Motohiro T, Oda K, Aramaki M, Kawakami A, Tanaka K, Koga T, Sakata Y, Fujimoto T, Yokochi K, Yamashita F
Department of Pediatrics, School of Medicine, Kurume University.
Jpn J Antibiot. 1989 Jul;42(7):1629-66.
Cefpodoxime proxetil (CPDX-PR, CS-807) is a new oral cephem derivative drug in which carboxylic acid was esterified to the 4-position of CPDX (oxime type cephem antibiotic). CPDX-PR is hydrolyzed mainly with esterase in intestinal wall and CPDX exists as an active form in body fluid. While there are numerous study reports using CPDX-PR in tablet forms in Japan, the dry syrup formula for pediatric use was newly developed. The dry syrup of CPDX-PR was orally administered 20 minutes after meal to the 6 boys of ages from 8 years and 1 month to 10 years and 10 months, with doses of 3 and 6 mg/kg, respectively, for 3 cases each. Serum concentrations and urinary concentrations and recovery rate of the drug were investigated. In addition to the above, the clinical and bacteriological studies were performed in a total of 105 cases consisting of children with ages ranging from 2 months to 11 years and 8 months, upon administering an average dose of 3.4 mg/kg, 3 to 4 times per day (96 cases of 3 times and 9 cases of 4 times). The 105 cases included 13 cases of pharyngitis, 21 cases of tonsillitis, 4 cases of acute bronchitis, 6 cases of pneumonia, 1 case of pleurisy, 13 cases of scarlet fever, 41 cases of urinary tract infection, 3 cases of posthitis and 3 cases of bacillary dysentery. Drug sensitivity test was performed for the following strains: (i) Strains retained by our department; 52 strains of Streptococcus pyogenes, 18 strains of Streptococcus agalactiae, and 11 strains of Bordetella pertussis, and (ii) strains isolated from cases to which CPDX-PR was administered; 2 strains of Staphylococcus aureus, 8 strains of S. pyogenes, 2 strains of Haemophilus influenzae, 10 strains of Escherichia coli, and 1 strain of Proteus mirabilis. Drug sensitivities of the strains retained by our department were tested with the inoculum sizes of 10(8) and 10(6) cfu/ml for R-3746 (Na-salt of CPDX), cefaclor (CCL), cephalexin (CEX), amoxicillin (AMPC), and methicillin (DMPPC), and those against strains separated from the cases to which CPDX-PR was administered were tested with the same inoculum sizes for R-3746, CCL, CEX, cefadroxil, ampicillin (ABPC), DMPPC and cloxacillin (MCIPC). Adverse reactions and abnormal clinical laboratory test results were also examined.(ABSTRACT TRUNCATED AT 400 WORDS)
头孢泊肟酯(CPDX-PR,CS-807)是一种新型口服头孢烯衍生物药物,其中羧酸被酯化到CPDX(肟型头孢烯抗生素)的4位。CPDX-PR主要在肠壁中被酯酶水解,CPDX以活性形式存在于体液中。在日本,虽然有许多关于使用片剂形式的CPDX-PR的研究报告,但新开发了用于儿科的干糖浆剂型。对年龄在8岁1个月至10岁10个月的6名男孩在饭后20分钟口服CPDX-PR干糖浆,剂量分别为3mg/kg和6mg/kg,各3例。研究了药物的血清浓度、尿浓度和回收率。除此之外,对年龄在2个月至11岁8个月的105例儿童进行了临床和细菌学研究,平均剂量为3.4mg/kg,每天3至4次(3次的96例,4次的9例)。这105例包括13例咽炎、21例扁桃体炎、4例急性支气管炎、6例肺炎、1例胸膜炎、13例猩红热、41例尿路感染、3例尿道炎和3例细菌性痢疾。对以下菌株进行了药敏试验:(i)本部门保存的菌株;52株化脓性链球菌、18株无乳链球菌和11株百日咳博德特氏菌,以及(ii)从接受CPDX-PR治疗的病例中分离出的菌株;2株金黄色葡萄球菌、8株化脓性链球菌、2株流感嗜血杆菌、10株大肠埃希菌和1株奇异变形杆菌。用10(8)和10(6)cfu/ml的接种量对本部门保存的菌株进行R-3746(CPDX钠盐)、头孢克洛(CCL)、头孢氨苄(CEX)、阿莫西林(AMPC)和甲氧西林(DMPPC)的药敏试验,对从接受CPDX-PR治疗的病例中分离出的菌株用相同接种量进行R-3746、CCL、CEX、头孢羟氨苄、氨苄西林(ABPC)、DMPPC和氯唑西林(MCIPC)的药敏试验。还检查了不良反应和异常的临床实验室检查结果。(摘要截取自400字)