模拟女性生殖道的体外模型在提高阴道内给药效率方面的最新进展。

Expert opinion on drug delivery Pub Date : 2024-07-01 Epub Date: 2024-07-22 DOI:10.1080/17425247.2024.2380338
Bruna Silva, Eduardo F Marques, Andreia C Gomes
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引用次数: 0

摘要

导言:阴道内给药已成为治疗全身性和局部性女性生殖道(FGT)疾病的一种前景广阔的途径,它利用生物材料作为载体或支架,实现有针对性的高效给药。为了解这一途径的天然屏障并改进给药系统以实现有效的治疗反应,人们付出了巨大的努力:在这篇综述中,我们利用多个数据库(PubMed Scopus Web of Science Google Scholar)进行了全面的文献检索,讨论了阴道内给药的潜力以及这一途径所特有的障碍。然后分析了 FGT 的体外细胞模型,以及如何将其应用于阴道内给药的研究。我们进一步探讨了现有模型的局限性,以及使其更有希望用于给药研究或生物材料验证的可能性。体外细胞技术提供了补充信息,可揭示粘液与药物的相互作用:三维模型和细胞培养的进步加深了我们对 FGT 的了解,但它们仍无法复制所有变量。未来的研究应以使用互补方法、确保稳定性和制定一致的方案为目标,以改进治疗评估并为妇女健康创建更好的预测性体外模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent advances in in vitro models simulating the female genital tract toward more effective intravaginal therapeutic delivery.

Introduction: Intravaginal drug delivery has emerged as a promising avenue for treating a spectrum of systemic and local female genital tract (FGT) conditions, using biomaterials as carriers or scaffolds for targeted and efficient administration. Much effort has been made to understand the natural barriers of this route and improve the delivery system to achieve an efficient therapeutic response.

Areas covered: In this review, we conducted a comprehensive literature search using multiple databases (PubMed Scopus Web of Science Google Scholar), to discuss the potential of intravaginal therapeutic delivery, as well as the obstacles unique to this route. The in vitro cell models of the FGT and how they can be applied to probing intravaginal drug delivery are then analyzed. We further explore the limitations of the existing models and the possibilities to make them more promising for delivery studies or biomaterial validation. Complementary information is provided by in vitro acellular techniques that may shed light on mucus-drug interaction.

Expert opinion: Advances in 3D models and cell cultures have enhanced our understanding of the FGT, but they still fail to replicate all variables. Future research should aim to use complementary methods, ensure stability, and develop consistent protocols to improve therapy evaluation and create better predictive in vitro models for women's health.

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