Nikolić M, Petrović D
Vojnomedicinska akademija, Institut za farmaciju, Zavod za preventivnu medicinu.
Vojnosanit Pregl. 1991 Jul-Aug;48(4):325-30.
A fast and sensitive method of high-performance liquid chromatography (HPLC) for determination of acetylsalicylic acid (ASA) and products of salicylic acid (SA) hydrolysis in tablets has been elaborated. Extraction was done with the mixture of methanol: formic acid (98:2 v/v) and separation of the components was achieved by using the colon of Ultropac Lichrosorb RP-18, 10 um, 4 cm x 250 mm and diode array detector. The mobile phase of methanol:water: :mol/1 H3PO4 (60:35:5) v/v, pP = 2.6 and safe flow of 1 ml/min were used. Follow up of chromatographic separation of ASA, SA and internal standard beta-naphtole (ITS) was performed at the wave length of 290 microns. The threshold of ASA was 0.5 mg/ml and of SA 0.0025 mg/ml.
已制定了一种快速灵敏的高效液相色谱法(HPLC),用于测定片剂中的乙酰水杨酸(ASA)和水杨酸(SA)水解产物。用甲醇:甲酸(98:2 v/v)混合物进行萃取,并使用10μm、4cm×250mm的Ultropac Lichrosorb RP - 18柱和二极管阵列检测器实现各组分的分离。使用甲醇:水:0.01mol/1 H3PO4(60:35:5)v/v的流动相,pH = 2.6,流速为1ml/min。在290微米波长下对ASA、SA和内标β-萘酚(ITS)进行色谱分离跟踪。ASA的检测限为0.5mg/ml,SA的检测限为0.0025mg/ml。