Yang Chu-Ya, Brooks Evan, Li Yang, Denny Paul, Ho Chih-Ming, Qi Fengxia, Shi Wenyuan, Wolinsky Lawrence, Wu Benjamin, Wong David T W, Montemagno Carlo D
UCLA's Department of Bioengineering, 7523 Boelter Hall, Los Angeles, CA 90095, USA.
Lab Chip. 2005 Oct;5(10):1017-23. doi: 10.1039/b504737d. Epub 2005 Aug 18.
Researchers at UCLA have discovered that the levels of interleukin-8 (IL-8) protein in the saliva of healthy individuals and patients with oropharyngeal squamous cell carcinoma (OSCC) are 30 pM and 86 pM, respectively. In this study, we present the development of the first immunoassay for the quantification of picomolar IL-8 concentrations in human saliva using Biacore surface plasmon resonance (SPR) in a microfluidic channel. A sandwich assay using two monoclonal antibodies, which recognize different epitopes on the antigen (IL-8), was used. Only 13 minutes were required to determine the quantity of pure IL-8 added to just 100 microL of either buffer or saliva-based samples. The limit of detection (LOD) of this immunoassay in buffer was 2.5 pM, and the precision of the response for each concentration was <3% of the coefficient of variation. When first analyzing the saliva supernatants, non-specific binding to the surface was observed. By adding carboxymethyl dextran sodium salt (10 mg mL(-1)) to compete with the surface dextran and primary antibody for non-specific interactions, the signal to noise ratio was greatly improved. The LOD of this immunoassay in saliva was 184 pM. A minimum concentration of 250 pM of exogenous IL-8 could then be consistently detected in a salivary environment. The precision of the response for each IL-8 concentration tested was <7% of the coefficient of variation. Diagnostic sensitivity for oral cancer can be achieved by pre-concentrating the saliva samples 10 fold prior to SPR analysis, making the target levels of IL-8 300 pM for healthy individuals and 860 pM for oral cancer patients.
加州大学洛杉矶分校的研究人员发现,健康个体以及患有口咽鳞状细胞癌(OSCC)的患者唾液中白细胞介素-8(IL-8)蛋白的水平分别为30皮摩尔/升和86皮摩尔/升。在本研究中,我们展示了首个使用微流控通道中的Biacore表面等离子体共振(SPR)技术对人唾液中皮摩尔浓度的IL-8进行定量的免疫测定方法的开发过程。采用了一种夹心测定法,使用两种识别抗原(IL-8)上不同表位的单克隆抗体。仅需13分钟就能测定添加到仅100微升缓冲液或唾液样本中的纯IL-8的量。该免疫测定法在缓冲液中的检测限(LOD)为2.5皮摩尔/升,每个浓度响应的精密度变异系数<3%。在首次分析唾液上清液时,观察到与表面的非特异性结合。通过添加羧甲基葡聚糖钠盐(10毫克/毫升)来与表面葡聚糖和一抗竞争非特异性相互作用,信噪比得到了极大提高。该免疫测定法在唾液中的LOD为184皮摩尔/升。然后在唾液环境中能够始终如一地检测到最低浓度为250皮摩尔/升的外源性IL-8。所测试的每个IL-8浓度响应的精密度变异系数<7%。通过在SPR分析前将唾液样本预浓缩10倍,可以实现对口腔癌的诊断敏感性,使健康个体的IL-8目标水平为300皮摩尔/升,口腔癌患者为860皮摩尔/升。