Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El-Aini St, Cairo 11562, Egypt.
Talanta. 2010 Sep 15;82(4):1604-7. doi: 10.1016/j.talanta.2010.07.024. Epub 2010 Jul 16.
New, simple, rapid and precise reversed phase liquid chromatographic (RP-LC) method has been developed for the simultaneous determination of diclofenac potassium (DP) and methocarbamol (MT) in ternary mixture with guaifenesin (GF), degradation product of methocarbamol. Chromatographic separation was achieved on a Symmetry Waters C18 column (150 mm x 4. 6mm, 5 microm). Gradient elution based on phosphate buffer pH (8)-acetonitrile at a flow rate of 1 mL min(-1) was applied. The UV detector was operated at 282 nm for DP and 274 nm for MT and GF. Linearity, accuracy and precision were found to be acceptable over the concentration ranges of 0.05-16, 0.5-160 and 0.5-160 microg mL(-1) for DP, MT and GF, respectively. The optimized method proved to be specific, robust and accurate for the quality control of the cited drugs in pharmaceutical preparation.
已开发出一种新的、简单的、快速的和精确的反相液相色谱(RP-LC)方法,用于同时测定含有愈创甘油醚(GF,美索卡巴莫的降解产物)的三元混合物中的双氯芬酸钾(DP)和甲氨蝶呤(MT)。色谱分离在 Waters C18 柱(150mmx4.6mm,5μm)上进行。基于磷酸盐缓冲液 pH(8)-乙腈以 1mLmin(-1)的流速进行梯度洗脱。对于 DP 和 MT 和 GF,UV 检测器在 282nm 和 274nm 处操作。DP、MT 和 GF 的浓度范围分别为 0.05-16、0.5-160 和 0.5-160μgmL(-1)时,发现线性、准确性和精密度均可以接受。该优化方法被证明对于药物制剂中引用药物的质量控制具有特异性、稳健性和准确性。