Separation and Determination ofd-Allose in Presence of Process-Related Impurities by Capillary Electrophoresis

被引:2
作者
Surapureddi, Sri Rama Krishna [1 ,2 ]
Ravindhranath, Kunta [1 ]
Sameer Kumar, Ghantasala S. [2 ]
Sappidi, Sreedhar Reddy [2 ]
机构
[1] Koneru Lakshmaiah Educ Fdn, Dept Chem, Guntur 522502, Andhra Pradesh, India
[2] Vimta Labs Ltd, Hyderabad 500085, Telangana, India
关键词
Carbohydrate analysis using capillary electrophoresis; d-Allose with processed impurities; d-Psicose; Enzymatic conversion of rare sugars; d-Altrose; L-RHAMNOSE ISOMERASE; D-PSICOSE; CONTINUOUS BIOREACTOR; D-FRUCTOSE; D-TAGATOSE; SUGARS; QUANTIFICATION; BIOSYNTHESIS;
D O I
10.1007/s12161-020-01842-z
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A simple and effective capillary electrophoresis (CE) method for the separation and quantification ofd-allose in the presence of its process impurities, namely sucrose,d-glucose,d-fructose,d-psicose, andd-altrose, has been developed and validated. The optimum conditions for the separation with an acceptable resolution are found to be as follows: background electrolyte (BGE): 36 mM of Na(2)HPO(4)and 130 mM NaOH; pH: 12.6; and voltage: 18 kV with direct UV detection at 265 nm. The present method overcomes the limitations of existing analytical method like sample preparation, poor resolution, and sensitivity. The method is optimized with the established standard curves ford-allose and its related impurities in the concentration range 0.25 to 3.0 mM with coefficient of determinations > 0.99 and the limit of detection (LOD) in the range of 0.11 to 0.20 mM. Separation ofd-allose and its impurities present in the mixture is achieved using the current method with good resolution, linearity, and reproducibility. The present method is suitable for the analysis of the final product in the enzymatically synthesizedd-allose and also for reaction monitoring of in-process samples.
引用
收藏
页码:2269 / 2278
页数:10
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