A new pH-sensitive CS/Zn-MOF@GO ternary hybrid compound as a biofriendly and implantable platform for prolonged 5-Fluorouracil delivery to human breast cancer cells

生物相容性 核化学 微球 材料科学 扫描电子显微镜 药物输送 三元运算 纳米技术 化学 化学工程 冶金 复合材料 计算机科学 工程类 程序设计语言
作者
Malihe Pooresmaeil,Elnaz Aghazadeh Asl,Hassan Namazi
出处
期刊:Journal of Alloys and Compounds [Elsevier]
卷期号:885: 160992-160992 被引量:83
标识
DOI:10.1016/j.jallcom.2021.160992
摘要

In the current work, we investigated and compared the capability of the monodispersed chitosan (CS) microspheres, CS coated zinc-based metal-organic framework (CS/Zn-MOF) microspheres, and CS coated the hybrid of Zn-MOF with graphene oxide (CS/[email protected]) microspheres as an anticancer drug carrier. The prepared samples were characterized through the common characterization techniques. The morphologies, sizes, and drug loading efficiency of the prepared compounds respectively were well-characterized, obtained, and compared with each other. The scanning electron microscopy (SEM) analysis displayed the particle size of the prepared microspheres in the range of 20–40 µm. The highest amount of 5-fluorouracil (5-Fu) loading was found for the ternary hybrid of CS/[email protected] microspheres; ~45%. The 5-Fu loaded CS microspheres ([email protected]/[email protected] microspheres) with rough surfaces exhibited a pH-sensitive and sustained release pattern for loaded 5-Fu. So, the cumulative drug release amount at pH 5.0 was relatively two times greater than pH 7.4. Eventually, CS/[email protected] microspheres exhibited acceptable enzymatic biodegradability and also good biocompatibility toward MDA-MB 231 cells line as an epithelial, human breast cancer cell. 41.2% cell viability after 48 treatment with [email protected]/[email protected] microspheres confirmed the capability of 5-Fu loaded CS/[email protected] microspheres in the tumor cell treatment. Based on the founded interesting results the CS/[email protected] ternary hybrid microspheres could be proposed as a promising and hopeful candidate to applied in the localized anticancer delivery.
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