干眼病患者当前和新兴的药物治疗选择。

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Feyza Cukurova, Giulia Coco, Filippo Lixi, Giuseppe Giannaccare
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引用次数: 0

摘要

干眼病(DED)是一种多因素且日益流行的眼表疾病,旨在提供干眼病的最新药理治疗和有希望的新疗法。覆盖领域:使用PubMed、Scopus、ClinicalTrials.gov和其他在线资源进行有针对性的文献检索,以确定DED药理学管理的最新进展。审查的重点是主要监管机构批准的治疗方法,以及后期临床开发的研究药物。特别关注新的药物传递平台和创新的治疗机制。专家意见:治疗靶点和给药技术的快速创新正在改变DED的治疗前景。先进的配方,如纳米胶束、粘液穿透颗粒和不含防腐剂的乳剂,正在改善眼部生物利用度,减少不良反应,并增强患者的依从性。DED药物治疗的未来在于个性化,多模式策略,解决疾病机制的全谱,包括炎症,泪膜不稳定,神经感觉功能障碍和上皮损伤。最近FDA批准的TRPM8激动剂AR-15512,体现了机制特异性治疗的趋势,旨在提供症状缓解和疾病改变。随着治疗设备在全球范围内的扩展,持续的临床试验和现实世界的研究对于确保持久的疗效和优化患者的结果至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current and emerging pharmacological treatment options for patients with dry eye disease.

Introduction: To provide an up-to-date overview of current pharmacological treatments and promising emerging therapies for dry eye disease (DED), a multifactorial and increasingly prevalent ocular surface disorder.

Areas covered: A targeted literature search was conducted using PubMed, Scopus, ClinicalTrials.gov, and additional online sources to identify recent advances in the pharmacological management of DED. The review focuses on therapies approved across major regulatory bodies, as well as investigational agents in late-stage clinical development. Special attention is given to novel drug delivery platforms and innovative therapeutic mechanisms.

Expert opinion: Rapid innovation in both therapeutic targets and drug delivery technologies is transforming the treatment landscape for DED. Advanced formulations, such as nanomicelles, mucus-penetrating particles, and preservative-free emulsions, are improving ocular bioavailability, reducing adverse effects, and enhancing patient adherence. The future of DED pharmacotherapy lies in personalized, multimodal strategies that address the full spectrum of disease mechanisms, including inflammation, tear film instability, neurosensory dysfunction, and epithelial damage. The recent FDA approval of AR-15512, a TRPM8 agonist, exemplifies the trend toward mechanism-specific therapies designed to deliver both symptomatic relief and disease modification. As the therapeutic armamentarium expands globally, continued clinical trials and real-world studies will be essential to ensure durable efficacy and optimize patient outcomes.

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来源期刊
Expert Review of Clinical Pharmacology
Expert Review of Clinical Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.30
自引率
2.30%
发文量
127
期刊介绍: Advances in drug development technologies are yielding innovative new therapies, from potentially lifesaving medicines to lifestyle products. In recent years, however, the cost of developing new drugs has soared, and concerns over drug resistance and pharmacoeconomics have come to the fore. Adverse reactions experienced at the clinical trial level serve as a constant reminder of the importance of rigorous safety and toxicity testing. Furthermore the advent of pharmacogenomics and ‘individualized’ approaches to therapy will demand a fresh approach to drug evaluation and healthcare delivery. Clinical Pharmacology provides an essential role in integrating the expertise of all of the specialists and players who are active in meeting such challenges in modern biomedical practice.
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