Revolutionizing ocular drug delivery: recent advancements in in situ gel technology

Susanta Paul, Subhabrota Majumdar, Mainak Chakraborty
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Abstract

Abstract Background Ophthalmic in situ gel is a novel preparation. It can be instilled into the eye as a liquid but gels upon contact with the ocular surface, generating a sustained-release depot of the drug. The main body of the abstract Among drug delivery modalities, ocular drug administration requires careful study and parameter assessment. This is because the eyes are sensitive and require careful care. Conventional ocular administration techniques quickly eliminate formulated compounds, minimizing epithelial interaction. This review covers polymers used in ocular medication delivery, their uses, and their drawbacks. The in situ gelling mechanism converts liquid formulations into gels under certain physiological or environmental conditions. When they contact the ocular surface, in situ ocular gels undergo this transformation for medication administration. Different mechanisms drive this change, depending on the gel's formulation and desired properties. Temperature-, pH-, and ion-induced gelation are common processes of in situ ocular gel formation. The medicine's physicochemical qualities, desired drug release kinetics, ocular environment, and patient comfort determine the mechanism. Researchers can create ocular gels that transport medications, improve bioavailability, and increase patient compliance by carefully formulating and understanding the in situ gelation mechanism. These polymers are useful in prodrug research and ocular penetration enhancement. The article thoroughly discusses polymeric systems and creates a viable ophthalmic drug delivery formulation. Short conclusion In conclusion, in situ ocular gels advance ocular medication delivery. These gels overcome various difficulties of current delivery strategies for ocular therapeutics and provide a diverse and effective platform. In situ gelling, where the liquid formulation becomes a gel when it contacts ocular tissues, improves medication retention, bioavailability, and contact time.
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革命性的眼部药物输送:原位凝胶技术的最新进展
摘要背景眼原位凝胶是一种新型的眼用凝胶。它可以作为液体注入眼睛,但与眼表面接触后会形成凝胶,产生药物的缓释库。摘要在给药方式中,眼部给药需要仔细研究和参数评估。这是因为眼睛很敏感,需要小心照顾。传统的眼部给药技术可以快速消除配方化合物,最大限度地减少上皮相互作用。本文综述了用于眼部给药的聚合物,它们的用途和它们的缺点。原位凝胶机制在一定的生理或环境条件下将液体制剂转化为凝胶。当它们接触眼表面时,原位眼凝胶经历这种转化以供药物施用。不同的机制驱动这种变化,取决于凝胶的配方和所需的性能。温度、pH值和离子诱导的凝胶形成是眼部原位凝胶形成的常见过程。药物的理化性质、期望的药物释放动力学、眼环境和患者舒适度决定了其作用机制。研究人员可以通过仔细制定和了解原位凝胶机制来制造运输药物、提高生物利用度和增加患者依从性的眼凝胶。这些聚合物在药物前研究和眼穿透增强方面很有用。本文深入讨论了聚合物体系,并创造了一个可行的眼科给药配方。总之,原位眼凝胶促进眼部给药。这些凝胶克服了目前眼部治疗的各种困难,提供了一个多样化和有效的平台。原位凝胶,当液体配方接触眼组织时变成凝胶,改善药物保留,生物利用度和接触时间。
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