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Transcript
c. DIACETYL MATHOD
Because of Instability of Diacetyl, Use Diacetyl Monoxide, add Acid 
Diacetyl
CH3COCOCH + UREA  CH3C-C-CH3
Diacetyl
N N
C
O
Diazine yellow
F. URIC ACID
Test for Kidney and Renal(Gout) Function
Normal- Males 2.5 to 7mg%
Females – 1.5 to 6mg%
In gout goes to 10mg%(Reflection of Nucleic Acid Breakdown)
METHODS
a.PHOSPHOTUNGSTIC ACID
URIC ACID + H3PW13O40  ALLANTOIN BLUE
b. ENZYMATIC
URIC ACID + URICASE PEROXIDE + ALLANTOIN
-Measure decrease in absorbance at 290nm of Uric Acid
OR – Use o-dianisidine + Peroxide Red Color
G. CREATININE
Better method for Kidney Function. No dietary effects.Difficulty-only very low
concentrations(approx. 1 mg%) in serum
BASIC EQUILIBRIUM:
CREATINE + ACID  CREATININE + BASE  CREATINE
NORMAL: Men= 0.6 to 1.2mg%; Women= 0.50 to 1 mg%
If Creatinine rises to 2 to 4mg% -Moderate to severe kidney damage
ASSAY: JAFFE METHOD
Alkaline picrate + Creatinine Red Color at 500 nm
To do Creatine add Acid  Creatinine, assay as above
H. PROTEIN
Proteins provide a Nutritive role
If protein level changes=disease of kidney
Normal rate is 6 to 8mg% in serum
ASSAY
l. TOTAL PROTEIN BY FOLIN-CIOCALTEAU REAGENT
ADD PHOSPHOTUNGSTIC ACID, OXIDIZE THE –OH GROUP
IN TYROSINE RING(COLOR CHANGE FROM YELLOW TO
BLUE
2. KJELDAHL METHOD : PROTEIN NH3 on digestion with acid/catalyst.Distill
NH3 into Boric Acid H2BO3-(titrate with Acid)
3. BIURET METHOD:
Cu(II) + PROTEIN  BLUE COLOR (530nm) DUE TO REACTION OF
Cu(II) WITH C=O and =NH GROUPS OF PROTEIN
CALLED BIURET BECAUSE OF ANALOGY OF Cu(II) REACTION WITH
BIURET
I.
ALBUMIN -ONE OF KEY PROTEINS IN BODY
ASSAY: ALBUMIN + METHYL ORANGE OR HYDROXYAZOBENZENE
COLOR at 540nm.
NORMAL LEVELS: 3.8 to 4.7 g%.
J. FIBRINOGEN
A PLASMA PROTEIN FACTOR NECESSARY FOR COAGULATION.
NORMAL: 200 to 400 ng%
GOES TO 700 ng% IN TUBERCULOSIS, PNEUMONIA
ASSAY – CLOT WITH THROMBIN AND MEASURE
DIFFRACTION OF LIGHT
K. AMINO ACIDS -3 ARE IMPORTANT IN CLINICAL:
1. PHENYLALANINE = BENZENE-CH2CHCOOH
NH2
2. TYROSINE = HO-BENZENE-CH2CHCOOH
NH2
3. TRYPTOPHAN = INDOLE-CH2CHCOOH
NH2
TOTAL AMINO ACIDS = 2.5 to 4.5mg% in Serum(Large Increase
indicates severe liver damage)
ASSAY: NINHYDRIN + AMINOACID  DEEP RED COLOR
L. l-PHENYLALANINE
MOST IMPORTANT AMINO ACID – PHENYLKETONURIA
(PKU) TEST=MEASURES BUILDUP OF PHENYLALANINE IN
NEWBORN BABIES. BUILD UP DUE TO LACK OF ENZYME lPHENYLALANINE HYDROXYLASE  l-TYROSINE, AN
IMPORTANT STEP IN METABOLISM OF BODY.
BUILD UP LEADS TO MENTAL RETARDATION IN BRAIN=ONE
OF KEY CAUSES OF MENTAL RETARDATION IN NEWBORNS.
ASSAY: PHENYLALANINE + Fe(III) GREEN COLOR
OR PHENYLALANINE + NINHYDRIN + LEUCYLALANINE
FLUORESCENCE(EXCITATION 365nm,EMISSION 525nm)
INFANTS: 2.1mg% AT BIRTH, 4.5mg% 3-4 DAYS,
20-30mg% 10 days=SERIOUS
M. CHOLESTEROL/TRIGLYCERIDES/HDL/LDL TESTS
IMPORTANCE=DIAGNOSIS OF POSSIBILITY OF
MYOCARDIAL INFARCTION.
SOME CHOLESTEROL NECESSARY FOR BODY
FUNCTIONING. BODY SYNTHESIZES 2 gram a day(3X level that
is taken in):Acetate radicals + Amino Acids,Carbohydrates and Fatty
Acids Cholesterol
ATTEMPTS TO LOWER CHOLESTEROL WITHOUT LIMIT OF
DIETARY INTAKE = UNSUCCESSFUL
PROBLEM: CHOLESTEROL IS INSOLUBLE AND CANNOT
ENTER BLOOD STREAM BY CROSSING GI TRACT WITHOUT
LIPOPROTEINS WHICH SOLUBILIZE CHOLESTEROL.THESE
ARE IMPORTANT HDL AND LDL MOLECULES.
TRIGLYCERIDES ARE FATTY MOLECULES THAT AFFECT MI
BY BUIDING UP IN BLOODSTREAM.
ALL OF THESE ARE IMPORTANT AND MUST BE ASSAYED.
l. CHOLESTEROL
NORMAL 150 to 180 mg%
at up to 850mg% =GOOD CHANCES OF MI
Cholesterol is removed by liver  Bile Acids(Hydroxylation Reaction)
METHODS OF ANALYSIS:
a. ENZYMATIC:
TOTAL CHOLESTEROL + ESTERASE CHOLESTEROL + OXIDASE 
PEROXIDE + o-DIANISIDINE (RED COLOR)
OR CAN MEASURE IN NOVA OR YELLOWSPRINGS INSTRUMENT WITH
IMMOBILIZED ENZYMES IN BIOSENSOR
b. LIEBERMAN-BURCHARD METHOD
CHOLESTEROL + SULFURIC ACID  GREEN COLOR(Bis Chlosteradienyl
Monosulfonic Acid)
c. CHOLESTEROL INSTRUMENT(SEE NEXT PICTURE)
2. TRIGLYCERIDES
TRIGLYCERIDES= ESTERS OF HIGH M.W., CONSTITUTE 95%
OF FAT STORED IN TISSUES.
TERMED POLYUNSATURATED FATA
UNDERGO DIGESTION IN DUODENDUM AND ILEUM.
THEY ARE HYDROLYZED TO GLYCEROL + FATTY ACIDS BY
LIPASES. DANGER: IN BLOOD STREAM, RESTRICT FLOW OF
BLOOD SINCE THEY ARE INSOLUBLE.
THE BAD LDL AND VLDL LIPOPROTEINS CAUSE ELEVATED
TRIGLYCERIDES AND HENCE INCREASED POSSIBILITY OF MI.
THE GOOD HDL CAUSES ONLY NORMAL LEVELS-LOWER MI
NORMAL 40-160 mg% Male; 35-135 mg% Female.ABOVE 200 BAD
ASSAY: ADD LIPASEFATTY ACIDS(MEASURE WITH DYE)
3. LIPOPROTEINS
- TRANSPORT INSOLUBLE LIPIDS
- PLAY KEY ROLE IN CHOLESTEROL/TRIGLYCERIDE
METABOLISM.
a. GOOD = HDL(HIGH DENSITY LIPOPROTEIN)
- Important in removing Cholesterol from Tissues,thereby reducing the
amount of cholesterol stored in body
- Involved in returning cholesterol from arteries to liver for removal as
bile acids(Reverse Cholesterol transport)
- Plays a major role as scavenger of lipid and apolipid proteins
MEASUREMENT: USE ANTIBODY TO HDL
Higher Value the better(low risk of MI)->35 mg% best
b. BAD = Low Density Lipoproten(LDL)and Very Low Density
Lipoprotein(VLDL)
-Causes Increased Uptake of Cholesterol by allowing Transport
Across GI Tract. Cholesterol deposits in arterial walls leading to
premature athersclerosis.
- Patients with Genetic Disorder Familial Hypercholesterolemia(FH)
have a gene that codes fopr the LDL receptor.
HIGH LDL and VLDL = GRAVE RISK
Range of LDL 0 to 150mg%. Above 150 BAD
K. THYROID GLAND = Size of Butterfly, Synthesizes Hormones
TEST FOR FUNCTIONING CALLED PBI(Protein Bound IodineAv PBI = 3.5 to 8.0 microgram %)
T3 and T4 Important-Assayed by Immunology,old method
RadioImmunoassay,Now Enzyme Immunoassay with Antibodies
AUTOMATION
a. First Machine called AUTOANALYZER. Developed by Leonard
Skeggs at Oak Ridge Labs in 1960’s.
ONE OF BIG ADVANCES IN CLINICAL ANALYSIS
TWO BIG FACTORS IN INSTRUMENT
- USE OF DIALYZER MEMBRANE TO SEPARATE 2
GROUPS(WATER SOLUBLE-DIFFUSABLE-AND NON
DIFFUSABLE)
- USE OF AIR BUBBLES TO SEPARATE SAMPLES FOR RAPID
INTRODUCTION INTO INSTRUMENT
ORIGINAL INSTRUMENT(SMA) 60 samples/hour with 12 tests
Then New SMAC – Computer Linked 24 assays with 240/hour
See Next View
SAMPLE  DIALYZER  Non-Diffusable:
Total Protein(Folin Calcateau Reagent)
Albumin(Dye)
Billirubin(dye)
Alkaline Phosphatase(Color)
LDH,CK,Transaminases etc
 DIFFUSABLE:
Electrolyes(Na+,K+,Ca++,Cl-)-ISE’s
Urea(Diaceyl Reaction)
Glucose (Enzymatic)
Bicarbonate(Acid Base)
l-Phenylalanine(dye)
Cholesterol(LB Reaction)
RESULTS DISPLACED AUTOMATICALLY AS SHOWN.
2. DUPONT AUTOMATIC CLINICAL ANALYZER:
SAMPLE
 CRUSHER INCUBATE READ PACK
INJECTED INTO PACK
AS CUVETTE
EACH TEST HAD SEPARATE COMPUTER LABELED PACK.ALL PACKS
LOADED ON CONVEYER BELT. TEST RESULTS COMPUTER REPORTED.
USUAL METHODS USED.
3. OTHER INSTRUMENTS
a. PERKIN ELMER CLINICAL ANALYZER – PROGRAMMED FOR 35 TESTS,
300/HOUR:
GLUCOSE = HEXOKINASE/NADH; UREA = NITROPRUSSIDE REACTION;
CREATININE=JAFFE REACTION; CHLORIDE = Hg++ + Fe+++ + SCN- ;
PHOSPHATE = MOLYBDATE; URIC ACID = URICASE;TOTAL PROTEIN =
Cu++ COMPLEX; ALBUMIN= COMPLEX; LDH and CK = NADH
PRODUCTION; TRANSAMINASES = NADH; Ca,K and Na by ISE’s; ETC
b. MASS SPEC CENTER OF USPHS –WORLDWIDE DATA BASE FOR
POISONS. ANYTHING CAN BE IDENTIFIED=CHILD?
c. DADE STRATUS – DRUGS, CLINICAL METABOLITES(LIKE PSA, T3,T4
ETC BY AUTOMATED IMMUNOASSAY=LATER)
d. BLOOD GAS ANALYZER= RESPIRATORY SYSTEM BY pH,
BICARBONATE, FREE CO2 ETC) = VERY BIG IN CLINICAL LAB
e. NOVA INSTRUMENT FOR
ELECTROLYTES/GLUCOSE/UREA/CHOLESTEROL/LACTATE
- USES ISE’s ON WHOLE BLOOD FOR ELECTROLYTES
- BIOSENSORS FOR GLUCOSE, UREA, CHOLESTEROL, LACTATE
f. TODAY BIGGEST ARE (1)NOVA (2)BLOOD GAS (3) LARGE CLINICAL
ANALYZERS LIKE OLYMPUS AND ROCHE(FORMERLY BOEHRINGER
ANALYZER). FOUND IN ALL CLINICAL LABS
CLINICAL LAB IS BIGGEST EMPLOYER OF ANALYTICAL CHEMIST. WHY?
Over 10,000 Hospitals Worldwide each with lab(Some very big) plus private labs that
do only blood work worldwide=estimate at least 5000 large ones.Sommerville N.J.eg.
IMMUNOASSAYS
ANTIGEN + ANTIBODY(LINKED TO ENZYME)  COMPLEX.
CALLED ENZYME IMMUNOASSAY = REPLACES OLD RIA OF
ROSEMOND YALLOW WHO WON NOBEL PRIZE FOR THIS
WORK in 1950’s
ACTIVITY OF ENZYME
CONC OF ANTIGEN
CONCEPT: ON BINDING TO ANTIGEN, THE ANTIBODY-ENZYME COMPLEX
LOSES ACTIVITY BECAUSE BINDING SITE OF ENZYME IS COVERED BY
ANTIGEN. HENCE ACTIVITY DECREASES WITH TIME AND ACTIVITY IS
RELATED TO ANTIGEN CONCENTRATION>
LARGE USEAGE IN CLINICAL ANALYSIS TODAY:
l. PSA(PROSTATE SPECIFIC ANTIGEN). USE KIT WITH
ANTIBODY TO PSA LABELED WITH ENZYME. LOOK AT
COLOR – RELATE TO PSA ACTIVITY.
2. ISOENZYMES. THERE ARE SPECIFIC ANTIBODIES TO LDH
1,2 and LDH 4,5, TO CK MB,
3. LIPOROTEINS – HDL, LDL and now VLDL
4. THYROID FUNCTION – T3 and T4
DADE STRATUS MACHINE FOR IMMUNOASSAY:
Labeled Pack for I
SERUM  PACKAGE FOR EACH IMMUNOASSAY CRUSH
MIX  ADD SUBSTRATE READ FLUORESCENCE
In reagent pack we have Antibody for each test labeled to Alkaline
Phosphatase. Add substrate(naphthol phosphate),read fluorescence
IMMUNOASSAY IS IMPORTANT IN
- FOOD .ASSAY FOR BACTERIA(E.COLI,SALMONELLA,
LISTERIA)
-ENVIRONMENTAL( ALL PESTICIDES DONE IN KITS
TODAY.CHEAPER, NO NEED FOR CLEAN UP)
- CLINICAL – IMMUNOASSAY IS THE SECOND GENERATION
TEST
NEXT STEP WILL BE RECEPTORS DIRECTLY
but LACK OF LARGE SUPPLY WILL HINDER THIS
ALREADY DONE BY PHARMACEUTICAL COMPANIES FOR
DRUG DEVELOPMENT
REVIEW
MUST KNOW:
l. SIGNIFICANE/METHODOLOGY FOR
4 SUBSTRATE AND 4 ENZYMES
GRADED ON RECOGNIZING MOST IMPORTANT
2. ISOENZYMES – WHAT ARE THEY, WHAT ARE THEY USED
FOR, EXAMPLES
3. AUTOMATION IN CLINICAL LAB – HISTORY, TYPES OF
INSTRUMENTS, WHAT DO THEY DO
4. FUTURE – WHERE ARE WE GOING??
5. VALIDATION
6. SET UP OF CLINICAL LAB
7. HISTORY OF CLINICAL ANALYSIS(IMPORTANT MARKER)