A novel pH-sensitive polymeric prodrug was prepared by SPAAC click chemistry for intracellular delivery of doxorubicin and evaluation of its anti-cancer activity in vitro
Authors:
- Jiahui HeJHJiahui He
- Wei WangWWWei Wang
- Huicong ZhouHZHuicong Zhou
- Pan ShePSPan She
- Pantian ZhangPZPantian Zhang
- Yi CaoYCYi Cao
- Xuefei ZhangXZXuefei Zhang
- 1 October 2019
- journal article
- research article
- Published by Elsevier in Journal of Drug Delivery Science and Technology
- Vol. 53
Abstract
No abstract availableKeywords
Funding Information
- National Natural Science Foundation of China
This publication has 36 references indexed in Scilit:
- Post‐Functionalization of Polymers via Orthogonal Ligation ChemistryMacromolecular Rapid Communications, 2013
- Hydrophobic blocks of PEG-conjugates play a significant role in the accelerated blood clearance (ABC) phenomenonJournal of Controlled Release, 2013
- Blood–Nanoparticle Interactions andin VivoBiodistribution: Impact of Surface PEG and Ligand PropertiesMolecular Pharmaceutics, 2012
- Strain‐Promoted Alkyne–Azide Cycloadditions (SPAAC) Reveal New Features of Glycoconjugate BiosynthesisChemBioChem, 2011
- Synthesis of glycopolymers via click reactionsEuropean Polymer Journal, 2011
- Synthesis and Characterization of Novel Biodegradable Poly(carbonate ester)s with Photolabile Protecting GroupsBiomacromolecules, 2007
- Polymer–drug conjugation, recent achievements and general strategiesProgress in Polymer Science, 2007
- Physical stimuli-responsive polymeric micelles for anti-cancer drug deliveryProgress in Polymer Science, 2007
- Recent advances in shell cross-linked micellesChemical Communications, 2007
- On the Mechanism of Schiff Base Formation and HydrolysisJournal of the American Chemical Society, 1962