Method of determining consumption of decayed drug through drug taggants
We disclose a method of using taggants to assess how and to what extent a drug in a drug composition that a user has consumed has decayed in response to storage conditions and time. The taggants may decay in response to environmental conditions which cause different drugs to lose their efficacy. These environmental conditions may include light, temperature, oxidation, and age. The taggants may be detected in biological samples, including urine and feces. By identifying the taggants, the drug composition and other information relating to the drug may be identified. Additionally, quantification of the different taggants may be used to determine whether the drug in the drug composition has been exposed to environmental conditions which may reduce its efficacy.
1. A method of tagging a drug composition to detect decay of an active ingredient in the drug composition comprising the steps of:
a. providing a drug composition, the drug composition comprising a drug;
b. providing a first taggant, wherein the first taggant is photosensitive;
c. providing a second taggant, wherein the second taggant is heat sensitive and resistant to light; and
d. adding the first taggant and the second taggant to the drug composition, wherein both the first taggant and the second taggant are detectable in a biological sample after consumption; and wherein the first taggant and the second taggant are independently selected from the following: polyethylene glycol, copovidone, povidone, propylparaben, methyl paraben, steviol glucuronide, sucralose, oleic acid, trans-anethole, 1,8-eucalyptol, limonene-2D, riboflavin, and tartaric acid, and salts of tartaric acid.
2. The method of claim 1 , wherein the first taggant and the second taggant are added in a defined ratio.
3. The method of claim 2 , wherein the defined ratio is indicative of one of the following: drug composition manufacturer, drug, drug composition, manufacturing batch, dispensing pharmacy, prescribing healthcare provider, healthcare provider's institution, and prescribed user.
4. The method of claim 1 , wherein either the first taggant, the second taggant, or both the first and second taggant consist of polyethylene glycol, and wherein the polyethylene glycol comprises polymers of one or more of the following average molecular weights: 400, 600, 1000, 1500, and 2000.
5. The method of claim 1 , wherein either the first taggant, the second taggant, or both the first and second taggant consist of polyethylene glycol, and wherein the polyethylene glycol comprises polymers with an average molecular weight of between about 400 and about 2000.
6. The method of claim 1 , wherein either the first taggant, the second taggant, or both the first and second taggant consists of povidone molecules, and wherein the povidone molecules consist of one or more of the following number of monomers: 25, 30, and 90.
7. The method of claim 1 , wherein the biological sample comprises one or more of the following: urine, feces, whole blood, serum, plasma, cerebrospinal fluid, ascites, mucous, gastric gavage, saliva, and breast milk.
8. The method of claim 1 , wherein the first taggant and the second taggant are detectable in the biological sample using one or more of the following analytical techniques: gas chromatography-mass spectrometry, liquid chromatography, capillary zone electrophoresis with UV absorbance, high performance liquid chromatography with UV absorbance, reverse-phase chromatography, fluorescence spectroscopy, high performance thin layer chromatography, UV spectroscopy, infrared spectroscopy, near IR spectroscopy, mid-IR spectroscopy, visible spectroscopy, nuclear magnetic resonance, ion mobility spectrometry, liquid chromatography-ion mobility spectroscopy, liquid chromatography-electrochemical detection, liquid chromatography-UV spectroscopy with a normal UV photodetector, thin layer chromatography, liquid chromatography, Raman spectroscopy, colorimetric assay, and mass spectrometry.
9. The method of claim 8 , wherein the analytical technique is performed by an instrument connected to a medical toilet.
10. The method of claim 1 , wherein at least one of the first taggant and the second taggant are detectable using a near IR absorption spectroscopy technique and at least one excitation wavelength of between about 1 micron and about 2.5 microns.
11. The method of claim 1 , wherein at least one of the first taggant and the second taggant are detectable using an absorption spectroscopy technique and at least one excitation wavelength of between about 250 nm and about 800 nm.
12. The method of claim 1 , wherein the first taggant has a first decay characteristic and the second taggant has a second decay characteristic which are independently selected from the following: decay due to light sensitivity, decay due to temperature sensitivity, and decay due to chemical degradation over time.
13. The method of claim 1 , wherein a concentration of the first taggant, a concentration of the second taggant, or the concentration of both the first and the second taggant is approximately the same as a concentration of the drug.
14. The method of claim 12 , wherein the first decay characteristic, the second decay characteristic, or both the first and the second decay characteristics are approximately the same as a decay characteristic of the drug.
15. The method of claim 14 , which further includes a third taggant, wherein the third taggant is stable in response to light, extreme temperature, oxygen exposure, and time relative to the first and second taggants.
16. The method of claim 15 , wherein the third taggant is cleared by the same biological system as the drug.
17. The method of claim 15 , providing each of the first taggant, second taggant, and third taggant with a distinct visual color or combination of visual colors corresponding to their respective decay characteristics.