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Modified dipeptide-based nanoparticles: vehicles for targeted tumor drug delivery

机译:修饰的基于二肽的纳米颗粒:靶向肿瘤药物递送的载体

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Aim: Different nanoparticles have been investigated to deliver chemotherapeutic agents, but complex synthesis procedures and biocompatibility issues raise concerns in developing them for safe human usage. The aim of this work is to develop a,(3-dehydrophenylalanine-containing, self-assembled, amphipathic dipeptide nanoparticles for tumor-targeted drug delivery and therapy. Materials & methods: Solution-phase peptide synthesis was used to synthesize dipeptides. Nanoparticles were prepared by molecular self-assembly. A tumor distribution study was carried out using a radiolabeling method. Tumor regression studies were carried out in murine ascitic tumors in BALB/c mice and breast tumor xenografts in nonobese diabetic/severe combined immunodeficiency mice. Results: Arg-a,(3-dehydrophenylalanine formed self-assembled nanoparticles that could be easily derivatized with folic acid. Folic acid-derivatized nanoparticles showed enhanced cellular uptake and, when loaded with doxorubicin, showed enhanced tumor regression compared with underivatized nanoparticles or native drug, without any adverse side effects, both in vitro and in vivo.
机译:目的:已经研究了不同的纳米颗粒来递送化学治疗剂,但是复杂的合成程序和生物相容性问题引起了人们对其开发安全性的担忧。这项工作的目的是开发一种用于肿瘤靶向药物递送和治疗的含(3-脱氢苯丙氨酸的,自组装的,两亲性的)二肽纳米颗粒。材料与方法:采用溶液相肽合成法合成二肽。用分子自组装法制备肿瘤,用放射标记法进行肿瘤分布研究,对BALB / c小鼠的小鼠腹水肿瘤和非肥胖/严重合并免疫缺陷小鼠的乳腺异种移植进行肿瘤消退研究。 -a,(3-脱氢苯丙氨酸形成的自组装纳米颗粒可以很容易地用叶酸衍生。叶酸衍生的纳米颗粒与未衍生的纳米颗粒或天然药物相比,细胞吸收增加,与阿霉素相比,载有阿霉素的肿瘤消退增强体内和体外的任何不良副作用。

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