Development and evaluation of a chromatographic procedure for partial purification of substance P with quantitation by an enzyme immunoassay

被引:25
作者
Fehder, WP
Ho, WZ
Campbell, DE
Tourtellotte, WW
Michaels, L
Cutilli, JR
Uvaydova, M
Douglas, SD
机构
[1] Childrens Hosp Philadelphia, Clin Immunol Labs, Div Infect Dis & Immunol, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Pediat, Div Infect Dis & Immunol, Philadelphia, PA 19104 USA
[3] Joseph Stokes Jr Res Inst, Philadelphia, PA USA
[4] Vet Affairs Med Ctr, Multiple Sclerosis Human Neurospecimen Bank, Los Angeles, CA USA
关键词
D O I
10.1128/CDLI.5.3.303-307.1998
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:303 / 307
页数:5
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