Otun Sarah O, Meehan Elizabeth, Qi Sheng, Craig Duncan Q M
School of Pharmacy, University of East Anglia, Earlham Road, Norwich, Norfolk, NR4 7TJ, UK.
Pharm Res. 2015 Apr;32(4):1316-24. doi: 10.1007/s11095-014-1535-8. Epub 2014 Oct 18.
Slow or incomplete crystallization may be a significant manufacturing issue for solid lipid-based dosage forms, yet little information is available on this phenomenon. In this investigation we suggest a novel means by which slow solidification may be monitored in Gelucire 44/14 using quasi-isothermal modulated temperature DSC (QiMTDSC).
Conventional linear heating and cooling DSC methods were employed, along with hot stage microscopy (HSM), for basic thermal profiling of Gelucire 44/14. QiMTDSC experiments were performed on cooling from the melt, using a range of incremental decreases in temperature and isothermal measurement periods.
DSC and HSM highlighted the main (primary) crystallization transition; solid fat content analysis and kinetic analysis were used to profile the solidification process. The heat capacity profile from QiMTDSC indicated that after an initial energetic primary crystallisation, the lipid underwent a slower period of crystallization which continued to manifest at much lower temperatures than indicated by standard DSC.
We present evidence that Gelucire 44/14 undergoes an initial crystallization followed by a secondary, slower process. QIMTDSC appears to be a promising tool in the investigation of this secondary crystallization process.
对于基于固体脂质的剂型而言,缓慢或不完全结晶可能是一个重大的生产问题,但关于这一现象的信息却很少。在本研究中,我们提出了一种新方法,可利用准等温调制温度差示扫描量热法(QiMTDSC)监测Gelucire 44/14中的缓慢固化过程。
采用传统的线性加热和冷却差示扫描量热法以及热台显微镜(HSM)对Gelucire 44/14进行基本的热分析。从熔体冷却过程中进行QiMTDSC实验,采用一系列温度增量降低和等温测量周期。
差示扫描量热法和热台显微镜突出了主要(初级)结晶转变;利用固体脂肪含量分析和动力学分析对固化过程进行了分析。QiMTDSC的热容量曲线表明,在初始的高能初级结晶之后,脂质经历了一个较慢的结晶阶段,该阶段在比标准差示扫描量热法所示温度低得多的温度下仍会持续出现。
我们提供的证据表明,Gelucire 44/14经历了初始结晶,随后是一个较慢的二次过程。准等温调制温度差示扫描量热法似乎是研究这种二次结晶过程的一种很有前景的工具。