DISACCHARIDE ANALYSIS BY SAX-HPLC OF 1 CHONDROITIN SULFATE SAMPLE

通过 SAX-HPLC 对 1 个硫酸软骨素样品进行二糖分析

• 批准号: 8361852
• 负责人: Parastoo Azadi
• 金额: $ 0.18万
• 依托单位: UNIVERSITY OF GEORGIA
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-02-01 至 2012-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8361852
• 关键词: Buffers; Chondroitin Sulfates; Chondroitinases; Detection; Digestion; Disaccharides; Fluorescence; Funding; GAG Gene; Grant; Heating; High Pressure Liquid Chromatography; Hyaluronidase; Incubated; Injection of therapeutic agent; Methods; National Center for Research Resources; Particle Size; Principal Investigator; Pump; Reaction; Research; Research Infrastructure; Resources; Sampling; Solutions; Solvents; Source; System; United States National Institutes of Health; Water; cost; detector; inorganic phosphate

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Methods: Chondroitinase digestion A solution (100 ¿L total volume) containing 0.1 mg/mL GAG, 50 mM NH4OAc buffer, pH 7, and 0.1 mU/mL chondroitinase AC (A. aurescens, Sigma) or ABC (F. heparinum, Sigma) was incubated at 37 ¿C for 18 h. SAX-HPLC SAX-HPLC was carried out on an Agilent system using a 4.6¿250 mm Waters Spherisorb analytical column with 5 ¿m particle size at 25 ¿C. Solvent A: 2.5 mM Na-phosphate, pH 3.5 Solvent B: 2.5 mM Na-phosphate, pH 3.5, 1.2 M NaCl. The flow rate was 1.0 mL/min. Injection volume was 10 ¿L. Detection was performed by post-column derivatization. Briefly, to the eluent from the column was added, from a binary HPLC pump, a 1:1 mixture of 0.25 M NaOH and 1 % 2-cyanoacetamide at 0.5 mL/min. The eluent was then heated to 120 ¿C in a 10-m reaction coil, followed by cooling in a 50-cm cooling coil, and directed into a Shimadzu fluorescence detector. Excitation wavelength was 346 nm and emission wavelength was 410 nm.

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