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尿中3 - O - 甲基多巴胺的特异性离子交换色谱法和荧光测定法。

Specific ion-exchange chromatography and fluorimetric assay for urinary 3-O-methyldopamine.

作者信息

Dalmaz Y, Peyrin L

出版信息

J Chromatogr. 1976 Jan 21;116(2):379-941. doi: 10.1016/s0021-9673(00)89908-2.

Abstract

A technique for the selective extraction of 3-O-methyldopamine, normetanephrine and metanephrine from a single urine sample has been investigated. After hydrolysis of the conjugates, the diluted mixture is passed through a Dowex 50W-X2 column and the methoxylated amines are eluted by means of concentrated ammonia. The eluate, containing metanephrine, normetanephrine and 3-O-methyldopamine is evaporated, and a solution of the residue in borate buffer is fractionated under strictly controlled conditions on an Amberlite CG-50 column. The three amines so separated are estimated by specific fluorimetric methods. The extraction recovery is 80 +/- 3% for pure solutions and 78 +/- 4% for 3-O-methyldopamine added to urine. The fluorimetric procedure, carried out under well-defined conditions, allows the estimation of 10 ng of 3-O-methethyldopamine. The spectral characteristics of the fluorescent derivative are similar to those obtained with dopamine, so that it can be assumed that iodine oxidation of 3-O-methyldopamine demethylates this compound and oxidises the resulting dopamine to the dopamine fluorophore (5,6-dihydroxy-indole). Of the compounds that might interfere in the fluorimetric procedure, dopamine, DOPA and alpha-methyl-DOPA are destroyed by the ammoniacal elution from the Dowex column and 3-O-methyl-DOPA is eliminated in the effluent from the Amberlite column. The elimination of interfering compounds and the improved separation on Amberlite ensure high specificity for this procedure. We have applied the method to normal urine and to pathological urines from patients with adrenergic tumours or untreated and treated parkinsonian subjects; vital information has been obtained on the prognosis of adrenergic tumours. The presence of large amounts of dopamine, normetanephrine and/or metanephrine does not affect the assay for 3-O-methyldopamine. The method is also applicable to rat and dog urine, and can be applied to tissue extracts with little modification.

摘要

已对从单一尿液样本中选择性提取3 - O - 甲基多巴胺、去甲变肾上腺素和变肾上腺素的技术进行了研究。结合物水解后,将稀释后的混合物通过Dowex 50W - X2柱,并用浓氨洗脱甲氧基化胺类。含有变肾上腺素、去甲变肾上腺素和3 - O - 甲基多巴胺的洗脱液经蒸发后,将残渣溶于硼酸盐缓冲液,在严格控制的条件下于Amberlite CG - 50柱上进行分离。如此分离得到的三种胺类通过特定的荧光法进行测定。纯溶液的提取回收率为80±3%,向尿液中添加3 - O - 甲基多巴胺后的回收率为78±4%。在明确的条件下进行的荧光法可测定10 ng的3 - O - 甲基多巴胺。荧光衍生物的光谱特征与多巴胺的相似,因此可以认为3 - O - 甲基多巴胺的碘氧化使其脱甲基,并将生成的多巴胺氧化为多巴胺荧光团(5,6 - 二羟基吲哚)。在可能干扰荧光法的化合物中,多巴胺、多巴和α - 甲基多巴通过Dowex柱的氨洗脱被破坏,3 - O - 甲基多巴在Amberlite柱的流出物中被去除。干扰化合物的去除以及在Amberlite上分离效果的改善确保了该方法具有高特异性。我们已将该方法应用于正常尿液以及患有肾上腺素能肿瘤的患者、未经治疗和经治疗的帕金森病患者的病理性尿液;已获得有关肾上腺素能肿瘤预后的重要信息。大量多巴胺、去甲变肾上腺素和/或变肾上腺素的存在不影响3 - O - 甲基多巴胺的测定。该方法也适用于大鼠和狗的尿液,稍加修改即可应用于组织提取物。

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