PENETAPAN KADAR KETAMIN HIDROKLORIDA DALAM SEDIAAN INJEKSI DENGAN METODE KROMATOGRAFI CAIR KINERJA TINGGI
<br /> An ion pair high performance liquid chromatographic method was developed for determination of ketamine hydrochloride in injection dosage form. Result showed that high performance liquid chromatographic method using a mixture of acetonitrrle-0.05 M phosphate buffer of pH 4.5 containing...
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id-itb.:52552006-03-20T13:34:05ZPENETAPAN KADAR KETAMIN HIDROKLORIDA DALAM SEDIAAN INJEKSI DENGAN METODE KROMATOGRAFI CAIR KINERJA TINGGI Kurnia Setiawan , Henry Farmakologi dan terapeutik Indonesia Theses INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/5255 <br /> An ion pair high performance liquid chromatographic method was developed for determination of ketamine hydrochloride in injection dosage form. Result showed that high performance liquid chromatographic method using a mixture of acetonitrrle-0.05 M phosphate buffer of pH 4.5 containing 0.05% sodium hexane sulphonate (25:75) as mobile phase, flow rate of 1.0 mL/minute, C-18 column, and detection wavelength of 215 nm. The method validation with an external standard showed that the accuracy was 99.50±0.66 %, the limit of detection and limit of quantitation were 0.93 and 3.09 pg/mL, respectively. The method validation with atropine sulphate as an internal standard showed that the accuracy was 100.84±1.92 %, the limit of detection and limit of quantitation were 1.46 and 4.87 gg/mL, respectively. text |
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Farmakologi dan terapeutik Kurnia Setiawan , Henry PENETAPAN KADAR KETAMIN HIDROKLORIDA DALAM SEDIAAN INJEKSI DENGAN METODE KROMATOGRAFI CAIR KINERJA TINGGI |
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An ion pair high performance liquid chromatographic method was developed for determination of ketamine hydrochloride in injection dosage form. Result showed that high performance liquid chromatographic method using a mixture of acetonitrrle-0.05 M phosphate buffer of pH 4.5 containing 0.05% sodium hexane sulphonate (25:75) as mobile phase, flow rate of 1.0 mL/minute, C-18 column, and detection wavelength of 215 nm. The method validation with an external standard showed that the accuracy was 99.50±0.66 %, the limit of detection and limit of quantitation were 0.93 and 3.09 pg/mL, respectively. The method validation with atropine sulphate as an internal standard showed that the accuracy was 100.84±1.92 %, the limit of detection and limit of quantitation were 1.46 and 4.87 gg/mL, respectively. |
format |
Theses |
author |
Kurnia Setiawan , Henry |
author_facet |
Kurnia Setiawan , Henry |
author_sort |
Kurnia Setiawan , Henry |
title |
PENETAPAN KADAR KETAMIN HIDROKLORIDA DALAM SEDIAAN INJEKSI DENGAN METODE KROMATOGRAFI CAIR KINERJA TINGGI |
title_short |
PENETAPAN KADAR KETAMIN HIDROKLORIDA DALAM SEDIAAN INJEKSI DENGAN METODE KROMATOGRAFI CAIR KINERJA TINGGI |
title_full |
PENETAPAN KADAR KETAMIN HIDROKLORIDA DALAM SEDIAAN INJEKSI DENGAN METODE KROMATOGRAFI CAIR KINERJA TINGGI |
title_fullStr |
PENETAPAN KADAR KETAMIN HIDROKLORIDA DALAM SEDIAAN INJEKSI DENGAN METODE KROMATOGRAFI CAIR KINERJA TINGGI |
title_full_unstemmed |
PENETAPAN KADAR KETAMIN HIDROKLORIDA DALAM SEDIAAN INJEKSI DENGAN METODE KROMATOGRAFI CAIR KINERJA TINGGI |
title_sort |
penetapan kadar ketamin hidroklorida dalam sediaan injeksi dengan metode kromatografi cair kinerja tinggi |
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https://digilib.itb.ac.id/gdl/view/5255 |
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