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舒他西林细粒剂在儿科的临床及药代动力学研究

[Clinical and pharmacokinetic studies on sultamicillin fine granules in pediatrics].

作者信息

Sato H, Narita A, Matsumoto K, Nakazawa S, Suzuki H, Nakanishi Y, Niino K, Nakazawa S

机构信息

Department of Pediatrics, Tokyo Metropolitan Ebara General Hospital.

出版信息

Jpn J Antibiot. 1988 Dec;41(12):1855-62.

PMID:3249359
Abstract

Sultamicillin (SBTPC) is a mutual prodrug of sulbactam (SBT) and ampicillin (ABPC). A study has been performed to evaluate pharmacokinetic properties and clinical usefulness of SBTPC fine granules in the treatment of pediatric infections. After an oral dose of 5-15 mg/kg of SBTPC fine granules, peak serum concentrations of ABPC and SBT were 1.18-3.26 micrograms/ml and 0.97-3.05 micrograms/ml, respectively at 1 hour. Serum half-lives for elimination (T 1/2 (beta] of ABPC and SBT were 0.83-1.83 hours and 0.94-1.71 hours, respectively. Serum concentrations of ABPC at 1-6 hours after an oral administration of SBTPC fine granules were similar to those of SBT. Serum concentrations of ABPC and SBT were proportional to dose levels of SBTPC fine granules. Following oral administrations of 5-15 mg/kg, 33.9-64.8% of ABPC and 38.1-76.6% of SBT were recovered in urine in 6 hours. SBTPC fine granules were administered in a daily dose of approximately 30 mg/kg divided into 3 doses to 14 pediatric patients with bacterial infections. All 14 were cured with 11 excellent and 3 good clinical response to this drug. Microbiological eradication was obtained in 85.7%. beta-Lactamase-producing ABPC-resistant strains were eradicated. Adverse effects including laboratory test values that may be attributed to the administration of SBTPC fine granules were not observed except a treatment episode of diarrhea in 1 patient.

摘要

舒他西林(SBTPC)是舒巴坦(SBT)和氨苄西林(ABPC)的复方前体药物。已开展一项研究以评估SBTPC细颗粒在治疗儿童感染方面的药代动力学特性和临床效用。口服5 - 15mg/kg的SBTPC细颗粒后,1小时时ABPC和SBT的血清峰值浓度分别为1.18 - 3.26微克/毫升和0.97 - 3.05微克/毫升。ABPC和SBT的血清消除半衰期(T 1/2(β))分别为0.83 - 1.83小时和0.94 - 1.71小时。口服SBTPC细颗粒后1 - 6小时ABPC的血清浓度与SBT相似。ABPC和SBT的血清浓度与SBTPC细颗粒的剂量水平成正比。口服5 - 15mg/kg后,6小时内尿液中回收了33.9 - 64.8%的ABPC和38.1 - 76.6%的SBT。以每日约30mg/kg的剂量将SBTPC细颗粒分3次给予14例患有细菌感染的儿科患者。所有14例患者均治愈,其中11例临床反应极佳,3例良好。微生物清除率为85.7%。产β-内酰胺酶的耐ABPC菌株被清除。除1例患者出现腹泻治疗情况外,未观察到可能归因于SBTPC细颗粒给药的不良反应,包括实验室检查值异常。

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