Licozinat基质片的处方及评价

D. Otgonsuren, Davaasuren Ts, B. Enkhtuul, D. Davaadagva, D. Jambaninj
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引用次数: 2

摘要

目的:甘草的甘草酸一铵具有祛痰、解毒、抗过敏、抗氧化等作用。日本研究人员已经确定它对甲型肝炎、乙型肝炎、丙型肝炎和丁型肝炎具有抗病毒活性。我们已经从蒙古种植的甘草根中分离出甘草酸一铵,通过先前研究中提出的方法。本研究的目的是研制具有保肝作用的缓释基质片,并对其药物技术质量和体内性能进行评价。甘草酸一铵Licozinat基质片140mg;甘氨酸50毫克;ld -蛋氨酸50mg /片。方法:采用HPMC - K4000、乳糖、葡萄糖、微晶纤维素、PVP-K30、滑石粉、硬脂酸镁按不同比例制备基质片。采用湿造粒法制备基质片,并对其进行重量变化、硬度、脆性、体外释放度和体内研究。结果:基质片选用合适的辅料:乳糖作为稀释剂,5%的PVP-K30作为粘合剂,HPMC作为基质成形剂,3%的滑石粉和1%的硬脂酸镁作为滑脂剂或润滑剂。采用湿造粒法制备基质片剂,并以2.5 kPa的压力对片剂混合物进行压缩。体外试验确定配方5 (F5)为最合适的片剂设计,且释放时间较长。研究了基质片与甘草酸片对CCl4致大鼠肝毒性的保护作用。比较Licozinat基质片与甘草素片对CCl4治疗大鼠的作用。甘草齐那特基质片可降低丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、总胆红素和碱性磷酸酶(ALP)水平。结论:研制并评价了具有保肝作用的缓释/控释基质片。Licozinat基质片符合质量标准。口服甘草嗪基片可降低血清丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、总胆红素和碱性磷酸酶(ALP)水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and Evaluation of Licozinat Matrix Tablet
Objective: Monoammonium glycyrrhizinate of Glycyrrhiza root has been used as an expectorant, detoxificator, anti-allergic, and antioxidant. Japanese researchers have been determined it has anti-viral activity in case of hepatitis A, B, C, D. We have isolated monoammonium glycyrrhizinate from Glycyrrhiza root, grown in Mongolia through a method presented in a previous study. The objective of the study was to develop prolonged release matrix tablet with hepatoprotective effect and to evaluate their pharmacotechnical qualities and the in vivo performance. Licozinat matrix tablets contained monoammonium glycyrrhizinate 140 mg; glycine 50 mg; LD-methionin 50 mg in each tablet. Methods: In the present study the matrix tablet were prepared using HPMC K4000, lactose, glucose, microcrystalline cellulose, PVP-K30, talc and magnesium stearate in different ratios. The matrix tablet were prepared by wet granulation method and evaluated for weight variation, hardness, friability, in-vitro release, and in vivo study. Results: Appropriate excipients were chosen for the matrix tablets: lactose as a diluent, 5% of PVP-K30 as a binder, HPMC as a matrix former, 3% of talc and 1% of magnesium stearate as a glidiant or lubricant. We have prepared the matrix tablets by wet granulation method and compressed the tablet mixture by a 2.5 kPa pressure. Formulation 5 (F5) was determined to be the most appropriate tablet design and it released the drug in a prolonged way during the in vitro testing. The hepatoprotective effect of matrix tablet in comparison to Glycyron tablet, were studied on CCl4 induced hepatotoxicity in rats. The effect of Licozinat matrix tablet were compared with the Glycyron tablet that were administered to CCl4 treated rats. On administration Licozinat matrix tablet decreased the levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), total bilirubin and alkaline phosphatise (ALP). Conclusion: We have developed and evaluated prolonged/controlled release matrix tablets with hepatoprotective effect. The Licozinat matrix tablets satisfied the quality criteria. On administration Licozinat matrix tablet decreased the level of alanine aminotransferase (ALT), aspartate aminotransferase (AST) and total bilirubin and alkaline phosphatise (ALP).
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