Objective: To establish a method for determining nucleosides (adenoside and guanoside) in Siweilingzhi Mixture by HPCE.
Method: Adenoside and guanoside were separated within 25 min using an 20 mmol.L-1 borate buffer with 30 mmol.L-1 SDS and 5% Ethanol (adjusted to pH 10.0 with sodium hydroxide solution), with an operation voltage of 10 kV, temperature of 20 degrees C and a hydrodynamic injection time of 15 s. Seperations were carried out in a fused-silica capillary 75 microns id x 57 cm (effective length 50 cm) with peak detection by direct UV at 254 nm.
Result: Regression equation of adenoside and that of guanoside were Y = 0.0705 + 0.01707X (r = 0.9995) and Y = 0.0232 + 0.01864X (r = 0.9999) respectively. The average recovery rate was 99.22% (RSD = 3.66%) and 104.3% (RSD = 1.91%) respectively. Nine samples were determined with the method.
Conclusion: The method is simple, rapid and accurate with good repeatability and it can be used to determine nucleosides.
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Zhongguo Zhong Yao Za Zhi
September 2002
Hebei Provincial Institute for Drug Control, Shijiazhuang 050011, Hebei, China.
Objective: To establish a method for determining nucleosides (adenoside and guanoside) in Siweilingzhi Mixture by HPCE.
Method: Adenoside and guanoside were separated within 25 min using an 20 mmol.L-1 borate buffer with 30 mmol.
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