نتایج جستجو برای: Ofloxacin
تعداد نتایج: 2097 فیلتر نتایج به سال:
The penetration of an optically active ofloxacin isomer [(-)-ofloxacin] into human neutrophils and different tissue culture cells (HEp-2, McCoy, MDCK, and Vero) was studied and compared with that of ofloxacin by a fluorometric assay. The cellular-to-extracellular-concentration ratios (C/E) of (-)-ofloxacin were always higher than 6, significantly greater than those of ofloxacin at extracellular...
Ofloxacin is an important drug with anti-bacterial effects, and (–)-ofloxacin has been shown to have better activity than racemic ofloxacin. But the chiral resolution of compounds a major challenge worldwide. Many methods do not show high specificity target molecules, causing errors in separation these pharmaceutical thus affecting purity drugs. The paper mainly researches on method for quick o...
بررسی کارایی پر سولفات سدیم فعال شده با پرتو فرا بنفش در حذف آنتی بیوتیک آفلوکساسین از محیط های آبی
Background and purpose: Pharmaceutical products, particularly antibiotics are emerging contaminants that cause major environmental challenges due to cumulative effects, different adverse effects, and leading to drug resistance. The aim of this experimental study was to evaluate the efficiency of advanced oxidation process by persulfate activated by UV in removal of ofloxacin from aqueous soluti...
The distribution behavior of ofloxacin enantiomers was examined in the aqueous and organic solvent of a two-phase system containing chiral selector L-tartarate. The effect of extraction equilibrium time, buffer pH, organic solvents and length of alkyl chain of L-tartarate on the partition coefficients and enantioselectivity of racemic ofloxacin were investigated, respectively. The L-tartara...
the distribution behavior of ofloxacin enantiomers was examined in the aqueous and organic solvent of a two-phase system containing chiral selector l-tartarate. the effect of extraction equilibrium time, buffer ph, organic solvents and length of alkyl chain of l-tartarate on the partition coefficients and enantioselectivity of racemic ofloxacin were investigated, respectively. the l-tartarate f...
BACKGROUND/AIMS Gold-standard treatment of spontaneous bacterial peritonitis currently involves 3rd generation cephalosporins. To evaluate the efficacy of ofloxacin in this infection, we compared a combined therapy with intravenous and oral ofloxacin to intravenous cefotaxime. METHODS Thirty cirrhotic patients with spontaneous bacterial peritonitis were assigned to receive either intravenous ...
We compared the safety and efficacy of a single 400-mg dose of ofloxacin, ofloxacin (200 mg) once daily for 3 days, and trimethoprim-sulfamethoxazole (160:800 mg) twice daily for 7 days for the treatment of acute uncomplicated cystitis (urinary tract infection [UTI]) in women. At 5 weeks posttreatment, 35 (81%) of 43 patients treated with single-dose ofloxacin, 40 (89%) of 45 treated with 3 day...
BACKGROUND Infection with Salmonella enterica serovar Typhi (S. Typhi) with reduced susceptibility to fluoroquinolones has been associated with fluoroquinolone treatment failure. We studied the relationship between ofloxacin treatment response and the ofloxacin minimum inhibitory concentration (MIC) of the infecting isolate. Individual patient data from seven randomised controlled trials of ant...
BACKGROUND This study aimed to analyze the association of mutation patterns in gyrA and gyrB genes and the ofloxacin resistance levels in clinical Mycobacterium tuberculosis isolates sampled in 2009 from East China. METHODS The quinolone resistance-determining region of gyrA/B were sequenced in 192 M. tuberculosis clinical isolates and the minimal inhibitory concentrations (MICs) of 95 ofloxa...
Two optically active (100% enantiomeric excess) isomers of ofloxacin [(+/-)-ofloxacin; DL-8280; (+/-)-9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7 H-pyrido[1,2,3-de] [1,4] benzoxazine-6-carboxylic acid] were prepared by use of their optically resolved synthetic intermediates. One of the isomers, (-)-ofloxacin, was 8 to 128 times more potent in inhibiting the multiplication ...
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