دورية أكاديمية

Effect of surfactant on the in vitro dissolution and the oral bioavailability of a weakly basic drug from an amorphous solid dispersion.

التفاصيل البيبلوغرافية
العنوان: Effect of surfactant on the in vitro dissolution and the oral bioavailability of a weakly basic drug from an amorphous solid dispersion.
المؤلفون: Tung NT; Department of Pharmaceutics, Hanoi University of Pharmacy, Vietnam. Electronic address: nguyenthachtung@hup.edu.vn., Tran CS; National Institute for Food Control, Vietnam., Nguyen TL; Department of Pharmaceutics, Hanoi University of Pharmacy, Vietnam., Pham TM; Department of Pharmaceutics, Hanoi University of Pharmacy, Vietnam., Chi SC; Gachon National University, Korea., Nguyen HA; Department of Pharmacology, Hanoi University of Pharmacy, Vietnam., Bui QD; National Institute for Food Control, Vietnam., Bui DN; Department of Pharmaceutics, Hanoi University of Pharmacy, Vietnam., Tran TQ; Department of Pharmaceutics, Hanoi University of Pharmacy, Vietnam.
المصدر: European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences [Eur J Pharm Sci] 2021 Jul 01; Vol. 162, pp. 105836. Date of Electronic Publication: 2021 Apr 20.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Elsevier Science B.V Country of Publication: Netherlands NLM ID: 9317982 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0720 (Electronic) Linking ISSN: 09280987 NLM ISO Abbreviation: Eur J Pharm Sci Subsets: MEDLINE
أسماء مطبوعة: Publication: Amsterdam : Elsevier Science B.V
Original Publication: Amsterdam ; New York : Elsevier, c1993-
مواضيع طبية MeSH: Pharmaceutical Preparations* , Surface-Active Agents*, Animals ; Biological Availability ; Chromatography, Liquid ; Rabbits ; Solubility ; Tandem Mass Spectrometry
مستخلص: This study aimed to investigate the effect of a surfactant on the liquid-liquid phase separation, dissolution, diffusion, and the oral bioavailability of a weakly basic drug (l-tetrahydropalmatine; l-THP) from an amorphous solid dispersion (ASD). The carrier used in the ASD was optimized by the application of casting film, solvent shift, and pH shift methods. The interaction between the optimized carrier (HPMCP) and l-THP was then evaluated by Fourier transform-infrared spectroscopy and powder X-ray diffraction. The impact of the surfactant on ASD prepared by the spray-drying method was evaluated by both in vitro and in vivo studies. The results of in vitro studies, including liquid-liquid phase separation, drug diffusion, and pH-shift dissolution, indicated that the addition of a surfactant at a certain concentration below critical micelle concentration to ASD caused the precipitation of and a reduction in the membrane diffusion of l-THP in pH 6.8. This observation was confirmed in an in vivo study in which the drug concentration of l-THP in rabbit plasma was determined by the LC-MS/MS analysis method. Then the absolute and relative bioavailability of l-THP was calculated from the obtained pharmacokinetic parameters. Specifically, the addition of 1.5% surfactant (Poloxamer 188) to the binary ASD decreased the relative bioavailability of l-THP by approximately 2.4 times compared with the original binary ASD. Besides, the study proved that l-THP had low absolute bioavailability (around 1.24%), and the application of binary ASD was meaningful in enhancing the oral bioavailability of l-THP by around 334.77% compared to the raw material. The study is expected to provide a better understanding of how different dosage forms influence the bioavailability of l-THP, thereby allowing the selection of the optimal approach for this weakly basic drug.
(Copyright © 2021. Published by Elsevier B.V.)
فهرسة مساهمة: Keywords: Bioavailability; Diffusion; Dissolution; Liquid-liquid phase separation; Surfactant; l-tetrahydropalmatine;∙Amorphous solid dispersion
المشرفين على المادة: 0 (Pharmaceutical Preparations)
0 (Surface-Active Agents)
تواريخ الأحداث: Date Created: 20210414 Date Completed: 20210621 Latest Revision: 20210621
رمز التحديث: 20231215
DOI: 10.1016/j.ejps.2021.105836
PMID: 33852972
قاعدة البيانات: MEDLINE
الوصف
تدمد:1879-0720
DOI:10.1016/j.ejps.2021.105836