Ukonaho Telle, Rantanen Terhi, Jämsen Laura, Kuningas Katri, Päkkilä Henna, Lövgren Timo, Soukka Tero
Department of Biotechnology, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland.
Anal Chim Acta. 2007 Jul 16;596(1):106-15. doi: 10.1016/j.aca.2007.05.060. Epub 2007 Jun 8.
Research in the field of immunoassays and labels used in the detection has been recently focused on particulate reporters, which possess very high specific activity that excludes the label as a sensitivity limiting factor. However, the large size and shape of the particulate labels may produce additional problems to immunoassay performance. The aim of this work was to study with two identical non-competitive two-site immunoassays whether up-converting phosphor (UCP) particles are comparable in performance with europium(III) chelate-dyed nanoparticles as particulate labels. In addition we strived to verify the common assumption of the photostability of up-converting phosphor particles supporting their potential applicability in imaging. Detection limits in two-site immunoassay for free prostate-specific antigen (free-PSA) were 0.53 ng L(-1) and 1.3 ng L(-1) using two different up-converting phosphors and 0.16 ng L(-1) using europium(III) nanoparticle. Large size distribution and non-specific binding of up-converting phosphor particles caused assay variation in low analyte concentrations and limited the analytical detection limit. The non-specific binding was the major factor limiting the analytical sensitivity of the immunoassay. The results suggests the need for nanoscaled and uniformly sized UCP-particles to increase the sensitivity and applicability of up-converting phosphor particles. Anti-Stokes photoluminescence of up-converting phosphor particles did not photobleach when measured repeatedly, on the contrary, the time-resolved fluorescence of europium nanoparticles photobleached relatively rapidly.
免疫分析及检测中所用标记领域的研究近来聚焦于颗粒状报告分子,其具有非常高的比活性,从而排除了标记作为灵敏度限制因素。然而,颗粒状标记的大尺寸和形状可能给免疫分析性能带来额外问题。本研究的目的是通过两种相同的非竞争性双位点免疫分析来研究上转换磷光体(UCP)颗粒作为颗粒状标记在性能上是否与铕(III)螯合物染色的纳米颗粒相当。此外,我们努力验证关于上转换磷光体颗粒光稳定性的普遍假设,以支持其在成像中的潜在适用性。使用两种不同的上转换磷光体,双位点免疫分析中游离前列腺特异性抗原(游离PSA)的检测限分别为0.53 ng L⁻¹和1.3 ng L⁻¹,而使用铕(III)纳米颗粒时检测限为0.16 ng L⁻¹。上转换磷光体颗粒的大尺寸分布和非特异性结合在低分析物浓度下导致分析变化,并限制了分析检测限。非特异性结合是限制免疫分析灵敏度的主要因素。结果表明需要纳米级且尺寸均匀的UCP颗粒来提高上转换磷光体颗粒的灵敏度和适用性。上转换磷光体颗粒的反斯托克斯光致发光在重复测量时不会发生光漂白,相反,铕纳米颗粒的时间分辨荧光相对较快地发生光漂白。