The interrelation effect of slaughtering, drying, and defatting methods of BSFL on the oxidative quality of the derived fat was studied. Blanching and freezing were compared as slaughtering methods, followed by oven or freeze-drying for drying and mechanical pressing or SFE for defatting. The oxidative state and stability of the extracted fat and defatted meals were monitored immediately after their production, using peroxide value (PV) and Rancimat test, and over 24 weeks of storage. Slaughtering and drying methods had an independent effect on PV, with freezing and freeze-drying being the best methods. Mechanical pressing and SFE were comparable and superior to conventional hexane defatting. Interactions were observed between slaughtering and defatting, drying and defatting, and between all three factors. Generally, freeze-drying combined with any of the slaughtering and defatting methods resulted in the lowest PVs, with mechanical pressing being preferred. Freeze-drying plus mechanical pressing also produced the most stable fats during storage according to the evolution of PV, while the combination of blanching and SFE produced the least stable. A significant correlation was found between the PV at 24 weeks and the antioxidant activity of the fats. Contrary to storage assays, in accelerated Rancimat assays, freeze-dried samples were the least stable, which was partially attributed to the significant correlation with the acid values of the samples. Defatted meals followed a similar pattern to the extracted fat, except for worse oxidation for SFE defatting. Therefore, the different processing methods of slaughtering, drying, and defatting of BSFL differently affect lipid oxidation, with interactions between such successive steps.

The supercritical defatting of H. illucens was scaled up at 450 bar and 60 °C from a 270 cm³ extraction cell to a vessel five times larger. Then, eight different H. illucens larvae batches, with variable content of oil (16.80–29.17% w/w) and moisture (4.45–15.95% w/w) were defatted. The effect of these parameters on yield and oil composition was analyzed. The presence of moisture in the larvae batch, in the range of the values studied, had no negative effect on the oil recovery efficiency, which was mainly determined by the initial content of oil in the larvae samples. Furthermore, no differences were determined in the fatty acid profile of the oils recovered, which were rich in saturated fatty acids, mainly lauric acid (ca. 50% w/w). Minor lipids, such as squalene and phytosterols, were determined in all the oil samples. The moisture content in the oils extracted was in the range of 0.118–1.706% w/w. Therefore, some samples exceeded the limits recommended for volatile matter in edible fats and oils (0.2%, including moisture). Yet, concerning the oil peroxide index, values were much lower than those corresponding to the oil extracted using hexane.

Synsepalum dulcificum (Richardella dulcifica) is a berry fruit from West Africa with the ability to convert the sour taste into a sweet taste, and for this reason, the fruit is also known as the “miracle berry” (MB). The red and bright berry is rich in terpenoids. The fruit’s pulp and skin contain mainly phenolic compounds and flavonoids, which correlate with their antioxidant activity. Different polar extracts have been described to inhibit cell proliferation and transformation of cancer cell lines in vitro. In addition, MB has been shown to ameliorate insulin resistance in a preclinical model of diabetes induced by a chow diet enriched in fructose. Herein, we have compared the biological activities of three supercritical extracts obtained from the seed—a subproduct of the fruit—and one supercritical extract obtained from the pulp and the skin of MB. The four extracts have been characterized in terms of total polyphenols content. Moreover, the antioxidant, anti-inflammatory, hypo-lipidemic, and inhibition of colorectal cancer cell bioenergetics have been compared. Non-polar supercritical extracts from the seed are the ones with the highest effects on the inhibition of bioenergetic of colorectal (CRC) cancer cells. At the molecular level, the effects on cell bioenergetics seems to be related to the inhibition of main drivers of the de novo lipogenesis, such as the sterol regulatory element binding transcription factor (SREBF1) and downstream molecular targets fatty acid synthase (FASN) and stearoyl coenzyme desaturase 1 (SCD1). As metabolic reprograming is considered as one of the hallmarks of cancer, natural extracts from plants may provide complementary approaches in the treatment of cancer. Herein, for the first time, supercritical extracts from MB have been obtained, where the seed, a by-product of the fruit, seems to be rich in antitumor bioactive compounds. Based on these results, supercritical extracts from the seed merit further research to be proposed as co-adjuvants in the treatment of cancer.

The nutritional composition of insect-derived meals is strongly influenced by insect diet, while defatting can further modulate nutritional quality. However, some defatting methods, such as supercritical CO₂ extraction, depend on sample properties, including density and macromolecule distribution. Therefore, diet-induced changes may affect lipid extraction efficiency and kinetics, a relationship that remains unexplored. This study evaluated the impact of feeding Hermetia illucens larvae with by-products from olive oil industry (olive leaves, OL, at 15, 30 or 50%; dry full-fat olive pomace, OP, at 30, 50, 70, 90%) or quinoa processing (husk, QH, at 15, 30 or 50%) on supercritical CO₂ defatting performance, meal composition, amino acid profile and digestibility. Despite diet-induced variations in lipid accumulation, defatted kinetics mainly depended on the content and solubility of extractable material, while differences in packed bed microstructure had a minor effect. Protein-rich meals were obtained (25–35%), although most diets reduced protein content, except OP50. QH15 and OP30 worsened essential amino acids in meals, whereas OP50 improved them. Chitin content increased, especially for OP-based meals. Digestibility slightly improved with OP30, OP70, QH15, and QH50. These results show the potential of olive oil and quinoa by-products to be up-cycled by H. illucens into high-value insect meals, without compromising the processing by supercritical CO₂ defatting, supporting sustainable insect-based food and feed production.

The aim of this study was to investigate the suitability of Pressurized Liquid Extraction (PLE) and Supercritical Fluid Extraction (SFE) for Quercus robur bark and Artemisia vulgaris extraction. PLE of Q. robur and A. vulgaris were carried out at different temperatures with water, ethanol and several hydroalcoholic mixtures. SFE of A. vulgaris was performed at different pressures and ethanol concentrations. The anti-inflammatory activity of Q. robur extracts, the antibacterial activity of A. vulgaris extracts and the antioxidant activity of the extracts from both materials were determined. The highest phenolic compound content and antioxidant activity of Q. robur extracts were achieved with water at 100 °C (487.97 mg GAE/g and 3741 µg trolox/g). The highest values for A. vulgaris extracts were obtained with ethanol at 200 °C (149.16 mg/g and 437.13 µmol/g). The ethanolic extract at 150 °C from A. vulgaris had a noticeable anti-inflammatory activity (inhibition of TNF-α and IL-6 secretion near basal values and inhibition of IL-1β higher than 80% at 20 µg/mL). A. vulgaris extracts obtained by SFE exerted antibacterial activity against E. coli (IC₅₀ of 1388 µg/mL with neat SCCO₂ at 15 MPa) and S. aureus (1406 µg/mL using SCCO₂ with 10% ethanol).