Exam 4: QC and other photometric methods Flashcards

1
Q

Quality Control

A

Includes regular operational activities that ensure high quality test results
What we do each day to ensure valid results

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2
Q

Quality Assurance

A

Monitoring/evaluation of QC to identify and correct problems

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3
Q

Statistical QC

A

Quantitative/qualitative controls

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4
Q

Non-statistical QC

A

Maintenance procedures, monitoring, checks

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5
Q

Random error

A

Bad precision, good accuracy

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6
Q

Systematic error

A

Good precision, bad accuracy

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7
Q

Gross error

A

Bad precision, bad accuracy

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8
Q

Which type of error is represented by bad precision, good accuracy?

A

Random error

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9
Q

Which type of error is represented by good precision, bad accuracy?

A

Systematic error

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10
Q

Coefficient of variation (%CV)

A

Another description of spread; the SD expressed as a percentage
Independent of units, allows for the comparison of different data sets

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11
Q

A lower CV indicates:

A

better precision

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12
Q

Analytical run

A

A set interval that we can expect performance (accuracy and precision) to remain stable

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13
Q

Basic troubleshooting approach to a potential system issue

A

FIRED - Figure out what is going on (repeat), Isolate the cause, Resolve the issue, Evaluate the resolution, Document all steps and outcomes

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14
Q

Stages of the quality hierarchy from top to bottom

A
TQM - total quality management
QM - quality management
QS - quality system
QA - quality assurance (assessment)
QC - quality control
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15
Q

Examples of non-statistical quality control

A

Production/monitoring of high quality water for use in analytical procedures
Regular calibration of lab equipment
Ensuring the stability of the electrical power supply
Regular monitoring of temps
Performance and documentation of maintenance and troubleshooting
Monitoring the prep and storage of reagents and standards
Performance of linearity checks

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16
Q

Wavelength isolated to measure sodium in flame emission photometry

17
Q

Wavelength isolated to measure potassium in flame emission photometry

18
Q

Wavelength isolated to measure lithium in flame emission photometry

19
Q

Four sources of error in light scattering measurements

A

Variations in particle size
Matrix effects
Dust particles in the reagents and dirt on the cuvets
Fluorescence

20
Q

Stokes shift

A

The difference between the maximum wavelength absorbed and the maximum wavelength emitted
A measure of the energy lost

21
Q

In fluorometry, what does the primary monochromator do?

A

Isolates the excitation wavelength

22
Q

In fluorometry, what does the secondary monochromator do?

A

Isolates the emission wavelength

23
Q

Six limitations of fluorescence measurements

A
Inner filter effect
Quenching
Light scattering
Solvent effects
Sample matrix effects
Temperature
24
Q

Interferences in flame emission photometry

A

Spectral - other emitting substances, self-absorption, mutual excitation
Ionization - too high of flame temp
Physical - large sample droplets will reduce flame temp

25
How do we account for self-absorption in flame emission photometry?
Initial dilution of all samples
26
How do we account for mutual excitation in flame emission photometry?
Using both Na and K in standards, also internal standard acts as a radiation buffer
27
How do we control ionization in flame emission photometry?
By keeping the flame temperature low
28
How do we control the size of sample droplets in flame emission photometry?
By using a wetting agent to control the surface tension, creating smaller sample droplets
29
Difference between turbidimetry and nephelometry
Turbidimetry measures the decrease in incident light due to scatter (inverse relationship to concentration). Nephelometry measures the amount of light that is scattered (direct relationship to concentration).
30
Clinical uses of turbidimetry
Coagulation analyzers, antibiotic sensitivities
31
Clinical uses of nephelometry
Hematology cell counters, immune complexes
32
Interferences in turbidimetry and nephelometry
Lipemia, particulates, fibrin clots, dirty cuvettes, fluorescence NOT colour interferences (eg hemolysis)
33
Principle of fluorometry
Atoms excited by a short wavelength (high energy) of light will emit a longer wavelength (lower energy) Typically uses UV light to excite, and measures in the visible spectrum
34
Clinical uses of fluorometry
Immunoassays, hematology cell counters/flow cytometry, micro
35
Interferences in fluorometry
``` Inner filter effect Self-absorption Light scatter Solvent effects Sample matrix effects Temperature ```
36
How to we control for inner filter effect and self-absorption in fluorometry?
By diluting samples
37
How do we control for light scatter in fluorometry?
By careful selection of wavelengths measured
38
Minimum number of times we run a control to get a control range
20
39
Principle of flame emission photometry
Excited atoms are generated by heat, and light energy liberated during the fall to the ground state is measured