ptt 202 organic chemistry for biotechnology lecture 1: general principles of analytical organic...
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PTT 202 Organic Chemistry for
BiotechnologyLecture 1: General Principles of Analytical Organic Chemistry
for Biotechnology
[email protected] Mohamed Idris
Semester 1 2013/2014
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Introduction Analytical organic chemistry involves the
use of laboratory methods to determine the composition of biological or organic samples.
The information gained from the analysis can be reported in two ways:
1. Qualitative report: indicates the presence of substance detected in a sample (Identification). 2. Quantitative report: states the amount or concentration of the substance present in a sample (Quantification).
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HPLC elution profile of ethanol extracts from petals of P. subulata for carbohydrates. (Left) standards, and (right) sample (stage 5): (1) sucrose, (2) glucose, (3) fructose, (4) myo-inositol, (5) sorbitol, A is 2-C-methyl-d-erythritol.
Example: Qualitative report (Identification of carbohydrate sugars in unknown sample)
Identification of sugars present in the unknown sample was made by the comparison with the retention times (tr) of the standard sugars (sucrose, glucose, fructose, etc…)
HPLC (High Performance Liquid Chromatography)
tr=
30
min
tr=
30
min
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Example: Quantitative report (Quantification of carbohydrate sugars in unknown sample)
Organ Concentrations (µg/ml))
Glucose Fructose Sucrosemyo-
InositoSorbitol
2-C-Methyl-erythritol
Petal 8.1±0.8 4.8±0.3 1.1±0.2 1.0±0.0 1.1±0.2 15.4±0.6
Glucose concentration (µg/ml)
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Selection of a valid method of analysis
To choose a suitable analytical method it is essential to know the chemical and physical properties of the test substance .
Not all methods that are suitable for qualitative analysis are also suitable for quantitative analysis.
Most analytical methods involve preparative steps before final measurement can be made.
Analytical methods validity (in terms of sensitivity, selectivity, accuracy/precision needed)
Need to consider the cost of the instrumentation and reagent required and also the time taken.
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Instrumental methodsMost convenient methods are those that
permit both identification and quantification but these types of methods are relatively few in number.
Atomic emission and absorption spectroscopy are good examples of instrumental methods that provide both qualitative and quantitative analysis. The wavelength of the radiation is used to identify the substance while the intensity of the radiation is used for its quantification.
If the substance is not easily detectable, some modification is done by chemical reaction to produce a substance that can be measured more easily.
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Most of the classical methods (using complex reagents) have been superseded by the improved instrumental methods, but some very reliable still remain in use such as Folin Ciocalteu’s reagent for the detection of phenolic compounds.
Interference occurs when other substances as well as the test substance are detected by the method led to errors. If it is major problem, the sample must be partially purified before analysis.
Gas and liquid chromatography are analytical techniques that can be used to separate (purification) and quantify test substance in the sample sequentially.
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Folin Ciocalteu assay-produce dark blue color when phenolic compounds are present.
Colorless when no phenolic compounds are detected
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Physiological methods Involve a bioassay that measures the
response of an organism or target organ to the test compound.
Can be conducted in vivo using animals or in vitro using isolated organ or tissue preparations.
Many bioassays are quantitative but those that give only positive or negative result are to be quantal in nature (either qualitative or quantitative).
Bioassays must be designed to consider variations in measurements (since different animals/cells respond in different way to the same stimulus) and replicate measurement must be made using different animals/cells.
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Due to the cost and ethical conflict of using animals in bioassays, the cell culture techniques (using cell lines) are introduced. Examples of bioassays using cell lines:Hormone System used Parameter
measured
Prolactin Rat lymphoma cells Cell growth
Interleukin 1 Human myeloma cells Cell growth
VSCell lines grown in petri dish and
then the physiological studies done by in vitro assays
Directly injected to animals
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Assay kits Developed methods marketed by reagent and
instrument manufacturers. Examples: colorimetric assays - which
require the additional of chemical solutions to the test sample.
The kits include all the necessary standards and assay components.
Designed to be used in manual procedures or on particular automated instruments.
Full assay protocols, details of the composition of all reagents, hazard data, and specified storage conditions are given in the kits.
Reduced the necessity for individual laboratories to develop their own methods.
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Glucose assay kits: a plate-based colorimetric enzymatic appraisal for the assurance of glucose in serum samples.
Malaria rapid test kit: is a rapid chromatographic immunoassay for the qualitative detection of Human Malaria antigen in whole blood.
Assay kits (Examples)
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The quality of data All data (particularly numerical) are subject to
errors. These types of errors should be quantified.
Variability in analytical data are due to random and systematic errors.
Random error: Represents the experimental uncertainty that
occurs in any measurement (due to instrument design and use, e.g. frictional effects on balance, reading fluctuating signals).
Causes variation between replicate measurements and cannot be predicted and estimated.
Cannot be avoided but can’t be reduced by carefully technique and the use of good quality instruments.
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Random error: Follows a normal distribution or Gaussian distribution about the mean.
HistogramNormal distribution curve
Fre
qu
ency
Class interval
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Random error: This type of error can be calculated
statistically as standard deviation (s) of the data:
where x is an individual measurement and n is the number of replicates. For any number of replicates less than 30, s
can be calculated as following:
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Random error: If limited number of replicates were done
instead of single measurement, a greater degree of confidence could be placed in the resulting mean value and can be expressed as following (SEM = Standard Error of the Mean):
Replicates analyses have an advantage against single analysis by improving the degree of confidence, but the increased time and effort involved should be considered.
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Relationship between standard deviation and the proportion of measurements about the mean value
Random error: Standard deviation permits a precise
statement to be made regarding the distribution of the replicates measurements about the mean value.
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Systematic error: Constant in character and can be either avoided
or corrected. Cannot be measured or calculated by
statistically. Cause the shifting of the position of the
mean of set of measurements relative to the original mean.
Such error shows bias towards either positive (an increase in the mean) or negative (a decrease in the mean).
This type of error due to instrumental factors (faulty equipment or uncalibrated instruments) and errors of method (failure to consider the limitations and constrains of a method or operate at different experimental conditions) that may result lower or greater reading than they should be.
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Assessment of analytical methods Analytical methods should be precise, accurate,
sensitive and specific but due to errors, all methods fail to meet this criteria fully.
Precision: Reproducibility of results: a number of replicate
measurements of a sample agree with one another.
Precision can be expressed in term of standard deviation.
Coefficient of variation (V) or relative standard deviation can be calculated as following :
where s is standard deviation and is the mean value (see Procedure 1.1 in the Handout for example) .
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Precision: Variance ratio or ‘F’ test is used to
compare the relative precision between two methods and can be calculated as following:
If the calculated value of F exceeds the critical value for F, (value from table) then it can be concluded that a significant difference does exist between the precision of the two methods (see Procedure 1.2 in the Handout for example).
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Accuracy: The closeness of the mean of set of replicate
analyses to the true value of the sample. The accuracy of the means of replicates of the
one sample (e.g. same conc.) of two methods can be compared by ‘t’ test that can be calculated as following:
If the calculated value of t does not exceeds the critical value for t (value from table) then it can be concluded that no significant difference does exist between the accuracy of the two methods (see Procedure 1.3 in the Handout for example).
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Accuracy: The accuracy of series of different samples (e.g.
different conc.) of two methods can be compared by the paired ‘t’ test that can be calculated as following:
Where is the mean value for the difference between the pairs (d), If the calculated value of t does not exceeds the critical value for t (value from table) then it can be concluded that no significant difference does exist between the accuracy of the two methods (see Procedure 1.4 in the Handout for example).
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Accuracy: The accuracy of series of different samples (e.g.
different conc.) of two methods can also be compared by the correlation coefficient (r) that can be calculated as following:
If the calculated value of r is greater than 0.9 indicates fair to good correlation and together with an acceptable result for the paired ‘t’ test would provide strong evidence for a common degree of accuracy between the two methods (see Procedure 1.5 in the Handout for example).
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Linear regression analysis: The equation of straight line and the values for
the slope and intercept can be calculated as following:
Where a is the slope and b is the intercept. If these values differ from 1.0 and 0 respectively,
the two methods differs from their accuracy (see Procedure 1.6 in the Handout for example).
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Precision vs Accuracy
bias
bias
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Sensitivity: The ability of a method to detect small
amount of the test substance. The slope of the calibration graph is a
conventional way of expressing sensitivity and particularly useful when comparing two methods.
Specificity: The ability to detect only the test substance. Lack of specificity (due to interference effects)
will result in false positive results if the methods is qualitative and positive bias in quantitative results (higher mean value than the true mean value).
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Quality control in analytical methods
Control charts: A quality control chart (see Procedure 1.7 for example) is a
time plot of a measured quantity that is assumed to be constant (with a Gaussian distribution) for the purpose of ascertaining that the measurement remains within a statistically acceptable range.
The control chart consists of a central line representing the known or assumed value of the control and either one or two pairs of limit lines, the inner control limit (warning limit) and outer control limit (action limit).
Warning limits: the max. and min. values within which a single control sample result is normally expected to lie (results are satisfactory and can be reported).
Action limits: specified max. and min. values outside which a single control sample result is extremely unlikely to lie without there being a serious error in the analysis (results are discarded, fresh standard are prepared, and the control sample re-analyzed).
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Control charts:
Warning limits
Action limits
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Accreditation of laboratories Recognizes that a laboratory is competent to
carry out its analytical services and a necessary requirement.
Several specific aspects of laboratory management which are essential in the process of accreditation as following:
1. Health and safety: Provide a procedure hazard form (or material
safety data sheets (MSDS)) that contain all the necessary information regarding potential hazards, mode of disposal and first aid procedures for all the chemicals.
Chemical hazards are classified into explosive, flammable, toxic, corrosive and irritant, and radioactive.
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2. Standard operating procedures (SOPs): A written details of the protocol that must be
followed for any particular procedure being undertaken.
Include details of the procedures for collecting and handling the samples, performing the analysis, storing and retrieving data, and preparing report.
3. Computerization: Computers plays a major role in modern
laboratory. LIMS: Laboratory Information Management
System is a system that link various operations associated with both analytical and organization aspects.
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4. Good laboratory practice (GLP): Is a set of procedures within which the overall
performance of a laboratory can be monitored.
Compliance with GLP may be required accreditation of a laboratory by external regulating agency.
The features of GLP: Staff- adequately trained with designated
responsibilities and appropriate qualifications. Equipment- adequate standard and full
records of all maintenance and faults must be kept for 10 years.
Procedures-must in the form of SOP. Data- details of the method, equipment, SOP
and raw results must be stored for 10 years.
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Sample of Analysis The collection and storage of sample prior to
analysis also affect the validity of a laboratory report.
The collection procedure must not adversely affect the analytical process.
The storage conditions should preserve the integrity of biological components.Examples of storage conditions of biological
samples:Possible change in the sample
Methods of prevention
Microbial degradation Addition of anti-microbial agent
Denaturation of enzymes Store in 50% glycerol at low temperatures
Oxidation Add antioxidant, store in dark
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The production of results The results of analysis should be presented in a clear
manner to enable valid conclusion to be made. Certain aspects of reporting analytical results that
should be considered as following:1. Choice of units:
SI units provide a system of universal units that consists primarily of 7 base units from which others may be derived.
SI base unitsPhysical quantity SI base unit Symbol
Length Meter m
Mass Kilogram kg
Time Second S
Electric current Ampere A
Thermodynamic temperature
Kelvin K
Luminous intensity Candela Cd
Amount of substance Mole mol
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Derived units
Physical quantity
Derived unit Symbol Name
Area Square meter
Volume Cubic meter
Velocity Meter per second
Density Kilogram per cubic meter kg
ForceKilogram meter per second per
secondkg Newton
Pressure Newton per square meter N Pascal
Substance concentration
Mole per cubic meter mol
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Prefixes
Factor PrefixName
Symbol
Factor PrefixName
Symbol
deca- da
deci- d
hecto- h
centi- c
kilo- k
milli- m
mega- M
micro- µ
giga- G
nano- n
tera- T
pico- p
femto- f
atto- a
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2. Calibration: Involves analyzing solutions that contain a range of
known concentrations (standard solutions) of the specified analyte in parallel with the test sample.
Determines the relationship between the reading and the concentration of the standard analyte (by plotting the calibration graph), and from this relationship, the amount of analyte in the test sample can be calculated.
Can be prepared by series of standard solutions (see Procedure 1.10 in Handout for example).
3. Graphical presentation of data: Graphs produced for qualitative analytical purposes
must be dated and include adequate information on the method analysis (such as SOP serial number, the analyte and the units of measurement).
The scale of each axis should be carefully chosen. The linear relationship between two set of data can be
expressed by linear equation derived from linear regression analysis.
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4. Laboratory report: The report of any measurement must always include enough information to avoid misunderstanding and should contain specific details about the sample (e.g. see Table 1.10 as following):