Quantification of circulating 1,25-dihydroxyvitamin D by radioimmunoassay with an I-125-labeled tracer

被引:1
|
作者
Hollis, BW
Kamerud, JQ
Kurkowski, A
Beaulieu, J
Napoli, JL
机构
[1] MED UNIV S CAROLINA,DEPT BIOCHEM,CHARLESTON,SC 29425
[2] MED UNIV S CAROLINA,DEPT MOLEC BIOL,CHARLESTON,SC 29425
[3] INCSTAR CORP,STILLWATER,MN 55082
[4] SUNY BUFFALO,SCH MED & BIOMED SCI,DEPT BIOCHEM,BUFFALO,NY 14214
关键词
nutritional status; vitamin D and metabolites; cholecalciferol; calcium metabolism;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
We report here the first RIA for 1,25-dihydroxyvitamin D utilizing a radioiodinated (I-125) tracer. This is also the first validated RIA for 1,25-dihydroxyvitamin D [1,25(OH)(2)D] that does not require sample prepuriiication by HPLC before the binding assay. The assay involves acetonitrile extraction, treatment of the crude extract supernate with sodium periodate, extraction and purification of endogenous 1,25(OH)(2)D by solid-phase chromatography, and finally, quantification by RIA. Calibrators were prepared in stripped human serum and processed exactly the same as samples, eliminating the need for internal control for procedural losses of endogenous 1,25(OH)(2)D. The assay consists of a 2-h room temperature incubation with the primacy antibody, a 20-min incubation with a second antibody, and separation of bound from free by centrifugation. Assay results can be in hand within 5 h. The detection limit of the assay is 2.4 ng/L 1,25-dihydroxyvitamin D-3. Results compare well with those from an accepted radioreceptor assay. Sample pretreatment with sodium periodate is absolutely essential before quantification by RIA; otherwise, concentrations of endogenous 1,25(OH)(2)D may be greatly overestimated.
引用
收藏
页码:586 / 592
页数:7
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