Clinical Laboratory Medicine, Anhui University of Science & Technology, Huainan, 232001, China.
Department of Blood Transfusion, Guangzhou 8th People's Hospital, Guangzhou Medical University, Guangzhou, 510440, People's Republic of China.
J Biomed Nanotechnol. 2021 Aug 1;17(8):1690-1698. doi: 10.1166/jbn.2021.3132.
The metabolic product of type I collagen synthesis, intact procollagen type I N propeptide (intact PINP), is a potential marker of bone formation and osteoporosis, which is not affected by kidney function. We sought to establish a chemiluminescent immunoassay method for the detection of serum intact PINP with previously prepared paired monoclonal antibodies and to evaluate the diagnostic value of the assay in osteoporosis. Using the capture molecule and monoclonal antibody as detection molecule, a diagnostic reagent was developed to detect intact PINP in serum with magnetic nanosphere carriers by the chemiluminescence method, and its analytical performance in the laboratory was evaluated. Serum intact PINP was measured in 142 healthy people and 115 osteoporosis patients. Results were matched with results of a similar test kit, Roche total PINP Elecsys Chemiluminescent Immunoassay Assay. Compared with the performance of the Roche PINP assay product, our method had higher sensitivity (0.02 ng/mL), wider linear range (0.02-1500 ng/mL), and anti-interference. Serum intact PINP values in osteoporosis patients were significantly higher than in healthy subjects (p < 0.001). Our method had good consistency compared with the Roche PINP assay ( = 0.9794). This chemiluminescence method for detecting serum intact PINP (CLIA-intact PINP) with magnetic nanosphere carrier technology meets the requirements of a clinical testing reagent and is expected to have clinical application after further evaluation and can compete with expensive imported kits on the market.
I 型胶原合成的代谢产物,完整的前胶原 I N 端肽( intact PINP),是骨形成和骨质疏松症的潜在标志物,其不受肾功能影响。我们试图建立一种化学发光免疫分析方法,用于检测血清中完整的 PINP,该方法使用先前制备的配对单克隆抗体,并评估该检测方法在骨质疏松症中的诊断价值。使用捕获分子和单克隆抗体作为检测分子,通过化学发光法开发了一种诊断试剂,用于检测血清中带有磁性纳米球载体的完整 PINP,并评估其在实验室中的分析性能。测量了 142 名健康人和 115 名骨质疏松症患者的血清完整 PINP。将结果与罗氏总 PINP Elecsys 化学发光免疫分析试剂盒的结果相匹配。与罗氏 PINP 检测试剂盒产品的性能相比,我们的方法具有更高的灵敏度(0.02ng/mL)、更宽的线性范围(0.02-1500ng/mL)和抗干扰性。骨质疏松症患者的血清完整 PINP 值明显高于健康受试者(p<0.001)。与罗氏 PINP 检测试剂盒相比,我们的方法具有良好的一致性( = 0.9794)。这种使用磁性纳米球载体技术检测血清完整 PINP(CLIA-intact PINP)的化学发光方法符合临床检测试剂的要求,预计在进一步评估后具有临床应用前景,并可以与市场上昂贵的进口试剂盒竞争。