Evidence map›Paper›PMID 39966367›Full record

ArticleRecent advances in drug delivery and formulation2025

Agomelatine Transdermal System Product Cycle: Development, Material/ Process Screening, Optimization, Characterization, Delivery Mechanics and Irritation study on Rat.

Punitkumar Rathod, Anita Lalwani

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Article in Recent advances in drug delivery and formulation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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2 authors.

Punitkumar RathodDepartment of Pharmaceutics, K. B. Institute of Pharmaceutical Education and Research, (University: Kadi Sarva Vishwavidyalaya), Gandhinagar, Gujarat, 382023, India.
Anita LalwaniDepartment of Pharmaceutics, K. B. Institute of Pharmaceutical Education and Research, (University: Kadi Sarva Vishwavidyalaya), Gandhinagar, Gujarat, 382023, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAgomelatine (AGT) is used for the treatment of major depressive disorder in adults. Agomelatine is highly susceptible to first-pass metabolism, and it has less than 5% oral bioavailability. Therapy for major depressive disorder extends for a long period and every time, additional caregivers are required to remind and manage the timely dosing of oral medicine to patients. In such cases, once a week, administration of agomelatine via transdermal patch dosage form provides major patient benefits and lowers overall therapy costs.

methodsAn agomelatine transdermal patch was prepared using the solvent evaporation method using the LTE-S Werner Mathis AG coater and dryer. A patch was prepared using silicon adhesive after screening different pressure-sensitive adhesives like acrylate, polyisobutylene, and silicon. To make a crystal-free patch, the concentration of povidone k-29/32 was optimized in preliminary trials. To deliver the drug over a 7-day period, propylene glycol monolaurate (PGML) was identified from different penetration enhancers. Three factors optimization was carried out, like the concentration of povidone k-29/32, the concentration of PGML, and the mixing time of the blend using the Box Behnken design. 3D surface response curves and contour plots were derived using Design Expert and Minitab software. From overlay plots, design spaces were identified.

resultsThe optimized AGT patch has good adhesion properties along with a desirable flux of 4.63 μg/cm

conclusionIt was concluded that agomelatine transdermal patches can be manufactured using silicon adhesive, povidone k-29/32, and propylene glycol monolaurate for the treatment of major depressive disorder and will be the most convenient and cost-effective therapy for the patient.

Indexed as

AcetamidesAntidepressive AgentsTransdermal PatchAdministration, CutaneousAnimalsDrug Delivery SystemsMaleNaphthalenesPropylene GlycolRatsRats, WistarSkinSkin AbsorptionAcetamidesagomelatineAntidepressive AgentsNaphthalenesPropylene GlycolAgomelatinebox behnken designheat flux studypressure sensitive adhesiveskin irritation studytransdermal patchwistar albino rats.

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.