grant

An Affordable and Versatile Two-Dimensional Cell Isolation and Tracking Platform Based on Image Machine Learning and Maskless Photolithography Single Cell Encapsulation

Organization LEHIGH UNIVERSITYLocation BETHLEHEM, UNITED STATESPosted 1 Sept 2022Deadline 30 Jun 2026
NIHUS FederalResearch GrantFY20232-dimensionalAcousticAcousticsAntibodiesBiological MarkersBiomedical ResearchBlood Precursor CellBlood SampleBlood monocyteBlood specimenCancer cell lineCapsulesCell BodyCell Communication and SignalingCell CountCell DifferentiationCell Differentiation processCell IsolationCell NumberCell SegregationCell SeparationCell Separation TechnologyCell SignalingCell SizeCellsCellular MorphologyCellular injuryChargeClassificationClinical Medical SciencesClinical MedicineCodeCoding SystemComplexComputer softwareCore FacilityDataData SetDependenceDetectionDevicesDropsEducation ModuleEducational ModuleEncapsulatedEquipmentFluorescenceFluorescence Activated Cell Sorting FractionationFluorescence Light MicroscopyFluorescence MicroscopyFluorescence-Activated Cell SortingFluorescence-Activated Cell SortingsHematopoietic Progenitor CellsHematopoietic stem cellsHydrogelsImageIn SituIndividualIntelligenceInternetInterruptionIntracellular Communication and SignalingLabelLaboratoriesLearningLearning ModuleLightLiquid substanceMachine LearningMagnetismMarrow monocyteMethodsMicrofluidic DeviceMicrofluidic Lab-On-A-ChipMicrofluidic MicrochipsMicrofluidicsMicroscopeModelingNeoplasm Circulating CellsOpticsPatternPerformancePhenotypePhotoradiationPopulationPriceProceduresProgenitor CellsPropertyRecoveryResearchResolutionSample SizeSamplingShapesSignal TransductionSignal Transduction SystemsSignalingSoftwareSortingSpeedStressSystemSystematicsSystems AnalysesSystems AnalysisTeaching ModuleTechnologyTimeTrainingUV laboratory microscopeUltraviolet MicroscopesUpdateWWWWorkbio-markersbiocompatibilitybiologic markerbiological researchbiological signal transductionbiomarkerbiomaterial compatibilityblood stem cellcapsulecell damagecell imagingcell injurycell morphologycell sortingcell typecellular damagecellular imagingcirculating neoplastic cellcirculating tumor cellcostcost estimatecost estimationdamage to cellsdata sharingdesigndesigningdigitalelectric fieldfluidfluorescence imagingfluorescence microscopefluorescence/UV microscopefluorescent imagingfluorescent microscopehematopoietic progenitorhematopoietic stem progenitor cellhemopoietic progenitorhemopoietic stem cellimagingin situ imaginginjury to cellslaboratory fluorescence light microscopeliquidlithographymachine based learningmachine learned algorithmmachine learning algorithmmachine learning based algorithmmachine learning based modelmachine learning modelmagneticmicrofluidic chipmonocyteopen sourceoperationoperationsopticalpricingresolutionsshear stressstem cellstooltwo-dimensionalvibrationvoltagewebworld wide webµfluidic
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Full Description

An Affordable and Versatile Two-Dimensional Cell Isolation and Tracking Platform Based on Image Machine
Learning and Maskless Photolithography Single Cell Encapsulation

Current commercial cell sorters typically use sheath flow to align cells into a single profile and sort cells based

on fluorescence signal or images. The single profile alignment limits the throughput and requires complex

hardware and expensive equipment for high-speed sorting. The usage of high-speed sheath flow also generates

high stress on cells, which makes it not suitable for fragile or sensitive cells such as stem cells for downstream

application. Some sticky cells such as monocytes or too many dead cells in the sample can interrupt or even

clog the flow. Such cell sorter also usually requires a significant amount of starting cell number. Considering the

yield, purity, and fluid dead volume, it is challenging to sort out cells of rare population such as subset of stem

cells or circulating tumor cells in blood sample. There are strong needs from small labs for an affordable and

versatile cell sorting platform applicable to a variety of cell types. The objectives of the proposed work are to: 1.

Develop a high-speed machine learning-based cell classification module. The module will enable real-time

detection of target cells inside a wide microfluidic channel based on brightfield or fluorescent images. 2. Develop

a stop flow lithography-based 2D cell sorting platform in combination with acoustic field cell array patterning that

will generate encoded encapsulations of target cells of different sizes. 3. Integrate the machine learning detection

and maskless lithography with the size-based filtering/sorting of the cell into an affordable cell sorter. The setup

can be mounted onto existing microscope and high-resolution camera, along with a web-lab flow controller and

a UV projector, makes a versatile and affordable cell sorter.

The proposed method can sort multiple cell types based on high content image information and machine learning.

This eliminates the dependency on specific antibody types which is the basis of fluorescence-activated cell

sorting (FACS) or magnetics-activated cell sorting (MACS). The proposed method can use simple microfluidic

devices for sorting different types of target cells in high purity with minimum requirement on starting cell number,

thus is applicable to rare subset of a large sample or rare cells. Maskless lithography based on digital micromirror

device (DMD) is used to stamp encoded ID to track individual cells which is convenient for downstream analysis.

The 2D wide platform can avoid high shear flow-induced cell damage or property change in the cell sorting

channel, thus is suitable for gentle cells such as stem cells. The wide channel can also avoid the potential cell

clogging problem in a regular cell sorter. By updating the machine learning algorithm and sharing datasets and

pre-trained models, as well as the availability of cameras and projectors of better resolution, the proposed project

leads to an affordable, expandable, powerful, and universal cell sorting platform.

Grant Number: 5R21EB033102-02
NIH Institute/Center: NIH

Principal Investigator: YEVGENY BERDICHEVSKY

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