Department of Pharmaceutics and Drug Delivery, School of Pharmacy, The University of Mississippi, University, Mississippi, 38677, USA.
Department of Pharmaceutics, School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab, India.
AAPS PharmSciTech. 2023 Sep 19;24(7):189. doi: 10.1208/s12249-023-02646-0.
The rationale for the current investigation is to study the crude banana peel (CBP) powder efficiency as a novel natural time-dependent polymer along with a pH-sensitive polymer to develop flurbiprofen colon-specific tablets. The direct compression method is utilized to prepare the flurbiprofen-CBP matrix tablets using 9 mm punches on the rotary tableting machine and subsequently coated with Eudragit® S 100 by a dip coating method. The tablets were evaluated for various tableting properties and in vitro drug release studies. From the results of dissolution studies, the F6 formulation showed negligible drug release (5.76% in 5 h) in the upper gastrointestinal tract and progressive release in the colon (99.08% in 24 h). Mean dissolution time, T10%, and T80% were found to be 13.33 h, 5.8 h, and 20.7 h, respectively, which explains the efficiency of the present combination of polymers for colon-specific drug release. From the dissolution studies results of stability studies, the similarity index was calculated and found to be 74.75. In conclusion, utilizing CBP as a natural, time-dependent polymer in conjunction with Eudragit® S 100 to develop the flurbiprofen tablets seems like a promising approach for delivering drugs specifically to the colon.
本研究的基本原理是研究生香蕉皮(CBP)粉末作为一种新型天然时滞聚合物的效率,同时作为一种 pH 敏感聚合物,以开发氟比洛芬结肠特异性片剂。采用旋转压片机上的 9mm 冲模,直接压片法制备氟比洛芬-CBP 基质片,随后采用浸涂法用 Eudragit®S100 进行包衣。对各种压片性能和体外药物释放研究进行了评价。从溶出研究的结果来看,F6 制剂在上胃肠道中几乎没有药物释放(5 小时内释放 5.76%),而在结肠中则逐渐释放(24 小时内释放 99.08%)。平均溶出时间 T10%和 T80%分别为 13.33 小时、5.8 小时和 20.7 小时,这表明了本研究中组合使用的聚合物在结肠特异性药物释放方面的效率。从稳定性研究的溶出研究结果来看,计算了相似度指数,发现为 74.75。总之,将 CBP 用作天然时滞聚合物,与 Eudragit®S100 结合开发氟比洛芬片剂,似乎是一种将药物专门递送到结肠的有前途的方法。