Daleva L, Ognianova V
Eksp Med Morfol. 1978;17(4):231-4.
Tempidone is original Bulgarian preparation, synthetized in NIHFI (Zelayskov Bikova). The plasma level of the preparation is determined after single oral administration in doses of 60 and 120 mg and for a period of five days in a dose of 20 mg three times daily per a person. It is shown that tempidone is quickly resorbed and is excreted unchanged mainly in urine. The preparation does not cumulate. The content of tempidone in plasma is determined by the method of thin-layer chromatography, but in urine-spectrophotometricaly.
坦匹酮是保加利亚原装制剂,由国立卫生和制药工业研究所(泽莱斯科夫·比科娃)合成。在单次口服60毫克和120毫克剂量后,以及每人每天三次、每次20毫克、持续五天的剂量下,测定该制剂的血浆水平。结果表明,坦匹酮吸收迅速,主要以原形经尿液排泄。该制剂不会蓄积。血浆中坦匹酮的含量通过薄层色谱法测定,而尿液中的含量则通过分光光度法测定。