OpenMicrowell Based Biosensor with Dielectrophorec … fine secondo... · OpenMicrowell Based...

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OpenMicrowellBasedBiosensor

with

Dielectrophore4cCellManipula4on

andImpedanceMonitoring

Tutor:

Prof.RobertoGuerrieriPhDStudent:AndreaFaenza

2ndyearpresenta4on

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OutlineLab‐on‐a‐chipisanadvancedtechnologythatintegratesamicrofluidicsystemonamicroscalechip.

Itistheminiaturiza4onofalaboratorytoasmalldevice.The'laboratory'iscreatedbymeansofchannels,mixers,reservoirs,diffusionchambers,integratedelectrodes,pumps,valvesandmore.

Goals:• Automatestandardlaboratoryprocesses.

FastandcostefficientImproveddataquality

Increasedsepara4onability

• ImproveResearchinvariousareasoflifesciences(e.g.Immunotherapy,Stemcells,Cancerresearch,etc…)

Individuallycontrollingsinglecellsandpar4cles

Issues:

‐Incompa4bilitywithsmallvolumeandrare(1/106)cells(e.g.CellSorter)‐Cellrecoveryimpossibleortooslow(e.g.ClosedMicroCage)

2ndyearpresenta4on

OurplaWormisabiosensorbasedonOpenMicrowelldesignedforHighThroughputrecoverywithintegratedelectrodesfor:

dielectrophore4ccellmanipula4onimpedancemonitoringwithsinglecellresolu4on

OurplaWorm:

Steps:

‐ Infusion:PhysiologicalSolu4on+cells(typicalflowrate:1ul/min)

‐ CellSor4ng

‐ ControlledCellDeliveryusingDEP

‐ Forcecell2cellinterac4onusingDEPfocusing

‐ Par4clescoun4ngusingimpedancemeasurements

‐ Cellrecovery

 PlaWormdescrip4on Controlleddelivery Cell2cellinterac4onusingDEPfocusing Impedancemonitoring

Dielectrophoresis(DEP)

Thedielectrophore4cforcedependson:

•  Themediumandpar4cles'electricalproper4es•  Thepar4cles'shapeandsize•  Thefrequencyandmagnitudeoftheelectricfield

Aphenomenoninwhichaforceisexertedonadielectricpar7clewhensubjectedtoanon‐uniformelectricfield.Thisforcedoesnotrequirethepar4cletobecharged.

Allpar4clesexhibitdielectrophore4cac4vityinthepresenceofelectricfields.

V+ V‐

ElectricField

‐‐‐‐‐+

++

‐‐‐‐

‐‐

‐‐

‐‐‐

+++

+

++++++

+++

pDEP

V+ V‐

ElectricField

‐‐‐

‐++

+

‐‐‐‐

‐‐

‐‐

‐‐‐

++

+

+

++++++

+++

nDEP

εp > εm εp < εm

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Fluidicchanneldimensions(HxWxL) 50μmX400μmXDevicelength

Flowrate0.5‐1μL/min(LAMINARFLOW)

Par4clevelocity(cellwith10‐15μmdiameter) 100μm/sec(StokesDragForce)

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Mul4LayerKapton®FlexPCBdesign

Microfluidicinterfacefabrica4on Result:

Geometricalproper4es:Devicethickness200μmMicrowelldiameter70‐100μmMicrowellpitchStandardMicro4tercompa4bility(2.25mm,mul4pleandsubmul4ple)

PlaWormdescrip4on

Bojom

Middle

Top

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Microchannel

Microwell

Air

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Controlleddelivery

Focaliza4onStructures:

DEPForce+DragForce:

Biosensor

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Normallythefreefallofthepar4cleswithinthewellischaracterizedbya

randomposi4oningNOCONTACT! Bojom

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Cell‐cellinterac4onthroughDEPfocusing

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Animportantrequirementofthebiosensoristoforcethecell‐cellinterac4on

DEPFocusingThe par4cles are pushed awayfromtheboundariesof thewellwhere the electric field ismaximum and drop along thecentralver4calaxis

Electrode Amplitude(V) Frequency(HZ)

Top GND ‐

Middle GND ‐

Bojom 2 100KHz

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a)

b)

c)

d)

e)

f)

a)

b)

c)

d)

e)

f)

Par4clesdockatthesameposi4ononthemeniscusandarefoundincontactbetweeneachothers.FocusLevel

FocusLevel

FocusLevel

FocusLevel

FocusLevel

FocusLevel

Cell‐cellinterac4onthroughDEPfocusing‐Results

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Par4clescoun4ngusingimpedancemeasurementsModel:

BIOSENSOR

MUX32:1 MUX32:1 MUX32:1

8x4Padsexample

Labviewinterface

freqє[100KHz–1MHz]Amplitude=250mV

Sensingboard

1.I/VConversionandpreamp 2.Mixersanddivider

Systemschema4za4on:

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SensingBoardBlockDiagram

I/Vconversion PreAmplifier X

DividerLPF

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I/Vconversion PreAmplifier X LPF

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VoutαZmidZtop

VirtualGND

(I/Vstage)

SovwarePostProcessingFeaturesPreservingSmoothing

Filter

DetrendFilter

PeakDetector

Savitzky–Golaylocalpolynomial

regression

Mul4resolu4ondetrendfilter

Mul4parametercriteria

Electrode Amplitude(V) Frequency(HZ)

Top VirtualGND ‐

Middle VirtualGND ‐

Bojom 0.25 100KHz–1MHz

Worksindependentlyoftheaxisthecellsfollowduringthedescent

(Integra4onwithDEPFocusing)

Compensatesfornoisyphenomena,suchastemperaturedrivorconduc4vitychanges,typicallyfoundinopenstructuresatair‐liquidinterfaces

2ndyearpresenta4on

Time (step= 0.1 s)

Time (step= 0.1 s)

Volta

gVe

(V)

Rel

ativ

e Va

riatio

n

WorstCasetest:Temperatureinduceddriv74messmaller

Rel

ativ

e Va

riatio

n

Time (step= 0.1 s)

Sta<s<cs*

OutputPeakVaria4on

0.84±0.57%

Pulsewidth 9.0±3.0s

*K562leukemiacells

Results:

2ndyearpresenta4on

Conclusions:

Wepresented:OpenMicrowellBasedBiosensorforcell2cellinterac4onstudy,abletoworkatsinglecelllevelanddesigntoallowcellrecovery

ControlledcelldeliveryusingDEPforce

Cell2cellinterac4onforcedusingDEPfocusing

Systemmonitoringandcellcoun4ngusingimpedancemeasurements

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Publica7ons:

“Dielectrophore<ctrappinginmicrowellformanipula<onofsinglecellsandsmallaggregatesofpar<cles”M.Bocchi,M.Lombardini,A.Faenza,L.Rambelli,L.Giulianelli,N.Pecorari,R.Guerrieri.Biosensors(Vol.24,Issue5),January2009

“Biocompa<bleLab‐On‐SubstrateTechnologyPlaJorm”,T.Braun,L.Böjcher, J.Bauer,M.Bocchi,A.Faenza,R.Guerrieri,R.Gambari,K.‐F.Becker,E. Jung,A.Ostmann,M.Koch,R.Kahle,R.Aschenbrenner,H.Reichl,Proc.ECTC2009,SanDiego,CA,USA.

“Con<nuousimpedancemonitoringofsinglecellsdeliveredinopenmicrowellarrays”,A.Faenza,N.Pecorari,M.Bocchi,E.Franchi,R.Guerrieri,MicroTas2009,Jeju,Korea,November2009

Conferences:

Biosensor2008Shangai,China,14‐16May2008.

XNa<onalBiotechnologyCongressPerugia,Italy,17‐19September2008

ECTC2009‐ElectronicComponentsandTechnologyConferenceSanDiego,CaliforniaUSA,26‐29May2009.

MicroTas2009Jeju,Korea,1‐5November2009.

2ndyearpresenta4on

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