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For: Shao W, Miao K, Liu H, Ye C, Du J, Zhao Y. Acid and reduction dually cleavable amphiphilic comb-like copolymer micelles for controlled drug delivery. Polym Chem 2013;4:3398. [DOI: 10.1039/c3py00252g] [Cited by in Crossref: 37] [Cited by in F6Publishing: 38] [Article Influence: 3.7] [Reference Citation Analysis]
Number Citing Articles
1 Raj W, Hałagan K, Kadłubowski S, Maczugowska P, Szutkowski K, Jung J, Pietrasik J, Jurga S, Sikorski A. The structure and dynamics of bottlebrushes: Simulation and experimental studies combined. Polymer 2022;261:125409. [DOI: 10.1016/j.polymer.2022.125409] [Reference Citation Analysis]
2 Wang Z, Lan Y, Liu P, Li X, Zhao Y. Rational design of a multi-in-one heterofunctional agent for versatile topological transformation of multisite multisegmented polystyrenes. Polym Chem 2022;13:4198-211. [DOI: 10.1039/d2py00662f] [Reference Citation Analysis]
3 Tian J, Xia L, Wu J, Huang B, Cao H, Zhang W. Linear Alternating Supramolecular Photosensitizer for Enhanced Photodynamic Therapy. ACS Appl Mater Interfaces 2020;12:32352-9. [PMID: 32584539 DOI: 10.1021/acsami.0c07333] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 5.7] [Reference Citation Analysis]
4 Zhang H, Liu X, Xu T, Xu K, Du B, Li Y. Biodegradable reduction and pH dual-sensitive polymer micelles based on poly(2-ethyl-2-oxazoline) for efficient delivery of curcumin. RSC Adv 2020;10:25435-45. [DOI: 10.1039/d0ra02779k] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
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6 Neugebauer D. Grafted polymethacrylate nanocarriers in drug delivery. Nanomaterials for Clinical Applications 2020. [DOI: 10.1016/b978-0-12-816705-2.00009-6] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
7 Jazani AM, Oh JK. Development and disassembly of single and multiple acid-cleavable block copolymer nanoassemblies for drug delivery. Polym Chem 2020;11:2934-54. [DOI: 10.1039/d0py00234h] [Cited by in Crossref: 22] [Cited by in F6Publishing: 24] [Article Influence: 7.3] [Reference Citation Analysis]
8 Yuan J, Deng A, Yang D, Li H, Chen J, Gao Y. Redox-responsive Pickering emulsion derived from the fabricated sheddable polymeric micelles. Polymer 2018;158:1-9. [DOI: 10.1016/j.polymer.2018.10.043] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 2.4] [Reference Citation Analysis]
9 Zhao Y. Facile Synthesis and Topological Transformation of Multicomponent Miktoarm Star Copolymers. Macromol Rapid Commun 2019;40:1800571. [DOI: 10.1002/marc.201800571] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 3.6] [Reference Citation Analysis]
10 You C, Wu H, Wang M, Gao Z, Sun B, Zhang X. Synthesis and biological evaluation of redox/NIR dual stimulus-responsive polymeric nanoparticles for targeted delivery of cisplatin. Mater Sci Eng C Mater Biol Appl 2018;92:453-62. [PMID: 30184771 DOI: 10.1016/j.msec.2018.06.044] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 3.6] [Reference Citation Analysis]
11 Ma G, Liu J, He J, Zhang M, Ni P. Dual-Responsive Polyphosphoester-Doxorubicin Prodrug Containing a Diselenide Bond: Synthesis, Characterization, and Drug Delivery. ACS Biomater Sci Eng 2018;4:2443-52. [DOI: 10.1021/acsbiomaterials.8b00429] [Cited by in Crossref: 38] [Cited by in F6Publishing: 38] [Article Influence: 7.6] [Reference Citation Analysis]
12 Liu F, Zhao X, Zhang X, Zhang X, Peng J, Yang H, Deng K, Ma L, Chang C, Wei H. Fabrication of theranostic amphiphilic conjugated bottlebrush copolymers with alternating heterografts for cell imaging and anticancer drug delivery. Polym Chem 2018;9:4866-74. [DOI: 10.1039/c8py01221k] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 3.8] [Reference Citation Analysis]
13 Jazani AM, Oh JK. Dual Location, Dual Acidic pH/Reduction-Responsive Degradable Block Copolymer: Synthesis and Investigation of Ketal Linkage Instability under ATRP Conditions. Macromolecules 2017;50:9427-36. [DOI: 10.1021/acs.macromol.7b02070] [Cited by in Crossref: 21] [Cited by in F6Publishing: 21] [Article Influence: 3.5] [Reference Citation Analysis]
14 Lin Y, Wang S, Yu Y, Lee R. Thermoresponsive and acid-cleavable amphiphilic copolymer micelles for controlled drug delivery. International Journal of Polymeric Materials and Polymeric Biomaterials 2017;66:943-54. [DOI: 10.1080/00914037.2017.1291514] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
15 Guan Y, Su Y, Zhao L, Meng F, Wang Q, Yao Y, Luo J. Biodegradable polyurethane micelles with pH and reduction responsive properties for intracellular drug delivery. Mater Sci Eng C Mater Biol Appl 2017;75:1221-30. [PMID: 28415410 DOI: 10.1016/j.msec.2017.02.124] [Cited by in Crossref: 34] [Cited by in F6Publishing: 35] [Article Influence: 5.7] [Reference Citation Analysis]
16 Chi X, Ji X, Shao L, Huang F. A Multiresponsive Amphiphilic Supramolecular Diblock Copolymer Based on Pillar[10]arene/Paraquat Complexation for Rate-Tunable Controlled Release. Macromol Rapid Commun 2017;38:1600626. [DOI: 10.1002/marc.201600626] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 3.0] [Reference Citation Analysis]
17 Fang J, Lin Y, Wang S, Yu Y, Lee R. Acid and light dual- stimuli-cleavable polymeric micelles. J Polym Res 2017;24. [DOI: 10.1007/s10965-016-1166-3] [Reference Citation Analysis]
18 Hu W, He C, Tan L, Liu B, Zhu Z, Gong B, Shen Y, Shao Z. Synthesis and micellization of redox-responsive dynamic covalent multi-block copolymers. Polym Chem 2016;7:3145-55. [DOI: 10.1039/c6py00326e] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 2.1] [Reference Citation Analysis]
19 Tong M, An X, Pan W, Liu H, Zhao Y. Synthesis and properties of stimuli-sensitive heterografted toothbrush-like terpolymers with a linear handle and two types of V-shaped grafts. Polym Chem 2016;7:2209-21. [DOI: 10.1039/c6py00182c] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 2.1] [Reference Citation Analysis]
20 Fang J, Lin Y, Wang S, Yu Y, Lee R. Dual-stimuli-responsive glycopolymer bearing a reductive and photo-cleavable unit at block junction. RSC Adv 2016;6:107669-82. [DOI: 10.1039/c6ra22207b] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
21 Yao Y, Xu D, Liu C, Guan Y, Zhang J, Su Y, Zhao L, Meng F, Luo J. Biodegradable pH-sensitive polyurethane micelles with different polyethylene glycol (PEG) locations for anti-cancer drug carrier applications. RSC Adv 2016;6:97684-93. [DOI: 10.1039/c6ra20613a] [Cited by in Crossref: 28] [Cited by in F6Publishing: 28] [Article Influence: 4.0] [Reference Citation Analysis]
22 Yao Y, Xu H, Liu C, Guan Y, Xu D, Zhang J, Su Y, Zhao L, Luo J. Biodegradable multi-blocked polyurethane micelles for intracellular drug delivery: the effect of disulfide location on the drug release profile. RSC Adv 2016;6:9082-9. [DOI: 10.1039/c5ra24903a] [Cited by in Crossref: 31] [Cited by in F6Publishing: 31] [Article Influence: 4.4] [Reference Citation Analysis]
23 Pan W, Liu H, Zhang H, Zhao Y. Synthesis and properties of an acid-labile dual-sensitive ABCD star quaterpolymer. Polym Chem 2016;7:2870-81. [DOI: 10.1039/c6py00267f] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.6] [Reference Citation Analysis]
24 Guragain S, Bastakoti BP, Malgras V, Nakashima K, Yamauchi Y. Multi-Stimuli-Responsive Polymeric Materials. Chemistry 2015;21:13164-74. [PMID: 26219746 DOI: 10.1002/chem.201501101] [Cited by in Crossref: 150] [Cited by in F6Publishing: 151] [Article Influence: 18.8] [Reference Citation Analysis]
25 Topete A, Barbosa S, Taboada P. Intelligent micellar polymeric nanocarriers for therapeutics and diagnosis. J Appl Polym Sci 2015;132:n/a-n/a. [DOI: 10.1002/app.42650] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 1.8] [Reference Citation Analysis]
26 Feng A, Yan Q, Zhang H, Peng L, Yuan J. Electrochemical redox responsive polymeric micelles formed from amphiphilic supramolecular brushes. Chem Commun (Camb) 2014;50:4740-2. [PMID: 24681929 DOI: 10.1039/c4cc00463a] [Cited by in Crossref: 68] [Cited by in F6Publishing: 68] [Article Influence: 8.5] [Reference Citation Analysis]
27 Mo B, Liu H, Zhou X, Zhao Y. Facile synthesis of photolabile dendritic-unit-bridged hyperbranched graft copolymers for stimuli-triggered topological transition and controlled release of Nile red. Polym Chem 2015;6:3489-501. [DOI: 10.1039/c5py00132c] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 2.5] [Reference Citation Analysis]
28 Peng L, Zhang H, Feng A, Huo M, Wang Z, Hu J, Gao W, Yuan J. Electrochemical redox responsive supramolecular self-healing hydrogels based on host–guest interaction. Polym Chem 2015;6:3652-9. [DOI: 10.1039/c5py00296f] [Cited by in Crossref: 81] [Cited by in F6Publishing: 82] [Article Influence: 10.1] [Reference Citation Analysis]
29 Liu H, Li C, Tang D, An X, Guo Y, Zhao Y. Multi-responsive graft copolymer micelles comprising acetal and disulfide linkages for stimuli-triggered drug delivery. J Mater Chem B 2015;3:3959-71. [DOI: 10.1039/c5tb00473j] [Cited by in Crossref: 35] [Cited by in F6Publishing: 35] [Article Influence: 4.4] [Reference Citation Analysis]
30 Fang G, Zeng F, Yu C, Wu S. Low molecular weight PEIs modified by hydrazone-based crosslinker and betaine as improved gene carriers. Colloids Surf B Biointerfaces 2014;122:472-81. [PMID: 25092585 DOI: 10.1016/j.colsurfb.2014.07.007] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 2.6] [Reference Citation Analysis]
31 Miao K, Shao W, Liu H, Zhao Y. Synthesis and properties of a dually cleavable graft copolymer comprising pendant acetal linkages. Polym Chem 2014;5:1191-201. [DOI: 10.1039/c3py01049j] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 2.6] [Reference Citation Analysis]
32 Liu H, Miao K, Zhao G, Li C, Zhao Y. Synthesis of an amphiphilic PEG-PCL-PSt-PLLA-PAA star quintopolymer and its self-assembly for pH-sensitive drug delivery. Polym Chem 2014;5:3071-80. [DOI: 10.1039/c3py01601c] [Cited by in Crossref: 27] [Cited by in F6Publishing: 28] [Article Influence: 3.0] [Reference Citation Analysis]
33 Tang D, Jiang X, Liu H, Li C, Zhao Y. Synthesis and properties of heterografted toothbrush-like copolymers with alternating PEG and PCL grafts and tunable RAFT-generated segments. Polym Chem 2014;5:4679-92. [DOI: 10.1039/c4py00332b] [Cited by in Crossref: 25] [Cited by in F6Publishing: 25] [Article Influence: 2.8] [Reference Citation Analysis]
34 Miao K, Liu H, Zhao Y. Thermo, pH and reduction responsive coaggregates comprising AB 2 C 2 star terpolymers for multi-triggered release of doxorubicin. Polym Chem 2014;5:3335-45. [DOI: 10.1039/c3py01767b] [Cited by in Crossref: 35] [Cited by in F6Publishing: 35] [Article Influence: 3.9] [Reference Citation Analysis]
35 Qiao Z, Qiao S, Fan G, Fan Y, Chen Y, Wang H. One-pot synthesis of pH-sensitive poly(RGD-co-β-amino ester)s for targeted intracellular drug delivery. Polym Chem 2014;5:844-53. [DOI: 10.1039/c3py01117h] [Cited by in Crossref: 46] [Cited by in F6Publishing: 46] [Article Influence: 5.1] [Reference Citation Analysis]
36 Petrova S, Jäger E, Konefał R, Jäger A, Venturini CG, Spěváček J, Pavlova E, Štěpánek P. Novel poly(ethylene oxide monomethyl ether)-b-poly(ε-caprolactone) diblock copolymers containing a pH-acid labile ketal group as a block linkage. Polym Chem 2014;5:3884-93. [DOI: 10.1039/c4py00114a] [Cited by in Crossref: 26] [Cited by in F6Publishing: 26] [Article Influence: 2.9] [Reference Citation Analysis]
37 Zhao J, Wang H, Liu J, Deng L, Liu J, Dong A, Zhang J. Comb-like amphiphilic copolymers bearing acetal-functionalized backbones with the ability of acid-triggered hydrophobic-to-hydrophilic transition as effective nanocarriers for intracellular release of curcumin. Biomacromolecules 2013;14:3973-84. [PMID: 24107101 DOI: 10.1021/bm401087n] [Cited by in Crossref: 52] [Cited by in F6Publishing: 54] [Article Influence: 5.2] [Reference Citation Analysis]