Comparative study of cavitands-based nanocapsule as a drug delivery vehicle for an anti-cancer and multiple sclerosis drug-A DFT study.

IF 2.9 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Royal Society Open Science Pub Date : 2025-09-10 eCollection Date: 2025-09-01 DOI:10.1098/rsos.250005
Annum Ahsan, Sehrish Sarfaraz, Malai Haniti S A Hamid, Nadeem S Sheikh, Khurshid Ayub
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引用次数: 0

Abstract

Nanoscale-assisted drug delivery systems give a platform to alter elementary properties associated with drug particles to limit their adverse effects. In this regard, deep benzimidazolone cavitand-based dimeric nanocapsule, which can act as good host for small guest molecules, is considered to be used as drug delivery vehicle. In the current study, we report the benzimidazolone cavitand-based nanocapsules as drug delivery systems for the drugs, i.e. ampyra (AM) and merceptopurine (MP) at M06-2x/6-31G(d,p) level of theory. AM and MP drugs interact with the nanocapsule with the interaction energies of -26.02 kcal mol-1 and -24.01 kcal mol-1, respectively. The results of quantum theory of atoms in molecules (QTAIM) and non-covalent index (NCI) analyses divulge that both the drug molecules are stabilized inside nanocapsule via the hydrogen bonding and van der Waals interactions. The transfer of charge is confirmed through electron density difference (EDD) analyses. Moreover, in the case of MP@cap slightly higher transfer of charge (natural bond orbital; NBO) is observed as compared with AM@cap. Furthermore, frontier molecular orbital (FMO) analyses show the higher energy gap reduction in the case of MP@cap as compared with nanocapsule. The FMO results are consistent with the results of interaction energies, NBO and EDD analyses. Additionally, we have employed ab initio molecular dynamics (AIMD) analysis to find the dynamical stability of drug delivery system after drug loading. Molecular docking has been performed for binding kinetics or the enzymatic interactions of the selected drugs. And, pH effect is studied for understanding the off-loading mechanism of the drugs, which clearly shows the decrease in Eint values pointing towards easier offloading. The analyses of values of dipole moment show that nanocapsule will carry MP drug more efficiently to the target site as compared with AM drug molecule. Overall, the results divulge that the benzimidazolone cavitand-based nanocapsule acts as better carrier for an anti-cancer drug molecule as compared with the other drugs.

基于空腔体的纳米胶囊作为抗癌和多发性硬化症药物递送载体的比较研究。
纳米辅助给药系统提供了一个平台来改变与药物颗粒相关的基本性质,以限制其副作用。因此,基于深苯并咪唑酮空腔体的二聚体纳米胶囊可以作为小客体分子的良好宿主,被认为可以作为药物递送载体。在本研究中,我们报道了基于苯并咪唑酮空腔体的纳米胶囊作为药物递送系统,即ampyra (AM)和merceptopurine (MP)在M06-2x/6-31G(d,p)水平的理论。AM和MP药物与纳米胶囊的相互作用能分别为-26.02 kcal mol-1和-24.01 kcal mol-1。分子原子量子理论(QTAIM)和非共价指数(NCI)分析结果表明,两种药物分子都是通过氢键和范德华相互作用在纳米胶囊内稳定的。通过电子密度差(EDD)分析证实了电荷的转移。此外,在MP@cap的情况下,观察到的电荷转移(自然键轨道;NBO)略高于AM@cap。此外,前沿分子轨道(FMO)分析表明,与纳米胶囊相比,MP@cap的能隙降低更高。FMO结果与相互作用能、NBO和EDD分析结果一致。此外,我们采用从头算分子动力学(ab initio molecular dynamics, AIMD)分析了载药后给药系统的动力学稳定性。所选药物的结合动力学或酶的相互作用进行了分子对接。通过研究pH效应来了解药物的卸荷机制,可以清楚地看到Eint值的降低表明更容易卸荷。偶极矩分析表明,纳米胶囊比AM药物分子更能有效地将MP药物携带到靶点。总的来说,研究结果表明,与其他药物相比,基于苯并咪唑酮空腔体的纳米胶囊是更好的抗癌药物分子载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Royal Society Open Science
Royal Society Open Science Multidisciplinary-Multidisciplinary
CiteScore
6.00
自引率
0.00%
发文量
508
审稿时长
14 weeks
期刊介绍: Royal Society Open Science is a new open journal publishing high-quality original research across the entire range of science on the basis of objective peer-review. The journal covers the entire range of science and mathematics and will allow the Society to publish all the high-quality work it receives without the usual restrictions on scope, length or impact.
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