Message Board

Respected readers, authors and reviewers, you can add comments to this page on any questions about the contribution, review,        editing and publication of this journal. We will give you an answer as soon as possible. Thank you for your support!

Name
E-mail
Phone
Title
Content
Verification Code

DONG Ling-ling, CAO Ying-ying, CHAI Yi-feng. Determination of trehalose in Candida albicans by HPLC-MS[J]. Journal of Pharmaceutical Practice and Service, 2010, 28(3): 186-188.
Citation: DONG Ling-ling, CAO Ying-ying, CHAI Yi-feng. Determination of trehalose in Candida albicans by HPLC-MS[J]. Journal of Pharmaceutical Practice and Service, 2010, 28(3): 186-188.

Determination of trehalose in Candida albicans by HPLC-MS

  • Received Date: 2010-01-25
  • Rev Recd Date: 2010-03-08
  • Objective To establish a high performance liquid chromatography-mass spectrum(HPLC-MS) method to determine trehalose in the biofilm of Candida albicans. Methods Shisheido CAPCELL NH2(150 mm×4.6 mm,5 μm) was used in this method and the mobile phase is 75% acetonitrile and 25% pure water.MS detector with an ESI ion source in negative mode was used. Results It has a good separation of trehalose and internal standard,and there is no interference of endogenous impurity.Linear was from 0.05~50 μg/ml(r=0.999 3),recovery was in the range of 81.50% to 96.29% and the RSD of precision is less than 2.1 %. Conclusion This method is a simple method for quantification of trehalose in fungus.
  • Created with Highcharts 5.0.7Amount of accessChart context menuAbstract Views, HTML Views, PDF Downloads StatisticsAbstract ViewsHTML ViewsPDF Downloads2024-052024-062024-072024-082024-092024-102024-112024-122025-012025-022025-032025-040246810Highcharts.com
    Created with Highcharts 5.0.7Chart context menuAccess Class DistributionFULLTEXT: 84.4 %FULLTEXT: 84.4 %META: 7.9 %META: 7.9 %PDF: 7.7 %PDF: 7.7 %FULLTEXTMETAPDFHighcharts.com
    Created with Highcharts 5.0.7Chart context menuAccess Area Distribution其他: 30.2 %其他: 30.2 %China: 0.2 %China: 0.2 %Korea Republic of: 0.2 %Korea Republic of: 0.2 %三明: 0.2 %三明: 0.2 %上海: 1.3 %上海: 1.3 %丽水: 0.2 %丽水: 0.2 %北京: 23.1 %北京: 23.1 %台州: 0.2 %台州: 0.2 %天津: 0.2 %天津: 0.2 %成都: 0.3 %成都: 0.3 %杭州: 1.7 %杭州: 1.7 %武汉: 0.5 %武汉: 0.5 %沈阳: 0.3 %沈阳: 0.3 %济南: 0.2 %济南: 0.2 %深圳: 0.3 %深圳: 0.3 %湖州: 0.2 %湖州: 0.2 %澳大利亚新南威尔士悉尼: 0.3 %澳大利亚新南威尔士悉尼: 0.3 %玉溪: 0.3 %玉溪: 0.3 %珀斯: 0.7 %珀斯: 0.7 %珠海: 0.2 %珠海: 0.2 %芒廷维尤: 9.4 %芒廷维尤: 9.4 %蚌埠: 0.2 %蚌埠: 0.2 %西宁: 26.6 %西宁: 26.6 %西安: 0.2 %西安: 0.2 %贵阳: 1.2 %贵阳: 1.2 %运城: 0.2 %运城: 0.2 %郑州: 0.2 %郑州: 0.2 %金华: 0.3 %金华: 0.3 %长沙: 0.8 %长沙: 0.8 %青岛: 0.3 %青岛: 0.3 %其他ChinaKorea Republic of三明上海丽水北京台州天津成都杭州武汉沈阳济南深圳湖州澳大利亚新南威尔士悉尼玉溪珀斯珠海芒廷维尤蚌埠西宁西安贵阳运城郑州金华长沙青岛Highcharts.com
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Article Metrics

Article views(2493) PDF downloads(585) Cited by()

Related
Proportional views

Determination of trehalose in Candida albicans by HPLC-MS

Abstract: Objective To establish a high performance liquid chromatography-mass spectrum(HPLC-MS) method to determine trehalose in the biofilm of Candida albicans. Methods Shisheido CAPCELL NH2(150 mm×4.6 mm,5 μm) was used in this method and the mobile phase is 75% acetonitrile and 25% pure water.MS detector with an ESI ion source in negative mode was used. Results It has a good separation of trehalose and internal standard,and there is no interference of endogenous impurity.Linear was from 0.05~50 μg/ml(r=0.999 3),recovery was in the range of 81.50% to 96.29% and the RSD of precision is less than 2.1 %. Conclusion This method is a simple method for quantification of trehalose in fungus.

DONG Ling-ling, CAO Ying-ying, CHAI Yi-feng. Determination of trehalose in Candida albicans by HPLC-MS[J]. Journal of Pharmaceutical Practice and Service, 2010, 28(3): 186-188.
Citation: DONG Ling-ling, CAO Ying-ying, CHAI Yi-feng. Determination of trehalose in Candida albicans by HPLC-MS[J]. Journal of Pharmaceutical Practice and Service, 2010, 28(3): 186-188.

Catalog

/

DownLoad:  Full-Size Img  PowerPoint
Return
Return