The use of the autoanalyzer to determine the acetylator phenotype.
نویسندگان
چکیده
It has been pointed out (Rao et al, 1970) that with the advent of intermittent treatment regimens the determination of the acetylator phenotype has become of practical importance. It has recently been shown that rapid acetylators have an inferior response to slow acetylators when their tuberculosis is treated with once weekly treatment regimens (Menon, 1968; Tuberculosis Chemotherapy Centre, Madras, 1970). Sulfamethazine is polymorphically acetylated in man by the same N-acetyl transferase as isoniazid (Evans and White, 1964). The stable storage properties, easy analysis, and speedy availability of results have led to sulfamethazine acetylation being developed as a phenotyping test in preference to isoniazid (Evans and White, 1964; Evans, 1969; Rao et al, 1970). It has been shown that a single small dose of 40 mg sulfamethazine per kg body weight is sufficient (Evans, 1969); and either a single urine specimen (Rao et al, 1970), or alternatively one urine and one serum (or plasma) specimen (Evans, 1969) are required for analysis. The purpose of the present communication is to show that a Technicon AutoAnalyzer can be used to perform the analyses required in the acetylator phenotyping procedure.
منابع مشابه
A simplified and rapid test for acetylator phenotyping by use of the peak height ratio of two urinary caffeine metabolites.
We describe a simplified liquid-chromatographic test in which acetylator phenotype is determined by measuring the peak height ratio of two urinary caffeine metabolites, 5-acetylamino-6-formylamino-3-methyluracil and 1-methylxanthine. We applied this test to determine the acetylator phenotypes of 52 subjects who regularly drink coffee, tea, or caffeinated beverages. Also, we determined the acety...
متن کاملPlasma concentration and acetylator phenotype determine response to oral hydralazine.
The vasodepressor response to single and multiple oral doses of hydralazine, 1 mg/kg, was studied in hypertensive patients. The concentration of hydralazine in plasma was measured both by a newly developed specific and a nonspecific assay similar to those used in previous studies. Acetylator phenotype was determined following oral sulfamethazine. Plasma hydralazine concentration peaked at 1 hou...
متن کاملSurvey of the human acetylator polymorphism in spontaneous disorders.
There is ample evidence that the human acetylator phenotypes are associated with drug induced phenomena. It is principally the slow acetylators who exhibit toxic adverse effects because of their relative inability to detoxify the original drug compounds. In rare instances, however, it is the rapid acetylators who are at a disadvantage. In the matter of association of spontaneous disease with ei...
متن کاملThe association of the slow acetylator phenotype with bladder cancer.
There is an association between exposure to aromatic amines and the development of bladder cancer. Aromatic amines such as are known to occur in tobacco smoke are polymorphically acetylated. One hundred bladder cancer patients have been acetylator phenotyped. Only three of them were non-smokers at the time of diagnosis. This new series, together with four previous series (each with its own cont...
متن کاملPharmacokinetic studies on the drug-related lupus syndrome. Differences in antinuclear antibody development and drug-induced DNA damage in rapid and slow acetylator animal models.
Pharmacogenetic study of an inbred mouse model system derived from A/J (slow acetylator) and C57BL/6J (rapid acetylator) parental strains shows that spontaneous occurrence of antinuclear antibodies is associated with the slow acetylator phenotype although the development of spontaneous and procainamide-induced antinuclear antibodies is a dissociable process. In another study using primary cultu...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of medical genetics
دوره 9 1 شماره
صفحات -
تاریخ انتشار 1972