Mojaverian P, Green P J, Jhangiania R K, Chase G D
Department of Medicine, Jefferson Medical College, Philadelphia, Pennsylvania.
J Pharm Biomed Anal. 1989;7(5):585-92. doi: 10.1016/0731-7085(89)80224-9.
Digoxin-like immunoreactive substance (DLIS) was measured in 34 samples obtained from subjects not receiving digoxin: 10 uremic, 10 third trimester pregnancy, seven cord blood and seven normal. DLIS concentration was measured by four commercial polyclonal radioimmunoassay (RIA) systems: Clinical Assay (CA), Corning Immophase (CI), Diagnostic Products Double Antibody (DP), Kallestad Quantitope (KK), a monoclonal antibody (MA) assay and a Fluorescence Polarization Immunoassay (FPIA). In general, the cord blood samples were richer in DLIS. Digoxin immunoassays, MA and DP showed minimal interference by DLIS in all samples, whereas FPIA and CA exhibited the maximal cross-reactivity with DLIS. In cord blood samples, mean +/- SD DLIS concentration ranged from 0.41 +/- 0.13 (by CA) to 0.034 +/- 0.02 ng ml-1 as measured by MA assay. In uremics, the mean DLIS concentration was below the detection limit of all RIA assays. The FPIA method showed a higher degree of cross-reactivity to DLIS, especially in the cord and pregnancy samples (0.42 +/- 0.13 and 0.4 +/- 0.14 ng ml-1, respectively). DLIS in uremics was below the FPIA detection limit of 0.2 ng ml-1. Overall, the degree of interference by DLIS in decreasing order was FPIA greater than CA greater than CI greater than or equal to KQ greater than DP greater than or equal to MA. The cord blood samples were re-analysed by FPIA (Digoxin-II assay) 4 months later, resulting in 2-4-fold higher DLIS concentrations for these samples. This appears to be due to the substitution of 5-sulphosalicylic acid as a protein precipitating reagent and this effect may have been accentuated by freeze-thaw cycles.
在34份未接受地高辛治疗的受试者样本中检测了地高辛样免疫反应物质(DLIS):10份尿毒症患者样本、10份孕晚期孕妇样本、7份脐带血样本和7份正常样本。通过四种商用多克隆放射免疫分析(RIA)系统检测DLIS浓度:临床分析(CA)、康宁免疫相(CI)、诊断产品双抗体(DP)、卡莱斯塔德定量表位(KK)、一种单克隆抗体(MA)分析和一种荧光偏振免疫分析(FPIA)。总体而言,脐带血样本中的DLIS含量更高。地高辛免疫分析中,MA和DP在所有样本中受DLIS的干扰最小,而FPIA和CA与DLIS的交叉反应性最大。在脐带血样本中,通过CA检测的平均±标准差DLIS浓度范围为0.41±0.13(ng/ml),通过MA分析检测为0.034±0.02 ng/ml。在尿毒症患者中,平均DLIS浓度低于所有RIA分析的检测限。FPIA方法对DLIS的交叉反应性更高,尤其是在脐带血和孕妇样本中(分别为0.42±0.13和0.4±0.14 ng/ml)。尿毒症患者中的DLIS低于FPIA的检测限0.2 ng/ml。总体而言,DLIS的干扰程度从高到低依次为:FPIA>CA>CI≥KQ>DP≥MA。4个月后,通过FPIA(地高辛-II分析)对脐带血样本进行重新分析,这些样本的DLIS浓度升高了2至4倍。这似乎是由于用5-磺基水杨酸替代了蛋白质沉淀剂,而冻融循环可能加剧了这种效应。