Issue 2, 2017

Enhanced cytotoxicity by a benzothiazole-containing cisplatin derivative in breast cancer cells

Abstract

In recent years, the concept of nanoparticles being used as an intelligent drug carrier has gained great attention. In this paper, the formulation of a liposome delivery system loaded with a novel benzothiazole-containing cisplatin derivative (CJM-Pt) was carried out. The particle size distributions were determined using dynamic light scattering, and the prepared liposomes showed a suitable size of around 98 nm. Stability studies showed that the CJM-Pt loaded liposomes were stable at 4 °C for more than four weeks. Investigation of triggered release indicated that the release performance of the prepared liposomes was controllable and the releasing effect was remarkable under low pH (<pH 6.8) and high temperature (>42 °C). To test the suitability of the chosen formulation, CJM-Pt loaded liposomes were investigated against several tumor cell lines: MGC-803, SGC-7901, MCF-7 and MDA-MB-231. Furthermore, the cell cycle arrest was examined. The CJM-Pt loaded liposomes have the potential to be applied in drug delivery systems (DDS) for breast cancer therapy.

Graphical abstract: Enhanced cytotoxicity by a benzothiazole-containing cisplatin derivative in breast cancer cells

Supplementary files

Article information

Article type
Paper
Submitted
06 Sep 2016
Accepted
12 Dec 2016
First published
14 Dec 2016

New J. Chem., 2017,41, 773-785

Enhanced cytotoxicity by a benzothiazole-containing cisplatin derivative in breast cancer cells

C. You, J. Yu, Y. Sun, Y. Luo, X. Zhang, J. Zhu and B. Sun, New J. Chem., 2017, 41, 773 DOI: 10.1039/C6NJ02753A

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