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利用 FACE 分析方法,可快速、可靠地监测临床重要生物样本中硫酸软骨素的硫酸化和总量。

FACE analysis as a fast and reliable methodology to monitor the sulfation and total amount of chondroitin sulfate in biological samples of clinical importance.

机构信息

Department of Surgical and Morphological Sciences, University of Insubria, 21100 Varese, Italy.

Laboratory of Biochemistry, Department of Chemistry, University of Patras, 26504 Patras, Greece.

出版信息

Molecules. 2014 Jun 12;19(6):7959-80. doi: 10.3390/molecules19067959.

Abstract

Glycosaminoglycans (GAGs) due to their hydrophilic character and high anionic charge densities play important roles in various (patho)physiological processes. The identification and quantification of GAGs in biological samples and tissues could be useful prognostic and diagnostic tools in pathological conditions. Despite the noteworthy progress in the development of sensitive and accurate methodologies for the determination of GAGs, there is a significant lack in methodologies regarding sample preparation and reliable fast analysis methods enabling the simultaneous analysis of several biological samples. In this report, developed protocols for the isolation of GAGs in biological samples were applied to analyze various sulfated chondroitin sulfate- and hyaluronan-derived disaccharides using fluorophore-assisted carbohydrate electrophoresis (FACE). Applications to biologic samples of clinical importance include blood serum, lens capsule tissue and urine. The sample preparation protocol followed by FACE analysis allows quantification with an optimal linearity over the concentration range 1.0-220.0 µg/mL, affording a limit of quantitation of 50 ng of disaccharides. Validation of FACE results was performed by capillary electrophoresis and high performance liquid chromatography techniques.

摘要

糖胺聚糖(GAGs)由于其亲水性和高阴离子电荷密度,在各种(病理)生理过程中发挥重要作用。在病理条件下,鉴定和定量生物样品和组织中的 GAGs 可能是有用的预后和诊断工具。尽管在开发用于测定 GAGs 的灵敏和准确方法方面取得了显著进展,但在样品制备方面仍存在显著的方法学差距,缺乏可靠的快速分析方法,无法同时分析多个生物样品。在本报告中,应用开发的生物样品 GAGs 分离方案,使用荧光辅助碳水化合物电泳(FACE)分析各种硫酸软骨素和透明质酸衍生的二糖。应用于具有临床重要性的生物样品,包括血清、晶状体囊组织和尿液。采用 FACE 分析的样品制备方案,可在 1.0-220.0 µg/mL 的浓度范围内实现最佳线性定量,二糖的定量限为 50 ng。通过毛细管电泳和高效液相色谱技术对 FACE 结果进行了验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a5f/6271866/76718277c304/molecules-19-07959-g001.jpg

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