Alshehri Sultan, Hussain Afzal, Ahsan Mohd Neyaz, Ali Raisuddin, Siddique Mohd Usman Mohd
Department of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.
Department of Medical Laboratory Technology University Polytechnic, Birla Institute of Technology, Mesra, Ranchi 835215, Jharkhand, India.
ACS Omega. 2021 Feb 11;6(7):5033-5045. doi: 10.1021/acsomega.0c06234. eCollection 2021 Feb 23.
The study aimed to select a suitable solvent capable to solubilize ketoconazole (KETO) and serve as a permeation enhancer across the skin. Experimental solubility and Hansen solubility parameters were obtained in ethanol, dimethyl sulfoxide (DMSO), ethylene glycol, oleic acid, span 80, limonene, eugenol, transcutol (THP), labrasol, and propylene glycol. Thermodynamic functional parameters and computational models (van't Hoff and Apelblat) validated the determined solubility in various solvents at = 298.2 K to 318.2 K and = 0.1 MPa. The HSPiP software estimated the solubility parameters in the solvents. The maximum mole fractional solubility values of KETO were found to be in an order as oleic acid (8.5 × 10) > limonene (7.3 × 10) > span 80 (6.9 × 10) > THP (4.9 × 10) > eugenol (4.5 × 10) at = 318.2 K. The results of the apparent thermodynamic analysis confirmed that the dissolution rate was endothermic and entropy driven. The GastroPlus program predicted significantly high permeation of KETO (79.1%) in human skin from the KETO-THP construct as compared to drug solution (38%) and excellent immediate release from THP-solubilized construct (90% < 1 h). Hence, THP could be a better option for topical, transdermal, and oral formulation.
该研究旨在选择一种能够溶解酮康唑(KETO)并作为皮肤渗透促进剂的合适溶剂。在乙醇、二甲基亚砜(DMSO)、乙二醇、油酸、吐温80、柠檬烯、丁香酚、肉豆蔻酸异丙酯(THP)、Labrasol和丙二醇中获得了实验溶解度和汉森溶解度参数。热力学函数参数和计算模型(范特霍夫和阿佩尔布拉特)验证了在298.2 K至318.2 K温度和0.1 MPa压力下各种溶剂中测定的溶解度。HSPiP软件估算了溶剂中的溶解度参数。在318.2 K时,酮康唑的最大摩尔分数溶解度值顺序为:油酸(8.5×10)>柠檬烯(7.3×10)>吐温80(6.9×10)>肉豆蔻酸异丙酯(4.9×10)>丁香酚(4.5×10)。表观热力学分析结果证实溶解速率是吸热的且由熵驱动。GastroPlus程序预测,与药物溶液(38%)相比,酮康唑 - 肉豆蔻酸异丙酯制剂在人皮肤中的渗透量显著较高(79.1%),且肉豆蔻酸异丙酯增溶制剂具有优异的速释效果(90%<1小时)。因此,肉豆蔻酸异丙酯可能是局部、透皮和口服制剂的更好选择。