INQUISAL, Departamento de Química, Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco 917, San Luis, Argentina.
Instituto Tecnológico de Chascomús (IIB-INTECH) CONICET-Universidad Nacional de General San Martín, Camino de Circunvalación Laguna Km. 6 CC 164, B7130IWA, Chascomús, Provincia de Buenos Aires, Argentina.
Anal Biochem. 2019 Jan 1;564-565:116-122. doi: 10.1016/j.ab.2018.10.025. Epub 2018 Oct 28.
This article describes a microfluidic LIF immunosensor for the quantitative determination of anti-Toxoplasma gondii IgG (anti-T. gondii) specific antibodies. The serological detection of these antibodies plays a crucial role in the clinical diagnosis of toxoplasmosis. Zinc oxide nanoparticles (ZnO-NPs) obtained by wet chemical procedure were covered with chitosan and then used to conjugate T-gondii antigens into the central microfluidic channel. Serum samples containing anti-T-gondii IgG antibodies were injected into the immunosensor where they interact immunologically with T. gondii antigens. Bound antibodies were quantified by the addition of anti-IgG antibodies labeled whit alkaline phosphatase (ALP). ALP enzymatically converts the non-fluorescent 4-methylumbelliferyl phosphate (4-MUP) to soluble fluorescent methylumbelliferone that was measured using excitation at 355 nm and emission at 440 nm. The relative fluorescent response of methylumbelliferone is proportional to the concentration of anti-T. gondii IgG antibodies. The coefficients of variation are less than 4.73% for within-day assays and less than 6.34% for between-day assays. Results acquired by LIF immunosensor agree with those obtained by enzyme-linked immunosorbent assay method, suggesting that the designed sensor represents a promising tool for the quantitative determination of anti-T. gondii IgG antibodies of clinical samples.
本文介绍了一种用于定量测定抗弓形虫 IgG(抗-T. gondii)特异性抗体的微流控 LIF 免疫传感器。这些抗体的血清学检测在弓形虫病的临床诊断中起着至关重要的作用。通过湿化学程序获得的氧化锌纳米粒子(ZnO-NPs)被壳聚糖覆盖,然后用于将 T-gondii 抗原共轭到中央微流控通道中。含有抗-T-gondii IgG 抗体的血清样本被注入免疫传感器中,在那里它们与 T. gondii 抗原发生免疫相互作用。结合的抗体通过添加碱性磷酸酶(ALP)标记的抗 IgG 抗体进行定量。ALP 酶促将非荧光的 4-甲基伞形酮磷酸盐(4-MUP)转化为可溶的荧光甲基伞形酮,通过以 355nm 激发和 440nm 发射来测量。甲基伞形酮的相对荧光响应与抗-T. gondii IgG 抗体的浓度成正比。日内检测的变异系数小于 4.73%,日间检测的变异系数小于 6.34%。LIF 免疫传感器获得的结果与酶联免疫吸附测定法获得的结果一致,表明设计的传感器代表了一种用于定量测定临床样本中抗-T. gondii IgG 抗体的有前途的工具。