Development of spray-dried amorphous solid dispersions of tadalafil using glycyrrhizin for enhanced dissolution and aphrodisiac activity in male rats

被引:18
作者
Ahmed, Mohammed Muqtader [1 ]
Fatima, Farhat [1 ]
Kalam, Mohd Abul [2 ]
Alshamsan, Aws [2 ]
Soliman, Gamal A. [3 ]
Shaikh, Abdul Azim [4 ]
Alshahrani, Saad M. [1 ]
Aldawsari, Mohammed F. [1 ]
Bhatia, Saurabh [5 ,6 ]
Anwer, Md. Khalid [1 ]
机构
[1] Prince Sattam Bin Abdulaziz Univ, Dept Pharmaceut, Coll Pharm, Al Kharj 11942, Saudi Arabia
[2] King Saud Univ, Dept Pharmaceut, Coll Pharm, Nanobiotechnol Unit, POB 2457, Riyadh 11451, Saudi Arabia
[3] Prince Sattam Bin Abdulaziz Univ, Dept Pharmacol, Coll Pharm, Al Kharj 11942, Saudi Arabia
[4] Riyadh Pharma Med & Cosmet Co Ltd, Riyadh, Saudi Arabia
[5] Amity Univ Haryana, Amity Inst Pharm, Gurgaon 122413, India
[6] Univ Nizwa, Nat & Med Sci Res Ctr, Nizwa, Oman
关键词
Spray-drying; Dissolution enhancement; Stability study; Aphrodisiac activity; TRANSDERMAL DELIVERY; ERECTILE DYSFUNCTION; FORMULATION; DRUG; BEHAVIOR;
D O I
10.1016/j.jsps.2020.11.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tadalafil (TDL) is a phosphodiesterase-5 inhibitor (PDE5I), indicated for erectile dysfunction (ED). However, TDL exhibits poor aqueous solubility and dissolution rate, which may limit its application. This study aims to prepare amorphous solid dispersion (ASD) by spray-drying, using glycyrrhizin-a natural drug carrier. Particle and physicochemical characterizations were performed by particle size, polydispersity index measurement, yield, drug content estimation, Fourier Transformed Infrared (FTIR) spectroscopy, Differential scanning calorimetry (DSC), X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and dissolution study. In order to evaluate the aphrodisiac activity of the prepared ASD, sexual behavior study was performed in male rats. It is further considered for the stability study. Our results revealed that TDL-GLZ spray-dried dispersion was a successful drug-carrier binary mixture. XRD and SEM showed that ASD of TDL with GLZ presented in the amorphous state and dentedspherical shape, unlike the drug indicating crystalline and spiked shaped. The optimized ASD3 formulation with particle size (1.92 mm), PDI (0.32), yield (97.78%) and drug content (85.00%) showed 4.07 folds' increase in dissolution rate compared to pure TDL. The results obtained from the in vivo study exhibit significantly improved aphrodisiac activity with ASD3. The stability study revealed that the prepared ASD3 did not show any remarkable changes in the dissolution and drug content for 1 month storage at room temperature. (c) 2020 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:1817 / 1826
页数:10
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