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Sensitive spectrophotometric method for determining methadone in biological specimens

Identifieur interne : 003B23 ( Main/Exploration ); précédent : 003B22; suivant : 003B24

Sensitive spectrophotometric method for determining methadone in biological specimens

Auteurs : Jack E. Wallace [États-Unis] ; Horace E. Hamilto [États-Unis] ; James T. Payte [États-Unis] ; Kenneth Blum [États-Unis]

Source :

RBID : ISTEX:C496276015EF6B94665A7D53CF8BD6ADD9E030A3

English descriptors

Abstract

The extensive use of methadone for the treatment of opiate addiction increases significantly the need for quantitative determination of methadone in urine and tissues. Existing spectrophotometric methods are limited in sensitivity by the low molar absorptivity of this compound(λ = 554 in 0.1 N HCI, ∈ = 292 nm.). Results demonstrate that a markedly enhanced sensitivity may be achieved by oxidizing the methadone to benzophenone (λ = 18,713 in n‐heptane, ∈ = 247 nm.). Methadone is extracted into n‐hexane at an alkaline pH and then back‐extracted into dilute sulfuric acid. Refluxing the acid solution with barium peroxide and n‐heptane oxidizes the methadone to benzophenone, which is immediately extracted into the heptane. The heptane layer is removed and washed, and the benzophenone is measured spectrophotometrically. The method is sufficiently sensitive to quantitate therapeutic levels of methadone in small volumes of urine.

Url:
DOI: 10.1002/jps.2600610911


Affiliations:


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Le document en format XML

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<term>Absorbance</term>
<term>Alkaline permanganate oxidation</term>
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<term>Barium</term>
<term>Barium acid</term>
<term>Barium acid oxidation</term>
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<term>Benzophenone</term>
<term>Biological specimens</term>
<term>Blank absorbance</term>
<term>Chemical pharmacology</term>
<term>Drug dependence</term>
<term>Extraction efficiency</term>
<term>Heating mantles</term>
<term>Heptane</term>
<term>Hexane</term>
<term>Kier</term>
<term>Methadone</term>
<term>Methadone concentration</term>
<term>Methadone hydrochloride</term>
<term>Methadone oxidation product</term>
<term>Molar absorptivity</term>
<term>National academy</term>
<term>Optimum conditions</term>
<term>Oxidation product</term>
<term>Peroxide</term>
<term>Physiological salt solution</term>
<term>Preliminary extraction</term>
<term>Quantitative determination</term>
<term>Reflux</term>
<term>Research council</term>
<term>Sodium hydroxide</term>
<term>Spectrophotometric methods</term>
<term>Sulfuric</term>
<term>Sulfuric acid</term>
<term>Unchanged methadone</term>
<term>Urine</term>
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<div type="abstract" xml:lang="en">The extensive use of methadone for the treatment of opiate addiction increases significantly the need for quantitative determination of methadone in urine and tissues. Existing spectrophotometric methods are limited in sensitivity by the low molar absorptivity of this compound(λ = 554 in 0.1 N HCI, ∈ = 292 nm.). Results demonstrate that a markedly enhanced sensitivity may be achieved by oxidizing the methadone to benzophenone (λ = 18,713 in n‐heptane, ∈ = 247 nm.). Methadone is extracted into n‐hexane at an alkaline pH and then back‐extracted into dilute sulfuric acid. Refluxing the acid solution with barium peroxide and n‐heptane oxidizes the methadone to benzophenone, which is immediately extracted into the heptane. The heptane layer is removed and washed, and the benzophenone is measured spectrophotometrically. The method is sufficiently sensitive to quantitate therapeutic levels of methadone in small volumes of urine.</div>
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