Department of Industrial and Physical Pharmacy, College of Pharmacy, Purdue University, 575 Stadium Mall Drive, West Lafayette, Indiana 47907, USA.
Pharm Res. 2011 Jul;28(7):1643-52. doi: 10.1007/s11095-011-0399-4. Epub 2011 Mar 4.
To critically evaluate the effect of submicron and micron-sized organic particulates on the ultraviolet (UV) absorption spectra of aqueous systems and assess the applicability of UV/Vis fiber-optic probes for in-situ concentration monitoring in the presence of particles of different sizes.
UV absorbance spectra were obtained for aqueous felodipine suspensions containing a range of particle sizes (300 nm-400 μm) and suspension concentrations and for methanolic solutions of different concentrations and amorphous films of different thicknesses. Select suspensions were further characterized using nuclear magnetic resonance (NMR) experiments. Mie theory was used to provide insight into the role of particle size on scattering and absorption of UV radiation.
Large increases in absorbance as a function of total suspension concentration were observed for nanosuspensions but not for the other particle sizes evaluated. NMR measurements of solution concentration indicated that the observed increases in UV absorbance values for these systems were not caused by increases in the concentration of dissolved molecules, implying that nanoparticles of felodipine might absorb UV light. Mie theory-based calculations enabled reconstruction of the experimental observations and supported this hypothesis.
For solutions containing small (submicron) felodipine particles, UV spectra were influenced by absorption of the particles and contributions from absorption of dissolved molecules and scattering of the particles. Caution should be applied when using in situ UV/VIS-probes to monitor the amount of dissolved material during dissolution, in particular when small particles are present (e.g. dissolution of nanoparticulate formulations) or generated (e.g. precipitation of supersaturated solutions) in the dissolution medium.
批判性评估亚微米和微米级有机颗粒对水相体系中紫外线(UV)吸收光谱的影响,并评估 UV/Vis 光纤探头在存在不同大小颗粒时用于原位浓度监测的适用性。
获得了含有一系列粒径(300nm-400μm)和悬浮浓度的水溶液非洛地平悬浮液以及不同浓度的甲醇溶液和不同厚度无定形薄膜的 UV 吸光度光谱。使用核磁共振(NMR)实验对部分悬浮液进行了进一步表征。米氏理论用于深入了解粒径对紫外线辐射散射和吸收的作用。
对于纳米悬浮液,观察到总悬浮浓度的增加导致吸光度大幅增加,但对于评估的其他粒径则没有观察到这种情况。溶液浓度的 NMR 测量表明,这些系统中 UV 吸光度值的增加不是由于溶解分子浓度的增加引起的,这意味着非洛地平纳米颗粒可能吸收紫外线。基于米氏理论的计算能够重建实验观察结果,并支持这一假设。
对于含有小(亚微米)非洛地平颗粒的溶液,UV 光谱受到颗粒吸收以及溶解分子吸收和颗粒散射的影响。在溶解过程中使用原位 UV/VIS 探头监测溶解物质的量时应谨慎,特别是当存在小颗粒(例如纳米颗粒制剂的溶解)或在溶解介质中生成(例如过饱和溶液的沉淀)时。