Enhanced Stability of Polymeric Micelles Based on Postfunctionalized Poly(ethylene glycol)-b-poly(γ-propargyl l-glutamate): The Substituent Effect
- 1 March 2012
- journal article
- research article
- Published by American Chemical Society (ACS) in Biomacromolecules
- Vol. 13 (5), 1315-1322
- https://doi.org/10.1021/bm201873u
Abstract
One of the major obstacles that delay the clinical translation of polymeric micelle drug delivery systems is whether these self-assembled micelles can retain their integrity in blood following intravenous (IV) injection. The objective of this study was to evaluate the impact of core functionalization on the thermodynamic and kinetic stability of polymeric micelles. The combination of ring-opening polymerization of N-carboxyanhydride (NCA) with highly efficient “click” coupling has enabled easy and quick access to a family of poly(ethylene glycol)-block-poly(γ-R-glutamate)s with exactly the same block lengths, for which the substituent “R” is tuned. The structures of these copolymers were carefully characterized by 1H NMR, FT-IR, and GPC. When pyrene is used as the fluorescence probe, the critical micelle concentrations (CMCs) of these polymers were found to be in the range of 10–7–10–6 M, which indicates good thermodynamic stability for the self-assembled micelles. The incorporation of polar side groups in the micelle core leads to high CMC values; however, micelles prepared from these copolymers are kinetically more stable in the presence of serum and upon SDS disturbance. It was also observed that these polymers could effectively encapsulate paclitaxel (PTX) as a model anticancer drug, and the micelles possessing better kinetic stability showed better suppression of the initial “burst” release and exhibited more sustained release of PTX. These PTX-loaded micelles exerted comparable cytotoxicity against HeLa cells as the clinically approved Cremophor PTX formulation, while the block copolymers showed much lower toxicity compared to the cremophor–ethanol mixture. The present work demonstrated that the PEG-b-PPLG can be a uniform block copolymer platform toward development of polymeric micelle delivery systems for different drugs through the facile modification of the PPLG block.Keywords
This publication has 32 references indexed in Scilit:
- Polymeric supramolecular systems for drug deliveryJournal of Materials Chemistry, 2009
- Block copolymer micelles for delivery of cancer therapy: Transport at the whole body, tissue and cellular levelsJournal of Controlled Release, 2009
- Preclinical and clinical studies of anticancer agent‐incorporating polymer micellesCancer Science, 2009
- Polymeric nanomedicine for cancer MR imaging and drug deliveryChemical Communications, 2009
- Nanoparticle therapeutics: an emerging treatment modality for cancerNature Reviews Drug Discovery, 2008
- Pluronic block copolymers: Evolution of drug delivery concept from inert nanocarriers to biological response modifiersJournal of Controlled Release, 2008
- Poly (amino acid) micelle nanocarriers in preclinical and clinical studiesAdvanced Drug Delivery Reviews, 2008
- Nano-engineering block copolymer aggregates for drug deliveryColloids and Surfaces B: Biointerfaces, 1999
- Polymeric micelles – a new generation of colloidal drug carriersEuropean Journal of Pharmaceutics and Biopharmaceutics, 1999
- Block copolymer micelles as vehicles for drug deliveryJournal of Controlled Release, 1993