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MICROBIVORES
GUIDED BY:
PARVATHY S B
ASSISTANT PROFESSOR
DEPARTMENT OF ECE
ACE COLLEGE OF ENGINEERING
PRESENTED BY:
AMAL B R
ROLL NO -14441003
S7-ECE
OUTLINE
AIM
 INTRODUCTION
VARIOUS CONDITIONS IN BODY
PRIMARY PHAGOCYTIC SYSTEMS
APPLICATIONS
 ADVANTAGES
DISADVANTAGES
CONCLUSION
REFERENCES
2
AIM
To know about the ideal nanotechnology-based
drug delivery system and its various features.
3
INTRODUCTION
Microbivores in simple terms means microbiological pathogens destroyer.
 It is an ideal nanotechnology-based drug delivery system which is—self- powered, computer-controlled medical
nanorobot system capable of digitally precise transport, timing, and targeted delivery of pharmaceutical agents to
specific cellular and intracellular destinations within the human body.
VARIOUS CONDITIONS
IN BODY
 SEPSIS
 SEPTICEMIA
 BACTEREMIA
 PHAGE THERAPY
5
MICROBIVORE
Artificial white blood cell or nanorobotic phagocytes.
Spheroid device 3.4 µm in diameter.
Consist of 610 billion precisely arranged atoms.
Traps blood pathogens & breaks them.
1000 times faster than white blood cells.
6
PRIMARY PHAGOCYTIC
SYSTEMS
Reversible microbial binding sites
Telescoping grapples
Morcellation chamber
Digestion chamber
Ejection piston and exhaust port
Power supply and fuel buffer tankage
Sensors
7
REVERSIBLE
MICROBIAL BINDING
SITES
Acquire a pathogen to be digested.
 A collision between a bacterium and the
nanorobotic device allows to recognize reversible
binding sites.
 Bacteria employ right-handed amino acids in
their cellular coats.
8
TELESCOPING
GRAPPLES
Telescoping robotic grapples establish secure
anchorage to the microbe's plasma membrane.
Grapple force sensors inform the onboard
computer of the captive microbe's footprint size
and orientation.
9
MORCELLATION
CHAMBER & DIGESTION
CHAMBER
The bacterium is internalized into the
morcellation chamber.
Bacterium is minced into nanoscale pieces.
Remains are pistoned into the digestion
chamber which consists of a pre-programmed set
of digestive enzymes.
These enzymes are injected and extracted 6
times during a single digestion cycle.
10
EJECTION PISTON AND
EXHAUST PORT
Egestion is an annular-shaped ejection piston
comprised of a 20-nm thick piston pusher plate
driven by at least two 2-micron long.
Afterwards, the piston is retracted, effectively
pulling a vacuum in the DC in preparation to
receive the next batch of morcellate from the MC.
Exhaust port door must be opened prior to
activation of the ejection piston to allow the
digesta to escape.
11
SENSORS
The microbivore needs a variety of external
and internal sensors to complete its tasks.
 External sensors include chemical sensors for
glucose, oxygen, carbon dioxide.
Acoustic communication sensors mounted
within the nanorobot hull permit the microbivore
to receive external instructions from the
attending physician.
12
Want big impact?
Use big image.
13
APPLICATIONS
14
Drug delivery
Body surveillance
Surgery
Cancer detection and treatment
Gene therapy
 Diabetes treatment
ADVANTAGES
15
Most animal cells are 10,000 to 20,000 nm in diameter so microbivores are easy to inject.
 Glucose or natural body sugars and oxygen might be a source for propulsion.
1000 times faster & 80 times more efficient than natural phagocytes.
Completely destroy one pathogen in just 30 seconds.
DISADVANTAGES
16
Change in behaviour at nano level,may not be suitable for body.
High cost
Larger nanoparticles may accumulate in vital organs.
Nanorobots of larger size will block capillary flow.
The concept of microbivores is just a
theoretical justification till now.
But the recent advancement in the field of
nanotechnology gives the hope of the
effective use of this technology in medical
field.
Diseases like AIDs , cancer can be treated
permanently at any stage using these
technologies.
.17
CONCLUSION
REFERENCES
www.ijtra.com Special Issue 41 (AVALON) (March 2016), PP. 70-74
http://www.imm.org/publications/reports/rep025/
http://www.kurzweilai.net/meme/frame.html?main=/articles/art0453.html?
http://www.rfreitas.com/Nano/Microbivores.htm
Soft Machines: Nanotechnology and Life by Richard Anthony Lewis Jones
www.nanomedicine.org
www.nanorobots.com
18
19
Thanks!

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Btech Final Seminar Topic Microbivore

  • 1. MICROBIVORES GUIDED BY: PARVATHY S B ASSISTANT PROFESSOR DEPARTMENT OF ECE ACE COLLEGE OF ENGINEERING PRESENTED BY: AMAL B R ROLL NO -14441003 S7-ECE
  • 2. OUTLINE AIM  INTRODUCTION VARIOUS CONDITIONS IN BODY PRIMARY PHAGOCYTIC SYSTEMS APPLICATIONS  ADVANTAGES DISADVANTAGES CONCLUSION REFERENCES 2
  • 3. AIM To know about the ideal nanotechnology-based drug delivery system and its various features. 3
  • 4. INTRODUCTION Microbivores in simple terms means microbiological pathogens destroyer.  It is an ideal nanotechnology-based drug delivery system which is—self- powered, computer-controlled medical nanorobot system capable of digitally precise transport, timing, and targeted delivery of pharmaceutical agents to specific cellular and intracellular destinations within the human body.
  • 5. VARIOUS CONDITIONS IN BODY  SEPSIS  SEPTICEMIA  BACTEREMIA  PHAGE THERAPY 5
  • 6. MICROBIVORE Artificial white blood cell or nanorobotic phagocytes. Spheroid device 3.4 µm in diameter. Consist of 610 billion precisely arranged atoms. Traps blood pathogens & breaks them. 1000 times faster than white blood cells. 6
  • 7. PRIMARY PHAGOCYTIC SYSTEMS Reversible microbial binding sites Telescoping grapples Morcellation chamber Digestion chamber Ejection piston and exhaust port Power supply and fuel buffer tankage Sensors 7
  • 8. REVERSIBLE MICROBIAL BINDING SITES Acquire a pathogen to be digested.  A collision between a bacterium and the nanorobotic device allows to recognize reversible binding sites.  Bacteria employ right-handed amino acids in their cellular coats. 8
  • 9. TELESCOPING GRAPPLES Telescoping robotic grapples establish secure anchorage to the microbe's plasma membrane. Grapple force sensors inform the onboard computer of the captive microbe's footprint size and orientation. 9
  • 10. MORCELLATION CHAMBER & DIGESTION CHAMBER The bacterium is internalized into the morcellation chamber. Bacterium is minced into nanoscale pieces. Remains are pistoned into the digestion chamber which consists of a pre-programmed set of digestive enzymes. These enzymes are injected and extracted 6 times during a single digestion cycle. 10
  • 11. EJECTION PISTON AND EXHAUST PORT Egestion is an annular-shaped ejection piston comprised of a 20-nm thick piston pusher plate driven by at least two 2-micron long. Afterwards, the piston is retracted, effectively pulling a vacuum in the DC in preparation to receive the next batch of morcellate from the MC. Exhaust port door must be opened prior to activation of the ejection piston to allow the digesta to escape. 11
  • 12. SENSORS The microbivore needs a variety of external and internal sensors to complete its tasks.  External sensors include chemical sensors for glucose, oxygen, carbon dioxide. Acoustic communication sensors mounted within the nanorobot hull permit the microbivore to receive external instructions from the attending physician. 12
  • 13. Want big impact? Use big image. 13
  • 14. APPLICATIONS 14 Drug delivery Body surveillance Surgery Cancer detection and treatment Gene therapy  Diabetes treatment
  • 15. ADVANTAGES 15 Most animal cells are 10,000 to 20,000 nm in diameter so microbivores are easy to inject.  Glucose or natural body sugars and oxygen might be a source for propulsion. 1000 times faster & 80 times more efficient than natural phagocytes. Completely destroy one pathogen in just 30 seconds.
  • 16. DISADVANTAGES 16 Change in behaviour at nano level,may not be suitable for body. High cost Larger nanoparticles may accumulate in vital organs. Nanorobots of larger size will block capillary flow.
  • 17. The concept of microbivores is just a theoretical justification till now. But the recent advancement in the field of nanotechnology gives the hope of the effective use of this technology in medical field. Diseases like AIDs , cancer can be treated permanently at any stage using these technologies. .17 CONCLUSION
  • 18. REFERENCES www.ijtra.com Special Issue 41 (AVALON) (March 2016), PP. 70-74 http://www.imm.org/publications/reports/rep025/ http://www.kurzweilai.net/meme/frame.html?main=/articles/art0453.html? http://www.rfreitas.com/Nano/Microbivores.htm Soft Machines: Nanotechnology and Life by Richard Anthony Lewis Jones www.nanomedicine.org www.nanorobots.com 18