Camptothecin-polylactide conjugates (CMPT-PLA) were synthesized by covalent incorporation of CMPT into PLA of different microstructure, i.e., atactic PLA and atactic-block-isotactically enriched PLA (Pm = 0.79) via urethane bonds. The kinetic release of CPMT from CMPT-PLA conjugates, tested in vitro under different conditions, is possible in both cases and notably, strongly dependent on PLA microstructure. It shows that release properties of drug-PLA conjugates can be tailored by controlled design of the PLA microstructure, and allow in the case of CMPT-PLA conjugates for the development of highly controlled biodegradable CMPT systems-important delivery systems for anti-cancer agents.
CITATION STYLE
Oledzka, E., Horeglad, P., Gruszczyńska, Z., Plichta, A., Nałęcz-Jawecki, G., & Sobczak, M. (2014). Polylactide conjugates of camptothecin with different drug release abilities. Molecules, 19(12), 19460–19470. https://doi.org/10.3390/molecules191219460
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