TY - JOUR
T1 - Application of hydrophilic polymers for the preparation of tadalafil solid dispersions
T2 - micromeritics properties, release and erectile dysfunction studies in male rats
AU - Ahmed, Mohammed Muqtader
AU - Anwer, Md Khalid
AU - Soliman, Gamal A.
AU - Aldawsari, Mohammed F.
AU - Mohammed, Abdul Aleem
AU - Alshehri, Sultan
AU - Ghoneim, Mohammed M.
AU - Alali, Amer S.
AU - Alshetaili, Abdullah
AU - Alalaiwe, Ahmed
AU - Bukhari, Sarah I.
AU - Zafar, Ameeduzzafar
N1 - Publisher Copyright:
Copyright 2022 Ahmed et al.
PY - 2022/5
Y1 - 2022/5
N2 - 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 R VA64, and Kollidon R 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.
AB - 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 R VA64, and Kollidon R 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.
KW - Aphrodisiac activity
KW - Kollidon
KW - Kolliphor
KW - Micromeritics
KW - Solid dispersion
KW - Tadalafil
UR - http://www.scopus.com/inward/record.url?scp=85131170209&partnerID=8YFLogxK
U2 - 10.7717/peerj.13482
DO - 10.7717/peerj.13482
M3 - Article
AN - SCOPUS:85131170209
SN - 2167-8359
VL - 10
JO - PeerJ
JF - PeerJ
M1 - e13482
ER -