Determination of Salivary Theophylline Concentration by SLFIA Method and Pharmacokinetics in Saliva
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概要
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Recently, we have reported that theophylline concentrations in plasma as determined by substratelabeled fluorescent immunoassay (SLFIA) well correlated (r=0.96) with the concentrations by high-pressure liquid chromatography, and that SLFIA procedure had considerable advantages over hitherto available method. Methods for measuring theophylline in saliva previously reported were spectrophotometry gas-liquid and high-pressure liquid chromatographs. Here, we used the SLFIA for the determination of theophylline concentrations in saliva. It was possible to determine salivary theophylline in low concentrations by using salivary altered first dilution rates with SLFIA method. The concentrations of theophylline in the plasma and saliva in 7 normal adults and 3 asthmatic patients who were administered aminophylline were determined by SLFIA method. In normal adults, the time-course of plasma and salivary theophylline levels showed a parallel relationship, and theophylline concentrations in the saliva as determined 2 and 4 hours after administration were about 44% lower than those in the plasma. In asthmatic patients, theophylline concentrations in saliva 2,4,6and 8 hours after administration were also 32% lower than those in the plasma. These results suggested that monitoring patients by means of salivary theophylline level is effective way to predict plasma levels and to help patients avoid pain of bloodletting.
- 日本医療薬学会の論文
- 1982-06-20
著者
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Takagi K
Department Of Medical Technology Nagoya University School Of Health Sciences
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Kondo Takaaki
Department Of Cardiology Nagoya University Graduate School Of Medicine
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HASEGAWA Takaaki
Department of Pharmacy and Pharmacokinetics, Aichi Medical University School of Medicine
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Satake Tatsuo
Second Department of Internal Medicine, Nagoya university School of Medicine, Nagoya
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Iwata Hitoshi
Second Department Of Internal Medicine Nagoya University School Of Medicine
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Satake Tatsuo
Third Division Of The Research Laboratory For Development Of Medicine School Of Pharmacy Hokuriku Un
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TAKAGI Kenzo
Second Department of Internal Medicine
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HASEGAWA TAKAAKI
Pharmacy, Nagoya University Hospital
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OGURA YOZO
Pharmacy, Nagoya University Hospital
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YAMADA SHIGEKI
Pharmacy, Nagoya University Hospital
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KOZAKI TAKESHI
Department of Pediatrics, Nagoya National Hospital
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Kawaguchi Takeshi
Kyoto University Center For Student Health
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Hasegawa Takaaki
Department Of Pharmacy And Pharmacokinetics Aichi Medical University School Of Medicine
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Hasegawa Takaaki
Third Division Of The Research Laboratory For Development Of Medicine School Of Pharmacy Hokuriku Un
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Ogura Yozo
Pharmacy Nagoya University Hospital
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Kozaki Takeshi
Department Of Pediatrics Nagoya National Hospital
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Yamada Shigeki
Pharmacy Nagoya University Hospital
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Hasegawa Takaaki
Pharmacy Nagoya University Hospital
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SATAKE Tatsuo
Second Department of Internal Medicine, Nagoya University School of Medicine
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