Department of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Division of Biochemistry, Department of Basic Medical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
F1000Res. 2023 Jun 27;12:468. doi: 10.12688/f1000research.132841.2. eCollection 2023.
: Posaconazole is a widely used antifungal drug, and its accurate quantification is essential for quality control and assessment of its pharmaceutical products. This study aimed to develop and validate a reverse-phase high-performance liquid chromatography (HPLC) analytical method for quantifying Posaconazole in bulk and dosage form. : The HPLC method was developed and validated based on International Conference on Harmonisation (ICH) guidelines. The developed method was then applied to quantify Posaconazole in a marketed tablet formulation. The method's specificity, linearity, precision, accuracy, robustness, and stability were evaluated. : The developed HPLC method showed good linearity over a 2-20 μg/mL concentration range. The percentage recovery of Posaconazole from the bulk and marketed formulations was found to be 99.01% and 99.05%, respectively. The intra-day and inter-day precisions were less than 1%, and the method was stable under different conditions. The HPLC method was successfully applied to quantify Posaconazole in the marketed formulation. : The developed and validated HPLC method is reliable and efficient for analyzing Posaconazole in bulk and dosage forms. The method's accuracy, precision, specificity, linearity, robustness, and stability demonstrate its effectiveness. The method can be used for the quality control and assessment of Posaconazole-containing pharmaceutical products.
泊沙康唑是一种广泛使用的抗真菌药物,其准确的定量分析对于质量控制和药物产品评估至关重要。本研究旨在开发和验证一种反相高效液相色谱(HPLC)分析方法,用于定量测定泊沙康唑原料药和制剂中的含量。
该 HPLC 方法是根据国际人用药品注册技术协调会(ICH)指南开发和验证的。然后将所开发的方法应用于市售片剂制剂中泊沙康唑的定量分析。评估了方法的专属性、线性、精密度、准确度、耐用性和稳定性。
所开发的 HPLC 方法在 2-20μg/mL 的浓度范围内显示出良好的线性关系。从原料药和市售制剂中回收的泊沙康唑的百分比分别为 99.01%和 99.05%。日内和日间精密度均小于 1%,且该方法在不同条件下稳定。该 HPLC 方法成功地应用于市售制剂中泊沙康唑的定量分析。
所开发和验证的 HPLC 方法可靠且高效,可用于分析原料药和制剂中的泊沙康唑。该方法的准确性、精密度、专属性、线性、耐用性和稳定性证明了其有效性。该方法可用于泊沙康唑药物产品的质量控制和评估。