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Development and Screening of a Series of Antibody-Conjugated and Silica-Coated Iron Oxide Nanoparticles for Targeting the Prostate-Specific Membrane Antigen

机译:一系列针对前列腺特异性膜抗原的抗体偶联和二氧化硅包覆的氧化铁纳米粒子的开发和筛选。

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The prostate-specific membrane antigen (PSMA) is an established target for the delivery of cancer therapeutic and imaging agents due to its high expression on the surface of prostate cancer cells and within the neovasculature of other solid tumors. Here, we describe the synthesis and screening of antibody-conjugated silica-coated iron oxide nanoparticles for PSMA-specific cell targeting. The humanized anti-PSMA antibody, HuJ591, was conjugated to a series of nanoparticles with varying densities of polyethylene glycol and primary amine groups. Customized assays utilizing iron spectral absorbance and enzyme-linked immunoassay (ELISA) were developed to screen microgram quantities of nanoparticle formulations for immunoreactivity and cell targeting ability. Antibody and PSMA-specific targeting of the optimized nanoparticle was evaluated using an isogenic PSMA-positive and PSMA-negative cell line pair. Specific nanoparticle targeting was confirmed by iron quantification with inductively coupled plasma mass spectrometry (ICP-MS). These methods and nanoparticles support the promise of targeted theranostic agents for future treatment of prostate and other cancers.
机译:前列腺特异性膜抗原(PSMA)由于在前列腺癌细胞表面和其他实体瘤的新脉管系统中高表达,因此是递送癌症治疗剂和显像剂的既定目标。在这里,我们描述了针对PSMA特异性细胞靶向的抗体偶联的二氧化硅包被的氧化铁纳米颗粒的合成和筛选。人源化抗PSMA抗体HuJ591与一系列具有不同密度的聚乙二醇和伯胺基团的纳米颗粒偶联。开发了利用铁光谱吸收和酶联免疫测定(ELISA)的定制测定法,以筛选微克量的纳米颗粒制剂的免疫反应性和细胞靶向能力。使用同基因的PSMA阳性和PSMA阴性细胞系对评估了优化纳米颗粒的抗体和PSMA特异性靶向。通过电感耦合等离子体质谱法(ICP-MS)对铁进行定量,确定了特定的纳米粒子靶向性。这些方法和纳米颗粒支持靶向治疗药物有望用于将来治疗前列腺癌和其他癌症。

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