对磺基[4]炔介导的吗啉水合物输送系统的实验和计算表征

Q2 Medicine
Sunaina Chaurasiya , Raghu Solanki , Mohd Athar , Ashok Kumar Jangid , Sunita Patel , Prakash C. Jha , Deep Pooja , Hitesh Kulhari
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引用次数: 0

摘要

钙[n]炔是一类大环化合物,已被研究用于改善水不溶性分子的物理化学特性。在这项工作中,使用对磺酰钙[4]炔(SC[4]A)作为络合剂制备了水合吗啉(MH)药物的络合物,以提高其水溶性、溶解速率和稳定性。采用甲醇溶剂蒸发法制备纯 MH 与 SC[4]A 之间的包合物(MH-SC[4]A),并通过傅立叶变换红外光谱、核磁共振、紫外光谱、DLS、TEM 和 DSC 技术进行分析。浓度依赖性溶解度研究表明,当 SC[4]A 浓度为 8 mM 时,MH 的溶解度提高了 22 倍。络合物形成后,MH 对 A549 细胞的体外抗癌效果增强。AO/EtBr 染色研究表明,与原生 MH 相比,MH 具有更强的介导细胞凋亡的抗癌活性。利用扩展伞状取样法计算的平均力势(PMF)描述了复合物的分子几何形状、稳定相互作用、释放行为和完全解旋途径。综合计算和实验数据证实,我们设计的 MH-SC[4]A 复合物可用作疏水性 MH 的药物递送载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Experimental and computational characterization of p-Sulfocalix[4]arene mediated delivery system for morin hydrate

Experimental and computational characterization of p-Sulfocalix[4]arene mediated delivery system for morin hydrate

Calix[n]arene is a class of macrocyclic compounds and has been investigated to improve the physicochemical properties of water insoluble molecules. In this work, a complex of morin hydrate (MH) drug was prepared using p-sulfocalix[4]arene (SC[4]A) as complexing agent to increase its water solubility, dissolution rate and stability. Solvent evaporation methanol was used to prepare the inclusion complex (MH-SC[4]A) between pure MH and SC[4]A and analysed by FTIR, NMR, UV, DLS, TEM, and DSC techniques. Concentration-dependent solubility study showed 22 folds enhancement of MH at 8 mM concentration of SC[4]A. The in vitro anticancer efficacy of MH against A549 cells was increased after complex formation. AO/EtBr staining study showed the more apoptosis mediated anticancer activity than native MH. Molecular geometry, stabilizing interactions, release behaviour and full-unwinding pathway of the complex were characterized by the computed Potential of Mean Force (PMF) using extended umbrella sampling. The combined computational and experimental data confirmed that our designed MH-SC[4]A complex could be utilized as a promising drug delivery carrier for hydrophobic MH.

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来源期刊
Medicine in Drug Discovery
Medicine in Drug Discovery Medicine-Pharmacology (medical)
CiteScore
8.30
自引率
0.00%
发文量
30
审稿时长
21 days
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