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Antitumor activity of PEGylated biodegradable nanoparticles for sustained release of docetaxel in triple-negative breast cancer.

作者信息

Palma Giuseppe, Conte Claudia, Barbieri Antonio, Bimonte Sabrina, Luciano Antonio, Rea Domenica, Ungaro Francesca, Tirino Pasquale, Quaglia Fabiana, Arra Claudio

机构信息

Animal Facility, National Cancer Institute - Foundation "G. Pascale", Via Mariano Semmola, 80131 Napoli, Italy; Institute of Experimental Endocrinology and Oncology, CNR, Via Pansini, 80131 Napoli, Italy.

Drug Delivery Laboratory, Department of Pharmacy, University of Napoli Federico II, Via Domenico Montesano 49, 80131 Napoli, Italy.

出版信息

Int J Pharm. 2014 Oct 1;473(1-2):55-63. doi: 10.1016/j.ijpharm.2014.06.058. Epub 2014 Jun 30.


DOI:10.1016/j.ijpharm.2014.06.058
PMID:24992317
Abstract

With the aim to find novel therapeutical approaches for triple-negative breast cancer (TNBC) treatment, we have developed a powder for i.v. injection based on cyclodextrins and docetaxel (DTX)-loaded polyethyleneglycol-poly(epsilon-caprolactone) nanoparticles (DTX-NPs). Nanoparticles are designed to concentrate at tumor level by enhanced permeability and retention effect and release drug cargo at a sustained rate in the blood and in tumor interstitium. DTX-NPs of around 70 nm, shielding proteins and allowing a sustained DTX release for about 30 days, were produced by melting sonication technique. DTX-NPs were associated to hydroxypropyl-β-cyclodextrin to give a powder for injection with excellent dispersibility and suitable for i.v. administration. DTX-NPs were as efficient as free DTX in inhibiting cell growth of MDA-MB231 cells, even at low concentrations, and displayed a comparable in vivo antitumor efficacy and better survival in a TNBC animal model as compared with DTX commercial formulation (Taxotere(®)). In conclusion, PEGylated biodegradable DTX-NPs highlighted their potential in the treatment of aggressive TNBC providing a foundation for future clinical studies.

摘要

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