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磷脂的分离纯化及高效毛细管电泳分析 被引量:9

Fractionation and High Performance Capillary Electrophoretic Analysis of Phospholipids
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摘要 采用溶剂提取和柱色谱法分离纯化市售大豆粉末磷脂(卵磷脂含量14.05%),得到高纯度的卵磷脂产品(纯度92.80%)。重点建立了磷脂的胶束电动毛细管色谱(MECC)分离分析方法。以分离度和峰面积为优化指标,对表面活性剂及其浓度、电泳缓冲液pH、有机改性剂及其含量、缓冲液浓度、温度等条件进行优化,确定了最优化电泳条件:电泳缓冲液为35mmol/L脱氧胆酸钠-1mmol/L硼砂缓冲液/正丙醇(体积比为57:43)(pH8.30),柱温44℃,操作电压25kV,检测波长200nm;内加法定性磷脂组分.外标法定量卵磷脂。结果表明,MECC法能有效分离5种磷脂组分;0.1~1g/L的质量浓度范围内卵磷脂的线性关系良好(r=0.9990),平均回收率为98.0%,日内、日间精密度分别为1.36%和3.27%,定性结果与薄层色谱法、红外光谱法的定性结果相符。 Phosphatidylcholine of high purity ( PC, content 92.80% ) was prepared from market soybean power phospholipids (PC content 14.05% ) by using solvent extraction and column chromatography. As the main objective, micellar electrokinetic capillary chromatography (MECC) was established for the separation and analysis of phospholipids. MECC conditions such as surfactant and its concentration, pH of running buffer solution, organic modifier and its volume content, concentration of buffer solution, temperature etc were optimized to provide good separation and larger peak area of phospholipids. The optimum MECC conditions were as follows: running buffer system of 35 mmoL/L sodium deoxycholate (SDC)-1 mmol/L borax buffer solution/n-propanol (57: 43, v/v) with pH 8.30, column temperature of 44 ℃, applied voltage of 25 kV and ultraviolet (UV) detection at 200 nm. Addition of standards was used to identify the components of phospholipids. External standard method was used to determine PC content. As the results shown, five components of phospholipids could be effectively separated under the optimum MECC conditions. Correlation coefficient within 0. 1 - 1 g/L PC concentration reached 0. 999 0. The average recovery of PC was 98.0%. The intra-day relative standard deviation (RSD) and inter-day RSD of peak area of PC were 1.36% and 3.27%, respectively. The qualitative result of PC obtained by MECC was consistent with that determined by thin layer chromatography and infrared analysis, respectively. So MECC can be used as an effective tool for the separation, analysis and quality control of phospholipids.
机构地区 武汉大学药学院
出处 《色谱》 CAS CSCD 北大核心 2006年第1期30-34,共5页 Chinese Journal of Chromatography
基金 武汉大学回国留学人员启动基金资助项目(502-276130)
关键词 高效毛细管电泳 胶束电动毛细管色谱 分离纯化 磷脂 卵磷脂 high performance capillary electrophoresis (HPCE) micellar electrokinetic capillary chromatography (MECC) fractionation phospholipids phosphatidylcholine
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  • 1胡援,闫春,崔彦.大豆磷脂乳饮料的开发及疗效[J].食品科学,1993,14(11):37-39. 被引量:7
  • 2胡佳惠,马国营,张喜玲,刘德强.阿霉素脂质体中磷脂含量测定[J].西北药学杂志,1996,11(5):195-196. 被引量:4
  • 3傅小芸,吕建德,竺安.乙醇-水混合溶剂体系毛细管胶束电动色谱的研究[J].分析化学,1990,18(9):791-795. 被引量:3
  • 4[1]New RRC.Liposomes:a practical approach,oxford,England,Information Press Ltd,1990∶113.
  • 5[2]New RRC.Liposomes:a Practical approach,Oxford,England,Information Press Ltd,1990∶105.
  • 6[3]US Pharmacopeia/National formulary ⅩⅩⅢ,1995∶2259.
  • 7Terabe S, Otsuka K, Ichikawa K, et al. Electrokinetic separations with micellar solutions and open-tubular capillaries. Anal Chem, 1984, 56(1): 111-113.
  • 8Kaneta T, Tanaka S, Taga M, et al. Migration behavior of inorganic anions in micellar electrokinetic capillary chromatography using cationic surfactant. Anal Chem, 1992, 64(7): 798-801.
  • 9Bjergegaard C, Michaelsen S, Sorensen H. Determination of phenolic carboxylic acids by micellar electrokinefic capillary chromatography and evaluation of factors affecting the method. J Chromatogr A, 1992, 608(1-2): 403-411.
  • 10Corran P H, Sutcliffe N. Identification of gonadorelin (LHRH) derivatives: Comparison of reversed-phase high-performance liquid chromatography and micellar electrokinetic chromatography. J Chromatogr A, 1993,636(1): 87-94.

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