首页> 外文期刊>Biomaterials Science >Green synthesis of methoxy-poly(ethylene glycol)-block-poly(l-lactide-co-glycolide) copolymer using zinc proline as a biocompatible initiator for irinotecan delivery to colon cancer in vivo
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Green synthesis of methoxy-poly(ethylene glycol)-block-poly(l-lactide-co-glycolide) copolymer using zinc proline as a biocompatible initiator for irinotecan delivery to colon cancer in vivo

机译:甲氧基聚(乙二醇)的绿色合成 - 用锌脯氨酸作为氨基甘替康的生物相容性引发剂在体内递送至结肠癌的生物相容性引发剂的共聚物

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摘要

Poly(lactic-co-glycolic acid) (PLGA) is the most commonly described biocompatible copolymer used in biomedical applications. In this work, a green synthetic approach based on the biocompatible zinc proline complex, as an initiator for PLGA synthesis, is reported for the first time for the synthesis of methoxy-poly(ethylene glycol)-block-poly(l-lactic-co-glycolic acid) (mPEG-PLGA). mPEG-PLGA with controlled molecular weight and narrow polydispersity was synthesised. Its potential for delivery of irinotecan (Ir), a poorly water-soluble chemotherapeutic drug used for the treatment of colon and pancreatic cancer, was studied. Nanoparticles of controlled size (140-160 nm), surface charge (similar to-10 mV), release properties and cytotoxicity against CT-26 (colon) and BxPC-3 (pancreatic) cancer cells, were prepared. Tumor accumulation was confirmed by optical imaging of fluorescently labelled nanoparticles. Unlike Tween (R) 80 coated NP-Ir, the Pluronic (R) F-127 coated NP-Ir exhibits significant tumor growth delay compared to untreated and blank formulation treated groups in the CT-26 subcutaneous tumor model, after 4 treatments of 30 mg irinotecan per kg dose. Overall, this proof-of-concept study demonstrates that the newly synthesized copolymer, via a green route, is proven to be nontoxic, requires fewer purification steps and has potential applications in drug delivery.
机译:聚(乳酸二乙醇酸)(PLGA)是最常用于生物医学应用中的生物相容性共聚物。在这项工作中,首次向PLGA合成引发剂的基于生物相容性锌脯氨酸复合物的绿色合成方法是用于合成甲氧基 - 聚(乙二醇)-Block-poly(L-Lactic-Co - 乙醇酸)(MPEG-PLGA)。合成了具有受控分子量和窄多分散性的MPEG-PLGA。研究了Irinotecan(IR)的潜力,用于治疗结肠和胰腺癌的水溶性不良化学治疗药物。制备了控制尺寸(140-160nm),表面电荷(类似于-10mV),对CT-26(结肠)和BxPC-3(胰腺)癌细胞的释放性质和细胞毒性的纳米颗粒。通过荧光标记的纳米颗粒的光学成像证实了肿瘤积累。与吐温(R)80涂覆的NP-IR不同,与CT-26皮下肿瘤模型中的未处理和空白配方处理的组相比,PluronicF-127涂覆的NP-IR表现出显着的肿瘤生长延迟,在30例治疗后4例Mg每kg剂量的Mg Irinotecan。总体而言,这种概念证明研究表明,通过绿色途径,新合成的共聚物被证明是无毒的,需要较少的纯化步骤并具有药物递送中的潜在应用。

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  • 来源
    《Biomaterials Science》 |2021年第3期|共12页
  • 作者单位

    CSIR Natl Chem Lab Polymer Sci &

    Engn Div Pune 411008 Maharashtra India;

    Kings Coll London Fac Life Sci &

    Med Sch Canc &

    Pharmaceut Sci London SE1 9NH England;

    Kings Coll London Fac Life Sci &

    Med Sch Canc &

    Pharmaceut Sci London SE1 9NH England;

    CSIR Natl Chem Lab Polymer Sci &

    Engn Div Pune 411008 Maharashtra India;

    Kings Coll London Fac Life Sci &

    Med Sch Canc &

    Pharmaceut Sci London SE1 9NH England;

    Kings Coll London Fac Life Sci &

    Med Sch Canc &

    Pharmaceut Sci London SE1 9NH England;

    Kings Coll London Fac Life Sci &

    Med Sch Canc &

    Pharmaceut Sci London SE1 9NH England;

    Kings Coll London Fac Life Sci &

    Med Sch Canc &

    Pharmaceut Sci London SE1 9NH England;

    CSIR Natl Chem Lab Polymer Sci &

    Engn Div Pune 411008 Maharashtra India;

    Kings Coll London Fac Life Sci &

    Med Sch Canc &

    Pharmaceut Sci London SE1 9NH England;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
  • 关键词

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