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Synthesis, self-assembly in water, and cytotoxicity of MPEG-block-PLLA/DX conjugates.

Journal of biomedical materials research. Part A (2008-02-21)
Zhigang Xie, Tiancheng Lu, Xuesi Chen, Yonghui Zheng, Xiabin Jing
RÉSUMÉ

Docetaxel (DX) is one of the most effective antineoplastic drugs. Its current clinical administration is limited because of its hydrophobicity and serious side effects. A polymer/DX conjugate is designed and successfully prepared to solve these problems. It is monomethoxy-poly(ethylene glycol)-block-poly(L-lactide)/DX (MPEG-PLLA/DX). It was synthesized by reacting DX with carboxyl-terminated copolymer MPEG-PLLA, which was prepared by reacting succinic anhydride with hydroxyl-terminated copolymer monomethoxy-poly(ethylene glycol)-block-poly(L-lactide) (MPEG-PLLA). Its structure and molecular weight was confirmed by (1)H NMR and GPC. The MPEG-PLLA/DX micelles in aqueous solution were prepared using a solvent displacement method and characterized by dynamic light scattering for size and size distribution, and by transmission electron microscopy for surface morphology. Its antitumor activity against HeLa cancer cells evaluated by MTT assay showed that it had a similar antitumor activity to pure DX at the same drug content.

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Sigma-Aldrich
Methoxy poly(ethylene glycol)-b-poly(L-lactide), 5k-10k