AS-924, a novel, orally active, bifunctional prodrug of ceftizoxime: physicochemical properties, oral absorption in animals, and antibacterial activity

被引:20
作者
Mori, N
Kodama, T
Sakai, A
Suzuki, T
Sugihara, T
Yamaguchi, S
Nishijima, T
Aoki, A
Toriya, M
Kasai, M
Hatano, S
Kitagawa, M
Yoshimi, A
Nishimura, K
机构
[1] Asahi Kasei Corp, Life Sci Res Inst, Shizuoka 4102321, Japan
[2] Kyoto Pharmaceut Ind Co Ltd, Res Labs, Nakakyo Ku, Kyoto 6048444, Japan
关键词
cephalosporin; ceftizoxime; bifunctional prodrug; antibacterial activity; lipophilicity; water solubility; AS-924;
D O I
10.1016/S0924-8579(01)00444-7
中图分类号
R51 [传染病];
学科分类号
100401 [流行病与卫生统计学];
摘要
AS-924 is an oral prodrug of the antibiotic ceftizoxime (CTIZ), a parenteral use cephalosporin. This novel prodrug, produced by esterifying CTIZ with a lipophilic pivaloyloxymethyl (POM) group and introducing a water soluble L-alanyl group, is expected to increase the bioavailability and thereby, augment the antibacterial activity of CTIZ in vivo compared with existing prodrugs. To study the effect of the L-alanyl group in AS-924 on its bioavailability, the plasma concentration profiles of CTIZ in dogs were examined following the dosing of AS-924 and CTIZ-POM, in powder form, after pretreatment with the antacid ranitidine, and following the dosing of AS-924 after pretreatment with a gastrointestinal motility stimulant metoclopramide or suppressant scopolamine butylbromide. The absorption rate of AS-924 was constant under these different conditions due to its unique balance of lipophilicity and water solubility. CTIZ is as antibacterially active as pre-existing oral cephalosporins against Gram-positive clinical isolates, while being more active against all Gram-negative isolates-particularly Enterobacteriaceae and Haemophilus influenzae. A simulation model for the eradication profile of bacteria in computer programmed pharmacokinetic (PK) system was carried out to study the antibacterial action of CTIZ in human. CTIZ was proven to eradicate Streptococcus pneumoniae and H. influenzae effectively, while cefpodoxime (CPOD), the active moiety of CPOD proxetil, eradicated S. pneumoniae, but not H. influenzae. These results confirm that, AS-924 is a potent oral antibiotic and would be expected to be clinically effective and efficient. (C) 2001 Published by Elsevier Science B.V. and International Society of Chemotherapy.
引用
收藏
页码:451 / 461
页数:11
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