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Development of docetaxel-loaded PEG–PLA nanoparticles using surfactant-free method for controlled release studies

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Version 2 2017-08-29, 13:40
Version 1 2017-07-19, 14:39
journal contribution
posted on 2017-08-29, 13:40 authored by Prajna Mishra, Ratan Kumar Dey

Docetaxel (DTX)-loaded poly(ethylene glycol)–poly(D,L-lactide) is prepared by nanoprecipitation method in the absence of any surfactants. The average particle size of the copolymer was found to be 101 nm. The drug entrapment efficiency (%) and drug loading (%) of polymer were found to be 9.471 ± 0.047 and 94.71 ± 0.466, respectively. The in vitro drug release characteristics show the controlled release of 98% of docetaxel in 72 h. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and apoptosis measured in terms of cleaved Poly(ADP-ribose) Polymerase (PARP) and cleaved caspase-3 protein expression shows that the copolymer has better cytotoxicity effect and apoptosis in comparison to free DTX in HeLa cells.

Funding

This work was supported by the Department of Science and Technology, New Delhi [Grant Number SR/S1/PC-24/2009].

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    International Journal of Polymeric Materials and Polymeric Biomaterials

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