Formulation and In Vitro Evaluation of Levetiracetam Transdermal Patches

Authors

  • Bariki Rajasekhar St John’s College of Pharmaceutical Sciences, Yemmiganur, Kurnool , Andhrapradesh .
  • Avula Bhojaraju St John’s College of Pharmaceutical Sciences, Yemmiganur, Kurnool , Andhrapradesh .
  • G Vinod Kumar Reddy St John’s College of Pharmaceutical Sciences, Yemmiganur, Kurnool , Andhrapradesh .
  • Gudipogula Susmitha St John’s College of Pharmaceutical Sciences, Yemmiganur, Kurnool , Andhrapradesh .
  • Harijana James St John’s College of Pharmaceutical Sciences, Yemmiganur, Kurnool , Andhrapradesh .
  • Kammara Jyothi St John’s College of Pharmaceutical Sciences, Yemmiganur, Kurnool , Andhrapradesh .

Abstract

Long-term epilepsy management requires maintaining stable therapeutic plasma concentrations, which is often challenging with orally administered Levetiracetam because of its short dosing interval requirements and extensive hepatic first-pass metabolism. The present investigation aimed to formulate and evaluate a novel matrix-type transdermal drug delivery system (TDDS) employing a synergistic combination of natural Ficus carica fruit mucilage and synthetic polymers, namely HPMC K100 and Eudragit S100, to achieve sustained and controlled drug release. Five formulations (LTP1–LTP5) were prepared using the solvent casting method. The developed transdermal patches were evaluated for various physicochemical parameters, including weight variation, thickness, folding endurance, and drug content uniformity. Compatibility and possible molecular interactions between the drug and polymers were analyzed using FT-IR spectroscopy, while in vitro drug diffusion studies were performed using a Franz diffusion cell over a 24-hour period.FT-IR analysis confirmed the absence of significant drug–polymer interactions, indicating the chemical stability of Levetiracetam within the polymeric matrix. The prepared patches demonstrated satisfactory uniformity, with drug content ranging from 97.5% to 99.4% and thickness values between 138 and 148 μm. Mechanical characterization revealed good flexibility and durability, with folding endurance values reaching up to 172 folds. Among all formulations, LTP4 containing an optimized ratio of natural and synthetic polymers showed the best performance, exhibiting a cumulative drug release of 98.85% over 24 hours, following matrix diffusion-controlled release kinetics.The study concludes that the optimized LTP4 transdermal patch successfully provided sustained release of Levetiracetam and may serve as a promising non-invasive alternative to conventional oral therapy, potentially improving therapeutic efficacy, patient compliance, and long-term epilepsy management.

 

Downloads

Download data is not yet available.

References

Rang HP, Dale MM, Ritter JM, Flower RJ. Rang and Dale’s Pharmacology. 8th ed. London: Elsevier; 2016.

Brunton LL, Hilal-Dandan R, Knollmann BC. Goodman and Gilman’s The Pharmacological Basis of Therapeutics. 13th ed. New York: McGraw-Hill; 2018.

Tripathi KD. Essentials of Medical Pharmacology. 8th ed. New Delhi: Jaypee Brothers Medical Publishers; 2019.

Brahmankar DM, Jaiswal SB. Biopharmaceutics and Pharmacokinetics: A Treatise. 3rd ed. New Delhi: Vallabh Prakashan; 2012.

Allen LV, Popovich NG, Ansel HC. Ansel’s Pharmaceutical Dosage Forms and Drug Delivery Systems. 10th ed. Philadelphia: Lippincott Williams & Wilkins; 2014.

Aulton ME, Taylor K. Aulton’s Pharmaceutics: The Design and Manufacture of Medicines. 5th ed. Edinburgh: Elsevier; 2018.

Guy RH, Hadgraft J. Transdermal Drug Delivery. 2nd ed. New York: Marcel Dekker; 2003.

Prausnitz MR, Langer R. Transdermal drug delivery. Nat Biotechnol. 2008;26(11):1261–

Barry BW. Novel mechanisms and devices to enable successful transdermal drug delivery. Eur J Pharm Sci. 2001;14(2):101–14.

Williams AC, Barry BW. Penetration enhancers. Adv Drug Deliv Rev. 2012; 64:128–37.

Rowe RC, Sheskey PJ, Quinn ME. Handbook of Pharmaceutical Excipients. 7th ed. London: Pharmaceutical Press; 2012.

Siepmann J, Peppas NA. Higuchi equation: Derivation, applications, use and misuse. Int J Pharm. 2011;418(1):6–12.

Korsmeyer RW, Gurny R, Doelker E, Buri P, Peppas NA. Mechanisms of solute release from porous hydrophilic polymers. Int J Pharm. 1983;15(1):25–35.

Higuchi T. Mechanism of sustained-action medication. J Pharm Sci. 1963;52(12):1145–9.

Shargel L, Yu ABC. Applied Biopharmaceutics and Pharmacokinetics. 7th ed. New York: McGraw-Hill; 2016.

Patel RP, Baria AH. Formulation and evaluation of transdermal patches of aceclofenac. Int J Drug Dev Res. 2011;3(1):296–301.

Kulkarni RV, Sreedhar V, Mutalik S. Natural polymers in drug delivery systems. Int J Pharm Sci Rev Res. 2012;17(2):54–62.

Singh MC, Naik AS, Sawant SD. Transdermal drug delivery systems: A review. J Pharm Res. 2010;3(7):1644–7.

Published

2026-06-15

How to Cite

Bariki Rajasekhar, Avula Bhojaraju, G Vinod Kumar Reddy, Gudipogula Susmitha, Harijana James, & Kammara Jyothi. (2026). Formulation and In Vitro Evaluation of Levetiracetam Transdermal Patches. Asian Journal of Pharmaceutical Research and Development, 14(3), 37–42. Retrieved from https://mail.ajprd.com/index.php/journal/article/view/1756