Department of Methodology, Pharco Pharmaceuticals Company, Alexandria, Egypt.
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Alexandria, Alexandria, Egypt.
Drug Dev Ind Pharm. 2020 Aug;46(8):1278-1288. doi: 10.1080/03639045.2020.1788064. Epub 2020 Jul 8.
A stability-indicating high performance liquid chromatography method with diode array detection (HPLC-DAD) was developed and validated for simultaneous determination of phenylephrine hydrochloride (PHR), dimetindene maleate (DMD) and benzalkonium chloride (BZM) in nasal drops and gel dosage forms. Effective liquid chromatographic separation was accomplished by employing Venusil XBP Cyano column (4.6 × 250 mm, 5 µm particle size) with gradient elution of the mobile phase consisting of buffer solution of potassium dihydrogen phosphate (0.025 M) and sodium 1-butane sulfonate (SBS) (0.025 M) (adjusted to pH 6.0) and acetonitrile. Peak areas of PHR, DMD and BZM at 271, 256 and 206 nm, respectively were measured and correlated to their concentrations. Peaks of PHR and DMD eluted at retention times 3.76 and 9.06 min, respectively, while BZM eluted as a couple of peaks at 11.88 and 12.51 min. The proposed HPLC procedure was carefully validated in terms of system suitability, linearity, ranges, precision, accuracy, specificity, robustness, detection and quantification limits. The linearity range for both PHR and BZM was 10-400 μg/mL and DMD was 5-300 μg/mL with correlation coefficients >0.9999. The studied compounds were subjected to stress conditions of neutral, acidic and alkaline hydrolysis, oxidation and thermal degradation. Good resolution of the three compounds from their forced degradation products proves specificity and stability-indicating merits of the proposed method. In addition, resolution of the three drugs under investigation from some pharmaceutical compounds of different medicinal categories showed the high specificity of the described method.
建立并验证了一种高效液相色谱二极管阵列检测法(HPLC-DAD),用于同时测定滴鼻剂和凝胶制剂中盐酸苯福林(PHR)、马来酸二甲茚定(DMD)和苯扎氯铵(BZM)的含量。采用 Venusil XBP Cyano 柱(4.6×250mm,5μm 粒径),以由磷酸二氢钾缓冲液(0.025M)和 1-丁烷磺酸钠(0.025M)(调至 pH 6.0)与乙腈组成的梯度洗脱流动相,实现了有效液相分离。在 271nm、256nm 和 206nm 处分别测量了 PHR、DMD 和 BZM 的峰面积,并与它们的浓度相关联。PHR 和 DMD 的保留时间分别为 3.76min 和 9.06min,而 BZM 则以 11.88min 和 12.51min 处的一对峰洗脱。该 HPLC 方法在系统适用性、线性、范围、精密度、准确度、特异性、稳健性、检测限和定量限方面进行了仔细验证。PHR 和 BZM 的线性范围均为 10-400μg/mL,DMD 的线性范围为 5-300μg/mL,相关系数均>0.9999。研究的化合物在中性、酸性和碱性水解、氧化和热降解条件下进行了受力降解。三种化合物与其强制降解产物的良好分离证明了该方法的特异性和稳定性指示优点。此外,所研究的三种药物与不同药用类别的一些药物化合物的分离显示了所描述方法的高特异性。