Sood S P, Green V I, Norton Z M
University of Kansas Medical Center, Division of Clinical Pharmacology, Kansas City 66103.
Ther Drug Monit. 1987 Dec;9(4):484-8. doi: 10.1097/00007691-198712000-00021.
A highly specific, sensitive, and rapid microscale method is described for determining furosemide levels in plasma and urine. Monitoring furosemide levels has been recommended in patients with impaired renal function and in premature infants since furosemide has been known to cause ototoxicity. The method described here is simple, easy to run, takes only 7 min per sample, and can be set up for routine monitoring of furosemide by clinical laboratories. The method uses ion-pairing high performance liquid chromatography and detection of furosemide by fluorescence, which gives excellent separation and high sensitivity with minimal sample preparation. The method requires only 25 microliters of plasma or urine and, thus, is suitable for use in newborn intensive care units.
本文描述了一种高度特异、灵敏且快速的微量方法,用于测定血浆和尿液中的呋塞米水平。由于已知呋塞米会导致耳毒性,因此建议对肾功能受损患者和早产儿进行呋塞米水平监测。这里描述的方法简单,易于操作,每个样品仅需7分钟,并且临床实验室可以将其设置为呋塞米的常规监测方法。该方法采用离子对高效液相色谱法,并通过荧光检测呋塞米,只需最少的样品前处理就能实现出色的分离和高灵敏度。该方法仅需25微升血浆或尿液,因此适用于新生儿重症监护病房。