Application of hydrophilic polymers for the preparation of tadalafil solid dispersions: micromeritics properties, release and erectile dysfunction studies in male rats

Author:

Ahmed Mohammed Muqtader1,Anwer Md Khalid1,Soliman Gamal A.23,Aldawsari Mohammed F.1,Mohammed Abdul Aleem4,Alshehri Sultan56,Ghoneim Mohammed M.5,Alali Amer S.1,Alshetaili Abdullah1,Alalaiwe Ahmed1,Bukhari Sarah I.6,Zafar Ameeduzzafar7

Affiliation:

1. Pharmaceutics, Prince Sattam Bin Abdulaziz University, Alkharj, Saudi Arabia

2. Department of Pharmacology and Toxicology, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Alkharj, Saudi Arabia

3. Department of Pharmacology, College of Veterinary Medicine, Cairo University, Giza, Egypt

4. Department of Pharmaceutics, College of Pharmacy, Najran University, Najran, Saudi Arabia

5. Department of Pharmaceutical Sciences, College of Pharmacy, AlMaarefa University, Ad Diriyah, Saudi Arabia

6. Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia

7. Department of Pharmaceutics, College of Pharmacy, Jouf University, Sakaka, Al-Jouf Saudi Arabia

Abstract

The objective of the present study was to improve the dissolution rate and aphrodisiac activity of tadalafil by using hydrophilic polymers. Solid dispersions were prepared by solvent evaporation-Rota evaporator using Koliphore 188, Kollidon® VA64, and Kollidon® 30 polymers in a 1:1 ratio. Prepared tadalafil-solid dispersions (SDs) evaluated for yield, drug content, micromeritics properties, physicochemical characterizations, and aphrodisiac activity assessment. The optimized SDs TK188 showed size (2.175 ± 0.24 µm), percentage of content (98.89 ± 1.23%), yield (87.27 ± 3.13%), bulk density (0.496 ± 0.005 g/cm3), true density (0.646 ± 0.003 g/cm3), Carr’s index (23.25 ± 0.81), Hausner ratio (1.303 ± 0.003) and angle of repose (<25°). FTIR spectrums revealed tadalafil doesn’t chemically interact with used polymers. XRD and DSC analysis represents TK188 SDs were in the amorphous state. Drug release was 97.17 ± 2.43% for TK188, whereas it was 32.76 ± 2.65% for pure drug at the end of 2 h with 2.96-fold increase in dissolution and followed release kinetics of Korsmeyer Peppa’s model. MDT and DE were noted to be 17.48 minutes and 84.53%, respectively. Furthermore, TK188 SDs showed relative improvement in the sexual behavior of the male rats. Thus the developed SDs TK188 could be potential tadalafil carriers for the treatment of erectile dysfunction.

Funder

Researchers Supporting Program (TUMA-Project-2021-2), AlMaarefa University, Riyadh, Saudi Arabia

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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