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基于分子动力学模拟的青藤碱凝胶处方设计

Prescription Design of Sinomenine Gel Based on Molecular Dynamics Simulations.

作者信息

Kang Yiran, Shen Wei, Pan Shili, Lian Haiying, Ding Xuehui, Li Jingying, Zhu Jiaoyue, Wang Lin, Xu Wei

机构信息

School of Pharmacy, Changchun University of Chinese Medicine, Changchun 130117, China.

出版信息

Int J Mol Sci. 2024 Nov 29;25(23):12863. doi: 10.3390/ijms252312863.

Abstract

Sinomenine (SIN) is a drug for the treatment of rheumatoid arthritis, most of which is administered orally, but it is prone to adverse gastrointestinal effects. Gel can overcome the gastrointestinal adverse effects caused by oral administration. In this paper, a multiscale computational pharmaceutics strategy was developed to guide the systematic study of formulation factors of a SIN gel and, further, to guide the formulation design. A molecular dynamics (MD) simulations method was utilized to successfully screen the optimal prescription of SIN gel and to elucidate the molecular mechanisms affecting the quality of SIN gel. The optimal prescription was 3.0% of SIN, 1.0% of Carbopol (Cp), 30% of Ethanol (Eth), 5.0% of Glycerine (Gly) and 10.0% of Menthol (Men). The influence mechanism can be explained by the combination of multiple parameters, such as the microstructure diagram, the radius of gyration (Rg) and the radial distribution function (RDF). In vitro transdermal studies were carried out using a modified Franz diffusion cell method to evaluate the quality of the screened and reference prescriptions. The results showed that the cumulative penetration and penetration rate of the screening of prescription were better than the reference formulation. Most important of all, the simulation results are in good agreement with the in vitro release experiment, indicating that the strategy has good applicability. This study was able to accurately optimize the formulation and elucidate the molecular mechanism, which would provide a reference for further research on SIN and gel.

摘要

青藤碱(SIN)是一种用于治疗类风湿性关节炎的药物,大多通过口服给药,但它容易产生胃肠道不良反应。凝胶剂可以克服口服给药引起的胃肠道不良反应。本文开发了一种多尺度计算药物学策略,以指导对SIN凝胶剂处方因素的系统研究,并进一步指导处方设计。利用分子动力学(MD)模拟方法成功筛选出SIN凝胶剂的最佳处方,并阐明影响SIN凝胶剂质量的分子机制。最佳处方为3.0%的SIN、1.0%的卡波姆(Cp)、30%的乙醇(Eth)、5.0%的甘油(Gly)和10.0%的薄荷醇(Men)。其影响机制可以通过多种参数的组合来解释,如微观结构图、回转半径(Rg)和径向分布函数(RDF)。采用改良的Franz扩散池法进行体外透皮研究,以评估筛选出的处方和参比处方的质量。结果表明,筛选处方的累积渗透量和渗透率均优于参比制剂。最重要的是,模拟结果与体外释放实验结果吻合良好,表明该策略具有良好的适用性。本研究能够准确优化处方并阐明分子机制,为SIN及凝胶剂的进一步研究提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0695/11640992/f878fc280521/ijms-25-12863-g001.jpg

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