药物输送和hesperidin的配方开发:一个系统的审查
Thi Phuong Nga Hoang1, Peter Timmins1, Alan M Smith1
1Department of Pharmacy, School of Applied Sciences, University of Huddersfield, Huddersfield, UK.
Expert opinion on drug delivery
|October 27, 2025
概括
配方策略显著增强西的作用.
科学领域:
- 药理学和药物输送 药理学和药物输送
- 自然产品化学 自然产品化学
背景情况:
- 素是类植物中的天然生物黄,具有强大的抗氧化,抗炎,抗癌和神经保护性质.
- 赫斯佩里丁的临床使用受到溶解性差,生物可用性低以及稳定性挑战的阻碍.
研究的目的:
- 系统地审查旨在改善hesperidin生物制药性质的配方策略.
- 确定领先的配方方法及其对赫斯佩里丁生物可用性和治疗潜力的影响.
主要方法:
- 在主要的科学数据库 (PubMed,MEDLINE,Scopus,Google Scholar) 中按照PRISMA指南进行系统的文献搜索,截至2025年1月10日.
- 包括专注于素配方和报告生物制药或生物结果的原始研究.
- 独立选,数据提取,以及由两名审稿人进行偏差风险评估.
主要成果:
- 69项研究符合资格标准,评估了各种配方平台,包括包容复合物,固体分散,SMEDDS,微粒,凝和各种纳米配方.
- 大多数配方改善了hesperidin的溶解和/或暴露.
- 脂质和聚合物纳米系统表现出最显著和最一致的改善,在血管,代谢和瘤指标方面有前途的早期临床数据.
结论:
- 先进的配方,特别是基于脂质的系统,聚合物纳米粒子和植物体,可以有效地克服hesperidin的生物制药限制.
- 未来的翻译需要强大的稳定性和免疫毒性数据,质量设计制造和经过精心设计的临床试验,具有标准化的终点.
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