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05 - BOE - Module 3 - Anatomical Principal BD Part 1

The document discusses the adaptation of anatomical principles for bioengineering design, highlighting the human body's organ systems and their functions. It covers bio-design, brain-computer interfaces, the nervous system, signal transmission, and advancements in prosthetics, particularly in relation to Parkinson's disease. Additionally, it compares the human eye to a camera, detailing optical corrections and lens materials used for vision correction.

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Sahana G
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0% found this document useful (0 votes)
17 views96 pages

05 - BOE - Module 3 - Anatomical Principal BD Part 1

The document discusses the adaptation of anatomical principles for bioengineering design, highlighting the human body's organ systems and their functions. It covers bio-design, brain-computer interfaces, the nervous system, signal transmission, and advancements in prosthetics, particularly in relation to Parkinson's disease. Additionally, it compares the human eye to a camera, detailing optical corrections and lens materials used for vision correction.

Uploaded by

Sahana G
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd
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BIOLOGY FOR ENGINEERS

MODULE - 3

ADAPTATION OF ANATOMICAL
PRINCIPLES FOR
BIOENGINEERING DESIGN
MODULE-3 (5 HOURS)

ADAPTATION OF ANATOMICAL PRINCIPLES FOR


BIOENGINEERING DESIGN:
 Brain As A CPU System.
 Eye As A Camera System.
 Heart As A Pump System.
 Lungs As Purification System.
 Kidney As A Filtration System.
HUMAN ORGAN SYSTEMS
The Human Body Is A
Biological Machine
Made Of Body Systems;
Groups Of Organs That Work Together
To Produce & Sustain Life.
ORGAN SYSTEMS
BIO-DESIGN
BIO-DESIGN

 Bio Design Is Use Of Living Organisms In Design.


 Its Processes Can Be Used In Creation Of Fashion,
Textiles, Furniture & Architecture.
 Its An Emerging Design Movement Which Incorporates
The Use Of Living Materials, Or ‘Moist Media,’ Such As
Fungi, Algae, Yeast, Bacteria, & Cultured Tissue.
 The Idea Is To Create A Product Whose Properties Are
Enhanced As A Result Of The Use Of These Living
Materials.
BIO-DESIGN

 Transforming Engineered Yeast Cells Into


Collagen Leather & Spider Silk Threads.
 Making Mycelium (Mushroom Fungus) Into
Leather & Chairs.
 A Leather Substitute Made Of Shells From
Seafood Waste & Coffee Grounds.
BRAIN AS A CPU SYSTEM
BRAIN AS A CPU SYSTEM

 Both CPU & Brain Use Electrical Signals


To Send Messages.
 The Brain Uses Chemicals To Transmit
Information & Computer Uses Electricity.
 Both Transmit Information.
BRAIN COMPUTER INTERFACE
BRAIN COMPUTER INTERFACE

A BCI System Is A Computer Based System


That Takes Brain Signals,
Analyses Them & Translates Them
Into Commands That Are Relayed To
A Device To Trigger; A Desired Action.
BRAIN COMPUTER INTERFACE
 A BCI System Is Used To Measure Signals Produced By Central
Nervous System.
 It Allow Users To Act In Their Environment When They Want It
By Reading Their Brain Signals Rather Than Muscles.
 The User, After A Training Session, Produces Brain Signals
Encoded By BCI System.
 The BCI Then Translates These Commands & Transmits Them
Into An Output Device.
 Thus, A Sensor That Is Activated By Voice Or Movement Of
Muscle Is Not A BCI System.
BRAIN COMPUTER INTERFACE
NERVOUS SYSTEM
NERVOUS SYSTEM

 The Nervous System Has 2 Main Parts:


 The Central Nervous System Is Made Up Of The
Brain & Spinal Cord.
 The Peripheral Nervous System Is Made Up Of
Nerves That Branch Off From The Spinal Cord &
Extend To All Parts Of Body.
NERVOUS SYSTEM: CNS

 CNS Includes Brain & Spinal Cord.


 The Brain Is Body’s “Control Center”.
 The CNS Has Various Centers Located Within It That
Carry Out The Sensory, Motor & Integration Of Data.
 These Centers Can Be Subdivided To Lower Centers
(Including The Spinal Cord & Brain Stem) & Higher
Centers Communicating With The Brain Via Effectors.
NERVOUS SYSTEM: CNS
NERVOUS SYSTEM: PNS

 PNS Is A Vast Network Of Spinal & Cranial


Nerves That Are Linked To Brain & Spinal Cord.
 It Contains Sensory Receptors Which Help In
Processing Changes In Internal & External
Environment.
 This Information Is Sent To The CNS Via Afferent
Sensory Nerves.
NERVOUS SYSTEM: PNS

 The PNS Is Then Subdivided Into Autonomic


Nervous System & Somatic Nervous System.
 The Autonomic Has Involuntary Control Of
Internal Organs, Blood Vessels, Smooth & Cardiac
Muscles.
 The Somatic Has Voluntary Control Of Skin,
Bones, Joints, & Skeletal Muscle.
NERVOUS SYSTEM: PNS
SIGNAL TRANSMISSION
SIGNAL TRANSMISSION

 A Neuron Sending A Signal (Presynaptic Neuron)


Releases A Chemical Called A Neurotransmitter, Which
Binds To A Receptor On The Surface Of Receiving;
Postsynaptic Neuron.
 Neurotransmitters Are Released From Presynaptic
Terminals, Which May Branch To Communicate With
Several Postsynaptic Neurons.
 Axon Terminals Are Where Neurotransmission Begins.
SIGNAL TRANSMISSION

 At Axon Terminals Where The Neuron Sends Its


OUTPUT To Other Neurons.
 At Electrical Synapses, The OUTPUT Will Be The
Electrical Signal Itself.
 At Chemical Synapses, The OUTPUT Will Be
Neurotransmitter.
 The Correct Outline For The Sequence Of Transmission
Of An Electrical Impulse Through A Neuron Is
Dendrites, Cell Body, Axon, Axon Terminal.
SIGNAL TRANSMISSION
ELECTRO ENCEPHALO GRAM
ELECTRO ENCEPHALO GRAM
 An Electroencephalogram (EEG) Is A Test That
Measures Electrical Activity In Brain Using Small, Metal
Discs (Electrodes) Attached To The Scalp.
 Brain Cells Communicate Via Electrical Impulses & Are
Active All The Time, Even During Asleep.
 This Activity Shows Up As Wavy Lines On An EEG
Recording.
 EEG Can Detect Abnormal Electrical Discharges Such
As Sharp Waves, Spikes Or Spike & Wave Complexes
That Are Seen In People With Epilepsy.
ELECTRO ENCEPHALO GRAM
ELECTRO ENCEPHALO GRAM
 An EEG Might Also Be Helpful For Diagnosing Or
Treating:
 Epilepsy Or Another Seizure Disorder.
 Brain Tumors.
 Brain Damage From Head Injury.
 Brain Dysfunction That Can Have A Variety Of Causes
(Encephalopathy).
 Sleep Disorders.
 Inflammation Of Brain (Herpes Encephalitis).
 Stroke.
 Brain Death In A Persistent Coma.
ELECTRO ENCEPHALO GRAM
 Derivatives Of The EEG Technique Include :
 Evoked Potentials (EP):
• Involves Averaging EEG Activity Time Locked To
Presentation Of A Stimulus Of Some Sort e.g. Visual,
Somatosensory Or Auditory.
 Event Related Potentials (ERPS):
• Refer To Averaged EEG Responses That Are Time
Locked To More Complex Processing Of Stimuli; This
Technique Is Used In Cognitive Science, Cognitive
Psychology, & Psychophysiological Research.
ELECTRO ENCEPHALO GRAM
ROBOTIC ARMS
FOR PROSTHETICS
ROBOTIC ARMS FOR PROSTHETICS

Robotic Prosthetic Limb Is A Well Established


Research Area That Integrates
Advanced Mechatronics, Intelligent Sensing
& Control For Achieving Higher Order Lost
Sensorimotor Functions While Maintaining
The Physical Appearance Of Amputated Limb.
ROBOTIC ARMS FOR PROSTHETICS
 Robotic Prosthetic Limbs Are Expected To Replace The
Missing Limbs Of An Amputee Restoring The Lost
Functions & Providing Aesthetic Appearance.
 The Main Aspects Are Enhanced Social Interaction,
Comfortable Amputee’s Life & Productive Amputee To
Society.
 Most Current Robotic Prostheses Work By Recording
From Surface Of Skin Electrical Signals From Muscles
Left Intact After An Amputation.
ROBOTIC ARMS FOR PROSTHETICS
 Robotic Arms Can Be Used To Automate The
Process Of Placing Goods Or Products Onto
Pallets.
 By Automating The Process, Palletizing Becomes
More Accurate, Cost Effective & Predictable.
 The Use Of Robotic Arms Also Frees Human
Workers From Performing Tasks That Present A
Risk Of Bodily Injury.
ROBOTIC ARMS FOR PROSTHETICS
ROBOTIC ARMS FOR PROSTHETICS
ROBOTIC ARMS FOR PROSTHETICS
PARKINSON’S DISEASE
PARKINSON’S DISEASE

 Parkinson’s Disease Is A Progressive Disorder


That Affects The Nervous System & The Parts Of
Body Controlled By Nerves.
 In Parkinson’s Disease, Certain Nerve Cells
(Neurons) In Brain Gradually Break Down Or Die.
 Many Of The Symptoms Are Due To A Loss Of
Neurons That Produce A Chemical Messenger In
Brain Called ‘Dopamine’.
PARKINSON’S DISEASE

 Symptoms Start Slowly.


 The First Symptom May Be A Barely Noticeable Tremor In
Just One Hand.
 Tremors Are Common, But Disorder May Also Cause
Stiffness Or Slowing Of Movement.
 Parkinson’s Disease Can’t Be Cured, But Medications Can
Help Control Symptoms, Often Dramatically.
 In Some More Advanced Cases, Surgery May Be Advised.
ENGINEERING SOLUTIONS
FOR THIS DISEASE
PARKINSON’S DISEASE

ENGINEERING SOLUTIONS

DEEP BRAIN STIMULATION


DEEP BRAIN STIMULATION
 Deep Brain Stimulation (DBS) Involves Surgically Implanting
A Neurotransmitter That Sends Electrical Impulses To Specific
Areas Of Brain.
 This Procedure Has Helped Many People With Parkinson’s
Reduce Symptoms Such As Tremor, Rigidity & Bradykinesia.
 There Are 6 Main Types Of Medications Available To Treat
Symptoms Of Parkinson Disease:
 Levodopa, Dopamine Agonists, Inhibitors Of Enzymes That
Inactivate Dopamine Inhibitors, Catechol-O-Methyl
Transferase (COMT) Inhibitors, Anti-Cholinergic Drugs &
Amantadine.
DEEP BRAIN STIMULATION
ENGINEERING NEURONS
ENGINEERING NEURONS

 Transplantation Of Embryonic Neurons Can


Restore Functional Dopaminergic Neurons In
Brains Of Patients With Parkinson’s Disease.
 But While Promising, Cell Transplantation
Therapy Is Still Out Of Reach To Most Patients, In
Part Because Of The Inaccessibility Of Human
Embryonic Tissue.
ENGINEERING NEURONS

 First Obtained Neuronal Stem Cells From Mouse Cells


Transfected With A Transcription Factor That Encourages
Cells To Adopt A Neuronal Fate.
 Then Co-cultured The Cells With Astrocytes, Which
Release A Factor That Induces Development Into
Dopaminergic Neurons.
 The Engineered Cells Released Dopamine & Some
Maintained Characteristics Of Dopaminergic Neurons For
Up To 2 Weeks After Implantation Into Mouse Brains.
ENGINEERING NEURONS
THE HUMAN EYE
EYE VS CAMERA
THE HUMAN EYE VS CAMERA

 He Human Eye Is A Wonderful Instrument,


Relying On Refraction & Lenses To Form
Images.
 There Are Many Similarities Between The
Human Eye & A Camera, Including:
THE HUMAN EYE VS CAMERA

 A Diaphragm To Control The Amount Of Light That


Gets Through To The Lens:
 This Is The Shutter In A Camera, & The Pupil, At
The Centre Of The Iris, In The Human Eye.
THE HUMAN EYE VS CAMERA

 A Lens To Focus The Light & Create An Image.


 The Image Is Real & Inverted.
THE HUMAN EYE VS CAMERA

 A Method Of Sensing The Image.


 In A Camera, Film Is Used To Record The Image; In
The Eye, The Image Is Focused On The Retina.
RODS & CONES
RODS & CONES
 Photoreceptors In Eye Are Localized Around An Area
Near Centre Of Retina Called Macula, Which Is
Functional Centre Of Retina.
 The Fovea Is Located In Centre Of The Macula.
 The Macula Is Responsible For High Resolution,
Colour Vision, Provided By Different Types Of
Photoreceptors.
 Photoreceptors In The Retina Are Classified Into 2
Groups, Named After Their Physical Morphologies.
RODS & CONES

 Rod Cells Are Highly Sensitive To Light &


Function In Night Vision.
 Whereas Cone Cells Are Capable Of Detecting
A Wide Spectrum Of Light Photons & Are
Responsible For Colour Vision.
 Rods & Cones Are Structurally
Compartmentalized.
RODS & CONES
 They Consist Of 5 Principal Regions:
 Outer Segment.
 Connecting Cilium.
 Inner Segment.
 Nuclear Region.
 Synaptic Region.
RODS & CONES
 Rods Are Responsible For Vision At Low Light Levels
(Scotopic Vision), They Do Not Mediate Colour
Vision & Have A Low Spatial Acuity.
 Cones Are Active At Higher Light Levels (Photopic
Vision), Are Capable Of Colour Vision & Are
Responsible For High Spatial Acuity.
 The Central Fovea Is Populated Exclusively By
Cones.
 Visible Spectrum For Human Eye Is From About 380
To About 750 Nanometers.
RODS & CONES
 There Are 3 Types Of Cones:
 The Short-Wavelength Sensitive Cones (S-Cone).
 The Middle-Wavelength Sensitive Cones (M-Cones).
 The Long-Wavelength Sensitive Cones (L-Cones).
OPTICAL CORRECTIONS
OPTICAL CORRECTIONS
 The Ability To See Images Or Objects With Clear,
Sharp Vision Results From Light Entering The Eye.
 Light Rays Bend Or Refract When They Hit The
Retina, Sending Nerve Signals To The Optic Nerve,
Which Then Sends These Signals To The Brain.
 The Brain Processes Them Into Images, Allowing You
To Understand What You See.
 When These Light Rays Bend Incorrectly, It Results In
A Refractive Error & Typically Causes Blurry Or
Cloudy Vision.
OPTICAL CORRECTIONS

 Since The Primary Cause Of Vision Problems Is


Caused By Light Bending Incorrectly As It Enters The
Eye, Virtually Any Method Of Treatment That Changes
This Can Be Categorized As A Form Of Vision
Correction.
 A Slight Modification Of Geometrically Correct Lines
For Purpose Of Making Them Appear Correct To The
Eye.
OPTICAL CORRECTIONS

 Eyeglasses & Contact Lenses:


 The Most Common Types Of Corrective Measures,
Always Recommended As First Course Of
Treatment For Vision Problems.
 While They Are Considered Very Basic Method Of
Vision Correction, They Are Unable To Control The
Refractive Error From Progressing.
 Patients Whose Vision Worsens Over Time Need
New Glasses Or Contacts Lenses.
LENS MATERIALS
LENS

 Corrective Sphero-Cylindrical Lenses Are Commonly


Used To Treat Refractive Errors Such As Myopia,
Hyperopia, Presbyopia, & Astigmatism.
 Both Lenses & Prisms Are Also Frequently Used To
Improve Eye Alignment & Treat Diplopia In
Strabismus.
 Eyeglasses Also Serve An Important Role In Protecting
The Eyes From Physical Trauma & Harmful
Radiation.
LENS MATERIALS
 Lenses Can Be Produced Using A Variety Of Materials
& Designed With Several Optical Profiles To Optimize
Use In Specific Applications.
 Critical Lens Properties Include Refractive Index,
Abbe Number (Chromatic Dispersion), Specific
Gravity, & Ultraviolet (<400nm) Absorption.
LENS MATERIALS
 The Most Common Lens Material Is, Of Course,
Optical Glass, But Crystals & Plastics Are Frequently
Used.
 There Are 5 Main Types Of Lens Materials For
Eyeglasses & Sunglasses.
 Each Type Of Lens Material Can Help Correct
Refractive Errors Such As Near-Sightedness
(Myopia), Far-Sightedness (Hyperopia), Astigmatism,
Or Presbyopia.
LENS MATERIALS: CR-39
 The Most Used Plastic Lens Material For Years Was CR-39.
 It Was First Developed As A Replacement For Glass Lenses
During World War II.
 It Still Has 55% Of World Market At Age 60.
 The Patent Was Awarded To Muskat & Strain Of Pittsburgh
Plate Glass Company (Now Named PPG) in 1946.
LENS MATERIALS: CR-39
 CR-39 Is Available In All Lens Styles & From Multiple
Manufacturers.
 The Basic Monomer Comes From PPG, & Then Each
Company Adds Their Own Materials To Create Their
Lenses.
 Advantages Include Light Weight, Good Optical
Properties, & Tinting Well.
 Disadvantages Of CR-39 Are That It Is The Thickest
Material & Scratches Easily.
CROWN GLASS
 Is The Most Commonly Used Clear Glass For
Ophthalmic Lenses.
 In General, Glass Is Most Durable Material Used For
Lenses.
 Crown Glass Is Used Mainly For Single Vision Lenses
& Distance Carrier For Most Glass Bifocals &
Trifocals.
CROWN GLASS

 It Has An Index Of Refraction Of 1.523 & An Abbe


Value Of 59.
 It Is Approximately 4% Thinner Than CR-39 Resin
Lenses & Is 40% Heavier Than Polycarbonate Lenses
& Is Slightly Lighter Than High Index Glass.
 It Blocks Out About 10% Of UV Light.
FLINT GLASS
 Uses Lead Oxides In Its Chemical Make Up To
Increase Its Index Of Refraction To Approximately
1.58 To 1.69.
 Its Abbe Value Ranges From 30 To 40.
 This Material Is Relatively Soft, Displays A Brilliant
Lustre & Has Chromatic Aberration.
FLINT GLASS
 It Was Used In Past As Single Vision Alternative For
Higher Rx Lenses, Its Use Today Is Often Limited To
Segments For Some Fused Bifocals.
 The Advantages Of Glass Lenses Include Optical
Clarity, Resistance To Scratches, & It Is The Least
Susceptible To Chemicals.
 The Disadvantages Include That It Is The Heaviest
Material & It Is Less Impact Resistant Than Other
Materials.
POLYCARBONATE LENSES

 Polycarbonate Lenses Were First Developed By


Company Named Gentex.
 Polycarbonate Is A Thermoplastic Which Means It Is
Mouldable Under Sufficient Heat.
 In The 1950’s It Was Marketed Under Name Lexan &
Due To Its Extraordinary Resistance To Impact Was
Originally Manufactured For Safety Devices.
CATARACT
CATARACT
 The Lens Is Positioned Behind The Coloured Part Of Eye
(Iris).
 The Lens Focuses Light That Passes Into Eye, Producing
Clear, Sharp Images On Retina (Light Sensitive
Membrane) In Eye That Functions Like The Film In A
Camera.
 As You Age, Lenses In Your Eyes Become Less Flexible,
Less Transparent & Thicker.
 Age Related & Other Medical Conditions Cause Proteins
& Fibers Within Lenses To Break Down & Clump
Together, Clouding The Lenses.
CATARACT

 A Cataract Is A Clouding Of Normally Clear Lens Of


The Eye.
 At First, Cloudiness In Vision Caused By A Cataract
May Affect Only A Small Part Of Eye’s Lens & May
Be Unaware Of Any Vision Loss.
 As Cataract Continues To Develop, The Clouding
Becomes Denser.
 This May Lead To More Noticeable Symptoms.
CATARACT
 A Cataract Scatters; Distorts & Blocks The Light
As It Passes Through The Lens, Preventing A
Sharply Defined Image From Reaching Retina.
 As A Result, Vision Becomes Blurred.
CATARACT

 Cataracts Generally Develop In Both Eyes, But Not


Always At The Same Rate.
 In One Eye May Be More Advanced Than The Other,
Causing A Difference In Vision Between Eyes.
 Cataracts May Be Partial Or Complete, Stationary Or
Progressive, Hard Or Soft.
 Histologically, The Main Types Of Age-Related
Cataracts Are Nuclear Sclerosis, Cortical, & Posterior
Sub-Capsular.
CATARACT: NUCLEAR SCLEROSIS
 Nuclear Sclerosis Is Most Common Type Of Cataract
& Involves Central Or ‘Nuclear’ Part Of Lens.
 This Eventually Becomes Hard, Or ‘Sclerotic’, Due To
Condensation On Lens Nucleus & Deposition Of
Brown Pigment Within The Lens.
 In Its Advanced Stages, It Is Called A ‘Brunescent
Cataract’.
CATARACT: CORTICAL

 Cortical Cataracts Are Due To The Lens Cortex


(Outer Layer) Becoming Opaque.
 They Occur When Changes In Fluid Contained In
Periphery Of The Lens Causes Fissuring.
 Symptoms Often Include Problems With Glare &
Light Scatter At Night.
CATARACT: CORTICAL

 When These Cataracts Are Viewed Through An


Ophthalmoscope The Appearance Is Similar To
White Spokes Of A Wheel
CATARACT: POSTERIOR SUBCAPSULAR
 Posterior Subcapsular Cataracts Are Cloudy At
The Back Of Lens Adjacent To The Capsule (Or
Bag) In Which The Lens Sits.
 Because Light Becomes More Focused Toward
Back Of The Lens, They Can Cause
Disproportionate Symptoms For Their Size.
CATARACT

 An Immature Cataract Has Some Transparent


Protein, But With A Mature Cataract, All The
Lens Protein Is Opaque.
 In A Hyper-Mature Or ‘Morgagnian Cataract’,
The Lens Proteins Have Become Liquid.
 Congenital Cataract, Which May Be Detected In
Adulthood, Has A Different Classification &
Includes Lamellar, Polar, & Sutural Cataracts.
BIONIC EYES
BIONIC EYES

Bionic Eye, Electrical Prosthesis Surgically


Implanted Into A Human Eye In Order To
Allow For Transduction Of Light In People
Who Have Sustained Severe Damage To The
Retina.
BIONIC EYES

 Technology Provided By This Helps Blind People To


Get Vision Again.
 The Bionic Eye Is An Artificial Eye Which Provide
Visual Sensations To The Brain.
 It Comprises An External Camera, Transmitter & An
Internal Microchip.
 Image Captured By Camera Are Focused To Chip
Which Converts It Into Electronic Signal That Brain
Can Interpret.
BIONIC EYES

 It Consist Of Electronic Systems Having:


 Image Sensors (Camera).
 Radio Transmitter.
 Receiver.
 Microprocessors.
 Retinal Chips.
BIONIC EYES

 The Camera Is Mounted On A Pair Of


Eyeglasses, Where It Serves To Organize Visual
Stimuli Of Environment Before Emitting High
Frequency Radio Waves.
 The Stimulator Microchip Consists Of An
Electrode Array That Is Surgically Implanted
Into The Retina, That Functions As An Electrical
Relay In Place Of Degenerated Retinal Cells.
BIONIC EYES

 The Radio Waves That Are Emitted By The


External Camera & Transmitter Are Received
By The Stimulator, Which Then Fires Electrical
Impulses.
 The Impulses Are Relayed By Few Remaining
Retinal Cells Through Implanted Retinal Chip &
Are Transduced As Normal To The Optic Nerve
Pathway, Resulting In Vision.
BIONIC EYES

 It Is An Expensive Treatment & Not Everyone Can


Afford It.
 Since Research Is Still Going On Results Are Yet Not
100% Successful.
 The Images Produced By Bionic Eye Were Not Be Too
Much Perfect But They Could Be Clear Enough To
Recognize.
 The Implant Bypasses The Diseased Cells In The
Retina & Go Through The Remaining Possible Cells.
Any Query?

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