scholarly journals Using real-time fluorescence and deformability cytometry and deep learning to transfer molecular specificity to label-free sorting

2019 ◽  
Author(s):  
Ahmad Ahsan Nawaz ◽  
Marta Urbanska ◽  
Maik Herbig ◽  
Martin Nötzel ◽  
Martin Kräter ◽  
...  

The identification and separation of specific cells from heterogeneous populations is an essential prerequisite for further analysis or use. Conventional passive and active separation approaches rely on fluorescent or magnetic tags introduced to the cells of interest through molecular markers. Such labeling is time- and cost-intensive, can alter cellular properties, and might be incompatible with subsequent use, for example, in transplantation. Alternative label-free approaches utilizing morphological or mechanical features are attractive, but lack molecular specificity. Here we combine image-based real-time fluorescence and deformability cytometry (RT-FDC) with downstream cell sorting using standing surface acoustic waves (SSAW). We demonstrate basic sorting capabilities of the device by separating cell mimics and blood cell types based on fluorescence as well as deformability and other image parameters. The identification of blood sub-populations is enhanced by flow alignment and deformation of cells in the microfluidic channel constriction. In addition, the classification of blood cells using established fluorescence-based markers provides hundreds of thousands of labeled cell images used to train a deep neural network. The trained algorithm, with latency optimized to below 1 ms, is then used to identify and sort unlabeled blood cells at rates of 100 cells/sec. This approach transfers molecular specificity into label-free sorting and opens up new possibilities for basic biological research and clinical therapeutic applications.


Lab on a Chip ◽  
2020 ◽  
Vol 20 (13) ◽  
pp. 2306-2316 ◽  
Author(s):  
Konstanze Aurich ◽  
Bob Fregin ◽  
Raghavendra Palankar ◽  
Jan Wesche ◽  
Oliver Hartwich ◽  
...  

Real-time deformability cytometry is a unique tool for quality assessment of therapeutic blood cells utilizing their mechanical properties.



2020 ◽  
Author(s):  
Hossein Tavassoli ◽  
Prunella Rorimpandey ◽  
Young Chan Kang ◽  
Michael Carnell ◽  
Chris Brownlee ◽  
...  

AbstractTo advance our understanding of cardiomyocyte identity and function, we need appropriate tools to isolate pure primary cardiomyocytes. We have developed a label-free method to purify viable cardiomyocytes from mouse neonatal hearts using a simple inertial microfluidics biochip. Cardiomyocytes were sorted from neonatal hearts and isolated to >90% purity and their physico-mechanical properties were evaluated using real time deformability cytometry. Purified cardiomyocytes were viable and retained their identity and function as depicted by expression of cardiac specific markers and contractility. Furthermore, we showed that cardiomyocytes have a distinct physico-mechanical phenotype that could be used as an intrinsic biophysical marker to distinguish these cells from other cell types within the heart. Taken together, this cardiomyocyte isolation and phenotyping method could serve as a valuable tool to progress our understanding of cardiomyocyte identity and function, which will ultimately benefit many diagnostic development and cardiac treatment studies.



2012 ◽  
Vol 22 (10) ◽  
pp. 105037 ◽  
Author(s):  
Guofeng Guan ◽  
Peter C Y Chen ◽  
Weng Kung Peng ◽  
Ali Asgar Bhagat ◽  
Chong Jin Ong ◽  
...  


2020 ◽  
Author(s):  
Shah R. Ali ◽  
Dan Nguyen ◽  
Brandon Wang ◽  
Steven Jiang ◽  
Hesham A. Sadek

ABSTRACTProper identification and annotation of cells in mammalian tissues is of paramount importance to biological research. Various approaches are currently used to identify and label cell types of interest in complex tissues. In this report, we generated an artificial intelligence (AI) deep learning model that uses image segmentation to predict cardiomyocyte nuclei in mouse heart sections without a specific cardiomyocyte nuclear label. This tool can annotate cardiomyocytes highly sensitively and specifically (AUC 0.94) using only cardiomyocyte structural protein immunostaining and a global nuclear stain. We speculate that our method is generalizable to other tissues to annotate specific cell types and organelles in a label-free way.



Micromachines ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 52 ◽  
Author(s):  
Jin-Chen Hsu ◽  
Chih-Hsun Hsu ◽  
Yeo-Wei Huang

We present a numerical and experimental study of acoustophoretic manipulation in a microfluidic channel using dual-wavelength standing surface acoustic waves (SSAWs) to transport microparticles into different outlets. The SSAW fields were excited by interdigital transducers (IDTs) composed of two different pitches connected in parallel and series on a lithium niobate substrate such that it yielded spatially superimposed and separated dual-wavelength SSAWs, respectively. SSAWs of a singltablee target wavelength can be efficiently excited by giving an RF voltage of frequency determined by the ratio of the velocity of the SAW to the target IDT pitch (i.e., f = cSAW/p). However, the two-pitch IDTs with similar pitches excite, less efficiently, non-target SSAWs with the wavelength associated with the non-target pitch in addition to target SSAWs by giving the target single-frequency RF voltage. As a result, dual-wavelength SSAWs can be formed. Simulated results revealed variations of acoustic pressure fields induced by the dual-wavelength SSAWs and corresponding influences on the particle motion. The acoustic radiation force in the acoustic pressure field was calculated to pinpoint zero-force positions and simulate particle motion trajectories. Then, dual-wavelength SSAW acoustofluidic devices were fabricated in accordance with the simulation results to experimentally demonstrate switching of SSAW fields as a means of transporting particles. The effects of non-target SSAWs on pre-actuating particles were predicted and observed. The study provides the design considerations needed for the fabrication of acoustofluidic devices with IDT-excited multi-wavelength SSAWs for acoustophoresis of microparticles.



1980 ◽  
Vol 35 (1) ◽  
pp. 37-41 ◽  
Author(s):  
A. Alippi ◽  
A. Palma ◽  
L. Palmieri ◽  
G. Socino ◽  
E. Verona


2005 ◽  
Vol 44 (6B) ◽  
pp. 4292-4296 ◽  
Author(s):  
Oliver B. Wright ◽  
Osamu Matsuda ◽  
Yoshihiro Sugawara


Lab on a Chip ◽  
2013 ◽  
Vol 13 (21) ◽  
pp. 4210 ◽  
Author(s):  
Ghulam Destgeer ◽  
Kyung Heon Lee ◽  
Jin Ho Jung ◽  
Anas Alazzam ◽  
Hyung Jin Sung


2016 ◽  
Vol 2 (7) ◽  
pp. e1600089 ◽  
Author(s):  
David J. Collins ◽  
Citsabehsan Devendran ◽  
Zhichao Ma ◽  
Jia Wei Ng ◽  
Adrian Neild ◽  
...  

Micrometer-scale acoustic waves are highly useful for refined optomechanical and acoustofluidic manipulation, where these fields are spatially localized along the transducer aperture but not along the acoustic propagation direction. In the case of acoustic tweezers, such a conventional acoustic standing wave results in particle and cell patterning across the entire width of a microfluidic channel, preventing selective trapping. We demonstrate the use of nanosecond-scale pulsed surface acoustic waves (SAWs) with a pulse period that is less than the time of flight between opposing transducers to generate localized time-averaged patterning regions while using conventional electrode structures. These nodal positions can be readily and arbitrarily positioned in two dimensions and within the patterning region itself through the imposition of pulse delays, frequency modulation, and phase shifts. This straightforward concept adds new spatial dimensions to which acoustic fields can be localized in SAW applications in a manner analogous to optical tweezers, including spatially selective acoustic tweezers and optical waveguides.



2021 ◽  
Author(s):  
Matthew Lindley ◽  
Julia Gala de Pablo ◽  
Jorgen Walker Peterson ◽  
Akihiro Isozaki ◽  
Kotaro Hiramatsu ◽  
...  

Cell sorting is the workhorse of biological research and medicine. Cell sorters are commonly used to sort heterogeneous cell populations based on their intrinsic features. Raman-activated cell sorting (RACS) has recently received considerable interest by virtue of its ability to discriminate cells by their intracellular chemical content, in a label-free manner. However, broad deployment of RACS beyond lab-based demonstrations is hindered by a fundamental trade-off between throughput and measurement bandwidth (i.e., cellular information content). Here we overcome this trade-off and demonstrate broadband RACS in the fingerprint region (300 - 1,600 cm-1) with a record high throughput of ~50 cells per second. This represents a 100x throughput increase compared to previous demonstrations of broadband fingerprint-region RACS. To show the utility of our RACS, we demonstrate real-time label-free sorting of microalgal cells based on their accumulation of carotenoids and polysaccharide granules. These results hold promise for medical, biofuel, and bioplastic applications.



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