Original ArticleIndian Journal of Pharmaceutical Education and ResearchVol. 56 | Issue 2s | 2022 | pp. S253–S264Open access
Effect of Solutol HS 15 and Cremophor RH 40 on Dissolution and Bioavailability of Nateglinide through Solid Dispersions
- 1*,
- 2
- 1 Department of Pharmaceutics, School of Pharmaceutical Sciences, Siksha O Anusandhan (Deemed to be University), Bhubaneswar, Odisha, INDIA.
- 2 Drug Development and Analysis Laboratory, School of Pharmaceutical Sciences, Siksha O Anusandhan (Deemed to be University), Bhubaneswar, Odisha, INDIA.
Published in Indian Journal of Pharmaceutical Education and Research
Correspondence: Ranjit Prasad Swain
Department of Pharmaceutics, School of Pharmaceutical Sciences, Siksha O Anusandhan (Deemed to be University), Bhubaneswar, Odisha, INDIA.
Email: ranjit.prasad797@gmail.com
Copyright: © 2022 Manuscript Technomedia. This is an open access article.
- Published:
- Jan 1, 2022
- Received:
- Jun 25, 2021
- Accepted:
- Apr 21, 2022
- DOI:
- 10.5530/ijper.56.2s.96
How to cite
Swain, R. P., & Subudhi, B. B. (2022). Effect of Solutol HS 15 and Cremophor RH 40 on Dissolution and Bioavailability of Nateglinide through Solid Dispersions. Indian Journal of Pharmaceutical Education and Research, 56(2s), S253–S264. https://doi.org/10.5530/ijper.56.2s.96
Abstract
Introduction: To improve the aqueous solubility and bioavailability of nateglinide, we have earlier used poloxamer 188 and 407. Since solutol HS 15 and cremophor RH 40 are compatible and scalable polymers for industrial applications. Materials and Methods: We developed solid dispersions using these polymers. All data including Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetry analysis, x-ray diffraction and scanning electron microscopy suggested loss of crystallinity and amorphization. The stability of these was demonstrated as per the International Council for Harmonisation norms. Results and Discussion: Cremophor RH 40 (melting method) and solutol HS 15 based (solvent evaporation method) solid dispersions showed the highest saturation solubility (~ 65 fold). The significant difference (p < 0.05) in dissolution efficiency, time taken to release 50 % of drug, mean dissolution time and similarity factor signifies the remarkable enhancement of dissolution in these solid dispersions. Following oral administration of solid dispersions to rabbits, an increase of ~ 2.4 and ~ 1.8 folds in peak plasma concentration, area under curve respectively and decrease in time to reach peak plasma concentration (1 hr) of nateglinide, suggested the effectiveness of solid dispersions to improve the bioavailability. A 170% and 179% increase in relative bioavailability was demonstrated compared to the marketed formulation (Natiz 60) for these solid dispersions. Conclusion: Cremophor RH 40 solid dispersion showed relatively late release but a higher In vitro-in vivo correlation. It may be suggested that cremophor RH 40 promotes better absorption as compared to solutol HS 15 based solid dispersion.
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Article metadata
| Title | Effect of Solutol HS 15 and Cremophor RH 40 on Dissolution and Bioavailability of Nateglinide through Solid Dispersions |
|---|---|
| Authors | Ranjit Prasad Swain; Bharat Bhusan Subudhi |
| Affiliations | Department of Pharmaceutics, School of Pharmaceutical Sciences, Siksha O Anusandhan (Deemed to be University), Bhubaneswar, Odisha, INDIA.; Drug Development and Analysis Laboratory, School of Pharmaceutical Sciences, Siksha O Anusandhan (Deemed to be University), Bhubaneswar, Odisha, INDIA. |
| Corresponding author | ranjit.prasad797@gmail.com |
| Journal | Indian Journal of Pharmaceutical Education and Research |
| Volume / Issue | Vol. 56, Issue 2s (2022) |
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