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bioavailability after different routes of administration vs bioavailability following different routes of administration

Both phrases are correct and can be used interchangeably. They both refer to the concept of bioavailability in relation to various routes of administration. The choice between 'after' and 'following' is a matter of personal preference or style, as they convey the same meaning in this context.

Last updated: March 23, 2024 • 419 views

bioavailability after different routes of administration

This phrase is correct and commonly used in scientific and medical contexts to describe the availability of a drug after it has been administered through various routes.

This phrase is used to discuss the extent to which a drug becomes available in the body after being administered through different routes such as oral, intravenous, or topical.
  • There was no evidence of a difference in risk between the different routes of administration.
  • Different mechanism of binding, different route of administration and different site of action to oral alternative bismuth.
  • At least two different routes of administration should normally be studied. One of these may be the same as, or similar to, that proposed for the target species.
  • This may be the result, inter alia, of different modes of actions, different pharmacokinetic or pharmacodynamic profiles, different lengths of treatment or different routes of administration.
  • At least two different routes of administration shall normally be used, one being identical with or similar to that proposed for use in human beings and the other ensuring systemic exposure to the substance.
  • Interaction with zalcitabine is unlikely due to different routes of metabolism and excretion.
  • and for different routes of exposure.
  • Special consideration shall be given to the different routes of ingestion.
  • Further repeat dose studies including testing on a second species (non-rodent), studies of longer duration or through a different route of administration shall be undertaken in case of:
  • the relative hazards associated with the different routes of exposure, and
  • the relative hazard associated with the different routes of exposure.
  • The usual routes of administration are oral intubation or intraperitoneal injection.
  • Routes of administration are usually oral intubation or intraperitoneal injection.
  • The two main routes of administration are oral and inhalation.
  • Subdivide the information according to the different routes of exposure, i.e. inhalation, skin and eye contact and ingestion, under different subheadings.
  • Subdivide the information according to the different routes of exposure, i.e. inhalation, skin and eye contact and ingestion, under different subheadings.
  • Subdivide the information according to the different routes of exposure, i.e. inhalation, skin and eye contact and ingestion, under different subheadings.
  • Include information on the different routes of exposure (inhalation, ingestion, skin and eye contact), and describe the symptoms related to the physical, chemical and toxicological characteristics.
  • Further repeat dose studies Further repeat dose studies including testing on a second species (non-rodent), studies of longer duration or through a different route of administration shall be undertaken in case of:
  • It is preferable that animal studies are conducted using appropriate routes of administration which relate to the potential route of human exposure.

Alternatives:

  • bioavailability following different routes of administration
  • bioavailability with different routes of administration
  • bioavailability across different routes of administration
  • bioavailability via different routes of administration
  • bioavailability from different routes of administration

bioavailability following different routes of administration

This phrase is also correct and commonly used in scientific and medical contexts to describe the availability of a drug following its administration through various routes.

This phrase is used to discuss the extent to which a drug becomes available in the body following its administration through different routes such as oral, intravenous, or topical.
  • There was no evidence of a difference in risk between the different routes of administration.
  • Different mechanism of binding, different route of administration and different site of action to oral alternative bismuth.
  • At least two different routes of administration should normally be studied. One of these may be the same as, or similar to, that proposed for the target species.
  • This may be the result, inter alia, of different modes of actions, different pharmacokinetic or pharmacodynamic profiles, different lengths of treatment or different routes of administration.
  • At least two different routes of administration shall normally be used, one being identical with or similar to that proposed for use in human beings and the other ensuring systemic exposure to the substance.
  • Bioavailability following subcutaneous and intramuscular injection in humans is high and similar for the two routes of administration (71% and 66%, respectively).
  • Interaction with zalcitabine is unlikely due to different routes of metabolism and excretion.
  • and for different routes of exposure.
  • Special consideration shall be given to the different routes of ingestion.
  • Further repeat dose studies including testing on a second species (non-rodent), studies of longer duration or through a different route of administration shall be undertaken in case of:
  • the relative hazards associated with the different routes of exposure, and
  • the relative hazard associated with the different routes of exposure.
  • The usual routes of administration are oral intubation or intraperitoneal injection.
  • Routes of administration are usually oral intubation or intraperitoneal injection.
  • The two main routes of administration are oral and inhalation.
  • Subdivide the information according to the different routes of exposure, i.e. inhalation, skin and eye contact and ingestion, under different subheadings.
  • Subdivide the information according to the different routes of exposure, i.e. inhalation, skin and eye contact and ingestion, under different subheadings.
  • Subdivide the information according to the different routes of exposure, i.e. inhalation, skin and eye contact and ingestion, under different subheadings.
  • Include information on the different routes of exposure (inhalation, ingestion, skin and eye contact), and describe the symptoms related to the physical, chemical and toxicological characteristics.
  • Further repeat dose studies Further repeat dose studies including testing on a second species (non-rodent), studies of longer duration or through a different route of administration shall be undertaken in case of:

Alternatives:

  • bioavailability after different routes of administration
  • bioavailability with different routes of administration
  • bioavailability across different routes of administration
  • bioavailability via different routes of administration
  • bioavailability from different routes of administration

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