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Pharmacokinetics of rokitamycin after single administration to healthy volunteers.

作者信息

Broggini M, Bottà V, Benvenuti C, Fonio W, Congedo M, Parini J

机构信息

Department of Medicine, Filippo Del Ponte Hospital, Varese, Italy.

出版信息

Eur J Drug Metab Pharmacokinet. 1991 Apr-Jun;16(2):137-40. doi: 10.1007/BF03189950.

DOI:10.1007/BF03189950
PMID:1936073
Abstract

The pharmacokinetics of rokitamycin tablets were studied in 12 healthy volunteers in a randomized cross-over design. The doses tested were 200 mg, 300 mg, 400 mg and 600 mg, as single oral administration. Rokitamycin was absorbed quickly with Tmax for all doses around 30 min after drug intake. Total AUC and Cmax values were linearly related to the administered dose. The buffer formulation determined a low interindividual variation. The overall findings show a good similarity with the data obtained in Japanese subjects. Tolerability was very good.

摘要

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本文引用的文献

1
Acyl derivatives of 16-membered macrolides. I. Synthesis and biological properties of 3"-O-propionylleucomycin A5 (TMS-19-Q).16元大环内酯的酰基衍生物。I. 3"-O-丙酰基柱晶白霉素A5(TMS-19-Q)的合成与生物学性质
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2
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