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明胶对含泊沙康唑的岩藻依聚糖微球药物特性的影响

The Impact of Gelatin on the Pharmaceutical Characteristics of Fucoidan Microspheres with Posaconazole.

作者信息

Szekalska Marta, Citkowska Aleksandra, Wróblewska Magdalena, Winnicka Katarzyna

机构信息

Department of Pharmaceutical Technology, Medical University of Białystok, Mickiewicza 2c, 15-222 Białystok, Poland.

出版信息

Materials (Basel). 2021 Jul 22;14(15):4087. doi: 10.3390/ma14154087.

Abstract

Fungal infections and invasive mycoses, despite the continuous medicine progress, are an important globally therapeutic problem. Multicompartment dosage formulations (e.g., microparticles) ensure a short drug diffusion way and high surface area of drug release, which as a consequence can provide improvement of therapeutic efficiency compared to the traditional drug dosage forms. As fucoidan is promising component with wide biological activity , the aim of this study was to prepare fucospheres (fucoidan microparticles) and fucoidan/gelatin microparticles with posaconazole using the one-step spray-drying technique. Pharmaceutical properties of designed fucospheres and the impact of the gelatin addition on their characteristics were evaluated. An important stage of this research was in vitro evaluation of antifungal activity of developed microparticles using different species. It was observed that gelatin presence in microparticles significantly improved swelling capacity and mucoadhesiveness, and provided a sustained POS release. Furthermore, it was shown that gelatin addition enhanced antifungal activity of microparticles against tested spp. strains. Microparticles formulation GF6, prepared by the spray drying of 20% fucoidan, 5% gelatin and 10% Posaconazole, were characterized by optimal mucoadhesive properties, high drug loading and the most sustained drug release (after 8 h 65.34 ± 4.10% and 33.81 ± 5.58% of posaconazole was dissolved in simulated vaginal fluid pH 4.2 or 0.1 M HCl pH 1.2, respectively).

摘要

尽管医学不断进步,但真菌感染和侵袭性真菌病仍是全球重要的治疗难题。多室剂型(如微粒)可确保药物扩散路径短且药物释放表面积大,因此与传统药物剂型相比,可提高治疗效果。由于岩藻依聚糖是具有广泛生物活性的有前景的成分,本研究的目的是采用一步喷雾干燥技术制备泊沙康唑岩藻球(岩藻依聚糖微粒)和岩藻依聚糖/明胶微粒。评估了所设计岩藻球的药学性质以及明胶添加对其特性的影响。本研究的一个重要阶段是使用不同菌种对所制备微粒的抗真菌活性进行体外评估。观察到微粒中存在明胶可显著提高溶胀能力和黏膜粘附性,并实现泊沙康唑的持续释放。此外,结果表明添加明胶可增强微粒对受试菌种的抗真菌活性。通过喷雾干燥20%岩藻依聚糖、5%明胶和10%泊沙康唑制备的微粒制剂GF6具有最佳的黏膜粘附性能、高载药量和最持久的药物释放特性(在pH 4.2的模拟阴道液或pH 1.2的0.1 M HCl中,8小时后分别有65.34±4.10%和33.81±5.58%的泊沙康唑溶解)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d47/8347644/f9b025f70879/materials-14-04087-g001.jpg

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