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β-环糊精金属有机骨架的超分子结构优化了碘的稳定性及其与 l-薄荷醇的共递送,用于抗菌应用。

Supramolecular Structure of the β-Cyclodextrin Metal-Organic Framework Optimizes Iodine Stability and Its Co-delivery with l-Menthol for Antibacterial Applications.

机构信息

Anhui University of Chinese Medicine, Hefei 230012, China.

Center for Drug Delivery Systems, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201210, China.

出版信息

ACS Appl Mater Interfaces. 2024 May 15;16(19):24235-24247. doi: 10.1021/acsami.4c02258. Epub 2024 Apr 30.

Abstract

The spread of upper respiratory tract (URT) infections harms people's health and causes social burdens. Developing targeted treatment strategies for URT infections that exhibit good biocompatibility, stability, and strong antimicrobial effects remains challenging. The dual antimicrobial and antiviral effects of iodine (I) in combination with the cooling sensation of l-menthol in the respiratory tract can simultaneously alleviate URT inflammation symptoms. However, as both I and l-menthol are volatile, addressing stability issues is crucial. In this study, a potassium iodide β-cyclodextrin metal-organic framework [β-CD-POF(I)] with appropriate particle size was used to coload and deliver I and l-menthol. Primarily, β-CD-POF(I) was employed as the most efficient carrier to significantly enhance the stability of I, surpassing any other known protection strategies in the pharmaceutical field (CD complexations, PVP conjugations, and cadexomer iodine). The mechanism underlying the improvement in stability of I by β-CD-POF(I) was investigated through scanning electron microscopy with energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, and molecular docking. The results revealed that the key processes involved in improving stability were the inclusion of I by β-CD cavities in β-CD-POF(I) and the formation of polyiodide anion between iodine ions and I. Furthermore, the potential of β-CD-POF(I) to load and deliver drugs was validated, and coloading of l-menthol and I demonstrated reliable stability. β-CD-POF(I) achieved a rate of URT deposition ≥95% in vitro, and the combined antibacterial effects of coloaded I and l-menthol was better than I or PVP-I alone, with no irritation noted following URT administration in rabbits. Therefore, the stable coloading of drugs by β-CD-POF(I), leading to enhanced antimicrobial effects, provides a new strategy for treating URT infections.

摘要

上呼吸道(URT)感染的传播危害人们的健康并造成社会负担。开发针对 URT 感染的靶向治疗策略,具有良好的生物相容性、稳定性和强大的抗菌作用,仍然具有挑战性。碘(I)与 l-薄荷醇在呼吸道中的冷却感觉相结合,具有双重抗菌和抗病毒作用,可同时缓解 URT 炎症症状。然而,由于 I 和 l-薄荷醇都是挥发性的,解决稳定性问题至关重要。在这项研究中,使用具有适当粒径的碘化钾β-环糊精金属有机骨架 [β-CD-POF(I)] 来共载和输送 I 和 l-薄荷醇。首先,β-CD-POF(I)被用作最有效的载体,显著提高了 I 的稳定性,超过了药物领域中任何其他已知的保护策略(CD 络合、PVP 缀合和 cadexomer 碘)。通过扫描电子显微镜与能量色散 X 射线光谱、X 射线光电子能谱、拉曼光谱和分子对接研究了 β-CD-POF(I)提高 I 稳定性的机制。结果表明,提高稳定性的关键过程包括 I 被β-CD 腔包含在β-CD-POF(I)中,以及碘离子和 I 之间形成多碘阴离子。此外,验证了β-CD-POF(I)负载和输送药物的潜力,并且 l-薄荷醇和 I 的共载显示出可靠的稳定性。β-CD-POF(I)在体外实现了 URT 沉积率≥95%,共载的 I 和 l-薄荷醇的联合抗菌效果优于单独的 I 或 PVP-I,并且在兔子的 URT 给药后没有观察到刺激。因此,β-CD-POF(I)的稳定共载药物导致增强的抗菌作用,为治疗 URT 感染提供了新的策略。

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