scholarly journals Application of High-performance Cation-exchange Chromatography for Characterization of Stinging Insect Venoms.

1983 ◽  
Vol 37b ◽  
pp. 252-254 ◽  
Author(s):  
Roland Einarsson ◽  
Ing-Mari Åstrand ◽  
Per Ålin ◽  
Bengt Mannervik ◽  
Jan-Eric Berg ◽  
...  
Keyword(s):  
Cation Exchange ◽  
High Performance ◽  
Exchange Chromatography ◽  
Cation Exchange Chromatography ◽  
Stinging Insect

Characterization of the Acidic Species of a Monoclonal Antibody Using Weak Cation Exchange Chromatography and LC-MS

2015 ◽  
Vol 87 (17) ◽  
pp. 9084-9092 ◽  
Author(s):  
Gomathinayagam Ponniah ◽  
Adriana Kita ◽  
Christine Nowak ◽  
Alyssa Neill ◽  
Yekaterina Kori ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Cation Exchange ◽  
Exchange Chromatography ◽  
Cation Exchange Chromatography ◽  
Weak Cation Exchange

Effect of temperature on quantifying glycated (glycosylated) hemoglobin by cation-exchange chromatography.

1985 ◽  
Vol 31 (1) ◽  
pp. 114-117 ◽  
Author(s):  
R Flückiger ◽  
T Woodtli
Keyword(s):  
Ionic Strength ◽  
Cation Exchange ◽  
High Performance ◽  
Glycated Hemoglobin ◽  
Operating Temperature ◽  
Glycosylated Hemoglobin ◽  
Regression Line ◽  
Exchange Chromatography ◽  
Effect Of Temperature ◽  
Cation Exchange Chromatography

Abstract As a consequence of nonideal chromatographic conditions, values for stable glycated hemoglobin (HbA1c) determined by cation-exchange chromatography in a commercial minicolumn system (y) or by "high-performance" liquid chromatography (x) differ markedly, yielding the regression line y = 0.82x + 0.6. With use of the protocol specified by the manufacturer, 20% of the HbA1c peak is not collected in the HbA1c fraction. Increasing the ionic strength of the eluting buffer by increasing the operating temperature to 28 degrees C increases the rate of elution from the minicolumn, making results of the two methods more closely comparable (y = 0.98x - 0.22). Because at a given pH the elution volume is determined primarily by the ionic strength, close limits on the composition of the eluting buffer are set by the temperature-dependence of its ionic strength. At a specified temperature and pH the position of a peak can be judged to within a volume of 1 mL if the conductivity of the eluent does not vary by more than +/- 0.05 mS.

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