Development of a Solid Self-emulsifying Drug Delivery System of Boswellia serrata

نویسندگان

چکیده

Pharmacognosy Research,2022,14,4,429-441.DOI:10.5530/pres.14.4.63Published:October 2022Type:Original ArticleAuthors:Vidhi Bhatia, and MS Arohi Paul Author(s) affiliations: Vidhi Bhatia*, Vivekanand Education Society’s College of Pharmacy Chembur, Mumbai, Maharashtra, INDIA. Abstract:Background: Self-emulsifying drug delivery system (SEDDS) solid-SEDDS Boswellia serrata extract (BSE) was aimed at overcoming the problems poor solubility bioavailability. Materials Methods: The formulation strategy included a selection oil phase, surfactant co-surfactant based on qualitative quantitative saturated studies. A ternary phase diagram constructed to identify self-emulsifying region using water uptake Pseudoternary diagrams were plotted 1:1, 2:1 3:1 ratios maximum micro-emulsification region. prepared formulations SEDDS evaluated for their physical appearance, stability, content, globule size determination. Solid-SEDDS by adsorption technique mannitol (4.5% w/w) size. In-vitro studies performed compare release solid drugs, S-SEDDS. Results: containing (200 mg), Capmul MCM C8 (15% w/w), Tween 20 (33.333% Transcutol HP (16.666% concluded be optimized. pattern signified more than 80% in 30 min case S-SEDDS SEDDS, 40% after 120 drug. may considered better oral dosage form as solidified are ideal liquid ones terms stability. Conclusion: Results suggest potential use improve dissolution hence bioavailability poorly water-soluble drugs like through route. Keywords:Bioavailability, serrata, Phase diagram, Solid-self-emulsifying systemView:PDF (1.56 MB)

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Design, Development and In Vitro Characterization of Self Emulsifying Drug Delivery System for Irbesartan

The objectives of present investigations were to optimize concentration of oil, surfactant and cosurfactant by pseudoternary phase diagrams and to develop a stable formulation of self emulsifying drug delivery system (SEDDS) in order to enhance the dissolution rate of poorly soluble Irbesartan (IBS) by SEDDS. Pseudoternary phase diagrams were constructed to identify the self emulsifying region....

متن کامل

Development and Characterization of Solid Self-emulsifying Drug Delivery System of Cilnidipine.

The present investigations highlight the development of solid self-emulsifying drug delivery system (solid-SEDDS) for improved oral delivery of the poorly water-soluble drug; cilnidipine. Liquid SEDDS of the drug were formulated using Capryol 90 as the oil phase, Tween 80 as the surfactant, and Transcutol HP as the co-surfactant after screening various vehicles. The prepared systems were charac...

متن کامل

Development and characterization of rozuvastatin loaded self emulsifying drug delivery system for the effective management of hypolipidemia

The present work was aimed to develop and characterize rosuvastatin loaded self emulsifying drug delivery system for the effective management of hypolipidemia (RSEDDS) for improving bioavailability, to enhance solubility, to prolong residence time and to provide sufficient amount of drug to a target site in a sustained release manner. Self-emulsifying drug delivery system was prepared by simple...

متن کامل

Solid Sirolimus Self-microemulsifying Drug Delivery System: Development and Evaluation of Tablets with Sustained Release Property

The clinical application of sirolimus (SRL) as an immunosuppressive agent is largely hampered by its narrow therapeutic range. This study focused on developing SRL tablets with a sustained release profile for better safety. SRL was highly water insoluble and its solubility has been efficiently enhanced by preparing self-microemulsifying drug delivery system (SMEDDS). The SRL-SMEDDS was physical...

متن کامل

Solid Sirolimus Self-microemulsifying Drug Delivery System: Development and Evaluation of Tablets with Sustained Release Property

The clinical application of sirolimus (SRL) as an immunosuppressive agent is largely hampered by its narrow therapeutic range. This study focused on developing SRL tablets with a sustained release profile for better safety. SRL was highly water insoluble and its solubility has been efficiently enhanced by preparing self-microemulsifying drug delivery system (SMEDDS). The SRL-SMEDDS was physical...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Pharmacognosy Research

سال: 2022

ISSN: ['0974-8490', '0976-4836']

DOI: https://doi.org/10.5530/pres.14.4.63