| Literature DB >> 6874860 |
B Winograd, M J Oosterbaan, E van der Kleijn, R M Liskamp, H C Ottenheijm, D J Wagener.
Abstract
Sparsomycin--an antibiotic with marked cytostatic activity--was the subject of a clinical Phase I study in 1964. The structure of sparsomycin was elucidated in 1970 and its first total synthesis was reported in 1981. Here we describe a sensitive high-performance liquid chromatographic method of determination. The detection limit was found to be 10 ng/ml of plasma and 20 ng/ml of urine. With this procedure sparsomycin and isosparsomycin can readily be separated. In addition, we performed a first pharmacokinetic study in the dog and found a half-life time t1/2 beta of 1.1 h. Only 25% of the administered dose could be recovered in the urine as sparsomycin. We consider that by now many prerequisites for further preclinical studies have been achieved, and the results of these studies will determine whether sparsomycin deserves reintroduction into clinical use.Entities:
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Year: 1983 PMID: 6874860 DOI: 10.1016/s0378-4347(00)84353-4
Source DB: PubMed Journal: J Chromatogr