Unraveling the Mechanisms, Clinical Impact, Comparisons, and Safety Profiles of Slow-Release Therapies in Glaucoma.

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Marco Zeppieri, Caterina Gagliano, Daniele Tognetto, Mutali Musa, Federico Bernardo Rossi, Angelo Greggio, Giuliano Gualandi, Alessandro Galan, Silvia Babighian
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Abstract

Glaucoma, a primary cause of irreversible blindness, is most effectively managed by reducing intraocular pressure (IOP). Topical eye drops, which are conventional treatments, frequently encounter constraints regarding patient compliance, inconsistent dosage, and tolerability. Slow-release drug delivery systems have emerged as a promising innovation in response to these challenges. The objective of these systems is to enhance the efficacy of treatment and patient compliance by ensuring the consistent and sustained delivery of therapeutic agents over extended periods. Implantable devices, injectable formulations, and external applications are all categorized as slow-release therapies. By delivering medication directly to the target tissues in a controlled manner, these technologies have the potential to circumvent common issues associated with traditional regimens, such as forgotten doses or improper administration. These systems have been shown to obtain clinically meaningful reductions in IOP in studies, with some demonstrating efficacy that is comparable to that of established daily topical treatments. Despite their potential, slow-release therapies encounter obstacles that necessitate resolution. Potential complications during implantation or removal, long-term biocompatibility, and the cost of treatment are all areas of concern. Furthermore, further investigation is required to comprehensively assess their relative economic feasibility, patient acceptability, and long-term safety profiles in comparison to conventional treatments. This review summarizes the most recent findings in the scientific literature, underlining the role and possible limits of slow-release therapies in glaucoma with the aim of offering a comprehensive understanding of their potential clinical applications and challenges. This emphasizes the potential for these innovations to revolutionize care by addressing current knowledge gaps, while also emphasizing the areas in which further development and research are required.

青光眼缓释治疗的机制、临床影响、比较和安全性分析。
青光眼是不可逆失明的主要原因,通过降低眼压(IOP)是最有效的治疗方法。局部滴眼液作为常规治疗方法,经常遇到患者依从性、剂量不一致和耐受性方面的限制。缓释给药系统已成为应对这些挑战的一项有前途的创新。这些系统的目标是通过确保在较长时间内持续和持续地提供治疗剂来提高治疗效果和患者的依从性。可植入装置、可注射制剂和外用药物都被归类为缓释疗法。通过以可控的方式将药物直接输送到目标组织,这些技术有可能避免与传统方案相关的常见问题,例如忘记剂量或给药不当。在研究中,这些系统已被证明可以获得临床意义上的IOP降低,其中一些显示出与既定的日常局部治疗相当的疗效。尽管有潜力,但缓释疗法遇到了需要解决的障碍。植入或移除过程中的潜在并发症、长期生物相容性和治疗费用都是值得关注的领域。此外,与传统治疗相比,需要进一步的调查来全面评估其相对经济可行性、患者可接受性和长期安全性。本综述总结了科学文献中的最新发现,强调了缓释治疗在青光眼中的作用和可能的局限性,旨在全面了解其潜在的临床应用和挑战。这强调了这些创新有可能通过解决目前的知识差距来彻底改变护理,同时也强调了需要进一步开发和研究的领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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