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7996469 Carbon Nanotubes for Experimental Biology Abdennour ABBAS

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  • 8/8/2019 7996469 Carbon Nanotubes for Experimental Biology Abdennour ABBAS

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    Carbon nanotubesfor

    experimental biology

    Presented by:

    Abdennour ABBAS

    Institute of Electronic, Microelectronic and Nanotechnology

    University of Lille1

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    Table of contents

    IntroductionI- What are carbon nanotubes ?

    II- Fabrication techniques

    III- General applications

    IV- Interest in biology

    V- Perspectives

    Conclusion

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    Introduction

    Living organisms are built of cells that are typically 10m across. Even smaller are the proteins with a typical

    size of just 5 nm, which is comparable with thedimensions of smallest manmade nanomateriel. Thissimple size comparison gives an idea of using

    nanomateriel especially Carbon NanoTubesas very smallprobes.

    In fact, since carbon nanotubes has been discovered,there is an elevated interest in performing single-cellexperimentation and manipulation including single-cellsurgery, precise drug release, and spatially resolved cell

    function monitoring.

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    I- What are carbon nanotubes?

    Carbon nanotubes (CNTs), long, thin

    cylinders of carbon, were discovered in1991 by S. Iijima.

    Nanotubes are formed by rolling up agraphene (one-atom-thick layer of graphite)sheet into a cylinder and capping eachend with half of a fullerene molecule(simillar to half C60).

    S. Iijima.

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    CNTs properties

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    Structural properties

    diameter = nanometers

    length = centimeters

    TEM image of nanotube filled with samarium oxide

    There are two main types of nanotubes:

    single-walled nanotubes (SWNTs) and

    multi-walled nanotubes (MWNTs).

    A nanotube (also known as abuckytube) is a member of the fullerene

    structural family,

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    Single-walled nanotubes

    (SWNTs):

    Diameter = 1nm Tube length = 10mic.m

    => aspect ratios (length/diameter) ofover ten million, which is extremelyadvantageous.

    They exhibit important electric

    properties that are not shared by themulti-walled carbon nanotube.

    SWNTs are the best candidate for

    miniaturizing electronics past themicroelectromechanical scale.

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    Multi-walled nanotubes (MWNTs):

    MWNT possess severalgraphitic concentric layers.

    Distance between each layer

    is 0.34 nm, with diameters from10 to 200 nm and lengths up tohundreds of microns

    MWNT are mainlymonodispersed

    Electron microscopy of raw MWNTsimaged by: (a) SEM; and (b)TEM.(R.P. Raffaelle et al. / Materials

    Science and Engineering B 116(2005) 233243)

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    Assembled CNTs:

    Until recently, assembly of individualnanotubes reproducibly into submicron

    diameter bundles was not feasible.

    The dense bundling (in SWNTs) is

    attributed to a strong van der Waalsinteraction.

    the assembly process is irreversible.D: microscope imageconfirming excellent stabilityof CNT-probe uponimmersion in a water droplet.(Kouklin et al. Appl. Phys.Lett. 87, 173901 2005).

    CNTs bundle

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    Schematics of the assembly mechanismby modified dielectrophoretique basedtechnique (Kouklin et al. Appl. Phys. Lett.

    87, 173901 2005).

    SEM images of MWNT-bundle left coated withsilicone.

    The inset shows a detailed view of a typicalMWNT bundle-electrode contact area with no

    coating applied, bar is 1 m.

    Assembly technique:

    Ethanol solution (90%)

    Electrode(electric fieldof 105 V/m)

    Droplets surface tension

    CNTs Probe

    CNTs

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    very good thermal conductors along the tube "ballisticconduction,

    Electrical properties

    SWNT ===>

    MWNT ===> only semi-conducting

    Large Youngs modulus (=1,1 million MPa , Fe=

    196 000) High strength

    non-biodegradable.

    Physical properties(Ajayan et al. PNAS u December 7, 1999 u vol. 96 u no. 25 u 1419914200)

    semi-conducting (Zigzag (7,0) nanotube )

    metallic (Armchair (5,5) nanotube )

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    Chemical properties

    Nanotubes are composed entirely of sp bonds, similarto graphite.

    Nanotubes naturally align themselves into "ropes" heldtogether by Van der Waals forces.

    Under high pressure, nanotubes can merge together.

    Nonpolar properties:this nonpolarity enables thecoupling of membrane-constituent lipids to the surface ofthe CNT probes.

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    II- Synthesis techniques

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    Fullerenes and carbon nanotubesare commonly formed in such mundaneplaces as candle flames. However,

    these naturally occurring varieties are:

    highly irregular in size and quality,

    the high degree of uniformitynecessary to meet the needs of

    research,

    industry is impossible in such an

    uncontrolled environment.

    Naturally synthetisied CNTs

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    CNTs synthesis techniques:

    High-Pressure CO Conversion (HiPCO) Pulsed-Laser Vaporisation (PLV) Carbon Arc Discharge (CA)

    Chemical Vapor Deposition (CVD)

    The CVD method has shown themost promise in being able toproduce larger quantities ofnanotube (compared to the othermethods) at lower cost. This isusually done by reacting a carbon-containing gas (such as acetylene,ethylene, ethanol, etc.) with a metal

    catalyst particle (usually cobalt,nickel, iron) at temperatures above600C.

    Nanotube production by CVD(J.H. Hafner et al. / Progress in Biophysics &Molecular Biology 77 (2001) 73110)

    catalyst nanoparticles

    Hydrocarbon carbon

    heat

    adsorbtion and precipitation

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    III- General applications

    For nanoelectromechanical systems(NEMS).

    CNT offers possibilities to create futurenanoelectronics devices: transistors, circuits,and computers.

    Great interest in quantum physics.

    Use of nanotubes in incandescent lamps, replacing atungsten filament (Louisiana State University 2004)

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    IV- Interest in biology

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    ===> before any further use for biology, CNTs mustundergo:

    purification (chromatography, centrifugation, filtration)

    Solubilization (covalent or noncovalent functionalizationwith surfactant: SDS, ..)

    ===> BiocompatibilityCytotoxic (C. Klumpp et al. / Biochimica et Biophysica Acta, (2005) -

    article in press-)

    good biocompatibility (J. Chopek et al. / Carbon - article in press-(2006))

    That depends on : purity, composition of CNTs, kind ofcell.

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    Typical configurations utilised in nano-biomaterials applied to medical or biological

    problems (OV Salata, Journal of Nanobiotechnology2004, 2).

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    Overview of possible reactions for the functionalisation of the carbon nanotubesidewall.

    (Z.P. Xu et al. / Chemical Engineering Science 61 (2006) 1027 1040)

    Functionalisation of the carbon nanotube

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    Free of permeabilisation and precise delivery:

    Permeabilisation protocols Undesirable side effects (apoptosis,

    necrosis)Dont diffuse in sufficient

    quantity CNTprobe penetrate easily the membrane of epithelial cell andcontact the nuclear membrane.

    Fluorescent left andphase-contrast imagesof the cell afterpenetration with aCNT probe onto the tipof which Alexa 1363

    fluoresceinyl glycineamide was adsorbed

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    Nanovectors for drug delivery:

    The ability of f-CNT to penetrate into the cells offers the potential of using f-CNT as vehicles for the delivery of small drug molecules

    (Alberto Bianco et al.,Current Opinion in Chemical Biology 2005, 9:674679)

    A- Covalent attachmentof amphotericin B andfluorescein

    isothiocyanate to CNT.

    B- CNT labelled with a

    fluorescent agent were easilyinternalised and could betracked into the cytoplasm orthe nucleus usingepifluorescence and confocal

    microscopy

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    Carbon nanotubes as electronic devices for sensing inaqueous solutions. An AFM image of a portion of thenanotube network (0.5 m on a side) is shown. (Chen et al.,PNAS April 29, 2003 vol. 100 no. 9)

    Sensing in aqueous solutions

    100 nm

    Carbon

    fiber

    Biosensor for amperometricmeasurement (M. Yang et al. /Biomaterials 27 (2006) 246255)

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    (A) Real-time electronic sensing of specific biological recognitionon nanotubes. Scheme for SA recognition with a nanotubecoated with biotinylated Tween.

    Protein and pathogen detection

    Specific detection ofmAbs binding to arecombinant humanautoantigen with a

    nanotube device coatedwith a U1A antigenTween conjugate.

    (Chen et al., PNAS April 29, 2003 vol. 100 no. 9)

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    Structural imaging with carbon nanotube AFM probes(Adam T Woolley et al, Chemistry & Biology 2000, Vol 7 No 11)

    Schematic of an atomic forcemicroscope.

    Isolated IgG molecule imaged with a pore growth MWNT tip(J.H. Hafner et al., 2001 )

    Individual GroES molecule detected with asurface growth SWNT tip

    Covalent functionalization of carbon nanotube AFM tips:

    Surface growth methodforCVD nanotube tip preparation.

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    SEMmicrograph shows the nanoscale interactionbetween the neurite and the nanotube bundles. The

    arrows show the direction of deformation of thenanotube bundles by the extending neurite.

    SEM micrograph indicating guided neurite growthalong long MWNT scaffolds. Neurons show preferentialadhesion as well as proliferation along the MWNTpattern

    Scanning electron micrograph demonstratingguided neurite growth along the MWNT array

    pattern.

    vertical carbon nanotubearrays as support platforms forguiding neurite growth. They can befunctionalized with different biomolecules like neurongrowth factors and adhesion agents ( X. Zhang et al.

    / Sensors and Actuators B 106 (2005) 843850)

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    IV- Perspectives

    Single-cell experimentation

    The attributes, along with their reduced dimensions,make carbon nanotubes a highly attractive platformfor future-generation ultra-sensitive minimally

    invasive bio-molecular probing, single-cellexperimentation, and delivery.

    Nanoscale imaging and measurementsImproved resolution, sensitivity, and reducedartifact effects in nanoscale imaging andmeasurements.

    Best control of CNTs synthesis and purification

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    Conclusion

    The rediscovery of carbon nanotubes has openednew frontiers in the field of nanotechnology and

    nanoscience.

    The future experimental biology will rest onmicrodevices and microsystems built fromnanomaterials like carbon nanotubes.

    Bibli h

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    Bibliography

    Ajayan P. M. etal., Carbon nanotubes: From macromolecules

    to nanotechnology.

    PNAS December 7, 1999 vol. 96 no. 25 u 1419914200

    Bianco Alberto et al., Applications of carbon nanotubes in

    drug delivery.

    Current Opinion in Chemical Biology 2005, 9:674679

    Chen Robert J. et al., Noncovalent functionalization of

    carbon nanotubes for highly specific electronic biosensors.

    PNAS April 29, 2003 ; vol. 100 ; no. 949844989

    Chopek J. et al., In vitro studies of carbon nanotubes

    biocompatibility.

    Carbon (2006) Article in press-

    Hafner J.H. et al., Structural andfunctional imaging with

    carbon nanotube AFM probes

    Progress in Biophysics & Molecular Biology 77 (2001) 73

    110

    Klumpp Cedric et al ., Functionalized carbon nanotubes as

    emerging nanovectors for the delivery of therapeutics.

    Biochimica et Biophysica Acta (2005)- Article in press-

    Kouklin N. A. etal, Carbon nanotube probes for single-cell

    experimentation and assays.

    Applied physics letters 87, 173901 2005

    Panhuis Marc in het, Vaccine Delivery by Carbon

    Nanotubes.

    Chemistry & Biology, Vol. 10, October, 2003,

    Patolsky Fernando et al., Electrical detection of single

    viruses.

    PNAS _ September 28, 2004 , vol. 101, no. 39 , 1401714022

    Raffaellea R.P. et al., Carbon nanotubes for power

    applications.

    Materials Science and Engineering B 116 (2005) 233243

    Salata OV etal., Applications of nanoparticles in biology and

    medicine.

    Journal of Nanobiotechnology 2004, 2

    Woolley Adam T et al, Structural biology with carbonnanotube AFM probes.

    Chemistry & Biology 2000, 7:R193-R204

    Xua Zhi Ping et al., Inorganic nanoparticles as carriers for

    efficient cellular delivery.

    Chemical Engineering Science 61 (2006) 1027 1040

    Zhanga Xuan et al., Guided neurite growth on patterned

    carbon nanotubes.

    Sensors and Actuators B 106 (2005) 843850

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