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负载药物的油酸接枝介孔二氧化硅纳米颗粒与α-乳白蛋白偶联,类似BAMLET样抗癌剂,具有改善的生物相容性和治疗效果。

Drug-loaded oleic-acid grafted mesoporous silica nanoparticles conjugated with α-lactalbumin resembling BAMLET-like anticancer agent with improved biocompatibility and therapeutic efficacy.

作者信息

Pei Wei, Cai Ling, Gong Xing, Zhang Li, Zhang Jiarong, Zhu Ping, Jiang Huijun, Wang Chao, Wang Shoulin, Chen Jin

机构信息

Center for Global Health, School of Public Health, Nanjing Medical University, 211166, Nanjing, China.

School of Chemistry and Chemical Engineering, Southeast University, Nanjing, 211189, China.

出版信息

Mater Today Bio. 2022 May 4;15:100272. doi: 10.1016/j.mtbio.2022.100272. eCollection 2022 Jun.

Abstract

Despite its prominent therapeutic efficacy, chemotherapy has raised serious concerns due to the severe adverse effects and multidrug resistance evoked, which propels the search for safe and green therapeutic agents. BAMLET (bovine α-lactalbumin made lethal against tumor cell) is a well-known protein-based anticancer agent of selective tumoricidal activity. Here, we prepared oleic acid-modified mesoporous silica nanoparticles (OA-MSNs) conjugated with bovine α-lactalbumin, a lipoprotein complex resembling BAMLET formed on the surface of MSNs (MSN-BAMLET) to load the anticancer drug of docetaxel (DTX). Compared to that of OA-MSNs/DTX, the obtained MSN-BAMLET/DTX with a sustained and pH-responsive drug release behaviors exhibited good biocompatibility and enhanced cytotoxic effect against cancer cells. Moreover, the presence of lipoprotein complex in MSN-BAMLET contributed to the improved dispersion of the composite in solution and the inhibitory effect on the migration of cancer cells. Furthermore, the adsorption profiles of protein corona on the obtained nanoparticles were analyzed. It was found that the marked low amount and abundance of plasma proteins were adsorbed on the α-lactalbumin coated siliceous composite demonstrated its long circulation property. Finally, study showed that MSN-BAMLET/DTX contributed to the effective cancer ablation and the prolonged survival. Therefore, the constructed MSN-BAMLET of the mesoregular structure and peculiar tumoricidal effect provides a manipulable nanoplatform as drug nanocarrier for therapeutic applications.

摘要

尽管化疗具有显著的治疗效果,但由于其引发的严重不良反应和多药耐药性,已引起了人们的严重关注,这推动了对安全、绿色治疗剂的探索。BAMLET(牛α-乳白蛋白对肿瘤细胞具有致死性)是一种著名的具有选择性杀肿瘤活性的基于蛋白质的抗癌剂。在此,我们制备了与牛α-乳白蛋白共轭的油酸修饰介孔二氧化硅纳米颗粒(OA-MSNs),在MSNs表面形成了一种类似于BAMLET的脂蛋白复合物(MSN-BAMLET),用于负载抗癌药物多西他赛(DTX)。与OA-MSNs/DTX相比,所获得的具有持续和pH响应药物释放行为的MSN-BAMLET/DTX表现出良好的生物相容性和增强的对癌细胞的细胞毒性作用。此外,MSN-BAMLET中脂蛋白复合物的存在有助于提高复合材料在溶液中的分散性以及对癌细胞迁移的抑制作用。此外,还分析了所得纳米颗粒上蛋白质冠层的吸附情况。结果发现,血浆蛋白在α-乳白蛋白包被的硅质复合材料上的吸附量显著较低且丰度较低,这表明其具有长循环特性。最后,研究表明MSN-BAMLET/DTX有助于有效的癌症消融和延长生存期。因此,构建的具有介观规则结构和独特杀肿瘤作用的MSN-BAMLET为治疗应用提供了一种可操控的作为药物纳米载体的纳米平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0afb/9123267/2972588dea96/ga1.jpg

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