1997
DOI: 10.1039/a608152e
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Determination of Disodium Cromoglycate in Human Urine by High-performance Liquid Chromatography With Post-column Photoirradiation–Fluorescence Detection

Abstract: For the determination of disodium cromoglycate in urine, a fluorimetric method using HPLC post-column photoirradiation has been developed. The mobile phase consisted of a 35 mmol l-1 phosphate buffer (pH 8)-methanol (7 + 3, %v/v) containing 75 mmol l-1 hydrogen peroxide and 20 mmol l-1 18-crown-6. The 18-crown-6 was used for separation adjustment of the disodium cromoglycate in the urine sample. Photoirradiation was carried out in tubing wound around a germicidal light in a reactor equipped with an air-cooling… Show more

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Cited by 18 publications
(3 citation statements)
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References 17 publications
(18 reference statements)
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“…Quantification of cromolyn sodium, nedocromil, and albuterol in urine can be done but must be performed with high-performance liquid chromatographic techniques that are relatively complex and expensive. [36][37][38] Using urinary excretion of tobramycin as a bioassay to document pulmonary delivery is not without limitations. The most obvious is that it does not describe the location in the airways where absorption of tracer occurs.…”
Section: Discussionmentioning
confidence: 99%
“…Quantification of cromolyn sodium, nedocromil, and albuterol in urine can be done but must be performed with high-performance liquid chromatographic techniques that are relatively complex and expensive. [36][37][38] Using urinary excretion of tobramycin as a bioassay to document pulmonary delivery is not without limitations. The most obvious is that it does not describe the location in the airways where absorption of tracer occurs.…”
Section: Discussionmentioning
confidence: 99%
“…It have been reported that the retention time usually becomes longer by the addition of CE in mobile phase. 11,12 The mechanism of reduction on the retention time is still not clear; however, it is speculated that the ion of phosphate buffer affects the retention time of KYNA. For separate of KYN and KYNA from components in the serum, the pH of phosphate buffer was adopted to 8.0, which gave retention times for KYN and KYNA of 18 and 24 minutes, respectively.…”
Section: Atsumi Et Almentioning
confidence: 99%
“…Both drugs are co-formulated in a nasal spray dosage form and are widely used for effective treatment of nasal congestion and allergy. Several methods have been reported for the determination of SCG in pharmaceutical preparations such as spectrophotometry [3,4], electrophoresis [5], electrochemical [6,7] and HPLC methods [8][9][10][11][12][13][14]. OXMT has also been analyzed by several methods in pharmaceutical preparations such as spectrophotometry [3,[15][16][17][18][19][20][21][22][23], capillary electrophoresis [24,25], gas chromatography [26,27] and HPLC [28][29][30][31][32][33][34][35].…”
Section: Introductionmentioning
confidence: 99%