王晋, 张汝华. 用渗滤理论研究乙基纤维素骨架片的最适压片力范围J. 药学学报, 2000, 35(7): 531-534.
引用本文: 王晋, 张汝华. 用渗滤理论研究乙基纤维素骨架片的最适压片力范围J. 药学学报, 2000, 35(7): 531-534.
WANG Jin, ZHANG Ru-Hua. OPTIMUM TABLETING PRESSURE RANGE OF ASPIRIN-ETHYLCELLULOSE TABLETS USING PERCOLATION THEORYJ. Acta Pharmaceutica Sinica, 2000, 35(7): 531-534.
Citation: WANG Jin, ZHANG Ru-Hua. OPTIMUM TABLETING PRESSURE RANGE OF ASPIRIN-ETHYLCELLULOSE TABLETS USING PERCOLATION THEORYJ. Acta Pharmaceutica Sinica, 2000, 35(7): 531-534.

用渗滤理论研究乙基纤维素骨架片的最适压片力范围

OPTIMUM TABLETING PRESSURE RANGE OF ASPIRIN-ETHYLCELLULOSE TABLETS USING PERCOLATION THEORY

  • 摘要: 目的 用渗滤理论研究制备阿司匹林-乙基纤维素骨架片的最适压片力范围。方法 使用不同的压片力(3~30 kN)制备了含阿司匹林40%的阿司匹林-乙基纤维素骨架片,测定了溶出曲线,用Higuchi方程和Ritger-Peppas方程对溶出数据进行拟合。将拟合的Higuchi方程的斜率b值和计算得到的片剂的孔隙率ε,代入渗滤理论推导出的公式中,可计算出表观扩散系数D和片剂溶出性能参数β,分别以D对ε及β对ε回归,可得到临界孔隙率εc,由β-ε,D-ε和β-ε0曲线可推知最适压片力范围。结果 压片力在9~18 kN时,药物释放遵从Higuchi模型方程,片剂以骨架扩散机制释药,且释药速度适中,因此9~18 kN为最适压片力范围。低于9 kN时,片子的初始孔隙率太大,药物溶出过快;高于18 kN时,药物溶出过慢,呈异常扩散机制释放药物。结论 渗滤理论可较清楚地阐明阿司匹林骨架片的释药机制,并可得到制备阿司匹林片的最适压片力范围。

     

    Abstract: AIM To study the optimum tableting pressure of aspirin-ethylcellulose (EC) matrix tablets using percolation theory. METHODS To prepare aspirin-EC tablets which contain 40% aspirin using different tableting pressures. The dissolution curves of tablets were determined, the dissolution data were model-fitted with Higuchi and Ritger-Peppas equations. Putting the values of slope b of model-fitted and total porosity of tablets ε to the formula derived from percolation theory, the apparent diffusivity D and tablet dissolution parameter β could be calculated. Regression with D versus ε, β versus ε and β versus ε0 could be obtained. RESULTS The release of drug prepared under 9~18 kN obeyed Higuchi model equation, the tablets released aspirin with matrix diffusion mechanism, the drug release was moderate. When the pressure was lower than 9 kN, the drug release was too fast; when the pressure was higher than 18 kN, the drug release was too slow. CONCLUSION Percolation theory could elucidate drug release mechanism more clearly. The optimum tableting pressure range of aspirin could be calculated, then tablets prepared under the pressure in this range could have a suitable dissolution rate.

     

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