, Y. Sun, H. Zhu, and Q. Fu, “Stimuli-Responsive Polymer-Based Nanosystems for Cancer Theranostics,” ACS Nano 17, no. 23 (2023): 23223–23261.

[7]

P. Yang, F. Zhu, Z. Zhang, Y. Cheng, Z. Wang, and Y. Li, “Stimuli-Responsive Polydopamine-Based Smart Materials,” Chemical Society Reviews 50, no. 14 (2021): 8319–8343.

[8]

W. Wang, P.-F. Li, R. Xie, X.-J. Ju, Z. Liu, and L.-Y. Chu, “Designable Micro-/Nano-Structured Smart Polymeric Materials,” Advanced Materials 34, no. 46 (2022): 2107877.

[9]

F. Fan, S. Ji, C. Sun, et al., “Wavelength-Controlled Dynamic Metathesis: A Light-Driven Exchange Reaction Between Disulfide and Diselenide Bonds,” Angewandte Chemie International Edition 57, no. 50 (2018): 16426–16430.

[10]

Y. Jin, C. Yu, R. J. Denman, and W. Zhang, “Recent Advances in Dynamic Covalent Chemistry,” Chemical Society Reviews 42, no. 16 (2013): 6634–6654.

[11]

D. Komáromy, M. C. A. Stuart, G. Monreal Santiago, M. Tezcan, V. V. Krasnikov, and S. Otto, “Self-Assembly Can Direct Dynamic Covalent Bond Formation Toward Diversity or Specificity,” Journal of the American Chemical Society 139, no. 17 (2017): 6234–6241.

[12]

F. Karandish, B. Mamnoon, L. Feng, et al., “Nucleus-Targeted, Echogenic Polymersomes for Delivering a Cancer Stemness Inhibitor to Pancreatic Cancer Cells,” Biomacromolecules 19, no. 10 (2018): 4122–4132.

[13]

B. Li, P.-F. Cao, T. Saito, and A. P. Sokolov, “Intrinsically Self-Healing Polymers: From Mechanistic Insight to Current Challenges,” Chemical Reviews 123, no. 2 (2023): 701–735.

[14]

T. J. Bechtel and E. Weerapana, “From Structure to Redox: The Diverse Functional Roles of Disulfides and Implications in Disease,” Proteomics 17, no. 6 (2017): 1600391.

[15]

Y. Xu, Y. Liu, X. Hu, et al., “The Synthesis of a 2D Ultra-Large Protein Supramolecular Nanofilm by Chemoselective Thiol–Disulfide Exchange and Its Emergent Functions,” Angewandte Chemie International Edition 59, no. 7 (2020): 2850–2859.

[16]

Z. Shao, K. Li, H. Guo, Y. Cheng, and S. Zhang, “An Oral H2S Nanotherapeutics for Hypertensive Chronic Kidney Disease via Synergistic Antihypertensive and Renoprotective Activities,” Journal of Controlled Release 389 (2026): 114419.

[17]

Y. Liu, Y. Jia, Q. Wu, and J. S. Moore, “Architecture-Controlled Ring-Opening Polymerization for Dynamic Covalent Poly(Disulfide)s,” Journal of the American Chemical Society 141, no. 43 (2019): 17075–17080.

[18]

E. J. Goethals and C. Sillis, “Oxidation of Dithiols to Polydisulfides by Means of Dimethylsulfoxide,” Die Makromolekulare Chemie 119, no. 1 (1968): 249–251.

[19]

C. Lin, Z. Zhong, M. C. Lok, et al., “Novel Bioreducible Poly(Amido Amine)s for Highly Efficient Gene Delivery,” Bioconjugate Chemistry 18, no. 1 (2007): 138–145.

[20]

C. Yan, F. Yang, M. Wu, Y. Yuan, F. Chen, and Y. Chen, “Phase-Locked Dynamic and Mechanoresponsive Bonds Design Toward Robust and Mechanoluminescent Self-Healing Polyurethanes: A Microscopic View of Self-Healing Behaviors,” Macromolecules 52, no. 23 (2019): 9376–9382.

[21]

R. Zhang, T. Nie, Y. Fang, H. Huang, and J. Wu, “Poly(Disulfide)s: From Synthesis to Drug Delivery,” Biomacromolecules 23, no. 1 (2022): 1–19.

[22]

B.-S. Wang, Q. Zhang, Z.-Q. Wang, et al., “Inside Cover: Acid-Catalyzed Disulfide-Mediated Reversible Polymerization for Recyclable Dynamic Covalent Materials (Angew. Chem. Int. Ed. 11/2023),” Angewandte Chemie International Edition 62, no. 11 (2023): e202215329.

[23]

J. G. Felber, L. Poczka, K. C. Scholzen, et al., “Cyclic 5-membered Disulfides Are Not Selective Substrates of Thioredoxin Reductase, but Are Opened Nonspecifically,” Nature Communications 13, no. 1 (2022): 1754.

[24]

R. Singh and G. M. Whitesides, “Degenerate Intermolecular Thiolate-Disulfide Interchange Involving Cyclic Five-Membered Disulfides Is Faster by. apprx.103 Than That Involving Six- or Seven-Membered Disulfides,” Journal of the American Chemical Society 112, no. 17 (1990): 6304–6309.

[25]

A. Mondal, S. Kolay, S. Santra, et al., “Cascade Initiation of Ring Opening Polymerization for Dynamic Covalent Poly(Disulfide)s: One-Step Double Modification and Copoly(Disulfide) Synthesis by Living Polymerization,” Macromolecules 57, no. 24 (2024): 11350–11360.

[26]

G. A. Barcan, X. Zhang, and R. M. Waymouth, “Structurally Dynamic Hydrogels Derived From 1,2-Dithiolanes,” Journal of the American Chemical Society 137, no. 17 (2015): 5650–5653.

[27]

A. Maczurek, K. Hager, M. Kenklies, et al., “Lipoic Acid as an Anti-Inflammatory and Neuroprotective Treatment for Alzheimer's Disease,” Advanced Drug Delivery Reviews 60, no. 13 (2008): 1463–1470.

[28]

Q. Zhang, D.-H. Qu, B. L. Feringa, and H. Tian, “Disulfide-Mediated Reversible Polymerization Toward Intrinsically Dynamic Smart Materials,” Journal of the American Chemical Society 144, no. 5 (2022): 2022–2033.

[29]

P. Tan, W. Gu, Y. Zou, et al., “Harnessing Dynamic Covalent Chemistry in Sustainable Biomass-Based Polymers: Synthesis, Dynamic Functionalities and Potential of Dithiolane-Containing Supramolecular Polymers,” Progress in Polymer Science 160 (2025): 101920.

[30]

S. Kim, K. I. Wittek, and Y. Lee, “Synthesis of Poly(Disulfide)s With Narrow Molecular Weight Distributions via Lactone Ring-Opening Polymerization,” Chemical Science 11, no. 19 (2020): 4882–4886.

[31]

F. N. Behrendt and H. Schlaad, “Entropy-Driven Ring-Opening Disulfide Metathesis Polymerization for the Synthesis of Functional Poly(Disulfide)s,” Macromolecular Rapid Communications 39, no. 6 (2018): e1700735.

[32]

Q. Zhang, C.-Y. Shi, D.-H. Qu, Y.-T. Long, B. L. Feringa, and H. Tian, “Exploring a Naturally Tailored Small Molecule for Stretchable, Self-Healing, and Adhesive Supramolecular Polymers,” Science Advances 4, no. 7 (2018): eaat8192.

[33]

Q. Zhang, Y. Deng, C.-Y. Shi, B. L. Feringa, H. Tian, and D.-H. Qu, “Dual Closed-Loop Chemical Recycling of Synthetic Polymers by Intrinsically Reconfigurable Poly(Disulfides),” Matter 4, no. 4 (2021): 1352–1364.

[34]

M. Raeisi and N. V. Tsarevsky, “Radical Ring-Opening Polymerization of Lipoates: Kinetic and Thermodynamic Aspects,” Journal of Polymer Science 59, no. 8 (2021): 675–684.

[35]

K. Endo and T. Yamanaka, “Copolymerization of Lipoic Acid With 1,2-Dithiane and Characterization of the Copolymer as an Interlocked Cyclic Polymer,” Macromolecules 39, no. 12 (2006): 4038–4043.

[36]

B. Sieredzinska, Q. Zhang, K. J. Berg, J. Flapper, and B. L. Feringa, “Photo-Crosslinking Polymers by Dynamic Covalent Disulfide Bonds,” Chemical Communications 57, no. 77 (2021): 9838–9841.

[37]

G. M. Scheutz, J. L. Rowell, S. T. Ellison, J. B. Garrison, T. E. Angelini, and B. S. Sumerlin, “Harnessing Strained Disulfides for Photocurable Adaptable Hydrogels,” Macromolecules 53, no. 10 (2020): 4038–4046.

[38]

Y. Deng, Q. Zhang, B. L. Feringa, H. Tian, and D.-H. Qu, “Toughening a Self-Healable Supramolecular Polymer by Ionic Cluster-Enhanced Iron-Carboxylate Complexes,” Angewandte Chemie International Edition 59, no. 13 (2020): 5278–5283.

[39]

R. Morodo, D. M. Dumas, J. Zhang, et al., “Ring-Opening Polymerization of Cyclic Esters and Carbonates With (Thio)Urea/Cyclopropenimine Organocatalytic Systems,” ACS Macro Letters 13, no. 2 (2024): 181–188.

[40]

B. R. Nelson, B. E. Kirkpatrick, C. E. Miksch, et al., “Photoinduced Dithiolane Crosslinking for Multiresponsive Dynamic Hydrogels,” Advanced Materials 36, no. 43 (2024): 2211209.

[41]

C.-Y. Shi, Q. Zhang, B.-S. Wang, M. Chen, and D.-H. Qu, “Intrinsically Photopolymerizable Dynamic Polymers Derived From a Natural Small Molecule,” ACS Applied Materials & Interfaces 13, no. 37 (2021): 44860–44867.

[42]

Y. Zhu, M. Lin, W. Hu, et al., “Controllable Disulfide Exchange Polymerization of Polyguanidine for Effective Biomedical Applications by Thiol-Mediated Uptake,” Angewandte Chemie International Edition 61, no. 23 (2022): e202200535.

[43]

D. Yu, Y. Wang, S. Qu, et al., “Controllable Star Cationic Poly(Disulfide)s Achieve Genetically Cascade Catalytic Therapy by Delivering Bifunctional Fusion Plasmids,” Advanced Materials 35, no. 52 (2023): 2307190.

[44]

J. Guo, S. Zhang, Y. Tao, B. Fan, and W. Tang, “Glutathione-Triggered Biodegradable Poly(Disulfide)s: Ring-Opening Copolymerization and Potent Antibacterial Activity,” Polymer Chemistry 13, no. 48 (2022): 6637–6649.

[45]

J. Guo, S. Zhang, Y. Tao, et al., “Synthesis of Cationic Cyclic Oligo(Disulfide)s Via Cyclo-Depolymerization: A Redox-Responsive and Potent Antibacterial Reagent,” Journal of the American Chemical Society 147, no. 8 (2025): 6772–6785.

[46]

J. Guo, T. Wan, B. Li, et al., “Rational Design of Poly(Disulfide)s as a Universal Platform for Delivery of CRISPR-Cas9 Machineries Toward Therapeutic Genome Editing,” ACS Central Science 7, no. 6 (2021): 990–1000.

[47]

R. Singh and G. M. Whitesides, “Comparisons of Rate Constants for Thiolate-Disulfide Interchange in Water and in Polar Aprotic Solvents Using Dynamic Proton NMR Line Shape Analysis,” Journal of the American Chemical Society 112, no. 3 (1990): 1190–1197.

[48]

S. Y. An, S. M. Noh, and J. K. Oh, “Multiblock Copolymer-Based Dual Dynamic Disulfide and Supramolecular Crosslinked Self-Healing Networks,” Macromolecular Rapid Communications 38, no. 8 (2017): 1600777.

[49]

H. Yu, Y. Wang, H. Yang, K. Peng, and X. Zhang, “Injectable Self-Healing Hydrogels Formed via Thiol/Disulfide Exchange of Thiol Functionalized F127 and Dithiolane Modified PEG,” Journal of Materials Chemistry B 5, no. 22 (2017): 4121–4127.

[50]

J. Houk and G. M. Whitesides, “Structure-Reactivity Relations for Thiol-Disulfide Interchange,” Journal of the American Chemical Society 109, no. 22 (1987): 6825–6836.

[51]

A. Carmine, Y. Domoto, N. Sakai, and S. Matile, “Comparison of Lipoic and Asparagusic Acid for Surface-Initiated Disulfide-Exchange Polymerization,” Chemistry – A European Journal 19, no. 35 (2013): 11558–11563.

[52]

T. Du, B. Shen, J. Dai, et al., “Controlled and Regioselective Ring-Opening Polymerization for Poly(Disulfide)s by Anion-Binding Catalysis,” Journal of the American Chemical Society 145, no. 50 (2023): 27788–27799.

[53]

E.-K. Bang, M. Lista, G. Sforazzini, N. Sakai, and S. Matile, “Poly(Disulfide)s,” Chemical Science 3, no. 6 (2012): 1752–1763.

[54]

A. Sadownik, J. Stefely, and S. L. Regen, “Polymerized Liposomes Formed Under Extremely Mild Conditions,” Journal of the American Chemical Society 108, no. 24 (1986): 7789–7791.

[55]

D. Lee, H. Wang, S.-Y. Jiang, and R. Verduzco, “Versatile Light-Mediated Synthesis of Degradable Bottlebrush Polymers Using α-Lipoic Acid,” Angewandte Chemie International Edition 63, no. 48 (2024): e202409323.

[56]

S. Huang, Y. Shen, H. K. Bisoyi, et al., “Covalent Adaptable Liquid Crystal Networks Enabled by Reversible Ring-Opening Cascades of Cyclic Disulfides,” Journal of the American Chemical Society 143, no. 32 (2021): 12543–12551.

[57]

T. Zhu, R. Lei, B. Wang, T. Du, W. Xia, and Y. Liu, “Bio-Sourced 4-Aryl-1,2-Dithiolanes for Recyclable Poly(Disulfide)s With High Performance,” Angewandte Chemie International Edition 64, no. 26 (2025): e202503677.

[58]

S. Nevejans, N. Ballard, J. I. Miranda, B. Reck, and J. M. Asua, “The Underlying Mechanisms for Self-Healing of Poly(Disulfide)s,” Physical Chemistry Chemical Physics 18, no. 39 (2016): 27577–27583.

[59]

M. Chen, R. Yang, H. Wu, et al., “Closed-Loop Recyclable Poly(Ester-Disulfide)s for Potential Alternatives to Engineering Plastic,” Angewandte Chemie International Edition 63, no. 38 (2024): e202409200.

[60]

J. Kamada, K. Koynov, C. Corten, et al., “Redox Responsive Behavior of Thiol/Disulfide-Functionalized Star Polymers Synthesized via Atom Transfer Radical Polymerization,” Macromolecules 43, no. 9 (2010): 4133–4139.

[61]

X. Wu, J. Li, G. Li, et al., “Heat-Triggered Poly(Siloxane-Urethane)s Based on Disulfide Bonds for Self-Healing Application,” Journal of Applied Polymer Science 135, no. 31 (2018): 46532.

[62]

Y. Amamoto, H. Otsuka, A. Takahara, and K. Matyjaszewski, “Self-Healing of Covalently Cross-Linked Polymers by Reshuffling Thiuram Disulfide Moieties in Air Under Visible Light,” Advanced Materials 24, no. 29 (2012): 3975–3980.

[63]

G. Deng, F. Li, H. Yu, et al., “Dynamic Hydrogels With an Environmental Adaptive Self-Healing Ability and Dual Responsive Sol–Gel Transitions,” ACS Macro Letters 1, no. 2 (2012): 275–279.

[64]

B. Niu, K. Liao, Y. Zhou, et al., “Application of Glutathione Depletion in Cancer Therapy: Enhanced ROS-Based Therapy, Ferroptosis, and Chemotherapy,” Biomaterials 277 (2021): 121110.

[65]

Z. Deng, J. Hu, and S. Liu, “Disulfide-Based Self-Immolative Linkers and Functional Bioconjugates for Biological Applications,” Macromolecular Rapid Communications 41, no. 1 (2020): 1900531.

[66]

G. S. Pulcu, N. S. Galenkamp, Y. Qing, et al., “Single-Molecule Kinetics of Growth and Degradation of Cell-Penetrating Poly(Disulfide)s,” Journal of the American Chemical Society 141, no. 32 (2019): 12444–12447.

[67]

Y. Wan, W. Wang, Q. Lai, M. Wu, and S. Feng, “Advances in Cell-Penetrating Poly(Disulfide)s for Intracellular Delivery of Therapeutics,” Drug Discovery Today 28, no. 8 (2023): 103668.

[68]

E.-K. Bang, G. Gasparini, G. Molinard, A. Roux, N. Sakai, and S. Matile, “Substrate-Initiated Synthesis of Cell-Penetrating Poly(Disulfide)s,” Journal of the American Chemical Society 135, no. 6 (2013): 2088–2091.

[69]

M.-W. Hei, Y.-R. Zhan, P. Chen, et al., “Lipoic Acid-Based Poly(Disulfide)s as Versatile Biomolecule Delivery Vectors and the Application in Tumor Immunotherapy,” Molecular Pharmaceutics 20, no. 6 (2023): 3210–3222.

[70]

W. Yang, C. Yu, C. Wu, S. Q. Yao, and S. Wu, “Cell-Penetrating Poly(Disulfide)-Based Star Polymers for Simultaneous Intracellular Delivery of miRNAs and Small Molecule Drugs,” Polymer Chemistry 8, no. 27 (2017): 4043–4051.

[71]

X. Li, C. Wang, L. Wang, et al., “A Glutathione-Responsive Silica-Based Nanosystem Capped With In-Situ Polymerized Cell-Penetrating Poly(Disulfide)s for Precisely Modulating Immuno-Inflammatory Responses,” Journal of Colloid and Interface Science 614 (2022): 322–336.

[72]

P. Yuan, X. Mao, K. C. Chong, et al., “Simultaneous Imaging of Endogenous Survivin mRNA and On-Demand Drug Release in Live Cells by Using a Mesoporous Silica Nanoquencher,” Small 13, no. 27 (2017): 1700569.

[73]

J. Fu, C. Yu, L. Li, and S. Q. Yao, “Intracellular Delivery of Functional Proteins and Native Drugs by Cell-Penetrating Poly(Disulfide)s,” Journal of the American Chemical Society 137, no. 37 (2015): 12153–12160.

[74]

L. Qian, J. Fu, P. Yuan, et al., “Intracellular Delivery of Native Proteins Facilitated by Cell-Penetrating Poly(Disulfide)s,” Angewandte Chemie International Edition 57, no. 6 (2018): 1532–1536.

[75]

Y. Zhang, J. J. Røise, K. Lee, J. Li, and N. Murthy, “Recent Developments in Intracellular Protein Delivery,” Current Opinion in Biotechnology 52 (2018): 25–31.

[76]

Z. Li, K. Xu, L. Qin, et al., “Hollow Nanomaterials in Advanced Drug Delivery Systems: From Single- to Multiple Shells,” Advanced Materials 35, no. 12 (2023): 2203890.

[77]

P. Zhang, Y. Wang, J. Lian, et al., “Engineering the Surface of Smart Nanocarriers Using a pH-/Thermal-/GSH-Responsive Polymer Zipper for Precise Tumor Targeting Therapy In Vivo,” Advanced Materials 29, no. 36 (2017): 1702311.

[78]

S. Bauhuber, C. Hozsa, M. Breunig, and A. Göpferich, “Delivery of Nucleic Acids via Disulfide-Based Carrier Systems,” Advanced Materials 21, no. 32–33 (2009): 3286–3306.

[79]

F. Wang, L. Gao, L. Y. Meng, J. M. Xie, J. W. Xiong, and Y. Luo, “A Neutralized Noncharged Polyethylenimine-Based System for Efficient Delivery of siRNA Into Heart Without Toxicity,” ACS Applied Materials & Interfaces 8, no. 49 (2016): 33529–33538.

[80]

Y.-W. Won, S.-M. Yoon, K.-M. Lee, and Y.-H. Kim, “Poly(Oligo-D-Arginine) With Internal Disulfide Linkages as a Cytoplasm-Sensitive Carrier for siRNA Delivery,” Molecular Therapy 19, no. 2 (2011): 372–380.

[81]

M. Ou, R. Xu, S. H. Kim, D. A. Bull, and S. W. Kim, “A Family of Bioreducible Poly(Disulfide Amine)s for Gene Delivery,” Biomaterials 30, no. 29 (2009): 5804–5814.

[82]

W. Lang, W. Tan, B. Zhou, et al., “Mitochondria-Targeted Gene Silencing Facilitated by Mito-CPDs,” Chemistry (Weinheim an der Bergstrasse, Germany) 29, no. 26 (2023): e202204021.

[83]

Y. Chen and Y. Ping, “Development of CRISPR/Cas Delivery Systems for In Vivo Precision Genome Editing,” Accounts of Chemical Research 56, no. 16 (2023): 2185–2196.

[84]

C. Wang, C. Pan, H. Yong, et al., “Emerging Non-Viral Vectors for Gene Delivery,” Journal of Nanobiotechnology 21, no. 1 (2023): 272.

[85]

L. Yu, Y. Xu, M. Al-Amin, et al., “CytoDirect: A Nucleic Acid Nanodevice for Specific and Efficient Delivery of Functional Payloads to the Cytoplasm,” Journal of the American Chemical Society 145, no. 50 (2023): 27336–27347.

[86]

L. Cheng, L. Yang, F. Meng, and Z. Zhong, “Protein Nanotherapeutics as an Emerging Modality for Cancer Therapy,” Advanced Healthcare Materials 7, no. 20 (2018): 1800685.

[87]

C. Chen, P. Gao, H. Wang, Y. Cheng, and J. Lv, “Histidine-Based Coordinative Polymers for Efficient Intracellular Protein Delivery via Enhanced Protein Binding, Cellular Uptake, and Endosomal Escape,” Biomaterials Science 11, no. 5 (2023): 1765–1775.

[88]

Y. Yang, S. Zuo, J. Zhang, et al., “Prodrug Nanoassemblies Bridged by Mono-/Di-/Tri-Sulfide Bonds: Exploration Is for Going Further,” Nano Today 44 (2022): 101480.

[89]

J. Lu, H. Wang, Z. Tian, Y. Hou, and H. Lu, “Cryopolymerization of 1,2-Dithiolanes for the Facile and Reversible Grafting-From Synthesis of Protein–Polydisulfide Conjugates,” Journal of the American Chemical Society 142, no. 3 (2020): 1217–1221.

[90]

J. Lu, Y. Dai, Y. He, et al., “Organ/Cell-Selective Intracellular Delivery of Biologics via N-Acetylated Galactosamine-Functionalized Polydisulfide Conjugates,” Journal of the American Chemical Society 146, no. 6 (2024): 3974–3983.

[91]

J. Guo, T. Wan, Z. Qi, et al., “Non-Covalent Delivery of Native Proteins and Peptides by Phenylboronic Cell-Penetrating Poly(Disulfide)s,” Nano Today 56 (2024): 102283.

[92]

S. Mu, Y. Zhu, Y. Wang, et al., “Cationic Polysaccharide Conjugates as Antibiotic Adjuvants Resensitize Multidrug-Resistant Bacteria and Prevent Resistance,” Advanced Materials 34, no. 41 (2022): 2204065.

[93]

A. Mondal, S. Das, S. M. Ali, S. Kolay, A. Sengupta, and M. R. Molla, “Bioderived Lipoic Acid-Based Dynamic Covalent Nanonetworks of Poly(Disulfide)s: Enhanced Encapsulation Stability and Cancer Cell-Selective Delivery of Drugs,” Bioconjugate Chemistry 34, no. 3 (2023): 489–500.

[94]

S. Santra, S. Das, S. Dey, A. Sengupta, B. Giri, and M. R. Molla, “Degradable Polymer-Based Nanoassemblies for Precise Targeting and Drug Delivery to Breast Cancer Cells Without Affecting Normal Healthy Cells,” Biomacromolecules 25, no. 3 (2024): 1724–1737.

[95]

R. Zhang, T. Nie, L. Wang, et al., “Facile Synthesis of Poly(Disulfide)s Through One-Step Oxidation Polymerization for Redox-Responsive Drug Delivery,” Biomaterials Science 11, no. 12 (2023): 4254–4264.

[96]

J. Lu, Z. Xu, H. Fu, Y. Lin, H. Wang, and H. Lu, “Room-Temperature Grafting From Synthesis of Protein–Polydisulfide Conjugates Via Aggregation-Induced Polymerization,” Journal of the American Chemical Society 144, no. 34 (2022): 15709–15717.

[97]

Z. Chen, “Small-Molecule Delivery by Nanoparticles for Anticancer Therapy,” Trends in Molecular Medicine 16, no. 12 (2010): 594–602.

[98]

A. Mondal, S. Sujauddin, D. Mondal, S. Kolay, S. Sarkar, and M. R. Molla, “Reducing Agent-Triggered Templated Synthesis of a Dynamic Covalent Poly(Disulfide)s Nanonetwork: Remarkable Tuning in Noncovalent Encapsulation Stabilities and Cargo Release,” Polymer Chemistry 15, no. 48 (2024): 5007–5015.

[99]

S. Son, R. Namgung, J. Kim, K. Singha, and W. J. Kim, “Bioreducible Polymers for Gene Silencing and Delivery,” Accounts of Chemical Research 45, no. 7 (2012): 1100–1112.

[100]

S. Zuo, T. Liu, L. Li, et al., “Tetrasulfide Bond Boosts the Anti-Tumor Efficacy of Dimeric Prodrug Nanoassemblies,” Cell Reports Medicine 5, no. 3 (2024): 101432.

[101]

Y. Yang, B. Sun, S. Zuo, et al., “Trisulfide Bond-Mediated Doxorubicin Dimeric Prodrug Nanoassemblies With High Drug Loading, High Self-Assembly Stability, and High Tumor Selectivity,” Science Advances 6, no. 45 (2020): eabc1725.

RIGHTS & PERMISSIONS

2026 The Author(s). MedComm – Biomaterials and Applications published by John Wiley & Sons Australia, Ltd on behalf of Sichuan International Medical Exchange & Promotion Association (SCIMEA).

PDF (5207KB)

1

Accesses

0

Citation

Detail

Sections
Recommended

/