Faroongsarng D, Kadejinda W, Sunthornpit A
Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, 90112 Thailand.
AAPS PharmSciTech. 2000 Jul 30;1(3):E23. doi: 10.1208/pt010323.
Thermal behavior of a series of acetaminophen (APAP) doped with p-aminophenol (PANP) was studied by differential scanning calorimetry (DSC) to determine whether it exhibited a eutectic system. Within the temperature range of 120 to 200 degrees C, accurately weighed (1-2 mg) samples sealed in hermetic pans were calorimetrically scanned with a low scanning rate of 1 degrees C/min. The mixture formed a single eutectic with the composition ratio APAP/PANP of 0.6/0.4 at a temperature of 138 degrees C, where it liquefied. Melting began as early as at the eutectic point, which was below the melting temperature of APAP (169 degrees C). The melting point as well as heat of APAP fusion was depressed with the increase in doped PANP. It was postulated that there might be a deficit heat of APAP fusion in APAP doped with PANP, which was coincident with the heat consumed by early liquefaction. The deficit heat was used to correct fraction molten in the van't Hoff law of purity determination. It was found that the purity determination of APAP doped with PANP was comparable to the UV-spectroscopic method up to the maximum doped PANP level of 8 mol percent. It was concluded that DSC was able to approach early heat of liquefaction of APAP doped with PANP. The van't Hoff law may be applicable to the determination of APAP with the presence of PANP as a eutectic impurity.
采用差示扫描量热法(DSC)研究了一系列对氨基酚(PANP)掺杂对乙酰氨基酚(APAP)的热行为,以确定其是否呈现低共熔体系。在120至200摄氏度的温度范围内,将精确称重(1 - 2毫克)并密封在密封盘中的样品以1摄氏度/分钟的低扫描速率进行量热扫描。该混合物在138摄氏度形成了一种单一低共熔物,其APAP/PANP的组成比为0.6/0.4,在此温度下它会液化。熔化早在低共熔点就开始了,该温度低于APAP的熔点(169摄氏度)。随着掺杂的PANP增加,APAP的熔点以及熔化热均降低。据推测,在PANP掺杂的APAP中可能存在APAP熔化热不足的情况,这与早期液化所消耗的热量一致。该不足的热量用于校正范特霍夫纯度测定定律中的熔融分数。结果发现,在PANP最大掺杂水平为8摩尔百分比之前,PANP掺杂的APAP的纯度测定与紫外光谱法相当。得出的结论是,DSC能够测定PANP掺杂的APAP的早期液化热。范特霍夫定律可能适用于存在作为低共熔杂质的PANP时APAP的纯度测定。