Примери за използване на Central compartment на Английски и техните преводи на Български
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Medicine
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Official
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Ecclesiastic
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Ecclesiastic
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Computer
First off, you have one large central compartment. .
Central compartment with Anti-Slip System for keyboard and accessories.
Mean volume of distribution of central compartment.
A large central compartment, two side pockets and a large front pocket.
A localised tumour(T1-3), with lymph node spread beyond the central compartment(N1b) but no distant spread(M0).
The central compartment volume was 2.62 L for patients with MBC and EBC and 3.63 L for patients with AGC.
Any localized tumour(T1-3)with spread to the central compartment of lymph nodes(N1a) but no distant spread(M0).
A large central compartment, two side mesh pockets and a large front pocket, mesh pocket on the underside of the lid and made a pocket flap.
Any localized tumor(T1, 2, or 3)with spread to the central compartment of lymph nodes(N1a) but no distant spread(M0).
The volume of the central compartment is 70% of body weight, probably reflecting very rapid tissue binding to formed elements of the blood.
Within 30 minutes to 2 hours after the end of inhalation, iloprost is not detectable in the central compartment(limit of quantification 25 picogram/ml).
Clearance(CL), the central compartment volume(Vc) and population-predicted steady-state exposures(Cmin, Cmax and AUC).
In patients with advanced solid tumours, Vd was 191 l for the apparent central compartment and 517 l for the apparent peripheral compartment. .
The volume of the central compartment(Vc) and clearance correspond to an initial half-life of 1.4 days and a terminal half-life of about 20 days.
A two-compartment model with parallel linear andnon-linear elimination from the central compartment described the trastuzumab concentration-time profile.
A large central compartment with two front pockets with flap, two side compartments with mesh front pocket and pouch for a mobile phone, GPS and more.
The cells of eukaryotes, on the other hand, have an organized central compartment, called the nucleus, and other structures, such as mitochondria and chloroplasts.
A population pharmacokinetic analysis for TOBI Podhaler in cystic fibrosis patients estimated the apparent volume of distribution of tobramycin in the central compartment to be 84.1 litres for a typical CF patient.
Four solid and three mesh pockets,combined with large central compartment provides plenty of space for accessories for specialized fishing.
Distribution Based on a population pharmacokinetic analysis of 491 subjects receiving Avastin weekly, every 2 weeks, or every 3 weeks, in doses ranging from 1 to 20 mg/ kg,the volume of the central compartment(Vc) was 2.92 l.
Measurements of volume of distribution of the central compartment after single intravenous doses were 110 ml/ kg at dose 0.03 mg/ kg and 58 ml/ kg at dose 10 mg/ kg.
The pharmacokinetics of decitabine following intravenous administration as a 1-hour infusion were described by a linear two-compartment model,characterised by rapid elimination from the central compartment and by relatively slow distribution from the peripheral compartment. .
A population pharmacokinetic analysis indicates that central compartment volume of distribution is 3.28 L and volume at steady-state is 6.91 L in the typical patient.
The pharmacokinetics of decitabine following intravenous administration as a 1-hour infusion were described by a linear two-compartment model,characterised by rapid elimination from the central compartment and by relatively slow distribution from the peripheral compartment. .
Based on the populationpharmacokinetic(PK) model, the volume of distribution of the central compartment(Vc/F) was estimated to be 212 L. Protein binding was not altered in subjects with mild or moderately impaired renal or hepatic function.
Due to avoiding the first-pass-metabolism in the liver after intravenous administration the drug reaches maximal plasma concentrations very rapidly and completely with a rapid biphasic consequent decline, which reflects generation of the distribution equilibrium between tissue,peripheral and central compartments.
MBC and EBC patients had similar PK parameters(e.g. clearance(CL),the central compartment volume(Vc)) and population-predicted steady-state exposures(Cmin, Cmax and AUC).
Based on a population pharmacokinetic analysis in 298 NHL patients who received single or multiple infusions of MabThera as a single agent or in combination with CHOP therapy(applied MabThera doses ranged from 100 to 500 mg/m2), the typical population estimates of nonspecific clearance(CL1), specific clearance(CL2) likely contributed by B cells ortumour burden, and central compartment volume of distribution(V1) were 0.14 l/day, 0.59 l/day, and 2.7 l, respectively.
The estimated formoterol Vc/F(volume of the central compartment), and Vp1/F(volume of the peripheral compartment) are 1030 L, and 647 L, respectively, via population pharmacokinetic analysis.
In a population pharmacokinetic analysis in 403 follicular lymphoma patients who received subcutaneous and/or intravenous MabThera, single or multiple infusions of MabThera as a single agent or in combination with chemotherapy, the population estimates of nonspecific clearance(CL1), initial specific clearance(CL2) likely contributed by B cells ortumour burden, and central compartment volume of distribution(V1) were 0.194 L/day, 0.535 L/day, and 4.37 L/day, respectively.