This is to ensure that the endogenous species overlapping with the internal standard at the spectral resolution is less than 1% of the most abundant species in the class of interest. For quantification of lipid species in a biological sample, prior to extraction, appropriate amounts of suitable internal standards are added based on a parameter that Inhibitors,research,lifescience,medical can be determined accurately and is least varied from sample to sample so that comparison of lipid content between samples can be made. The lipid content of the sample quantified by ratiometric comparison with

the internal standards can then be reported after normalization to the parameter. The protein, DNA or RNA content in tissue or cell samples, the tissue wet or dry weight, the cell number, the phosphorus content in the lipid extract, and the volumes of the body fluids are some of the parameters used most often by investigators. Each parameter has benefits and disadvantages. For example, determination of phosphorus content may carry a large experimental error and may be variable under BMS-345541 different physiological Inhibitors,research,lifescience,medical and pathological conditions.

Tissue samples may carry different amounts of water in preparation while it is time-consuming to obtain dry tissue weight. The volume of biofluid may vary with the fluid intake prior to sampling. The cell number counting may become difficult with the Inhibitors,research,lifescience,medical presence of aggregated cells. Accordingly, protein or DNA or RNA content as a normalization parameter is highly recommended. Note that although the levels of many proteins change from one state to another, the amounts of the structural proteins that account for most of the protein content of a biological sample Inhibitors,research,lifescience,medical do not change significantly. 5.2. Aggregation of Lipid Species and Dynamic Range of Quantification Lipids readily form aggregates (e.g., dimers, oligomers, or micelles) as the lipid concentration increases or the solvent of a lipid solution becomes more polar due to the unique high hydrophobicity of lipid species. The higher the hydrophobicity of a lipid species

Inhibitors,research,lifescience,medical (e.g., longer acyl chain or less unsaturation), the lower the concentration at which the lipids aggregate. Lipids in aggregated forms cannot be ionized efficiently. Accordingly, lipid species containing short and/or Idoxuridine polyunsaturated acyl chains might show higher apparent response factors than those in the same class containing long and/or saturated acyl chains at a concentration that lipid aggregates form. Therefore, lipid aggregation could substantially affect ionization efficiency in a species-dependent fashion. Subsequently, ionization of individual lipid species in a polar lipid class becomes not only charged head group-dependent but also species-dependent, which violates Equation 3. It is, therefore, critical to keep the total lipid concentration lower than the concentration that favors aggregate formation.