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一种改进的应用,用于在德灵-拜耳Dimension RxL Max临床化学系统上采用酶增强免疫测定技术检测咖啡因、阿米卡星和甲氨蝶呤。

An improved application for the enzyme multipled immunoassay technique for caffeine, amikacin, and methotrexate assays on the Dade-Behring Dimension RxL Max clinical chemistry system.

作者信息

Mendu Damodara Rao, Chou Peter P, Soldin Steven J

机构信息

Department of Medicine, Georgetown University and Georgetown Clinical Research Center, Washington, DC, USA.

出版信息

Ther Drug Monit. 2007 Oct;29(5):632-7. doi: 10.1097/FTD.0b013e3181570791.

Abstract

Caffeine is widely used in children's hospitals to treat neonatal apnea. Amikacin is used for treating hospital-acquired infections caused by Gram-negative bacteria resistant to other aminoglycosides. The blood levels, however, have to be monitored carefully because of its ototoxicity and nephrotoxicity. Methotrexate (MTX) is used as a chemotherapeutic agent in the treatment of leukemia and lymphoma as well as of certain solid tumors. Current enzyme multiplied immunoassay technique (EMIT) assays for caffeine, amikacin, and MTX lack low-end precision. In addition, the EMIT assays for MTX lack the sensitivity of reliable quantification to 0.05 micromol/L needed because of today's more rigorous requirements. The goal of the present study was to optimize the EMIT method parameters on the Dimension RxL Max, thereby providing applications with improved precision for all the three analytes and enhancing the sensitivity of the EMIT methotrexate assay. Serum samples were measured for caffeine, amikacin, and MTX by EMIT on the Dimension RxL Max and by EMIT (on the Olympus AU 600 for caffeine) and fluorescence polarization immunoassay [for MTX and amikacin (FPIA; TDx FLx)] at Quest Diagnostics. The new instrument method parameters that use larger sample volumes and longer observation of optical density changes (caffeine, MTX) provide improved sensitivity for MTX permitting reliable measurement at 0.05 micromol/L and improved precision for all three analytes. Within- and between-day imprecision were less than 6% for low to high concentrations of caffeine and amikacin controls and are less than 7.5% for MTX concentrations greater than 0.3 micromol/L and 12.3% at 0.06 micromol/L. The correlation coefficients for caffeine, amikacin, and MTX plotted for the Dimension RxL Max versus the methods used at Quest Diagnostics were 0.973, 0.986, and 0.992, respectively. These EMIT method applications now compare well with other established assays. The new Dimension RxL Max method parameters provide greatly improved precision and also meet today's clinical sensitivity guidelines (0.05 micromol/L) for MTX.

摘要

咖啡因在儿童医院被广泛用于治疗新生儿呼吸暂停。阿米卡星用于治疗由对其他氨基糖苷类耐药的革兰氏阴性菌引起的医院获得性感染。然而,由于其耳毒性和肾毒性,必须密切监测其血药浓度。甲氨蝶呤(MTX)用作化疗药物,用于治疗白血病、淋巴瘤以及某些实体瘤。目前用于检测咖啡因、阿米卡星和MTX的酶放大免疫分析技术(EMIT)缺乏低端精度。此外,由于当今要求更为严格,用于检测MTX的EMIT分析缺乏可靠定量至0.05微摩尔/升所需的灵敏度。本研究的目的是优化Dimension RxL Max上的EMIT方法参数,从而提高所有三种分析物检测的精度,并提高EMIT甲氨蝶呤分析的灵敏度。通过Dimension RxL Max上的EMIT以及在奎斯特诊断公司通过EMIT(咖啡因检测使用奥林巴斯AU 600)和荧光偏振免疫分析[用于MTX和阿米卡星(FPIA;TDx FLx)]对血清样本进行咖啡因、阿米卡星和MTX检测。使用更大样本量和更长光密度变化观察时间(咖啡因、MTX)的新仪器方法参数提高了MTX的灵敏度,使其能够在0.05微摩尔/升进行可靠测量,并提高了所有三种分析物检测的精度。低至高浓度的咖啡因和阿米卡星对照品的批内和批间不精密度均小于6%,MTX浓度大于0.3微摩尔/升时不精密度小于7.5%,0.06微摩尔/升时为12.3%。绘制的Dimension RxL Max与奎斯特诊断公司使用的方法之间的咖啡因、阿米卡星和MTX的相关系数分别为0.973、0.986和0.992。这些EMIT方法应用现在与其他既定检测方法相当。新的Dimension RxL Max方法参数大大提高了精度,也符合当今MTX的临床灵敏度指南(0.05微摩尔/升)。

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