نتایج جستجو برای: ofloxacin enantiomers

تعداد نتایج: 5479  

Journal: :The Journal of antimicrobial chemotherapy 2010
K A Angeby P Jureen C G Giske E Chryssanthou E Sturegård M Nordvall A G Johansson J Werngren G Kahlmeter S E Hoffner T Schön

OBJECTIVES To describe wild-type distributions of the MIC of fluoroquinolones for Mycobacterium tuberculosis in relation to current critical concentrations used for drug susceptibility testing and pharmacokinetic/pharmacodynamic (PK/PD) data. METHODS A 96-stick replicator on Middlebrook 7H10 medium was used to define the MICs of ciprofloxacin, ofloxacin, moxifloxacin and levofloxacin for 90 c...

Journal: :Antimicrobial agents and chemotherapy 1991
C Martin D Lambert B Bruguerolle P Saux J Freney J Fleurette H Meugnier F Gouin

The pharmacokinetics of ofloxacin were studied in 12 intensive care patients, 6 of whom were under controlled mechanical ventilation. All patients had a creatinine clearance of greater than 80 ml/min per 1.73 m2. They were given 3 mg of ofloxacin per kg of body weight intravenously at a constant flow rate in 30 min twice a day for 7 days. Pharmacokinetic studies were performed on days 1 and 7. ...

The electrochemical response of S- and R-naproxen enantiomers was investigated on L-cysteine/reduced graphene oxide modified glassy carbon electrode (L-Cys/RGO/GCE). The production of the reduced graphene oxide and L-cysteine on the surface of the glassy carbon electrode was done by using electrochemical processes. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were us...

Journal: :Biochemistry 2001
M Chen-Goodspeed M A Sogorb F Wu F M Raushel

The factors that govern the substrate reactivity and stereoselectivity of phosphotriesterase (PTE) toward organophosphotriesters containing various combinations of methyl, ethyl, isopropyl, and phenyl substituents at the phosphorus center were determined by systematic alterations in the dimensions of the active site. The wild type PTE prefers the S(P)-enantiomers over the corresponding R(P)-ena...

Journal: :Antiviral chemistry & chemotherapy 2000
Y L Qiu F Geiser T Kira E Gullen Y C Cheng R G Ptak J M Breitenbach J C Drach C B Hartline E R Kern J Zemlicka

A series of R and S enantiomers of 2-aminopurine methylenecyclopropane analogues of nucleosides was synthesized. Two diastereoisomeric lipophilic phosphate prodrugs derived from R and S enantiomers of 2,6-diaminopurine analogue were also prepared. Enantioselectivity (diastereoselectivity in case of prodrugs) of in vitro antiviral effects was investigated with human and murine cytomegalovirus (H...

Journal: :The Journal of antimicrobial chemotherapy 2009
Rose A Devasia Amondrea Blackman Carolyn May Svetlana Eden Teresa Smith Nancy Hooper Fernanda Maruri Charles Stratton Ayumi Shintani Timothy R Sterling

OBJECTIVES The aim of this study was to assess the sensitivity, specificity and time to results of mycobacterial growth indicator tube (MGIT) 960, microscopic observation drug susceptibility (MODS) assay and nitrate reductase assay (NRA) compared with the gold standard agar proportion method (PM), and to determine whether there is cross-resistance between older-generation fluoroquinolones and m...

Journal: :The Journal of antimicrobial chemotherapy 2006
Vincent Cattoir Philippe Lesprit Christine Lascols Erik Denamur Patrick Legrand Claude-James Soussy Emmanuelle Cambau

OBJECTIVES To investigate quinolone resistance mechanisms in an Escherichia coli clinical isolate (Ar2) resistant to ofloxacin but susceptible to nalidixic acid selected after 10 days of ofloxacin therapy in a patient with prostatitis. METHODS Molecular typing (ERIC-PCR and RAPD), antibiotic susceptibility and gyrA, gyrB, parC and parE QRDR sequences were compared for E. coli Ar2 and a wild-t...

Journal: :Antimicrobial agents and chemotherapy 2001
C K Naber M Hammer M Kinzig-Schippers C Sauber F Sörgel E A Bygate A J Fairless K Machka K G Naber

In a randomized crossover study, 16 volunteers (8 men, 8 women) received single oral doses of 320 mg of gemifloxacin and 400 mg of ofloxacin on two separate occasions in the fasting state to assess the urinary excretion and urinary bactericidal titers (UBTs) at intervals for up to 144 h. Ofloxacin showed higher concentrations in urine compared with those of gemifloxacin. The median (range) cumu...

2010
Manisha Puranik D. V. Bhawsar Prachi Rathi P. G. Yeole

The objective of this work was to develop and validate simple, rapid and accurate chromatographic methods for simultaneous determination of ofloxacin and ornidazole in solid dosage form. The first method was based on reversed phase high performance liquid chromatography, on Intersil C(18) column (250 mm, 4.6 i.d.), using acetonitrile:methanol: 0.025M phosphate buffer, pH 3.0 (30:10:60 % v/v/v) ...

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