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首页> 外文期刊>Nanotechnology >The effects of size and synthesis methods of gold nanoparticle-conjugated MαHIgG_4 for use in an immunochromatographic strip test to detect brugian filariasis
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The effects of size and synthesis methods of gold nanoparticle-conjugated MαHIgG_4 for use in an immunochromatographic strip test to detect brugian filariasis

机译:纳米金结合的MαHIgG_4的大小和合成方法对免疫丝氨酸条检验检测布鲁氏丝虫病的影响

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This study describes the properties of colloidal gold nanoparticles (AuNPs) with sizes of 20, 30 and 40 nm, which were synthesized using citrate reduction or seeding-growth methods. Likewise, the conjugation of these AuNPs to mouse anti-human IgG_4 (MαHIgG_4) was evaluated for an immunochromatographic (ICG) strip test to detect brugian filariasis. The morphology of the AuNPs was studied based on the degree of ellipticity (G) of the transmission electron microscopy images. The AuNPs produced using the seeding-growth method showed lower ellipticity (G ≤ 1.11) as compared with the AuNPs synthesized using the citrate reduction method (G ≤ 1.18). Zetasizer analysis showed that the AuNPs that were synthesized using the seeding-growth method were almost monodispersed with a lower polydispersity index (PDI; PDI≤0.079), as compared with the AuNPs synthesized using the citrate reduction method (PDI≤0.177). UV-visible spectroscopic analysis showed a red-shift of the absorbance spectra after the reaction with MαHIgG_4, which indicated that the AuNPs were successfully conjugated. The optimum concentration of the BmR1 recombinant antigen that was immobilized on the surface of the ICG strip on the test line was 1.0 mg ml ~(-1). When used with the ICG test strip assay and brugian filariasis serum samples, the conjugated AuNPs-MαHIgG_4 synthesized using the seeding-growth method had faster detection times, as compared with the AuNPs synthesized using the citrate reduction method. The 30 nm AuNPs- MαHIgG_4, with an optical density of 4 from the seeding-growth method, demonstrated the best performance for labelling ICG strips because it displayed the best sensitivity and the highest specificity when tested with serum samples from brugian filariasis patients and controls.
机译:这项研究描述了大小为20、30和40 nm的胶体金纳米颗粒(AuNP)的性质,这些纳米颗粒是使用柠檬酸盐还原法或种子生长法合成的。同样,对这些AuNP与小鼠抗人IgG_4(MαHIgG_4)的缀合进行了免疫色谱(ICG)剥离测试,以检测比利时丝虫病。基于透射电子显微镜图像的椭圆度(G)研究AuNPs的形态。与使用柠檬酸盐还原法合成的AuNPs(G≤1.18)相比,使用种子生长法生产的AuNPs的椭圆度较低(G≤1.11)。 Zetasizer分析表明,与使用柠檬酸盐还原法合成的AuNPs(PDI≤0.177)相比,使用种子生长法合成的AuNPs几乎单分散,具有较低的多分散指数(PDI;PDI≤0.079)。紫外可见光谱分析表明,与MαHIgG_4反应后,吸光度光谱发生红移,表明AuNPs已成功偶联。固定在测试线上ICG试纸条表面的BmR1重组抗原的最佳浓度为1.0 mg ml〜(-1)。当与ICG试纸条检测和布鲁氏丝虫病血清样品一起使用时,与使用柠檬酸盐还原法合成的AuNPs相比,使用种子生长法合成的缀合的AuNPs-MαHIgG_4具有更快的检测时间。 30 nmAuNPs-MαHIgG_4的种子生长法测光密度为4,显示了标记ICG条的最佳性能,因为用布鲁氏丝虫病患者和对照的血清样品测试时,它显示出最佳的灵敏度和最高的特异性。

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