Lakings D B, Lizarraga C, Haggerty W J, Williamson M J
J Pharm Sci. 1979 Sep;68(9):1113-6. doi: 10.1002/jps.2600680914.
A previously reported high-performance liquid chromatographic (HPLC) method for indoprofen determination in physiological fluids was modified and extended to provide quantitative data on drug concentrations in human milk samples at a low nanogram per milliliter level. The reversed-phase HPLC technique was modified to give a better separation of the drug and milk components. To achieve the necessary cleanup for low level determination, the milk samples required protein precipitation, liquid-liquid drug extraction, and concentration. Excellent indoprofen recovery was obtained with this technique; the average recovery from 20 milk samples spiked with various nanogram drug levels was 95%. The analytical technique showed excellent reproducibility; the calibration solutions over 15 days had a relative standard deviation of 3.2%. Results for indoprofen levels in milk and plasma samples from seven subjects who received either a single or multiple oral drug dose are presented.
一种先前报道的用于测定生理体液中吲哚美辛的高效液相色谱(HPLC)方法经过改进和扩展,以提供人乳样品中低纳克每毫升水平药物浓度的定量数据。反相HPLC技术经过改进,以更好地分离药物和乳汁成分。为实现低水平测定所需的净化,乳样需要进行蛋白质沉淀、液-液药物萃取和浓缩。采用该技术可获得出色的吲哚美辛回收率;在20个添加了不同纳克药物水平的乳样中的平均回收率为95%。该分析技术显示出出色的重现性;15天内校准溶液的相对标准偏差为3.2%。给出了7名接受单次或多次口服药物剂量的受试者的乳汁和血浆样品中吲哚美辛水平的结果。