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Graduation Project I

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A natural process in which blood cells and fibrin strands clump together to stop ... Resuming investigating the testing methods. Evaluating testing methods ... – PowerPoint PPT presentation

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Title: Graduation Project I


1
Graduation Project I
Device for controllable administration of drug
dosage
Prepared By - Mona
Ibrahim 200002091
- Azza Al Hassani 200002019
- Asma Ahmed
200002020 - Hamda Al
Ketbi 199902209
- Moza Al Shamsi 199908356 Advisers
name - Dr. Yousef Haik
2
Outline
  • Introduction
  • Background Theory
  • Methods and Techniques
  • Results and Discussions
  • Conclusion

3
Introduction
4
Project Description
5
Objectives
  • Design a blood testing mechanism
  • Design a drug dispensing mechanism
  • Design and construct a working prototype of the
    system

6
  • Motivation
  • Frequent Monitoring
  • Dose adjustment
  • Reduce patient error
  • Time saving
  • Availability of a patient medical history
  • Minimizing potential risks and liability
  • Reduce visiting appointments which will reduce
    insurance payments.

7
Background Theory
8
Blood Clotting
  • A natural process in which blood cells and fibrin
    strands clump together to stop bleeding

9
Blood Coagulation Mechanism
  • There are two well-recognized coagulation
    pathways
  • Extrinsic (thromboplastin)
  • Intrinsic (prothrombin/fibrongen)

10
Prothrombine Time PT
  • The time it takes plasma to clot.
  • PT is reported in seconds

11
International Normalization Ratio
  • The ratio of the patient's clotting time to the
    mean reference value.

12
Anticoagulants
  • Medications that delay the coagulation of blood
  • Some of these are
  • Heparin
  • Argatroban
  • Hirudin
  • Warfarin

13
Warfarin
  • Warfarin is probably the best known and
  • most widely used oral anticoagulant. It is a
    non-habit forming medication used to limit the
    size of existing blood clots and to prevent
    formation of new blood clots in high-risk
    patients

14
Methods and Techniques
15
Design Process
16
Market Analysis
  • The ProTime System-PT-INR Testing
  • The Harmony INR Monitoring System
  • Coaguchek System
  • INRatioPT Monitoring System

17
Function Structure
Global device function
Overall function structure
18
Specifications
  • Measuring System
  • Dispensing System

19
Measuring system
Small sample volume 20 µL
  • Disposable sample holder
  • Measuring time is less than one minute
  • Made of biocompatible materials
  • Sensitive can measure less than 1 mg/ mL of
    Prothrombin
  • Meet the International Biomedical Instrumentation
    standards

20
Measuring system
Portable and easy to use
  • Touch button operation
  • Large, easy to read reporting screen
  • Perform measurement automatically as soon as the
    sample is applied

Durable, Repeatable and Cost effective meter and
test strip
21
Dispensing system
Durable
Store medicine
Cost effective
Loading medicine dump
Dispense one tablet at the time
Patient interference to the device is negligible
Time for dispensing to be less than 2 minutes
22
Developing concepts
23
Testing Morphological Chart
24
Testing Methods
25
RLC Testing Method
26
Protein Separation Method
27
Cantilever Beam Method
28
Plasma Profile
29
Measuring the distance moved
30
Shear Stress
31
Light Intensity
32
Blood layer Thickness
33
Contact Angle
34
Flow in Pipes
35
Piezoelectric
36
Elisa
37
Viscosity
38
The charged Particle method
39
Resistance Measurement using Y tube
40
Drug Dispensing Device
41
Dispensing Morphological Chart
42
Dispensing Morphological Chart
43
Dispensing Morphological Chart
44
Dispensing Concept 1
45
Dispensing Concept 2
46
Dispensing Concept 3
47
Communication Part
48
Communication Morphological Chart
49
Results and Discussions
50
Feasibility study
  • Cantilever beam method
  • Light Intensity and plasma profile
  • Measuring the distance moved

51
Feasibility study
  • Capacitance measurements
  • Procedure 1 Measuring the voltage across the
    copper plates

  • with time

52
Feasibility study
  • Procedure 2 Measuring the capacitance across the
    copper
  • plates
    with time

53
Feasibility study
  • Procedure 2 Measuring the capacitance across the
    copper
  • plates
    with time for different INR values

54
Feasibility study
  • Contact angle measurements

Syringe
camera
sample stage
light source
Captive Bubble Contact Angle apparatus
55
Feasibility study
  • Surface Area method

56
Feasibility study
  • Protein Separation method

57
Conclusion
58
Future work
  • Resuming investigating the testing methods
  • Evaluating testing methods
  • Selecting the proper and suitable testing method
  • Selecting appropriate design for dispenser
  • Building a prototype for the whole device
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