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February 6, 2025Frontiers in Medical TechnologyOpen Access

Bioanalytical method development, in-vivo pharmacokinetic evaluation, ex-vivo platelet aggregation inhibition activity of a novel solid dispersion formulation of ticagrelor

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Why the study?

Ticagrelor use has been restricted due to poor aqueous solubility, prompting the development and evaluation of a formulation to improve oral bioavailability and antiplatelet activity.

Does a novel solid dispersion formulation of ticagrelor improve oral bioavailability and antiplatelet activity compared to the marketed formulation in Sprague Dawley rats?

Population

Sprague Dawley rats

Comparison

Developed ticagrelor formulation (SD1) at 10 mg/kg vs marketed formulation (RLD)

Design

Preclinical pharmacokinetic and ex-vivo pharmacodynamic study

Authors

ASAbhishek Kumar SrivastavaSBSimrata BediAMAbhishesh Kumar Mehata

Discussion

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Overview

Preclinical Ticagrelor formulation gains leave clinical translation uncertain; leaves open human bioavailability and antiplatelet trials.

Structured PICO

Does a novel solid dispersion formulation of ticagrelor improve oral bioavailability and antiplatelet activity compared to the marketed formulation in Sprague Dawley rats?

P
Population
Sprague Dawley rats
I
Intervention
Novel solid dispersion formulation of ticagrelor (SD1) at 10 mg/kg
C
Comparator
Marketed ticagrelor formulation (RLD)
O
Outcome
Pharmacokinetic profile (oral bioavailability) and ex-vivo antiplatelet aggregation activity (inhibition of ADP-induced platelet aggregation)surrogate

A novel solid dispersion formulation of ticagrelor significantly improved oral bioavailability and antiplatelet activity in a rat model compared to the marketed formulation.

Cite This Study

Srivastava et al. (2025) studied this question.

synapsesocial.com/papers/6a8798ba0bb327885a2c219chttps://doi.org/10.3389/fmedt.2025.1499189
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