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Biomedical subjects

M Emanuel

Publications and source records attributed to M Emanuel.

13 recordsLinked to original sources

Dose proportionality study of loperamide following oral administration of loperamide oxide.

The pharmacokinetics of loperamide, after oral administration of increasing doses (1 to 16 mg) of loperamide oxide, has been investigated in 10 healthy male volunteers, using a randomised cross-over design. Comparison of the maximum plasma loperamide concentration and AUC demonstrated that the bioavailability of loperamide was proportional to the dose of loperamide oxide administered.

Administration, Oral

On treating AIDS.

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Acquired Immunodeficiency Syndrome

A double-blind placebo controlled dose response study of noberastine on histamine induced weal and flare.

The antihistaminic effects of 7 days treatment with each of three doses of noberastine (10, 20 and 30 mg) were compared to placebo in 12 healthy male volunteers. The antihistaminic activity was assessed from the inhibition of weal and flare formation after intradermal histamine injections. For both weal and flare there was a highly significant effect of treatment with each of the three doses of noberastine, compared to placebo. The 30 mg daily dose produced the maximum inhibition of weal and flare. The daily mean values for the assessment of sedation by visual analogue scales at 09.00 h, 15.00 h and 21.00 h showed no significant treatment, or order, effect for any of the three doses of noberastine compared to placebo. The mean steady-state plasma concentrations of noberastine were significantly higher with increasing daily doses of noberastine (trough concentrations: 1.0, 1.6 and 2.2 ng.ml-1; peak concentrations: 3.5, 13.4 and 20.9 ng.ml-1 for 10, 20 and 30 mg daily dose, respectively). The percentage weal inhibition correlated (r = 0.77) with steady-state noberastine plasma trough levels. The percentage flare inhibition showed a weaker correlation (r = 0.35) with steady-state noberastine plasma trough levels.

Adult

A fragile X suppressor in the normal human blood?

Eberle et al. (1981, 1982a) reported diminished proportion of fragile X chromosomes in co-cultures of blood cells taken from fra(X) patients with normal blood cells. However, we did not observe any suppression of fra(X) in the blood of fra(X)-positive patients after co-cultivation with blood of fra(X)-negative subjects. Neither was any suppression caused by medium where fra(X)-negative cells had been previously cultivated for two days.

Cells, Cultured