Claims Analysis
Total Claims: 14
Claim 1
Independent Claim
159 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 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.
Claim 2
Dependent Claim
159 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 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.
Claim 3
Dependent Claim
13 words
A process as in claim 1 wherein said alkylene polyol is ethylene glycol.
Claim 4
Dependent Claim
13 words
A process as in claim 1 wherein said alkylene polyol is propylene glycol.
Claim 5
Dependent Claim
12 words
A process as in claim 1 wherein said alkylene polyol is glycerol.
Claim 6
Dependent Claim
13 words
A process as in claim 1 wherein said alkylene polyol is butylene glycol.
Claim 7
Dependent Claim
13 words
A process as in claim 1 wherein said alkylene polyol is pentane diol.
Claim 8
Dependent Claim
14 words
A process as in claim 1 wherein said biologically similar material is blood serum.
Claim 9
Dependent Claim
33 words
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.
Claim 10
Dependent Claim
20 words
A process as in claim 8 wherein said reduced pressure ranges from about 5 to about 10 millimeters of mercury.
Claim 11
Dependent Claim
25 words
A process as in claim 1 wherein said reconstituting composition of E. contains from about 20 to about 35 wt. % of said alkylene polyol.
Claim 12
Dependent Claim
13 words
A process as in claim 10 wherein said alkylene polyol is ethylene glycol.
Claim 13
Dependent Claim
57 words
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.
Claim 14
Dependent Claim
57 words
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.