Simoncic Z, Zupancic P, Roskar R, Gartner A, Kogej K, Kmetec V
Krka, d.d., Novo mesto, Smarjeska cesta 6, 8501 Novo mesto, Slovenia.
Int J Pharm. 2007 Sep 5;342(1-2):145-51. doi: 10.1016/j.ijpharm.2007.05.016. Epub 2007 May 18.
The stability properties of enalapril maleate (EM) and of different tablet formulations including EM were studied by isothermal microcalorimetry and by high performance liquid chromatography (HPLC). It was shown that water content of the sample and elevated temperature have a high impact on stability properties of the substance itself and of the formulations including this substance. The degradation is more extensive at higher water content and at elevated temperature. The type of the tablet formulation (5 or 20mg EM tablet formulation) also has an impact: the 5 EM tablet formulation is the less stable one. The heat output of individual tablet formulations was used to evaluate the enthalpy changes and to calculate the difference in the amount of degraded EM between various samples. These results agreed satisfactorily with those obtained by HPLC. Isothermal microcalorimetry proved to be a fast and predictive method that could be used in preformulation studies to accelerate the pharmaceutical development and shorten the time before launching the product to the market.
采用等温微量热法和高效液相色谱法(HPLC)研究了马来酸依那普利(EM)及包括EM在内的不同片剂制剂的稳定性。结果表明,样品的含水量和升高的温度对该物质本身以及包含该物质的制剂的稳定性有很大影响。在较高含水量和升高温度下,降解更为广泛。片剂制剂的类型(5或20mg EM片剂制剂)也有影响:5mg EM片剂制剂稳定性较差。利用各个片剂制剂的热输出评估焓变,并计算不同样品之间降解的EM量的差异。这些结果与HPLC获得的结果令人满意地一致。等温微量热法被证明是一种快速且具有预测性的方法,可用于处方前研究,以加速药物开发并缩短产品上市前的时间。