采用光荧光和阴极荧光方法 ,对 Ga N外延层中的黄色和蓝色发光进行测量分析 ;同时 ,采用原子力显微镜、扫描电镜及其能谱测量外延层中的缺陷。结果表明 ,黄色和蓝色发光与残留杂质有关。采用第一原理计算结果显示 ,残留 C、O杂质、本征...采用光荧光和阴极荧光方法 ,对 Ga N外延层中的黄色和蓝色发光进行测量分析 ;同时 ,采用原子力显微镜、扫描电镜及其能谱测量外延层中的缺陷。结果表明 ,黄色和蓝色发光与残留杂质有关。采用第一原理计算结果显示 ,残留 C、O杂质、本征缺陷等是黄色和蓝色的可能物理起源。采用原子力显微镜、扫描电镜、透射电镜及其能谱对 Ga N/Al Ga N异质结中的纳米管进行观测 ,了解了纳米管的形貌。结果表明 ,构成纳米管的小面可能是外延过程中表面吸附引起的 ;计算结果显示 ,纳米管形貌变化与 Ga N/Al Ga N界面处晶格失配应力有关。采用透射电镜观察外延层中沉积物及其周围位错的结构表明 。展开更多
A Novel stability indicating RP-UPLC chromatographic method was developed for analysis of Nevirapine in pharmaceutical formulations. The developed RP-UPLC method is superior in technology to conventional RP-HPLC with ...A Novel stability indicating RP-UPLC chromatographic method was developed for analysis of Nevirapine in pharmaceutical formulations. The developed RP-UPLC method is superior in technology to conventional RP-HPLC with respect to speed, resolution, solvent consumption and cost of analysis. Nevirapine was subjected to the stress conditions like acid, base, thermal, oxidative and photolytic degradation. Nevirapine was found to degrade significantly in acid and thermal degradation. In acid degradation relative retention time with 0.42 is found as unknown impurity. New impurity was identified, isolated using mass based auto purification system and characterized by <sup>1</sup>H NMR (<sup>1</sup>D and <sup>2</sup>D) and HRMS experiments. Isolated impurity was showing molecular weight of 244.10, molecular formula C<sub>12</sub>H<sub>12</sub>N<sub>4</sub>O<sub>2</sub> and its name as 2-(3-Amino-4-methylpyridin-2-ylamino)nicotinic acid. The calibration graph was linear and the method showed less deviation in accuracy results. The test solution was found to be stable for 20 days when stored in the refrigerator between 2°C to 8°C. The developed RP-UPLC method was validated and meets the requirements delineated by the International Conference on Harmonization (ICH) guidelines. The intra-day and inter-day variation was less than 1%. The method was reproducible and selective for the estimation of Nevirapine. Because the method could effectively separate the drug from its degradation products, it can be employed as a stability-indicating method.展开更多
文摘采用光荧光和阴极荧光方法 ,对 Ga N外延层中的黄色和蓝色发光进行测量分析 ;同时 ,采用原子力显微镜、扫描电镜及其能谱测量外延层中的缺陷。结果表明 ,黄色和蓝色发光与残留杂质有关。采用第一原理计算结果显示 ,残留 C、O杂质、本征缺陷等是黄色和蓝色的可能物理起源。采用原子力显微镜、扫描电镜、透射电镜及其能谱对 Ga N/Al Ga N异质结中的纳米管进行观测 ,了解了纳米管的形貌。结果表明 ,构成纳米管的小面可能是外延过程中表面吸附引起的 ;计算结果显示 ,纳米管形貌变化与 Ga N/Al Ga N界面处晶格失配应力有关。采用透射电镜观察外延层中沉积物及其周围位错的结构表明 。
文摘A Novel stability indicating RP-UPLC chromatographic method was developed for analysis of Nevirapine in pharmaceutical formulations. The developed RP-UPLC method is superior in technology to conventional RP-HPLC with respect to speed, resolution, solvent consumption and cost of analysis. Nevirapine was subjected to the stress conditions like acid, base, thermal, oxidative and photolytic degradation. Nevirapine was found to degrade significantly in acid and thermal degradation. In acid degradation relative retention time with 0.42 is found as unknown impurity. New impurity was identified, isolated using mass based auto purification system and characterized by <sup>1</sup>H NMR (<sup>1</sup>D and <sup>2</sup>D) and HRMS experiments. Isolated impurity was showing molecular weight of 244.10, molecular formula C<sub>12</sub>H<sub>12</sub>N<sub>4</sub>O<sub>2</sub> and its name as 2-(3-Amino-4-methylpyridin-2-ylamino)nicotinic acid. The calibration graph was linear and the method showed less deviation in accuracy results. The test solution was found to be stable for 20 days when stored in the refrigerator between 2°C to 8°C. The developed RP-UPLC method was validated and meets the requirements delineated by the International Conference on Harmonization (ICH) guidelines. The intra-day and inter-day variation was less than 1%. The method was reproducible and selective for the estimation of Nevirapine. Because the method could effectively separate the drug from its degradation products, it can be employed as a stability-indicating method.
