Method for increasing the sensitivity of assays

Claim 2

In an enzymatic method for the kinetic analysis of biological fluids in which the hydrolysis of a nitrophenol indicator from its respective substrate is effected at or about neutral pH, the improvement comprising: adding to said biological fluid a sensitization effective amount of cyclodextrin so as to effect a hypochromic shift in the wavelength in the unionized homologue of indicator compound thereby increasing the proportion of ionized homologue indicator in said biological fluid; and, measuring the level of ionized indicator in the biological fluid at the absorbance maxima of said ionized indicator.

Claim 3

In an enzymatic method for the kinetic analysis of biological fluids for alkaline phosphatase in which the hydrolysis of a nitrophenol indicator from its respective substrate is effected at a pH which produces the optimum rate of hydrolysis, the improvement comprising: adding to said biological fluid a sensitization effective amount of cyclodextrin so as to effect a shift in the absorbance maxima of the indicator and thereby reduce interference caused by the nitrophenol labeled substrate; and measuring the level of indicator in the biological fluid at the absorbance maxima of said indicator.

Claim 4

In an enzymatic method for the kinetic analysis of biological fluids for alkaline phosphatase in which the hydrolysis of a nitrophenol indicator from its respective substrate is effected at a pH which produces the optimum rate of hydrolysis, the improvement comprising: adding to said biological fluid a sensitization effective amount of cyclodextrin so as to effect a shift in the absorbance maxima of the indicator and thereby reduce interference caused by the nitrophenol labeled substrate; and measuring the level of indicator in the biological fluid at the absorbance maxima of said indicator.

Claim 5

In an enzymatic method for the analysis of biological fluids in which the hydrolysis of a nitrophenol indicator from its respective substrate produces a chromopore which has an absorbance maxima within a range of absorbance of interferring substances also present within said biological fluid, the improvement comprising: adding to said biological fluid a sensitization effective amount of cyclodextrin so as to effect a shift in the absorbance maxima of the indicator and thereby reduce the interference caused by other substances within said fluid having appreciable absorbance within the same range of absorbance of the indicator compound prior to shift of its absorbance maxima by said cyclodextrin; and measuring the level of indicator in the biological fluid at the absorbance maxima of said indicator.

Claim 6

In an enzymatic method for the analysis of biological fluids in which the hydrolysis of a nitrophenol indicator from its respective substrate produces a chromopore which has an absorbance maxima within a range of absorbance of interferring substances also present within said biological fluid, the improvement comprising: adding to said biological fluid a sensitization effective amount of cyclodextrin so as to effect a shift in the absorbance maxima of the indicator and thereby reduce the interference caused by other substances within said fluid having appreciable absorbance within the same range of absorbance of the indicator compound prior to shift of its absorbance maxima by said cyclodextrin; and measuring the level of indicator in the biological fluid at the absorbance maxima of said indicator.

Claim 7

In an enzymatic method for the kinetic analysis of biological fluids for amylase activity in which the enzymatic hydrolysis of a nitrophenol indicator from a nitrophenol oligoglycoside substrate produces a chromophore which can be correlated with the level of amylase activity in said biological fluid, the improvement comprising: adding to said biological fluid a sensitization effective amount of cyclodextrin so as to effect an increase in the proportion of chromophore at the optimum pH for the conduct of such analysis; and measuring the level of chromophore in the biological fluid at the absorbance maxima of said chromophore advantage.

Claim 8

In an enzymatic method for the kinetic analysis of biological fluids for amylase activity in which the enzymatic hydrolysis of a nitrophenol indicator from a nitrophenol oligoglycoside substrate produces a chromophore which can be correlated with the level of amylase activity in said biological fluid, the improvement comprising: adding to said biological fluid a sensitization effective amount of cyclodextrin so as to effect an increase in the proportion of chromophore at the optimum pH for the conduct of such analysis; and measuring the level of chromophore in the biological fluid at the absorbance maxima of said chromophore advantage.

Claim 9

The method of claim 1 wherein the substituted phenol compound is para- or meta-nitrophenol.

Claim 10

The method of claim 1 wherein the enzyme assay is for amylase or alpha-glucosidose in biological fluids.

Claim 11

The method of claim 1 wherein the concentration of cyclodextrin in the reagent is from about 0.1 to about 100 mg/ml.

Claim 12

The method of claim 1 wherein the concentration of cyclodextrin is from about 5 to about 50 mg/ml.

Claim 13

The method of claim 6 wherein the pH of the reagent is about 6.6.

Claim 14

The method of claim 6 wherein the enzyme assay is for the determination of amylase activity and the reagent further comprises: para-nitrophenylmaltoheptaoside as a substrate, and maltase.