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The chemical properties of the African palm weevil, Rhychophorus phoenicis (F.) (Coleoptera: Curculionidae), larvae were evaluated using standard methodology. The chloroform-methanol extract yielded 37.12% on a dry basis. The oil was liquid at room temperature with a flash point of 36.0 °C. Analysis of the physical constants indicated values of 192.25 Wijs and 427.70 mg KOH/g as iodine and saponification, respectively. Fatty acid analysis of the extracted oil showed the presence of unsaturated fatty acids at low levels. Palmitic acid and stearic acid constituted 35.3 and 60.5% of the oil, respectively. The usual behaviour of the oil at room temperature, irrespective of the level of unsaturation of its constituent fatty acid was noted. The total protein content of the defatted palm weevil larva (dry basis) was estimated at 66.3%. The amino acid values compared favourably to FAO reference protein, except for tryptophan, which was limiting. All the other essential amino acids were adequate. Mineral analysis revealed high levels of potassium (1025 mg/100 g) and phosphorus (685 mg/100 g). The dried and defatted palm weevil lava represents a very good source of protein, and a good complement of essential amino acids.

The chemical and antioxidant properties of the ethanolic extract of Tetrapleura tetraptera fruit peels were investigated. Dried peels of T. tetraptera fruits were extracted with ethanol. The extract was subjected to preliminary phytochemical screening using standard procedures. GC-MS was used in identifying the secondary metabolites. The antioxidant properties of the extract were determined by its ferric reducing activity, 2,2-diphenyl-1-picrylhydrazyl (DPPH) and nitric oxide (NO) radicals scavenging activities, and the inhibition of lipid peroxidation in hepatic tissues of albino male rats. Preliminary phytochemical screening revealed the presence of flavonoids, phenols, tannins, saponins, terpenoids and phlebotannin. GC-MS analysis revealed the presence of D-fructose, piperazine, octodrine, glycidol, glyceraldehydes, 6-octadecenoic acid and 9,12-octadecenoic acid, with D-fructose being the most predominant compound. The extract exhibited high antioxidant activities both in vitro and ex vivo, as indicated by its ability to scavenge DPPH and nitric oxide as well as inhibition of lipid peroxidation. This is further portrayed by its ferric reducing activity. These results suggest an antioxidant protective effect of the extract against oxidative hepatic damage and can be attributed to a synergetic action of the identified bioactive compounds.