CHEMOTHERAPY JUN Citrobacter freundii 27, Enterobacter aerogenes 26, Enterobacter cloacae 27, Proteus rettgeri 7, Proteus inconstans 20, Proteus

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VOL. 32 S-4 CHEMOTHERAPY Fig. 1 Chemical structure of sodium cefoperazone Fig. 2 Chemical structure of sodium cefoperazone

CHEMOTHERAPY JUN. 1984 Citrobacter freundii 27, Enterobacter aerogenes 26, Enterobacter cloacae 27, Proteus rettgeri 7, Proteus inconstans 20, Proteus morganii 27,Echerichia coli 27, Klebsiella aerogenes 27, Serratia marcescens 27) Fig. 3 MIC distribution of SBT/CPZ, CPZ and SBT S. aureus (106cell/ml) Fig. 4 MIC distribution of SBT/CPZ, CPZ and SBT C. freundii (106 cell f/ml)

VOL.32 S-4 CHEMOTHERAPY Fig. 5 MIC distribution of SBT/CPZ, CPZ and SBT Fig. 6 MIC distribution of SBT/CPZ, CPZ and SBT Fig. 7 MIC distribution of SBT/CPZ, CPZ and SBT

CHEMOTHERAPY JUN. 1984 Fig. 8 MIC distribution of SBT/CPZ, CPZ and SBT Fig. 9 MIC distribution of SBT/CPZ, CPZ and SBT Fig. 10 MIC distribution of SBT/CPZ, CPZ and SBT

VOL.32 S-4 CHEMOTHERAPY Fig. 11 MIC distribution of SBT/CPZ, CPZ and SBT Fig. 12 MIC distribution of SBT/CPZ, CPZ and SBT

CHEMOTHERAPY JUN. 1984 Fig. 13 Sputum and serum levels of CPZ and SBT Fig. 14 Sputum and serum levels of CPZ and SBT Case 1 Cystic bronchiectasis Case 2 Bronchiectasis

VOL.32 S-4 CHEMOTHERAPY Fig. 15 Sputum and serum levels of CPZ and SBT Fig. 16 Sputum and serum levels of CPZ and SBT Case 3 Chronic bronchitis Case 4 Chronic bronchitis

CHEMOTHERAPY JUN. 1984 Table 1. Clinical effect of SBT/CPZ

VOL.32 S-4 CHEMOTHERAPY * :Ĉ-lactamase (+)

CHEMOTHERAPY JUN. 1984 Table 2 Clinical efficacy of SBT/CPZ Efficacy rate : 16/20 (80.0%) Table 3 Bacteriological effect of SBT/CPZ Fig. 17 Laboratory findings before and after administration of SBT/CPZ RBC(x104/N) Hb (g/c1k) Platelet (x104/mi)

VOL.32 S-4 CHEMOTHERAPY Fig. 18 Laboratory findings before and after administration of SBT/CPZ GOT (I.U.) GPT (I.U.) Al-p (I.U.) Fig. 19 Laboratory findings before and after administration of SBT/CPZ T-Bilirubin (mg/de) BUN (mg/de) Creatinine (mg/de)

CHEMOTHERAPY JUN. 1984 Fig. 20 Case: K.M. 45y.o. M. Clinical diagnosis: Chronic bronchitis

VOL. 32 S-4 CHEMOTHERAPY LABORATORY AND CLINICAL STUDIES ON SBT/CPZ YOH SUZUYAMA, HIROKO NAKAZATO, HIRONOBU KOGA, HIROSHI TOMITA, KOICHI WATANABE, HIKARU TANAKA, NAOMI ITO, KIYO FUJITA, YOSHITERU SHIGENO, ATSUSHI SAITO, MUNETAKA KOMORI and KOHEI HARA The 2nd Department of Internal Medicine, Nagasaki University School of Medicine KEIZO YAMAGUCH I, MASUMI MATSUE, MITSUO KAKU Department of Clinical Laboratory Nagasaki University Hospital Laboratory and clinical studies on SBT/CPZ, a novel antibiotic which combine a broad-spectrum cephalosporin antibiotic, cefoperazone and a 0-lactamase inhibitor, sulbactam developed by Pfizer Co. Ltd., were carried out and the results were as follows. 1) Antibacterial activity: Minimum inhibitory concentrations (MICs) of SBT/CPZ against a total of 240 strains isolated from various specimens (Staphylococcus aureus 25, Citrobacter freundii 27, Enterobacter aerogenes 26, Enterobacter cloacae 27, Proteus rettgeri 7, Proteus inconstans 20, Proteus morganii 27, Escherichia coli 27, Klebsiella aerogenes 27, Serratiii marcescens 27) were compared with those of CPZ and SBT. MICs50 of SBT/CPZ against most of these organisms other than Serratia marcescens were somewhat inferior to those of CPZ. MICs100 of SBT/CPZ against Escherichia coli, Citrobacter freundii and Proteus species were superior to those of CPZ. SBT alone showed no remarkable antimicrobial activity against most of these organisms. 2) Serum and sputum levels in patients with chronic respiratory tract infections: SBT/CPZ was administered by intravenous drip infusion at a dose of 2 g to four patients. The peak serum levels were 71-130ƒÊg/ml for CPZ and 20-58 ƒêg/ml for SBT at the termination of infusion and the peak sputum levels were 5.6 ƒêg/ml for CPZ and 8.8ƒÊg/ml for SBT. 3) Clinical results: Twenty patients with respiratory tract infections (chronic bronchitis 3, bronchiectasis 7, pulmonary cyst 2, pneumonia 6, lung abscess 1, pleuritis 1) were treated with SBT/CPZ by intravenous drip infusion at a dose of 1-2g once or twice a day for 7-14 days and over all efficacy rate was 80%. Adverse reaction was noted in one case with slight elevation of S-GOT and S-GPT.