Liquid Chromatographic Determination of Plasma Ropivacaine for Assessing Pharmacokinetics of the Viscous Preparation
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- Kawata Takeshi
- Department of Pharmaceutical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba Faculty of Pharmaceutical Sciences, Josai University
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- Homma Masato
- Department of Pharmaceutical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba Department of Pharmacy, Tsukuba University Hospital
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- Kakiuchi Yoshihiro
- Department of Pharmacy, Tsukuba University Hospital
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- Inomata Shinichi
- Department of Anesthesiology, Graduate School of Comprehensive Human Sciences, University of Tsukuba
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- Miyabe Masayuki
- Department of Anesthesiology, Graduate School of Comprehensive Human Sciences, University of Tsukuba
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- Kobayashi Daisuke
- Faculty of Pharmaceutical Sciences, Josai University
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- Morimoto Yasunori
- Faculty of Pharmaceutical Sciences, Josai University
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- Kohda Yukinao
- Department of Pharmaceutical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba Department of Pharmacy, Tsukuba University Hospital
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We developed assay method for determination of plasma ropivacaine by using reversed-phase high performance liquid chromatography (HPLC) equipped with ordinary octadecylsilyl silica-gel (ODS) column. Plasma samples spiked with internal standard (bupivacaine) were treated by ethylacetate to extract ropivacaine and internal standard. The ropivacaine and internal standard separated on ODS column were detected by an ultra violet (UV) detector set at 215 nm. The mobile phase solvent consisted of acetonitrile, methanol and 0.05 M phosphate buffer adjusted to pH 4.0 (10 : 30 : 60, v/v) was pumped at a flow rate of 0.8 ml/min. The calibration curve of ropivacaine was linear at the concentration of 25—1000 ng/ml (r=0.9998). The recoveries of ropivacaine from plasma were greater than 87.9% with the coefficient of variations (CVs) less than 6.1%. The CVs for intra- and inter-day assay of ropivacaine were 2.0—12.0% and 1.7—14.8%, respectively. This HPLC method was applied to determining plasma ropivacaine in two healthy subjects after receiving 0.5% ropivacaine viscous preparation, which was prepared in our hospital. Our preliminary pharmacokinetic data showed that ropivacaine viscous could be used safely based on the plasma ropivacaine concentrations (Cmax: 89—125 ng/ml) for pain relief in oral mucosa.
収録刊行物
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- Biological & Pharmaceutical Bulletin
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Biological & Pharmaceutical Bulletin 28 (12), 2271-2273, 2005
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390282679601308928
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- NII論文ID
- 110004049130
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- NII書誌ID
- AA10885497
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- ISSN
- 13475215
- 09186158
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- NDL書誌ID
- 7721009
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- 本文言語コード
- en
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