Method of determining the nicotine content of tobacco

• US 4,783,418 A
• Filed: 01/13/1987
• Issued: 11/08/1988
• Est. Priority Date: 01/13/1986
• Status: Expired due to Fees

• Current Assignee: Imperial Tobacco Limited (Imperial Tobacco Group PLC)
• Original Assignee: Imperial Tobacco Limited (Imperial Tobacco Group PLC)
• Inventors: Johnson, Joseph C., Naylor, Maurice, Long, Terence M.
• Primary Examiner(s): Marcus, Michael S.
• Assistant Examiner(s): McMahon, Timothy M.
• Application Number:
  US07/002,931
• Time in Patent Office: 665 Days
• Field of Search: 436/96, 131/297
• US Class Current: 436/96
• CPC Class Codes: G01N 31/00 Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
• CPC Class Codes: G01N 31/22 using chemical indicators G01N31/02 takes precedence
• CPC Class Codes: Y10T 436/145555 Hetero-N

Abstract

A method of determining on a discrete analyzer the nicotine content of tobacco or a smoking-related product by preparing an aqueous extract of a sample of tobacco or smoking-related product, pre-reacting the extract with an acidic buffered solution of pH not more than 6 for at least two minutes, reacting the pre-reacted extract in the discrete analyzer with aniline and cyanogen bromide, measuring the intensity of yellow coloration generated, and comparing said intensity with that produced by a nicotine standard to determine the nicotine content of said sample.

Claims

1. A method of determining on a discrete analyzer the nicotine content of tobacco or a smoking-related product wherein the discrete analyzer includes a container for cyanogen bromide made of a polymeric material, the method including a prior step of passivating the container to cyanogen bromide by allowing a cyanogen bromide solution of high concentration to contact the interior of the container for a period of at least 24 hours before the first use of the container in the method, and including the further steps of,

(a) preparing a first aqueous extract of a sample of tobacco or smoking-related product,

(b) pre-reacting the extract with an acidic buffered solution of pH not more than 6 for at least two minutes,

(c) reacting the pre-reacted extract in the discrete analyzer with aniline and with cyanogen bromide from the passivated container,

(d) measuring the intensity of yellow coloration generated by step (c) and generating a first signal proportional to said intensity of coloration of said sample extract,

(e) preparing a second aqueous extract of a nicotine standard of known nicotine content,

(f) carrying out steps (b) and (c) on the extract of step (e),

(g) measuring the intensity of yellow coloration produced by step (c) during the performance of step (f) and generating a second signal proportional to said intensity of said standard extract, and

(h) comparing said first and second signals to determine the nicotine content of said sample.

2. The method as claimed in claim 1 wherein, when the sample is tobacco, the acidic buffered solution is based on citric acid.

3. The method as claimed in claim 1 wherein the nicotine standard is nicotine hydrogen tartrate.

4. The method as claimed in claim 1 wherein the intensity of the yellow coloration is measured spectrophotometrically at a wavelength of 460 nm.

5. The method as claimed in claim 1 wherein the first aqueous extract is prepared by acid extraction of said tobacco or smoking-related product.

6. The method as claimed in claim 5 wherein said acid of the first aqueous extraction step comprises is 1% v/v solution of acetic acid in water.

7. The method as claimed in claim 1 wherein, when the sample is a smoking-related product other than tobacco, the acidity of the acidic buffered solution is not more than 4 pH and the time taken for the pre-reaction is at least four minutes.

8. The method as claimed in claim 7 wherein the acid buffered solution comprises hydrochloric acid.