Department of Industrial and Physical Pharmacy, Purdue University, West Lafayette, IN 47907, USA.
Chemistry, Purdue University, West Lafayette, IN 47907, USA.
J Pharm Biomed Anal. 2017 Nov 30;146:86-95. doi: 10.1016/j.jpba.2017.07.066. Epub 2017 Aug 24.
Various techniques have been used to detect crystallization in amorphous solid dispersions (ASD). However, most of these techniques do not enable the detection of very low levels of crystallinity (<1%). The aim of the current study was to compare the sensitivity of second harmonic generation (SHG) microscopy with powder X-ray diffraction (XRPD) in detecting the presence of crystals in low drug loading amorphous solid dispersions. Amorphous solid dispersions of the poorly water soluble compounds, flutamide (FTM, 15wt.% drug loading) and ezetimibe (EZT, 30wt.% drug loading) with hydroxypropyl methylcellulose acetate succinate (HPMCAS) were prepared by spray drying. To induce crystallization, samples were subsequently stored at 75% or 82% relative humidity (RH) and 40°C. Crystallization was monitored by XRPD and by SHG microscopy. Solid state nuclear magnetic resonance spectroscopy (ssNMR) was used to further investigate crystallinity in selected samples. For flutamide, crystals were detected by SHG microscopy after 8days of storage at 40°C/82% RH, whereas no evidence of crystallinity could be observed by XRPD until 26days. Correspondingly, for FTM samples stored at 40°C/75% RH, crystals were detected after 11days by SHG microscopy and after 53days by XRPD. The evolution of crystals, that is an increase in the number and size of crystalline regions, with time could be readily monitored from the SHG images, and revealed the formation of needle-shaped crystals. Further investigation with scanning electron microscopy indicated an unexpected mechanism of crystallization, whereby flutamide crystals grew as needle-shaped projections from the surface of the spray dried particles. Similarly, EZT crystals could be detected at earlier time points (15days) with SHG microscopy relative to with XRPD (60days). Thus, SHG microscopy was found to be a highly sensitive method for detecting and monitoring the evolution of crystals formed from spray dried particles, providing much earlier detection of crystallinity than XRPD under comparable run times.
已经使用了各种技术来检测无定形固体分散体(ASD)中的结晶。然而,这些技术中的大多数都不能检测到非常低水平的结晶度(<1%)。本研究的目的是比较二次谐波产生(SHG)显微镜与粉末 X 射线衍射(XRPD)检测低药物负载无定形固体分散体中晶体存在的灵敏度。采用喷雾干燥法制备了疏水性差的化合物氟他胺(FTM,15wt.%药物负载)和依折麦布(EZT,30wt.%药物负载)与羟丙基甲基纤维素醋酸琥珀酸酯(HPMCAS)的无定形固体分散体。为了诱导结晶,随后将样品储存在 75%或 82%相对湿度(RH)和 40°C。通过 XRPD 和 SHG 显微镜监测结晶。固态核磁共振波谱(ssNMR)用于进一步研究选定样品的结晶度。对于氟他胺,在 40°C/82%RH 下储存 8 天后,通过 SHG 显微镜检测到晶体,而在 XRPD 下直到 26 天后才观察到结晶度的证据。相应地,对于在 40°C/75%RH 下储存的 FTM 样品,通过 SHG 显微镜在 11 天后和通过 XRPD 在 53 天后检测到晶体。通过 SHG 图像可以容易地监测晶体的演变,即结晶区域的数量和尺寸的增加,并且揭示了针状晶体的形成。进一步的扫描电子显微镜研究表明了一种意想不到的结晶机制,即氟他胺晶体从喷雾干燥颗粒的表面作为针状突起生长。同样,与 XRPD(60 天)相比,通过 SHG 显微镜可以更早地检测到 EZT 晶体(15 天)。因此,SHG 显微镜被发现是一种非常灵敏的方法,用于检测和监测从喷雾干燥颗粒形成的晶体的演变,与可比运行时间下的 XRPD 相比,提供了更早的结晶度检测。