Claims Analysis
Total Claims: 24
Claim 1
Independent Claim
94 words
A STABLE, LIQUID BIOLOGICAL REFERENCE CONTROL COMPOSITION FOR USE IN ANALYSIS OF BIOLOGICALLY SIMILAR UNKNOWNS, SAID COMPOSITION BEING STABLE AT -20*C. AND CAPABLE OF EXTENDED STORAGE IN THE LIQUID STATE AT SAID TEMPERATURE AND COMPRISING IN ITS NON-BIOLOGICAL COMPONENT FROM ABOUT 60 TO ABOUT 80 WEIGHT PER CENT WATER, FROM ABOUT 20 TO ABOUT 40 WEIGHT PER CENT OF AT LEAST ONE ALKYLENE POLYOL HAVING FROM 2 TO 5 CARBON ATOMS, THE REMAINDER BEING CHIEFLY AT LEAST ONE NATURAL BIOLOGICAL MATERIAL SELECTED FROM THE GROUP CONSISTING OF BLOOD SERUM, ENZYME, METABOLITES, ELECTROLYTES AND HORMONES.
Claim 2
Dependent Claim
94 words
A STABLE, LIQUID BIOLOGICAL REFERENCE CONTROL COMPOSITION FOR USE IN ANALYSIS OF BIOLOGICALLY SIMILAR UNKNOWNS, SAID COMPOSITION BEING STABLE AT -20*C. AND CAPABLE OF EXTENDED STORAGE IN THE LIQUID STATE AT SAID TEMPERATURE AND COMPRISING IN ITS NON-BIOLOGICAL COMPONENT FROM ABOUT 60 TO ABOUT 80 WEIGHT PER CENT WATER, FROM ABOUT 20 TO ABOUT 40 WEIGHT PER CENT OF AT LEAST ONE ALKYLENE POLYOL HAVING FROM 2 TO 5 CARBON ATOMS, THE REMAINDER BEING CHIEFLY AT LEAST ONE NATURAL BIOLOGICAL MATERIAL SELECTED FROM THE GROUP CONSISTING OF BLOOD SERUM, ENZYME, METABOLITES, ELECTROLYTES AND HORMONES.
Claim 3
Dependent Claim
14 words
A composition as in claim 1 wherein said biological material is human blood serum.
Claim 4
Dependent Claim
13 words
A composition as in claim 1 wherein said alkylene polyol is ethylene glycol.
Claim 5
Dependent Claim
13 words
A composition as in claim 1 wherein said alkylene polyol is propylene glycol.
Claim 6
Dependent Claim
13 words
A composition as in claim 1 wherein said alkylene polyol is butylene glycol.
Claim 7
Dependent Claim
12 words
A composition as in claim 1 wherein said alkylene polyol is pentanediol.
Claim 8
Dependent Claim
12 words
A composition as in claim 1 wherein said alkylene polyol is glycerol.
Claim 9
Dependent Claim
135 words
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 -20.degree.C. and capable of extended storage in the liquid stage 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 20 to about 40 per cent water therefrom, D. adding at least one alkylene polyol containing from about 2 to about 5 carbon atoms thereto in a concentration substantially the same as the removed water, E. mixing the components thereof, and F. reducing the freezing temperature thereof to from about 0.degree.C. to about -20.degree.C.
Claim 10
Dependent Claim
135 words
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 -20.degree.C. and capable of extended storage in the liquid stage 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 20 to about 40 per cent water therefrom, D. adding at least one alkylene polyol containing from about 2 to about 5 carbon atoms thereto in a concentration substantially the same as the removed water, E. mixing the components thereof, and F. reducing the freezing temperature thereof to from about 0.degree.C. to about -20.degree.C.
Claim 11
Dependent Claim
21 words
A process as in claim 8 wherein the temperature thereof is reduced in step (F) to a temperature of about -20.degree.C.
Claim 12
Dependent Claim
22 words
A process as in claim 8 wherein from about 25 to about 35 weight per cent water is removed in step (C).
Claim 13
Dependent Claim
13 words
A process as in claim 8 wherein said alkylene polyol is ethylene glycol.
Claim 14
Dependent Claim
13 words
A process as in claim 8 wherein said alkylene polyol is propylene glycol.
Claim 15
Dependent Claim
12 words
A process as in claim 8 wherein said alkylene polyol is glycerol.
Claim 16
Dependent Claim
13 words
A process as in claim 8 wherein said alkylene polyol is butylene glycol.
Claim 17
Dependent Claim
13 words
A process as in claim 8 wherein said alkylene polyol is pentane diol.
Claim 18
Dependent Claim
15 words
A process as in claim 8 wherein said biologically similar material is human blood serum.
Claim 19
Dependent Claim
33 words
A process as in claim 8 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.
Claim 20
Dependent Claim
20 words
A process as in claim 17 wherein said reduced pressure ranges from about 5 to about 10 millimeters of mercury.
Claim 21
Dependent Claim
45 words
A process as in claim 8 wherein removal of water is conducted by slowly and gradually raising the temperature of said frozen biologically similar material from a temperature of about -20.degree. to about 0.degree.C. over a period ranging from about 10 to about 30 hours.
Claim 22
Dependent Claim
24 words
A process as in claim 19 wherein said temperature is aobut 0.degree.C. and said time period ranges from about 10 to about 24 hours.
Claim 23
Dependent Claim
63 words
IN A PROCESS FOR PERFORMING AUTOMATED CONTINUOUS FLOW MULTICHANNEL ANALYSES OF UNKNOWN BIOLOGICALLY ACTIVE NATURALLY OCCURRING MATERIALS, THE IMPROVEMENT WHICH COMPRISES EMPLOYING THE STABLE LIQUID COMPOSITION OF CLAIM 1 AS A REFERENCE CONTROL IN STANDARDIZING THE AUTOMATED ANALYZER AND THEREAFTER CONDUCTING CONTINUOUS FLOW MULTICHANNEL ANALYSES UTILIZING SAID REFERENCE CONTROL COMPOSITION WHEREIN SAID REFERENCE CONTROL COMPOSITION CONTAINS THE SAME COMPONENT MATERIALS AS SAID UNKNOWNS.
Claim 24
Dependent Claim
60 words
In a process for performing automated continuous flow multichannel analysis on unknown biologically active human blood serum, the improvement which comprises employing the stable liquid composition of claim 2 as a reference control in standardizing the automated analyzer and thereafter conducting continuous flow multichannel analyses on human blood serum unknowns containing the same component materials as said reference control composition.