Puskar Ljiljana, Tuckermann Rudolf, Frosch Torsten, Popp Jürgen, Ly Vanalysa, McNaughton Don, Wood Bayden R
Centre for Biospectroscopy and School of Chemistry, Monash University, Wellington Road, 3800, Victoria, Australia.
Lab Chip. 2007 Sep;7(9):1125-31. doi: 10.1039/b706997a. Epub 2007 Aug 3.
Methods to probe the molecular structure of living cells are of paramount importance in understanding drug interactions and environmental influences in these complex dynamical systems. The coupling of an acoustic levitation device with a micro-Raman spectrometer provides a direct molecular probe of cellular chemistry in a containerless environment minimizing signal attenuation and eliminating the affects of adhesion to walls and interfaces. We show that the Raman acoustic levitation spectroscopic (RALS) approach can be used to monitor the heme dynamics of a levitated 5 microL suspension of red blood cells and to detect hemozoin in malaria infected cells. The spectra obtained have an excellent signal-to-noise ratio and demonstrate for the first time the utility of the technique as a diagnostic and monitoring tool for minute sample volumes of living animal cells.
探索活细胞分子结构的方法对于理解这些复杂动态系统中的药物相互作用和环境影响至关重要。将声悬浮装置与显微拉曼光谱仪耦合,可在无容器环境中对细胞化学进行直接分子探测,最大限度地减少信号衰减,并消除与壁和界面粘附的影响。我们表明,拉曼声悬浮光谱(RALS)方法可用于监测悬浮的5微升红细胞悬液的血红素动态,并检测疟疾感染细胞中的疟原虫色素。所获得的光谱具有出色的信噪比,并首次证明了该技术作为活动物细胞微量样品诊断和监测工具的实用性。