BIOCHEMISTRY 285 PHL Introduction Blood Glucose. Blood Blood is vascular tissue that circulates in the closed system of blood vessels Functions: TransportationTransportation.

Slides:



Advertisements
Similar presentations
Kidney Function Tests Contents: Kidney functions Functional units Renal diseases Routine kidney function tests Serum creatinine Creatinine clearance.
Advertisements

Experiments in Clinical Biochemistry
Determination of plasma enzymes using the clinical analyzer
Lab 6 Isolation Techniques
Sugar Water Screening Test
Blood Course 2 Blood Physiology Lecture 1 Composition of Blood, Plasma and Plasma Proteins 2 nd year Physiotherapy 2nd year Physiotherapy- November 2008.
DETERMINATION OF BLOOD GLUCOSE CONCENTRATION
Glucose test Ms. Ibtisam alaswad Ms. Nour A. taim.
BIOCHEMISTRY 285 PHL Introduction Blood Glucose
BIO 265 – Human A&P Chapter 17 - Blood. Preview of Circulation Figure 18.5.
Estimation of Serum Total Protein
Plasma Glucose. Glucose Glucose (MW: ) is a very important fuel source to generate universal energy molecules (ATP). Blood glucose regulation I-
All body tissues can utilize glucose, the principle and almost exclusive carbohydrate circulating in blood. Glucose is a reducing monosaccharide that.
EXPERIMENT SIX 1. Influence of Adrenalin and Insulin on Glucose Concentration in Serum 2. Determination of Glucose in Urine
BCH302 [Practical] 1. There are three main methods of estimation the reducing sugar content in solution : 1. Reduction of cupric to cuprous salts. 2.
Lecture -1 Dr. Zahoor Ali Shaikh 1. BLOOD We will discuss i). Compositions and Functions of Blood, Plasma ii). Hematocrit iii). Plasma Protein 2.
The use of LABORATORY ANALYSIS clinical practice.
BY : Dr. Beenish Zaki, Instructor Department of Biochemistry (15 February 2012)
Lab 4 M. Zaharna Clin. Chem. Lab.  All body tissues can utilize glucose, the principle and almost exclusive carbohydrate circulating in blood.  The.
BLOOD Islamic university. Blood Everybody is familiar with the sight of blood - the red fluid that oozes out of your body when you've sustained a cut.
Determination of triglyceride in serum Dept.of Biochemistry.
Determination of Total Serum Proteins By Biuret Method
Excretory System Urinary system Structures of the Urinary System 2 kidneys – produce urine, filter blood 180 L of blood per 24 hours filtered 2 ureters.
Experiment 6 Measurement of blood glucose (GOD-POD method )
224 PHL Lab#5. Non-protein nitrogen (NPN) NPN includes the nitrogen from all nitrogenous substances other than proteins. The NPN could be measured as.
Serum biochemical parameters glucose assay Biochemistry Clinical practice CLS 432 Dr. Samah Kotb Lecturer of Biochemistry 2015.
1 IBLS Module 2 nd year Medicine Phase II, MBBS 2nd year Medicine- IBLS Module May 2008.
TOTAL PROTEIN Definition of protein:- A large group of nitrogenous organic compounds that are essential constituents of living cells; consist of polymers.
The use of LABORATORY ANALYSIS clinical practice.
TYPES OF SPECIMENS. Blood is a suspension of cells in a protein-salt matrix. Plasma: The non cellularportion of blood contains a series of proteins, some.
Biochemistry Clinical practice Lecturer of Biochemistry
Office: Building 5, 3rd floor, T251
LABORATORY MEDICINE.
Clinical diagnostic biochemistry - 3 Dr. Maha Al-Sedik 2015 CLS 334.
285 PHL Lab # 2 Plasma Proteins. Proteins: Classification Proteins: Classification 1- Simple proteins e.g. albumin and globulin 2- Conjugated proteins.
Determination of serum urea Cls331,,,experiment (8):
 chemical hazards e.g: toxic,flammables, corrosives and reactive  biological hazards e.g: microbes and plants  Radiation  Physical hazards e.g:heating.
Clinical Biochemistry Lab 1 Introduction
Lab (7): Diabetic profile
Dr.n.n.kumari MBBS-Year I term1 MCBM 1 Element 2 Lec-16.
Introduction and Separation of Plasma and Serum from Whole Blood
Outline of Today’s lecture 1. Introduction of Triglyceride 2. Clinical significance of Triglyceride 3. Principle of Triglyceride estimation.
Whole blood was the sample of choice for analysis However, values for glucose in whole blood are less than in plasma since red blood cells contain only.
(Anticoagulant).
Oral Glucose Tolerance Test (OGTT)
prepared by Dr. Akaber Tarek Biochemistry Department Clinical Chemistry prepared by Dr. Akaber Tarek Biochemistry Department Clinical Chemistry prepared.
Outline of Today’s lecture 1. Introduction of Lipoproteins 2. Discuss the different types of Lipoproteins 3. Identify healthy HDL & LDL levels 4. Principle’s.
Hematology Unit 2 Chapter 7 Sample Collection and Handling Copyright © 2015 by Mosby, an imprint of Elsevier Inc. All rights reserved.
Determination Of Albumin In Serum By Bromocresol Green Method
Outline of Today’s lecture 1. Discuss the different types of cholesterol 2. Identify healthy cholesterol levels 3. Clinical significance of cholesterol.
Exp #1 Glucose Quantitative determination of glucose in serum or plasma.
Exp#2 Total Protein Quantitative determination of total protein in serum using a biuret reaction.
Triglyceride determination
Plasma Proteins a prelude.
Determination of Blood Glucose By Alkaline Copper Reduction Method
BLOOD Islamic university.
The Excretory System.
BIOCHEMISTRY Blood Glucose
Practical Analysis Using Spectrophotometer
بسم الله الرحمن الرحيم 285 PHL Lab# 1 Introduction Blood.
Blood Glucose Test By Fifth Stage Student 18 Dr. Sakar Karem Abdulla
Exp#4 Cholesterol Quantitative determination of total cholesterol in serum /plasma by enzymatic color/endpoint method.
The Excretory System.
Separation of Plasma and Serum and Their Proteins from Whole Blood
Determination of Serum Total Protein Concentration
Determination of plasma enzymes
The Excretory System.
Urine Analysis Protein. Protein: Urine normally contains a scant amount of protein, which derives both blood and urinary tract itself. Proteins present.
Exp 7 UREA Bio-systems Kit.
Separation of Plasma and Serum and Their Proteins from Whole Blood
Presentation transcript:

BIOCHEMISTRY 285 PHL Introduction Blood Glucose

Blood Blood is vascular tissue that circulates in the closed system of blood vessels Functions: TransportationTransportation Regulation of acid-base balanceRegulation of acid-base balance Regulation of body temperatureRegulation of body temperature Protection against infectionsProtection against infections CoagulationCoagulation

Blood: Composition Blood Plasma Formed Elements RBCs WBCs Platelets Water Solids : Diffusible - Anabolic - Catabolic Non- diffusible

Types of Samples Whole bloodWhole blood Liquid (plasma)+ cells (RBCs, WBCs, platelets) PlasmaPlasma Water + solids (e.g. glucose, urea, albumin, fibrinogen) No cells SerumSerum Serum = plasma – clotting factors

Preparation of sample: Plasma Plasma Cent. tube anticoagulan t Add venous blood Mix then centrifuge Transfer the clear supernatant to specimen tube cells

Preparation of sample: Serum Serum Venous Blood Cent. tube Allow blood to clot (20min.) Remove the clot and centrifuge Transfer the clear supernatant to specimen tube cells

Centrifuging tubes Centrifugator

Plasma vs. Serum Plasma Plasma Serum Serum - Anticoagulant - Contains clotting factors - Advantage: time saving - No anticoagulant - Contains no clotting factors - Advantage: less interference

Anticoagulants Definition: Anticoagulants are chemicals which prevent blood clotting Types : 1- Heparin MOA: Prevents conversion of prothrombin to thrombin Advantage: less interference with chemical tests Disadvantage: high cost

Anticoagulants: cont. 2-EDTA (ethylene diamine tetraacetic acid): MOA: Binds to calcium Advantage: prevents platelets clumping 3-Oxalates: (Na, K, Li, or NH4 salts) MOA: Form insoluble complex with calcium Disadvantage: interfere with lactate dehydrogenase N.B Na, K salts should not be used in electrolytes determination

Anticoagulants: cont. 4-Citrate: e.g. trisodium citrate Used in ESR 5-Na fluoride: (enzyme poison) Used in blood sugar determination b/c it inhibits glycolysis N.B: it inhibits urease enz., therefore it should not be used in urea determination

Deproteinization Purposes: 1- To precipitate protein & use the ppt. in plasma protein determination e.g. albumin 2- Proteins have UV absorption and could interfere with tests 3- Proteins are colloids which make the solution turbid & difficult to read 4- Determination of non-protein nitrogen & glucose

Deproteinization Agents Acids 1- Trichloroacetic acid 2- Tungestic acid MOA: ↓ pH, proteins become cations & ppt as insoluble salts of acids Bases 1- Zinc hydroxide 2- Cu, Ba, Cd hydroxide MOA: ↑ pH, proteins become anions & ppt as insoluble salts of heavy metals Organic substances e.g. ethanol or ether MOA: remove water from protein mol.

Determination of Blood Glucose (BG) BG is determined by 2 methods: 1- Oxidation method ( enzymatic method): Principle -Glucose +O 2 + H 2 O Glucose oxidase Gluconic acid + H 2 O 2 -H 2 O 2 + phenol + amino-4-antipyrine Peroxidase Quinoneimine +H 2 O

Determination of Blood Glucose: Oxidation Method Procedure Sample name Stand. name Serum Stand. Reagent 0.1 ml 1 ml Mix, then incubate at 37°C for 10 min. Read the absorbance of sample & stand. at λ= 505 nm against blank (reagent)

Calculation Glugose (mg/dl) = Sample absorbance x conc of standard Stand. Absorbance Stand. Absorbance Normal level Normal level Fasting: mg/dl ( mmol/L)

Interpretation of the results If BG >110 mg/dl HYPERGLYCEMIAIf BG >110 mg/dl HYPERGLYCEMIA Causes:Causes: 1-Diabetis mellitus 2-Acromegaly 3-Acute stress 4-Adrenal hyperactivity (Cushing's syndrome) 5- Hyperthyroidism 6- Pancreatic cancer or pancreatitis 7- Drugs: e.g. corticosteroids

Interpretation of the results: cont. If BG <70 mg/dl HYPOGLYCEMIA Causes: 1- Insulin overdose 2- Hypothyroidism & hypopituitarism 3- Adrenal insufficiency (Addison's disease) 4- Liver diseases 5- Starvation

Renal glucose threshold Definition: -The blood glucose concentration at which the kidneys start to excrete glucose into the urine -BG level of 180 mg/dl is called Renal Glucose Threshold Glucoseurea Appearance of glucose in urine (occurs when BG conc. > 180 mg/dl)

Renal glucose threshold