Development of Tapentadol Hydrochloride Loaded Proniosomal Gel using Main Effects Screening Design and in silico Verification using Parameter Sensitivity Analysis
Sangeetha G1★, Swamivel Manickam M2, Sanil Kumar P3, Chandramouli R4★ Corresponding author
- 1Department of Pharmaceutics, Krupanidhi College of Pharmacy, Bengaluru, Karnataka, INDIA.
- 2Department of Pharmacy, Faculty of Engineering and Technology, Annamalai University, Tamil Nadu, INDIA.
- 3Accenture, Bangalore, Karnataka, INDIA.
- 4Department of Quality Assurance, Krupanidhi College of Pharmacy, Bengaluru, Karnataka, INDIA.
CORRESPONDENCE
Sangeetha G
Department of Pharmaceutics, Krupanidhi College of Pharmacy, Bengaluru, Karnataka, INDIA.
Received: 13-02-2021; Revised: 28-07-2021; Accepted: 14-10-2021.
Volume 56, Issue 1 · pp. 65–76 · PUBLISHED 2022 · DOI: 10.5530/ijper.56.1.9
ABSTRACT
Aim: Tapentadol Hydrochloride is a centrally acting opioid analgesic of biopharmaceutical classification system class I drug. Oral administration of tapentadol hydrochloride undergoes extensive first-pass metabolism leads to poor bioavailability. The present study was aimed to screen the critical material attributes to deliver the tapentadol hydrochloride through the transdermal route using a carrier proniosomal gel. Methodology: Main effect screening design has been constructed to screen the choice of surfactant used for the formulation of tapentadol hydrochloride proniosomal gel. The critical material attributes selected were surfactant, cholesterol, and soya lecithin, with responses entrapment efficiency (%), vesicle size (nm), and zeta potential (mV). All 24 runs of experiments were performed and evaluated to check the model fit. The in silico verification was analyzed using parameter sensitivity analysis. Results: The prediction profiler showed maximum desirability for Kolliphore RH 40 against the set goals. The design diagnostic efficiency was measured better for the constructed MESD. Also, parameter sensitivity analysis confirms that the vesicle size would play a principal role in the permeation of tapentadol hydrochloride proniosomal gel. Conclusion: Hence, Kolliphore RH 40 was considered for the further optimization process. The tapentadol hydrochloride proniosomal gel would be a better alternative to oral therapy.
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G, S., M, S. M., P, S. K., & R, C. (2022). Development of Tapentadol Hydrochloride Loaded Proniosomal Gel using Main Effects Screening Design and in silico Verification using Parameter Sensitivity Analysis. Indian Journal of Pharmaceutical Education and Research, 56(1), 65–76. https://doi.org/10.5530/ijper.56.1.9
