Dose‐dependent pharmacokinetics of enprofylline and its renal handling in rats

Masayuki Nadai, Takaaki Hasegawa, Isao Muraoka, Kenzo Takagi, Toshitaka Nabeshima

研究成果: Article査読

14 被引用数 (Scopus)

抄録

The effect of dosage on the pharmacokinetics of the potent bronchodilator enprofylline (3‐propylxanthine; PX) and its renal handling were investigated in rats. Enprofylline (PX) was administered iv in dosages of 2.5, 10, 20, and 40 mg/kg, and PX concentration in plasma and urine was determined by HPLC. The pharmacokinetic parameters were estimated by model‐independent methods. The disappearance of PX from plasma was delayed as dosage was increased. The corresponding pharmacokinetic parameters also showed dose dependency; increases in the volume of distribution (Vd) and mean residence time (MRT) and a decrease in total body clearance (CLT) were observed as dosage was increased from 2.5 to 40 mg/kg. Approximately 80% of the dose, however, was excreted in urine as unchanged PX. Plasma protein binding studies of PX showed concentration dependency and allowed determination of binding parameters, with an apparent dissociation constant (Kd) of 162.50 μM and a binding capacity (nP) of 565.23 μM. Some pharmacokinetic parameters for unbound PX calculated by total plasma concentration and binding parameters also showed dosedependent characteristics. However, no significant change in Vd for unbound PX was observed among administered doses, indicating that the distribution of PX into the body tissues is not changed by an increase in dosage. Renal clearance of unbound PX significantly increased as plasma concentration decreased. The maximum transport capacity (Vmax) and the Michaelis‐Menten constant (Km) for tubular secretion were 60.53 μg/min and 2.27 μg/mL, respectively. The aim of the present study is to demonstrate that both saturable tubular secretion and concentration‐dependent protein binding are responsible for the dose‐dependent pharmacokinetics of PX in rats.

本文言語English
ページ(範囲)648-652
ページ数5
ジャーナルJournal of Pharmaceutical Sciences
80
7
DOI
出版ステータスPublished - 07-1991
外部発表はい

All Science Journal Classification (ASJC) codes

  • 薬科学

フィンガープリント

「Dose‐dependent pharmacokinetics of enprofylline and its renal handling in rats」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル