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Solvent-Free Click-Mechanochemistry for the Preparation of Cancer Cell Targeting Graphene Oxide

机译:无溶剂点击机械化学法制备靶向癌细胞的氧化石墨烯

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摘要

Polyethylene glycol-functionalized nanographene oxide (PEGylated n-GO) was synthesized from alkyne-modified n-GO, using solvent-free click-mechanochemistry, i.e., copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC). The modified n-GO was subsequently conjugated to a mucin 1 receptor immunoglobulin G antibody (anti-MUC1 IgG) via thiol-ene coupling reaction. n-GO derivatives were characterized with Fourier-transformed infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), Bradford assay, sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and atomic force microscopy (AFM). Cell targeting was confirmed in vitro in MDA-MB-231 cells, either expressing or lacking MUC1 receptors, using flow cytometry, confocal laser scanning microscopy (CLSM) and multiphoton (MP) fluorescence microscopy. Biocompatibility was assessed using the modified lactate dehydrongenase (mLDH) assay.
机译:使用无溶剂点击机制化学方法,即由铜(I)催化的叠氮化物-炔烃环加成反应(CuAAC),由炔烃修饰的n-GO合成聚乙二醇官能化的纳米氧化石墨烯(PEG化的n-GO)。修饰的n-GO随后通过硫醇-烯偶联反应与粘蛋白1受体免疫球蛋白G抗体(抗MUC1 IgG)偶联。 n-GO衍生物通过傅立叶变换红外(FT-IR)光谱,热重分析(TGA),布拉德福德测定,十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)和原子力显微镜(AFM)进行表征。使用流式细胞仪,共聚焦激光扫描显微镜(CLSM)和多光子(MP)荧光显微镜,在表达或缺乏MUC1受体的MDA-MB-231细胞中体外确定了细胞靶向性。使用改良的乳酸脱氢酶(mLDH)分析评估生物相容性。

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