关闭
 
读者在线:用户名 密码
首页 期刊简介 投稿须知 期刊目录 专家风采 编委会 特邀顾问 联系我们 移动出版
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5



刊物信息

期刊名称:药物分析杂志
主管单位:中国科学技术协会
主办单位:中国药学会
承办:中国食品药品检定研究院
主编:金少鸿
地址:北京天坛西里2号
邮政编码:100050
电话:010-67012819,67058427
电子邮箱:ywfx@nifdc.org.cn
国际标准刊号:ISSN 0254-1793
国内统一刊号:CN 11-2224/R
邮发代号:2-237
 

访问统计
您是第  1 1 7 8 5 9 5 0 位浏览者
您当前的位置:首页 >> 正文

单唾液酸四己糖神经节苷脂钠有关物质测定方法的研究

Study onmethods for related substances measurment in monosialotetrahexosyl ganglioside

分类号:
出版年·卷·期(页码):2013,33 (2):0-0
DOI: 10.16155/j.0254-1793.2017.01.01
-----摘要:-------------------------------------------------------------------------------------------

目的: 建立单唾液酸四己糖神经节苷脂钠(GM1)有关物质的检测方法。 方法: 采用COSMOSIL 5C8-MS柱(250 mm×4.6 mm,5 μm),以乙腈-0.01 mol·L-1四丁基硫酸氢铵(80: 20)为流动相,流速1.0 mL·min-1,在205 nm波长处,应用外标法对GM1中已知杂质GD1a和GD3进行检查,其他未知杂质用不加校正因子的主成分自身对照法进行检查。 结果: GD1a和GD3在15~240 μg·mL-1浓度范围内线性关系良好,相关系数均为0.9999;检测限分别为1.40 μg和1.41 μg;定量限分别为4.61 μg和4.60 μg;方法重复性的RSD分别为0.45%和0.51%;该方法与现行标准的对比测定结果显示, 现行标准测得的杂质总量和总数目明显低于该方法。 结论: 本方法专属性强,灵敏度高,精密度好,可用于质量控制以及GM1原料药中有关物质的研究。

-----英文摘要:---------------------------------------------------------------------------------------

Objective: To establish a method for monosialotetrahexosyl ganglioside(GM1)measurement. Method: The known impurities GD1a and GD3 in GM1 were analyzed by external standard method on a COSMOSIL 5C8-MS column(250 mm×4.6 mm,5 μm)with mobile phase consisted of acetonitrile-tetrabutylammonium acid(0.01 mol·L-1,80: 20)at a flow rate of 1.0 mL·min-1,and the detection wave-length was set at 205 nm;meanwhile,the unknown impurities were examined by the self-compare method but without calibration factors. Results: Good linear relations of GD1aand GD3 were obtained in the range of 15-240 μg·mL-1,and both of the correlation coefficients were 0.9999.The limits of detection were 1.40 μg and 1.41 μg,respectively.The limits of quality were 4.61 μg and 4.60 μg,respectively.Meanwhile,the reproducibility of RSD were 0.45%and 0.51%,respectively.Compared with the results using current criteria,the total impurity amount was higher with this method. Conclusion: The established method is specific,sensitive and accurate,which can be used for quality control and research in related substances of raw material GM1.

-----参考文献:---------------------------------------------------------------------------------------
1 ZHANG Wei-jie(张惟杰).Research Technology of Glyco-compound (糖复合生物生化研究技术).(2nd Ed(第2版))Zhejiang(浙江).Zhejiang University Press(浙江大学出版社),1999.445
2 Lars Svennerholm.The gangliosides.Lipid Res,1964.145
3 Svennerholm L .Chromatographic separation of human brain gangliosides.J Neuirochem,1963,10:613
4 Sabel BA,Slavin MD,Stine DG.GM1 ganglioside treatment facilitates behavioral recovery from bilateral brain damage.Science,1984,225(7):340
5 Geisler FH.GM-1 ganlioside and motor recovery following human spinal cord injury.J Emerg Med,1993,11(1)Suppl:49
6 Heaton MB et al.Ethanol neurotoxicity in vitro:effects of GM1 ganglioside and protein synthesis inhibition.Brain Res,1994,645(2):336
7 Favaron M,Manev H,Alho H,et al.Ganglisides prevent glutamate and kainite beurotoxicity in primary neuronal culture of neonatal rat cerebellum and cortex.Proc Natl Acad Sci USA,1988,85:7351
8 LIU Qin(刘勤),XIE Jian-wei(谢剑炜).Studies on determination of monosialoterahexosyl ganglioside sodium salt and its impurities(单唾液酸四己糖神经节苷脂钠杂质检查及含量测定方法研究).Chin J Pharm Anal(药物分析杂志),2005,25(2):153
9 Zeng G,Gao L,Birkle S,et al.Suppression of ganglioside GD3 expression in a rat F211 tumorcell line reduces tumor growth,angiogenesis,and vascular endothelial growth factor production.Cancer Res,2000,60:6670
10 Wang L,Talaku S,Yamagata T,et al.Ganglioside GD1a regulation of caveolin21 and Stim1 expression in mouse FBJ cells:augmented expression of caveolin21 and Stim1 in cells with increased GD1a content.Glycoconj J,2006,23:303
11 Criterion of the State Food and Drug Administration(Trail)(国家食品药品监督管理局标准)(试行).2004.YBH20692004
12 Criterion of the State Food and Drug Administration(Trail)(国家食品药品监督管理局标准)(试行).2006.YBH15322006

欢迎阅读《药物分析杂志》!您是该文第 1977位读者!

药物分析杂志 © 2009
地址:北京天坛西里2号 邮政编码:100050; 电子邮件:ywfx@nicpbp.org.cn