Irma Lerma Rangel College of Pharmacy, Texas A&M Health Science Center, Texas A&M University, College Station, TX, USA.
Department of Pharmaceutics, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt.
Pharm Dev Technol. 2021 Apr;26(4):455-463. doi: 10.1080/10837450.2021.1888978. Epub 2021 Mar 3.
The focus of present work was to prepare salt of aripiprazole (APZ) with dicarboxylic acids to improve physicochemical properties the drug. Dicarboxylic acids used in the study were malonic acid, maleic acid and succinic acid. The salts were prepared with solubilization-crystallization method. The salts were characterized for pH-solubility, dissolution, and stabilities. The Fourier infrared spectroscopy, X-ray powder diffraction, differential scanning calorimetry and near infrared chemical imaging indicated formation of new solid phase. pH-solubility profiles of the salts were similar to the drug except higher solubility were observed in the salts at all tested pH. The highest solubility was observed for APZ-Malonate salt among all the prepared salts. The solubility curve was inverted 'V' shape for APZ-maleate and APZ-succinate while it was inverted 'U' shape for APZ-malonate. The water solubility of APZ, APZ-malonate, APZ-maleate and APZ-succinate were 0.07 ± 0.02, 3503.9 ± 37.4, 269.3 ± 6.9 and 729.4 ± 9.4 µg/mL, respectively. The dissolution was 2.9 ± 0.4, 18.4 ± 3.9, 19.5 ± 1.4 and 36.6 ± 4.0% in 45 min for APZ, APZ-maleate, APZ-malonate, and APZ-succinate. The stabilities of the salts were similar to the drug. Thus, salts improved the physicochemical properties of the drug, and have similar stability profiles as that of APZ.
本工作的重点是制备阿立哌唑(APZ)与二元羧酸的盐,以改善药物的理化性质。研究中使用的二元羧酸为丙二酸、马来酸和琥珀酸。盐是通过溶析结晶法制备的。对盐的 pH-溶解度、溶解和稳定性进行了表征。傅里叶红外光谱、X 射线粉末衍射、差示扫描量热法和近红外化学成像表明形成了新的固相。盐的 pH-溶解度曲线与药物相似,但在所有测试的 pH 值下,盐的溶解度都较高。在所制备的盐中,APZ-丙二酸盐的溶解度最高。APZ-马来酸盐和 APZ-琥珀酸盐的溶解度曲线呈倒“V”形,而 APZ-丙二酸盐的溶解度曲线呈倒“U”形。APZ、APZ-丙二酸盐、APZ-马来酸盐和 APZ-琥珀酸盐的水溶解度分别为 0.07±0.02、3503.9±37.4、269.3±6.9 和 729.4±9.4μg/mL。在 45 分钟内,APZ、APZ-马来酸盐、APZ-丙二酸盐和 APZ-琥珀酸盐的溶解率分别为 2.9±0.4、18.4±3.9、19.5±1.4 和 36.6±4.0%。盐的稳定性与药物相似。因此,盐改善了药物的理化性质,且与 APZ 具有相似的稳定性特征。