| Literature DB >> 30954620 |
Ji Eun Park1, Joonyoung Park2, Yearin Jun1, Yunseok Oh1, Gongmi Ryoo1, Yoo-Seong Jeong1, Hytham H Gadalla2, Jee Sun Min3, Jung Hwan Jo4, Myung Geun Song5, Keon Wook Kang4, Soo Kyung Bae3, Yoon Yeo6, Wooin Lee7.
Abstract
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.Entities:
Keywords: Albumin; Breast cancer; Carfilzomib; Nanocrystal; Proteasome inhibitor
Year: 2019 PMID: 30954620 PMCID: PMC6638563 DOI: 10.1016/j.jconrel.2019.04.006
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776