Endale Abebe, Gebre-Mariam Tsige, Schmidt Peter C
Department of Pharmaceutics, School of Pharmacy, Addis Ababa University, PO Box 1176, Addis Ababa, Ethiopia.
AAPS PharmSciTech. 2008;9(1):31-8. doi: 10.1208/s12249-007-9027-3. Epub 2008 Jan 4.
The purpose of this research was to improve the hygroscopicity and poor flow properties of the crude dry extract of the seeds of Glinus lotoides and improve the disintegration time of the core-tablets for enteric coated formulation thereof. The liquid crude extract of the plant was adsorbed on granulated colloidal silicon dioxide (Aeroperl 300 Pharma) at 30% w/w and the dry extract preparation (DEP) was dry-granulated with roller-compaction using Micro-Pactor. Hygroscopicity, flow property and disintegration time were improved significantly due to the adsorption and granulation processes. Moreover, the DEP does not become mucilaginous even at higher relative humidity levels (above 65%). Oblong tablets (20 x 8.25 mm) containing 947 mg of the granulated DEP (equivalent to the traditional dose), 363 mg of Avicel PH101 and 90 mg of Ac-di-Sol as disintegrant were formulated using an instrumented eccentric tablet machine at 20 kN. The tablets showed a crushing strength of 195 N, a friability of 0.4% and disintegrated within 9 min. The tablets were then enteric coated using polymethacrylate co-polymers (Eudragit L 100-55 and Kollicoat MAE 100P). The coated tablets resisted disintegration or softening in simulated gastric fluid for a minimum of 2 h and disintegrated within 15 min in intestine simulated fluid at pH 6.8. In addition to controlling the release of the active agents, the enteric coating improved the strength and decreased friability of the core-tablets.
本研究的目的是改善沼生水马齿种子粗干提取物的吸湿性和不良流动性,并改善其肠溶制剂片芯的崩解时间。将该植物的液体粗提取物以30% w/w的比例吸附在颗粒状胶体二氧化硅(Aeroperl 300 Pharma)上,然后使用Micro-Pactor通过滚压进行干法制粒,制备干提取物制剂(DEP)。由于吸附和制粒过程,吸湿性、流动性和崩解时间得到了显著改善。此外,即使在较高相对湿度水平(高于65%)下,DEP也不会变得粘稠。使用装有仪器的偏心压片机在20 kN压力下制备了椭圆形片剂(20×8.25 mm),该片剂含有947 mg的制粒DEP(相当于传统剂量)、363 mg的微晶纤维素PH101和90 mg的Ac-di-Sol作为崩解剂。该片剂表现出195 N的抗压强度、0.4%的脆碎度,并在9分钟内崩解。然后使用聚甲基丙烯酸酯共聚物(Eudragit L 100 - 55和Kollicoat MAE 100P)对该片剂进行肠溶包衣。包衣片剂在模拟胃液中至少2小时内不会崩解或软化,在pH 6.8的模拟肠液中15分钟内崩解。除了控制活性剂的释放外,肠溶包衣还提高了片芯的强度并降低了脆碎度。