Stability of quinine dihydrochloride in commonly used intravenous solutions
The stability of quinine dihydrochloride at two concentrations, 1.2 and 3.6 mg/ml, in common intravenous solutions was studied. Admixtures of quinine in the following vehicles were prepared in glass containers: 5% dextrose in water, 5% dextrose in normal saline solution, 5% dextrose in half strength...
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Prince of Songkla University
2024
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th-psu.2016-193612024-02-14T09:03:52Z Stability of quinine dihydrochloride in commonly used intravenous solutions Sanguan Lerkiatbundit Faculty of Pharmaceutical Sciences (Clinical Pharmacy) คณะเภสัชศาสตร์ ภาควิชาเภสัชกรรมคลินิก Quinine The stability of quinine dihydrochloride at two concentrations, 1.2 and 3.6 mg/ml, in common intravenous solutions was studied. Admixtures of quinine in the following vehicles were prepared in glass containers: 5% dextrose in water, 5% dextrose in normal saline solution, 5% dextrose in half strength saline solution and normal saline solution. The solutions were kept under the fluorescent light at room temperature. Drug concentrations were monitored for 24 hours using stability-indicating high pressure liquid chromatographic method. More than 90 percent of the initial concentration of quinine remained in all solutions under the study condition and all samples remained clear and colourless over the entire 24 hr period. Admixtures containing quinine 1.2 and 3.6 mg/ml in four infusion solutions studied were stable for at least 24 hr and did not required protection from light during 24 hr period. Prince of Songkla University 2024-02-14T09:03:52Z 2024-02-14T09:03:52Z 1992 Technical Report http://kb.psu.ac.th/psukb/handle/2016/19361 en application/pdf Prince of Songkla University |
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Quinine Sanguan Lerkiatbundit Stability of quinine dihydrochloride in commonly used intravenous solutions |
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The stability of quinine dihydrochloride at two concentrations, 1.2 and 3.6 mg/ml, in common intravenous solutions was studied. Admixtures of quinine in the following vehicles were prepared in glass containers: 5% dextrose in water, 5% dextrose in normal saline solution, 5% dextrose in half strength saline solution and normal saline solution. The solutions were kept under the fluorescent light at room temperature. Drug concentrations were monitored for 24 hours using stability-indicating high pressure liquid chromatographic method.
More than 90 percent of the initial concentration of quinine remained in all solutions under the study condition and all samples remained clear and colourless over the entire 24 hr period. Admixtures containing quinine 1.2 and 3.6 mg/ml in four infusion solutions studied were stable for at least 24 hr and did not required protection from light during 24 hr period. |
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Faculty of Pharmaceutical Sciences (Clinical Pharmacy) |
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Faculty of Pharmaceutical Sciences (Clinical Pharmacy) Sanguan Lerkiatbundit |
format |
Technical Report |
author |
Sanguan Lerkiatbundit |
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Sanguan Lerkiatbundit |
title |
Stability of quinine dihydrochloride in commonly used intravenous solutions |
title_short |
Stability of quinine dihydrochloride in commonly used intravenous solutions |
title_full |
Stability of quinine dihydrochloride in commonly used intravenous solutions |
title_fullStr |
Stability of quinine dihydrochloride in commonly used intravenous solutions |
title_full_unstemmed |
Stability of quinine dihydrochloride in commonly used intravenous solutions |
title_sort |
stability of quinine dihydrochloride in commonly used intravenous solutions |
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Prince of Songkla University |
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2024 |
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http://kb.psu.ac.th/psukb/handle/2016/19361 |
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1792200106344185856 |