Plasma levels, heart rate, and blood pressure after intravenous, oral, and aerosol administration of reproterol in man

Abstract

Three healthy volunteers received single doses of reproterol (D 1959) by means of intravenous infusion, oral and aerosol application, respectively. Administrations were separated by at least 1 week. Plasma levels were measured by means of high performance liquid chromatography. After infusion, plasma levels showed a steep decline, indicative for a rapid distribution. Even though relatively large amounts of drug were given (up to 540 μg), this phenomenon caused reproterol levels to drop to values near or below the limit of reliable quantitation (1 ng ml−1) within 60 to 90 min. After oral administration of one or two tablets (containing 20 mg reproterol. HC1 per tablet), a very short lag time could be observed, indicating fast absorption. After one tablet, plasma level maxima (of plateau‐type) were 5.6 ng ml−1 and 2.3 ng ml−1 in two subjects, respectively. After two tablets, plateau level maxima around 18 ng ml−1 and 9 ng ml−1 were found, respectively. After inhalation of a metered aerosol (two puffs of 500 μg each) the drug appeared in plasma within minutes, albeit at very low levels, and usually remained detectable at the sub‐nanogram level during the time of the experiment (2 h). Due to the very low levels and to some oscillations in the plasma concentration‐time curves, a detailed pharmacokinetic assessment could not be carried out. Effects on heart rate and blood pressure were negligible. Only during the infusion of high doses (540 μg) was there an increase in heart rate of about 50 to 120 beats min−1. Other side‐effects were also negligible.