ABSTRACT
This study investigated the acetylation of starch to improve its processability and compatibility with poly(lactic acid). The temperature at the maximum rate of degradation increased by 3.2% for poly(lactic acid) blends containing acetylated starch degree of substitution 2.5 compared to the blend containing neat starch. A biphasic morphology with distinct dispersed phase was predicted and observed experimentally for all blends except the blend containing acetylated starch degree of substitution 3. Acetylated starch induced plasticization and nucleation for all degree of substitution. The blend containing acetylated starch degree of substitution 2.5 had higher tensile strength (26%), and toughness (29%) compared to the blend containing neat starch. The superior mechanical properties of the blend containing acetylated starch degree of substitution 2.5 are attractive for medical implant applications. The continuous microstructure and transparency characteristics of the blend containing acetylated starch degree of substitution 3 are attractive for packaging applications.
ABSTRACT
We describe a new technique that combines ultrasound and microfluidics to rapidly size and count cells in a high-throughput and label-free fashion. Using 3D hydrodynamic flow focusing, cells are streamed single file through an ultrasound beam where ultrasound scattering events from each individual cell are acquired. The ultrasound operates at a center frequency of 375 MHz with a wavelength of 4 µm; when the ultrasound wavelength is similar to the size of a scatterer, the power spectra of the backscattered ultrasound waves have distinct features at specific frequencies that are directly related to the cell size. Our approach determines cell sizes through a comparison of these distinct spectral features with established theoretical models. We perform an analysis of two types of cells: acute myeloid leukemia cells, where 2,390 measurements resulted in a mean size of 10.0 ± 1.7 µm, and HT29 colorectal cancer cells, where 1,955 measurements resulted in a mean size of 15.0 ± 2.3 µm. These results and histogram distributions agree very well with those measured from a Coulter Counter Multisizer 4. Our technique is the first to combine ultrasound and microfluidics to determine the cell size with the potential for multi-parameter cellular characterization using fluorescence, light scattering and quantitative photoacoustic techniques.
