Em. Grima et al., COMPARISON BETWEEN EXTRACTION OF LIPIDS AND FATTY-ACIDS FROM MICROALGAL BIOMASS, Journal of the American Oil Chemists' Society, 71(9), 1994, pp. 955-959
Seven solvent mixtures have been used to extract the lipid fraction of
lyophilized biomass of Isochrysis galbana. Six of them were composed
of biocompatible solvents. Each method was carried out under relaxed o
perating conditions (i.e., one hour at room temperature) with extracti
on in a nitrogen atmosphere to prevent autooxidation and degradation o
f polyunsaturated fatty acids (PUFAs). Apart from the well-established
Bligh and Dyer method [Can. J. Biochem. Physiol 37:911 (1959)] (Cl3CH
/MeOH/H2O, 1:2:0.8, vol/vol/vol), which rendered the highest yield of
lipids (93.8%), ethanol (96%) and hexanelethanol (96%), 1:2.5 vo/vol p
roduced the best results (84.4 and 79.6%, respectively). To obtain fre
e fatty acids, KOB was added to the solvent mixtures used to extract t
he total lipids, except for Cl3CH/MeOH/H2O, and direct saponification
was carried out at 60 degrees C for 1 h or at room temperature for 8 h
. The highest yields obtained by direct saponification were 81% with h
exanelethanol (96%), 1:2.5, vol/vol and 79.8% with ethanol (96%). Part
ial yields of the main n-3 PUFAs found in I. galbana, stearidonic acid
(SA), eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), wer
e calculated for both extraction methods. For lipid extraction with et
hanol (96%), yields of 91, 82 and 83% were obtained for SA, EPA and DH
A, respectively. When direct saponification was used, hexanelethanol (
96%; 1:2.5, vol/vol) produced the best yields of (91, 79 and 69% for S
A, EPA and DHA, respectively).