It has been demonstrated that microalgae play an important role in the food, agriculture and medicine industries. Additionally, the identification and counting of the microalgae are also a critical step in evaluating water quality, and some lipid-rich microalgae species even have the potential to be an alternative to fossil fuels. However, current technologies for the detection and analysis of microalgae are costly, labor-intensive, time-consuming and throughput limited. In the past few years, microfluidic chips integrating optical components have emerged as powerful tools that can be used for the analysis of microalgae with high specificity, sensitivity and throughput. In this paper, we review recent optofluidic lab-on-chip systems and techniques used for microalgal detection and characterization. We introduce three optofluidic technologies that are based on fluorescence, Raman spectroscopy and imaging-based flow cytometry, each of which can achieve the determination of cell viability, lipid content, metabolic heterogeneity and counting. We analyze and summarize the merits and drawbacks of these micro-systems and conclude the direction of the future development of the optofluidic platforms applied in microalgal research.
Biomolecular imaging of intracellular structures of a single cell and subsequent screening of the cells are of high demand in metabolic engineering to develop strains with the desired phenotype. However,...
In
order to obtain high yield of astaxanthin, a high-value compound
with ultrastrong antioxidant capacity, it is necessary to identify
the growth characteristics (biomass, morphology, and size) of Haematococcus pluvialis. The current detection methods have
the disadvantages of labor-consuming operation or complicated measurement
system. It is an urgent need to explore a simple and cost-effective
method for the detection of H. pluvialis with large
size distribution during its growth period. In this work, a digital
in-line holographic flow cytometry using a linear array sensor is
proposed to measure the growth characteristics of H. pluvialis in a two-dimensional (2-D) hydrodynamic focusing microfluidic chip.
Based on the modified angular spectrum method, the distorting holograms
caused by the asynchrony of sample flow velocity and acquisition speed
of the linear array sensor were rectified and reconstructed. In addition,
the depth-of-focus of the imaging system were digitally extended to
cover the entire depth of the microfluidic channel for optimized imaging
quality. We have utilized the proposed method to statistically investigate
the biomass, morphology and size of H. pluvialis under
different culture conditions and growth durations.
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