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具有高光热转换效率的钴铁氧体-棉酚配位纳米制剂,通过敏化化疗作用于 Bcl-2 诱导肿瘤细胞凋亡。

Cobalt Ferrite-Gossypol Coordination Nanoagents with High Photothermal Conversion Efficiency Sensitizing Chemotherapy against Bcl-2 to Induce Tumor Apoptosis.

机构信息

School of Life Science and Technology, Xidian University and Engineering Research Center of Molecular and Neuro Imaging, Ministry of Education, Xi'an, Shaanxi, 710126, P. R. China.

International Joint Research Center for Advanced Medical Imaging and Intelligent Diagnosis and Treatment and Xi'an Key Laboratory of Intelligent Sensing and Regulation of trans-Scale Life Information, School of Life Science and Technology, Xidian University, Xi'an, Shaanxi, 710126, P. R. China.

出版信息

Small. 2023 Aug;19(34):e2300104. doi: 10.1002/smll.202300104. Epub 2023 Apr 26.

Abstract

Gossypol is a chemotherapeutic drug that can inhibit the anti-apoptotic protein Bcl-2, but the existing gossypol-related nanocarriers cannot well solve the problem of chemotherapy resistance. Based on the observation that gossypol becomes black upon Fe coordination, it is hypothesized that encasing gossypol in glyceryl monooleate (GMO) and making it coordinate cobalt ferrite will not only improve its photothermal conversion efficiency (PCE) but also help it enter tumor cells. As the drug loading content and drug encapsulation efficiency of gossypol are 10.67% (w/w) and 96.20%, the PCE of cobalt ferrite rises from 14.71% to 36.00%. The synergistic therapeutic effect finally induces tumor apoptosis with a tumor inhibition rate of 96.56%, which is 2.99 and 1.47 times higher than chemotherapy or photothermal therapy (PTT) alone. PTT generated by the GMO nanocarriers under the irradiation of 808 nm laser can weaken tumor hypoxia, thereby assisting gossypol to inhibit Bcl-2. In addition, the efficacy of nanocarriers is also evaluated through T -weighted magnetic resonance imaging. Observations of gossypol-induced apoptosis in tissue slices provide definitive proof of chemotherapy sensitization, indicating that such coordination nanocarriers can be used as an effective preclinical agent to enhance chemotherapy.

摘要

棉酚是一种化疗药物,可抑制抗凋亡蛋白 Bcl-2,但现有的棉酚相关纳米载体并不能很好地解决化疗耐药问题。基于棉酚与铁配位后会变黑的观察结果,推测将棉酚包裹在单油酸甘油酯(GMO)中并使其与钴铁氧体配位,不仅可以提高其光热转换效率(PCE),还可以帮助其进入肿瘤细胞。由于棉酚的载药量和包封率分别为 10.67%(w/w)和 96.20%,钴铁氧体的 PCE 从 14.71%上升至 36.00%。协同治疗效果最终诱导肿瘤细胞凋亡,肿瘤抑制率达到 96.56%,是单独化疗或光热治疗(PTT)的 2.99 倍和 1.47 倍。在 808nm 激光照射下,GMO 纳米载体产生的 PTT 可以减弱肿瘤缺氧,从而协助棉酚抑制 Bcl-2。此外,还通过 T1 加权磁共振成像对纳米载体的疗效进行了评估。组织切片中观察到的棉酚诱导的细胞凋亡提供了化疗增敏的确凿证据,表明这种配位纳米载体可用作增强化疗的有效临床前药物。

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