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Bioequivalence in generic drugs, such as tablets and capsules, refers to their pharmaceutical equivalence to the brand-name counterparts. However, for therapeutic equivalence, manufacturers must also consider physical attributes like size, shape, and weight (FDA Guidance for Industry, December 2003). Discrepancies in these aspects could impact patient compliance and cause medication errors. For instance, swallowing difficulties, often experienced with larger tablets or capsules, can lead to...
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A medication’s effectiveness largely depends on its appropriate dosage and the route of administration. Dosage ensures that a sufficient drug concentration is maintained in the bloodstream to elicit the desired therapeutic effect without causing toxicity. The route of administration affects the drug's bioavailability, rate of absorption, and onset of action, which are crucial for achieving optimal therapeutic outcomes. Drug dosage calculations are critical to tailoring therapy to...
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Chewable Tablets for Precise Unit Dosing of Animals.

Reese E Landes1, Pradeep Valekar1, Muslim Abbas1

  • 1Duquesne University, Pittsburgh, PA USA.

Journal of Pharmaceutical Innovation
|January 1, 2026
PubMed
Summary
This summary is machine-generated.

Tablets offer a precise method for delivering preclinical drugs to laboratory mice, overcoming the distress of oral gavage and the imprecision of food formulations. Mice readily consumed bitter tablets after a habituation period, indicating their suitability for drug delivery.

Keywords:
OralOral gavagePeroralPest controlPreclinical researchTabletsVeterinary

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Area of Science:

  • Pharmacology
  • Animal Models
  • Drug Delivery Systems

Background:

  • Oral administration of preclinical drugs typically uses oral gavage or food formulations.
  • Oral gavage causes distress and is unsuitable for behavioral studies.
  • Food-based delivery methods lack precision in dosing.

Purpose of the Study:

  • To develop and evaluate tablets for precise peroral drug delivery in laboratory mice.
  • To assess the feasibility of using tablets for unit dosing in preclinical research.

Main Methods:

  • Tablet compositions were assessed for compactability and compressibility.
  • CD-1 mice were tested for voluntary tablet consumption.
  • Denatonium benzoate, a bitter compound, was added to tablets at escalating doses.
  • Tablet consumption was measured over four weeks in male and female mice.

Main Results:

  • Tablet consumption increased with exposure, indicating a need for habituation.
  • After a one-week habituation to placebo tablets, 9 of 11 mice consumed all bitter tablets.
  • Mice consumed 97% of tablet mass within one hour.
  • No significant changes in body weight were observed.

Conclusions:

  • Tablets are a viable and precise method for preclinical drug delivery in laboratory mice.
  • The habituation strategy enhances tablet acceptance in mice.
  • This method offers an alternative to less precise or distressing drug administration techniques.