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I need a procedure to measure the tocols activity after few days the tocols standard prepared. Its mentioned that then tocols conc in standard stock solution need to re-adjust the conc. of standard tocols. And I found one journal said like this...
Standards will be standardized using spectrophotometric measurements at the following wavelengths: 292 nm (α-tocopherol, α-tocotrienol), 296 nm (β-tocopherol, β-tocotrienol), 297 nm (γ-tocotrienol, δ-tocotrienol) and 298 nm (γ- tocopherol, δ-tocopherol). Absorbance difference (A-A0) of each working solution is measured with a spectrophotometer at defined above wavelength. A is the absorbance of a standard solution and A0 is absorbance of blank ethanol. The concentrations of standard solutions, made in ethanol matrix, will be corrected based on tabular data for extinction coefficient (E1cm 1%) of 75.8, 89.4, 91.4, 87.3, 86.0, 86.2, 91.0 and 85.8 for α-tocopherol β-tocopherol, γ-tocopherol, δ-tocopherol, α-tocotrienol, β-tocotrienol, γ-tocotrienol and δ-tocotrienol, respectively. Concentrations will be calculated from peak area determined by the spectrophotometer and linear regression.
How to calculate the conc. using spectrophotometer. IS there any source that give full explanation about this. Hope will get reply from you all.Thank You
