Examples of 'bioavailability of the drug' in a sentence
Meaning of "bioavailability of the drug"
bioavailability of the drug: The degree and rate at which an administered drug is absorbed by the body's circulatory system, making it available to produce its intended effects. Factors affecting bioavailability include the drug's formulation, route of administration, and interactions with other substances in the body
How to use "bioavailability of the drug" in a sentence
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bioavailability of the drug
The bioavailability of the drug is therefore improved.
This may reduce the bioavailability of the drug.
The bioavailability of the drug is decreased by dietary fiber.
The gel retards dissolution and bioavailability of the drug.
The bioavailability of the drug is minimally altered by the presence of food.
This reduction in drug transport represents an increase of the bioavailability of the drug.
Even bioavailability of the drug in the pharmaceutical dosage form may be improved.
The proper choice of polymer in turn affects the bioavailability of the drug.
EGCG may reduce the bioavailability of the drug sunitinib when they are taken together.
This is significant as smaller drug particles result in greater bioavailability of the drug.
Pulmonary deposition and systemic bioavailability of the drug depend on the nebulizer used.
The dissolution rate of a drug or composition thereof affects the bioavailability of the drug.
Therefore, the bioavailability of the drug depends on the route of administration.
The polymorphism and geometrical isomerism may also influence on the bioavailability of the drug.
This may result in a lowered systemic bioavailability of the drug as the drug is metabolized.
See also
The improved dissolution and dispersion properties of this formulation affords improved bioavailability of the drug.
Further, the invention provides for superior bioavailability of the drug in an aqueous use environment.
Interestingly, intravenous administration to patients undergoingenteral nutrition is associated with higher bioavailability of the drug.
Such a change generally, in turn, decreases the bioavailability of the drug when dosed to a mammal.
The systemic bioavailability of the drug by this ocular route of administration is 23 %.
This first pass through the liver thus greatly reduces the bioavailability of the drug.
Without a meal preceding dose, the bioavailability of the drug is reduced by approximately 50.
Lipophilic moieties can also improve site-specificity and bioavailability of the drug.
The bioavailability of the drug was > 98 % with no gender differences.
Thus, this characteristic allows an improved bioavailability of the drug to be released.
In a preferred embodiment, the composition comprising the solid dispersion provides enhanced bioavailability of the drug.
This, however, required sufficient bioavailability of the drug compound.
The cats showed hypothermia and lethargy after injection, indicative of the bioavailability of the drug.
In the case of intravenous injections the bioavailability of the drug is 100 %.
Physico-chemical factors and the pharmaco-technical formulation can have repercussions in the bioavailability of the drug.
Furthermore, the carrier may be used to improve the bioavailability of the drug.
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Examples of using Bioavailability
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Comparative bioavailability of ranitidine tablets and suspension
Scientific advisory committee on bioavailability and bioequivalence
The bioavailability is not affected by food intake
