Zafar Nadiah, Mahmood Asif, Ilyas Sehar, Ijaz Hira, Muhammad Sarfraz Rai, Mahdi Wael A, Salem-Bekhit Mounir M, Ibrahim Mohamed A, Benguerba Yacine, Ernst Barbara
Department of Pharmaceutics, Faculty of Pharmacy, Universiti Teknologi MARA (UiTM), Puncak Alam Campus, 42300 Bandar Puncak Alam, Selangor, Malaysia.
Department of Pharmacy, University of Chakwal, Chakwal, Pakistan.
Saudi Pharm J. 2023 Aug;31(8):101671. doi: 10.1016/j.jsps.2023.06.004. Epub 2023 Jun 12.
BACKGROUND & OBJECTIVES: This study aimed to create a controlled delivery system for Tapentadol Hydrochloride by developing interpenetrating networks (IPNs) of Natrosol-Pectin copolymerized with Acrylic Acid and Methylene bisacrylamide, and to analyze the effects of various ingredients on the physical and chemical characteristics of the IPNs.
Novel Tapentadol Hydrochloride-loaded Natrosol-Pectin based IPNs were formulated by using the free radical polymerization technique. Co-polymerization of Acrylic Acid (AA) with Natrosol and Pectin was performed by using Methylene bisacrylamide (MBA). Ammonium persulfate (APS) was used as the initiator of crosslinking process. The impact of ingredients i.e. Natrosol, Pectin, MBA, and Acrylic Acid on the gel fraction, porosity, swelling (%), drug loading, and drug release was investigated. FTIR, DSC, TGA, SEM and EDX studies were conducted to confirm the grafting of polymers and to evaluate the thermal stability and surface morphology of the developed IPNs.
Swelling studies exhibited an increase in swelling percentage from 84.27 to 91.17% upon increasing polymer (Natrosol and Pectin) contents. An increase in MBA contents resulted in a decrease in swelling from 85 to 67.63%. Moreover, the swelling was also observed to increase with higher AA contents. Significant drug release was noted at higher pH instead of gastric pH value. Oral toxicological studies revealed the nontoxic and biocompatible nature of Natrosol-Pectin IPNs.
INTERPRETATION & CONCLUSION: The developed IPNs were found to be an excellent system for the controlled delivery of Tapentadol Hydrochloride.
本研究旨在通过制备与丙烯酸和亚甲基双丙烯酰胺共聚的羟丙甲纤维素 - 果胶互穿网络(IPN),创建一种盐酸曲马多的控释系统,并分析各种成分对IPN物理和化学特性的影响。
采用自由基聚合技术制备了新型载盐酸曲马多的羟丙甲纤维素 - 果胶基IPN。丙烯酸(AA)与羟丙甲纤维素和果胶的共聚反应通过亚甲基双丙烯酰胺(MBA)进行。过硫酸铵(APS)用作交联过程的引发剂。研究了羟丙甲纤维素、果胶、MBA和丙烯酸等成分对凝胶分数、孔隙率、溶胀率(%)、载药量和药物释放的影响。进行了傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)、热重分析法(TGA)、扫描电子显微镜(SEM)和能谱分析(EDX)研究,以确认聚合物的接枝情况,并评估所制备IPN的热稳定性和表面形态。
溶胀研究表明,随着聚合物(羟丙甲纤维素和果胶)含量的增加,溶胀率从84.27%增加到91.17%。MBA含量的增加导致溶胀率从85%降至67.63%。此外,还观察到随着AA含量的增加溶胀也增加。在较高pH值而非胃内pH值下观察到显著的药物释放。口服毒理学研究表明羟丙甲纤维素 - 果胶IPN具有无毒和生物相容性。
所制备的IPN被发现是一种用于盐酸曲马多控释的优异系统。