Carfilzomib公司
乳腺癌
蛋白酶体抑制剂
癌症研究
癌症
硼替佐米
多发性骨髓瘤
药理学
体内
白蛋白
医学
化学
免疫学
生物
内科学
生物技术
作者
Ji Eun Park,Joonyoung Park,Yearin Jun,Yunseok Oh,Gongmi Ryoo,Yoo-Seong Jeong,Hytham H. Gadalla,Jee Sun Min,Jung Hwan Jo,Myung Geun Song,Keon Wook Kang,Soo Kyung Bae,Yoon Yeo,Wooin Lee
标识
DOI:10.1016/j.jconrel.2019.04.006
摘要
Carfilzomib (CFZ) is the second-in-class proteasome inhibitor with much improved efficacy and safety profiles over bortezomib in multiple myeloma patients. In expanding the utility of CFZ to solid cancer therapy, the poor aqueous solubility and in vivo instability of CFZ are considered major drawbacks. We investigated whether a nanocrystal (NC) formulation can address these issues and enhance anticancer efficacy of CFZ against breast cancer. The surface of NC was coated with albumin in order to enhance the formulation stability and drug delivery to tumors via interactions with albumin-binding proteins located in and near cancer cells. The novel albumin-coated NC formulation of CFZ (CFZ-alb NC) displayed improved metabolic stability and enhanced cellular interactions, uptake and cytotoxic effects in breast cancer cells in vitro. Consistently, CFZ-alb NC showed greater anticancer efficacy in a murine 4T1 orthotopic breast cancer model than the currently used cyclodextrin-based formulation. Overall, our results demonstrate the potential of CFZ-alb NC as a viable formulation for breast cancer therapy.
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