Micelles from Amphiphilic Block Copolyphosphates for Drug Delivery
β Scribed by Xiang Zhai; Wei Huang; Jinyao Liu; Yan Pang; Xinyuan Zhu; Yongfeng Zhou; Deyue Yan
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 499 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1616-5187
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β¦ Synopsis
Abstract
Amphiphilic block copolyphosphates (PEP__βbβPIPPs) are synthesized by twoβstep ROP of cyclic phosphate monomers with different pedant groups. They can spontaneously selfβassemble into approximately spherical micelles ranging in size between 89 and 198βnm in water. A typical hydrophobic antiβcancer drug DOX is encapsulated into the micelles. The release rate of DOX slows down with increasing hydrophobic block length of PIPP. DOXβloaded micelles are investigated for the proliferation inhibition of Hela cells and the DOX dose required for 50% cellular growth inhibition is found to be 0.8βΒ΅gβmL^β1^. It is demonstrated that PEPβbβ__PIPP micelles can be used as a safe and promising drug delivery system.magnified image
π SIMILAR VOLUMES
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 b
The CMCs of ABCs are typically on the order of 10 Γ6 -10 Γ7 M, 5,6 whereas those of low-molecular-weight surfactants are on the order of 10 Γ3 -10 Γ4 M. 7,8
## Abstract Wellβdefined amphiphilic PLA__βbβ__PMPC diblock copolymers were synthesized. Bimimetic micelles were prepared and applied for release of antiβcancer drugs (DOX). TEM and DLS analysis revealed a regular spherical shape with small diameter (less than 50βnm) of the micelle. The biocompatib