| Literature DB >> 27702529 |
Xueqiong Zhang1, Lianghong Li1, Chunfu Li1, Hua Zheng1, Haoyuan Song1, Fuliang Xiong1, Tong Qiu2, Jin Yang3.
Abstract
The delivery of combination chemotherapy by nanoscale platforms has been demonstrated to enhance cancer treatment in the clinic. Cisplatin (CDDP)-crosslinked, glutathione-sensitive, tumor-targeting micelles based on carboxymethyl chitosan were designed for synergistic cisplatin-doxorubicin (DOX) combination chemotherapy. In our study, DOX was conjugated to carboxymethyl chitosan through a disulfide bond, which was structurally characterized by 1H NMR. The micelles formed by self-assembly were spherical, with the mean diameter of 274nm. The in vitro release studies revealed that the micelles were highly glutathione-sensitive. Cytotoxicity analysis demonstrated that the cisplatin-crosslinked micelles loaded with DOX exhibited enhanced therapeutic efficacy compared with the DOX-loaded nanoparticles, free DOX, and free CDDP. Cellular uptake and intracellular release revealed that the cisplatin-crosslinked micelles loaded with DOX could efficiently deliver and release DOX into the cancer cells. These results clearly indicate that tumor-targeting and glutathione-sensitive micelles provide means for combination drug delivery in cancer treatment.Entities:
Keywords: Carboxymethyl chitosan; Cisplatin; Combination therapy; Doxorubicin; Drug delivery; Micelles
Mesh:
Substances:
Year: 2016 PMID: 27702529 DOI: 10.1016/j.carbpol.2016.08.072
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381