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口服液体制剂中16种邻苯二甲酸酯类塑化剂残留量的研究
引用本文:钟浩,葛德洲,刘浩,邓祖磊. 口服液体制剂中16种邻苯二甲酸酯类塑化剂残留量的研究[J]. 中国药师, 2014, 0(4): 556-560
作者姓名:钟浩  葛德洲  刘浩  邓祖磊
作者单位:蚌埠医学院药学系 安徽蚌埠 233030;蚌埠医学院药学系 安徽蚌埠 233030;蚌埠医学院药学系 安徽蚌埠 233030;蚌埠市食品药品检验所
基金项目:蚌埠医学院研究生科研创新计划项目(编号:Byycx1330)
摘    要:目的:建立气相色谱-质谱联用技术同时测定口服液体制剂中16种邻苯二甲酸酯类塑化剂的检测方法。比较液-液萃取和固相萃取对液体制剂的净化效果影响,并对操作参数进行优化,建立最佳试验条件。方法:分别采用液-液萃取和固相萃取两种样品前处理方式处理样品,采用选择离子监测,以碎片的丰度比定性,外标法定量。结果:采用液-液萃取方法前处理样品时基质的干扰大,杂质峰较多,故采用固相萃取方式对样品进行前处理,GC-MS检测口服液体制剂中16中邻苯二甲酸酯类塑化剂残留量,该方法检出限为0.02μg · g-1,在0.5~8.0μg · ml-1范围内,线性良好(相关系数 r 范围0.9907~0.9998),加标回收率在71.7%~95.6%范围内,RSD为2.1%~9.7%。结论:采用固相萃取,GC-MS的方法对口服液体制剂中16中邻苯二甲酸酯类塑化剂进行检测,方法简便、快速、准确、灵敏度高,适用于口服液体制剂中16中邻苯二甲酸酯类塑化剂的测定。

关 键 词:气质联用色谱法  邻苯二甲酸酯类  口服液体制剂  塑化剂
收稿时间:2013-11-19
修稿时间:2013-12-21

Research on Residues of 16 Phthalate Ester Plasticizers in Oral Liquid Preparations
Zhong Hao,Ge Dezhou,Liu Hao and Deng Zulei. Research on Residues of 16 Phthalate Ester Plasticizers in Oral Liquid Preparations[J]. China Pharmacist, 2014, 0(4): 556-560
Authors:Zhong Hao  Ge Dezhou  Liu Hao  Deng Zulei
Affiliation:1. Pharmacy Department of Bengbu Medical College, Anhui Bengbu 233030, China; 2. Bengbu Institute for Food and Drug Control)
Abstract:Objective:To establish a GC-MS method for the simultaneous determination of 16 phthalate ester plasticizers in oral liquid preparations, compare the purification effect of liquid preparations by liquid-liquid extraction and solid phase extraction and opti-mize the operating parameters to determine the optimal experimental conditions. Methods:The samples were operated by liquid-liquid extraction and solid phase extraction, respectively. Selective ion monitor ( SIM) was adopt, phthalate esters were identified by the rela-tive abundance of major characteristic ions and the content was determined by an external standard method. Results:When the samples were operated by liquid-liquid extraction, the interference was strong with many impurity peaks. Therefore, the solid phase extraction was adopted for the sample pretreatment. GC-MS was used to detect the residues of 16 phthalate ester plasticizers in oral liquid prepara-tions. The detection limit was 0. 02μg·g-1 ,while the calibration curve showed good linearity within the range of 0. 25-8. 0μg·ml-1 with the correlation coefficient between 0. 990 7 and 0. 999 8. The average recoveries were 76. 0%-95. 4%. The relative standard devi-ations were between 2. 3% and 9. 6%(n=6). Conclusion: Pretreated by solid phase extraction, the residues of 16 phthalate ester plasticizers in oral liquid preparations can be detected by GC-MS with the properties of simple, fast, precise and sensitive, and it is suitable for the determination of phthalate esters in oral liquid preparations.
Keywords:Gas chromatography tandem mass spectrometry   Phthalates   Oral liquid preparations   Plasticizer
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