Ahram Canadian University, Faculty of Pharmacy, Pharmaceutical Analytical Chemistry Department, Cairo 12556, Egypt.
Ain Shams University, Faculty of Pharmacy, Pharmaceutical Analytical Chemistry Department, Cairo 12556, Egypt.
J AOAC Int. 2023 Sep 1;106(5):1348-1360. doi: 10.1093/jaoacint/qsad037.
Nebivolol and valsartan (VAL) in combination with each other successfully control blood pressure and improve hypertension patient outcomes.
To develop and validate innovative, simple, and sustainable spectrophotometric methods for the simultaneous analysis of nebivolol and valsartan.
The new modified difference amplitude modulation (MD-AM) method uses only unified regression equation and does not require any resolution techniques. Other different approaches were also applied for the determination of the same mixture including univariate and multivariate spectrophotometric methods. The multivariate methods were PLS and PCR, whereas the univariate methods were derivative ratio (DD1), ratio difference (RD), constant center (CC), constant center spectrum subtraction (CC-SS), constant value coupled with amplitude difference (CV-AD), advanced concentration value (ACV), and amplitude difference (AD). The proposed methods use a green solvent; thus, the environmental impact of the presented procedures was evaluated qualitatively and quantitatively using six well-known evaluation tools.
All methods were applied successfully for the analysis of the studied drugs in their bulk powder, pharmaceutical dosage form Byvalson®, and in vitro release at intestinal pH (7.4) using a USP dissolution tester. Results obtained were compared statistically with the reported method and with each other using a one-way ANOVA statistical test, and no significant differences were found.
All green and white analytical chemistry evaluation tools results confirm the safety, sustainability, and cost-effectiveness of the approaches, indicating that the methods are regarded green and sustainable. Results were agreeable, encouraging their applicability in quality control laboratories for dosage form and making these methods an eco-friendly substitute for the analysis of this combined dosage form and for evaluating the dissolution profile.
For the first time, a severely overlapped spectrum was determined using a unified regression equation without the need of extended part or zero contribution regions by the novel method MD-AM. The proposed methods are the first study of in vitro dissolution profiling of nebivolol hydrochloride (NEB) and VAL and the first sustainable and green methods applied without compromising the analytical criteria.
比索洛尔和缬沙坦(VAL)联合使用成功地控制了血压,改善了高血压患者的预后。
开发和验证用于同时分析比索洛尔和缬沙坦的创新、简单和可持续分光光度法。
新的改进差分幅度调制(MD-AM)方法仅使用统一的回归方程,不需要任何分辨率技术。还应用了其他不同的方法来测定相同的混合物,包括单变量和多变量分光光度法。多变量方法是偏最小二乘法(PLS)和主成分回归(PCR),而单变量方法是导数比(DD1)、比值差(RD)、常数中心(CC)、常数中心光谱减法(CC-SS)、固定值与幅度差(CV-AD)、先进浓度值(ACV)和幅度差(AD)。所提出的方法使用绿色溶剂;因此,使用六个知名评估工具对所提出方法的程序进行了定性和定量的环境影响评估。
所有方法均成功地应用于研究药物的原料药、制剂 Byvalson®以及在肠 pH(7.4)下的体外释放的分析,使用 USP 溶解测试仪。用单向方差分析统计检验将获得的结果与报道的方法和彼此进行比较,没有发现显著差异。
所有绿色和白色分析化学评估工具的结果都证实了方法的安全性、可持续性和成本效益,表明这些方法被认为是绿色和可持续的。结果是一致的,鼓励将其应用于制剂的质量控制实验室,并使这些方法成为分析这种联合制剂和评估溶解曲线的环保替代品。
新方法 MD-AM 首次使用统一的回归方程,无需扩展部分或零贡献区域,即可确定严重重叠的光谱。所提出的方法是首次研究盐酸比索洛尔(NEB)和 VAL 的体外溶出度曲线,也是首次应用可持续和绿色方法,且不影响分析标准。