光动力疗法
体内
体内分布
阿霉素
适体
MTT法
离体
癌症研究
癌细胞
体外
化学
流式细胞术
光敏剂
乳腺癌
药理学
癌症
医学
化疗
分子生物学
免疫学
生物化学
内科学
生物
光化学
有机化学
生物技术
作者
Monireh Falsafi,Mahsa Zahiri,Amir Sh. Saljooghi,Khalil Abnous,Seyed Mohammad Taghdisi,Ameneh Sazgarnia,Mohammad Ramezani,Mona Alibolandi
标识
DOI:10.1016/j.micromeso.2021.111337
摘要
Nanoscale porphyrinic metal−organic frameworks have emerged as promising therapeutic system for photodynamic therapy (PDT) of cancer in recent years. Nevertheless, their low selectivity towards malignant tissues is a hindrance for highly efficient cancer photodynamic therapy. In this study, a nano metal-organic framework ([CuL-[AlOH]2]n (Cu MOF), with Cu (II) core, as a PDT active center, was coated with red blood cell (RBC) membrane after loaded with doxorubicin (DOX), to avoid immediate clearance from the bloodstream and persist for longer periods of time in circulation. Then, a carboxylic acid-end aptamer (MUC1) was decorated on the RBC-coated DOX-loaded MOF ([email protected]) in order to provide targeted chemo and photodynamic therapy. The MTT and flow cytometry experiments exhibited that [email protected] provided highly efficient DOX transportation and toxicity against 4T1 and MCF7 breast cancer cells in vitro in comparison to non-targeted [email protected]. On the other hand, the single dose intravenous injection of [email protected] considerably reduced the tumor growth in vivo. The desirable biodistribution, faster liver clearance, and higher tumor accumulation were confirmed by ex vivo fluorescent imaging. Moreover, under irradiation at 630 nm, the fabricated nanostructures exhibited effective synergistic chemo and photodynamic therapy, proved via in vitro MTT assay and tumor ablation in vivo. The developed [email protected] could serve as a potent platform in clinic for targeted chemo-photodynamic dual therapy.
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