topic 4 and 6 forensic chem analysis Flashcards

1
Q

what is a drug?

A

•Adrugisasubstance,wheningested,iscapable
ofinducingaphysiologicalchange.
•Alldrugsaretoxic.
•Itisthedose thatdifferentiatesatherapeuticdrugfrompoison.

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2
Q

what is the difference between drug and medicine?

A

Medicines are combinations of drugs and inert ingredients. drugs do not have combination on inert materials or stabilizers.

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3
Q

what are the 3 categories of drugs? what does each do and give some examples

A

Drugscanbeabused–‘pleasurableeffects’

Categorised into 3 areas according to impact on the central nervous system (CNS) especially the brain :

(a) Stimulant–stimulates brain activities–Amphetamines (ice), Cocaine
(b) Depressants –inhibits brain activity–Alcohol, Barbiturates (sleeping pills), Heroin, Morphine
(c) Hallucinogens–Changes perception and mood (without either stimulating or inhibiting brain activity)-causes hallucinations–Ecstasy, Lysergic acid diethylamide (LSD), Cannabis (mild effect)

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4
Q

what are the 4 legal uses of morphine?

A
  • general anesthesia, epidural ansesthesia
  • palliative care–alleviate pain without caring
  • antitussive for severe cough
  • antidiarrheal e.g in aids
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5
Q

what is the difference between morphine vs aspirin? why is morphine addictive?

A

•Aspirinreducespainbyinhibitingthepain inducingevent,
whereasmorphineinterceptsthepainsignalafteritisproduced.
•Aspirinstopsinflammationandpain,butitdoesnotproduceeuphoria.

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6
Q

explain the use of Fourier transformInfraredSpectroscopy. what can it be used to identify?

A
  • Analysethestructuresoforganicandinorganiccompounds
  • Organicfunctionalgroupswithreferencetocorrelationtable.
  • Identify powdereddrugs.
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7
Q

explain the use of chromatography? what can it be used to determine?

A

Drugssubmittedtolaboratoriesareroutinelyexaminedbychromatography todeterminetheirnature andpurity.

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8
Q

what is GC used for? what type of samples can be analysed using GC?

A

separationandanalysisofvolatileorganiccompounds(VOCs).

TypeofsamplesthatcanbeanalysedbyGC: •volatile,lowboilingpoint(lowmolecularweight) •thermallystableunderGCoperatingtemperatures

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9
Q

what is HPLC? why does it compliment GC?

A

HighperformanceLiquidChromatography is a separationtechnique thatusesaliquidmobilephase.

itallowsnon‐volatile,and/or thermallyunstable compoundstobeanalysed.
e.g Highmolecularweightorganiccompounds, Pharmaceuticalcompounds, Hormones

LChaswiderapplicationascomparedtoGCtechnique.

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10
Q

what is thin layer chromatography used for ? what surface is the technique carried out on?

A

initialscreeningtechniquetoscreenmostofthedrugsabuse.

Fast,providesrapididentificationaftertheillicitdrugswasseizedbylaw enforcementagencies.

TLCiscarriedoutonaglassplateorothersupportivebackingcoatedwithasolidphase.

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11
Q

what is the retention factor used in TLC? (Rf value)

A

TheRf valueofacompoundisequaltothedistancetravelledbythecompounddividedbythedistancetraveledbythesolventfront
Rf value: x/y
Xisthedistancefromthespottotheorigin. Yisthedistanceofthesolventfronttravelsfromtheorigin.

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12
Q

what can IonSelectiveElectrode(ISE) be used for?

A

ISEcanbeusedtodeterminetheconcentrations ofthefollowingionsinforensicsamples:
cations:
Ammonium(NH4+),Barium(Ba2+),Calcium(Ca2+),Cadmium(Cd2+),Copper(Cu2+),Lead(Pb2+),Mercury(Hg2+),Potassium(K+),Sodium(Na+),Silver(Ag+),Hydrogen(H+)
Anions:
Bromide(Br‐),Carbonate(CO3‐),Chloride(Cl‐),Cyanide(CN‐),Fluoride(F‐),Iodide(I‐),Nitrate(NO3),Nitrite(NO2‐),Perchlorate(ClO4‐),Sulphide(S‐),Thiocyanate(SCN‐),andCyanide(CN‐)

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13
Q

what are the 3 types of active materials used in ISE?

A
  1. Glass–pHmeasurement
  2. Insolubleinorganicsalts
  3. Long‐chainion‐exchangematerials
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14
Q

how does gas sensors operate? what does it do?

A

•Incorporateaconventionalion‐selectiveelectrode
•Real‐timemonitoringofgases–e.g.CO2,O2andNH3
greatimportanceinmanypracticalenvironmental,clinicalandindustrialsituations

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15
Q

what are the advantages and disadvantages of gas sensors?

A

Advantages:
•Non‐destructive
•Fast
•real‐timemonitoring
•Suitableforsingleelemental/gasanalysis
•Cheapercomparedtospectroscopyinstruments.

Disadvantages:
•Lesssensitive
•Interferenceduetopresentofothersionsinsamples.

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16
Q

what is spectroscopy? what kind of process is it?

A
  • interactionbetweenelectromagneticradiationandmatter.

* Excitation oremission process.

17
Q

what are the advantages and disadvantages of atomic absorption spectrometer (AAS)

A
advantages:
•Fast(singeelement)
•Sensitive(ppm–ppb) 
•Smallsamplesize 
•Qualitative&Quantitative analysis

disadvantages:
•Destructive
•Lowersamplethroughput compared to AESi.e.multiple elementsanalysis

18
Q

what are the advantages and disadvantages of atomic emission spectrometer (AES)

A
advantages:
•Fast(multipleelements)
•Sensitive(ppm–ppb) 
•Smallsamplesize 
•Highersamplethroughputi.e. multiple elementsanalysis 
•Qualitative&Quantitative analysis

disadvantage:
•Destructive
•Spectralinterference.

19
Q

what is ScanningElectronMicroscope(SEM)? what is its operating principal?

A

•Non‐destructive,qualitativeanalysis.
•Imagesthesamplesurfacebyscanningitwithahigh energybeamofelectronsinarasterscanpattern •Electronsinteractwiththeatomsthatmakeupthesampleproducing
signalsthatcontaininformationaboutthesample’ssurface
topography,composition etc.

20
Q

what is SEM‐EnergydispersiveX‐RaySpectroscopy(SEM‐EDX) ?

A

SEM can coupled with EnergydispersiveX‐RaySpectroscopy(EDX)
toprovidebothsurfacetopographyinformation(elementalidentification,qualitative)
andquantitativecompositionalinformation. •Non‐destructivetechnique.

21
Q

what is NeutronActivationAnalysis(NAA)? what is its advantage?

A

Thismethodrequiresirradiationofthesamplewithneutronsthat
transformtheelementsintoradioactiveisotopes.
•Non‐destructive
•Qualitative&quantitative
•Multi‐elementanalysissimultaneously
•Superioraccuracyandsensitivity

22
Q

what are the disadvantages of NAA?

A
  • Slow
  • Expensive
  • Requiresanuclearreactor
  • Radioactivewastedisposalsystem
23
Q

what are the two categories of NAA?

A

Inprinciple,therefore,withrespecttothetimeofmeasurement,NAAfallsintotwocategories:

PGNAA(Promptgamma‐rayneutronactivationanalysis)
–Measurementstakeplaceduringirradiation
‘de‐excite’intoamorestableconfigurationthroughtheemissionofcharacteristicgammaray.

•DGNAA(Delayedgamma‐rayneutronactivationanalysis)
Radioactivenucleus‘de‐excites’byemittingacharacteristicdelayedgammaray(ataslowerrateaccordingtotheuniquehalf‐lifeoftheradioactivenucleus.)
Measurementsfollowradioactivedecay(slowerrate)
Morecommonmode;thus,whenonementionsNAAitisgenerallyassumedthatmeasurementofthedelayedgammaraysisintended.
–About70%oftheelementshavepropertiessuitableformeasurementbyNAA.
•non-destructive
•slow
•requires a nuclear reactor
•bulk analysis