Determination of Phospholipid Oxidation by UV/VIS Spectroscopy
DEFINITION
The percent oxidation of a phospholipid can be determined by using Beer’s Law to calculate the peroxidized phospholipid’s concentration from its absorbance at 234 nm.
SCOPE
Applicable to all unsaturated phospholipids.
APPARATUS
- UV/VIS Spectrophotometer
- HELLMA UV Quartz Sample Cell (QS 1.000)
- Kimwipes
- Disposable Glass Tubes
REAGENTS
- Ethanol (200 proof, dehydrated USP)
- Deionized water
- #850355: Dipalmitoyl Phosphatidylcholine (DPPC) Avanti Cat. #850355
PROCEDURE
- Prepare the DPPC Sample. Prepare a minimum of 3 mL of a 1mg/mL solution of DPPC dissolved in ethanol/DI water (9:1).
- Prepare the Sample. Prepare a minimum of 3 mL of a 1mg/mL solution of the phospholipid sample dissolved in ethanol/DI water (9:1).
- Run the Blank. The blank (background) is the solvent used to dissolve the phospholipid samples.
- Rinse the sample cell with the solvent three times to remove any residual contaminants from the cell.
- Fill 3/4 of the sample cell with the reference.
- Use a Kimwipe to wipe off all fingerprints and contaminants on the exterior of the sample cell.
- Insert the sample cell into the spectrophotometer and run a blank spectrum.
- Run the DPPC Sample.
- Pour the blank solvent out of the sample cell.
- Fill 3/4 of the sample cell with the DPPC sample solution.
- Remove fingerprints from the exterior of the sample cell.
- Insert the sample cell into the spectrophotometer and run a DPPC spectrum.
- Run the Sample.
- Pour the DPPC sample out of the sample cell.
- Rinse the sample cell with the solvent three times to remove any residual DPPC from the cell.
- Fill 3/4 of the sample cell with the phospholipid sample.
- Remove fingerprints from the exterior of the sample cell. Insert the sample cell into the spectrophotometer and run a sample spectrum.
- Subtract the DPPC spectrum from the sample spectrum and record the phospholipid sample’s absorbance reading (OD) at 234 nm.
CALCULATIONS
Concentration of peroxidized lipid (D) = A/(B*C) A = Absorbance reading (OD) at 234 nm B = Extinction coefficient in (OD*mL)/(mmol*cm) (27,000 for peroxidized lipid) C = Path length in cm Percent oxidation = D/E * 100 D = Concentration of peroxidized lipid in mg/mL E = Concentration of lipid sample = 1.0 mg/mL
REFERENCES
- R.S. Kim & F.S. LaBella (1987). Comparison of analytical methods for monitoring autoxidation profiles of authentic lipids. J. Lipid Res. 28:1110-1117.