Measurement of lipoprotein particle sizes using dynamic light scattering

Toshihiro Sakurai, Suchin Trirongjitmoah, Yuka Nishibata, Takeshi Namita, Masahiro Tsuji, Shu Ping Hui, Shigeki Jin, Koichi Shimizu, Hitoshi Chiba

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)476-481
Number of pages6
JournalAnnals of Clinical Biochemistry
Volume47
Issue number5
DOIs
Publication statusPublished - 2010 Sep
Externally publishedYes

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Dynamic light scattering
Particle Size
Lipoproteins
Particle size
Ultracentrifugation
Clinical laboratories
Chromatography
Polystyrenes
oxidized low density lipoprotein
Dynamic Light Scattering
Serum
Gel Chromatography
Coronary Disease
Gels

ASJC Scopus subject areas

  • Clinical Biochemistry

Cite this

Sakurai, T., Trirongjitmoah, S., Nishibata, Y., Namita, T., Tsuji, M., Hui, S. P., ... Chiba, H. (2010). Measurement of lipoprotein particle sizes using dynamic light scattering. Annals of Clinical Biochemistry, 47(5), 476-481. https://doi.org/10.1258/acb.2010.010100

Measurement of lipoprotein particle sizes using dynamic light scattering. / Sakurai, Toshihiro; Trirongjitmoah, Suchin; Nishibata, Yuka; Namita, Takeshi; Tsuji, Masahiro; Hui, Shu Ping; Jin, Shigeki; Shimizu, Koichi; Chiba, Hitoshi.

In: Annals of Clinical Biochemistry, Vol. 47, No. 5, 09.2010, p. 476-481.

Research output: Contribution to journalArticle

Sakurai, T, Trirongjitmoah, S, Nishibata, Y, Namita, T, Tsuji, M, Hui, SP, Jin, S, Shimizu, K & Chiba, H 2010, 'Measurement of lipoprotein particle sizes using dynamic light scattering', Annals of Clinical Biochemistry, vol. 47, no. 5, pp. 476-481. https://doi.org/10.1258/acb.2010.010100
Sakurai T, Trirongjitmoah S, Nishibata Y, Namita T, Tsuji M, Hui SP et al. Measurement of lipoprotein particle sizes using dynamic light scattering. Annals of Clinical Biochemistry. 2010 Sep;47(5):476-481. https://doi.org/10.1258/acb.2010.010100
Sakurai, Toshihiro ; Trirongjitmoah, Suchin ; Nishibata, Yuka ; Namita, Takeshi ; Tsuji, Masahiro ; Hui, Shu Ping ; Jin, Shigeki ; Shimizu, Koichi ; Chiba, Hitoshi. / Measurement of lipoprotein particle sizes using dynamic light scattering. In: Annals of Clinical Biochemistry. 2010 ; Vol. 47, No. 5. pp. 476-481.
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AU - Sakurai, Toshihiro

AU - Trirongjitmoah, Suchin

AU - Nishibata, Yuka

AU - Namita, Takeshi

AU - Tsuji, Masahiro

AU - Hui, Shu Ping

AU - Jin, Shigeki

AU - Shimizu, Koichi

AU - Chiba, Hitoshi

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N2 - 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.

AB - 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.

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