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Raman detected differential scanning calorimetry of polymorphic transformations in acetaminophen.

机译:拉曼检测对乙酰氨基酚中多态性转变的差示扫描量热法。

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Acetaminophen is known to crystallize in three polymorphic forms. Thermally induced transformations between the crystalline forms and the super-cooled liquid have been observed by differential scanning calorimetry (DSC), but the assignment of calorimetric transitions to specific polymorphic transformations remains challenging, because the transition temperatures for several transformations are close to one another, and the characteristics of the observed transitions depend on experimental variables that are often poorly controlled. This paper demonstrates the simultaneous application of DSC and Raman microscopy for the observation of thermally driven transitions between polymorphs of pharmaceutical materials. Raman detected differential scanning calorimetry (RD-DSC) has been used to monitor the DSC thermograms of super-cooled liquid acetaminophen and confirms the assignment of two exothermic transitions to specific polymorphic transformations. Principal component analysis of the Raman spectra have beenused to determine the number of independent components that participate in the phase transformations, and multivariate regression has been used to determine transition temperatures from the spectral data. The influence of the laser excitation source on measured DSC thermograms has also been investigated, and it has been demonstrated that a baseline shift occurs in RD-DSC when a polymorphic transformation occurs between crystalline and amorphous forms. RD-DSC has been used to examine the influence of sample aging and sample pan configuration on the observed polymorphic transformations, and both of these variables were found to influence the thermal behavior of the sample. The results demonstrate the advantage of simultaneous Raman spectroscopy and differential scanning calorimetry for the unambiguous assignment of thermally driven polymorphic transformations.
机译:已知对乙酰氨基酚会以三种多晶型物形式结晶。通过差示扫描量热法(DSC)观察到了结晶形式和过冷液体之间的热诱导转变,但是将热量转变过渡到特定的多晶型转变仍然很困难,因为几种转变的转变温度彼此接近,以及观察到的过渡特征取决于实验变量,而这些变量通常难以控制。本文展示了DSC和拉曼显微镜的同时应用,用于观察药物材料多晶型物之间的热驱动转变。拉曼检测差示扫描量热法(RD-DSC)已用于监测过冷液态对乙酰氨基酚的DSC热谱图,并确认了两个放热转变为特定多晶型转变的分配。已使用拉曼光谱的主成分分析来确定参与相变的独立成分的数量,并且已使用多元回归从光谱数据确定转变温度。还研究了激光激发源对测得的DSC温度记录图的影响,并且已经证明,当在结晶形式和非晶形式之间发生多态转化时,RD-DSC中会发生基线偏移。 RD-DSC已用于检查样品老化和样品盘结构对观察到的多晶型转变的影响,并且发现这两个变量都影响样品的热行为。结果证明了同时拉曼光谱法和差示扫描量热法在热驱动多态转化的明确分配方面的优势。

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