Fatty Acid Positions in Triacylglycerol of Iridescent Shark Fish Oil (Pangasius sp.), Focusing on Omega-3 and Omega-6 Fatty Acids.

<b>Background and Objective:</b> Considering the many health benefits of fish oil, the potential of Indonesian fisheries needs to be mapped to find local fish oil sources that have the opportunity to be used as a source of omega-3 and 6. This research aimed to ascertain the glyceride profile of iridescent shark fish oil hydrolyzed by immobilized lipase from <i>Thermomyces lanuginosus</i> at the sn-1,3 position and identify the position of omega-3 and omega-6 fatty acids. <b>Materials and Methods:</b> To extract the fish oil from the iridescent shark, the soxhletation method was utilized. The analysis of the fatty acid composition that was carried out using gas chromatography (GC) was previously esterified with BF₃ before it was carried out to position the fatty acid hydrolysis that was carried out using lipase enzymes to position the fatty acid composition. <b>Results:</b> The sample had more unsaturated fatty acids than saturated ones. Omega-3 and omega-6 fatty acids are more concentrated in the fat molecule's sn-2 position than in the sn-1+sn-3 location. Iridescent shark fish oil meets the recommended ratio of omega-3 to omega-6 (1:1) or better (2:1). <b>Conclusion:</b> It has been discovered that iridescent shark fish oil is rich in omega-3 and omega-6 fatty acids, especially those in the sn-2 position. This makes it a great food choice for those trying to get more omega-3 unsaturated fatty acids into their diets.

Self-healing composite hydrogel with antibacterial and reversible restorability conductive properties.

Self-healable PAA/PPy-Fe composite hydrogels have been simply synthesized in one step and utilized for antibacterial and electrical conductivity application. The network of hydrogel is composed of polyacrylic acid (PAA) and Fe3+ ions with interlacing of the second polymeric chain of polypyrrole (PPy). In this study, ammonium persulfate (APS) was utilized to initiate the polymerization of both acrylic acid and pyrrole. Such hydrogels exhibited good mechanical properties and remarkable self-healing efficiency as well. The self-healing ability of the hydrogels was facilitated by ionic interaction between carboxylic anion groups (COO-) from polyacrylic acid (PAA) and Fe3+ ions. Moreover, the antibacterial activity of the composite hydrogels was examined on Escherichia coli via the disk diffusion method and the zone of inhibition was obtained in the range of 1.26-1.56 cm after incubation for 12 h. In addition, demonstration of the PAA/PPy-Fe composite hydrogels in electrical conductivity applications was performed in which the composite hydrogel was set up in an electrical circuit consisting of an LED and powered by 3 V batteries. The results showed that the electricity could light-up the LED through the PAA/PPy-Fe composite hydrogels and possessed reversible restorability, as indicated by the healed hydrogel consistently lighting-up the LED in the electrical circuit.

Preparation of In Situ Cross-Linked N-Maleoyl Chitosan-Oxidized Sodium Alginate Hydrogels for Drug Delivery Applications.

AIM: This study was aimed to prepare in situ cross-linked N-maleoyl chitosan - oxidised sodium alginate (MCS - OSA) hydrogel loaded with metronidazole (MTZ) for drug delivery applications. METHODS: The hydrogel was prepared by in situ cross-linking via Schiff base reaction between amine (-NH2) groups from MCS and aldehyde (-CHO) groups from OSA at the different ratio, and the MTZ was loaded into the hydrogels along with the gelatin processes. RESULTS: The highest drug entrapment efficiency (DEE) was exhibited by MTZ-H3 (5: 5) with DEE of 99.20% and a gel fraction of 97.52%. FTIR results revealed that Schiff base reaction was occurred by the absorption peak of -C = N- groups at 1628 cm-1 and indicated that there is insignificant alteration at different ratio of MCS and OSA. The best sustained of in vitro release profiles of MTZ was shown by MTZ-H3, which is 74.92% and 75.65% at pH 1.2 and 7.4 for 12 h of release, respectively. CONCLUSION: The optimised ratio between MCS and OSA to prepare in situ cross-linked hydrogels were found to be 5:5 according to the results of DEE and in vitro drug release profiles of MTZ and the MTZ loaded MCS-OSA hydrogels have a great potential which can be applied in biomedical applications.