Measurement of lipoprotein particle sizes using dynamic light scattering

被引:26
|
作者
Sakurai, Toshihiro
Trirongjitmoah, Suchin [2 ]
Nishibata, Yuka
Namita, Takeshi [2 ]
Tsuji, Masahiro [3 ]
Hui, Shu-Ping [4 ]
Jin, Shigeki
Shimizu, Koichi [2 ]
Chiba, Hitoshi [1 ]
机构
[1] Hokkaido Univ, Fac Hlth Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[2] Hokkaido Univ, Grad Sch Informat Sci & Technol, Sapporo, Hokkaido 0600812, Japan
[3] Hlth Sci Univ Hokkaido Hosp, Div Internal Med, Sapporo, Hokkaido, Japan
[4] Hlth Sci Univ Hokkaido, Fac Pharmaceut Sci, Ishikari, Hokkaido 06102, Japan
基金
日本学术振兴会;
关键词
LOW-DENSITY-LIPOPROTEIN; MAGNETIC-RESONANCE-SPECTROSCOPY; SERUM-LIPOPROTEINS; LDL PARTICLES; SUBCLASSES; PLASMA; RISK; QUANTIFICATION; IDENTIFICATION; DISTRIBUTIONS;
D O I
10.1258/acb.2010.010100
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: A simple method for the measurement of LDL particle sizes is needed in clinical laboratories because a predominance of small, dense LDL (sd LDL) has been associated with coronary heart disease. We applied dynamic light scattering (DLS) to measure lipoprotein particle sizes, with special reference to sd LDL. Methods: Human serum lipoproteins isolated by a combination of ultracentrifugation and gel chromatography, or by sequential ultracentrifugation, were measured for particle size using DLS. Results: The sizes of polystyrene beads, with diameters of 21 and 28 nm according to the manufacturer, were determined by DLS as 19.3 +/- 1.0 nm (mean +/- SD, n = 11) and 25.5 +/- 1.0 nm, respectively. The coefficients of variation for the 21 and 28 nm beads were 5.1% and 3.8% (within-run, n = 11), and 2.9% and 6.2% (between-run, n = 3), respectively. The lipoprotein sizes determined by DLS for lipoprotein fractions isolated by chromatography were consistent with the elution profile. Whole serum, four isolated lipoprotein fractions (CM + VLDL + IDL, large LDL, sd LDL and HDL) and a non-lipoprotein fraction isolated by sequential ultracentrifugation were determined by DLS to be 13.1 +/- 7.5, 37.0 +/- 5.2, 21.5 +/- 0.8, 20.3 +/- 1.1, 8.6 +/- 1.5 and 8.8 +/- 2.0 nm, respectively. Conclusions: The proposed DLS method can differentiate the sizes of isolated lipoprotein particles, including large LDL and sd LDL, and might be used in clinical laboratories in combination with convenient lipoprotein separation.
引用
收藏
页码:476 / 481
页数:6
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