Highly sensitive analysis of sterol profiles in human serum by LC-ESI-MS/MS

被引:135
作者
Honda, Akira [2 ]
Yamashita, Kouwa [3 ]
Miyazaki, Hiroshi [4 ]
Shirai, Mutsumi [5 ]
Ikegami, Tadashi [1 ]
Xu, Guorong [6 ]
Numazawa, Mitsuteru [3 ]
Hara, Takashi [5 ]
Matsuzaki, Yasushi [1 ]
机构
[1] Tokyo Med & Dent Univ, Kasumigaura Hosp, Dept Gastroenterol, Ibaraki 3000395, Japan
[2] Tokyo Med & Dent Univ, Kasumigaura Hosp, Ctr Collaborat Res, Ibaraki 3000395, Japan
[3] Tohoku Pharmaceut Univ, Fac Pharmaceut Sci, Sendai, Miyagi 9818558, Japan
[4] Pharmax Inst, Kanagawa 2130021, Japan
[5] Ibaraki Prefectural Inst Publ Hlth, Mito, Ibaraki 3100852, Japan
[6] Univ Med & Dent New Jersey, Dept Med, Sch Med, Newark, NJ 07103 USA
关键词
cholestanol; cholesterol precursors; congenital birth defect; liquid chromatography-electrospray ionizationtandem mass spectrometry; picolinic acid; plant sterols;
D O I
10.1194/jlr.D800017-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a highly sensitive and specific method for the analysis of serum sterol profiles. Sterols in 1 mu l of dried serum were derivatized into picolinyl esters (3 beta-picolinate) and analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) using the electrospray ionization (ESI) mode. In addition to cholesterol, 19 cholesterol precursors, cholestanol, campesterol, sitosterol, and sitostanol were identified simultaneously. Quantitative analyses for the picolinyl esters of 11 available sterols were performed, and detection limits were found to be less than 1 pg on-column. Reproducibilities and recoveries of 8 noncholesterol sterols were validated according to one-way layout and polynomial equation, respectively. The variances between sample preparations and between measurements by this method were calculated to be 1.6% to 8.2% and 2.5% to 16.5%, respectively. The recovery experiments were performed using 1 mu l aliquots of normal human serum spiked with 1 ng to 6 ng of sterols, and recoveries of the sterols ranged from 88.1% to 102.5% with a mean recovery of 98.1%. The present method provides reliable and reproducible results for the identification and quantification of neutral sterols, especially in small volumes of blood samples, which is useful for serological diagnosis of inherited disorders in cholesterol metabolism and for noninvasive evaluation of cholesterol biosynthesis and absorption in humans.-Honda, A., K. Yamashita, H. Miyazaki, M. Shirai, T. Ikegami, G. Xu, M. Numazawa, T. Hara, and Y. Matsuzaki. Highly sensitive analysis of sterol profiles in human serum by LC-ESIMS/MS.
引用
收藏
页码:2063 / 2073
页数:11
相关论文
共 45 条
  • [1] Simultaneous determination of plasmatic phytosterols and cholesterol precursors using gas chromatography-mass spectrometry (GC-MS) with selective ion monitoring (SIM)
    Ahmida, H. S. Mohamed
    Bertucci, Pierfrancesco
    Franzo, Letizia
    Massoud, Renato
    Cortese, Claudio
    Lala, Alberto
    Federici, Giorgio
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2006, 842 (01): : 43 - 47
  • [2] AXELSON M, 1991, J LIPID RES, V32, P1441
  • [3] Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters
    Berge, KE
    Tian, H
    Graf, GA
    Yu, LQ
    Grishin, NV
    Schultz, J
    Kwiterovich, P
    Shan, B
    Barnes, R
    Hobbs, HH
    [J]. SCIENCE, 2000, 290 (5497) : 1771 - 1775
  • [4] Berge KE, 2002, J LIPID RES, V43, P486
  • [5] BJORKHEM I, 1987, J LIPID RES, V28, P1137
  • [6] Mutations in the gene encoding 3β-hydroxysteroid-Δ8,Δ7-isomerase cause X-linked dominant Conradi-Hunermann syndrome
    Braverman, N
    Lin, P
    Moebius, FF
    Obie, C
    Moser, A
    Glossmann, H
    Wilcox, WR
    Rimoin, DL
    Smith, M
    Kratz, L
    Kelley, RI
    Valle, D
    [J]. NATURE GENETICS, 1999, 22 (03) : 291 - 294
  • [7] NSDHL, an enzyme involved in cholesterol biosynthesis, traffics through the Golgi and accumulates on ER membranes and on the surface of lipid droplets
    Caldas, H
    Herman, GE
    [J]. HUMAN MOLECULAR GENETICS, 2003, 12 (22) : 2981 - 2991
  • [8] CALI JJ, 1991, J BIOL CHEM, V266, P7779
  • [9] FitzPatrick DR, 1998, AM J MED GENET, V75, P145, DOI 10.1002/(SICI)1096-8628(19980113)75:2<145::AID-AJMG5>3.3.CO
  • [10] 2-1