{"title":"Formulation and evaluation of voriconazole loaded ophthalmic in situ gel using a natural polymer","authors":"Prerana Shantinath Husukale, Indrajeet Damodar Gonjari, Nikita Harekrishna Gurav","doi":"10.30574/wjbphs.2024.19.1.0411","DOIUrl":null,"url":null,"abstract":"The eyes are one of the body's most significant and intricate organs, able to capture visual images and send them as signals via the optic nerve to the brain. The ocular transport of the medicine has been one of the challenging tasks for drug researchers because of the amazing development of the eye, which stifles the part of the prescription molecules into the perfect spot. The external visual course is the most often used method of medicine administration for treating visual diseases. Drugs used intraocularly that are topically controlled have very little visual bioavailability. A significant amount of medication is lost as a result of dose structure spilling brought on by tear turnover and nasolacrimal seepage weakening. Therefore, 1–10% of the medicine reaches the cornea. Voriconazole is the drug used in the treatment of fungal keratitis. Various polymers are screened out & among them, K-Carrageenan & Xanthan gum were used for the preparation of various formulations. Drug loaded with voriconazole was optimized using DOE experimental design with concentration of K- Carrageenan (X1), concentration of Xanthan gum(X2) as a dependent variable while Viscosity (Y1), Percent drug release(Y2) as a dependable variable. All the formulated batches were characterized for clarity, pH, drug content, gelling capacity, viscosity, in vitro drug release, accelerated stability study. An optimized batch was evaluated & showed there was no significant difference between them. The stability study suggested the formulation did not show any significant changes in drug content, viscosity, pH, gelling capacity & percent drug release. Conclusion-An ion sensitive ophthalmic in situ gel of antifungal agent using natural polymer will be serves as an alternative dosage form to reduce frequent dosing & safe.","PeriodicalId":23738,"journal":{"name":"World Journal of Biology Pharmacy and Health Sciences","volume":"1 9","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"World Journal of Biology Pharmacy and Health Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30574/wjbphs.2024.19.1.0411","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The eyes are one of the body's most significant and intricate organs, able to capture visual images and send them as signals via the optic nerve to the brain. The ocular transport of the medicine has been one of the challenging tasks for drug researchers because of the amazing development of the eye, which stifles the part of the prescription molecules into the perfect spot. The external visual course is the most often used method of medicine administration for treating visual diseases. Drugs used intraocularly that are topically controlled have very little visual bioavailability. A significant amount of medication is lost as a result of dose structure spilling brought on by tear turnover and nasolacrimal seepage weakening. Therefore, 1–10% of the medicine reaches the cornea. Voriconazole is the drug used in the treatment of fungal keratitis. Various polymers are screened out & among them, K-Carrageenan & Xanthan gum were used for the preparation of various formulations. Drug loaded with voriconazole was optimized using DOE experimental design with concentration of K- Carrageenan (X1), concentration of Xanthan gum(X2) as a dependent variable while Viscosity (Y1), Percent drug release(Y2) as a dependable variable. All the formulated batches were characterized for clarity, pH, drug content, gelling capacity, viscosity, in vitro drug release, accelerated stability study. An optimized batch was evaluated & showed there was no significant difference between them. The stability study suggested the formulation did not show any significant changes in drug content, viscosity, pH, gelling capacity & percent drug release. Conclusion-An ion sensitive ophthalmic in situ gel of antifungal agent using natural polymer will be serves as an alternative dosage form to reduce frequent dosing & safe.
眼睛是人体最重要、最复杂的器官之一,能够捕捉视觉图像,并通过视神经将其作为信号发送到大脑。药物的眼部运输一直是药物研究人员面临的挑战性任务之一,因为眼睛的发育令人惊叹,它能将部分处方分子扼杀在最佳位置。外用视觉疗法是治疗视觉疾病最常用的给药方法。局部控制的眼内用药在视觉上的生物利用度非常低。由于泪液周转和鼻泪管渗出减弱导致剂量结构溢出,大量药物流失。因此,只有 1-10% 的药物到达角膜。伏立康唑是治疗真菌性角膜炎的药物。我们筛选了各种聚合物,其中 K 角叉菜胶和黄原胶被用于制备各种配方。采用 DOE 实验设计法对装载伏立康唑的药物进行了优化,K-卡拉胶浓度(X1)、黄原胶浓度(X2)为因变量,粘度(Y1)、药物释放百分比(Y2)为依赖变量。对所有配制的批次进行了透明度、pH 值、药物含量、胶凝能力、粘度、体外药物释放和加速稳定性研究。对优化批次进行了评估,结果表明它们之间没有显著差异。稳定性研究表明,该制剂在药物含量、粘度、pH 值、胶凝能力和药物释放率方面均无明显变化。结论--使用天然聚合物制成的抗真菌剂离子敏感眼用原位凝胶将作为一种替代剂型,可减少用药次数,且安全可靠。