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Technical Briefs |
Departments of
1
Cardiology and
2
Laboratory Medicine, All India Institute of Medical Sciences, N. Delhi-110029, India
aaddress correspondence to this author at: Department of Cardiology, CNC, All India Institute of Medical Sciences, N. Delhi-110029, India; fax 91-11-6862663, e-mail lakshmy_ram{at}yahoo.com
Dried blood on filter paper has been found to be suitable in large-scale population screening programs (1)(2)(3), but to the best of our knowledge, dried blood or serum on filter paper has not been used for lipid measurements. In the present study, we evaluated the stability of cholesterol and triglycerides in serum dried on filter paper.
Fifty-four patients coming to the centralized laboratory, CNC, All India Institute of Medical Sciences for lipid investigations were selected at random, and blood was collected by venipuncture into tubes without anticoagulant. Serum was separated within 2 h of collection. All procedures were in accordance with the ethics standards of our institution. An aliquot of each serum sample was analyzed immediately. Exact 10-µL replicates of the samples were also spotted onto 3M Whatman filter paper kept on a nonabsorbent surface (thermacol) and left at room temperature for 1 h for drying. The room temperature was 16–37 °C for the duration of the study.
After drying, one aliquot was eluted and analyzed on the day of collection. The remaining filter discs were kept in a sealed plastic bag to protect them from dust and moisture and stored at room temperature for different time periods. At 7, 14, 21, 28, and 35 days, entire dried serum spots corresponding to 10 µL were cut out with scissors and transferred to 1.0 mL of enzymatic reagent (described below). For fresh serum, 10 µL was added to 1 mL of the reagent. The enzymatic reagent for cholesterol contained cholesterol esterase, cholesterol oxidase, peroxidase, phenol, and 4-amino antipyrine in PIPES buffer (4) and was purchased from RANDOX. For fresh serum, the reaction was carried out at room temperature for 10 min; for dried serum on filter paper, the reaction time was 30 min. (We observed that 10 min was not sufficient for the reaction to reach completion.) The absorbance of the resulting product was measured at 500 nm on a Spectronic 20 spectrophotometer. Calibration was with calibrators dried on filter discs and treated the same way as samples. For triglyceride measurements in fresh serum (10 µL) or on filter discs, the enzymatic reagent contained lipase, glycerol kinase, glycerol-3-phosphate oxidase, peroxidase, ATP, 4-chlorophenol, and 4-amino antipyrine in PIPES buffer (5).
The interassay CV of the modified method for filter discs was 2.6% for cholesterol and 2.4% for triglycerides; these compared well with the original method (2.8% and 2.5%, respectively). For quality assurance, the laboratory is part of United Kingdom National External Quality Assessment Scheme (UKNEQAS) program for cholesterol and triglycerides. Statistical analysis was done by within-subject ANOVA.
Both cholesterol and triglycerides were completely released from the
filter discs in the respective enzymatic reagents within 30 min
(calibrators dried on filter discs gave 100% recovery). Total
cholesterol values in the 54 samples (fresh) were 2.57–7.05 mmol/L.
Forty-one samples had cholesterol values 
5.2 mmol/L, and 13 samples
had values >5.2 mmol/L. The mean recovery of cholesterol from dried
sera was 99.4–99.8% at different time points.
Triglyceride values in the 54 samples were 0.736–6.854 mmol/L.
Triglyceride values were 1.725 mmol/L in 22 samples and >1.725
mmol/L in 32 samples. One subject had a triglyceride concentration of
6.854 mmol/L. The mean recovery of triglycerides from dried serum at
different time points was 100.6–101.7%.
The mean cholesterol and triglyceride concentrations in fresh samples
and the dried serum samples at the end of the different storage times
are shown in Table 1
. Mean cholesterol in dried serum eluted and measured on the day
of sample collection (day 0) did not differ significantly from that in
fresh liquid serum (Table 1
), and the individual values obtained by the
two methods gave a highly correlated linear relationship (Fig. 1A
). Storage of filter discs at room temperature for 7, 14, 21,
28, and 35 days also did not significantly alter the mean cholesterol
values, as is apparent from the F statistic (0.97) and the
P value (0.45; Table 1
).
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The mean triglyceride concentrations given in Table 1
indicate that
dried serum is stable for triglyceride measurements and that storage
for different time periods at room temperature does not alter the mean
values significantly (F = 0.89; P =
0.50). An excellent correlation was observed between triglyceride
concentrations in fresh samples and samples dried on filter paper and
analyzed on day 0 (Fig. 1B
).
Dried blood on filter paper may be useful for cholesterol and triglycerides. It has been used extensively for mass screening programs (1)(2)(6)(7)(8) and for measurement of glucose, insulin, glycosylated hemoglobin (9)(10), and steroids (11).
The adaptation of lipid assays to dried blood is ideal for pediatric applications and in multicenter studies where the costs and safety of sample transportation to a distant laboratory are limiting considerations. However, because serum was used in the present study, this approach needs to be evaluated in whole blood, and the use of filter paper matrix as a means of sample transportation would also need to be validated in the context of a multicenter study.
We conclude that cholesterol and triglycerides are highly stable in dried serum and are readily transferable to a liquid phase. The good agreement between values in dried serum and fresh samples supports the validity of the measurement of these analytes in dried serum.
Acknowledgments
The Indian Council of Medical Research provided financial assistance for this study.
References
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