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血浆和血清中硫酸盐定量分析方法。

Analytical methods for quantitating sulfate in plasma and serum.

作者信息

Vijayakumar Prasidhee, Dawson Paul A

机构信息

Mater Research Institute, The University of Queensland, Woolloongabba QLD, Australia.

出版信息

Essays Biochem. 2024 Dec 4;68(4):383-389. doi: 10.1042/EBC20230092.

DOI:10.1042/EBC20230092
PMID:38699863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11625858/
Abstract

Circulating sulfate needs to be maintained at sufficiently high levels for healthy growth and development. Animal studies have shown the adverse physiological consequences of low circulating sulfate level on the skeletal, neurological and reproductive systems. However, sulfate is not routinely measured in clinical investigations, despite the importance of sulfate being documented over the past several decades. Several methods have been developed for measuring serum and plasma sulfate level in animals and humans, including a range of barium sulfate precipitation techniques that have been a major focus of sulfate analytics since the 1960s. Evaluation of an ion chromatography method demonstrated its utility for investigation of sulfate levels in human health. More recently, liquid chromatography-tandem mass spectrometry has been used to show hyposulfatemia in a human case of mild skeletal dysplasia. This article provides an overview of analytical methods for measuring sulfate in serum and plasma, highlighting the strengths and limitations of each method.

摘要

循环中的硫酸盐需要维持在足够高的水平以实现健康的生长和发育。动物研究表明,循环中硫酸盐水平过低会对骨骼、神经和生殖系统产生不良生理影响。然而,尽管在过去几十年中已经证明了硫酸盐的重要性,但在临床研究中并不常规测量硫酸盐。已经开发了几种用于测量动物和人类血清及血浆中硫酸盐水平的方法,包括一系列硫酸钡沉淀技术,自20世纪60年代以来,这些技术一直是硫酸盐分析的主要重点。对一种离子色谱法的评估证明了其在研究人类健康中硫酸盐水平方面的实用性。最近,液相色谱-串联质谱法已被用于显示一例轻度骨骼发育不良人类病例中的低硫酸盐血症。本文概述了测量血清和血浆中硫酸盐的分析方法,突出了每种方法的优缺点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8188/11625858/d3b6264d5aac/ebc-68-ebc20230092-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8188/11625858/09a061cdf439/ebc-68-ebc20230092-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8188/11625858/d3b6264d5aac/ebc-68-ebc20230092-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8188/11625858/09a061cdf439/ebc-68-ebc20230092-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8188/11625858/d3b6264d5aac/ebc-68-ebc20230092-g2.jpg

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本文引用的文献

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MethodsX. 2024 Apr 18;12:102712. doi: 10.1016/j.mex.2024.102712. eCollection 2024 Jun.
2
SLC26A1 is a major determinant of sulfate homeostasis in humans.SLC26A1 是人类硫酸盐稳态的主要决定因素。
J Clin Invest. 2023 Feb 1;133(3):e161849. doi: 10.1172/JCI161849.
3
Serum sulfate level and Slc13a1 mRNA expression remain unaltered in a mouse model of moderate vitamin D deficiency.血清硫酸盐水平和 Slc13a1mRNA 表达在中度维生素 D 缺乏症的小鼠模型中保持不变。
Mol Cell Biochem. 2023 Aug;478(8):1771-1777. doi: 10.1007/s11010-022-04634-7. Epub 2022 Dec 25.
4
Liquid chromatography-tandem mass spectrometry for clinical diagnostics.用于临床诊断的液相色谱-串联质谱法。
Nat Rev Methods Primers. 2022;2(1):96. doi: 10.1038/s43586-022-00175-x. Epub 2022 Dec 8.
5
Biallelic variants in the SLC13A1 sulfate transporter gene cause hyposulfatemia with a mild spondylo-epi-metaphyseal dysplasia.SLC13A1 硫酸盐转运基因的双等位基因突变可导致低硫酸血症伴轻度脊椎-骨骺-干骺端发育不良。
Clin Genet. 2023 Jan;103(1):45-52. doi: 10.1111/cge.14239. Epub 2022 Oct 3.
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