评估用于阿昔洛韦缓释的阴道粘液片中的聚合物组合。

IF 4.3 3区 医学 Q1 PHARMACOLOGY & PHARMACY European Journal of Pharmaceutical Sciences Pub Date : 2024-09-30 DOI:10.1016/j.ejps.2024.106919
Laura Martín-Bartolomé , Roberto Ruiz-Caro , María Dolores Veiga , Fernando Notario-Pérez
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摘要

由 2 型单纯疱疹病毒(HSV-2)引起的生殖器疱疹影响着近 5 亿人,其中大部分是妇女。由于传播的主要途径是性接触,因此开发阿昔洛韦缓释阴道杀菌剂将是预防病毒传播的合适工具。在这项工作中,我们评估了三种具有不同特性的聚合物(壳聚糖、黄原胶和乙基纤维素)在获得阿昔洛韦缓释阴道片剂方面的潜力。通过组合这些聚合物,观察到了某些有用的协同作用,以改变其粘附能力并控制药物释放。在溶胀研究中发现,壳聚糖和黄原胶在酸性介质(模拟阴道液)中形成的聚电解质复合物具有更温和的溶胀和持续的凝胶作用。在对阴道粘膜进行的体内外研究中,这种复合物可延长药片的粘附性,从而在用药后更好地保留在阴道中。此外,壳聚糖和黄原胶的结合还能使阿昔洛韦在 5 天内得到控制释放,而不受介质 pH 值的影响,这就保证了即使在有精液存在的情况下也能继续释放药物。
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Evaluation of polymer combinations in vaginal mucoadhesive tablets for the extended release of acyclovir
Genital herpes, caused by herpes simplex virus type 2 (HSV-2), affects nearly 500 million people, mostly women. Since the main route of transmission is sexual contact, the development of an acyclovir extended-release vaginal microbicide would be a suitable tool for the prevention of virus transmission. In this work, we evaluated the potential of three polymers with different characteristics (chitosan, xanthan gum and ethyl cellulose) for obtaining acyclovir extended-release vaginal tablets. By combining the polymers, certain useful synergies were observed to modify their mucoadhesive capacity and control drug release. In the swelling studies, it observed that a polyelectrolyte complex with more moderate swelling and sustained gelation was formed between chitosan and xanthan gum exclusively in acidic medium (simulated vaginal fluid). This complex allowed prolonging the mucoadhesion of the tablets in ex vivo studies performed with vaginal mucosa, which would translate into better retention in the vagina after administration. In addition, the combination of chitosan and xanthan gum allowed obtaining a controlled release of acyclovir for 5 days, regardless of the pH of the medium, which would guarantee that drug release continues even in the presence of seminal fluid.
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来源期刊
CiteScore
9.60
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2.20%
发文量
248
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期刊介绍: The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development. More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making. Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.
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