Scienti!& Publishing Company, Amsterdti - printed in The N&e&u&
a wsevier
CHROM. 11,456 .’
_..
Note
:
.. ~..
%
.. .
.>L ._
_._..z _.___-:
.
“_‘.;[ :_ ::-
-.._. ..: _. . ..-.__.
. . _.y:_.-
: ; : 1:-;
Quantitative gas-liquid chromatagraphic methyi-nnilproxen SUK HAN WAN
and their
and SHAKEI
conjugates~in
analFir_
of
wine
~~aprcm&
;b_des_ .
I
,-
B. MATIN
; _ ; .: -_: i_ -.
llie School of Pkamracy, Universityof So&rem .Califomia:Los Angeles, Wifonka and tixe.Depw&ent ‘.,z:,; of De Me&o&m, Sytttex Research, Pdo. Alto, Calif. ( ff_S& .
(Receii
August gth,
1978)
“.:.
Naproxen [(+)-6-methoxy-a-methyl-2-naphthaleneacetic ,acidl _.& a-ne& ‘&n-~ steroidal, anti-inflammatory agent &at also has antipyretic and analgesic &.$&. Xi is well-absorbed orally and has an elimination haif-lifeofabout 14 h. IIXma_n;5%@0~~ of an orally administered dose of naproxen can be recovered in tine in-;&e form of naproxen, QO-desmethyi-naproxen and their giucuronide conjugate+3. A g&-Ii&&i chromatographic (GLC) technique has been reported for the analysis of naproxen in plasma in which methylation of the carboxylic a,cid group wit@ &,azo&&an~~ is achieved prior to chromatogr&phy 2*4_This method & not appti@&z. to .&&en ,.i analysis in urine bec+se of presence of m-&G +etabolites. _. Severai reports have described the successful application dfGJ.$ in&t; a&&& of barbituric acids, diphenylhydantoin, purines, p$imidi&s and u&ii ‘IBY