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用聚丙烯酸对ZIF-8纳米颗粒进行表面包覆:一种增强生物医学应用化学稳定性的简便方法。

Surface Coating of ZIF-8 Nanoparticles with Polyacrylic Acid: A Facile Approach to Enhance Chemical Stability for Biomedical Applications.

作者信息

Yamane Setsuko, Yusri Abdul Hadi Bin, Chen Po-Yu, van der Vlies André J, Mabrouk Amira Ben, Fetzer Isabelle, Hasegawa Urara

机构信息

Department of Materials Science and Engineering, The Pennsylvania State University, Steidle Building, 80 Pollock Road, University Park, PA, 16802, USA.

National Institute of Technology (KOSEN), Numazu College, 3600 Ooka, Numazu, Shizuoka, 410-8501, Japan.

出版信息

Macromol Biosci. 2025 Feb;25(2):e2400382. doi: 10.1002/mabi.202400382. Epub 2024 Nov 3.

Abstract

Nanoparticles of zeolitic imidazole framework-8 (ZIF-8 NPs), which are the subclass of metal-organic frameworks consisting of Zn ion and 2-methylimidazole, have been identified as promising drug carriers since their large microporous structure is suited for encapsulating hydrophobic drug molecules. However, one of the limitations of ZIF-8 NPs is their low stability in physiological solutions, especially in the presence of water and phosphate anions. These molecules can interact with the coordinatively unsaturated Zn sites at the external surface to induce the degradation of ZIF-8 NPs. In this study, herein a facile approach is reported to enhance the chemical stability of ZIF-8 NPs by surface coating with polyacrylic acid (PAA). The PAA-coated ZIF-8 (PAA-ZIF-8) NPs are prepared by mixing ZIF-8 NPs and PAA in water. PAA coating inhibits the degradation of ZIF-8 NPs in water as well as phosphate-buffered saline over 6 days, which seems to be due to the coordination of carboxyl groups of PAA to the reactive Zn sites. Furthermore, the PAA-ZIF-8 NPs loaded with the anticancer drug doxorubicin (Dox) show cytotoxicity in human colon cancer cells. These results clearly show the feasibility of the PAA coating approach to improve the chemical stability of ZIF-8 NPs without impairing their drug delivery capability.

摘要

沸石咪唑框架-8纳米颗粒(ZIF-8 NPs)是由锌离子和2-甲基咪唑组成的金属有机框架的子类,因其大微孔结构适合封装疏水性药物分子而被认为是有前途的药物载体。然而,ZIF-8 NPs的局限性之一是它们在生理溶液中的稳定性较低,尤其是在有水和磷酸根阴离子存在的情况下。这些分子可以与外表面配位不饱和的锌位点相互作用,从而诱导ZIF-8 NPs的降解。在本研究中,报道了一种通过用聚丙烯酸(PAA)进行表面包覆来提高ZIF-8 NPs化学稳定性的简便方法。通过将ZIF-8 NPs和PAA在水中混合制备了PAA包覆的ZIF-8(PAA-ZIF-8)NPs。PAA包覆在6天内抑制了ZIF-8 NPs在水以及磷酸盐缓冲盐溶液中的降解,这似乎是由于PAA的羧基与活性锌位点的配位作用。此外,负载抗癌药物阿霉素(Dox)的PAA-ZIF-8 NPs在人结肠癌细胞中显示出细胞毒性。这些结果清楚地表明了PAA包覆方法在不损害其药物递送能力的情况下提高ZIF-8 NPs化学稳定性的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5212/11827546/02b5731e7485/MABI-25-2400382-g003.jpg

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