Detection of nicotine metabolites
The present invention relates to assays for detection of nicotine metabolites, in particular cotinine, in fluid samples and uses of these assays in quantification of smoking habits. The assays comprise contacting a body fluid sample with a cyanogen halide and a pyrazolone compound and detecting a change in light absorbance of the pyrazolone compound which is associated with the presence of nicotine metabolites. Also provided are assay kits including a cyanogen halide or cyanogen halide-precursor(s) and a pyrazolone compound.
1. A method of detecting or measuring a nicotine metabolite in a sample comprising contacting the sample with a cyanogen halide and a pyrazolone compound and detecting a change in light absorbance of the pyrazolone compound; wherein the pyrazolone compound is a compound according to formula I
in which:
R 1 is —C(═O)—;
R 2 is —CH 2 —;
R 3 is —C(R 6 )—;
R 5 is phenyl substituted with —S(═O) 2 OH;
R 6 is C 1-6 alkyl;
z is a single bond and a is 1; and
y is a double bond and b is 0.
2. A method according to claim 1 , wherein the pyrazolone compound has formula III
3. A method according to claim 1 , wherein the pyrazolone compound is 1-(4-sulfophenyl)-3-methyl-5-pyrazolone (SPMP).
4. A method according to claim 1 , wherein the cyanogen halide is cyanogen chloride.
5. A method according to claim 1 , wherein the change in light absorbance is quantitatively correlated to the level of nicotine metabolite in the sample.
6. A kit for detection or measurement of a nicotine metabolite in a sample, the kit comprising:
a cyanogen halide or cyanogen halide-precursor(s);
and
a pyrazolone compound as defined in claim 1 .
7. A kit according to claim 6 , comprising reagents KCN, chloramine-T and SPMP.
8. A kit according to claim 7 , wherein the reagents of KCN, chloramine-T and SPMP are present in a KCN:chloramine-T:SPMP ratio of about 1:1:0.2 w/w.