Determination of iodoform in rabbit plasma by HPLC

A simple, rapid and reproducible method for the determination of iodoform in rabbit plasma by HPLC has been developed. Under the light-resistant condition, iodoform and diiodomethane (as internal standard) in 1.0 ml plasma were extracted with 1.0 ml diethylether. Twenty microliters of the organic ph...

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Published inBUNSEKI KAGAKU Vol. 42; no. 4; pp. 215 - 218
Main Authors NAGATA, Etsuko, YASUDA, Shuuichi, KASAHARA, Tomoyuki, KUBO, Hiroaki, MIURA, Sadanori
Format Journal Article
LanguageJapanese
English
Published Tokyo The Japan Society for Analytical Chemistry 1993
Nippon Bunseki Kagakkai
Japan Science and Technology Agency
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Abstract A simple, rapid and reproducible method for the determination of iodoform in rabbit plasma by HPLC has been developed. Under the light-resistant condition, iodoform and diiodomethane (as internal standard) in 1.0 ml plasma were extracted with 1.0 ml diethylether. Twenty microliters of the organic phase were injected into the HPLC system, consisted of a Model 510, U6K-injector, Model 481 UV detector setting at 336 nm (0.005 AUFS), an Ultrasphere ODS 5 μm guard column (45 mm × 4.6 mm i.d. ) and an analytical column (150 mm ×4.6 mm i.d.). The mobile phase was 60% methanol / pH 3.8, 5 mM potassium phosphate buffer. The flow rate was 1.0 ml/min. The retention time for iodoform and diiodomethane were 10.4 and 7.7 min, respectively. The limit of detection was 0.3 μg/ml (S/N=3) of plasma. Within-run reproducibility for 0.4 μg/ml was ± 2.1% (n=9). The HPLC separation can be completed in less than 11 min and had been applied for plasma of rabbit packed intraperitoneally by iodoform gauze.
AbstractList A simple, rapid and reproducible method for the determination of iodoform in rabbit plasma by HPLC has been developed. Under the light-resistant condition, iodoform and diiodomethane (as internal standard) in 1.0 ml plasma were extracted with 1.0 ml diethylether. Twenty microliters of the organic phase were injected into the HPLC system, consisted of a Model 510, U6K-injector, Model 481 UV detector setting at 336 nm (0.005 AUFS), an Ultrasphere ODS 5 μm guard column (45 mm × 4.6 mm i.d. ) and an analytical column (150 mm ×4.6 mm i.d.). The mobile phase was 60% methanol / pH 3.8, 5 mM potassium phosphate buffer. The flow rate was 1.0 ml/min. The retention time for iodoform and diiodomethane were 10.4 and 7.7 min, respectively. The limit of detection was 0.3 μg/ml (S/N=3) of plasma. Within-run reproducibility for 0.4 μg/ml was ± 2.1% (n=9). The HPLC separation can be completed in less than 11 min and had been applied for plasma of rabbit packed intraperitoneally by iodoform gauze.
Author KASAHARA, Tomoyuki
KUBO, Hiroaki
NAGATA, Etsuko
YASUDA, Shuuichi
MIURA, Sadanori
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Snippet A simple, rapid and reproducible method for the determination of iodoform in rabbit plasma by HPLC has been developed. Under the light-resistant condition,...
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SubjectTerms drug monitoring
HPLC
iodoform intoxication
plasma iodoform concentration
plasma of rabbit
Title Determination of iodoform in rabbit plasma by HPLC
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