Dhaneshwar Shep, Ashwini Ojha, Sweta Patel, Manish Nivsarkar, Vijaya Jaiswal and Harish Padh Pages 26-29 (4)
Methods: This two way randomized crossover study was performed in 14 healthy, adult, Indian, male human subjects to compare bioavailability. The formulations were administered intramuscularly (intragluteal) to the volunteers in a two way randomized fashion with a wash out period of 6 days. Blood samples were collected till 6.0 h following drug administration. The samples were analyzed using pre-validated HPLC method.
Results: The mean Cmax and Tmax for the test and reference formulations were 2.14 μg/mL, 1.91 μg/mL and 0.49 h, 0.50 h respectively. The mean AUC0-t for test and reference formulations were 3.79 μg.h/mL, and 3.43 μg.h/mL respectively. The mean AUC0-∞ for test and reference formulation were 4.03 μg.h/mL and 3.65 μg.h/mL respectively. The mean (90% CI) Cmax, AUC0-t and AUC0-∞ ratio (Test:Reference) were 1.15 (100.25 – 132.99), 1.10 (100.34 – 119.96) and 1.09 (100.78 – 118.88), respectively.
Conclusion: The test formulation shows a comparable AUC0-t and AUC0-∞ but a higher Cmax in comparison to the reference when given intra-gluteally. The lower volume of the test formulation offers advantage of injection at other sites, like deltoid region. Absence of propylene glycol in the test formulation could be advantageous in terms of improved tolerability. Hence, such formulations of previously well established molecules provide a new direction towards developing better and convenient dosing alternatives.
Bioavailability, diclofenac sodium, intragluteal, injection, pharmacokinetics, volume, leukocytes, Parameters, dichloromethaness, anti-inflammatory drug
Vice-President, Medical Services, Troikaa Pharmaceuticals Ltd, Commerce House-1, Satya Marg, Bodakdev, Ahmedabad-54.