Prakash Lakkireddy, Malipeddi Himaja, Subbaiah Bandaru Venkata
Department of Analytical Research and Development, Dr Reddy's Laboratories, Hyderabad 500 090, India Pharmaceutical Chemistry Division, School of Advanced Sciences, VIT University Vellore, Vellore, Tamil Nadu 632014, India
Pharmaceutical Chemistry Division, School of Advanced Sciences, VIT University Vellore, Vellore, Tamil Nadu 632014, India.
J Chromatogr Sci. 2015 Jan;53(1):122-6. doi: 10.1093/chromsci/bmu028. Epub 2014 May 15.
Nicorandil is a potent drug with a dual mechanism of action which results in its wide application in treating angina patients. Since the literature review showed no single preparative method for isolation and liquid chromatography-mass spectrometry (LC-MS) compatible [high-performance liquid chromatography (HPLC) or ultra performance liquid chromatography (UPLC)] method for identification for the impurities generated in process and by force degradation was reported. Thus an attempt was made to develop a single preparative method for isolation and HPLC and UPLC methods for identification of impurities of nicorandil in tablet dosage form. Ten degradants were found in the formulated drug under the stress conditions, [40°C/75% relative humidity for 2 months] in an LC-MS compatible method. A cost effective and high-throughput simple gradient preparative HPLC method was developed with a runtime of 30 min to isolate all the degradants. The method is capable and can be used to isolate further degradants. To detect these degradants, rapid and effecient HPLC and UPLC methods were developed and the same were identified by UPLC-time of flight mass spectrometry (TOF MS). The crux of this work involves a single preparative isolation method and UPLC identification method for all degradants with a very short runtime, i.e., 13.8 min, and, furthermore, the method has the potential to separate a wide range of degradants.
尼可地尔是一种具有双重作用机制的强效药物,这使其在治疗心绞痛患者方面得到广泛应用。由于文献综述显示,尚未有报道称存在用于分离的单一制备方法以及与液相色谱 - 质谱联用(LC - MS)兼容的[高效液相色谱(HPLC)或超高效液相色谱(UPLC)]方法来鉴定工艺过程中产生的杂质以及强制降解产生的杂质。因此,人们尝试开发一种单一的制备方法用于分离,并开发HPLC和UPLC方法来鉴定片剂剂型中尼可地尔的杂质。在[40°C/75%相对湿度,持续2个月]的加速条件下,通过一种与LC - MS兼容的方法在制剂中发现了10种降解产物。开发了一种经济高效且高通量的简单梯度制备型HPLC方法,运行时间为30分钟,可分离所有降解产物。该方法有能力且可用于分离更多的降解产物。为了检测这些降解产物,开发了快速高效的HPLC和UPLC方法,并通过UPLC - 飞行时间质谱(TOF MS)对其进行鉴定。这项工作的关键在于一种单一的制备分离方法和UPLC鉴定方法,可用于所有降解产物,运行时间非常短,即13.8分钟,此外,该方法有潜力分离多种降解产物。