Extracellular retention of a cyclopamine nanoformulation leveraging larger size and more negative charge for improved breast cancer treatment. Issue 12 (12th March 2018)

• Record Type: Journal Article
• Authors: Feng, Chan; Wang, Kun; Lin, Yun; Song, Zhiwang; Lu, Yonglin; Liu, Jie; Zhu, Donglei; Li, Yongyong; Dong, Chunyan
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 12(2018)
• Page Start: 1834
• Page End: 1843
• Publication Date: 2018-03-12
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Biomedical materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c7tb02777j
• Languages: English
• ISSNs: 2050-750X

Abstract

Abstract : We achieved greater extracellular retention of nanoparticles, by leveraging their larger size and negative charge, for improving the effects of a drug with extracellular targeting sites. Abstract : Compared with intracellular drug delivery, drugs with extracellular targeting sites are rarely considered. As one of these drugs, cyclopamine (CYC) is a promising anticancer drug that functions by targeting the cell membrane receptor. For improving therapeutic effect, an albumin-based nano-system (ABN) with the capacity for extracellular retention was developed. The ABN was formulated by incorporating bovine serum albumin (BSA) into nanoparticles at the denaturing temperature of BSA, with CYC acting as a hydrophobic nucleation site, followed by stabilization upon heat-induced disulfide cross-linking. The resultant ABNs are negatively charged with a nanoparticle size that can be delicately regulated by varying the reaction time. In MDA-MB-231 cells, the size and charge of ABNs significantly affected the extracellular retention capacity, with ABN-300 nm exhibiting an enhanced cytotoxic effect. In vivo fluorescence imaging revealed obvious and persistent tumor accumulation of ABNs. A therapeutic study in an orthotopic mammary fat pad tumor model shows that ABN-300 nm possesses the most remarkable antitumor effect compared with the control groups. These results provide a new strategy for improving the efficacy of drug targeting at extracellular sites.