Danyu Lv, , , Huanyu Xu, , , Ji Ma, , , Zhong Han*, , and , Yongguang Guan*,
{"title":"Spatial Confinement Mechanism for Developing Versatile Nonionic Guest-in-CD-MOF-1 Complexes to Generate Transparent Nonionic Guest in Aqueous Dispersion","authors":"Danyu Lv, , , Huanyu Xu, , , Ji Ma, , , Zhong Han*, , and , Yongguang Guan*, ","doi":"10.1021/acsanm.5c03482","DOIUrl":null,"url":null,"abstract":"<p >Understanding the universal encapsulation mechanism of nonionic guests in CD-MOF-1 is important to develop various stable nanosized nonionic guest-in-CD-MOF-1 complexes for improving the aqueous dispersity of hydrophobic nonionic guests. Herein, typal nonionic guests with different sizes and van der Waals volumes were encapsulated into CD-MOF-1. We found that urolithin A (Uro-A) could be effectively encapsulated into CD-MOF-1 compared to other guests. The long edge size of Uro-A (1.06 nm) exceeds the aperture size of CD-MOF-1 (0.78 nm), while its short edge size (0.62 nm) is slightly smaller than the aperture size. The van der Waals volume of Uro-A is 193.07 Å<sup>3</sup>, smaller than the A and B pore volumes of CD-MOF-1 (i.e., 2571.14 Å<sup>3</sup> and 381.51 Å<sup>3</sup>). Consequently, Uro-A can easily enter into the pores of CD-MOF-1 via free diffusion, while the noncovalent spatial confinement prevents the encapsulated Uro-A against escaping. Ellagic acid (EA) and caffeic acid phenethyl ester (CAPE) share similar molecular dimensions and van der Waals volumes compared to Uro-A, resulting in a reasonable loading capacity and are effectively difficult to escape from CD-MOF-1. However, the van der Waals volumes of Vitamin K1 (VK1) and coenzyme Q<sub>10</sub> (CoQ<sub>10</sub>) are significantly larger than the B pore volume of CD-MOF-1, stopping them from diffusing into CD-MOF-1. Alternatively, carvacrol, geranyl acetate, and nerol have excessively small dimensions and van der Waals volumes and thus are prone to escape from CD-MOF-1 during the washing process. Furthermore, the developed Uro-A-in-CD-MOF-1 presented desirable hydrolysis characteristics without significant residual nanostructures. This work provides a universal mechanism for developing nonionic guest-in-CD-MOF-1 to improve aqueous dispersibility of hydrophobic guests, providing potential applications in food, cosmetics, and pharmaceutical development.</p>","PeriodicalId":6,"journal":{"name":"ACS Applied Nano Materials","volume":"8 41","pages":"19910–19918"},"PeriodicalIF":5.5000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Nano Materials","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsanm.5c03482","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Understanding the universal encapsulation mechanism of nonionic guests in CD-MOF-1 is important to develop various stable nanosized nonionic guest-in-CD-MOF-1 complexes for improving the aqueous dispersity of hydrophobic nonionic guests. Herein, typal nonionic guests with different sizes and van der Waals volumes were encapsulated into CD-MOF-1. We found that urolithin A (Uro-A) could be effectively encapsulated into CD-MOF-1 compared to other guests. The long edge size of Uro-A (1.06 nm) exceeds the aperture size of CD-MOF-1 (0.78 nm), while its short edge size (0.62 nm) is slightly smaller than the aperture size. The van der Waals volume of Uro-A is 193.07 Å3, smaller than the A and B pore volumes of CD-MOF-1 (i.e., 2571.14 Å3 and 381.51 Å3). Consequently, Uro-A can easily enter into the pores of CD-MOF-1 via free diffusion, while the noncovalent spatial confinement prevents the encapsulated Uro-A against escaping. Ellagic acid (EA) and caffeic acid phenethyl ester (CAPE) share similar molecular dimensions and van der Waals volumes compared to Uro-A, resulting in a reasonable loading capacity and are effectively difficult to escape from CD-MOF-1. However, the van der Waals volumes of Vitamin K1 (VK1) and coenzyme Q10 (CoQ10) are significantly larger than the B pore volume of CD-MOF-1, stopping them from diffusing into CD-MOF-1. Alternatively, carvacrol, geranyl acetate, and nerol have excessively small dimensions and van der Waals volumes and thus are prone to escape from CD-MOF-1 during the washing process. Furthermore, the developed Uro-A-in-CD-MOF-1 presented desirable hydrolysis characteristics without significant residual nanostructures. This work provides a universal mechanism for developing nonionic guest-in-CD-MOF-1 to improve aqueous dispersibility of hydrophobic guests, providing potential applications in food, cosmetics, and pharmaceutical development.
期刊介绍:
ACS Applied Nano Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics and biology relevant to applications of nanomaterials. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important applications of nanomaterials.