Extraction of dried sage and coriander seed was carried out using near critical carbon dioxide to obtain oleoresin, non-volatile oil and essential oil extracts. Extractions were carried out in both a 4 litre and 75 litre extraction plant, to determine the effects of the particle size, carbon dioxide flow rate, bulk density and extraction temperature and pressure on the yield and extraction time. The rate of extraction of oleoresin from sage depended only on the particle diameter, and was limited by intra-particle diffusion. The rate of extraction of non-volatile oil from coriander seed was limited both by its solubility in carbon dioxide, and intra-particle diffusion. The results were satisfactorily correlated with a mathematical model. Scale-up calculations were performed to enable the economics of the extraction process to be evaluated.

Substituted phenols, anilines, pyridines and mononitrobenzenes can be classified as polar narcotics. These chemicals differ from non-polar narcotic compounds not only in their toxic potency (normalized by log Kₒw), but also in their Fish Acute Toxicity Syndrome profiles, together suggesting a different mode of action.For 97 polar narcotics, which are not ionized under physiological conditions, 11 physico-chemical and quantum-chemical descriptors were calculated. Using principal component analysis, 91 % of the total variance in this descriptor space could be explained by three principal components which were subsequently used as factors in a statistical design. Eleven compounds were selected based on a two-level full factorial design including three compounds near the center of the chemical domain (a 2³+3 design).QSARs were developed for both the design set and the whole set of 63 polar narcotics for which guppy and/or fathead minnow data were available in the literature. Both QSARs, based on partial least squares regression (3 latent variables), resulted in good models (R²=0.96 and Q²=0.82; R²=0.86 and Q²=0.83 respectively) and provided similar pseudo-regression coefficients. In addition, the model based on the design chemicals was able to predict the toxicity of the 63 compounds (R² =0.85).Models show that acute fish toxicity is determined by hydrophobicity, HOMO-LUMO energy gap and hydrogen-bond acceptor capacity.