Download Abstract: Ever since Giovanni Borelli`s seminal De Motu Animalium

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

Extracellular matrix wikipedia , lookup

Cell cycle wikipedia , lookup

Cellular differentiation wikipedia , lookup

Cytokinesis wikipedia , lookup

Cell growth wikipedia , lookup

Cytoplasmic streaming wikipedia , lookup

Mitosis wikipedia , lookup

Cell encapsulation wikipedia , lookup

Cell culture wikipedia , lookup

JADE1 wikipedia , lookup

Amitosis wikipedia , lookup

Mechanosensitive channels wikipedia , lookup

Tissue engineering wikipedia , lookup

List of types of proteins wikipedia , lookup

Organ-on-a-chip wikipedia , lookup

Transcript
Abstract:
Ever since Giovanni Borelli’s seminal De Motu Animalium of 1680 [1] the interpretation of
organismic structures as working machines has been a powerful tool in analysis of organismic
activities. Although this synergism expressed by Borelli long back were not really metaphorical
but more based on the fact that human and animal muscles were the actual workhorses of most
machines in his time, still scientists look at this as a seminal point for starting of a perfect
congruence or synergism between Biology and machines. Getting inspired by this synergism
many researchers of modern times have expressed great interest in finding out biological
macromolecules which would work as molecular machines and would do some useful and
important [2‐4]. So a whole new paradigm of biomimetics (literally meaning : copying life) have
emerged. This can be broadly defined as the translation of insights which one gets from pure
biological research into realizable technology. [5] Miniaturization technology starting with the
famous talk by Sir Richard Feynman, “There is plenty of room at the bottom” has lead to the
mimicking and realization of newer phenomena both physiological and physical at the micro and
nano scales. The advantages that miniaturization offers is the realization of physical systems at
scales and dimensions similar to biological entities such as bacterial and mammalian cells,
viruses, spores, etc. which further leads to enhancement in our capabilities to mimick biological
systems with better sensing capabilities, accuracy of physical manipulation and control. In this
respect it is worth mentioning that almost 70‐80% of any living organism is a fluid and thus
would need transport. The transport network that our vasculatures and other mechanisms provide
is either through hair like capillaries or in some cases through molecular channels. These flow
networks can easily be mimicked by a network of micro‐fluidic channel and so bio‐mimetics is
strongly synergistic with micro‐fluidics. Literature reviews several areas wherein the
micro‐fabrication technologies are bio‐inspired mimic some biological phenomena. Bitensky
et. al. [6] have demonstrated a set of micro‐channel architecture which is used to separate
leukocytes from whole blood samples. This architecture mimics the intrinsic features of blood
flow in microcirculation, such as plasma skimming and leukocyte margination as happens within
the vasculature and is able to generate a 34 fold enrichment of the leukocytes thus alternates the
time consuming buffy coat process of extracting leukocytes from blood samples. Wheleer et. al.
[7] have demonstrated a biomimetic micro‐channel invitro fertilization system which reduces
poly‐spermy and therefore increases the number of potentially viable embryos without reducing
the overall invitro production efficiency. In vivo the sperm is guided to the oocyte via a
narrowing fluid path in the oviduct . The micro‐channel design is made in PDMS with a
constriction of 20 microns thickness placed centrally in another 1000 microns X 250 microns X
38 mm channel which would hold the Oocytes in place near the center f the micro‐channels
while allowing the sperm and media to flow through the outlet. In a similar mode of cell culture
experiments we plan to incubate biological cells in microfabricated channels to study cell
proliferation using the microscopy technique. In particular, we plan to study a three dimensional
network of micro‐channels made within PDMS and agarose gels for observing a directional
growth of human Osteoblast and Fibroblast cells in vitro based on different flow directions of the
nutrient media. The experimental observations will be analysed in terms of the cell viability
index as well as the cell adhesion on the micro‐channel network and cell‐cell interactions will be
investigated. This is vital from a standpoint of mimicking the in vivo conditions of an
implantable material to get an idea of the pattern of cell growth within micro‐channels. We have
been able to synthesize a dense array of microchannels in PDMS using a simplistic replication
technique using chemically etched copper wires [8,9]. We are also currently trying to use
a microchannel architecture to study vibration isolation behavior. In another mode of
experiments we intend to design, fabricate and develop a biochip with a rapid
dielectrophoretically assisted concentration and molecular identification of food pathogens in
micro-channels. We have been able successfully able to get a very good dielectrophoretic
entrapment within these architectures using fluorescent microbeads and alternating electric fields
of 10 Volt peak to peak at an operational frequency of 10KHz.[14]Fluorescence techniques are
developed to rapidly quantitate the beads. This technology is currently also being tried in Green
fluorescent protein expressed E. Coli BL-21 cells. We are planning to add on the other molecular
identification modules to this biochip.[10,11, 12] We have also been able to do microscale
fluidic transport and mixing experiments which has produced some novel prototypes and
products capable of integration to biosensors and detectors. [13,14,15] Thus in a nutshell
bioinspired microfluidics can be applied to several important real life requirements and can also
enhance sensitivity, speed and accuracy of detection.
Brief Curriculum Vitae of Dr. Shantanu Bhattacharya:
Professor Shantanu Bhattacharya currently teaches at the Department of Mechanical Engineering
at the Indian Institute of Technology at Kanpur. He is running a MEMS program and is in the
process of setting up a state of the art Microsystems fabrication laboratory within the department
of Mechanical Engineering.
Dr. Bhattacharya has prior to this done his B. Tech. from the Delhi College of Engineering in
1996 and then an M.S. degree in Mechanical Engineering from Texas Tech University, Lubbock,
Texas in 2003. He completed his Ph.D.in Biomedical Engineering from The University of
Missouri at Columbia in 2006 and served as a Post Doctoral Research Associate at the Birck
Nanotechnology Center, Purdue University, Indiana, USA.
Dr. Bhattacharya has served as a senior engineer at Suzuki Motors Corporation for 6 years prior
to his MS degree. His research interests are BioMEMS, Nanotechnology, Novel Microfabrication Techniques, Nano-energetics and Microfluidics.