Phcog.Net logo

BROWSE ALL JOURNALS

    SEE ALL 6 JOURNALS
    Article

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

    Vidhi Bhatia1, MS Arohi Paul1 Corresponding author

    1. 1Vivekanand Education Society’s College of Pharmacy Chembur, Mumbai, Maharashtra, INDIA.

    CORRESPONDENCE

    Vidhi Bhatia

    Vivekanand Education Society’s College of Pharmacy Chembur, Mumbai, Maharashtra, INDIA.

    vidhi.bhatia@ves.ac.in

    Received: 12-07-2022; Revised: 25-08-2022; Accepted: 05-09-2022.

    Volume 14, Issue 4 · pp. 429–441 · PUBLISHED · DOI: 10.5530/pres.14.4.63

    View on Pharmacogn. Res. original site ↗

    ABSTRACT

    Background:Self-emulsifying drug delivery system (SEDDS) and solid-SEDDS of Boswellia serrataextract (BSE) was aimed at overcoming the problems of poor solubility and bioavailability. Materials and Methods:The formulation strategy included a selection of oil phase, surfactant and co-surfactant based on qualitative and quantitative saturated solubility studies. A ternary phase diagram was constructed to identify the self-emulsifying region using water uptake studies. Pseudoternary phase diagrams were plotted using 1:1, 2:1 and 3:1 ratios of surfactant and co-surfactant to identify the maximum micro-emulsification region. The prepared formulations of SEDDS were evaluated for their physical appearance, stability, drug content, and globule size determination. Solid-SEDDS were prepared by adsorption technique using mannitol (4.5% w/w) and were evaluated for physical appearance, stability, drug content, and globule size. In-vitrostudies were performed to compare the release of solid drugs, SEDDS and S-SEDDS. Results:The formulation containing Boswellia serrata(200 mg), Capmul MCM C8 (15% w/w), Tween 20 (33.333% w/w), Transcutol HP (16.666% w/w) was concluded to be optimized. The release pattern was signified more than 80% release in 30 min in case of S-SEDDS and SEDDS, and 40% release after 120 min in case of solid drug. Solid-SEDDS may be considered a better solid oral dosage form as solidified formulations are more ideal than liquid ones in terms of their stability. Conclusion:Results suggest the potential use of SEDDS and solid-SEDDS to improve the dissolution and hence oral bioavailability of poorly water-soluble drugs like Boswellia serratathrough oral route.

    KEYWORDS

    Open in new tab

    REFERENCES

    As published

    Showing references and in-text citations exactly as published.

      Cite this article

      SELECT FORMAT

      Bhatia, V., & Paul, M. A. (). Development of a Solid Self-emulsifying Drug Delivery System of Boswellia serrata. Pharmacognosy Research, 14(4), 429–441. https://doi.org/10.5530/pres.14.4.63