Process for preparing biological compositions for use as reference controls in diagnostic analyses

• US 4,121,905 A
• Filed: 08/22/1977
• Issued: 10/24/1978
• Est. Priority Date: 08/22/1977
• Status: Expired due to Term

• Current Assignee: Jonas Maurukas
• Original Assignee: Jonas Maurukas
• Inventors: Maurukas, Jonas
• Primary Examiner(s): Serwin, R.E.
• Application Number:
  US05/826,973
• Time in Patent Office: 428 Days
• Field of Search: 23/230 B, 23/230 R, 252/408
• US Class Current: 436/16
• CPC Class Codes: G01N 2496/05 containing blood cells or plasma
• CPC Class Codes: G01N 2496/80 Multi-analyte reference solutions containing cholesterol, glucose and the like
• CPC Class Codes: G01N 33/96 involving blood or serum control standard
• CPC Class Codes: Y10T 436/103332 Bilirubin or uric acid standard or control
• CPC Class Codes: Y10T 436/104165 Lipid, cholesterol, or triglyceride standard or control
• CPC Class Codes: Y10T 436/104998 Glucose, ketone, nitrate standard or control
• CPC Class Codes: Y10T 436/105831 Protein or peptide standard or control [e.g., hemoglobin, etc.]
• CPC Class Codes: Y10T 436/106664 Blood serum or blood plasma standard or control
• CPC Class Codes: Y10T 436/108331 Preservative, buffer, anticoagulant or diluent
• CPC Class Codes: Y10T 436/109163 Inorganic standards or controls

Abstract

The present disclosure is directed to the preparation of stable aqueous-containing biological compositions capable of use as liquid reference serums in diagnostic chemical analysis using multichannel automated analyzers and having improved storage stability and capable of storage in the liquid state for extended periods of time measured in weeks when stored at 2° to 8° C.; processes for preparing the reference serums and the process of automated analysis utilizing the improved reference serums. The subject materials are prepared by freezing the aqueous-containing labile biologicals rapidly at temperatures ranging from about -20° to about -30° C., removing from about 98 to 99 weight percent of the water therefrom and storing same (as a dehydrated solid) at 2° to 8° C. until desired use. The dehydrated material is then reconstituted by dissolving it in a medium containing from about 20 to about 50 wt. % of an alkylene polyol containing from 2 to 5 carbon atoms with the remainder being water. The thus reconstituted biological compositions can be stored in the liquid state at 2° to 8° C. for periods of 4 to 5 weeks or at -20° C. for months.

Claims

1. A process for preparing stable, liquid, biological reference control compositions for use in analysis of naturally occurring biologically similar unknowns, said compositions being stable at temperatures of about 8°

to -20°

C. and capable of extended storage in the liquid state at said temperature, comprising

A. obtaining a portion of biological materials similar in composition to and containing the same component materials as the unknown to be analyzed;

B. freezing said biological material over a period of about 10 to about 24 hours;

C. removing from about 98 to about 99 weight percent water therefrom to obtain dehydrated solid;

D. storing said dehydrated solid until it is to be used in analysis; and

E. reconstituting said freeze-dried dehydrated solid with an aqueous composition containing from about 20 to about 50 wt. % of at least one alkylene polyol containing from about 2 to about 5 carbon atoms in a concentration substantially equal to the water removed therefrom in C.

2. A process as in claim 1 wherein said alkylene polyol is ethylene glycol.

3. A process as in claim 1 wherein said alkylene polyol is propylene glycol.

4. A process as in claim 1 wherein said alkylene polyol is glycerol.

5. A process as in claim 1 wherein said alkylene polyol is butylene glycol.

6. A process as in claim 1 wherein said alkylene polyol is pentane diol.

7. A process as in claim 1 wherein said biologically similar material is blood serum.

8. A process as in claim 1 wherein the removal of water is conducted while said biologically similar material is frozen at reduced pressures ranging from about 1 to about 10 millimeters of mercury.

9. A process as in claim 8 wherein said reduced pressure ranges from about 5 to about 10 millimeters of mercury.

10. A process as in claim 1 wherein said reconstituting composition of E. contains from about 20 to about 35 wt. % of said alkylene polyol.

11. A process as in claim 10 wherein said alkylene polyol is ethylene glycol.

12. In a process for performing analyses on unknown biologically active naturally occurring materials, the improvement which comprises employing the stable, liquid, reconstituted composition of claim 1 as a reference control for comparison as a standard conducting the colorimetric analyses utilizing said reference control composition wherein said reference control composition contains the same component materials as said unknowns.

13. In a process for performing automated multichannel analysis on unknown biologically active human blood serum, the improvement which comprises employing the stable, liquid, reconstituted composition of claim 2 as a reference control in standardizing the automated analyzer and thereafter conducting multichannel analyses on human blood serum unknowns containing the same component materials as said reference control composition.