Hosny Khaled Mohamed, Mosli Hisham Ahmed, Hassan Ali Habiballah
Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia ; Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Beni Suef University, Beni Suef, Egypt.
Department of Urology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Drug Des Devel Ther. 2015 Jan 12;9:465-72. doi: 10.2147/DDDT.S76314. eCollection 2015.
Sildenafil citrate (SC), a drug used to treat erectile dysfunction, is available in tablet form but has three major problems. First, the drug displays inadequate aqueous solubility, which delays the onset of its action. Second, the drug undergoes extensive first-pass metabolism, resulting in a low (40%) bioavailability. Third, the gastrointestinal effects of SC include dyspepsia and a burning sensation. The aim of this research was to prepare SC as a sublingual tablet utilizing soy polysaccharide as novel superdisintegrant to mitigate the abovementioned problems. The solubility of SC in various hydrophilic carrier solutions was estimated in order to prepare the drug as a coprecipitate. Sublingual tablets were prepared and evaluated for hardness, friability, drug content, wetting time, water absorption ratio, in vitro dispersion time, dissolution rate, and stability study. The pharmacokinetic study of the tablets was carried out on healthy volunteers. The results indicated that the co-precipitation of SC with polyvinylpyrollidone K30 enhanced the solubility of SC by more than eight folds. The tablet contained 8% soy polysaccharide as a superdisintegrant and provided a wetting time of 25 seconds, and in vitro dispersion times of 55 seconds. The drug release was found to be 95.6%. The prepared SC sublingual tablet also exhibited a rapid onset of action, and its bioavailability was enhanced 1.68-fold compared with that of the marketed tablets. It can be concluded that SC sublingual tablet is a promising formulation that results in higher solubility, faster dispersion and onset of action, higher release rate, and higher systemic bioavailability.
枸橼酸西地那非(SC)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,该药物的水溶性不足,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,SC的胃肠道副作用包括消化不良和烧灼感。本研究的目的是利用大豆多糖作为新型超级崩解剂制备SC舌下片,以缓解上述问题。为了将药物制备成共沉淀物,评估了SC在各种亲水性载体溶液中的溶解度。制备了舌下片,并对其硬度、脆碎度、药物含量、湿润时间、吸水率、体外分散时间、溶出率和稳定性进行了研究。对健康志愿者进行了该片剂的药代动力学研究。结果表明,SC与聚乙烯吡咯烷酮K30的共沉淀使SC的溶解度提高了八倍多。该片剂含有8%的大豆多糖作为超级崩解剂,湿润时间为25秒,体外分散时间为55秒。药物释放率为95.6%。所制备的SC舌下片还表现出起效迅速,与市售片剂相比,其生物利用度提高了1.68倍。可以得出结论,SC舌下片是一种很有前景的制剂,具有更高的溶解度、更快的分散和起效速度、更高的释放率和更高的全身生物利用度。