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Merck

Blood-stable, tumor-adaptable disulfide bonded mPEG-(Cys)4-PDLLA micelles for chemotherapy.

Biomaterials (2012-10-20)
Seung-Young Lee, Sungwon Kim, Jacqueline Y Tyler, Kinam Park, Ji-Xin Cheng
RESUMO

Although targeted delivery mediated by ligand modified or tumor microenvironment sensitive nanocarriers has been extensively pursued for cancer chemotherapy, the efficiency is still limited by premature drug release after systemic administration. Herein we report a highly blood-stable, tumor-adaptable drug carrier made of disulfide (DS) bonded mPEG-(Cys)(4)-PDLLA micelles. Intravenously injected disulfide bonded micelles stably retained doxorubicin in the bloodstream and efficiently delivered the drug to a tumor, with a 7-fold increase of the drug in the tumor and 1.9-fold decrease in the heart, as compared with self-assembled (SA), non-crosslinked mPEG-PDLLA micelles. In vivo administration of disulfide bonded micelles led to doxorubicin accumulation in cancer cell nuclei, which was not observed after administration of self-assembled micelles. With a doxorubicin dose as low as 2 mg/kg, disulfide bonded micelles almost completely suppressed tumor growth in mice.

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Sigma-Aldrich
Poly(ethylene glycol) methyl ether, average Mn ~2,000
Sigma-Aldrich
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Methoxypolyethylene glycol 350, average mol wt 350
Sigma-Aldrich
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Sigma-Aldrich
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Sigma-Aldrich
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Sigma-Aldrich
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