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

机译:聚(苹果酸)的纳米缀合物具有用于药物递送的功能模块

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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:β-聚(L-苹果酸)(PMLA)的纳米缀合物已经用活性递送的模块,药物释放,通过反义寡核苷酸封闭肿瘤源核苷酸,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是无毒的,非免疫原性,可生物降解的,可生物降解,非常适合作为定制纳米缀合物化学的支架。 550 kDa的纳米缀合物允许植入小鼠的脑肿瘤和乳腺癌的荧光成像,靶向肿瘤组织固有的增强渗透性和保留(EPR)和抗体识别。纳米缀合物被设计成通过预防血管生成来抑制肿瘤生长。

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