LIPID ANALYSIS.ppt

LIPID ANALYSIS  Introduction  Some of the most important properties of concern to the food analyst are: 1. Total lipid concentration 2. Type of lipids present 3. Physicochemical properties of lipids 4. Structural organization of lipids within a food Why we are intereste...

LIPID ANALYSIS  Introduction  Some of the most important properties of concern to the food analyst are: 1. Total lipid concentration 2. Type of lipids present 3. Physicochemical properties of lipids 4. Structural organization of lipids within a food Why we are interested in lipid analysis? 1. Nutritional importance (omega 3, saturated fat, cholesterol, fat sol vitamins). 2. Oxidative stability of foods (stability of many foods is affected by fatty acid composition or presence of enzymes that act on lipids such as lipoxygenase, lipase etc). 3. Physical properties of foods (melting behavior in chocolate, margarine, etc.)  Components of Lipids in Foods  Triacylglycerol  Phospholipids  Diacylglycerol  Sterols  Monoacylglycerol  Carotenoids  Free Fatty Acids  Glycolipids  Waxes  Determination of Lipid Composition  Important reasons: 1. Legal – amount of saturated, unsaturated etc 2. Food quality – desirable characteristics 3. Lipid oxidation – unsaturated fatty acids prone to oxidation 4. Adulteration – lard in fat food  Sampling method  It depends on 1. Type of food – meat, milk, margarine 2. The nature of the lipid component – volatility, physical state 3. Type of analytical procedure used – solvent extraction, instrumental technique  Determination of Total Lipid Concentration  Reasons to analyze total lipid concentration: 1. Economic – not to give away expensive ingredients 2. Legal – to conform food regulations 3. Health - development of low fat foods 4. Quality – food properties depend on the total lipid content  Solvent Extraction Lipids – soluble in organic solvents but insoluble in water Sample Preparation Drying sample – solvent cannot easily penetrate foods containing water Particle size reduction – finely ground Acid hydrolysis – to release bound lipids into easily extractable forms Solvent selection – choose the best solvent for the extraction  Solvent Selection  Solvent selection is important since a solvent that is too polar will poorly extract non-polar lipids and will extract non-lipid materials (i.e carbohydrates)  Too non-polar will be inefficient for more polar lipids.  Ideal Solvent For Fat Extraction  High solvent power  Non flammable / for lipids not explosive  Low solvent power  Nontoxic for nonlipids  Low surface tension  No residue with food  Evaporate easily (low  Single compound heat of vaporization  Cheap  Low boiling point  Non-hygroscopic Ethyl ether is used  Petroleum ether is a lot but is an excellent solvent for lipids Very flammable  More selective for Explosion hazard more hydrophobic lipids Forms peroxides  Non hygroscopic Expensive  Less flammable  Cheaper  Batch Solvent Extraction Mixing sample with organic solvent in separating funnel Shake vigorously and allow the separation either by gravity or centrifugation Aqueous phase is decanted off and the concentration of lipid in the solvent is determined by evaporating off the solvent and measure the mass lipid remaining Have to be repeated a few times  Semi-Continuous Solvent Extraction Used to increase efficiency of lipid extraction from foods Common method: Soxhlet extraction Solvent extracts the lipids and carries them into the flask The lipids still remain in the solvent due to low volatility  Continuous Solvent Extraction Commonly used is Goldfisch method Similar to soxhlet method except the extraction chamber is designed. Solvent trickles through the sample rather than building up around it Disadvantage: channeling of the solvent can occur i.e. solvent may take certain routes through the sample GOLDFISH Accelerated Solvent Extraction  By increase the temperature and pressure normally used.  The effectiveness of the lipid extraction increases as its temperature increases, but the pressure must also be increased to keep the solvent in the liquid state.  Advantage: reduce the amount of solvent Supercritical Fluid Extraction  Pressurized CO2 is heated above a certain critical temperature to become supercritical fluid  This fluid behaves like a gas to easily penetrate into a sample and extract lipid while it also behaves like a liquid to dissolve a large quantity of lipids.  The CO2 extracts the lipid, and forms a separate solvent layer, which is separated from the aqueous components Non-solvent Liquid Extraction Methods 1. Babcock Method  A specified amount of milk is accurately pipetted into Babcock bottle  Sulfuric acid: breaks down the fat globule membrane than surrounds the droplet and thereby release the fat  Lipid is removed from the aqueous phase by centrifuging while it is hot (55- 60°C)  The neck is graduated to give the amount of milk fat present in the food. 2. Gerber Method Used mixture of sulfuric acid and isomyl alcohol and a slightly different shaped bottle Isomyl alcohol: prevent charring of the sugars by heat and sulfuric acid Difficult to read the fat content from graduated flask Faster and simpler than Babcock method 3. Detergent Method  Developed to overcome the inconvenience and safety concerns associated with sulfuric acid  A sample is mixed with a combination of surfactants  Surfactants displace the fat globule membrane which surrounds the emulsion droplets in milk and causes them to coalesce and separate  Amount of fat is read after centrifugation.  Separation and analysis by Chromatography The most powerful analytical procedures for separating and analyzing the properties of lipids Information can be used: Amount of saturated, unsaturated, polyunsaturated and cholesterol Degree of lipid oxidation Detect adulteration Determine the presence of antioxidants Lipid fractions by Thin Layer Chromatography (TLC) A TLC plate is coated with a suitable absorbing material and placed into an appropriate solvent. A small amount of lipid sample to be analyzed is spotted onto the TLC plate With time, the solvent moves up the plate due to capillary forces and separates different lipid fractions on the basis of their affinity for the absorbing material  At the end of the separation, the plate is sprayed with a dye so as to make the spots visible  Identification of lipid present can be done by comparing the distance that the spots move with standards of known composition  Spots can be scraped off and analyzed further using GC, NMR and HPLC Fatty acid Methyl Esters (FAMEs) by Gas Chromatography (GC) TAG are first saponified which breaks them down to glycerol and free fatty acids, and are then methylated Saponification reduces MW and methylation reduces the polarity, both of which increase the volatility of the lipids The FAMEs are dissolved in a suitable organic solvent that is injected into a GC injection chamber.  Chemical Techniques 1. Iodine Value (IV)  IV gives a measure of the average degree of unsaturation of a lipid: the higher the iodine value, the greater the number of C=C double bonds.  By definition the iodine value is expressed as grams of iodine absorbed per 100 g of lipid.  Commonly used methods: Wijs method.  General Procedure  The lipid to be analyzed is weighed and dissolved in a suitable organic solvent, to which a known excess of iodine chloride is added. Some of the ICl reacts with the double bonds in the unsaturated lipids, while the rest remains: R-CH=CH-R + IClexcess  R-CHI-CHCl-R + IClremaining  The amount of ICl that has reacted is determined by measuring the amount of ICl remaining after the reaction has gone to completion (IClreacted =IClexcess - IClremaining).  The amount of ICl remaining is determined by 1. adding excess potassium iodide to the solution to liberate iodine, and 2. then titrating with a sodium thiosulfate (Na2S2O3) solution in the presence of starch to determine the concentration of iodine released Iodine itself has a reddish brown color, but this is often not intense enough to be used as a good indication of the end-point of the reaction. For this reason, starch is usually used as an indicator because it forms a molecular complex with the iodine that has a deep blue color. Initially, starch is added to the solution that contains the iodine and the solution goes a dark blue. Then, the solution is titrated with a sodium thiosulfate solution of known molarity.  Saponification Number The saponification number is a measure of the average molecular weight of the triacylglycerols in a sample. Saponification is the process of breaking down a neutral fat into glycerol and fatty acids by treatment with alkali The saponification number is defined as the mg of KOH required to saponify one gram of fat. The smaller the saponification number, the larger the average MW of the TAG present Procedure: The lipid is first extracted and then dissolved in an ethanol solution which contains a known excess of KOH. This solution is then heated so that the reaction goes to completion. The unreacted KOH is then determined by adding an indicator and titrating the sample with HCl. Saponification Value of Fats and Oils Fat Saponification Value Milk fat 210-233 Coconut Oil 250-264 Cotton seed oil 189-198 Soybean Oil 189-195 Lard 190-202  Acid Value / free fatty ACIDS The acid value is a measure of the amount of free fatty acids present in a given amount of fat. The lipids are extracted from the food sample and then dissolved in an ethanol solution containing an indicator. This solution is then titrated with alkali (KOH) until a pinkish color appears. The acid value is defined as the mg of KOH necessary to neutralize the fatty acids present in 1g of lipid.  The acid value may be overestimated if other acid components are present in the system, e.g. amino acids or acid phosphates.  The acid value is often a good measure of the break down of the triacylglycerols into free fatty acids, which has an adverse effect on the quality of many lipids. Physical Properties of Fats and Oils  Solid Fat Content  The solid fat content (SFC) of a lipid influences many of its sensory and physical properties, such as spreadability, firmness, mouthfeel, processing and stability.  Food manufacturers often measure the variation of SFC with temperature when characterizing lipids that are used in certain foods, e.g., margarine and butter.  The solid fat content is defined as the percentage of the total lipid that is solid at a particular temperature. Principle: The density of solid fat is higher than the density of liquid oil, and so there is an increase in density when a fat crystallizes and a decrease when it melts. By measuring the density over a range of temperatures it is possible to determine the solid fat content - temperature profile Basically, the sample is placed into an NMR instrument and a radio frequency pulse is applied to it. This induces a NMR signal in the sample, whose decay rate depends on whether the lipid is solid or liquid. The signal from the solid fat decays much more rapidly than the signal from the liquid oil and therefore it is possible to distinguish between these two components  Techniques based on differential scanning calorimetry are also commonly used to monitor changes in SFC.  These techniques measure the heat evolved or absorbed by a lipid when it crystallizes or melts.  By making these measurements over a range of temperatures it is possible to determine the melting point, the total amount of lipid involved in the transition and the SFC-temperature profile.  Melting Point  Clear point. A small amount of fat is placed in a capillary tube and heated at a controlled rate. The temperature at which the fat completely melts and becomes transparent is called the "clear point".  Slip point. A small amount of fat is placed in a capillary tube and heated at a controlled rate. The temperature at which the fat just starts to move downwards due to its weight is called the "slip point".  Wiley melting point. A disc of fat is suspended in an alcohol-water mixture of similar density and is then heated at a controlled rate. The temperature at which the disc changes shape to a sphere is called the "Wiley melting point".  Cloud point  This gives a measure of the temperature at which crystallization begins in a liquid oil.  A fat sample is heated to a temperature where all the crystals are known to have melted (e.g., 130oC).  The sample is then cooled at a controlled rate and the temperature at which the liquid just goes cloudy is determined.  This temperature is known as the cloud point, and is the temperature where crystals begin to form and scatter light.  It is often of practical importance to have an oil which does not crystallize when stored at 0oC for prolonged periods.  A simple test to determine the ability of lipids to withstand cold temperatures without forming crystals, is to ascertain whether or not a sample goes cloudy when stored for 5 hours at 0oC.  Smoke point  Is the temperature at which the sample begins to smoke when tested under specified conditions.  A fat is poured into a metal container and heated at a controlled rate in an oven.  The smoke point is the temperature at which a thin continuous stream of bluish smoke is first observed.  Flash point  Is the temperature at which a flash appears at any point on the surface of the sample due to the ignition of volatile gaseous products.  The fat is poured into a metal container and heated at a controlled rate, with a flame being passed over the surface of the sample at regular intervals.  Fire point  Is the temperature at which evolution of volatiles due to the thermal decomposition of the lipids proceeds so quickly that continuous combustion occurs (a fire).  Methods of Analyzing Lipid Oxidation in Foods  High concentration of unsaturated fatty acid are particularly susceptible to lipid oxidation  This leads to the formation of off-flavours and potentially toxic compounds  Lipid oxidation process consists of  Reactants – unsaturated fatty acids and O2  Primary products – peroxides and conjugated dienes  Secondary products – ketones, aldehydes, alcohols and hydrocarbons  Oxygen Uptake  Measuring the oxygen uptake by the sample as the reaction proceeds  Lipids is placed in a sealed container and the amount of oxygen that must be input into the container to keep the O2 concentration in the head-space above the sample constant is measured  Peroxide Value (PV)  Peroxides (ROOH) are primary reaction products formed in the initial stages of oxidation, and therefore give an indication of the progress of lipid oxidation.  The lipid is dissolved in a suitable organic solvent and an excess of KI is added: ROOH + KIexcess  ROH + KOH + I2  Once the reaction has gone to completion, the amount of ROOH that has reacted can be determined by measuring the amount of iodine formed. This is done by titration with sodium thiosulfate and a starch indicator  The amount of sodium thiosulfate required to titrate the reaction is related to the concentration of peroxides in the original sample  There are a number of problems with the use of peroxide value as an indication of lipid oxidation. 1. Peroxides are primary products that are broken down in the latter stages of lipid oxidation. Thus, a low value of PV may represent either the initial or final stages of oxidation. 2. The results of the procedure are highly sensitive to the conditions used to carry out the experiment, and so the test must always be standardized.  Anasidine Value  Is a measure of secondary oxidation  Suitable to determine quality of crude oils and efficiency of the processing procedures  Not suitable to detect fat oxidation  Principle: ρ-anasidine reacts with aldehyde compounds in an oil, producing yellowish reaction products  Thiobarbituric Acid (TBA)  It measures the concentration of relatively polar secondary reaction products  The lipid to be analyzed is dissolved in a suitable non-polar solvent which is contained within a flask  An aqueous solution of TBA reagent is added to the flask and the sample is shaken which causes the polar secondary products to be dissolved in it.  The aqueous phase is then separated from the non-polar solvent, placed in a test-tube and heated for 20 minutes in boiling water which produces pink color  The intensity of the pink color is measured using UV-Vis spectrophotometer at absorbance 540 nm  Also referred as thiobarbituric acid reactive substances (TBARS) method  Accelerated Oxidation Tests  To determine the susceptibility of the fats or oils to oxidation as oxidation can take a long time to occur.  These methods artificially increase the rate of lipid oxidation by exposing the lipid to heat, oxygen, metal catalysts, light or enzymes  A typical accelerated oxidation test are  Active Oxygen Method (AOM) – a liquid sample is held at 98°C while air is constantly bubbled through it. Oxidation is determined by measuring the PV or detection of rancid odors  Schaal Oven Test – A known weight of oil is placed in an oven at a specified temperature and time until rancidity is detected by SE or measuring PV Fat crystals Temperature 30C