Babiker I E, Cooke P R, Gillett M G
Southmead General Hospital, Westbury-on-Trym, Bristol, England.
J Behav Med. 1989 Feb;12(1):25-38. doi: 10.1007/BF00844747.
A quantitative spectrofluorometer assay of urinary riboflavin is described. Using the method, levels produced by prescribed riboflavin are reliably distinguished from normal background levels without requiring dietary restrictions. The method is successfully used to verify the intake of a single 50-mg dose of riboflavin. However, when more frequent dosage is used, verification becomes unreliable because of a "spillover" effect produced by the slow rate of elimination of the substance. This seriously limits the utility of riboflavin as a tracer, as does its tendency to change the appearance of therapeutic compounds into which it is incorporated. The need for further work on validating combined measures of compliance is stressed.
本文描述了一种用于测定尿中核黄素的定量荧光分光光度计法。使用该方法,无需饮食限制,就能可靠地区分规定剂量核黄素产生的水平与正常背景水平。该方法已成功用于验证单次50毫克核黄素剂量的摄入量。然而,当使用更频繁的给药方式时,由于该物质消除速率缓慢产生的“溢出”效应,验证变得不可靠。这严重限制了核黄素作为示踪剂的效用,其掺入治疗性化合物中时改变其外观的趋势也有同样的限制。强调了进一步开展有效验证依从性综合措施的工作的必要性。