Literature DB >> 12820139

Amphiphilic block copolymers for drug delivery.

Monica L Adams1, Afsaneh Lavasanifar, Glen S Kwon.   

Abstract

Amphiphilic block copolymers (ABCs) have been used extensively in pharmaceutical applications ranging from sustained-release technologies to gene delivery. The utility of ABCs for delivery of therapeutic agents results from their unique chemical composition, which is characterized by a hydrophilic block that is chemically tethered to a hydrophobic block. In aqueous solution, polymeric micelles are formed via the association of ABCs into nanoscopic core/shell structures at or above the critical micelle concentration. Upon micellization, the hydrophobic core regions serve as reservoirs for hydrophobic drugs, which may be loaded by chemical, physical, or electrostatic means, depending on the specific functionalities of the core-forming block and the solubilizate. Although the Pluronics, composed of poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide), are the most widely studied ABC system, copolymers containing poly(L-amino acid) and poly(ester) hydrophobic blocks have also shown great promise in delivery applications. Because each ABC has unique advantages with respect to drug delivery, it may be possible to choose appropriate block copolymers for specific purposes, such as prolonging circulation time, introduction of targeting moieties, and modification of the drug-release profile. ABCs have been used for numerous pharmaceutical applications including drug solubilization/stabilization, alteration of the pharmacokinetic profile of encapsulated substances, and suppression of multidrug resistance. The purpose of this minireview is to provide a concise, yet detailed, introduction to the use of ABCs and polymeric micelles as delivery agents as well as to highlight current and past work in this area. Copyright 2003 Wiley-Liss, Inc. and the American Pharmacists Association

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Year:  2003        PMID: 12820139     DOI: 10.1002/jps.10397

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  128 in total

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Review 2.  Strategies in the design of nanoparticles for therapeutic applications.

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Review 4.  Polymeric micelles for ocular drug delivery: From structural frameworks to recent preclinical studies.

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5.  Polymer micelle formulations of proteasome inhibitor carfilzomib for improved metabolic stability and anticancer efficacy in human multiple myeloma and lung cancer cell lines.

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Review 6.  Oral bioavailability: issues and solutions via nanoformulations.

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7.  PEG branched polymer for functionalization of nanomaterials with ultralong blood circulation.

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8.  Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles.

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9.  Structural changes in block copolymer micelles induced by cosolvent mixtures.

Authors:  Elizabeth G Kelley; Thomas P Smart; Andrew J Jackson; Millicent O Sullivan; Thomas H Epps
Journal:  Soft Matter       Date:  2011-08-07       Impact factor: 3.679

10.  Multi-stimuli sensitive amphiphilic block copolymer assemblies.

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Journal:  J Am Chem Soc       Date:  2009-04-08       Impact factor: 15.419

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