Fabrication of pH responsive FU@Eu-MOF nanoscale metal organic frameworks for lung cancer therapy

纳米尺度 制作 肺癌 金属有机骨架 化学 癌症治疗 材料科学 纳米技术 医学 癌症 内科学 有机化学 病理 吸附 替代医学
作者
Prabhu Raju,Karthiyayini Balakrishnan,Monali Mishra,Thirumurugan Ramasamy,Natarajan Suganthy
出处
期刊:Journal of Drug Delivery Science and Technology [Elsevier BV]
卷期号:70: 103223-103223 被引量:57
标识
DOI:10.1016/j.jddst.2022.103223
摘要

Fabrication of biocompatible drug delivery systems (DDS) with enhanced permeation -retention effect and precise targeting is a major challenge in cancer therapy. The present study focused on fabrication of europium metal-organic framework (EuMOF) as pH responsive drug delivery system for sea weed polysaccharide fucoidan (FU@Eu-MOF) by one-pot synthesis method and assess its anticancer potential against lung cancer. Fabricated Eu-MOF exhibited high drug loading efficiency (22.15% by wt) and pH responsive controlled release of drug fucoidan (85.3 ± 0.02% in 48 h at pH 5.0). Material characterization revealed the formation of monodispersed uniform rod shaped structure decorated with fucoidan on the surface with average particle size of 71 ± 0.21 nm. Results of anticancer studies revealed that FU@Eu-MOF showed enhanced anticancer potential (IC 50 value 32.17 ± 0.06 μg/ml) in lung cancer cells (A549) when compared to fucoidan alone (IC 50 60.34 ± 0.03 μg/ml). Mechanism of anticancer potential revealed that FU@Eu-MOF enhanced ROS level inducing mitochondrial dysfunction and DNA damage leading to apoptosis. Safety evaluation studies revealed that FU@Eu-MOF showed neither cytotoxic, nor hemolytic activity under in vitro condition. To conclude the results of the study reveals FU@Eu-MOF as promising biocompatible material for drug delivery system for lung cancer therapy and other biomedical applications. • FU@Eu-MOF was synthesized by one pot synthesis method. • FU@Eu-MOF showed high drug loading efficiency and pH triggered release kinetics. • FU@Eu-MOF exhibited potent anticancer effect against A549 cells. • FU@Eu-MOF triggered ROS level leading to mitochondrial dysfunction mediated apoptosis. • FU@Eu-MOF is neither cytotoxic nor hemolytic indicating biocompatibility.
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