【24h】

Nanoconjugates of Poly(malic acid) with Functional Modules for Drug Delivery

机译:聚苹果酸与药物功能模块的纳米共轭物

获取原文

摘要

Nanoconjugates of β-poly(L-malic acid) (PMLA) have been synthesized with modules active in drug delivery, drug release, blocking of tumor-affiliated mRNA by antisense oligonucleotides, penetration of blood and cellular barriers, tissue targeting, membrane permeation, fluorescence, and protection. PMLA of microbial origin is non-toxic, non-immunogenic, biodegradable and highly suited as a scaffold for tailored nanoconjugate chemistry. The nanoconjugate of 550 kDa allowed fluorescence imaging of brain tumor and breast cancer implanted on mouse, targeted on the basis of tumor tissue-inherent enhanced permeability and retention (EPR) and antibody recognition. The nanoconjugates were designed to inhibit tumor growth by preventing angiogenesis.
机译:已合成了具有β-聚(L-苹果酸)(PMLA)纳米共轭物的模块,这些模块具有以下功能:药物递送,药物释放,反义寡核苷酸阻断肿瘤相关的mRNA,血液和细胞屏障的渗透,组织靶向,膜渗透,荧光和保护。微生物来源的PMLA无毒,无免疫原性,可生物降解,非常适合用于定制的纳米共轭物化学。 550 kDa的纳米共轭物可对植入小鼠的脑部肿瘤和乳腺癌进行荧光成像,其目标是基于肿瘤组织固有的增强的通透性和保留(EPR)和抗体识别。纳米缀合物被设计为通过预防血管生成来抑制肿瘤生长。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号