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M Kuchmak

Publications and source records attributed to M Kuchmak.

12 recordsLinked to original sources

International survey of apolipoproteins A1 and B measurements (1983-1984).

We report here results of a worldwide survey of apolipoprotein (apo) A1 and B measurements. A lyophilized pool of human serum was developed for the survey to test its suitability as a candidate Reference Material. Seventy-five laboratories from 18 countries responded to invitations to participate. Using several methods, they evaluated the mass concentration of apo A1 and B in the proposed Reference Material. The bias between laboratories and between analytical methods was then characterized. Fifty-five laboratories reported results before the deadline on measurement of at least one apolipoprotein by one method. Variation in apo A1 and B among collaborators constituted the largest source of error in the study (68% of the total variation for apo A1, 73% for apo B). Variation among method means was not significant for apo A1, but for apo B it constituted 20% of the total variation. Differences due to vials or in replicate measurements within vials were found to constitute 6% or less of the total variability. Within-laboratory, among-vial, and among-replicate CV values were less than 5% for the study. These results suggest that future standardization efforts can be successful.

Apolipoprotein A-I↗

Reference sera with graded levels of high density lipoprotein cholesterol.

A two-step procedure for the separation of low density lipoprotein (LDL)-rich fractions and high density lipoprotein (HDL)-rich fractions from human serum is presented. The isolated precipitates are combined separately with small volumes of human serum in order to stabilize the lipoproteins. Calculated volumes of concentrates are added to human serum or to delipidated human serum [1], so that reference sera with graded levels of high density lipoprotein cholesterol (HDLC) can be prepared. These reference sera resemble human serum in appearance, composition and fractionation by ultracentrifugation. Our evaluations of the materials described in this communication have shown them to be suitable for HDLC determinations, using the precipitation procedure with heparin-manganese chloride. Properties of these reference materials are discussed.

Chemical Precipitation↗

Suitability of frozen and lyophilized reference sera for cholesterol and triglyceride determinations.

Observations on the suitability of frozen and lyophilized reference sera stored at -20 degrees C are presented. These sera, intended for use as controls for both cholesterol and triglyceride determinations, covered ranges for cholesterols from 4 to 8 mmol/l and for triglyceride from 0.7 to 2.4 mmol/L. We observed no change in cholesterol or triglyceride concentration in either the frozen or lyophilized forms of serum during almost 5 years of storage. The suitability of these materials for cholesterol and triglyceride determinations is demonstrated by representative methods. Our results show that lyophilized reference sera can be shipped unprotected by dry ice without any effect on cholesterol or triglyceride concentration. Although the total cholesterol concentration was unchanged with storage, changes did occur in the lipoproteins carrying these lipid constituents.

Blood Preservation↗

Low lipid level reference sera with human serum matrix.

We describe a simple procedure for preparing low lipid level reference sera containing concentrations of nonlipid components similar to the concentrations in human serum. A portion of human serum is delipidized with colloidal silicic acid, and the delipidated serum, in selected proportions, is combined with the native serum. These reference materials can be used as internal or external quality controls in conjunction with low total cholesterol and low high-density lipoprotein (HDL) cholesterol determinations in serum or plasma. They can also be used as controls with low triglyceride determinations.

Blood Preservation↗

Preparation of reference sera with desired levels of cholesterol and triglyceride.

Simple methods for isolating cholesterol-rich protein fraction from human serum and triglyceride-rich fraction from hen egg yolk are presented. The isolated fractions are combined separately with small volumes of human serum in order to stabilize concentrated cholesterol and triglyceride. Precalculated volumes of concentrates are added to human serum in order to prepare reference sera with desired levels of cholesterol or triglyceride, or both. The reference sera resemble human serum in appearance, composition, and stability. Properties of preparations are discussed and stability of reference sera is illustrated.

Blood Proteins↗

Automated determination of total plasma cholesterol: a serum calibration technique.

The automated (AutoAnalyzer II) determination of cholesterol in nine serum pools in the concentration range 3.465-8.871 mmol/l, gave results that were approximately 10% higher than reference values when the analyses were based on unesterified cholesterol standards containing the same amount of water as the sample extracts (1963 analyses in 12 laboratories during a 12 month period; automated value = 0.032 + 1.10 X (Reference value)). A serum calibration procedure was successful ilues, and was equally effective in correcting the values observed for aliquots of 368 fresh-frozen plasma samples analyzed in each of the 12 laboratories during a 38 month period.

Autoanalysis↗