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KMID : 0370219970410020225
Yakhak Hoeji
1997 Volume.41 No. 2 p.225 ~ p.232
In vitro Antibacterial Activities of Novel Fluoroquinolone DWP20367
±èÁö¿¬/Kim JY
ÃÖ¹®Á¤/ÇѽÂÈñ/½ÉÁ¡¼ø/Á¤¿¬ÀÇ/¼ÕÈ£Á¤/ÀÌÀç¿í/À¯¿µÈ¿/¹Ú¸íȯ/Choi MJ/Han SH/Shim JS/Jung YE/Son HJ/Lee JW/Yu YH/Park MH
Abstract
The in vitro antibacterial activity of DWP20367 (1-Cyclopropyl-6-fluoro-8-chloro-7-(2,7-diazabicyclo[3,3,0]oct-4-ene-7-yl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid), a new broad-spectrum fluoroquinolone, was compared with those of ciprofloxacin (CPFX), sparfloxacin (SPFX) and ofloxacin (OFLX). DWP20367 was showed antibacterial activity much higher than CPFX, SPFX and OFLK against gram-positive bacteria, while it was slightly more superior to quinolones against gram-negative bacteria. DWP20367 was particularly effective against MRSA, and its MlC90 against clinical isolates of methicillin-susceptible S. aureus, low methicillin-resistant S. aureus and high methicillin-resistant S. aureus were 0.098, 0.781 and 1.563 micro g/ml, respectively. Against S. pneumoniae, MIC90 of DWP20367 was 2- to 8-fold higher than those of CPFX. With a view of MIC90, DWP20367 showed slightly more potent activity against P. aeruginosa and E. coli isolates than the control quinolones. DWP20367 activity was not affected by inoculum size and medium pH. But addition of Mg2+, Ca2+ or horse serum (25%) decreased its antibacterial activity. DWP20367 was showed rapidly bactericidal activity within 2 to 4 h, and regrowth was not observed even after 24 h incubation at concentrations near the 4-fold of MIC.
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