El-Gindy A, El-Zeany B, Awad T, Shabana M M
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
J Pharm Biomed Anal. 2001 Sep;26(2):211-7. doi: 10.1016/s0731-7085(01)00426-5.
Three methods are described for the determination of trazodone hydrochloride in pharmaceutical tablets. The spectrophotometric method was based on the formation of yellow ion pair complex between the basic nitrogen of the drug and bromophenol blue at pH 3.4. The formed complex was extracted with chloroform and measured at 414 nm. The spectrofluorimetric method was based on measurement of the native fluorescence of the drug in 50% acetic acid upon excitation at a maximum of 320 nm and the emission wavelength is 435 nm. The third method was based on the high performance liquid chromatographic determination of trazodone hydrochloride using a reversed phase, ODS column, with a mobile phase of acetonitrile--phosphate buffer at pH 4.5 (60:40, v/v). Quantization was achieved with UV detection at 250 nm based on peak area. The three methods were simple, accurate and suitable for quality control application.
本文描述了三种测定药片中盐酸曲唑酮的方法。分光光度法是基于在pH 3.4条件下,药物的碱性氮与溴酚蓝形成黄色离子对络合物。形成的络合物用氯仿萃取,并在414 nm处进行测定。荧光分光光度法是基于在50%乙酸中,药物在最大激发波长320 nm处激发时的固有荧光进行测定,发射波长为435 nm。第三种方法是基于使用反相ODS柱,以pH 4.5的乙腈 - 磷酸盐缓冲液(60:40,v/v)作为流动相,通过高效液相色谱法测定盐酸曲唑酮。基于峰面积,在250 nm处进行紫外检测实现定量。这三种方法简单、准确,适用于质量控制应用。