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基于穴状配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——一项密度泛函理论研究

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

作者信息

Ahsan Annum, Sarfaraz Sehrish, Hamid Malai Haniti S A, Sheikh Nadeem S, Ayub Khurshid

机构信息

Department of Chemistry, COMSATS University, Abbottabad Campus, KPK, 22060, Pakistan.

Chemical Sciences, Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, Gadong BE1410, Brunei Darussalam.

出版信息

R Soc Open Sci. 2025 Sep 10;12(9):250005. doi: 10.1098/rsos.250005. eCollection 2025 Sep.

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 and -24.01 kcal mol, 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 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 E 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.

摘要

纳米级辅助药物递送系统提供了一个平台,可改变与药物颗粒相关的基本性质,以限制其副作用。在这方面,基于深度苯并咪唑酮空穴体的二聚体纳米胶囊可作为小分子客体分子的良好宿主,被认为可作为药物递送载体。在当前研究中,我们在M06 - 2x/6 - 31G(d,p)理论水平下报道了基于苯并咪唑酮空穴体的纳米胶囊作为药物氨吡啶(AM)和巯嘌呤(MP)的药物递送系统。AM和MP药物与纳米胶囊相互作用,相互作用能分别为-26.02 kcal/mol和-24.01 kcal/mol。分子中的原子量子理论(QTAIM)和非共价指数(NCI)分析结果表明,两种药物分子均通过氢键和范德华相互作用在纳米胶囊内稳定存在。通过电子密度差(EDD)分析证实了电荷转移。此外,与AM@cap相比,在MP@cap情况下观察到电荷转移(自然键轨道;NBO)略高。此外,前线分子轨道(FMO)分析表明,与纳米胶囊相比,MP@cap情况下的能隙降低更高。FMO结果与相互作用能、NBO和EDD分析结果一致。此外,我们采用了分子动力学(AIMD)分析来研究药物负载后药物递送系统的动力学稳定性。已对所选药物的结合动力学或酶促相互作用进行了分子对接。并且,研究了pH效应以了解药物的卸载机制,这清楚地表明E值降低指向更容易卸载。偶极矩值分析表明,与AM药物分子相比,纳米胶囊将更有效地将MP药物携带至靶位点。总体而言,结果表明与其他药物相比,基于苯并咪唑酮空穴体的纳米胶囊作为抗癌药物分子的载体表现更好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd05/12419892/2980c60338d5/rsos.250005.f001.jpg

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