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1999
DOI: 10.1016/s0378-4347(99)00209-1
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Gas chromatographic–mass spectrometric analysis of urinary sugar and sugar alcohols during pregnancy

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Cited by 28 publications
(14 citation statements)
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“…GC analysis of the trimethylsilyl ether derivatives of sugars is a well-known procedure [9], as is the GC separation of sugars as alditol acetates [7]. However, sample preparation for GC is extensive, involving the derivatization of sugars with specialty reagents to render them more volatile [10]. Also, the sensitive chromatographic operating parameters for GC are not well suited for routine analysis.…”
mentioning
confidence: 99%
“…GC analysis of the trimethylsilyl ether derivatives of sugars is a well-known procedure [9], as is the GC separation of sugars as alditol acetates [7]. However, sample preparation for GC is extensive, involving the derivatization of sugars with specialty reagents to render them more volatile [10]. Also, the sensitive chromatographic operating parameters for GC are not well suited for routine analysis.…”
mentioning
confidence: 99%
“…Inexpensive derivatization reagents however, such as acetic anhydride, do not provide optimum volatility for carbohydrates, reducing sensitivity, limiting analysis to abundant species such as glucose. Increased sensitivity of carbohydrate detection by GC/MS has been achieved with specialty reagents for derivatization; however, they are significantly more expensive [8,10,16]. LC/ MS-based methods are potentially advantageous because of the simplification of sample processing [4 -6, 11].…”
mentioning
confidence: 99%
“…20,21) In the present study, it was found that FJHQ(SR) markedly decreases urinary glucose, sorbitol, fructose, myo-inositol and 1,5-anhydro-Dglucitol in STZ-diabetic mice. This indicates that FJHQ(SR) is effective in suppressing an excessively activated polyol pathway in diabetes, as well as hyperglycemia and reduced insulin deficiency.…”
Section: Discussionmentioning
confidence: 48%
“…Urine samples were prepared using a urease treatment method as follows: 20,21) One hundred µl of urine was incubated with 30 units of urease at 37°C for 30 min. After adding an internal standard (20 µl of n-heptadecanoic acid), the sample was mixed with 900 µl of ethanol and centrifuged to deproteinize it; the supernatant was collected and evaporated.…”
Section: Measurement Of Urinary Sugar and Sugarmentioning
confidence: 99%
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