Hosny Khaled Mohamed, El-Say Khalid Mohamed, Ahmed Osama Abdelhakim
a Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy , King Abdulaziz University , Jeddah , Saudi Arabia .
b Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy , Beni Suef University , Beni Suef , Egypt .
Drug Deliv. 2016;23(1):355-61. doi: 10.3109/10717544.2014.916763. Epub 2014 May 28.
Sildenafil citrate, a drug used to treat erectile dysfunction, is available in tablet form but has three major problems. First, the drug displays poor aqueous solubility, which delays its onset of action. Second, the drug undergoes extensive first-pass metabolism, resulting in a low (40%) bioavailability. Third, the gastrointestinal effects of sildenafil citrate include dyspepsia and a burning sensation. The objective of this study was to prepare sildenafil citrate using a fast orodissolvable film (ODF) containing the drug in a solid dispersion (SD) to mitigate the abovementioned problems. The solubility of sildenafil citrate in β-cyclodextrin derivatives was estimated, and SDs were prepared and characterized. To develop an ODF that disintegrates rapidly and releases the maximum amount of sildenafil citrate, a 3(3) Box-Behnken experimental design was used to estimate the effects of different concentrations of film forming polymer (X1), the film modifier (X2), and the plasticizer (X3) on the responses, i.e. the disintegration time (Y1) and the amount of drug released (Y2). Pharmacokinetic studies with the optimized (ODF) were conducted on human volunteers. SD prepared using hydroxybutyl-β-cyclodextrin enhanced the solubility of sildenafil citrate by more than eightfold. The Y1 for the optimized ODF was 89 seconds, and the Y2 was 86%; this formula also exhibited a rapid onset of action, and its bioavailability was enhanced by 2.25-fold compared with that of the marketed tablet. The ODF is a promising formulation for sildenafil citrate that results in higher solubility, a rapid onset of action, and enhanced systemic bioavailability.
枸橼酸西地那非是一种用于治疗勃起功能障碍的药物,有片剂形式,但存在三个主要问题。首先,该药物的水溶性较差,这会延迟其起效时间。其次,该药物会经历广泛的首过代谢,导致生物利用度较低(40%)。第三,枸橼酸西地那非的胃肠道副作用包括消化不良和烧灼感。本研究的目的是制备一种快速口腔崩解膜(ODF),该膜含有处于固体分散体(SD)中的药物,以缓解上述问题。估算了枸橼酸西地那非在β-环糊精衍生物中的溶解度,并制备和表征了固体分散体。为了开发一种能快速崩解并释放最大量枸橼酸西地那非的口腔崩解膜,采用3(3) Box-Behnken实验设计来估算不同浓度的成膜聚合物(X1)、膜改性剂(X2)和增塑剂(X3)对响应指标即崩解时间(Y1)和药物释放量(Y2)的影响。对人体志愿者进行了使用优化后的口腔崩解膜的药代动力学研究。使用羟丁基-β-环糊精制备的固体分散体使枸橼酸西地那非的溶解度提高了八倍多。优化后的口腔崩解膜的Y1为89秒,Y2为86%;该配方还表现出起效迅速,与市售片剂相比,其生物利用度提高了2.25倍。口腔崩解膜是枸橼酸西地那非一种很有前景的剂型,它能提高溶解度、起效迅速并增强全身生物利用度。