The effect of block copolymer structure on the internalization of polymeric micelles by human breast cancer cells

被引:72
作者
Mahmud, A [1 ]
Lavasanifar, A [1 ]
机构
[1] Univ Alberta, Fac Pharm & Pharmaceut Sci, Edmonton, AB T6G 2N8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
polymeric micelles; drug delivery; poly(ethylene oxide); poly(epsilon-caprolactone); endocytosis; fluorescent microscopy;
D O I
10.1016/j.colsurfb.2005.07.008
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The objective of this study was to assess the effect of hydrophilic/hydrophobic block chain lengths on the internalization of poly(ethylene oxide)-block-poly(epsilon-caprolactone) (PEO-b-PCL) micelles by cancer cells. PEO-b-PCL block copolymers with varied PEO and PCL chain lengths were synthesized, assembled to polymeric micelles and loaded with a hydrophobic fluorescent probe (DiI) through a co-solvent evaporation method of physical encapsulation. The slow release of the fluorescent probe from the micellar structure was evidenced following DiI transfer to lipid vesicles. The extent of micellar uptake by cancer cells was investigated through their incubation with MCF-7 cells followed by measurement of the fluorescent emission intensity of DiI (lambda = 550nm) in separated lysed cells. Cellular internalization of polymeric micelles was confirmed by laser scanning microscopy. The mechanism of micellar uptake was investigated by pretreatment of MCF-7 cells with chlorpromazine and cytochalasin B. Encapsulation of DiI in PEO-b-PCL micelles lowered the extent and rate of hydrophobic probe internalization by cancer cells. For polymeric micelles with 5000 a mol(-1) of PCL and varied PEO molecular weights of 2000, 5000 and 13,000 g mol(-1), maximum uptake was observed at a PEO molecular weight of 5000 a mol(-1). For polymeric micelles with 5000 g mol(-1) of PEO and varied PCL molecular weights of 5000, 13,000 and 24,000 g mol(-1), maximum uptake was observed at 13,000 g mol(-1) of PCL. Chlorpromazine reduced the cellular uptake of PEO-b-PCL micelles independent from the block copolymer structure, pointing to the involvement of clathrin mediated endocytosis mechanisms in the uptake of polymeric micelles by cancer cells. Inhibition of cellular uptake of PEO-b-PCL micelles by cytochalasin B, on the other hand, was found to be dependent on the chemical structure of the core/shell forming blocks. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:82 / 89
页数:8
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