Original ArtcileJournal of Young PharmacistsVol. 14 | Issue 3 | pp. 295–301Open access
Fabrication and Evaluation of Controlled Release Transdermal Drug Delivery System of Carvedilol using Design Expert® Software for the Management of Hypertension
- 1,
- 2,
- 3*,
- 1,
- 4
- 1 Department of Pharmaceutics, B.S. Anangpuria Institute of Pharmacy, Faridabad, Haryana, INDIA.
- 2 Department of Pharmaceutics, B.S. Anangpuria Educational Institute, Faridabad, Haryana, INDIA.
- 3 Department of Pharmacy, Noida Institute of Engineering and Technology, Greater Noida, Uttar Pradesh, INDIA.
- 4 Department of Pharmaceutics, Avadh Institute of Medical Technology and Hospital, Paikra Mau Behta, Lucknow-226018, U.P, INDIA.
Published in Journal of Young Pharmacists
Correspondence: Rupa Mazumder
Department of Pharmacy, Noida Institute of Engineering and Technology, Greater Noida, Uttar Pradesh, INDIA.
Email: rupa_mazumder@rediffmail.com
- Received:
- Apr 11, 2022
- Accepted:
- Jul 12, 2022
- DOI:
- 10.5530/jyp.2022.14.58
How to cite
Maan, S., Khar, R. K., Mazumder, R., Yadav, N., & Khan, U. A. Fabrication and Evaluation of Controlled Release Transdermal Drug Delivery System of Carvedilol using Design Expert® Software for the Management of Hypertension. Journal of Young Pharmacists, 14(3), 295–301. https://doi.org/10.5530/jyp.2022.14.58
Abstract
Objectives: Design, development and characterization of controlled release transdermal drug delivery system of carvedilol using Design Expert® software for managing hypertension. Materials and Methods: CV undergoes extensive first-pass metabolism due to low oral bioavailability approx ~24% and biological half-life ~6 hr. Available CV preparations have drawback of poor patient compliance due to increase in dosing frequency and making the therapy less effective. Phospholipid E80, glycerol and cholesterol were used for preparing CVGs via film hydration technique. Optimization was done using Central Composite Design under Design Expert software. While PVP and EC in a ratio of 4:1 in chloroform (5 mL) with plasticizer dibutyl phthalate (30%) were used for preparing Matrix type transdermal patch containing CVGs. Results: Optimized CVGs showed 115.7 nm particle size, and -16.4 mV zeta potential. TEM analysis also showed similar vesicle size and reveals globular structure of CVGs. Nearly 0.31 mm thickness, 0.14 % g weight variation, 99.13% flatness and 98.72% drug content was found in Matrix type transdermal patch having CVGs Transdermal patch with Franz diffusion cell showed approx. 90% release upto 48 hr during in-vitro permeation studies. In-vivo pharmacological assessment was done for efficacy estimation of GVs transdermal patch by N-nitro-L-arginine methyl ester which produced significant hypertension in rats. The application of CVGs transdermal patch resulted in a gradual decrease in BP, with the maximum effect from the patch observed at 10 hr (p < 0.001), the effect continued for 48 hr clearly indicating the gradual release of drug by transdermal patch for a long period. Conclusion: Developed novel transdermal patch having CV loaded glycerosomes may be considered as a promising approach for controlled release of drug with effective hypertension management.
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Article metadata
| Title | Fabrication and Evaluation of Controlled Release Transdermal Drug Delivery System of Carvedilol using Design Expert® Software for the Management of Hypertension |
|---|---|
| Authors | Saurabh Maan; Roop Krishen Khar; Rupa Mazumder; Nishant Yadav; Urooj Ahmed Khan |
| Affiliations | Department of Pharmaceutics, B.S. Anangpuria Institute of Pharmacy, Faridabad, Haryana, INDIA.; Department of Pharmaceutics, B.S. Anangpuria Educational Institute, Faridabad, Haryana, INDIA.; Department of Pharmacy, Noida Institute of Engineering and Technology, Greater Noida, Uttar Pradesh, INDIA.; Department of Pharmaceutics, Avadh Institute of Medical Technology and Hospital, Paikra Mau Behta, Lucknow-226018, U.P, INDIA. |
| Corresponding author | rupa_mazumder@rediffmail.com |
| Journal | Journal of Young Pharmacists |
| Volume / Issue | Vol. 14, Issue 3 |
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