A comparative study of floating drug delivery system of metronidazole formulated using effervescent and non effervescent techniques

C. Airemwen, M. Uhumwangho
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引用次数: 1

Abstract

This study was carried out to compare effervescent and non-effervescent gastro-floating matrix tablets (GFMT) of metronidazole formulated using Azadirachta indica (Neem) gum (AIG). Neem gum was extracted by a method previously described. Granules were prepared by wet granulation technique using the extracted neem gum at varying concentrations (2, 4, 6 and 8% w/w). Sodium bicarbonate and tartaric acid were used as the gas generating agents for the GFMTs, while ammonium bicarbonate was used as the sublimating agent for the non-effervescent GFMTs. Formulations were either prepared alone with the natural gum or with the addition of 1.0% w/w of acrylate methacrylate copolymer (Eudragit® RL100). All granules were evaluated for micromeritic properties. The granules were compressed at an optimized compression pressure of 30 arbitrary unit on the tableting machine load scale and the non-effervescent GFMTs were sintered at 70 °C for 12 h in a hot-air oven. Tablets were evaluated for hardness, friability, floating lag time, in vitro buoyancy and drug release profiles. Drug-excipient compatibility study was done using Fourier Transform Infra-red Spectroscopy (FTIR) and Differential Scanning Calorimetry (DSC). Scanning Electron Microscope (SEM) was used to analyze the pores and morphology of the tablets. Results revealed that all formulated floating matrix granules were free flowing, with angle of repose and Carr’s index ≤ 33.2o and ≤ 15.5% respectively. All floating matrix granules were compressible with tablet hardness ≤ 9.0 Kg/cm 2 . Generally, the percentage friability of the GFMTs decreased with increase in binder concentration (≤ 0.99%). The floating lag time for the effervescent GFMT tablets ranged from 2-7 min, while the non-effervescent formulations had zero floating lag time. FTIR and DSC studies showed that the excipients and the active pharmaceutical ingredient (API) i.e. metronidazole were compatible. SEM reveals the presence of pores and a smooth surface of the non-effervescent GFMTs, while smooth surface with no pores was revealed in the effervescent formulations. Gastro-floating matrix tablets of metronidazole were successfully formulated in this study using the effervescent and non-effervescent techniques and there was significant difference in the floating lag times (P 0.05). Keywords : Floating, matrix tablets, effervescent, non-effervescent, buoyancy.
用泡腾法和非泡腾法配制甲硝唑漂浮给药系统的比较研究
本研究对印楝胶配制的甲硝唑胃浮基质泡腾片和非泡腾片进行了比较。用前面描述的方法提取印楝胶。用不同浓度(2、4、6和8% w/w)提取印楝胶,采用湿造粒技术制备颗粒。采用碳酸氢钠和酒石酸作为气体生成剂,碳酸氢铵作为升华剂制备非起泡型石墨烯纳米管。配方要么单独使用天然胶,要么添加1.0% w/w的丙烯酸酯-甲基丙烯酸酯共聚物(Eudragit®RL100)。对所有颗粒进行微粒性评价。在压片机负荷量表上以任意30单位的优化压缩压力对颗粒进行压缩,并在热风烘箱中在70℃下烧结12 h。对其硬度、脆性、漂浮滞后时间、体外浮力和药物释放特性进行了评价。采用傅里叶变换红外光谱(FTIR)和差示扫描量热法(DSC)研究了药物赋形剂的配伍性。采用扫描电镜(SEM)对片剂的孔隙和形貌进行了分析。结果表明:配制的悬浮基质颗粒均为自由流动,休止角≤33.2,卡尔指数≤15.5%;所有漂浮基质颗粒均可压缩,片剂硬度≤9.0 Kg/ cm2。一般情况下,GFMTs的脆性百分比随粘结剂浓度的增加而降低(≤0.99%)。泡腾片的漂浮滞后时间为2 ~ 7 min,而非泡腾片的漂浮滞后时间为零。FTIR和DSC研究表明,赋形剂与活性药物成分(API)甲硝唑是相容的。扫描电镜显示,非泡腾配方的GFMTs表面光滑,表面有气孔,而泡腾配方的GFMTs表面光滑,没有气孔。采用泡腾法和非泡腾法制备了甲硝唑胃漂浮基质片,其漂浮滞后时间差异有统计学意义(p0.05)。关键词:漂浮,基质片,泡腾剂,非泡腾剂,浮力。
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