Fehder W P, Ho W Z, Campbell D E, Tourtellotte W W, Michaels L, Cutilli J R, Uvaydova M, Douglas S D
Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, USA.
Clin Diagn Lab Immunol. 1998 May;5(3):303-7. doi: 10.1128/CDLI.5.3.303-307.1998.
We have developed a simple chromatographic procedure for the partial purification of substance P (SP) from acidified plasma and serum samples. We have evaluated a sensitive antigen competition enzyme immunoassay (EIA) for the quantitation of SP. The chromatographic procedure has recovery efficiencies ranging from 94.8 to 125%. The immunoreactivity of unknown amounts of purified SP subjected to the preparative procedure yielded a coefficient of variance of 9.4%. The EIA yielded reproducible standard curves having an interassay (n = 8) correlation coefficient of 0.984. The evaluation of normal adult control serum yielded a mean value of 51 pg/ml (range, 35 to 61 pg/ml). The evaluation of 3.33 x concentrates of serum-derived partially purified SP provided uncorrected SP values of 117 to 201 pg/ml, which fell within the midpoint of the three-decalog standard curve. These studies indicate that both the preparative and quantitative procedures are required for the detection of SP in plasma or serum samples collected from patients with several clinical disorders.
我们已经开发出一种简单的色谱方法,用于从酸化的血浆和血清样本中部分纯化P物质(SP)。我们评估了一种灵敏的抗原竞争酶免疫测定法(EIA)用于定量SP。该色谱方法的回收率在94.8%至125%之间。经过制备程序的未知量纯化SP的免疫反应性产生了9.4%的变异系数。EIA产生了可重复的标准曲线,批间(n = 8)相关系数为0.984。对正常成人对照血清的评估得出平均值为51 pg/ml(范围为35至61 pg/ml)。对血清来源的部分纯化SP的3.33倍浓缩物的评估提供了未经校正的SP值为117至201 pg/ml,其落在十诫标准曲线的中点范围内。这些研究表明,对于从患有多种临床疾病的患者收集的血浆或血清样本中检测SP,制备和定量程序都是必需的。