Ding Hai-Yan, Li Gai-Ru, Yu Ying-Ge, Guo Wei, Zhi Ling, Li Xin-Xia
Guang Pu Xue Yu Guang Pu Fen Xi. 2014 Apr;34(4):1056-9.
A method for on-line monitoring the dissolution of Valsartan and hydrochlorothiazide tablets assisted by mathematical separation model of linear equations was established. UV spectrums of valsartan and hydrochlorothiazide were overlapping completely at the maximum absorption wavelength respectively. According to the Beer-Lambert principle of absorbance additivity, the absorptivity of Valsartan and hydrochlorothiazide was determined at the maximum absorption wavelength, and the dissolubility of Valsartan and hydrochlorothiazide tablets was detected by fiber-optic dissolution test (FODT) assisted by the mathematical separation model of linear equations and compared with the HPLC method. Results show that two ingredients were real-time determined simultaneously in given medium. There was no significant difference for FODT compared with HPLC (p > 0.05). Due to the dissolution behavior consistency, the preparation process of different batches was stable and with good uniformity. The dissolution curves of valsartan were faster and higher than hydrochlorothiazide. The dissolutions at 30 min of Valsartan and hydrochlorothiazide were concordant with US Pharmacopoeia. It was concluded that fiber-optic dissolution test system assisted by the mathematical separation model of linear equations that can detect the dissolubility of Valsartan and hydrochlorothiazide simultaneously, and get dissolution profiles and overall data, which can directly reflect the dissolution speed at each time. It can provide the basis for establishing standards of the drug. Compared to HPLC method with one-point data, there are obvious advantages to evaluate and analyze quality of sampling drug by FODT.
建立了一种基于线性方程数学分离模型辅助的缬沙坦氢氯噻嗪片溶出度在线监测方法。缬沙坦和氢氯噻嗪的紫外光谱在各自最大吸收波长处完全重叠。根据吸光度加和性的比尔-朗伯原理,在最大吸收波长处测定缬沙坦和氢氯噻嗪的吸光系数,并采用线性方程数学分离模型辅助的光纤溶出度试验(FODT)检测缬沙坦氢氯噻嗪片的溶出度,并与高效液相色谱法(HPLC)进行比较。结果表明,在给定介质中可同时实时测定两种成分。FODT与HPLC相比无显著差异(p>0.05)。由于溶出行为的一致性,不同批次的制备过程稳定且均匀性良好。缬沙坦的溶出曲线比氢氯噻嗪更快、更高。缬沙坦和氢氯噻嗪在30分钟时的溶出度符合美国药典标准。结论是,基于线性方程数学分离模型辅助的光纤溶出度试验系统能够同时检测缬沙坦和氢氯噻嗪的溶出度,并获得溶出曲线和总体数据,可直接反映各时刻的溶出速度。可为制定药品标准提供依据。与单点数据的HPLC方法相比,采用FODT评价和分析抽样药品质量具有明显优势。