Eric LECLERC

 

CNRS Researcher since November 2003

AFFILIATION

 

Université de Technologie de Compiègne

Biomechanics and Biomedical Engineering (CNRS-UMR 6600)

Bioengineering Department

Laboratory website: http://www.utc.fr/umr6600/

 

ADDRESS

 

Leclerc Eric

CNRS UMR 6600

Laboratoire de biomécanique et génie biomédical

Université de Technologie de Compiègne

B.P. 20529, 60205 Compiègne, France


CONTACT

 

Tel: 33 (0)3 44 23 79 43,    email: eric.leclerc@utc.fr

 

 

Publication list

 

Research interests

 

My research is focussed on the development of microfluidic and cellular microdevices for in vitro biology investigation. My interest is to build microtools as new tools and alternative methods to characterize biomechanical/biochemical/biological interactions involved in biological systems.  In this frame, I joined the Biomechanics and Biomedical Engineering group of the University and develop a research area at the interface of microtechnology, bioengineering and bioartificial organs groups.

 

 

Related publications

 

Baudoin R., Duval J.L., Griscom L., Baudoin R., Legallais C., Leclerc E., Selective control of liver and kidney cells migration  during organotypic co-cultures inside fibronectin coated rectangular  silicone microchannels,  Biomaterials, accepted , in press

Baudoin R., Corlu A., Griscom L., Legallais C., Leclerc E., Trends in the development of microfluidic cell biochips for in vitro hepatotoxicity, Toxicology in vitro, accepted, in press

Leclerc E., Corlu A., Griscom L., Baudoin R., Legallais C.,Guidance of liver and kidney organotipic cultures inside rectangular silicone microchannels,  Biomaterials, 27:22, 4109-4119, 2006

Leclerc E., David B., Griscom L., Lepioufle B., Fujii T., Sakai Y., Legallais C., Perfusion culture of mammalian cells in microfluidic environments for tissue engineering applications, La houille blanche, 3, 2006

Leclerc E., David B., Griscom L., Lepioufle B., Fujii T., Layrolle P., Legallais C.,  Study of osteoblastic cells in a microfluidic environment,  Biomaterials, 27:4, 586-595, 2006

 

 

 

PREVIOUS POSITION

                

02/2001 – 10/2003 junior researcher in the laboratory of the Pr Teruo Fujii at the Institute of Industrial Science at the Tokyo University in the frame of LIMMS (Laboratory of Integrated Micro-Mechatronic Systems)

 

 

EDUCATION

 

10/1997 - 11/2000      PhD Student in Fluids Mechanics and Energetics at the CEA (French Nuclear Energy Commission) at the Thermalhydraulics and Physics Department

   1996   -     1997       M.D. Student in Paris VI University (http://www.lmm.jussieu.fr/DEA/dea.html)

   1995   -     1996       Undergraduate Student in Marseille II University

 

 

 

PREVIOUS RESEARCH PROJECTS

 

 

   2003       Research Project (30 months):

 

Abstract

 

We fabricated various types of bioreactors composed of microstructured PolyDiMethylSiloxane (PDMS) or biodegradable (pCLLA acrylate) polymers layers for perfusion culture of mammalian cells such as hepatocytes.  During the perfusion culture of the bioreactors for one week to two weeks, cells showed good attachment, spreading and reached their confluence over the channels of the bioreactors.  In addition, the albumin production of the hepatocytes was significantly enhanced in the perfusion culture using the PDMS bioreactors when compared in dish-level static culture.  Although, the cellular activities of the cells are still low even compared to in vivo tissue, the conclusions of this work is encouraging toward future liver tissue engineering based on in vitro propagation and maturation of hepatocyte combined with microfabrication technologies.

 

Keywords: PDMS micro fabrication, bioreactors, tissue cell cultures, perfusion

 

Contact : eric.leclerc@utc.fr

Contact : tfujii@iis.u-tokyo.ac.jp

Related websites:

Pr Fujii laboratory

LIMMS

 

Linked publications:

 

Patends:

 

Fujii T, Sakai Y , Leclerc E, brevet japonais (en japonais, « cell culture chamber ») no 2002-321859

Fujii T, Sakai Y , Leclerc E, brevet japonais (en japonais, « cell culture device, bioreactor and cell culture chamber »)  no 2002-316136

 

Papers in journals

 

Leclerc E. Sakai Y., Fujii T., Cells culture in a three-dimensional network of PDMS (PolyDiMethylSiloxane) microchannels, biomedical microdevices, 5:2, 109-114, 2003

Leclerc E., Sakai Y. and Fujii T., A microfluidic PDMS (polydimethylsiloxane) bioreactor for large-scale culture of hepatocytes, in press, available on the web, Biotechnology Progress

Leclerc E., Sakai Y., Fujii T., Perfusion Culture of Fetal Human Hepatocytes in Microfluidic-Environments, in press, available on the web, Biochemical Engineering Journal

Leclerc E., Furukawa K.S., Miyata F., Sakai Y.,Ushida T., Fujii T., Fabrication of microstructures in photosensitive biodegradable polymers for tissue engineering applications,  Biomaterials, 25, 4683-4690, 2004

Leclerc E., Furukawa K.S., Miyata F., Sakai Y., Ushida T., Fujii T., Effect on liver cells of stepwise microstructures fabricated in a photosensitive biodegradable polymer by softlithography, Materials Science and Engineering: C, 24:3, 349-354, 2004

 

Lattest conferences:

 

Leclerc E., Sakai Y. and Fujii T., A Multi-Layer PDMS Microfluidic Device for Tissue Engineering Applications, Proc. of MEMS-2003, Kyoto, Japan, 2003

Leclerc E, Sakai Y, Fujii T, Fetal Human Hepatocytes and Endothelial Cells co-culture in a microfluidic environment, Proc of mTAS-2003, Tahoe Lake, USA, 2003

Leclerc E., Furukawa K. S., Miyata, F., Sakai, Y., and Fujii, T., A Bioreactor for Continuous Perfusion Cell Culture Fabricated with Photosensitive Biodegradable Polymer, Proc. of Transducers-2003, Boston, USA, 2003

 

 

2000                          Research Project (36 months):

 

“Study and simulation of the growing and propagation phases of a steam explosion in the

                   framework of severe accidents occurring in pressurized water nuclear reactor”

 

 

Abstract:

 

In hypothetical Severe Accident studies for a PWR, a large amount of molten corium may be poured into water. There is then a risk of Steam Explosion. After the premixing sequence in which the melt is more or less dispersed into water, a fine fragmentation process may start which can lead to an escalation. Such an event is generally triggered by the destabilization of the vapor film surrounding the hot melt droplets. In this work, an attempt to describe all the successive processes leading to this fine fragmentation is presented. First a critical analysis of previous models is performed, allowing us to propose a new sequence of events. As in the previous models, the film destabilization leads to the growth of cold liquids peaks induced by Rayleigh Taylor instability. As these peaks have a smaller density than the drop, they do not penetrate into the hot drop. At the cold liquid-hot liquid contacts, transient heat transfer leads to the explosive boiling of a small amount of coolant. The generated local pressurization deforms the hot melt interface. This can produce fine fragments from the filaments issued from the melt. Some of them may reach the vapor-coolant interface where intense and rapid vaporization occurs. A large bubble then develops and a new fragmentation sequence may again appear at the bubble collapse. The present model is supported by experimental results.

 

Keywords: Intense vaporization, thermal fragmentation, steam explosion

 

Contact : eric.leclerc@utc.fr

Contact : georges.berthoud@cea.fr

 

Linked publication:

 

 

Leclerc E, Berthoud G, Modeling of melt droplet fragmentation following vapor film destabilisation by a trigger pulse, Nuclear Technology,  144:2, 158-174, 2003

 

 

 

 

    1997            Master thesis keeping terms (4 months):

 

                   “Experimental and analytic study of the influence of downstream flow conditions on Mach stem

                    height”, Laboratoire du  CNRS d’Aérothermique de Meudon .

 

Abstract:

            An experimental work on the influence of downstream flow expansion process on Mach stem height has been carried out in steady hypersonic flows. The results showed clearly for the first time that the Mach stem height does not depend on the extent of expansion fan. These results contradict recent analytical findings from which a strong influence of downstream flow conditions on Mach stem height may be expected.

Keywords: Mach reflection, Mach stem, Expansion fan, Supersonic flow

Contact : eric.leclerc@utc.fr

Contact: A.Chpoun@iut.univ-evry.fr

Website: http://web.cnrs-orleans.fr/~webaero/index.html

 

 

Linked publication:

 

Chpoun A, Leclerc E, Experimental investigation of the influence of downstream flow conditions on Mach Stem height, Shock Waves, 9 : 269-271, 1999

 

 

 

    1996             Undergraduate project (4 months):

 

                     « Influence of hoar-frost on the helicopter rotor screw »

                     Laboratory of the University of Aix Marseille II, with a mentor of Eurocopter INC (http://www.eurocopter.com/)