基于溶剂交换的原位成形植入物:作为长效配方的进步和挑战。

IF 5.4
Irene Lozza, Ana Isabel Fraguas-Sánchez, Cristina Martín-Sabroso, Ana Isabel Torres-Suárez
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引用次数: 0

摘要

原位成形植入物(ISFIs)是长效药物输送系统,在注射部位固化,创建一个持续释放药物的仓库,从几天到几个月。与预制植入物相比,isfi具有独特的优势,包括更容易和更方便的管理和更简单的制造。在不同类型中,溶剂型isfi是最广泛研究和开发的配方。涵盖领域:本综述分析了溶剂型isfi在临床前和临床水平的进展,重点是配方策略和治疗应用。使用PubMed和WOS进行文献检索。还查阅了EMA和FDA的数据库。专家意见:溶剂型isfi是一种重要的策略,可以通过单次给药获得持久的效果,而不受患者依从性的影响。它们的主要影响是精神和物质使用障碍,但它们也对局部效果有用。迄今为止,一种制剂已被批准用于牙周炎,尽管预计将应用于眼部疾病和骨关节炎。一个关键的配方挑战是减少初始药物释放。大多数上市的配方是基于溶解在NMP中的PLGA/PLA。最近,DMSO和聚乙二醇基isfi已被批准,它们通常提供更好的药物释放控制,并可能导致新配方的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Solvent-exchange-based in situ forming implants: advances and challenges as long-lasting formulations.

Introduction: In situ forming implants (ISFIs) are long-acting drug delivery systems that solidify at the injection site, creating a depot for sustained drug release from days to months. Compared with preformed implants, ISFIs offer unique advantages, including easier and more convenient administration and simpler manufacturing. Among the different types, solvent-based ISFIs are the most extensively studied and developed formulations.

Areas covered: This review analyses advances in solvent-based ISFIs at both preclinical and clinical levels, with emphasis on formulation strategies and therapeutic applications. A literature search was conducted using PubMed and WOS. EMA and FDA databases were also consulted.

Expert opinion: Solvent-based ISFIs represent an important strategy for achieving long-lasting effects with a single administration independent of patient compliance. Their main impact has been in mental and substance use disorders, but they are also useful for local effects. To date, one formulation has been approved for periodontitis, though applications in ocular diseases and osteoarthritis are anticipated. A key formulation challenge is to reduce the initial drug release. Most marketed formulations are based on PLGA/PLA dissolved in NMP. Recently, DMSO and PEGylated-based-ISFIs have been approved, which generally provide better drug release control and will likely lead to the development of new formulations.

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