Pressurized liquid extraction-capillary electrophoresis-mass spectrometry for the analysis of polar antioxidants in rosemary extracts

被引:62
作者
Herrero, M
Arráez-Román, D
Segura, A
Kenndler, E
Gius, B
Raggi, MA
Ibáñez, E
Cifuentes, A
机构
[1] Univ Vienna, Inst Analyt Chem, A-1090 Vienna, Austria
[2] CSIC, Dept Food Anal, Inst Ind Fermentat, E-28006 Madrid, Spain
[3] Univ Granada, Fac Sci, Dept Analyt Chem, E-18071 Granada, Spain
[4] Univ Bologna, Fac Pharm, Alma Mater Studiorum, Dept Pharmaceut Sci, Bologna, Italy
关键词
antioxidants; rosemary; pressurized liquid extraction; capillary electrophoresis; electrospray mass spectrometry;
D O I
10.1016/j.chroma.2004.10.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method based on capillary electrophoresis-electrospray-mass spectrometry (CE-ESI-MS) was developed to qualitatively characterize natural antioxidants from rosemary (Rosmarinus officinalis L.) in different fractions obtained by pressurized liquid extraction (PLE) using subcritical water. The parameters of CE-ESI-MS were adjusted allowing the separation and characterization of different compounds from rosemary in the PILE fractions. These parameters for CE are kind, pH and concentration of the separation buffer, parameters for ESI-MS are dry gas temperature and flow, nebulizing gas pressure, and make-up flow. The following analytical conditions were found most favorable: aqueous CE buffer (40 mM ammonium acetate/ammonium hydroxide, pH 9); sheath liquid containing 2-propanol-water (60:40, v/v) and 0.1% (v/v) triethylamine at a flow rate of 0.24 mL/h; drying gas flow rate equal to 7 L/min at 350 degrees C, nebulizing gas pressure of 13.8 kPa (2 psi), using a compound stability of 50%. Different antioxidant compounds (e.g., rosmarinic acid and camosic acid) could be detected in the rosemary extracts by CE-ESI-MS without any additional treatment, enabling the determination of variations in the extract composition caused by the different PLE conditions (i.e., 60 and 100 degrees C). The results provide complementary information to HPLC analysis. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:54 / 62
页数:9
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