Bhupathyraaj Mullaicharam, Vijaya Rani K Reeta, Sridhar Sathvik B, Shareef Javed, Thomas Sabin, Halligudi Nirmala, Sockalingam Anbazhagan, Mohandoss Kiruba, Sundar Shyam
College of Pharmacy, National University of Science and Technology, Muscat 130, Oman.
Surya School of Pharmacy, Vikravandi, Villupuram 605652, Tamilnadu, India.
Polymers (Basel). 2022 May 13;14(10):1984. doi: 10.3390/polym14101984.
Quetiapine Fumarate is potent, and the daily therapeutic dose can be delivered easily across the skin with the help of permeation enhancers. Quetiapine Fumarate-loaded transdermal patches were prepared by solvent evaporation technique. Various formulation parameters, excipients, and their combinations were optimized to get thin, translucent, smooth, stable, and high permeable character patches. A total number of 10 formulations were prepared. All formulations were subjected to various physicochemical evaluations. Three different formulations were prepared and F1, F2, and F3. Various physicochemical studies were carried out and found no significant difference between the three batches. The in vitro release study showed 74.29%, 82.73%, and 77.27%, respectively, up to 24 h. From the results, F2 has been selected as an optimized formulation and evaluated for skin irritation test. The results revealed that there is no irritation produced. The stability study results showed that there is no significant change from its initial nature till the period of three months in both temperatures. Quetiapine Fumarate Transdermal Patch F2 has achieved the goal of extended-release, cost-effectiveness, lowering the dose and frequency of drug administration, and thus may improve patient compliance.
富马酸喹硫平药效显著,借助渗透促进剂,每日治疗剂量可轻松透过皮肤给药。采用溶剂蒸发技术制备了载有富马酸喹硫平的透皮贴剂。对各种制剂参数、辅料及其组合进行了优化,以获得薄、半透明、光滑、稳定且高渗透性的贴剂。共制备了10种制剂。所有制剂均进行了各种物理化学评价。制备了三种不同的制剂F1、F2和F3。进行了各种物理化学研究,发现这三批制剂之间无显著差异。体外释放研究表明,在24小时内,释放率分别为74.29%、82.73%和77.27%。根据结果,选择F2作为优化制剂并进行皮肤刺激性试验。结果显示未产生刺激。稳定性研究结果表明,在两种温度下,直至三个月期间,其初始性质均无显著变化。富马酸喹硫平透皮贴剂F2实现了缓释、成本效益、降低给药剂量和频率的目标,因此可能提高患者的依从性。