Diblock copolymer glyco-nanomicelles constructed by a maltoheptaose-based amphiphile for reduction- and pH-mediated intracellular drug delivery

Micellar Nanocontainers Distribute to Defined Cytoplasmic Organelles

Savić, R., Luo, L., Eisenberg, A., & Maysinger, D. (2003) · Science · doi:10.1126/science.1078192 · Cited by 1,113 · see citing works

pH-Responsive Supramolecular Vesicles Based on Water-Soluble Pillar[6]arene and Ferrocene Derivative for Drug Delivery

Duan, Q., Cao, Y., Li, Y., Hu, X., Xiao, T., Chen, L., Pan, Y., & Wang, L. (2013) · Journal of the American Chemical Society · doi:10.1021/ja405014r · Cited by 644 · see citing works

Acetal-Derivatized Dextran: An Acid-Responsive Biodegradable Material for Therapeutic Applications

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Disulfide-cross-linked PEG-poly(amino acid)s copolymer micelles for glutathione-mediated intracellular drug delivery

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Interlayer‐Crosslinked Micelle with Partially Hydrated Core Showing Reduction and pH Dual Sensitivity for Pinpointed Intracellular Drug Release

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Redox and pH-responsive degradable micelles for dually activated intracellular anticancer drug release

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Dimeric Drug Polymeric Nanoparticles with Exceptionally High Drug Loading and Quantitative Loading Efficiency

Cai, K., He, X., Song, Z., Yin, Q., Zhang, Y., Uckun, F. M., Jiang, C., & Cheng, J. (2015) · Journal of the American Chemical Society · doi:10.1021/ja513034e · Cited by 363 · see citing works

Synthesis of Poly(β-amino ester)s Optimized for Highly Effective Gene Delivery

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Cellular Internalization of Poly(ethylene oxide)-b-poly(ε-caprolactone) Diblock Copolymer Micelles

Luo, L., Tam, J., Maysinger, D., & Eisenberg, A. (2002) · Bioconjugate Chemistry · doi:10.1021/bc025524y · Cited by 199 · see citing works

Acid-Degradable Cationic Dextran Particles for the Delivery of siRNA Therapeutics

Cohen, J. L., Schubert, S., Wich, P. R., Cui, L., Cohen, J. A., Mynar, J. L., & Fréchet, J. M. J. (2011) · Bioconjugate Chemistry · doi:10.1021/bc100542r · Cited by 156 · see citing works

Glutathione- and pH-responsive nonporous silica prodrug nanoparticles for controlled release and cancer therapy

Xu, Z., Liu, S., Kang, Y., & Wang, M. (2015) · Nanoscale · doi:10.1039/c5nr00297d · Cited by 139 · see citing works

Redox-Responsive Polymer–Drug Conjugates Based on Doxorubicin and Chitosan Oligosaccharide-g-stearic Acid for Cancer Therapy

Su, Y., Hu, Y., Du, Y., Huang, X., He, J., You, J., Yuan, H., & Hu, F. (2015) · Molecular Pharmaceutics · doi:10.1021/mp500710x · Cited by 120 · see citing works

Acetal‐Modified Dextran Microparticles with Controlled Degradation Kinetics and Surface Functionality for Gene Delivery in Phagocytic and Non‐Phagocytic Cells

Cohen, J. A., Beaudette, T. T., Cohen, J. L., Broaders, K. E., Bachelder, E. M., & Fréchet, J. M. J. (2010) · Advanced Materials · doi:10.1002/adma.201000307 · Cited by 112 · see citing works

Synthesis and Characterization of Acetalated Dextran Polymer and Microparticles with Ethanol as a Degradation Product

Kauffman, K. J., Do, C., Sharma, S., Gallovic, M. D., Bachelder, E. M., & Ainslie, K. M. (2012) · ACS Applied Materials & Interfaces · doi:10.1021/am3008888 · Cited by 106 · see citing works

Intracellular pH-Sensitive PEG-block-Acetalated-Dextrans as Efficient Drug Delivery Platforms

Zhang, Z., Chen, X., Chen, L., Yu, S., Cao, Y. Z., He, C., & Chen, X. (2013) · ACS Applied Materials & Interfaces · doi:10.1021/am402840f · Cited by 95 · see citing works

Mannosylated Dextran Nanoparticles: A pH-Sensitive System Engineered for Immunomodulation through Mannose Targeting

Cui, L., Cohen, J. A., Broaders, K. E., Beaudette, T. T., & Fréchet, J. M. J. (2011) · Bioconjugate Chemistry · doi:10.1021/bc100596w · Cited by 92 · see citing works

Doxorubicin-loaded PEG-PCL copolymer micelles enhance cytotoxicity and intracellular accumulation of doxorubicin in adriamycin-resistant tumor cells

Han, M. Y., Diao, Fu, Hu, Y., Jiang, J., Tsutsumi, Wei, Chen, & Gao, J.-Q. (2011) · International Journal of Nanomedicine · doi:10.2147/ijn.s23099 · Cited by 91 · see citing works

Conjugation Chemistry through Acetals toward a Dextran-Based Delivery System for Controlled Release of siRNA

Cui, L., Cohen, J. L., Chu, C. K., Wich, P. R., Kierstead, P. H., & Fréchet, J. M. J. (2012) · Journal of the American Chemical Society · doi:10.1021/ja305552u · Cited by 91 · see citing works

Synthesis of pH-responsive tertiary amine methacrylate polymer brushes and their response to acidic vapour

Fielding, L. A., Edmondson, S., & Armes, S. P. (2011) · Journal of Materials Chemistry · doi:10.1039/c1jm11412c · Cited by 87 · 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

Acid-Degradable Polymer-Caged Lipoplex (PCL) Platform for siRNA Delivery: Facile Cellular Triggered Release of siRNA

Hong, B. J., Chipre, A. J., & Nguyen, S. T. (2013) · Journal of the American Chemical Society · doi:10.1021/ja404491r · Cited by 73 · see citing works

Fabrication of Dual-Redox Responsive Supramolecular Copolymers Using a Reducible β-Cyclodextran-Ferrocene Double-Head Unit

Zuo, C., Dai, X., Zhao, S., et al. (2016) · ACS Macro Letters · doi:10.1021/acsmacrolett.6b00450 · Cited by 69 · see citing works

Chemoselective Ligation in the Functionalization of Polysaccharide-Based Particles

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pH- and Reduction-Responsive Polymeric Lipid Vesicles for Enhanced Tumor Cellular Internalization and Triggered Drug Release

Wang, S., Zhang, S., Liu, J., et al. (2014) · ACS Applied Materials & Interfaces · doi:10.1021/am502579e · Cited by 61 · see citing works

Glyco-Nanoparticles Made from Self-Assembly of Maltoheptaose-block-Poly(methyl methacrylate): Micelle, Reverse Micelle, and Encapsulation

Zepon, Κ. M., Otsuka, I., Bouilhac, C., et al. (2015) · Biomacromolecules · doi:10.1021/acs.biomac.5b00443 · Cited by 44 · see citing works

Chemoenzymatic Synthesis of Amylose‐Grafted Cellulose

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Synthesis of chromogenic substrates of α-amylases on a cyclodextrin basis

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Biomimetic pH/redox dual stimuli‐responsive zwitterionic polymer block poly(L‐histidine) micelles for intracellular delivery of doxorubicin into tumor cells

John, J. V., Uthaman, S., Augustine, R., Lekshmi, K. M., Park, I., & Kim, I. (2017) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.28602 · Cited by 39 · see citing works

Double pH-responsive supramolecular copolymer micelles based on the complementary multiple hydrogen bonds of nucleobases and acetalated dextran for drug delivery

Kuang, H., Wu, Y., Zhang, Z., et al. (2015) · Polymer Chemistry · doi:10.1039/c5py00042d · Cited by 34 · see citing works

Core-crosslinked polymeric micelles with high doxorubicin loading capacity and intracellular pH- and redox-triggered payload release

Zhang, Y., Wang, C., Huang, Y., et al. (2015) · European Polymer Journal · doi:10.1016/j.eurpolymj.2015.04.033 · Cited by 31 · see citing works

Tumor microenvironment-specific nanoparticles activatable by stepwise transformation

Ko, H., Son, S., Jeon, J., Thambi, T., Kwon, S., Chae, Y. S., Kang, Y. M., & Park, J. H. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.05.009 · Cited by 28 · see citing works

Maltopentaose-Conjugated CTA for RAFT Polymerization Generating Nanostructured Bioresource-Block Copolymer

Togashi, D., Otsuka, I., Borsali, R., et al. (2014) · Biomacromolecules · doi:10.1021/bm501314f · Cited by 22 · see citing works

Recent Advances in Nanomicelles Delivery Systems.

Tawfik, S. M., Azizov, S., Elmasry, M. R., Sharipov, M., & Lee, Y.-I. (2020) · Nanomaterials · doi:10.3390/nano11010070 · Cited by 156 · see citing works

STUDY ON COPOLYMERIZATION OF D_3~F, D_4

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Reverse Micelles, Enzymes

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Anionic copolymerization of α,ω-dihydroxyoligodimethylsiloxane with organocyclosiloxanes

Шрагин, Д. И., Копылов, В. М., Ivanov, P. V., et al. (2008) · Polymer Science Series A · doi:10.1134/s0965545x08010069 · Cited by 2 · see citing works

Copolymerization of N-vinylformamid and N-vinylcaprolactam

Shaoqun, J., & Han-jiang, Y. (2006) · Journal of Tongji University

Synthesis of copolymers. I. Copolymers of styrene and of α‐methylstyrene

Cunliffe, A. V., Hubbert, W. J., & Richards, D. (1972) · Die Makromolekulare Chemie · doi:10.1002/macp.1972.021570103 · Cited by 12 · see citing works