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Competitive Binding Radioassay for the Determination of 5‐Fluorodeoxyuridine and 5‐Fluorodeoxyuridine‐5′‐monophosphate Levels in Plasma and Tumor Tissue

机译:竞争性结合放射分析法测定血浆和肿瘤组织中的5-氟脱氧尿苷和5-氟脱氧尿苷-5-单磷酸水平

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摘要

A competitive binding radioassay was developed to measure 5‐fluoro‐2′‐deoxyuridine (FUDR) as well as 5‐fluoro‐2′‐deoxyuridine monophosphate (FdUMP). FdUMP has been measured by a competitive binding radioassay with thymidylate synthase as the binding enzyme (TS assay). FUDR was enigmatically converted to FdUMP by thymidine kinase, and then the converted FdUMP was measured by the competitive binding assay to determine the concentration of FUDR in plasma and tumor tissue. As little as 100 pg/ml of FUDR or 50 pg/ml of FdUMP can be detected quantitatively by this method. When TS assay and high‐performance liquid chromatography were compared for the measurement of FUDR and FdUMP levels in plasma and tumor tissue of Ehrlich carcinoma (EQ‐bearing mice following administration of FUDR, a close agreement was observed for FUDR levels, though low FdUMP levels were detectable only by the TS assay method. The examination of intracellular metabolism of FUDR in EC cells by this method showed that metabolic conversion of FUDR into FdUMP or 5‐fluorouracil is rapid. Thus, we have established a highly sensitive method for measuring not only FdUMP but also FUDR with TS assay. This should be very useful for experimental and clinical studies on fluoropyrimidines.
机译:开发了一种竞争性结合放射测定法,用于测量5-氟-2'-脱氧尿苷(FUDR)以及5-氟-2'-脱氧尿苷单磷酸(FdUMP)。 FdUMP已经通过以胸苷酸合酶作为结合酶的竞争性结合放射测定法(TS测定法)进行了测定。通过胸苷激酶将FUDR神秘地转化为FdUMP,然后通过竞争结合测定法测量转化的FdUMP,以确定血浆和肿瘤组织中FUDR的浓度。通过这种方法可以定量检测出低至100 pg / ml的FUDR或50 pg / ml的FdUMP。当比较TS测定法和高效液相色谱法测量Ehrlich癌(荷瘤后荷EQ的小鼠)的血浆和肿瘤组织中FUDR和FdUMP的水平时,尽管FdUMP水平较低,但观察到的FUDR水平非常一致仅通过TS法即可检测到,通过这种方法检测EC细胞中FUDR的细胞内代谢表明,FUDR代谢转化为FdUMP或5-氟尿嘧啶的速度很快,因此,我们建立了一种高度灵敏的检测方法FdUMP以及TS分析的FUDR,这对于氟嘧啶的实验和临床研究应该非常有用。

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