首页> 外文学位 >Qualitative and quantitative analysis of Human Insulin, USP, by High-Performance Liquid Chromatography and Mass Spectroscopy.
【24h】

Qualitative and quantitative analysis of Human Insulin, USP, by High-Performance Liquid Chromatography and Mass Spectroscopy.

机译:通过高效液相色谱和质谱对人胰岛素USP进行定性和定量分析。

获取原文
获取原文并翻译 | 示例

摘要

The aim of this project was to develop and validate an analytical testing method for qualitative and quantitative analysis of Human Insulin, USP, by tandem High Performance Liquid Chromatography and Mass Spectroscopy Detection (LC/MS).;The experimental work was carried out by using a High Performance Liquid Chromatography unit coupled with a Mass Spectroscopic Detection system controlled by Chemstation, which was qualified to be in compliance of CFR part 11. Method conditions were established based on the physical characteristics of the Humana Insulin.;Once the chromatographic conditions were established, a single point standard calibration was developed. All of the responses of the Insulin in each replicate standard injection were used in the calculation of the mean standard response. Upon completion of the analytical testing, the overall relative standard deviation was included in the suitability requirements for reproducibility. A check standard at the nominal concentration was used as a part of the system suitability by comparing the concentration to area counts to that of the standard. Standard samples were injected in replicates at the beginning of the run and also at the end of the run to demonstrate the integrity of the system during function.;Validation parameters of Human Insulin, USP, with a molecular mass of 5807.58 m/z showed the calibration curve was linear in the range of 0.75 to 2.25 mg/mL and accurate using the following conditions. The chromatographic analysis for Human Insulin was performed on a reversed-phase C18 column. The flow rate was 0.3 mL/minute and the LC/MS positive detection scan range was 200 to 3000 m/z. Mobile phase A for consisted of 950 ml distilled water/50 ml acetonitrile/5 ml acetic acid (pH=3.04) and 950 ml distilled water/50 ml acetonitrile/5 ml acetic acid (pH=4.46). The retention time of Insulin was typically between 6.0 to 7.0 minutes.;This study shows that High Performance Liquid Chromatography unit coupled with a Mass Spectroscopic Detection system can be a useful way for analysis of Insulin, USP.
机译:该项目的目的是开发和验证一种通过串联高效液相色谱和质谱检测(LC / MS)对人胰岛素USP进行定性和定量分析的分析测试方法。高效液相色谱仪与由Chemstation控制的质谱检测系统相结合,符合CFR第11部分的要求。方法条件是根据Humana胰岛素的物理特性确定的;一旦确定了色谱条件,开发了单点标准校准。每次重复标准注射中胰岛素的所有反应都用于计算平均标准反应。分析测试完成后,总的相对标准偏差已包括在重复性的适用性要求中。通过将浓度,面积计数与标准浓度进行比较,将标称浓度的检查标准用作系统适用性的一部分。在运行开始和运行结束时重复进样标准样品,以证明系统在运行过程中的完整性。人胰岛素USP的验证参数(分子量为5807.58 m / z)表明:校正曲线在0.75至2.25 mg / mL的范围内呈线性,在以下条件下准确。人胰岛素的色谱分析是在反相C18柱上进行的。流速为0.3 mL / min,LC / MS阳性检测扫描范围为200至3000 m / z。流动相A由950 ml蒸馏水/ 50 ml乙腈/ 5 ml乙酸(pH = 3.04)和950 ml蒸馏水/ 50 ml乙腈/ 5 ml乙酸(pH = 4.46)组成。胰岛素的保留时间通常在6.0到7.0分钟之间。这项研究表明,高效液相色谱仪结合质谱检测系统可以作为分析USP胰岛素的有用方法。

著录项

  • 作者

    Maygoo, Eshwar.;

  • 作者单位

    Long Island University, The Brooklyn Center.;

  • 授予单位 Long Island University, The Brooklyn Center.;
  • 学科 Chemistry Analytical.;Health Sciences Pharmacy.
  • 学位 M.S.
  • 年度 2008
  • 页码 119 p.
  • 总页数 119
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号