Literature DB >> 26024817

Multifunctional Poly(methyl vinyl ether-co-maleic anhydride)-graft-hydroxypropyl-β-cyclodextrin Amphiphilic Copolymer as an Oral High-Performance Delivery Carrier of Tacrolimus.

Dong Zhang1, Xiaolei Pan1,2, Shang Wang1, Yinglei Zhai3, Jibin Guan1, Qiang Fu1, Xiaoli Hao1, Wanpeng Qi1, Yingli Wang1, He Lian3, Xiaohong Liu1, Yongjun Wang1, Yinghua Sun1, Zhonggui He1, Jin Sun1,4.   

Abstract

In order to improve oral bioavailability of tacrolimus (FK506), a novel poly(methyl vinyl ether-co-maleic anhydride)-graft-hydroxypropyl-β-cyclodextrin amphiphilic copolymer (CD-PVM/MA) is developed, combining the bioadhesiveness of PVM/MA, P-glycoprotein (P-gp), and cytochrome P450-inhibitory effect of CD into one. The FK506-loaded nanoparticles (CD-PVM/MA-NPs) were obtained by solvent evaporation method. The physiochemical properties and intestinal absorption mechanism of FK506-loaded CD-PVM/MA-NPs were characterized, and the pharmacokinetic behavior was investigated in rats. FK506-loaded CD-PVM/MA-NPs exhibited nanometer-sized particles of 273.7 nm, with encapsulation efficiency as high as 73.3%. FK506-loaded CD-PVM/MA-NPs maintained structural stability in the simulated gastric fluid, and about 80% FK506 was released within 24 h in the simulated intestinal fluid. The permeability of FK506 was improved dramatically by CD-PVM/MA-NPs compared to its solution, probably due to the synergistic inhibition effect of P-gp and cytochrome P450 3A (CYP3A). The intestinal biodistribution of fluorescence-labeled CD-PVM/MA-NPs confirmed its good bioadhesion to the rat intestinal wall. Two endocytosis pathways, clathrin- and caveolae-mediated endocytosis, were involved in the cellular uptake of CD-PVM/MA-NPs. The important role of lymphatic transport in nanoparticles' access to the systemic circulation, about half of the contribution to oral bioavailability, was observed in mesenteric lymph duct ligated rats. The AUC0-24 of FK506 loaded in nanoparticles was enhanced up to 20-fold compared to FK506 solutions after oral administration. The present study suggested that the novel multifunctional CD-PVM/MA is a promising efficient oral delivery carrier for FK506, due to its ability in solubilization, inhibitory effects on both P-gp and CYP 3A, high bioadhesion, and sustained release capability.

Entities:  

Keywords:  CYP 3A; P-gp; bioavailability; nanoparticles; tacrolimus (FK506)

Mesh:

Substances:

Year:  2015        PMID: 26024817     DOI: 10.1021/acs.molpharmaceut.5b00010

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  6 in total

Review 1.  Nanotechnology in Glycomics: Applications in Diagnostics, Therapy, Imaging, and Separation Processes.

Authors:  Erika Dosekova; Jaroslav Filip; Tomas Bertok; Peter Both; Peter Kasak; Jan Tkac
Journal:  Med Res Rev       Date:  2016-11-15       Impact factor: 12.944

2.  Preparation and evaluation of tacrolimus-loaded thermosensitive solid lipid nanoparticles for improved dermal distribution.

Authors:  Ji-Hyun Kang; Jinmann Chon; Young-Il Kim; Hyo-Jung Lee; Dong-Won Oh; Hong-Goo Lee; Chang-Soo Han; Dong-Wook Kim; Chun-Woong Park
Journal:  Int J Nanomedicine       Date:  2019-07-18

3.  Development of Liposome containing sodium deoxycholate to enhance oral bioavailability of itraconazole.

Authors:  Zhenbao Li; Meiyu Zhang; Chang Liu; Shiwei Zhou; Wenjuan Zhang; Tianyang Wang; Mei Zhou; Xiaohong Liu; Yongjun Wang; Yinghua Sun; Jin Sun
Journal:  Asian J Pharm Sci       Date:  2016-08-04       Impact factor: 6.598

4.  Tacrolimus-Loaded Solid Lipid Nanoparticle Gel: Formulation Development and In Vitro Assessment for Topical Applications.

Authors:  Abdul Shakur Khan; Kifayat Ullah Shah; Mohammed Al Mohaini; Abdulkhaliq J Alsalman; Maitham A Al Hawaj; Yousef N Alhashem; Shakira Ghazanfar; Kamran Ahmad Khan; Zahid Rasul Niazi; Arshad Farid
Journal:  Gels       Date:  2022-02-18

Review 5.  Strategies and Mechanism in Reversing Intestinal Drug Efflux in Oral Drug Delivery.

Authors:  Rong Lu; Yun Zhou; Jinqian Ma; Yuchen Wang; Xiaoqing Miao
Journal:  Pharmaceutics       Date:  2022-05-26       Impact factor: 6.525

6.  Luteinizing hormone-releasing hormone targeted poly(methyl vinyl ether maleic acid) nanoparticles for doxorubicin delivery to MCF-7 breast cancer cells.

Authors:  Jaleh Varshosaz; Ali Jahanian-Najafabadi; Jila Ghazzavi
Journal:  IET Nanobiotechnol       Date:  2016-08       Impact factor: 1.847

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.