Extended tacrolimus release via the combination of lipid-based solid dispersion and HPMC hydrogel matrix tablets

The objective of this study is to evaluate the feasibility of obtaining extended release of tacrolimus by a novel combination of lipid-based solid dispersion and matrix-type extended release tablet techniques. Tacrolimus solid dispersion was prepared using glycerylbehenate (Compritol® ATO888) and Pl...

Full description

Bibliographic Details
Main Authors: Hui Xu, Li Liu, Xuehui Li, Junyuan Ma, Rui Liu, Shaoning Wang
Format: Article
Language:English
Published: Elsevier 2019-07-01
Series:Asian Journal of Pharmaceutical Sciences
Online Access:http://www.sciencedirect.com/science/article/pii/S1818087618302617
id doaj-9ba8e2ed78814c15ad6470e3904d88ba
record_format Article
spelling doaj-9ba8e2ed78814c15ad6470e3904d88ba2020-11-24T21:24:04ZengElsevierAsian Journal of Pharmaceutical Sciences1818-08762019-07-01144445454Extended tacrolimus release via the combination of lipid-based solid dispersion and HPMC hydrogel matrix tabletsHui Xu0Li Liu1Xuehui Li2Junyuan Ma3Rui Liu4Shaoning Wang5School of Pharmacy, Shenyang Pharmaceutical University, Benxi 117004, ChinaSchool of Pharmacy, Shenyang Pharmaceutical University, Benxi 117004, ChinaSchool of Pharmacy, Shenyang Pharmaceutical University, Benxi 117004, ChinaSchool of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Benxi 117004, ChinaSchool of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Benxi 117004, ChinaSchool of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Benxi 117004, China; Corresponding author: School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, No. 26 Huatuo Road, High & New Technology Development Zone, Benxi 117004, China. Tel.: +86 24 43520203The objective of this study is to evaluate the feasibility of obtaining extended release of tacrolimus by a novel combination of lipid-based solid dispersion and matrix-type extended release tablet techniques. Tacrolimus solid dispersion was prepared using glycerylbehenate (Compritol® ATO888) and Pluronic F127 as the carrier materials with hot-melt method, which was then blended with hydrogel matrix materials, such as HPMC and lactose, the powders were directly compressed into tablets. In vitro drug release tests were carried out to evaluate the performance of the solid dispersions and the tablets. The dissolution rate of tacrolimus was significantly improved by the lipid-based solid dispersion, and the incorporation of HPC into the solid dispersion obviously improved its stability after storage. Extended release tablets loaded with tacrolimus solid dispersion showed prolonged drug release patterns over 24 h, the release patterns of the tablets can be tailored by the compositions of the matrix materials, including the types and content of HPMCs. A modified processing method that directly mixed the melted solid dispersion with HPMC powders improved the uniformity of the solid dispersion inside the tablet matrix and release profile. The release data of the extended release tablet fitted well to the Korsmeyer–Peppas model with n value of 0.85, which suggested diffusion- and erosion-controlled release mechanism. The combination of lipid-based solid dispersion and HPMC hydrogel matrix may find wide applications in the extended release dosage forms of high potent, water-insoluble drugs. Keywords: Tacrolimus, Solid dispersion, Lipid, Extended-release tablethttp://www.sciencedirect.com/science/article/pii/S1818087618302617
collection DOAJ
language English
format Article
sources DOAJ
author Hui Xu
Li Liu
Xuehui Li
Junyuan Ma
Rui Liu
Shaoning Wang
spellingShingle Hui Xu
Li Liu
Xuehui Li
Junyuan Ma
Rui Liu
Shaoning Wang
Extended tacrolimus release via the combination of lipid-based solid dispersion and HPMC hydrogel matrix tablets
Asian Journal of Pharmaceutical Sciences
author_facet Hui Xu
Li Liu
Xuehui Li
Junyuan Ma
Rui Liu
Shaoning Wang
author_sort Hui Xu
title Extended tacrolimus release via the combination of lipid-based solid dispersion and HPMC hydrogel matrix tablets
title_short Extended tacrolimus release via the combination of lipid-based solid dispersion and HPMC hydrogel matrix tablets
title_full Extended tacrolimus release via the combination of lipid-based solid dispersion and HPMC hydrogel matrix tablets
title_fullStr Extended tacrolimus release via the combination of lipid-based solid dispersion and HPMC hydrogel matrix tablets
title_full_unstemmed Extended tacrolimus release via the combination of lipid-based solid dispersion and HPMC hydrogel matrix tablets
title_sort extended tacrolimus release via the combination of lipid-based solid dispersion and hpmc hydrogel matrix tablets
publisher Elsevier
series Asian Journal of Pharmaceutical Sciences
issn 1818-0876
publishDate 2019-07-01
description The objective of this study is to evaluate the feasibility of obtaining extended release of tacrolimus by a novel combination of lipid-based solid dispersion and matrix-type extended release tablet techniques. Tacrolimus solid dispersion was prepared using glycerylbehenate (Compritol® ATO888) and Pluronic F127 as the carrier materials with hot-melt method, which was then blended with hydrogel matrix materials, such as HPMC and lactose, the powders were directly compressed into tablets. In vitro drug release tests were carried out to evaluate the performance of the solid dispersions and the tablets. The dissolution rate of tacrolimus was significantly improved by the lipid-based solid dispersion, and the incorporation of HPC into the solid dispersion obviously improved its stability after storage. Extended release tablets loaded with tacrolimus solid dispersion showed prolonged drug release patterns over 24 h, the release patterns of the tablets can be tailored by the compositions of the matrix materials, including the types and content of HPMCs. A modified processing method that directly mixed the melted solid dispersion with HPMC powders improved the uniformity of the solid dispersion inside the tablet matrix and release profile. The release data of the extended release tablet fitted well to the Korsmeyer–Peppas model with n value of 0.85, which suggested diffusion- and erosion-controlled release mechanism. The combination of lipid-based solid dispersion and HPMC hydrogel matrix may find wide applications in the extended release dosage forms of high potent, water-insoluble drugs. Keywords: Tacrolimus, Solid dispersion, Lipid, Extended-release tablet
url http://www.sciencedirect.com/science/article/pii/S1818087618302617
work_keys_str_mv AT huixu extendedtacrolimusreleaseviathecombinationoflipidbasedsoliddispersionandhpmchydrogelmatrixtablets
AT liliu extendedtacrolimusreleaseviathecombinationoflipidbasedsoliddispersionandhpmchydrogelmatrixtablets
AT xuehuili extendedtacrolimusreleaseviathecombinationoflipidbasedsoliddispersionandhpmchydrogelmatrixtablets
AT junyuanma extendedtacrolimusreleaseviathecombinationoflipidbasedsoliddispersionandhpmchydrogelmatrixtablets
AT ruiliu extendedtacrolimusreleaseviathecombinationoflipidbasedsoliddispersionandhpmchydrogelmatrixtablets
AT shaoningwang extendedtacrolimusreleaseviathecombinationoflipidbasedsoliddispersionandhpmchydrogelmatrixtablets
_version_ 1725989913231360000