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- W2389356431 abstract "To Investigate the stability of cefuroxime sodium and vitamin C in 5% GS transfusion. RP HPLC was applied to quantitative analysis of cefuroxime sodium and vitamin C in 5% GS transfusion, using cefotaxime sodium as an internal standard. Chromatographic conditions were Novapak C 18 Column(3 9 mm×150 mm, 5 μm), mobile phase: water methanol acetic acid (71∶28∶1), flow rate: 0 6 ml/min and UV detection wavelength: 274 nm. At 37 ℃, 4 hours after cefuroxime sodium and vitamin C were mixed in 5% GS transfusion, the contents of cefuroxime sodium and vitamin C were 95% or more and 93.55% respectively. After 8 hours, their contents were only 89 95% and 86.57% respectively [CONCLUSION]In clinical practice, if it is required that cefuroxime sodium is mixed with vitamin C, the mixture should be used within 4 hours." @default.
- W2389356431 created "2016-06-24" @default.
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- W2389356431 date "2003-01-01" @default.
- W2389356431 modified "2023-09-23" @default.
- W2389356431 title "The Stability of Cefuroxime Sodium and Vitamin C in 5% GS Transfusion" @default.
- W2389356431 hasPublicationYear "2003" @default.
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