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采用液相色谱串联质谱法测定干血斑和尿液中作为丹磺酰腙的琥珀酰丙酮。

Determination of succinylacetone in dried blood spots and liquid urine as a dansylhydrazone by liquid chromatography tandem mass spectrometry.

作者信息

Al-Dirbashi Osama Y, Rashed Mohamed S, Brink Herman J Ten, Jakobs Cornelis, Filimban Najlaa, Al-Ahaidib Lujane Y, Jacob Minnie, Al-Sayed Moeen M, Al-Hassnan Zuhair, Faqeih Eissa

机构信息

Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Takhsussi Road, MBC-03, Riyadh 11211, Saudi Arabia.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Feb 2;831(1-2):274-80. doi: 10.1016/j.jchromb.2005.12.010. Epub 2005 Dec 27.

Abstract

Succinylacetone (SA) is a specific marker for the inherited metabolic disease, hepatorenal tyrosinemia. We developed a stable-isotope dilution liquid chromatography tandem mass spectrometry for the determination of SA in dried blood spots (DBS) and liquid urine using a (13)C(4)-SA as internal standard. SA was extracted, converted to the butyl ester and derivatized with dansylhydrazine (Dns-H). Calibration curves in DBS and urine calibrators were linear up to 100 and 30 microM, respectively. At a signal-to-noise ratio of 3, the limits of detection in DBS and urine were 0.2 and 0.005 microM, respectively. Total run time was 5 min. Intra- and inter-assay precision expressed as coefficient of variation were better than 9.1% with more than 96% recovery. The method was applied retrospectively and prospectively for the diagnosis of hepatorenal tyrosinemia and for follow-up of patients under treatment.

摘要

琥珀酰丙酮(SA)是遗传性代谢疾病肝肾酪氨酸血症的一种特异性标志物。我们开发了一种稳定同位素稀释液相色谱串联质谱法,以(13)C(4)-SA作为内标,用于测定干血斑(DBS)和液体尿液中的SA。SA被提取出来,转化为丁酯并用丹磺酰肼(Dns-H)进行衍生化。DBS和尿液校准品中的校准曲线分别在高达100和30 microM时呈线性。在信噪比为3时,DBS和尿液中的检测限分别为0.2和0.005 microM。总运行时间为5分钟。以变异系数表示的批内和批间精密度优于9.1%,回收率超过96%。该方法被回顾性和前瞻性地应用于肝肾酪氨酸血症的诊断以及治疗中患者的随访。

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