Recent advances in stimuli-responsive polymeric micelles via click chemistry

Stimuli-responsive nanocarriers for drug delivery

Mura, S., Nicolas, J., & Couvreur, P. (2013) · Nature Materials · doi:10.1038/nmat3776 · Cited by 6,289 · see citing works

The growing applications of click chemistry

Moses, J. E., & Moorhouse, A. D. (2007) · Chemical Society Reviews · doi:10.1039/b613014n · Cited by 2,376 · see citing works

Click Chemistry for Drug Development and Diverse Chemical–Biology Applications

Prakasam, T., Matosiuk, D., & Jóźwiak, K. (2013) · Chemical Reviews · doi:10.1021/cr200409f · Cited by 1,907 · see citing works

‘Click’ Chemistry in Polymer and Materials Science

Binder, W. H., & Sachsenhofer, R. (2007) · Macromolecular Rapid Communications · doi:10.1002/marc.200600625 · Cited by 1,560 · see citing works

Glutathione-responsive nano-vehicles as a promising platform for targeted intracellular drug and gene delivery

Cheng, R., Feng, F., Meng, F., Deng, C., Feijén, J., & Zhong, Z. (2011) · Journal of Controlled Release · doi:10.1016/j.jconrel.2011.01.030 · Cited by 1,367 · see citing works

pH-Sensitive nano-systems for drug delivery in cancer therapy

Liu, J., Huang, Y., Kumar, A., Tan, A., Jin, S., Mozhi, A., & Liang, X.-J. (2014) · Biotechnology Advances · doi:10.1016/j.biotechadv.2013.11.009 · Cited by 1,121 · see citing works

Advances in polymeric micelles for drug delivery and tumor targeting

Kedar, U., Phutane, P., Shidhaye, S., & Kadam, V. (2010) · Nanomedicine: Nanotechnology, Biology and Medicine · doi:10.1016/j.nano.2010.05.005 · Cited by 791 · see citing works

‘Click’ Chemistry in Polymer and Material Science: An Update

Binder, W. H., & Sachsenhofer, R. (2008) · Macromolecular Rapid Communications · doi:10.1002/marc.200800089 · Cited by 756 · see citing works

Enzyme-responsive nanomaterials for controlled drug delivery

Hu, Q., Katti, P. S., & Gu, Z. (2014) · Nanoscale · doi:10.1039/c4nr04249b · Cited by 683 · see citing works

Click Chemistry and Bioorthogonal Reactions: Unprecedented Selectivity in the Labeling of Biological Molecules

Best, M. D. (2009) · Biochemistry · doi:10.1021/bi9007726 · Cited by 643 · see citing works

“Click”‐Chemistry in Polymer and Material Science: the Update

Binder, W. H. (2008) · Macromolecular Rapid Communications · doi:10.1002/marc.200800332 · Cited by 568 · see citing works

Biodegradable polymeric micelles for targeted and controlled anticancer drug delivery: Promises, progress and prospects

Deng, C., Jiang, Y., Cheng, R., Meng, F., & Zhong, Z. (2012) · Nano Today · doi:10.1016/j.nantod.2012.08.005 · Cited by 562 · see citing works

Redox-responsive polymers for drug delivery: from molecular design to applications

Huo, M., Yuan, J., Tao, L., & Wei, Y. (2014) · Polym. Chem. · doi:10.1039/c3py01192e · Cited by 561 · see citing works

Temperature-responsive smart nanocarriers for delivery of therapeutic agents: applications and recent advances

Karimi, M., Sahandi Zangabad, P., Ghasemi, A., Amiri, M., Bahrami, M., Malekzad, H., Ghahramanzadeh Asl, H., Mahdieh, Z., Bozorgomid, M., Ghasemi, A., et al. (2016) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b00371 · Cited by 500 · see citing works

Recent advances in polymeric micelles for anti-cancer drug delivery

Biswas, S., Kumari, P., Lakhani, P. M., & Ghosh, B. (2015) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2015.12.031 · Cited by 475 · see citing works

Stimuli-responsive polymeric micelles for drug delivery and cancer therapy

Zhou, Q., Zhang, L., Yang, T., & Wu, H. Y. (2018) · International Journal of Nanomedicine · doi:10.2147/ijn.s158696 · Cited by 415 · see citing works

“Click” reactions: a versatile toolbox for the synthesis of peptide-conjugates

Tang, W., & Becker, M. L. (2014) · Chemical Society Reviews · doi:10.1039/c4cs00139g · Cited by 377 · see citing works

Schiff's base as a stimuli-responsive linker in polymer chemistry

Xin, Y., & Yuan, J. (2012) · Polymer Chemistry · doi:10.1039/c2py20290e · Cited by 368 · see citing works

Polymeric micelles: nanocarriers for cancer-targeted drug delivery

Zhang, Y., Huang, Y., & Li, S. (2014) · AAPS PharmSciTech · doi:10.1208/s12249-014-0113-z · Cited by 367 · see citing works

Field responsive materials: photo-, electro-, magnetic- and ultrasound-sensitive polymers

Manouras, T., & Vamvakaki, M. (2016) · Polymer Chemistry · doi:10.1039/c6py01455k · Cited by 330 · see citing works

Evolution of macromolecular complexity in drug delivery systems

Kakkar, A. K., Traverso, G., Farokhzad, O. C., Weissleder, R., & Langer, R. (2017) · Nature Reviews Chemistry · doi:10.1038/s41570-017-0063 · Cited by 325 · see citing works

Recent Advances in light-responsive on-demand drug-delivery Systems

Linsley, C. S., & Wu, B. M. (2017) · Therapeutic Delivery · doi:10.4155/tde-2016-0060 · Cited by 270 · see citing works

Endogenous pH-responsive nanoparticles with programmable size changes for targeted tumor therapy and imaging applications

Wu, W., Luo, L., Wang, Y., Wu, Q., Dai, H.-B., Li, J., Durkan, C., Wang, N., & Wang, G. (2018) · Theranostics · doi:10.7150/thno.23459 · Cited by 247 · see citing works

Polymeric micelles: Basic research to clinical practice

Deshmukh, A. S., Chauhan, P. N., Noolvi, M. N., Chaturvedi, K., Ganguly, K., Shukla, S. S., Nadagouda, M. N., & Aminabhavi, T. M. (2017) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2017.09.005 · Cited by 244 · see citing works

Polymeric Micelles: Recent Advancements in the Delivery of Anticancer Drugs

Gothwal, A., Khan, I., & Gupta, U. D. (2015) · Pharmaceutical Research · doi:10.1007/s11095-015-1784-1 · Cited by 233 · see citing works

“Click” chemistry in polymeric scaffolds: Bioactive materials for tissue engineering

Zou, Y., Zhang, L., Yang, L., Zhu, F., Ding, M., Lin, F., Wang, Z., & Li, Y. (2018) · Journal of Controlled Release · doi:10.1016/j.jconrel.2018.01.023 · Cited by 219 · see citing works

Oxime Linkage: A Robust Tool for the Design of pH-Sensitive Polymeric Drug Carriers

Jin, Y., Song, L., Su, Y., Zhu, L., Pang, Y., Qiu, F., Tong, G., Yan, D., Zhu, B., & Zhu, X. (2011) · Biomacromolecules · doi:10.1021/bm200956u · Cited by 216 · see citing works

Temperature-responsive polymeric micelles for optimizing drug targeting to solid tumors

Akimoto, J., Nakayama, M., & Okano, T. (2014) · Journal of Controlled Release · doi:10.1016/j.jconrel.2014.06.062 · Cited by 206 · see citing works

Enzyme-Sensitive and Amphiphilic PEGylated Dendrimer-Paclitaxel Prodrug-Based Nanoparticles for Enhanced Stability and Anticancer Efficacy

Li, N., Cai, H., Jiang, L., Hu, J., Bains, A., Hu, J., Gong, Q., Luo, K., & Gu, Z. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b15505 · Cited by 189 · see citing works

Redox-Responsive, Core-Cross-Linked Micelles Capable of On-Demand, Concurrent Drug Release and Structure Disassembly

Wang, H., Tang, L., Tu, C., Song, Z., Yin, Q., Yin, L., Zhang, Z., & Cheng, J. (2013) · Biomacromolecules · doi:10.1021/bm401086d · Cited by 173 · see citing works

Photo-responsive polymeric micelles

Huang, Y. L., Dong, R., Zhu, X., & Yan, D. (2014) · Soft Matter · doi:10.1039/c4sm00871e · Cited by 172 · see citing works

Photo-Triggered Release of Caged Camptothecin Prodrugs from Dually Responsive Shell Cross-Linked Micelles

Hu, X., Tian, J., Liu, T., Zhang, G., & Liu, S. (2013) · Macromolecules · doi:10.1021/ma400691j · Cited by 160 · see citing works

Potential and problems in ultrasound-responsive drug delivery systems

Lu, C., Zhao, Y.-Z., Ge, S., Jin, Y., & Du, L. (2013) · International Journal of Nanomedicine · doi:10.2147/ijn.s43589 · Cited by 156 · see citing works

Block Copolymer Micelles with a Dual-Stimuli-Responsive Core for Fast or Slow Degradation

Han, D., Tong, X., & Zhao, Y. (2012) · Langmuir · doi:10.1021/la204930n · Cited by 150 · see citing works

Synthesis of Amphiphilic Tadpole-Shaped Linear-Cyclic Diblock Copolymers via Ring-Opening Polymerization Directly Initiating from Cyclic Precursors and Their Application as Drug Nanocarriers

Wan, X., Liu, T., & Liu, S. (2011) · Biomacromolecules · doi:10.1021/bm101463d · Cited by 142 · see citing works

Redox-Responsive, Core Cross-Linked Polyester Micelles

Zhang, Z., Yin, L., Tu, C., Song, Z., Zhang, Y., Xu, Y., Tong, R., Zhou, Q., Ren, J., & Cheng, J. (2012) · ACS Macro Letters · doi:10.1021/mz300522n · Cited by 126 · see citing works

Matrix metalloproteinase 2-responsive micelle for siRNA delivery

Wang, H., Yang, X., Sun, C., Mao, C., Zhu, Y., & Wang, J. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.05.050 · Cited by 123 · see citing works

One‐Pot Synthesis of an Acid‐Labile Amphiphilic Triblock Copolymer and its pH‐Responsive Vesicular Assembly

Dan, K., & Ghosh, S. (2013) · Angewandte Chemie International Edition · doi:10.1002/anie.201302722 · Cited by 123 · see citing works

Micelles Based on Acid Degradable Poly(acetal urethane): Preparation, pH-Sensitivity, and Triggered Intracellular Drug Release

Huang, F., Cheng, R., Meng, F., Deng, C., & Zhong, Z. (2015) · Biomacromolecules · doi:10.1021/acs.biomac.5b00625 · Cited by 114 · see citing works

Click Chemistry-Mediated Nanosensors for Biochemical Assays

Chen, Y., Xianyu, Y., Wu, J., Yin, B., & Jiang, X. (2016) · Theranostics · doi:10.7150/thno.14856 · Cited by 108 · see citing works

Endogenous Stimuli-responsive Nanocarriers for Drug Delivery

Chen, H., Liu, D., & Guo, Z. (2016) · Chemistry Letters · doi:10.1246/cl.151176 · Cited by 103 · see citing works

Recent Advances in Endogenous and Exogenous Stimuli-Responsive Nanocarriers for Drug Delivery and Therapeutics

Hatakeyama, H. (2017) · Chemical and Pharmaceutical Bulletin · doi:10.1248/cpb.c17-00068 · Cited by 88 · see citing works

Clickable and imageable multiblock polymer micelles with magnetically guided and PEG-switched targeting and release property for precise tumor theranosis

Wei, J., Shuai, X., Wang, R., He, X., Li, Y., Ding, M., Li, J., Tan, H. S., & Fu, Q. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.08.005 · Cited by 88 · see citing works

“Y”-shape armed amphiphilic star-like copolymers: design, synthesis and dual-responsive unimolecular micelle formation for controlled drug delivery

Fan, X., Wang, X., Cao, M., Wang, C., Hu, Z., Wu, Y., Li, Z., & Loh, X. J. (2017) · Polymer Chemistry · doi:10.1039/c7py00999b · Cited by 84 · see citing works

A polyphosphoester-conjugated camptothecin prodrug with disulfide linkage for potent reduction-triggered drug delivery

Zhang, Q., He, J., Zhang, M., & Ni, P. (2015) · Journal of Materials Chemistry B · doi:10.1039/c5tb00623f · Cited by 80 · see citing works

Matrix Metalloproteinase-Responsive Multifunctional Peptide-Linked Amphiphilic Block Copolymers for Intelligent Systemic Anticancer Drug Delivery

Ke, W., Zha, Z., Mukerabigwi, J. F., Chen, W., Wang, Y., He, C., & Ge, Z. (2017) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.7b00330 · Cited by 79 · see citing works

Design of reversibly core cross-linked micelles sensitive to reductive environment

Cajot, S., Lautram, N., Passirani, C., & Jérôme, C. (2011) · Journal of Controlled Release · doi:10.1016/j.jconrel.2011.03.026 · Cited by 76 · see citing works

Reduction-Responsive Polymeric Micelles and Vesicles for Triggered Intracellular Drug Release

Sun, H., Meng, F., Cheng, R., Deng, C., & Zhong, Z. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5733 · Cited by 75 · see citing works

Thermo-responsive “hairy-rod” polypeptides for smart antitumor drug delivery

Ding, J., Zhao, L., Li, D., Xiao, C., Zhuang, X., & Chen, X. (2013) · Polymer Chemistry · doi:10.1039/c3py00144j · Cited by 73 · see citing works

Dual-Stimuli-Responsive Micelle of an ABC Triblock Copolymer Bearing a Redox-Cleavable Unit and a Photocleavable Unit at Two Block Junctions

Xuan, J., Han, D., Xia, H., & Zhao, Y. (2013) · Langmuir · doi:10.1021/la404493n · Cited by 72 · see citing works

Enzyme-Degradable Self-Assembled Nanostructures from Polymer–Peptide Hybrids

Bacinello, D., Garanger, É., Taton, D., Tam, K. C., & Lecommandoux, S. (2014) · Biomacromolecules · doi:10.1021/bm500296n · Cited by 69 · see citing works

Redox-responsive core cross-linked micelles based on cypate and cisplatin prodrugs-conjugated block copolymers for synergistic photothermal–chemotherapy of cancer

Han, Y., Li, J., Zan, M., Luo, S., Ge, Z., & Liu, S. (2014) · Polymer Chemistry · doi:10.1039/c4py00064a · Cited by 67 · see citing works

Miktoarm Amphiphilic Block Copolymer with Singlet Oxygen-Labile Stereospecific β-Aminoacrylate Junction: Synthesis, Self-Assembly, and Photodynamically Triggered Drug Release

Saravanakumar, G., Park, H., Kim, J., Park, D., Pramanick, S., Kim, D. H., & Kim, W. J. (2018) · Biomacromolecules · doi:10.1021/acs.biomac.8b00290 · Cited by 65 · see citing works

Recent development of functional aliphatic polycarbonates for the construction of amphiphilic polymers

Dai, Y., & Zhang, X. (2017) · Polymer Chemistry · doi:10.1039/c7py01815k · Cited by 64 · see citing works

Polymeric prodrugs conjugated with reduction-sensitive dextran–camptothecin and pH-responsive dextran–doxorubicin: an effective combinatorial drug delivery platform for cancer therapy

Cao, D., He, J., Xu, J., Zhang, M., Zhao, L., Duan, G., Cao, Y., Zhou, R., & Ni, P. (2016) · Polymer Chemistry · doi:10.1039/c6py00701e · Cited by 61 · see citing works

Modular Design and Facile Synthesis of Enzyme-Responsive Peptide-Linked Block Copolymers for Efficient Delivery of Doxorubicin

Ke, W., Li, J., Zhao, K., Zha, Z., Han, Y., Wang, Y., Yin, W., Zhang, P., & Ge, Z. (2016) · Biomacromolecules · doi:10.1021/acs.biomac.6b00997 · Cited by 59 · see citing works

Amphiphilic Polysaccharide Block Copolymers for pH-Responsive Micellar Nanoparticles

Breitenbach, B. B., Schmid, I., & Wich, P. R. (2017) · Biomacromolecules · doi:10.1021/acs.biomac.7b00771 · Cited by 59 · see citing works

Redox-stimuli responsive micelles from DOX-encapsulating polycaprolactone-g-chitosan oligosaccharide

Guerry, A., Cottaz, S., Fleury, É., Bernard, J., & Halila, S. (2014) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2014.06.052 · Cited by 56 · see citing works

Recent Advances in Cyclodextrin‐Based Light‐Responsive Supramolecular Systems

Zhang, X., Ma, X., Wang, K., Lin, S., Zhu, S., Dai, Y., & Xia, F. (2018) · Macromolecular Rapid Communications · doi:10.1002/marc.201800142 · Cited by 56 · see citing works

Reduction-responsive cross-linked micelles based on PEGylated polypeptides prepared via click chemistry

Cheng, Y., He, C., Xiao, C., Ding, J., Ren, K., Yu, S., Zhuang, X., & Chen, X. (2013) · Polymer Chemistry · doi:10.1039/c3py00364g · Cited by 55 · see citing works

Polycarbonate-based biodegradable copolymers for stimuli responsive targeted drug delivery

Ganivada, M. N., Kumar, P., Kanjilal, P., Dinda, H., Sarma, J. D., & Shunmugam, R. (2016) · Polymer Chemistry · doi:10.1039/c6py00615a · Cited by 52 · see citing works

Ultrasound responsive block copolymer micelle of poly(ethylene glycol)–poly(propylene glycol) obtained through click reaction

Li, F., Xie, C. L., Cheng, Z., & Xia, H. (2015) · Ultrasonics Sonochemistry · doi:10.1016/j.ultsonch.2015.11.023 · Cited by 50 · see citing works

Synthesis, Self-Assembly, and Photoresponsive Behavior of Tadpole-Shaped Azobenzene Polymers

Wang, X., Yang, Y., Gao, P., Yang, F., Shen, H. Y., Guo, H., & Wu, D. (2015) · ACS Macro Letters · doi:10.1021/acsmacrolett.5b00698 · Cited by 50 · see citing works

Polyphosphoester-Camptothecin Prodrug with Reduction-Response Prepared via Michael Addition Polymerization and Click Reaction

Du, X., Sun, Y. L., Zhang, M., He, J., & Ni, P. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.7b02281 · Cited by 49 · see citing works

Stimuli-Responsive Polymers and Colloids under Electric and Magnetic Fields

Zhang, W., & Choi, H. J. (2014) · Polymers · doi:10.3390/polym6112803 · Cited by 48 · see citing works

Facile preparation of pH-responsive polyurethane nanocarrier for oral delivery

Nabid, M. R., & Omrani, I. (2016) · Materials Science and Engineering C · doi:10.1016/j.msec.2016.07.017 · Cited by 47 · see citing works

A co-delivery system based on a reduction-sensitive polymeric prodrug capable of loading hydrophilic and hydrophobic drugs for combination chemotherapy

Yi, X., Zhao, D., Zhang, Q., Xu, J., Yuan, G., Zhuo, R., & Li, F. (2016) · Polymer Chemistry · doi:10.1039/c6py00900j · Cited by 46 · see citing works

Redox-responsive, core-crosslinked degradable micelles for controlled drug release

Xia, Y., He, H., Liu, X., Hu, D. Y., Yin, L., Lu, Y., & Xu, W. (2016) · Polymer Chemistry · doi:10.1039/c6py01423b · Cited by 42 · see citing works

Photo-responsive reversible micelles based on azobenzene-modified poly(carbonate)s via azide–alkyne click chemistry

Hu, D. Y., Li, Y., Niu, Y., Li, L., He, J., Liu, X., Xia, X., Lu, Y., Xiong, Y., & Xu, W. (2014) · RSC Advances · doi:10.1039/c4ra07345b · Cited by 41 · see citing works

Facile synthesis and self-assembly behaviour of pH-responsive degradable polyacetal dendrimers

Huang, D., Yang, F., Wang, X., Shen, H. Y., You, Y., & Wu, D. (2016) · Polymer Chemistry · doi:10.1039/c6py01511e · Cited by 41 · see citing works

Light/temperature dual-responsive ABC miktoarm star terpolymer micelles for controlled release

Huo, H., Ma, X., Dong, Y., & Qu, F. (2017) · European Polymer Journal · doi:10.1016/j.eurpolymj.2016.12.038 · Cited by 40 · see citing works

Dual-responsive core-crosslinked polyphosphoester-based nanoparticles for pH/redox-triggered anticancer drug delivery

Sun, Y. L., Du, X., He, J., Hu, J. Q., Zhang, M., & Ni, P. (2017) · Journal of Materials Chemistry B · doi:10.1039/c7tb00440k · Cited by 39 · see citing works

Click Chemistry in Functional Aliphatic Polycarbonates

Dai, Y., Zhang, X., & Xia, F. (2017) · Macromolecular Rapid Communications · doi:10.1002/marc.201700357 · Cited by 39 · see citing works

Synthesis and photochemical properties of spiropyran graft and star polymers obtained by ‘click’ chemistry

Ventura, C., Thornton, P. D., Giordani, S., & Heise, A. (2014) · Polymer Chemistry · doi:10.1039/c4py00778f · Cited by 38 · see citing works

Reduction-triggered release of paclitaxel from in situ formed biodegradable core-cross-linked micelles

Zhu, W., Wang, Y., Cai, X., Zha, G., Luo, Q., Sun, R., Li, X., & Shen, Z. (2015) · Journal of Materials Chemistry B · doi:10.1039/c4tb01834f · Cited by 38 · see citing works

Redox‐responsive core cross‐linked micelles of poly(ethylene oxide)‐b‐poly(furfuryl methacrylate) by Diels‐Alder reaction for doxorubicin release

Le, C. M. Q., Thi, H. H. P., Cao, X. T., Kim, G., Oh, C., & Lim, K. T. (2016) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.28271 · Cited by 38 · see citing works

Amphiphilic photosensitive dextran-g-poly(o-nitrobenzyl acrylate) glycopolymers

Soliman, S. M. A., Colombeau, L., Nouvel, C., Babin, J., & Six, J. (2015) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2015.09.061 · Cited by 37 · see citing works

Redox‐Responsive Micelles with Cores Crosslinked via Click Chemistry

Zhang, X., Dong, H. R., Fu, S., Zhong, Z., & Zhuo, R. (2016) · Macromolecular Rapid Communications · doi:10.1002/marc.201600049 · Cited by 37 · see citing works

Visible light-triggered disruption of micelles of an amphiphilic block copolymer with BODIPY at the junction

Patil, N. G., Basutkar, N. B., & Ambade, A. V. (2015) · Chemical Communications · doi:10.1039/c5cc06820g · Cited by 36 · see citing works

Thermosensitive Peptide-Hybrid ABC Block Copolymers Obtained by ATRP: Synthesis, Self-Assembly, and Enzymatic Degradation

de Graaf, A. J., Mastrobattista, E., Vermonden, T., van Nostrum, C. F., Rijkers, D. T. S., Liskamp, R. M. J., & Hennink, W. E. (2012) · Macromolecules · doi:10.1021/ma2024667 · Cited by 35 · see citing works

One-pot syntheses of dual-responsive core cross-linked polymeric micelles and covalently entrapped drug by click chemistry

Cao, X. T., Kim, Y. H., Park, J. M., & Lim, K. T. (2016) · European Polymer Journal · doi:10.1016/j.eurpolymj.2016.03.039 · Cited by 35 · see citing works

Reversibly light‐responsive biodegradable poly(carbonate) micelles constructed via C u AAC reaction

Hu, D. Y., Peng, H., Niu, Y., Li, Y., Xia, Y., Li, L., He, J., Liu, X., Xia, X., Lu, Y., et al. (2014) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.27499 · Cited by 34 · see citing works

Matrix metalloproteases-responsive nanomaterials for tumor targeting diagnosis and treatment

Xiong, J., & Gao, H. (2017) · Journal of Microencapsulation · doi:10.1080/02652048.2017.1343873 · Cited by 34 · see citing works

Modular Synthetic Approach for Adjusting the Disassembly Rates of Enzyme-Responsive Polymeric Micelles

Harnoy, A. J., Buzhor, M. G., Tirosh, E., Shaharabani, R., Beck, R., & Amir, R. J. (2017) · Biomacromolecules · doi:10.1021/acs.biomac.6b01906 · Cited by 33 · see citing works

In situ fabrication of paclitaxel‐loaded core‐crosslinked micelles via thiol‐ene “click” chemistry for reduction‐responsive drug release

Huang, Y., Sun, R., Luo, Q., Wang, Y., Zhang, K., Deng, X., Zhu, W., Li, X., & Shen, Z. (2015) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.27778 · Cited by 31 · see citing works

Novel hydroxyl-containing reduction-responsive pseudo-poly(aminoacid) via click polymerization as an efficient drug carrier

Wu, Y., Kuang, H., Xie, Z., Chen, X., Jing, X., & Huang, Y. (2014) · Polymer Chemistry · doi:10.1039/c4py00227j · Cited by 26 · see citing works

Synthesis of aliphatic polycarbonates with a tuneable thermal response

Thomas, A. W., Kuroishi, P. K., Pérez‐Madrigal, M. M., Whittaker, A. K., & Dove, A. P. (2017) · Polymer Chemistry · doi:10.1039/c7py00358g · Cited by 25 · see citing works

ROMP synthesis of benzaldehyde-containing amphiphilic block polynorbornenes used to conjugate drugs for pH-responsive release

Qiu, G., Zhao, L., Liu, X., Zhao, Q., Liu, F., Liu, Y., Liu, Y., & Gu, H. (2018) · Reactive and Functional Polymers · doi:10.1016/j.reactfunctpolym.2018.03.010 · Cited by 25 · see citing works

Preparation of Light‐Responsive Polyester Micelles via Ring‐Opening Polymerization of O‐Carboxyanhydride and Azide–Alkyne Click Chemistry

Li, Y., Niu, Y., Hu, D. Y., Song, Y., He, J., Liu, X., Xia, X., Lu, Y., & Xu, W. (2014) · Macromolecular Chemistry and Physics · doi:10.1002/macp.201400406 · Cited by 24 · see citing works

Amphiphilic Peptide–Polymer Conjugates with Side‐Conjugation

Dube, N., Presley, A. D., Shu, J. Y., & Xu, T. (2011) · Macromolecular Rapid Communications · doi:10.1002/marc.201000603 · Cited by 24 · see citing works

Photo‐responsive amphiphilic poly(α‐hydroxy acids) with pendent o‐nitrobenzyl ester constructed via copper‐catalyzed azide‐alkyne cycloaddition reaction

Liu, X., He, J., Niu, Y., Li, Y., Hu, D. Y., Xia, X., Lu, Y., & Xu, W. (2015) · Polymers for Advanced Technologies · doi:10.1002/pat.3472 · Cited by 20 · see citing works

Polycaprolactone-b-poly(N-isopropylacrylamide) nanoparticles: Synthesis and temperature induced coacervation behavior

Vandewalle, S., Walle, M. V. D., Chattopadhyay, S., & Prez, F. D. (2017) · European Polymer Journal · doi:10.1016/j.eurpolymj.2017.11.027 · Cited by 20 · see citing works

Synthesis and properties of couplable ABCDE star copolymers by orthogonal CuAAC and Diels–Alder click reactions

Liu, H., Pan, W., Tong, M., & Zhao, Y. (2016) · Polymer Chemistry · doi:10.1039/c5py01960e · Cited by 19 · see citing works

Temperature and pH dual stimuli responsive PCL-b-PNIPAAm block copolymer assemblies and the cargo release studies

Patil, S. S., & Wadgaonkar, P. P. (2017) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.28508 · Cited by 19 · see citing works

Redox-responsive core cross-linked prodrug micelles prepared by click chemistry for pH-triggered doxorubicin delivery

Cao, X. T., Le, C. M. Q., Thi, H. H. P., Kim, G.-D., Gal, Y.-S., & Lim, K. T. (2017) · eXPRESS Polymer Letters · doi:10.3144/expresspolymlett.2017.79 · Cited by 19 · see citing works

Spiropyran-decorated light-responsive amphiphilic poly(α-hydroxy acids) micelles constructed via a CuAAC reaction

Niu, Y., Li, Y., Lu, Y., & Xu, W. (2014) · RSC Advances · doi:10.1039/c4ra11550c · Cited by 17 · see citing works

Polyion complex micelles prepared by self-assembly of block-graft polycation and hyperbranched polyanion

Dai, Y., Wang, H., & Zhang, X. (2017) · Journal of Nanoparticle Research · doi:10.1007/s11051-017-3997-1 · Cited by 14 · see citing works

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