Liquid lipoprotein control

Abstract

An accurate, stable, liquid lipoprotein control composition is provided. The control composition of the present invention preferably contains lipoprotein, surfactant and a divalent cation. The control may further contain an anti-oxidant agent and a chelating agent. The control composition of the present invention is stable for up to about 12 months at room temperature and up to about 24 months when refrigerated. Methods of making and using the control composition are also provided.

Description

FIELD OF THE INVENTION

The present invention relates generally to lipoprotein controls and more particularly, to a stable, liquid, lipoprotein control composition, and methods of making and using the same.

BACKGROUND OF THE INVENTION

Lipoproteins are water soluble conjugated proteins. They are conjugated with lipids--substances such as cholesterol, triglycerides and phospholipids. Cholesterol, triglycerides and phospholipids are all insoluble in aqueous solutions. They are conjugated to proteins which make them soluble in serum.

The association of cholesterol and lipoproteins with arteriosclerosis has led to the frequent evaluation of cholesterol and lipoprotein in human serum. It is known that elevated total cholesterol and elevated low density lipoprotein (LDL) cholesterol levels may lead to poor cardiovascular health while elevated high density lipoprotein (HDL) cholesterol does not have a negative influence on cardiovascular health and may even improve the condition of cardiovascular health. Because of the association of cholesterol and lipoproteins with cardiovascular health and because it has been demonstrated that LDL cholesterol can be decreased and HDL cholesterol increased by diet, exercise and drugs, several clinical assays have been developed to measure lipoprotein, triglycerides and cholesterol.

A typical assay for lipid analysis often includes values for cholesterol, triglycerides, HDL cholesterol, LDL cholesterol, phospholipids, cholesterol esters, free fatty acids, apolipoprotein A1 and apolipoprotein B. In routine practice, LDL cholesterol is estimated using the Friedwald equation wherein LDL cholesterol is calculated by subtracting measured HDL cholesterol and estimated very low density lipoprotein (VLDL) cholesterol (approximated as one-fifth of the serum triglyceride) from total cholesterol. HDL cholesterol may be measured by various methods such as density separation using ultracentrifugation, electrophoresis or enzyme-linked methods employing cholesterol oxidase and photometric measurement. When the latter method is employed, the VLDL and LDL cholesterol is first precipitated from the serum with reagents such as heparin, dextran sulfate and magnesium ion or phosphotungstate. The HDL cholesterol remaining in the supernatant can then be measured.

Controls are used to objectively evaluate the accuracy and precision of lipoprotein testing procedures. Unfortunately, the freezing and lyophilization of lipoprotein controls leads to aggregation and turbidity of lipoprotein solutions. Another disadvantage in lipoprotein controls is reconstitution of lyophilized controls which can lead to inaccuracies due to volumetric measurements. Various approaches to improving lipid controls (triglycerides and total cholesterol) have thus been developed.

For example, in U.S. Pat. Nos. 4,816,411 and 4,503,146 (incorporated by reference), turbidity in biological fluid such as plasma or serum is reduced by adding a surfactant and cholesterol esterase or lipase, to degrade the lipoproteins. These patents describe photometric assays for cholesterol and triglycerides, wherein clear samples are essential. U.S. Pat. Nos. 4,626,511 and 5,310,679 (incorporated by reference), also disclose reduction of turbidity by the addition of a surfactant and lipolytic enzyme to degrade the lipoproteins.

In U.S. Pat. No. 4,011,045 (incorporated by reference), lipoproteins are precipitated from serum by the addition of divalent cations and dextran sulfate. The large lipoproteins are discarded and the short chain triglycerides are added back to the serum. The added triglycerides in serum are then emulsified by using the surfactant alkylphenoxypolyethoxyethanol. The serum is then lyophilized and reconstituted to produce a clear preparation.

Similarly, in U.S. Pat. No. 3,955,925 (incorporated by reference), a clear, lyophilized control product is prepared by precipitating lipoproteins from serum with dextran sulfate and divalent cations and adding back to the serum, bovine high density lipoprotein which has been purified. Surfactant is also used to remove turbidity in U.S. Pat. Nos. 5,258,315, 4,579,825 and 4,708,939 (incorporated by reference), although no control product is disclosed. Similarly in U.S. Pat. No. 4,289,649 (incorporated by reference), non-ionic and ionic detergent is used to remove turbidity in a control for triglycerides and total cholesterol.

In U.S. Pat. No. 4,127,502 (incorporated by reference), the addition of arabinose, sorbitol, sucrose or glucosamine was shown to reduce the turbidity of lyophilized serum and U.S. Pat. Nos. 4,298,441, 4,045,176 and 4,216,117 (incorporated by reference), disclose that lyophilized control serum which contains non-reducing sugars is stable.

The following United States Patents and journal article, which are incorporated by reference herein, relate generally to lipid preparations: U.S. Pat. Nos. 3,751,381, 3,853,465, 4,189,400, 4,290,774, 3,260,648, 4,414,326 and Hirst, C. F. et al., J. Clin. Pathol 45:701-703 (1992).

None of the above patents describe stable lipoprotein controls; they are all used for cholesterol and triglyceride standards only. Several recent journal articles make it clear that there is no lipoprotein control which adequately behaves like human serum. In particular, Naito et al., Arch. Pathol. Lab. Med. 117:345-351 (1993), describes the "matrix effects" of known lipoprotein controls used in proficiency studies. Matrix is defined by the National Committee for Clinical Laboratory Standards, Document EP10-T, Vol. 9, No. 3, November, 1988, as "all properties other than the property to be measured, that can have an effect on a measured value, " and matrix effects is defined as "an analytic bias due to the matrix of the processed specimen being measured, that is exclusive of calibration." Naito points out that the matrix problems associated with lipoprotein controls severely hamper interlaboratory accuracy, standardization efforts, and monitoring of laboratory performance. It is thus suggested that efforts be made to improve lipoprotein controls so they behave more like human serum.

Likewise, in Kroll, M.H. et al., Clin. Chem. 40:389-394 (1994), it was shown that there is a lack of linearity in high density lipoprotein measurements. Available commercial controls were not linear and it was suggested that the non-linearity is due to alteration of the lipoproteins during lyophilization. Rej. R., Clin. Chem. 40:345-346 (1994) also addresses the inadequacy of available lipoprotein controls and stresses the importance of developing adequate preparations for standardization of methods. The level of importance of this issue is further indicated by an Omnibus Solicitation of the National Institutes of Health, PHS 95-1 (Dec. 1, 1994 Application Receipt Date). The title of the solicitation is "Development of proficiency testing materials free of the matrix effects that compromise accurate measurement of total cholesterol, HDL cholesterol, and LDL cholesterol."

It would thus be desirable to provide an accurate, stable, lipoprotein control. It would further be desirable to provide an accurate, stable, liquid, lipoprotein control that is not lyophilized and reconstituted or frozen and thawed. It would also be desirable to provide an accurate, complete, chemistry control which includes all lipoproteins.

SUMMARY OF THE INVENTION

An accurate, stable, liquid lipoprotein control composition is provided. The control composition of the present invention preferably comprises lipoprotein, surfactant and a divalent cation. It has been surprisingly found that when surfactant and a divalent cation are added to lipoprotein, it behaves like native lipoprotein in human serum, i.e. not aggregated and not subject to matrix effects. The control of the present invention may thus provide all of the lipid parameters: HDL cholesterol, LDL cholesterol, phospholipids, cholesterol esters, free fatty acids, apolipoprotein A1 and apolipoprotein B. Surprisingly, the control composition of the present invention is stable for up to about 12 months at room temperature (about 22.degree. C.) and up to about 24 months refrigerated (about 2.degree. C. to about 10.degree. C.), preferably up to about 6 months at room temperature and up to about 12 months refrigerated. Methods of making and using the control composition are also provided.

Additional objects, advantages, and features of the present invention will become apparent from the following description and appended claims, taken in conjunction with the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

The various advantages of the present invention will become apparent to one skilled in the art by reading the following specification and subjoined claims and by referencing the following drawings in which:

FIG. 1 is a graph illustrating triglyceride stability;

FIG. 2 is a graph illustrating LDL cholesterol stability;

FIG. 3 is a graph illustrating HDL cholesterol stability;

FIG. 4 is a graph illustrating HDL cholesterol stability at various concentration levels;

FIG. 5 is a graph illustrating LDL cholesterol stability at various concentration levels; and

FIG. 6 is a graph illustrating triglyceride stability at various concentration levels.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

An accurate, stable, liquid, lipoprotein control composition is provided. The control composition of the present invention preferably comprises lipoprotein, surfactant and a divalent cation. The control may further comprise an anti-oxidant and a chelating agent. In a preferred embodiment, the control composition comprises by weight from about 0.1% to about 1.5% lipoprotein, from about 0.01% to about 0.5% surfactant and from about 0.05% to about 1.0% divalent cation, the amount of which may vary with the particular antioxidant used. In a preferred embodiment, the control composition comprises by weight from about 0.001% to about 0.1% antioxidant. Methods of making and using the controls described herein are also provided.

The lipoprotein control composition of the present invention performs like native lipoprotein in serum and, unlike native lipoprotein in serum, is stable. The lipoprotein control is not lyophilized or frozen and therefore does not require thawing or reconstitution. The control composition of the present invention is stable for up to about 12 months at room temperature (about 22.degree. C.) and up to about 24 months refrigerated (about 2.degree. C. to about 10.degree. C.).

Although the control composition of the present invention is described with respect to use as a lipoprotein control, it will be appreciated that the control composition may be used in other applications such as in a complete chemistry control which contains other constituents. For example, analytes such as bilirubin, glucose, potassium, urea, creatinine, sodium, uric acid, ALT (alanine aminotransferase), GGT (.gamma.-glutamyltransferase) may be included in the control composition.

A broad range of surfactants may be employed in the control of the present invention including anionic, ionic, non-ionic and zwitterionic surfactants. In a preferred embodiment, the surfactant produces a surface tension similar to serum, i.e., approximately 70 dynes/cm. The following surfactants are preferred: Triton X705 (Sigma), Silwet 7614 (Union Carbide), Diazopon SS 837 (GAF Chemicals Corp.), Pluronic F-68 (BASF), Polyethylene Glycol (PEG) 400-20,000 (Union Carbide) and dioctyl sodium sulfosuccinate. Triton X705, PEG-1500 and Pluronic F-68 are most preferred. In addition, although it is believed that any cation may be employed in the control of the present invention, divalent cations are preferred and manganese (Mn.sup.++), calcium (Ca.sup.++) and magnesium (Mg.sup.++) divalent cations are most preferred. Mg.sup.++ is highly preferred.

As noted above, chelating agents may also be added to the control of the present invention. Preferred chelating agents include ethylenediaminetetraacetic acid (EDTA), ethyleneglycol-bis-(.beta.-aminoethyl ether) N,N,N.sup.1,N.sup.1 -tetraacetic acid (EGTA) and sodium citrate. EDTA is most preferred in an amount of up to about 12 mmol.

Also, as noted above, anti-oxidants may also be added to the control of the present invention to further increase the stability of the control. Preferred anti-oxidants include sulfasalazine at a concentration of about 0.1 mg/dl to about 50 mg/dl, preferably about 0.001M, uric acid at a concentration of about 0.1 mg/dl to about 25 mg/dl, preferably about 1 mg/dl to about 20 mg/dl, most preferably about 10 mg/dl and alpha-tocopherol (.alpha.-tocopherol) at a concentration of about 0.01 mg/dl to about 5 mg/dl, preferably about 5 mg/dl. A mixture of antioxidants may also be employed.

It has been found that the amount of surfactant employed in the composition of the present invention is directly related to the amount of divalent cation employed. Surprisingly, the amount of divalent cation employed is inversely related to the amount of lipoprotein employed. It would be expected that more divalent cation would be required at a higher lipoprotein concentrations. Hence, when the concentration of lipoprotein is increased, the concentration of divalent cation is decreased and when the concentration of surfactant is increased, the amount of divalent cation is likewise increased. For example, when Triton X705 is increased from about 0.175% to about 0.350%, the optimum Mg.sup.++ concentration increases from about 6 mM to about 25 mM.

Without wishing to be bound by theory, it is believed that the surfactant of the composition of the present invention acts as a stabilizer of the lipoprotein in solution and the divalent cation eliminates the matrix problems of currently available controls by maintaining the lipoprotein structure to prevent dissolution by the surfactant. That is, the surfactant stabilizes the lipoproteins and prevents the development of aggregation, and the divalent cation allows the lipoproteins to act like native lipoprotein in human serum, i.e. the difference between the way the lipoprotein in the control and the lipoprotein in serum react to various manipulations such as precipitation, is the same. It is also believed that the chelating agent stabilizes the divalent cation and inhibits any oxidation of lipoprotein caused by cations such as Fe.sup.++ which may be present in traces.

Because the lipoprotein of the control substance composition behaves substantially similar to native lipoprotein in serum, the control composition of the present invention may be used with any known method of lipoprotein measurement. For example, total cholesterol and triglyceride control concentrations may be measured by known techniques. The VLDL and LDL cholesterol may then be precipitated from the control with reagents such as heparin, dextran sulfate and magnesium ion and the HDL cholesterol may then be measured by photometric techniques. The LDL cholesterol may then be calculated by subtracting the measured HDL cholesterol concentration and the estimated VLDL cholesterol (approximated as one-fifth of the triglyceride concentration) from total cholesterol. The measured and calculated values of the various lipoprotein components may then be compared to the known values of the control composition, in order to objectively evaluate the accuracy and precision of the lipoprotein testing procedure.

Lp(a) is a lipoprotein which is similar to LDL but has apolipoprotein (a) linked to Apo B. This lipoprotein has been found to be a marker for atherosclerosis. In addition, Apo A.sub.1 and Apo B are commonly assayed in the laboratory to assess the risk of coronary heart disease. While not wishing to be bound by theory, it is believed that these components are stabilized by the antioxidant in the composition.

It will be appreciated that as used herein the term "stable" generally refers to maintaining consistency and more particularly, maintaining consistent values for various parameters over a determined period of time. The term "accurate" as referred to herein means providing consistent results substantially similar to known values.

It will also be appreciated by those skilled in the art that the composition of the present invention may include other additives such as antimicrobial agents. It will further be understood that with the teachings of the present application, the skilled artisan will, and without undue experimentation, be enabled to alter concentrations of various components of the composition of the present invention to achieve a desired result.

The following Specific Examples will further describe the present invention.

SPECIFIC EXAMPLE 1

A. Prior Art

Concentrates were prepared from human plasma using dextran sulfate and Mg.sup.++ as precipitating agents. The methods for preparing high density and low density lipoproteins have been described in Burstein, M., Advan. Lipid. Res. 11:67-108 (1973). The HDL concentrate had an HDL cholesterol of 550 mg/dl. The LDL concentrate had an LDL cholesterol of 950 mg/dl. For these studies, the lipoprotein concentrates were added to a HEPES buffered 0.5% NaCI, pH 7.4, containing 2% bovine serum albumin (BSA). The LDL and HDL concentrates were added to the buffered saline to give the various concentrations of LDL and HDL desired.

To measure cholesterol, an Abbott CCX or a Boehringer Mannheim Reflotron was employed. The LDL and VLDL cholesterol was precipitated and the HDL cholesterol was measured in the supernatant. Several methods of precipitation are known and the most common methods employ either phosphotungstic acid or dextran sulfate with Mg.sup.++. Four different phosphotungstic acid reagents were obtained from Sigma, Baxter, Beckman, and DuPont. Each reagent is slightly different in composition. In addition, three different dextran sulfate reagents were obtained from Sigma, Abbott, and DMA.

When the various precipitating agents were compared using the lipoprotein preparation of HDL and LDL, very large differences in HDL cholesterol were obtained. The standard deviation for the six reagents was 15.8. The C.V. was 18 Values as low as 72 mg/dl and as high as 111 mg/dl were found. This is an illustration of the "matrix effect" observed with traditional lipoprotein preparations.

B. Control Composition

A hypothesis was made that lipids tend to coalesce or aggregate in aqueous solutions. To keep them suspended, surfactants or wetting agents were added. The following surfactants were tested: Triton X705 (Sigma), Silwet 7614 (Union Carbide), Diazopon SS837 (GAF Chemicals Corp.), Pluronic F-68 (BASF), Polyethylene Glycol 400-20,000 (Union Carbide), and dioctyl sodium sulfosuccinate (Sigma). These surfactants were found to provide lipoprotein stability, i.e. the cholesterol levels were stable and the HDL and LDL cholesterol values were stable. The values are shown in FIGS. 1-3. The values set forth in FIGS. 1-3 were obtained using 150 mg/dl of dioctyl sodium sulfosuccinate. No significant change occurred over 200 days at 22.degree. C. It is thus clear that a broad range of surfactants will stabilize the lipoprotein values for extended periods of time at room temperature.

The effect of varying the concentration of surfactant was examined by testing different concentrations of surfactant using the same concentration of lipoprotein. The results of this experiment is shown in Table 1 below. As shown in Table 1, as the concentration of Triton X705 is increased, the HDL cholesterol is increased. The higher concentrations of surfactant are thus inhibiting the precipitation of the LDL and VLDL and therefore the surfactants are stabilizing the lipoproteins. However, with surfactant alone, the lipoproteins do not behave in a manner similar to human serum and a severe matrix problem is produced as evidenced by the values in Table 1.

TABLE 1______________________________________Effect of Concentration of SurfactantPrecipitating Measured HDL Cholesterol mg/dlReagent 0.05% X705 0.25% X705 0.50% X705______________________________________Sigma (PTA) 34 76 193Baxter (PTA) 41 103 224Beckman (PTA) 25 44 64DuPont (PTA) 42 103 216Sigma (DEX) 38 47 48Abbott (DEX) 32 46 45DMA (DEX) 36 47 45Mean: 35.5 66.4 119S.D.: 5.76 27.1 86.5C.V.: 16.2% 40.8% 72.6%______________________________________

It was discovered that the addition of a divalent cation such as Mg.sup.++, Ca.sup.++, of Mn.sup.++ will eliminate the matrix problems. In addition, it was discovered that the use of a chelating agent and in particular EDTA, stabilizes the divalent cation and also inhibits oxidation of the lipoprotein. (It is known that Fe.sup.+++ ions in traces will cause oxidation of lipoproteins). The results of a study investigating the effect of divalent cation and EDTA are set forth in Table 2 below. In Table 2, Sample 1 is the control and thus contained no surfactant, no MgCl.sub.2, and no EDTA. Sample 2 contained 0.175 g/dI Triton X705, no MgCl.sub.2 and no EDTA. Sample 3 contained no Triton X705, 8 mM MgCl.sub.2 and 3 mM EDTA. Sample 4 contained 0.175 g/dl Triton X705, 8 mM MgCl.sub.2 and 3 mM EDTA.

TABLE 2______________________________________Effect of Surfactant (Triton X705) and a Divalent Cation (MgCl.sub.2)on the Precipitation of LDLValues HDL Cholesterol mg/dlPrecipitatingAgent Sample 1 Sample 2 Sample 3 Sample 4______________________________________Sigma (PTA) 37 44 18 45DuPont (PTA) 43 94 25 48Abbott (Dex) 35 46 37 47Sigma (Dex) 42 49 40 49Mean: 39.2 58.2 30.0 47.2C.V.: 10.2% 41.6% 34.3% 3.53%______________________________________

The effect of varying the concentration of divalent cation was also investigated. Various concentrations of MgCl.sub.2 were tested and the results are set forth in Tables 3 and 4 below. These data indicate that at 0.175 mg/dl of Triton X705, the optimum Mg.sup.++ is approximately 6 mM. (Table 3: CV=5.6%) These data also indicate that as the concentration of lipoprotein is increased, the level of Mg.sup.++ required decreased. This can be seen in Tables 3, 4A and 4B. As shown in Table 3, at the highest level of lipoprotein, the optimum Mg.sup.++ concentration is 6 mM (HDLC cholesterol=80 mg/dl). As shown in Table 4A, at the intermediate level of lipoprotein, wherein the HDL cholesterol concentration is 48 mg/dl, the optimum concentration is 8 mM Mg.sup.++. As shown in Table 4B, at the lowest level of HDL cholesterol wherein the lipoprotein concentration is 24 mg/dl, the optimum concentration is 20 mM Mg.sup.++.

TABLE 3______________________________________Effect of Divalent Cation ConcentrationValues HDL Cholesterol mg/dlPrecipitating MgCl at MgCl at MgCl atReagent No Mg.sup.++ 6 mM 20 mM 30 mM______________________________________Sigma (PTA) 94 75 40 50Baxter (PTA) 106 81 47 40Beckman (PTA) 73 75 69 17DuPont (PTA) 111 83 54 44Sigma (DEX) 75 82 81 79Abbott (DEX) 76 82 84 83DMA (DEX) 78 87 82 83Mean: 87.6 80.5 65.1 56.6S.D.: 15.8 4.50 18.0 25.5C.V.: 18.0% 5.60% 27.7% 45.2%______________________________________ TABLE 4A______________________________________Intermediate Lipoprotein LevelValues HDL Cholesterol mg/dlPrecipitating MgCl at MgCl at MgCl atReagent No Mg.sup.++ 8 mM 20 mM 30 mM______________________________________Sigma (PTA) 76 45 35 32Baxter (PTA) 103 48 35 30Beckman (PTA) 44 44 41 39DuPont (PTA) 193 49 36 30Sigma (DEX) 47 50 45 41Abbott (DEX) 46 48 48 46DMA (DEX) 47 49 45 43Mean: 66.4 47.4 40.5 37.3S.D.: 27.1 2.21 5.38 6.53C.V.: 40.8% 4.70% 13.3% 17.5%______________________________________ TABLE 4B______________________________________Low Lipoprotein LevelValues HDL Cholesterol mg/dlPrecipitating MgCl at MgCl at MgCl atReagent No Mg.sup.++ 10 mM 20 mM 30 mM______________________________________Sigma (PTA) 103 78 23 24Baxter (PTA) 114 25 23 22Beckman (PTA) 21 24 22 24DuPont (PTA) 123 24 23 22Sigma (DEX) 23 23 25 24Abbott (DEX) 23 24 26 25DMA (DEX) 24 23 25 25Mean: 61.5 31.3 23.8 23.8S.D.: 48.7 20.5 1.35 1.29C.V.: 78.9% 65.3% 5.70% 5.44%______________________________________

The effect of varying the concentration of chelating agent was also examined. In particular, various concentrations of EDTA were tested and the results are set forth in Table 5. It has been found that a higher concentration of surfactant requires more divalent cation. As the level of chelating agent is increased the Mg.sup.++ is less available and the CV rises.

TABLE 5______________________________________Effect of Chelating Agent ConcentrationValues HDL Cholesterol mg/dlPrecipitationReagent No EDTA 3 mM EDTA 12 mM EDTA 15 mM EDTA______________________________________Sigma 39 37 33 22Baxter 38 38 35 23Beckman 39 39 37 25Abbott 41 40 41 41Mean: 39.3 mg/dl 38.5 mg/dl 36.5 mg/dl 27.7 mg/dlS.D.: 1.3 1.4 3.6 8.9C.V.: 3.2% 3.6% 9.8% 32.0%______________________________________

The effect of varying the type of anti-oxidant was also examined. In particular, controls containing no anti-oxidant, sulfasalazine at a concentration of 0.001M, uric acid at a concentration of 10 mg/dl and alpha-tocopherol at a concentration of 5 mg/dl were examined. The results are set forth in Table 5A.

TABLE 5A______________________________________No AntioxidantPercent Change From Initial ConcentrationSample Total HDLC HDLC# Cholesterol (Dextran) (PTA) Trigs Apo A-1 Apo B______________________________________1 -13% -19% -20% -13% -25% -3%2 -14% -20% -21% -16% -23% -3%3 -10% -16% -16% -11% -24% -3%______________________________________ Using the antioxidants described above, all the changes in the analytes described are less than 2% over 6 months stored at 6.degree. C.

When the concentration of surfactant is increased from the level shown as optimum, the lipoproteins are stable but do not precipitate as they should. Therefore, the HDL values are not correct and vary depending on the precipitating agent. However, it is possible to correct for the elevated surfactant by increasing the divalent cation concentration. To illustrate, Triton X705 was increased from 0.175% to 0.350% with the elevated level of lipoprotein (80 mg/dl). Table 6 below shows the results. Instead of the optimum Mg.sup.++ concentration being 6 mM, the optimum is increased to 25 mM when the surfactant level is increased to 0.350%.

TABLE 6______________________________________Requirement for Increased Divalent Cation Concentration with anIncrease in Surfactant ConcentrationValues HDL Cholesterol mg/dlPrecipitating Concentration MgCl.sub.2Reagent No Mg.sup.++ 6 mM 15 mM 25 mM______________________________________Sigma (PTA) 195 115 83 74Baxter (PTA) 211 125 80 78Beckman (PTA) 144 122 105 86Dupont (PTA) 211 136 82 76Sigma (DEX) 79 81 82 81Abbott (DEX) 79 81 80 82DMA (DEX) 80 80 82 77Mean: 143 106 84.8 78.9S.D.: 63.3 24.4 8.93 4.11C.V.: 44.4% 23.1% 10.5% 5.20%______________________________________

Materials and Methods

The following materials and methods were used in carrying out the experiments described herein.

Preparation of LDL cholesterol and triglyceride control. To 0.5 liter H.sub.2 O, add 11.91 g HEPES, 1.11 g EDTA, 0.1 g nalidixic acid, 0.3 g chloramphenicol, 0.4 g methylparaben, 5.0 g sodium chloride, 2.7 g Triton X705 and 20.0 g bovine serum albumin. Components stirred at 22.degree. C. until dissolved. After addition of desired lipoprotein, volume is brought to 1.0 liter with H.sub.2 O.

______________________________________ IntermediateComponent Low Level Level Elevated Level______________________________________.sup.1 Avian Triglyceride 12 ml 16 ml 36 mlConcentrate 4925mg/dl.sup.2 LDL Cholesterol 185 ml 265 ml 365 mlConcentrate 950mg/dl______________________________________ .sup.1 Miles Pentex: Triglyceride Concentrate Triglycerides: 4925 mg/dl Cholesterol: 213 mg/dl .sup.2 LDL Cholesterol Concentrate LDL Cholesterol: 960 mg/dl HDL Cholesterol: <10 mg/dl Triglycerides: 390 mg/dl

Preparation of LDL cholesterol, HDL cholesterol, and triglyceride control. To 0.5 liter H.sub.2 O, add 11.91 HEPES, 1.11 g EDTA, 0.1 g nalidixic acid, 0.3 g chloramphenicol, 0.4 g methylparaben, 5.0 g sodium chloride, 2.7 g Triton X705 and 20.0 g bovine serum albumin. Components stirred at 22.degree. C. until dissolved. After addition of desired lipoprotein, volume is brought to 1.0 liter with H.sub.2 O.

______________________________________ Intermediate ElevatedComponent Low Level Level Level______________________________________MgCl.sub.2 1.90 g 0.76 g 0.57 g.sup.1 Avian Triglyceride 38.8 ml 12.2 ml 17.4 mlConcentrate 4925 mg/dl.sup.2 LDL Cholesterol 164 ml 225 ml 283 mlConcentrate.sup.3 HDL Cholesterol 46.0 ml 88.0 ml 146 mlConcentrate 550 mg/dl______________________________________ .sup.1 Miles Pentex: Triglyceride Concentrate Triglycerides: 4925 mg/dl Cholesterol: 213 mg/dl .sup.2 LDL Cholesterol Concentrate LDL Cholesterol: 960 mg/dl HDL Cholesterol: <10 mg/dl Triglycerides: 390 mg/dl .sup.3 HDL Cholesterol Concentrate HDL Cholesterol: 550 mg/dl LDL Cholesterol: <10 mg/dl Triglycerides: 130 mg/dl

Lipoprotein control prepared from human serum. It will be appreciated that human serum may be used in the composition of the present invention, instead of purified lipoprotein fractions. For example, to 1 liter human serum, add 1.11 g EDTA, 0.1 g nalidixic acid, 0.3 g chloramphenicol, 0.4 g methylparaben, MgCl.sub.2, 10.0 g of PEG-1500 and 0.1 g of uric acid to produce a liter batch. Components are stirred at 22.degree. C. until dissolved. Levels may be adjusted by adding lipoprotein concentrate.

SPECIFIC EXAMPLE 2

STABILITY

Based on the above studies, using the appropriate concentration of lipoprotein, surfactant and divalent cation, liquid lipoprotein controls were prepared and their stability examined. It was found that the control composition of the present invention is stable for up to about 12 months at about 2.degree. C. to about 10.degree. C. and preferably at 6.degree. C. (refrigeration temperature). Moreover, at about 22.degree. C. (approximately room temperature), the control composition of the present invention is stable for up to about 5 months. FIGS. 4, 5 and 6 show the HDL cholesterol, LDL cholesterol and triglyceride stability, respectively, when low, mid and elevated levels of lipoprotein are present in the control. The control composition of the present invention may thus be stored as a liquid without hindering stability.

SPECIFIC EXAMPLE 3

MATRIX EFFECTS

As noted above, lyophilized and frozen lipid controls known in the art have matrix problems. In order to demonstrate this, a study was performed to compare various commercially-available controls with fresh human serum and the control of the present invention. The results of the study are set forth in Tables 7A-7E below. The data illustrates the matrix problems associated with the use of available commercial controls, in contrast to the results with human serum and the control of the present invention. In addition, three samples of human serum were tested with several precipitating agents. As shown, all the reagents perform equally well with human serum (see Table 7A). The C.V. between methods is 3%-4%. The control of the present invention gives a C.V. between methods that is close to normal serum (see Table 7B). The C.V. between methods using Sigma, CIBA-Coming, and Bio-Rad lipid controls illustrate the large matrix values in these prior art controls (see Tables 7C-7E).

TABLE 7A______________________________________Human SerumValues HDL Cholesterol mg/dlPrecipitating Reagent Sample 1 Sample 2 Sample 3______________________________________Sigma (PTA) 22 44 58Baxter (PTA) 22 46 59Beckman (PTA) 23 42 58DuPont (PTA) 23 45 63Sigma (DEX) 25 45 62Abbott (DEX) 24 42 58DMA (DEX) 24 45 60Mean: 23.3 44.2 59.7S.D.: 1.03 1.55 2.10C.V.: 4.42% 3.52% 3.51%______________________________________ TABLE 7B______________________________________Control of InventionValues HDL Cholesterol mg/dlPrecipitatingReagent Level 1 Level 2 Level 3______________________________________Sigma (PTA) 23 45 76Baxter (PTA) 23 48 81Beckman (PTA) 22 44 75DuPont (PTA) 23 49 83Sigma (DEX) 25 50 82Abbott (DEX) 26 48 82DMA (DEX) 25 49 87Mean: 23.8 47.4 80.5S.D.: 1.35 2.21 4.50C.V.: 5.70% 4.70% 5.59%______________________________________ TABLE 7C______________________________________Sigma Control*Values HDL Cholesterol mg/dlPrecipitating Reagent Level 1 Level 2 Level 3______________________________________Sigma (PTA) 23 45 56Baxter (PTA) 23 56 80Beckman (PTA) 24 56 64DuPont(PTA) 23 54 77Sigma (DEX) 25 52 72Abbott (DEX) 18 29 54DMA (DEX) 27 43 67Mean: 23.3 47.8 67.0S.D.: 2.99 9.61 9.85C.V.: 12.8% 20.1% 14.7%______________________________________ *Lyophilized TABLE 7D______________________________________Ciba-Corning ControlValues HDL Cholesterol mg/dlPrecipitating Reagent Level 1 Level 2 Level 3______________________________________Sigma (PTA) 26 33 65Baxter (PTA) 43 56 129Beckman (PTA) 27 37 91DuPont (PTA) 45 55 129Sigma (DEX) 31 46 118Abbott (DEX) 23 33 81DMA (DEX) 25 38 92Mean: 31.4 42.6 100S.D.: 8.91 9.89 25.1C.V.: 28.4% 23.2% 24.9%______________________________________ TABLE 7E______________________________________Bio-Rad ControlValues HDL Cholesterol Mg/dlPrecipitating Reagent Level 1 Level 2______________________________________Sigma (PTA) 17 53Baxter (PTA) 45 58Beckman (PTA) 18 55DuPont (PTA) 39 57Sigma (DEX) 11o 116Abbott (DEX) 22 53DMA (DEX) 59 58Mean: 44.1 64.1S.D.: 32.8 22.9C.V.: 74.3% 35.7%______________________________________

SPECIFIC EXAMPLE 4

PREFERRED PROCEDURE

The following is a detailed description of the preparation of a preferred control composition of the present invention.

A tri-level lipoprotein control is prepared containing clinically significant concentration levels for cholesterol, triglycerides and HDL cholesterol. Table 8 summarizes the constituent concentration of the control.

TABLE 8______________________________________Measured Analytes Level 1 Level 2 Level 3______________________________________Cholesterol (mg/dl) 150-200 230-280 330-380Triglycerides (mg/dl) 120-150 170-200 290-350HDL Cholesterol (mg/dl) 15-25 30-45 55-80______________________________________ Stock Solution: 50 mM HEPES buffer with Nalidixic acid (sodium salt at 10 mg %. 250 mM EDTA disodium in HEPES buffer, (93.06 g/l). 500 mM Magnesium Chloride (MgCl.sub.2) in HEPES buffer, (47.62 g/l). 500 mM Nalidixic Acid (sodium salt) in HEPES buffer, (5.00 g/l). 250 mM chloramphenicol in HEPES buffer, (2.50 g/l) 30.0% BSA, Protease Free 5.0% Sodium Chloride in HEPES buffer, (50.00 g/l). 10% Triton X705 in HEPES buffer. Avian Triglyceride Concentrate (Miles). Human LDL & HDL Cholesterol (Continental Services). 30% Triton X705 in HEPES buffer, (.apprxeq.462.9 g/l).

It should be noted that the control is sensitive to microbial contamination and prolonged exposure to excessive heat (>30.degree. C.). Any microbial contamination or prolonged exposure to high temperatures will compromise the stability of some components.

One liter of each level of control may be made using the stock solutions at the concentrations set forth in Table 9, combined in the order set forth in Table 9.

TABLE 9______________________________________Stock Solution Level 1 Level 2 Level 3Lipid Control 1 Liter 1 Liter 1 Liter______________________________________A. Preferred Lipoprotein ControlVolumes of Stock Solution to Make 1 Liter of ControlMgCl.sub.2 * 40.0 ml 16.0 ml 12.0 mlEDTA Disodium* 12.0 ml 12.0 ml 12.0 mlHEPES Buffer 488. ml 429. ml 325. mlNalidixic Acid 5.55 ml 7.65 ml 10.3 mlChloramphenicol 86.6 ml 74.2 ml 58.1 mlTriton X705 13.8 ml 12.0 ml 10.0 mlSodium Chioride 75.4 ml 67.0 ml 57.0 mlAvian 2.00 ml 2.50 ml 20.0 mlTriglyceridesAlbumin 66.7 ml 66.7 ml 66.7 mlMethylparaben 0.288 g 0.246 g 0.185 gLDL Cholesterol 164. ml 225. ml 283. ml.apprxeq.950.0 mg/dlHDL Cholesterol 46.0 ml 88.0 ml 146. ml.apprxeq.550.0 mg/dlB. Preferred Lipoprotein ControlMgCl.sub.2 1.90 g .75 g .06 gEDTA Disodium 1.00 g 1.00 g 1.00 gHEPES Bufter 11.90 g 11.90 g 11.90 gNalidixic Acid 0.03 g 0.04 g 0.05 gChloramphenicol 0.20 g 0.20 g 0.20 gPEG 1500 at 1% 10.0 g 10.0 g 10.0 gSodium Chioride 3.80 g 3.35 g 2.85 gAvian Triglycerides 0.10 g 0.15 g 1.00 gAlbumin 20.0 g 20.0 g 20.0 gMethylparaben 0.30 g 0.25 g 0.19 gLDL Cholesterol 1.55 g 2.15 g 2.70 g.apprxeq.950.0 mg/dlHDL Cholesterol 0.25 g 0.50 g 0.80 g.apprxeq.555.0 mg/dlUric Acid .10 g .10 g .10 g______________________________________ *Th MgCl.sub.2 and EDTA Disodium are allowed to chelate for 10 minutes.

SPECIFIC EXAMPLE 5

MULTI-ANALYTE CONTROL

As described above, additional constituents such as analytes may be combined with the control composition of the present invention. Thus, a "multi-analyte" or "complete chemistry" control is also within the scope of the present invention. The following is a list of tests which may be performed with a control composition of the present invention containing the appropriate constituents: potassium, BUN, glucose, uric acid, bilirubin, creatinine, sodium, alanine aminotransferase, .gamma.-glutamyltransferase.

Table 10 indicates the various constituents and concentrations employed in a two level control to be used on chemistry analyzers (e.g. analogous to the Boehringer Reflotron, Abbott Vision and Kodak Ektachem).

TABLE 10______________________________________Measured Analyte (Units) Level 1 Level 2______________________________________Cholesterol (mg/dl) 170-190 250-270HDL Cholesterol (mg/dl) 45-52 20-27Triglycerides (mg/dl) 170-200 280-320Bilirubin (mg/dl) 1.10-1.40 4.60-5.20Creatinine (mg/dl) 1.30-1.60 4.90-5.50Glucose (mg/dl) 90.0- 105 40.0-50.0Potassium (mmol/l) 3.0-4.0 7.0-9.0Urea (mg/dl) 27.0-33.0 47.0-55.0Uric Acid (mg/dl) 6.00-7.00 8.00-9.00______________________________________ Stock Solution: 50 mM HEPES buffer with Nalidixic Acid (sodium salt) at 10 mg %. 225 mM EDTA Disodium in HEPES buffer, (83.75 g/l). 500 mM Magnesium Chloride (MgCl.sub.2) in HEPES buffer, (47.60 g/l). 0.50% Nalidixic Acid (sodium salt) in .sub.d H.sub.2 O, (5.00 g/l). 250 mg % Chloramphenicol in HEPES buffer, (2.50 g/l). 1M Potassium Chloride (KCL) in HEPES buffer, (74.55 g/l). 3% Urea (BUN) in HEPES buffer, (30.00 g/l). 0.5% ANS (Bilirubin) in HEPES buffer, (5.00 g/l). 20% Glucose in HEPES buffer, (200.00 g/l). 1.0% Uric Acid in HEPES buffer, (1.00 g/l). 30.0% BSA, Protease Free, (Hematology Grade). 5.0% Sodium Chloride in HEPES buffer, (50.00 g/l). 10% Triton X705 in HEPES buffer. Avian Triglyceride Concentrate (Miles) Human LDL and HDL Cholesterol. (Continental Services) 30% Triton X705 in HEPES buffer, (.apprxeq.462.9 g/l).

One liter of each level of control may be made using the stock solutions as the concentrations set forth in Table 11, combined in the order set forth in Table 11.

TABLE 11______________________________________Multi-Analyte Control With LipoproteinsVolumes of Stock Solution to Add to Make 1 Liter of ControlStock Solution Level 1 Level 2Multi-Analyte 1 Liter 1 Liter______________________________________MgCl.sub.2 * 330.0 ml 30.0 mlEDTA Disodium* 12.0 ml 12.0 mlHEPES Buffer 398. ml 277. mlNalidixic Acid 5.90 ml 7.45 mlChloramphenicol 84.5 ml 75.3 mlKCL (Potassium) 4.50 ml 7.00 mlUrea (BUN) 22.0 ml 40.0 mlANS (Biulirubin) 1.40 ml 7.50 mlGlucose 5.00 ml 2.50 mlCreatinine 1.20 ml 5.60 mlUric Acid 70.0 ml 100. mlTriton X705 13.6 ml 12.4 mlSodium Chloride 57.0 ml 51.0 mlAvian Triglycerides 2.50 ml 15.0 mlAlbumin 66.7 ml 66.7 mlMethylparaben 0.280 g 0.250 gLDL Cholesterol 138. ml 248. mlHDL Cholesteroi 88.0 ml 43.0 ml______________________________________ *The MgCl.sub.2 and EDTA Disodium are allowed to chelate for 10 minutes.

Again it should be noted that the control is sensitive to microbial contamination and excessive heat. Any microbial contamination or prolonged exposure to high temperatures will compromise the stability of some components.

The foregoing discussion discloses and describes merely exemplary embodiments of the present invention. One skilled in the art will readily recognize from such discussion, and from the accompanying drawings and claims, that various changes, modifications and variations can be made therein without departing from the spirit and scope of the invention as defined in the following claims.

All patents and references cited herein are incorporated by reference.

Claims

1. A liquid lipoprotein control composition comprising:

a) a lipoprotein;

b) a surfactant present in an amount directly proportional to the amount of lipoprotein;

c) a divalent cation present in an amount inversely proportional to the amount of lipoprotein; and

d) an anti-oxidant.

2. The composition of claim 1, wherein the lipoprotein is selected from the group consisting of HDL cholesterol, LDL cholesterol and triglyceride.

3. The composition of claim 2, wherein at least a portion of the lipoprotein is from human serum.

4. The composition of claim 1, wherein the divalent cation is selected from the group consisting of Mg.sup.++, Ca.sup.++ and Mn.sup.++.

5. The composition of claim 1, wherein the lipoprotein comprises from about 0.1% to about 1.5% by weight of the composition, the surfactant comprises from about 0.01% to about 0.5% by weight of the composition, the divalent cation comprises from about 0.05% to about 1.0% by weight of the composition, and the anti-oxidant comprises from about 0.001% to about 0.1% by weight of the composition.

6. The composition of claim 1, further comprising a chelating agent.

7. The composition of claim 6, wherein the chelating agent is selected from the group consisting of EDTA, EGTA and sodium citrate.

8. The composition of claim 1, further comprising a compound selected from the group consisting of glucose, bilirubin, potassium, urea, creatinine, sodium, uric acid, alanine aminotransferase and .gamma.-glutamyltransferase.

9. The composition of claim 1, wherein the anti-oxidant is selected from the group consisting of sulfasalazine, uric acid and .alpha.-tocopherol.

10. A method of determining the accuracy of a lipoprotein determination method comprising the steps of:

a) providing a liquid lipoprotein control composition having a known lipoprotein concentration, wherein the composition comprises a lipoprotein, a surfactant present in an amount directly proportional to the amount of lipoprotein, a divalent cation present in an amount inversely proportional to the amount of lipoprotein and an anti-oxidant;

b) determining the lipoprotein concentration of the control composition; and

c) comparing the concentration of lipoprotein obtained in step b) with the known lipoprotein concentration.

11. The method of claim 10, wherein the lipoprotein is selected from the group consisting of HDL cholesterol, LDL cholesterol and triglyceride.

12. The method of claim 11, wherein at least a portion of the lipoprotein is from human serum.

13. The method of claim 10, wherein the divalent cation is selected from the group consisting of Mg.sup.++, Ca.sup.++ and Mn.sup.++.

14. The method of claim 10, wherein the lipoprotein comprises from about 0.1% to about 1.5% by weight of the composition, the surfactant comprises from about 0.01% to about 0.5% by weight of the composition, the divalent cation comprises from about 0.05% to about 1.0% by weight of the composition, and the anti-oxidant comprises from about 0.001% to about 0.1% by weight of the composition.

15. The method of claim 10, wherein the anti-oxidant is selected from the group consisting of sulfasalazine, uric acid and .alpha.-tocopherol.

16. A liquid lipoprotein control composition comprising:

a) HDL cholesterol;

b) LDL cholesterol;

c) a surfactant present in an amount directly proportional to the amount of HDL cholesterol and the amount of LDL cholesterol;

d) a divalent cation present in an amount inversely proportional to the amount of HDL cholesterol and the amount of LDL cholesterol;

e) up to about 12 mmol chelating agent, and

f) an anti-oxidant,

wherein the control is stable for up to about twelve months at about 2.degree. C. to about 10.degree. C.

17. The control of claim 16, wherein the divalent cation is selected from the group consisting of Mg.sup.++, Ca.sup.++ and Mn.sup.++.

18. The control of claim 16, wherein the chelating agent is selected from the group consisting of EDTA, EGTA and sodium citrate.

19. The control of claim 16, further comprising a compound selected from the group consisting of glucose, bilirubin, potassium, urea, creatinine, sodium, uric acid, alanine aminotransferase and .gamma.-glutamyltransferase.

20. The control of claim 16, wherein the anti-oxidant is selected from the group consisting of sulfasalazine, uric acid and .alpha.-tocopherol.

21. The control of claim 16, wherein a portion of the HDL cholesterol is from human serum.

22. The control of claim 16, wherein a portion of the LDL cholesterol is from human serum.