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Thermal and dissolution studies of Cefpodoxime proxetil drug and tablets

机译:头孢泊肟酯类药物和片剂的热学和溶出度研究

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Cefpodoxime proxetil is commonly used antibacterial drug. Thermal analysis and dissolution studies are routinely conducted by pharmaceutical industries in order to evaluate the drug stability, the drugexcipient interaction and compatibility. In this study dynamic thermogravimetry (TG) experiments were performed in flowing dry air atmosphere (20 ml min-1) to investigate the thermal decomposition of cefpodoxime proxetil drug and tablets (A, B and C) containing different excipients. The TG curve of cefpodoxime proxetil drug shows single decomposition process while tablets (A, B and C) display two. Decomposition activation energies and thermal rate constant (kT) were determined using model-free methods viz. Kissinger, Friedman, Flynn-Wall-Ozawa, and modified Coats-Redfern. The dissolution study of samples was carried out in accordance of United State Pharmacopeia (USP 32) and Kitazawa equation was used for kinetics. Samples are found to have following sequence of the thermal stability: tablet B cefpodoxime proxetil drug tablet A tablet C and the dissolution order: tablet B cefpodoxime proxetil drug tablet A tablet C. The thermal rate constant (kT) and dissolution rate constant (kD) were also correlated graphically and found to have very good correlation with regression coefficient close to 1.
机译:头孢泊肟酯是常用的抗菌药物。制药行业通常进行热分析和溶出度研究,以评估药物稳定性,药物赋形剂相互作用和相容性。在这项研究中,动态热重分析(TG)实验是在干燥的空气流通环境(20 ml min-1)中进行的,以研究头孢泊肟酯Proxetil药物和含有不同赋形剂的片剂(A,B和C)的热分解。头孢泊肟普罗塞特药物的TG曲线显示单个分解过程,而片剂(A,B和C)显示两个分解过程。分解活化能和热速率常数(kT)使用无模型方法确定。基辛格,弗里德曼,弗林·沃尔·小泽和改良的高士·雷德芬。根据美国药典(USP 32)进行样品的溶出度研究,并将Kitazawa方程用于动力学。发现样品具有以下热稳定性顺序:片剂B <头孢泊肟肟酯药物<片剂A <片剂C和溶出顺序:片剂B <头孢泊肟肟醚酮药物<片剂A <片剂C。热速率常数(kT)和溶出速率常数(kD)也通过图形相关,发现与回归系数接近1时具有很好的相关性。

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