Self-assembled micelles based on N-octyl-N'-phthalyl-O-phosphoryl chitosan derivative as an effective oral carrier of paclitaxel. (1st March 2019)

• Record Type: Journal Article
• Authors: Qu, Guowei; Hou, Siyuan; Qu, Ding; Tian, Chunli; Zhu, Jingcheng; Xue, Lingjing; Ju, Caoyun; Zhang, Can
• Is Part Of: Carbohydrate polymers. Volume 207(2019)
• Page Start: 428
• Page End: 439
• Publication Date: 2019-03-01
• Subjects: N-octyl-N'-phthalyl-O-phosphoryl chitosan -- Micelles -- P-glycoprotein -- Oral drug delivery -- Paclitaxel; Polysaccharides -- Periodicals; Polysaccharides -- Periodicals; Polysaccharides -- Périodiques; Electronic journals; 547.78
• DOI: 10.1016/j.carbpol.2018.11.099
• Languages: English
• ISSNs: 0144-8617

Abstract

Highlights: N -octyl- N '-phthalyl- O -phosphoryl chitosan (OPPC) possesses good water solubility. OPPC micelles possess substantial loading capacity for paclitaxel (PTX). OPPC micelles significantly improve oral bioavailability of PTX. OPPC micelles enhance PTX absorption via transcytosis and P-gp efflux inhibition. Abstract: Herein, we describe a novel amphipathic chitosan derivative ( N -octyl- N '-phthalyl- O -phosphoryl chitosan, abbreviated as OPPC) as an effective oral delivery platform for P-gp substrates, especially paclitaxel (PTX). OPPC could readily self-assemble into micelles, solubilize and encapsulate PTX into the hydrophobic inner core of OPPC with superior loading capacity to chitosan. PTX/OPPC micelles possessed improved intestinal epithelial permeability and oral bioavailability of PTX evaluated by in situ perfusion and pharmacokinetic studies. In vivo fluorescence imaging revealed enhanced stability and integrity of OPPC micelles in mice gastrointestine. Furthermore, cellular uptake studies revealed effective transport and accumulation of OPPC micelles loading PTX or rhodamine-123 into Caco-2 cells via clathrin/cavelin-mediated endocytosis and OPPC-mediated P-gp inhibition. Mechanistically, the inhibition of P-gp efflux pumps by OPPC resulted from the reduction of membrane fluidity and decreased P-gp ATPase activity. In summary, OPPC micelles may serve as an efficient and promising delivery system for enhancing oral bioavailability of P-gp substrates.