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盐酸精氨酸减轻七叶皂苷钠对直肠黏膜的刺激:分子对接、物理性质、抗痔活性、安全性及局部凝胶制剂研究

Arginine Hydrochloride Reduce Rectal Mucosal Irritation of Sodium Aescinate: Molecular Docking, Physical Properties, Anti-Hemorrhoidal Activity, Safety and Topical Gel Formulations Investigation.

作者信息

Hu Di, Zeng Qiuyang, Wang Huanrong, Jiang Wei

机构信息

School of Life Science and Technology, Wuhan Polytechnic University, Wuhan 430023, China.

出版信息

Pharmaceutics. 2024 Nov 22;16(12):1498. doi: 10.3390/pharmaceutics16121498.

Abstract

: Sodium aescinate (SA) is commonly used topically due to its anti-inflammatory, anti-edematous, and anti-swelling properties. However, the clinical application of SA is limited by strong irritation, and cannot be used on the damaged skin and mucous membrane. This study aimed to investigate whether arginine hydrochloride (Arg·HCl) could reduce the rectal mucosal irritation of SA through the formation of a gel. : Molecular docking was first used to explore potential interactions between SA and Arg·HCl. Gels for rectal administration were then formulated by combining SA with various ratios of Arg·HCl (from 1:0 to 1:10). In vitro tests, including pH, centrifuge stability, viscosity, and spreadability analysis, were conducted. The optimal gel formulation was determined based on rectal mucosal irritation tests and anti-inflammatory experiments. Additionally, the anti-hemorrhoidal characteristics and safety of the optimal gel in terms of acute toxicity and dermal sensitivity were evaluated. : The optimal SA to Arg·HCl ratio of 1:6 (F5-SA gel) was identified, significantly reducing rectal mucosal irritation while enhancing anti-inflammatory activity. The F5-SA gel demonstrated high efficacy against hemorrhoids, notably promoting anal ulcer healing. When administered rectally to rabbits at a dose of 132 mg·kg·d (198 times the recommended therapeutic dose), no other obvious side effects were observed except a significant reduction in food intake on the day of administration. In addition, the gel did not induce dermal sensitivity. : The F5-SA gel is a promising formulation that can reduce irritation and toxic side effects, and enhance the therapeutic effect to some extent, ultimately achieving a safer and more effective rectal delivery system for SA.

摘要

七叶皂苷钠(SA)因其抗炎、抗水肿和消肿特性而常用于局部给药。然而,SA的临床应用受到强烈刺激性的限制,不能用于受损皮肤和黏膜。本研究旨在探讨盐酸精氨酸(Arg·HCl)是否能通过形成凝胶来减轻SA对直肠黏膜的刺激。首先采用分子对接技术探索SA与Arg·HCl之间的潜在相互作用。然后将SA与不同比例的Arg·HCl(从1:0到1:10)混合制备直肠给药凝胶。进行了包括pH值、离心稳定性、粘度和铺展性分析在内的体外试验。根据直肠黏膜刺激试验和抗炎实验确定最佳凝胶配方。此外,还评估了最佳凝胶在急性毒性和皮肤敏感性方面的抗痔特性和安全性。确定了SA与Arg·HCl的最佳比例为1:6(F5-SA凝胶),显著降低了直肠黏膜刺激,同时增强了抗炎活性。F5-SA凝胶对痔疮显示出高效,尤其能促进肛门溃疡愈合。以132 mg·kg·d的剂量直肠给药于兔子(为推荐治疗剂量的198倍)时,除给药当天食物摄入量显著减少外,未观察到其他明显副作用。此外,该凝胶未诱发皮肤敏感性。F5-SA凝胶是一种有前景的制剂,可减少刺激和毒副作用,并在一定程度上增强治疗效果,最终为SA实现更安全有效的直肠给药系统。

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