「bioavailability」の共起表現一覧(1語右で並び替え)
該当件数 : 56件
rectal, and injectable formulations, with | bioavailability above 97 per cent after oral administrati |
fference between the two substances is in | bioavailability and pharmacodynamic potency. |
agnesium are considered essential for the | bioavailability and absorption of Vitamin D and calcium. |
ne include longer half-life, greater oral | bioavailability and no observed dose-dependent liver toxi |
Reflecting this link between iron | bioavailability and bacterial growth, the taking of iron |
le taken with a high fat meal exceeds 90% | bioavailability and increases the concentration by 4 time |
subjects have confirmed the low systemic | bioavailability and favourable safety profile of single a |
Formestane has poor oral | bioavailability and as such is no longer popular as many |
compound, noopept displays both high oral | bioavailability and good blood-brain barrier penetration, |
The relatively poor oral | bioavailability and blood-brain barrier penetration of CX |
umans, although THIQ itself has poor oral | bioavailability and a short duration of action so improve |
od in vivo properties including high oral | bioavailability and good brain penetration. |
re potent than CX-717 and has better oral | bioavailability, and is being trialled for treatment of s |
acokinetic factors, such as its high oral | bioavailability and long duration of action, but several |
ersion of resveratrol exhibiting a higher | bioavailability as it is more easily transported into the |
It is well absorbed with absolute oral | bioavailability between 80 and 100%. |
Food does not alter the | bioavailability, but may increase the resorption. |
OX1 over OX2 receptors, and improved oral | bioavailability compared to the older OX1 antagonist SB-3 |
-alkylated; instead it has increased oral | bioavailability due to its cyclopentenyl ether group. |
Bioavailability following subcutaneous and intramuscular | |
and selective in vitro and had good oral | bioavailability in vivo, but had poor penetration across |
Bioavailability is almost complete. | |
Losartan's | bioavailability is about 32%. |
Despite this, absolute | bioavailability is relatively poor at 15% (candesartan ci |
Oral | bioavailability is estimated to be about 10%, but food do |
le it contains antimony and nickel, their | bioavailability is very low, so the pigment is relatively |
ot meet additional requirements, and that | bioavailability is the only test FDA can require. |
erectile dysfunction, although poor oral | bioavailability means alternative drugs such as ABT-670 m |
Poor water solubility and | bioavailability of silymarin led to the development of en |
The | bioavailability of Nelfinavir is increased 2.5 to 5 times |
Studies suggest that the | bioavailability of curcumin and possibly its derivatives |
st-pass-metabolization leading to an oral | bioavailability of 50 to 95%. |
The use of a prodrug form increases the | bioavailability of candesartan. |
In many individuals, | bioavailability of calcium is found to be equal to that o |
es extensive first-pass metabolism, has a | bioavailability of 34-38 percent, and is 95 percent bound |
oephedrine, it has a reduced and variable | bioavailability of only up to 38 percent. |
However, it is well known that oral | bioavailability of opioids is heavily dependent on the su |
gs that are targeted to increase the oral | bioavailability of other drugs. |
ation with entacapone, which enhances the | bioavailability of carbidopa and levodopa. |
fect over this enzyme and as a result the | bioavailability of the drug increases, raising the risk f |
s, which may damage tissues and alter the | bioavailability of limiting trace metals. |
Another disadvantage is that the | bioavailability of oral or sublingual formulations can be |
ious drugs and an improvement of the oral | bioavailability of drugs with poor absorption characteris |
oted that methasterone possessed the oral | bioavailability of methyl-testosterone while being 400% a |
It was designed for increased oral | bioavailability over gabapentin, and human trials showed |
urgery, calcium citrate may have improved | bioavailability over calcium carbonate in Roux-en-Y gastr |
y and anorexia; however, due to poor oral | bioavailability, Ro 64-6198 will most likely not be pursu |
Calcium citrate malate's | bioavailability stems from its water-solubility and its m |
There are no specific | bioavailability studies that were made available on this |
It has a somewhat higher oral | bioavailability than THC itself but is otherwise very sim |
t resveratrol from wine could have higher | bioavailability than resveratrol from a pill has been ref |
and longer lasting, and also have higher | bioavailability than codeine. |
y used in medicine, but may have a higher | bioavailability than hydromorphone due to its greater lip |
he use of tacrine is limited by poor oral | bioavailability, the necessity for four-times daily dosin |
ve extra genes inserted; it also has high | bioavailability when taken orally, so it is useful for de |
hone, metopon is less potent and its oral | bioavailability, while higher than that of morphine, is s |
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