Shrivastav Tulsidas G
Department of Reproductive Biomedicine, National Institute of Health and Family Welfare, New Delhi, India.
J Immunoassay Immunochem. 2004;25(3):295-304. doi: 10.1081/ias-200028096.
Peroxidase hydrazides were prepared by conjugating horseradish peroxidase (HRP) to adipic acid dihydrazide (ADH) by carbodiimide or periodate oxidation method. The resulting HRP hydrazides (ADH-HRP) were conjugated to cortisol-21-hemisuccinate (cortisol-21-HS) by forming diimide bonds using the N-hydroxysuccinimide (NHS) carbodiimide mediated reaction. The prepared cortisol-21-HS-ADH-HRP enzyme conjugates were utilized for the development of an enzyme linked immunosorbent assay (ELISA) for direct estimation of cortisol. To the cortisol antibody coated microtiter wells, standard or serum sample (50 microL), along with 100 microL of cortisol-21-HS-ADH-HRP enzyme conjugate (ADH-HRP used is prepared by either carbodiimide or periodate oxidation method), was incubated for 1 hr at 37 degrees C. Bound enzyme activity was measured by using tetramethyl benzidine/hydrogen peroxide (TMB/H202) as substrate. The sensitivity, specificity, and recovery of the assays were found to be identical when ELISAs were employed with cortisol enzyme conjugates prepared by conjugating cortisol-21-HS to HRP hydrazide, made either by the carbodiimide method or periodate oxidation method.
通过碳二亚胺法或高碘酸盐氧化法将辣根过氧化物酶(HRP)与己二酸二酰肼(ADH)偶联制备过氧化物酶酰肼。通过N-羟基琥珀酰亚胺(NHS)碳二亚胺介导的反应形成二酰亚胺键,将所得的HRP酰肼(ADH-HRP)与皮质醇-21-半琥珀酸酯(皮质醇-21-HS)偶联。制备的皮质醇-21-HS-ADH-HRP酶偶联物用于开发直接测定皮质醇的酶联免疫吸附测定(ELISA)。向包被有皮质醇抗体的微量滴定孔中加入标准品或血清样品(50微升),以及100微升皮质醇-21-HS-ADH-HRP酶偶联物(所用的ADH-HRP通过碳二亚胺法或高碘酸盐氧化法制备),在37℃孵育1小时。使用四甲基联苯胺/过氧化氢(TMB/H2O2)作为底物测量结合的酶活性。当ELISA使用通过碳二亚胺法或高碘酸盐氧化法将皮质醇-21-HS与HRP酰肼偶联制备的皮质醇酶偶联物时,发现该测定的灵敏度、特异性和回收率相同。