Siraj Ebrahim Abdela, Mulualem Yohannes, Molla Fantahun, Yayehrad Ashagrachew Tewabe, Belete Anteneh
Department of Pharmaceutics and Social Pharmacy, School of Pharmacy, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
Department of Pharmacy, College of Medicine and Health Sciences, Bahir Dar University, P.O. Box 79, Bahir Dar, Ethiopia.
Sci Rep. 2025 May 14;15(1):16704. doi: 10.1038/s41598-025-95732-1.
Natural polymers such as pectin have garnered significant interest in recent years due to their potential applications in gastroretentive drug delivery systems. Gastroretentive dosage forms are intended to extend the emptying time of drugs in the gastrointestinal tract. Accordingly, this study was aimed to examine the use of pectin as a floating and mucoadhesive polymer using furosemide as a model drug. The citrus peel pectin was extracted from local Citrus aurantifolia tree fruit peel using hot water extraction technique. FTIR and DSC analyses were performed to investigate the compatibility of the pectin extracted with furosemide. C. aurantifolia peel yielded 34.4% (w/w) purified pectin with a degree of esterification of 85.49%. FTIR and DSC analysis revealed that the citrus peel pectin powder is compatible with furosemide. Based on preliminary study, pectin and effervescent agent concentration were identified as significant independent variables. Hence, their influence on five response variables (floating duration, bioadhesive strength, swelling index, drug release at 1 h, and drug release rate) were further studied and optimized using central composite design (CCD). Accordingly, the CCD model predicted an optimum formulation at 22.3% of pectin concentration and 5% of effervescent agent. Under this condition, the Design-Expert software predicted floating duration (14.07 s), bioadhesive strength (28.57 g), swelling index (254.08%), drug release at 1 h (27.86%), and drug release rate (28.045%/h). The validity of the predicted optimum formulation was confirmed experimentally. The optimized tablet formulation showed pharmacopeial acceptable characteristics. In conclusion, the results of this study suggest that waste-derived citrus pectin can be considered as an abundant alternative pharmaceutical excipient in the formulation and manufacture of floating and bioadhesive matrix tablets with favorable floating and bioadhesion characteristics.
近年来,诸如果胶等天然聚合物因其在胃滞留型药物递送系统中的潜在应用而备受关注。胃滞留型剂型旨在延长药物在胃肠道中的排空时间。因此,本研究旨在以呋塞米为模型药物,研究果胶作为漂浮和粘膜粘附聚合物的用途。采用热水提取技术从当地酸橙树果皮中提取柑橘皮果胶。进行了傅里叶变换红外光谱(FTIR)和差示扫描量热法(DSC)分析,以研究提取的果胶与呋塞米的相容性。酸橙皮产生了34.4%(w/w)的纯化果胶,酯化度为85.49%。FTIR和DSC分析表明,柑橘皮果胶粉末与呋塞米相容。基于初步研究,果胶和泡腾剂浓度被确定为显著的自变量。因此,使用中心复合设计(CCD)进一步研究并优化了它们对五个响应变量(漂浮持续时间、生物粘附强度、溶胀指数、1小时药物释放率和药物释放速率)的影响。据此,CCD模型预测果胶浓度为22.3%、泡腾剂浓度为5%时为最佳配方。在此条件下,Design-Expert软件预测的漂浮持续时间为14.07秒、生物粘附强度为28.57克、溶胀指数为254.08%、1小时药物释放率为27.86%、药物释放速率为28.045%/小时。实验证实了预测的最佳配方的有效性。优化后的片剂配方显示出符合药典要求的特性。总之,本研究结果表明,源自废弃物的柑橘果胶可被视为一种丰富的替代药用辅料,用于制备具有良好漂浮和生物粘附特性的漂浮和生物粘附基质片剂。