检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:汪元亮 常亮 辜倩 熊马剑 朱碧君 赵霞[3] WANG Yuanliang;CHANG Liang;GU Qian;Xiong Majian;ZHU Bijun;ZHAO Xia(Jiangxi Institute for Drug Control,NMPA Key Laboratory for Quality Evaluation of Traditional Chinese Patent Medicine,Jiangxi Province Engineering Research Center of Drug and Medical Device Quality,Nanchang 330029,China;Jiangxi University of Traditional Chinese Medicine,Nanchang 330004,China;National Institutes for Food and Drug Control,Beijing 100050,China)
机构地区:[1]江西省药品检验检测研究院,国家药品监督管理局中成药质量评价重点实验室,江西省药品与医疗器械质量工程技术研究中心,南昌330029 [2]江西中医药大学,南昌330004 [3]中国食品药品检定研究院,北京100050
出 处:《中国药学杂志》2023年第23期2120-2126,共7页Chinese Pharmaceutical Journal
基 金:江西省药品监督管理局科研项目资助(2021KY31);中国食品药品检定研究院中青年发展研究基金项目资助(2023C6)。
摘 要:目的建立同时测定药用复合软膏管中10种光引发剂的定量分析方法。方法对剪碎的药用复合软膏管超声30 min,利用GC-MS技术对样品进行检测。色谱柱为DB17-MS毛细管色谱柱(0.25 mm×30 m,0.25μm),进样口:300℃,流速:1 mL·min^(-1),柱温:初始70℃,保持0.5 min,再以10℃·min^(-1)升至300℃,保持7 min。进样类型:液体进样,进样体积:1μL。离子源:EI,温度:290℃,电压:70 eV,溶剂延迟5 min。结果10种光引发剂分离度良好,在浓度0.05~10μg·mL^(-1)内线性关系良好,相关系数r^(2)在0.9945~0.9988之间;平均回收率(n=9)在84.9%~94.6%之间,相对标准偏差(RSD)在3.9%~8.5%之间,检测限在0.2~0.5μg·g^(-1),定量限在0.5~1.0μg·g^(-1)。结论该方法经方法学验证,操作简便,方法准确性、重复性好,可用于复合软膏管中10种光引发剂的筛查。OBJECTIVE To develop a quantitative analytical method for simultaneous determination of 10 photoinitiators in medicinal compound ointment tubes.METHODS Ultrasound was used to ultrasonicate the shredded medicinal compound ointment tube for 30 min,and the samples were detected by GC-MS technology.Chromatographic column was DB17-MS capillary column(0.25 mm×30 m,0.25μm),injection port:300℃,flow rate:1 mL·min^(-1),column temperature:initial 70℃,hold for 0.5 min,and then rise at 10℃·min^(-1) to 300℃,keeping for 7 min.Injection type:liquid injection,injection volume:1μL.Ion source:EI,temperature:290℃,voltage:70 eV,solvent delay 5 min.RESULTS The 10 kinds of photoinitiators were well separated,with good linear relationship in the concentration range of 0.05-10μg·mL^(-1).The correlation coefficient r^(2) was between 0.9945-0.9988;the average recoveries(n=9)were 84.9%-94.6%,and the RSDs were between 3.9% and 8.5%.The limits of detection were between 0.2 and 0.5μg·mL^(-1),and the limits of quantification were between 0.5 and 1.0μg·mL^(-1).CONCLUSION This method is validated to have good method accuracy and reproducibility,is easy to operate,and can be used for the determination of 10 photoinitiators in compound ointment tubes.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.75