| Literature DB >> 22681126 |
Yingchao Han1, Zhijian He, Anita Schulz, Tatiana K Bronich, Rainer Jordan, Robert Luxenhofer, Alexander V Kabanov.
Abstract
Many effective drugs for cancer treatment are poorly water-soluble. In combination chemotherapy, needed excipients in additive formulations are often toxic and restrict their applications in clinical intervention. Here, we report on amphiphilic poly(2-oxazoline)s (POx) micelles as a promising high capacity delivery platform for multidrug cancer chemotherapy. A variety of binary and ternary drugs combinations of paclitaxel (PTX), docetaxel (DTX), 17-allylamino-17-demethoxygeldanamycin (17-AAG), etoposide (ETO) and bortezomib (BTZ) were solubilized in defined polymeric micelles achieving unprecedented high total loading capacities of up to 50 wt % drug per final formulation. Multidrug loaded POx micelles showed enhanced stability in comparison to single-drug loaded micelles. Drug ratio dependent synergistic cytotoxicity of micellar ETO/17-AAG was observed in MCF-7 cancer cells and of micellar BTZ/17-AAG in MCF-7, PC3, MDA-MB-231 and HepG2 cells.Entities:
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Year: 2012 PMID: 22681126 PMCID: PMC3534837 DOI: 10.1021/mp300159u
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939