Examples of 'terminal half-life' in a sentence

Meaning of "terminal half-life"

Terminal half-life is the time it takes for the concentration or amount of a substance in the body to be reduced by half

How to use "terminal half-life" in a sentence

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terminal half-life
The terminal half-life of lomitapide was not affected.
No significant variation in mean terminal half-life was observed.
However the terminal half-life was not significantly altered.
No significant variation in mean terminal half-life is observed.
The terminal half-life of esketamine was not affected by clarithromycin pre-treatment.
Following subcutaneous administration, the terminal half-life is slightly prolonged.
The terminal half-life of esketamine was not affected by ticlopidine pre-treatment.
Rolapitant is slowly eliminated with a mean terminal half-life of approximately 7 days.
The terminal half-life was twice as long for rFVIIIFc compared to rFVIII.
Pharmacokinetic analysis indicated a small distribution volume, slow plasma clearance and terminal half-life of approximately 2 days.
The terminal half-life is long population value of the terminal elimination phase.
A multiexponential decline in ADC serum concentrations was observed with a terminal half-life of approximately 4 to 5 days.
Terminal half-life increases with increasing dose and with repeated dosing.
This corresponds to a mean terminal half-life of approximately 11 days.
The terminal half-life and renal clearance of dabigatran were not affected by dronedarone.

See also

Pradofloxacin is eliminated from serum with a terminal half-life of 7 hours.
The terminal half-life of methadone is decreased during second and third trimesters.
In contrast to dutasteride, finasteride has a short terminal half-life of only 5 to 8 hours.
This terminal half-life is similar to the pharmacokinetics of endogenous cortisol that also is secretion-controlled.
When injected intravenously, the terminal half-life of dibotermin alfa was 16 minutes in rats.
This terminal half-life provides effective blood concentrations for the entire duration of the inter-dosing interval.
For example they have a very long terminal half-life when administered i . v.
The estimated terminal half-life for a typical patient from the population pharmacokinetic analysis is approximately 1 day.
The total body clearance of vardenafil is 56 l / h with a resultant terminal half-life of approximately.
The exceptionally long terminal half-life suggests the existence of storage sites within the organism.
Following subcutaneous administration, the absolute bioavailability is approximately 60 % ; the terminal half-life is slightly prolonged.
Elimination The terminal half-life is determined by the rate of absorption from the subcutaneous tissue.
Following an initial more rapid distribution phase, the terminal half-life of asenapine is approximately 24 h.
The terminal half-life is approximately 4 weeks.
Following an initial more rapid distribution phase, the mean terminal half-life is approximately 24 hrs.
Its terminal half-life is about one day.
As another non-limiting example, the derivative of the invention has a terminal half-life after i . v.
The mean terminal half-life is approximately 9 days.
Vincristine has a multiphasic pattern of clearance from the plasma ; the terminal half-life is about 24 hours.
Terminal half-life days.
In addition, the mean terminal half-life appeared to be shortened.
Elimination of buprenorphine from Buvidal is release-rate limited with a terminal half-life ranging from 3 to 5 days.
The terminal half-life of cysteamine bitartrate is approximately 4 hours.
The N-desmethyl metabolite is further metabolised, with a terminal half-life of approximately 4 h.
The terminal half-life is approximately 9 hours after administration of a single 40 mg dose.
In some embodiments, a plasma half-life is a terminal half-life after administration of a single IV dose.
The terminal half-life is between 5 and 7 hours depending on the dose.
More specifically, these compound had improved AUC, Cmax and terminal half-life.
Apparent terminal half-life.
Terminal half-life hrs.
In addition, the mean terminal half-life appears to be shortened.
Terminal half-life following an intravenous single microdose is 2.6 hours.
Efavirenz has a relatively long terminal half-life of at least 52 hours after single doses and.
The terminal half-life for radioactivity was about 130 h indicating that elimination of metabolites is very slow.
Meloxicam is eliminated with a terminal half-life of 7.7 hours.

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