Preparation and pharmacokinetics in vivo of linarin solid dispersion and liposome.

ABSTRACT:

Objective

The current investigation aimed to determine the appropriate dosage form by comparing solid dispersion and liposome to achieve the purpose of improving the solubility and bioavailability of linarin.

Methods

Linarin solid dispersion (LSD) and linarin liposome (LL) were developed via the solvent method and the thin film hydration method respectively. The Transwell chamber model of Caco-2 cells was established to evaluate the absorption of drug. The pharmacokinetics of linarin, LSD and LL in rats after ig administration were carried out by high performance liquid chromatography (HPLC) method.

Results

The solubility of LSD and LL was severally 3.29 times and 3.09 times than that of linarin. The permeation coefficients of LSD and LL were greater than 10

SUBMITTER: Huang Y 

PROVIDER: S-EPMC9476784 | biostudies-literature | 2022 Apr

REPOSITORIES: biostudies-literature