Noncompartmental Determination of the Steady-State Volume of Distribution During Multiple Dosing

1984 ◽  
Vol 73 (2) ◽  
pp. 281-282 ◽  
Author(s):  
Ian L. Smith ◽  
Jerome J. Schentag
Keyword(s):  
Steady State ◽  
Volume Of Distribution ◽  
Multiple Dosing

Noncompartmental Determination of the Steady‐State Volume of Distribution

1979 ◽  
Vol 68 (8) ◽  
pp. 1071-1074 ◽  
Author(s):  
Leslie Z. Benet ◽  
Renato L. Galeazzi
Keyword(s):  
Steady State ◽  
Volume Of Distribution

Method for the determination of the arteriovenous muscle protein balance during non-steady-state blood and muscle amino acid concentrations

2005 ◽  
Vol 289 (6) ◽  
pp. E1064-E1070 ◽  
Author(s):  
Christos S. Katsanos ◽  
David L. Chinkes ◽  
Melinda Sheffield-Moore ◽  
Asle Aarsland ◽  
Hisamine Kobayashi ◽  
...  
Keyword(s):  
Steady State ◽  
Amino Acid ◽  
Muscle Protein ◽  
Volume Of Distribution ◽  
Protein Balance ◽  
Nonsteady State ◽  
Balance Technique ◽  
Amino Acid Concentrations ◽  
Rate Of Accumulation

We describe a method based on the traditional arteriovenous balance technique in conjunction with muscle biopsies for the determination of leg muscle protein balance during the nonsteady state in blood amino acid concentrations. Six young, healthy individuals were studied in the postabsorptive state (pre-Phe) and after a bolus ingestion of ∼0.5 g phenylalanine (post-Phe). Post-Phe free phenylalanine concentrations in blood and muscle increased ( P < 0.05), but the respective concentrations of the amino acid threonine did not change. The average post-Phe leg net balance (NB) for threonine decreased from basal ( P < 0.05), but that for phenylalanine did not change. A volume of distribution for free phenylalanine in the leg was calculated based on the leg lean mass and the relative muscle water content and used to estimate the rate of accumulation of free phenylalanine in the leg. When the post-Phe NB for phenylalanine was corrected for the rate of accumulation of free phenylalanine in the leg, the post-Phe NB for phenylalanine decreased from basal ( P < 0.05). This corrected value was not different ( P > 0.05) from the value predicted for the phenylalanine NB based on the pre- and post-Phe NB responses for threonine. We conclude that the protein NB in non-steady-state blood phenylalanine concentrations can be determined from the arteriovenous phenylalanine NB by accounting for changes in free phenylalanine within its volume of distribution.

scholarly journals Double-Blind Evaluation of the Safety and Pharmacokinetics of Multiple Oral Once-Daily 750-Milligram and 1-Gram Doses of Levofloxacin in Healthy Volunteers

1998 ◽  
Vol 42 (4) ◽  
pp. 885-888 ◽  
Author(s):  
Shu-Chean Chien ◽  
Frank A. Wong ◽  
Cynthia L. Fowler ◽  
Susan V. Callery-D’Amico ◽  
R. Rex Williams ◽  
...  
Keyword(s):  
Steady State ◽  
Healthy Volunteers ◽  
Washout Period ◽  
Volume Of Distribution ◽  
Controlled Study ◽  
High Dose ◽  
Multiple Dosing ◽  
Double Blind ◽  
Once Daily ◽  
Dose Levels

ABSTRACT The safety and pharmacokinetics of once-daily oral levofloxacin in 16 healthy male volunteers were investigated in a randomized, double-blind, placebo-controlled study. Subjects were randomly assigned to the treatment (n = 10) or placebo group (n = 6). In study period 1, 750 mg of levofloxacin or a placebo was administered orally as a single dose on day 1, followed by a washout period on days 2 and 3; dosing resumed for days 4 to 10. Following a 3-day washout period, 1 g of levofloxacin or a placebo was administered in a similar fashion in period 2. Plasma and urine levofloxacin concentrations were measured by high-pressure liquid chromatography. Pharmacokinetic parameters were estimated by model-independent methods. Levofloxacin was rapidly absorbed after single and multiple once-daily 750-mg and 1-g doses with an apparently large volume of distribution. Peak plasma levofloxacin concentration (C max) values were generally attained within 2 h postdose. The mean values of C max and area under the concentration-time curve from 0 to 24 h (AUC0–24) following a single 750-mg dose were 7.1 μg/ml and 71.3 μg · h/ml, respectively, compared to 8.6 μg/ml and 90.7 μg · h/ml, respectively, at steady state. Following the single 1-g dose, mean C max and AUC0–24 values were 8.9 μg/ml and 95.4 μg · h/ml, respectively; corresponding values at steady state were 11.8 μg/ml and 118 μg · h/ml. These C maxand AUC0–24 values indicate modest and similar degrees of accumulation upon multiple dosing at the two dose levels. Values of apparent total body clearance (CL/F), apparent volume of distribution (V ss/F), half-life (t 1/2), and renal clearance (CLR) were similar for the two dose levels and did not vary from single to multiple dosing. Mean steady-state values for CL/F,V ss/F,t 1/2, and CLR following 750 mg of levofloxacin were 143 ml/min, 100 liters, 8.8 h, and 116 ml/min, respectively; corresponding values for the 1-g dose were 146 ml/min, 105 liters, 8.9 h, and 105 ml/min. In general, the pharmacokinetics of levofloxacin in healthy subjects following 750-mg and 1-g single and multiple once-daily oral doses appear to be consistent with those found in previous studies of healthy volunteers given 500-mg doses. Levofloxacin was well tolerated at either high dose level. The most frequently reported drug-related adverse events were nausea and headache.

STEADY-STATE DETERMINATION OF FUEL-BOND NITROGEN IN DIESEL AND INDUSTRIAL GAS OIL

Clean Air ◽  
2007 ◽  
Vol 8 (4) ◽  
pp. 359-371
Author(s):  
A. Medeiros ◽  
R. Edenhofer ◽  
K. Lucka ◽  
H. Kohne
Keyword(s):  
Steady State ◽  
Gas Oil ◽  
State Determination
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