Suppr超能文献

用于个性化癌症治疗的包裹协同药物的肿瘤靶向荧光类蛋白纳米胶囊

Tumor-Targeted Fluorescent Proteinoid Nanocapsules Encapsulating Synergistic Drugs for Personalized Cancer Therapy.

作者信息

Itzhaki Ella, Hadad Elad, Moskovits Neta, Stemmer Salomon M, Margel Shlomo

机构信息

Department of Chemistry, Institute of Nanotechnology and Advanced Materials (BINA), Bar-Ilan University, Ramat-Gan 5290002, Israel.

Davidoff Center, Rabin and Felsenstein Medical Center, Beilinson Campus, Petach Tikva 49100, Israel.

出版信息

Pharmaceuticals (Basel). 2021 Jul 6;14(7):648. doi: 10.3390/ph14070648.

Abstract

Personalized cancer treatment based on specific mutations offers targeted therapy and is preferred over "standard" chemotherapy. Proteinoid polymers produced by thermal step-growth polymerization of amino acids may form nanocapsules (NCs) that encapsulate drugs overcoming miscibility problems and allowing passive targeted delivery with reduced side effects. The arginine-glycine-glutamic acid (RGD) sequence is known for its preferential attraction to αvβ3 integrin, which is highly expressed on neovascular endothelial cells that support tumor growth. Here, tumor-targeted RGD-based proteinoid NCs entrapping a synergistic combination of Palbociclib (Pal) and Alpelisib (Alp) were synthesized by self-assembly to induce the reduction of tumor cell growth in different types of cancers. The diameters of the hollow and drug encapsulating poly(RGD) NCs were 34 ± 5 and 22 ± 3 nm, respectively; thereby, their drug targeted efficiency is due to both passive and active targeting. The encapsulation yield of Pal and Alp was 70 and 90%, respectively. In vitro experiments with A549, MCF7 and HCT116 human cancer cells demonstrate a synergistic effect of Pal and Alp, controlled release and dose dependence. Preliminary results in a 3D tumor spheroid model with cells derived from patient-derived xenografts of colon cancer illustrate disassembly of spheroids, indicating that the NCs have therapeutic potential.

摘要

基于特定突变的个性化癌症治疗提供了靶向治疗,比“标准”化疗更受青睐。通过氨基酸热逐步生长聚合产生的类蛋白聚合物可形成纳米胶囊(NCs),其包裹药物可克服混溶性问题,并实现副作用减少的被动靶向递送。精氨酸-甘氨酸-谷氨酸(RGD)序列因其对αvβ3整合素的优先吸引力而闻名,αvβ3整合素在支持肿瘤生长的新生血管内皮细胞上高度表达。在此,通过自组装合成了包裹帕博西尼(Pal)和阿培利司(Alp)协同组合的基于RGD的肿瘤靶向类蛋白NCs,以诱导不同类型癌症中肿瘤细胞生长的减少。中空和包裹药物的聚(RGD)NCs的直径分别为34±5和22±3nm;因此,它们的药物靶向效率归因于被动靶向和主动靶向。Pal和Alp的包封率分别为70%和90%。对A549、MCF7和HCT116人癌细胞进行的体外实验证明了Pal和Alp的协同作用、控释和剂量依赖性。在由结肠癌患者来源的异种移植瘤细胞构建的三维肿瘤球体模型中的初步结果表明球体解体,这表明NCs具有治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6065/8308547/1cd1895a8ee1/pharmaceuticals-14-00648-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验