Zobrazeno 1 - 10
of 20
pro vyhledávání: '"S. J. Kohlhepp"'
Publikováno v:
Antimicrobial Agents and Chemotherapy. 38:1065-1070
Dietary calcium supplements attenuate experimental aminoglycoside nephrotoxicity. In cultured renal tubular cells, intracellular calcium levels have been reported to rise with aminoglycoside addition to the culture medium. In experiments designed to
Publikováno v:
Antimicrobial Agents and Chemotherapy. 37:2678-2683
Scant data exist on intracellular events during aminoglycoside-induced postantibiotic effect (PAE). We examined DNA, RNA, and protein syntheses after tobramycin exposure using [3H]thymidine, [14C]uracil, and [14C]alanine incorporation in a clinical E
Publikováno v:
Antimicrobial Agents and Chemotherapy. 35:2591-2595
Polyaspartic Acid (PAA) protects the kidney from experimental gentamicin nephrotoxicity despite large increases in renal cortical gentamicin content. In these experiments, prominent cytoplasmic vacuoles were noted in all animals that received PAA wit
Publikováno v:
Antimicrobial Agents and Chemotherapy. 38:2169-2171
The surface membrane properties of LLC-PK1 cells grown with and without various amounts of gentamicin or tobramycin for various lengths of time were determined by measuring the diffusion coefficient of N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)dipalmitoyl
Autor:
D N, Gilbert, S J, Kohlhepp, K A, Slama, G, Grunkemeier, G, Lewis, R J, Dworkin, S E, Slaughter, J E, Leggett
Publikováno v:
Antimicrobial agents and chemotherapy. 45(3)
The phenotypic resistance of selected organisms to ciprofloxacin, levofloxacin, and trovafloxacin was defined as a MIC ofor =4 microg/ml. The dynamics of resistance were studied after single and sequential drug exposures: clinical isolates of methici
Autor:
P. W. Kohnen, S. J. Kohlhepp, David N. Gilbert, William M. Bennett, James E. Leggett, Suzanne K. Swan
Publikováno v:
Antimicrobial Agents and Chemotherapy. 36:2556-2558
It is known that daily polyaspartic acid (PAA) protects the kidney from gentamicin nephrotoxicity in a standardized rat model despite marked cortical accumulation of the aminoglycoside. The present experiments address the duration of PAA protection.
Publikováno v:
Antimicrobial agents and chemotherapy. 40(2)
The pharmacokinetics and tolerability of 1-g doses of ceftriaxone diluted in sterile water, 1% lidocaine, or buffered lidocaine were investigated. No difference in bioequivalence was noted between the three treatments. No difference in peak creatine
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 263(3)
The in vitro interaction of polyaspartic acid (PAA) with aminoglycosides was evaluated using double diffusion in agar, dialysis chambers and changes in the optical density of test solutions. The results document a reversible, presumably electrostatic
Autor:
D, Kremer, M Y, Munar, S J, Kohlhepp, S K, Swan, E A, Stinnett, D N, Gilbert, E W, Young, W M, Bennett
Publikováno v:
Pharmacotherapy. 12(1)
A few reports in the literature describe zidovudine (AZT) pharmacokinetics in patients undergoing hemodialysis; however, the effect of continuous ambulatory peritoneal dialysis (CAPD) on the drug's disposition has not been studied. The pharmacokineti
Publikováno v:
Antimicrobial Agents and Chemotherapy. 37:347-348
Polyaspartic acid (PAA) ameliorates experimental gentamicin nephrotoxicity despite marked accumulation of gentamicin in the renal cortex. The experiments described here probe the extent of PAA's nephroprotective action when increasing doses of gentam