ABSTRACT
Lubricating oils are composed of base oils (>85% v/v) and enriching additives (<15% v/v). Three types of base oils may be distinguished: 1) traditional bases (obtained by low-volatile fractions from crude oil distillation refining), 2) synthetic bases (mainly poly-alpha-olefins, sometimes esters, especially succinic acid esters), 3) bases of natural origin (especially obtained from refined plant oils). The bases of natural origin are the only ones recommended for application when lubricating oil may be emitted to the environment (e.g. when the machine with an open cutting system is used). Group-type separation and analysis of group-type composition of base and lubricating oils are of significant importance in quality control and environmental monitoring. Due to the potentially wide range of polarity of the components of base and lubricating oils, group- type separation becomes a difficult separation problem. It is also a serious analytical problem due to the considerable diversity of physicochemical properties. The authors propose a new procedure for the separation and determination of the group-type composition of base and lubricating oils using thin-layer liquid chromatography in normal phase systems (abr. NP-TLC) on silica gel plates impregnated with berberine salt/in the coupling of thin-layer chromatography with flame ionization detection (abr. TLC-FID). A new, effective procedure of TLC plates impregnation with berberine sulphate was presented. The proposed procedure ensures the visualization of all groups of base oils. Extensive experimental research showed that a 2-step development procedure with application of n-hexane up to 100% height of development +15 min and further n-hexane: isopropanol: tri-fluoroacetic acid 96.25: 3: 0.75 (v: v: v) up to 75% height of development is advantageous for the group-type separation, both in TLC-FID and TLC.
Subject(s)
Chromatography, Thin Layer/methods , Lubricants , Oils , Petroleum/analysis , Berberine/chemistry , Flame Ionization , Lubricants/analysis , Lubricants/chemistry , Lubricants/isolation & purification , Oils/analysis , Oils/chemistry , Oils/isolation & purificationABSTRACT
Oil extracted from spent coffee grounds (SCG) [yield 16.8 % (w/w)] was discovered to be a highly suitable carbon substrate for the biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) [P(3HB-co-3â¯HV)] copolymers by Cupriavidus necator DSM 545 in the absence of any traditional 3â¯HV precursors. Cells cultivated in a 3â¯L bioreactor (batch) reached a total biomass concentration of 8.9â¯g L-1 with a P(3HB-co-3â¯HV) (6.8â¯mol% 3â¯HV) content of 89.6 % (w/w). In contrast, cells grown on sunflower oil reached a total biomass concentration of 9.4â¯gL-1 with a P(3HB-co-3â¯HV) (0.2â¯mol% 3â¯HV) content of 88.1 % (w/w). It is proposed that the organism could synthesize 3â¯HV monomers from succinyl CoA, an intermediate of the tricarboxylic acid (TCA) cycle, via the succinate-propionate metabolic pathway.
Subject(s)
Coffee/chemistry , Cupriavidus necator/metabolism , Oils/chemistry , Polyesters/metabolism , Coffee/metabolism , Cupriavidus necator/chemistry , Molecular Structure , Oils/isolation & purification , Oils/metabolism , Polyesters/chemistryABSTRACT
Ganoderma lucidum (Leyss. ex Fr.) Karst. is a valuable dietary supplement used worldwide for promoting health as well as a medicinal fungus for handling fatigue, immunological disorders, and cancer. Previous studies have revealed the immunoenhancing effect of G. lucidum and the polysaccharide extract, with potential involvement of gut microbiome. The oil of G. lucidum spores (GLSO)is one of the well-known G. lucidum-related products. However, there is little evidence supporting the immune promotion activity and the underlying mechanisms. The present study aims to investigate the immunoenhancing effect of GLSO in mice. GLSO enhanced macrophage phagocytosis and NK cell cytotoxicity of mice. Further microbiome and metabolomics studies showed that GLSO induced structural rearrangement of gut microbiota, mediating alterations in a wide range of metabolites. By clustering, multivariate and correlation analysis, the immunoenhancing effect of GLSO was found to be highly correlated with elevated abundance of several bacterial genera (Lactobacillus, Turicibacter and Romboutsia) and species (Lactobacillus_intestinalis and Lactobacillus_reuteri), and decreased level of Staphylococcus and Helicobacter, which resulted in the regulation of a range of key metabolites such as dopamine, prolyl-glutamine, pentahomomethionine, leucyl-glutamine, l-threonine, stearoylcarnitine, dolichyl ß-d-glucosyl phosphate, etc. These results provide new insights into the understanding of the modulatory effect of GLSO on immune system.
Subject(s)
Adjuvants, Immunologic/pharmacology , Gastrointestinal Microbiome/physiology , Metabolomics/methods , Oils/pharmacology , Reishi , Spores, Fungal , Adjuvants, Immunologic/isolation & purification , Animals , Cell Line , Dietary Supplements , Gastrointestinal Microbiome/drug effects , Male , Mice , Mice, Inbred ICR , Oils/isolation & purification , Sheep , Spores, Fungal/isolation & purificationABSTRACT
Brain aging is commonly associated with neurodegenerative disorders, but the ameliorative effect of krill oil and the underlying mechanism remain unclear. In this study, the components of krill oil were measured, and the antiaging effects of krill oil were investigated in mice with d-galactose (d-gal)-induced brain aging via proteomics and gut microbiota analysis. Krill oil treatment decreased the expression of truncated dopamine- and cAMP-regulated phosphoproteins and proteins involved in the calcium signaling pathway. In addition, the concentrations of dopamine were increased in the serum (p < 0.05) and brain (p > 0.05) due to the enhanced expressions of tyrosine-3-monooxygenase and aromatic l-amino acid decarboxylase. Moreover, krill oil alleviated gut microbiota dysbiosis, decreased the abundance of bacteria that consume the precursor tyrosine, and increased the abundance of Lactobacillus spp. and short-chain fatty acid producers. This study revealed the beneficial effect of krill oil against d-gal-induced brain aging and clarified the underlying mechanism through proteomics and gut microbiota analysis.
Subject(s)
Aging/drug effects , Brain/physiopathology , Euphausiacea/chemistry , Galactose/adverse effects , Gastrointestinal Microbiome/drug effects , Oils/administration & dosage , Aging/physiology , Animals , Bacteria/classification , Bacteria/drug effects , Bacteria/genetics , Bacteria/isolation & purification , Brain/drug effects , Dietary Supplements/analysis , Humans , Intestines/drug effects , Intestines/microbiology , Male , Mice , Oils/isolation & purificationABSTRACT
Polyhydroxyalkanoates (PHAs) are three-level group of biodegradable polymers and attractive substitutes over conventional plastics to avoid the pollution problems. The yeast strain isolated from sugarcane juice, identified as Wickerhamomyces anomalus VIT-NN01, was used for the production of polyhydroxyalkanoates (PHA). Response surface methodology (RSM), three-level six variables Box-Behnken design (BBD), was employed to optimize the factors such as pH 8.0, temperature 37°C, sugarcane molasses (35g/L) supplemented with co-substrate palm oil (0.5%),corn steep liquor (2%) after a period of 96h of incubation for the maximum yield (19.50±0.3g/L) of PHA. It was well in close agreement with the predicted value obtained by RSM model yield (19.55±0.1g/L).Characterization of the extracted polymer was done using FTIR, GC-MS, XRD, TGA and AFM analysis. NMR spectroscopic analysis revealed that the biopolymer was poly (3-hydroxybutyrate-co-3-hydroxyvalerate), copolymer of PHA. This is the first report on optimization of PHA production using yeast strain isolated from natural sources.
Subject(s)
Biotechnology/methods , Polyhydroxyalkanoates/biosynthesis , Statistics as Topic , Yeasts/metabolism , Analysis of Variance , Carbon/analysis , Fatty Acids/analysis , Gas Chromatography-Mass Spectrometry , Magnetic Resonance Spectroscopy , Microscopy, Atomic Force , Nitrogen/analysis , Oils/isolation & purification , Phylogeny , Reproducibility of Results , Spectroscopy, Fourier Transform Infrared , Thermogravimetry , X-Ray DiffractionABSTRACT
Cyclic lipopeptides (CLPs) are non-ribosomal biosurfactants produced by Bacillus species that exhibit outstanding interfacial activity. The synthesis of CLPs is under genetic and environmental influence, and representatives from different families are generally co-produced, generating isoforms that differ in chemical structure and biological activities. This study to evaluate the effect of low and high NaCl concentrations on the composition and surface activity of CLPs produced by Bacillus strains TIM27, TIM49, TIM68, and ICA13 towards microbial enhanced oil recovery (MEOR). The strains were evaluated in mineral medium containing NaCl 2.7, 66, or 100 g L-1 and growth, surface tension and emulsification activity were monitored. Based on the analysis of 16S rDNA, gyrB and rpoB sequences TIM27 and TIM49 were assigned to Bacillus subtilis, TIM68 to Bacillus vallismortis, and ICA13 to Bacillus amyloliquefaciens. All strains tolerated up to 100-g L-1 NaCl, but only TIM49 and TIM68 were able to reduce surface tension at this concentration. TIM49 also showed emulsification activity at concentrations up to 66-g L-1 NaCl. ESI-MS analysis showed that the strains produced a mixture of CLPs, which presented distinct CLP profiles at low and high NaCl concentrations. High NaCl concentration favored the synthesis of surfactins and/or fengycins that correlated with the surface activities of TIM49 and TIM68, whereas low concentration favored the synthesis of iturins. Taken together, these findings suggest that the determination of CLP signatures under the expected condition of oil reservoirs can be useful in the guidance for choosing well-suited strains to MEOR.
Subject(s)
Bacillus/chemistry , DNA Fingerprinting , Lipopeptides/biosynthesis , Peptides, Cyclic/biosynthesis , Surface-Active Agents/chemistry , Bacillus/genetics , Bacillus amyloliquefaciens/chemistry , Bacillus amyloliquefaciens/genetics , Bacillus subtilis/chemistry , Bacillus subtilis/genetics , Bacterial Proteins/genetics , Culture Media/chemistry , DNA Gyrase/genetics , Oils/isolation & purification , Petroleum/microbiology , Salt Tolerance , Sodium Chloride/pharmacology , Surface TensionABSTRACT
Starfish oil (SO) is characterized by functional lipids, including n-3 polyunsaturated fatty acid (both in the form of triacylglycerol and in the form of phospholipid), and carotenoids, which may exert beneficial effects on metabolic disorders in obesity-associated diseases. In the present study, the effect of SO on dysregulation of lipid metabolism was examined using C57BL/6N mice treated with high-fat (HF) diet. Mice were fed HF, HF with 2% SO, or HF with 5% SO diet for 8 weeks. Weight gain, blood glucose, serum and hepatic lipid contents, and hepatic fatty acid composition were measured. Fatty acid ß-oxidation activity was monitored by measuring the catabolic rate of 13C-labeled fatty acid, assessed as 13CO2/12CO2 ratio using isotope ratio mass spectrometry (IR-MS). Although there were no differences in body weight or white adipose tissue weight among the test groups, dietary SO reduced blood glucose, and dose-dependently improved hyperlipidemia and decreased hepatic lipid accumulation. Analysis of hepatic fatty acid composition revealed a significant decrease in the ratio of monounsaturated fatty acid to saturated fatty acid, which is attributed to stearoyl-CoA desaturase activity. IR-MS analysis suggested that ß-oxidation activity was enhanced in the mice treated with 5% SO. These results demonstrate that dietary SO improves lipid metabolism measures in HF diet-induced obese mice, suggesting that SO holds promise as an agent for the prevention and treatment of lipid metabolism disorders in the liver.
Subject(s)
Diet, High-Fat/adverse effects , Dietary Supplements , Fatty Liver/prevention & control , Hyperlipidemias/prevention & control , Oils/administration & dosage , Oils/isolation & purification , Starfish/chemistry , Animals , Body Weight/drug effects , Carotenoids/administration & dosage , Carotenoids/isolation & purification , Carotenoids/pharmacology , Fatty Acids/metabolism , Fatty Acids, Omega-3/administration & dosage , Fatty Acids, Omega-3/isolation & purification , Fatty Acids, Omega-3/pharmacology , Fatty Liver/etiology , Hyperlipidemias/etiology , Liver/metabolism , Male , Mice, Inbred C57BL , Obesity/etiology , Obesity/metabolism , Oils/chemistry , Oils/pharmacologyABSTRACT
Industrial vegetable oil production in Viet Nam depends on oil seeds and crude plant oils that are currently more than 90% imported. As the first step in investigating the feasibility of using microalgae to provide Viet Nam with a domestic source of oil for food and edible oil industries, fifty lipid-producing microalgae were isolated and characterized. The microalgae were isolated from water sources ranging from freshwater to brackish and marine waters from a wide geographic distribution in Viet Nam. Initial analyses showed that 20 of the 50 strains had good growth rates, produced high biomass and had high lipid content, ranging up to 50% of dry weight biomass. 18S rRNA gene sequence analyses of the 50 strains showed a great diversity in this assemblage of microalgae, comprising at least 38 species and representatives of 25 genera: Chlamydomonas, Poterioochromonas, Scenedesmus, Desmodesmus, Chlorella, Bracteacoccus, Monoraphidium, Selenastrum, Acutodesmus, Mychonastes, Ankistrodesmus, Kirchneriella, Raphidocelis, Dictyosphaerium, Coelastrella, Schizochlamydella, Oocystidium, Nannochloris, Auxenochlorella, Chlorosarcinopsis, Stichococcus, Picochlorum, Prasinoderma, Chlorococcum, and Marvania. Some of the species are closely related to well-known lipid producers such as Chlorella sorokiniana, but some other strains are not closely related to the strains found in public sequence databases and likely represent new species. Analysis of oil quality showed that fatty acid profiles of the microalgal strains were very diverse and strain-dependent. Fatty acids in the microalgal oils comprised saturated fatty acids (SFAs), poly-unsaturated fatty acids (PUFAs), and mono-unsaturated fatty acids (MUFAs). The main SFA was palmitic acid. MUFAs and PUFAs were dominated by oleic acid, and linoleic and linolenic acids, respectively. Some strains were especially rich in the essential fatty acid α-linolenic acid (ALA), which comprised more than 20% of the fatty acids in these strains. Other strains had fatty acid compositions similar to that of palm oil. Several strains have been selected on the basis of their suitable fatty acid profiles and high lipid content for further chemical and physical characterization, toxicity and organoleptic tests of their oils, and for scale-up.
Subject(s)
Fatty Acids/isolation & purification , Lipids/isolation & purification , Microalgae/metabolism , Oils/isolation & purification , Biomass , Fatty Acids/chemistry , Fatty Acids, Unsaturated/chemistry , Fatty Acids, Unsaturated/isolation & purification , Feasibility Studies , Genes, rRNA , Lipids/chemistry , Microalgae/genetics , Oils/chemistry , RNA, Ribosomal, 18S/genetics , VietnamABSTRACT
Bullfrog oil is a natural product extracted from the Rana catesbeiana Shaw adipose tissue and used in folk medicine for the treatment of several diseases. The aim of this study was to evaluate the extraction process of bullfrog oil, to develop a suitable topical nanoemulsion and to evaluate its efficacy against melanoma cells. The oil samples were obtained by hot and organic solvent extraction processes and were characterized by titration techniques and gas chromatography mass spectrometry (GC-MS). The required hydrophile-lipophile balance and the pseudo-ternary phase diagram (PTPD) were assessed to determine the emulsification ability of the bullfrog oil. The anti-tumoral activity of the samples was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay for normal fibroblast (3T3) and melanoma (B16F10) cell lines. Both extraction methods produced yielded around 60% and the oil was mainly composed of unsaturated compounds (around 60%). The bullfrog oil nanoemulsion obtained from PTPD presented a droplet size of about 390 nm and polydispersity = 0.05 and a zeta potential of about -25 mV. Both the bullfrog oil itself and its topical nanoemulsion did not show cytotoxicity in 3T3 linage. However, these systems showed growth inhibition in B16F10 cells. Finally, the bullfrog oil presented itself as a candidate for the development of pharmaceutical products free from cytotoxicity and effective for antineoplastic therapy.
Subject(s)
Antineoplastic Agents/isolation & purification , Biological Products/therapeutic use , Melanoma, Experimental/drug therapy , Oils/therapeutic use , Rana catesbeiana , 3T3 Cells , Animals , Antineoplastic Agents/therapeutic use , Antineoplastic Agents/toxicity , Biomedical Research/trends , Cell Line, Tumor , Drug Screening Assays, Antitumor , Emulsions , HeLa Cells , Humans , Mice , Oils/chemistry , Oils/isolation & purification , Oils/toxicityABSTRACT
Marine oil spills constitute an environmental disaster with severe adverse effects on the economy and ecosystem. Phase-selective organogelators (PSOGs), molecules that can congeal oil selectively from oil-water mixtures, have been proposed to be useful for oil-spill recovery. However, a major drawback lies in the mode of application of the PSOG to an oil spill spread over a large area. The proposed method of using carrier solvents is impractical for various reasons. Direct application of the PSOG as a solid, although it would be ideal, is unknown, presumably owing to poor dispersion of the solid through the oil. We have designed five cheap and easy-to-make glucose-derived PSOGs that disperse in the oil phase uniformly when applied as a fine powder. These gelators were shown to selectively congeal many oils, including crude oil, from oil-water mixtures to form stable gels, which is an essential property for efficient oil-spill recovery. We have demonstrated that these PSOGs can be applied aerially as a solid powder onto a mixture of crude oil and sea water and the congealed oil can then be scooped out. Our innovative mode of application and low cost of the PSOG offers a practical solution to oil-spill recovery.
Subject(s)
Environmental Restoration and Remediation/methods , Gels/chemistry , Glucose/chemistry , Petroleum Pollution/analysis , Petroleum/analysis , Water Pollutants, Chemical/isolation & purification , Hydrogen Bonding , Oils/isolation & purification , Seawater/analysisABSTRACT
Northern shrimp (Pandalus borealis) oil, which is rich in omega-3 fatty acids, was recovered from the cooking water of shrimp processing facilities. The oil contains significant amounts of omega-3 fatty acids in triglyceride form, along with substantial long-chain monounsaturated fatty acids (MUFAs). It also features natural isomeric forms of astaxanthin, a nutritional carotenoid, which gives the oil a brilliant red color. As part of our efforts in developing value added products from waste streams of the seafood processing industry, we present in this paper a comprehensive characterization of the triacylglycerols (TAGs) and astaxanthin esters that predominate in the shrimp oil by using HPLC-HRMS and MS/MS, as well as 13C-NMR. This approach, in combination with FAME analysis, offers direct characterization of fatty acid molecules in their intact forms, including the distribution of regioisomers in TAGs. The information is important for the standardization and quality control, as well as for differentiation of composition features of shrimp oil, which could be sold as an ingredient in health supplements and functional foods.
Subject(s)
Chromatography, High Pressure Liquid/methods , Oils/analysis , Pandalidae/chemistry , Tandem Mass Spectrometry/methods , Animals , Fatty Acids, Omega-3/analysis , Fatty Acids, Omega-3/isolation & purification , Magnetic Resonance Spectroscopy/methods , Oils/chemistry , Oils/isolation & purification , Triglycerides/analysis , Triglycerides/chemistry , Triglycerides/isolation & purification , Xanthophylls/analysis , Xanthophylls/chemistry , Xanthophylls/isolation & purificationABSTRACT
By using a novel hydrophilic cellulose acetate butyrate (CAB) as the membrane material for the hollow fiber substrate and modifying its outer surface by polydopamine (PDA) coating and inner surface by interfacial polymerization, we have demonstrated that the thin-film composite (TFC) membranes can be effectively used for sustainable water reclamation from emulsified oil/water streams via forward osmosis (FO) under the pressure retarded osmosis (PRO) mode. The newly developed TFC-FO hollow fiber membrane shows characteristics of high water flux, outstanding salt and oil rejection, and low fouling propensity. Under the PRO mode, the newly developed TFC-FO membrane exhibits a water flux of 37.1 L m(-2) h(-1) with an oil rejection of 99.9% using a 2000 ppm soybean oil/water emulsion as the feed and 1 M NaCl as the draw solution. Remarkable anti-fouling behaviors have also been observed. Under the PRO mode, the water flux decline is only 10% of the initial value even after a 12 h test for oil/water separation. The water flux of the fouled membrane can be effectively restored to 97% of the original value by water rinses on the fiber outer surface without using any chemicals. Furthermore, the flux declines are only 25% and 52% when the water recovery of a 2000 ppm soybean oil/water emulsion and a 2000 ppm petroleum oil/water emulsion containing 0.04 M NaCl reaches 82%, respectively. This study may not only provide insightful guidelines for the fabrication of effective TFC-FO membranes with high performance and low fouling behaviors for oily wastewater under the PRO mode but also add an alternative perspective to the design of new materials for water purification purposes.
Subject(s)
Membranes, Artificial , Oils/isolation & purification , Waste Disposal, Fluid/methods , Wastewater/chemistry , Water Purification/methods , Cellulose/analogs & derivatives , Cellulose/chemistry , Emulsions , Hydrophobic and Hydrophilic Interactions , Indoles/chemistry , Industrial Waste , Osmosis , Petroleum , Polymers/chemistry , Soybean Oil/isolation & purification , Water Purification/instrumentationABSTRACT
CONTEXT: The toad Rhinella jimi (Stevaux, 2002) (Bufonidae) is used in traditional medicine to treat a number of illnesses (inflammation, infections, and wounds) in humans as well as animals. OBJECTIVES: The present work examined the antimicrobial actions of the extracted oils from the body fat of R. jimi (ORJ) against fungi and standard and multi-resistant lines of bacteria, as well as their effects when combined with aminoglycosides. MATERIALS AND METHODS: The toads were collected in the municipality of Exu in Pernambuco State, Brazil, and their body fat oils extracted in a Soxhlet apparatus using hexane. A gas chromatograph coupled to a mass spectrometer was used to identify the fatty acids, based on their methyl esters. The antimicrobial activities of the oil were analyzed against standard and multi-resistant lines of Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa, as well as against fungal lines of Candida albicans and Candida krusei using the broth micro-dilution method. RESULTS: The minimum inhibitory concentrations (MIC) of ORJ were 512 µg/mL for Candida krusei and ≥1024 µg/mL for the other microorganisms. When associated with amikacin, ORJ demonstrated an increase in its ability to inhibit E. coli growth (from 156.25 to 39.06 µg/mL), indicating synergistic interaction. In the same way, when allied with amikacin, gentamicin, and neomycin, the ORJ reduced the MICs meaningly, against P. aeruginosa. CONCLUSIONS: These data will enable searches to be made to obtain new products in combination with antibiotics, enhancing the efficacy of these drugs against drug-resistant microorganisms.
Subject(s)
Anti-Infective Agents/chemistry , Anti-Infective Agents/pharmacology , Bufonidae , Fat Body/chemistry , Oils/chemistry , Oils/pharmacology , Animals , Anti-Infective Agents/isolation & purification , Brazil , Candida/drug effects , Drug Resistance, Multiple, Bacterial/drug effects , Drug Synergism , Escherichia coli/drug effects , Medicine, Traditional , Microbial Sensitivity Tests , Oils/isolation & purification , Pseudomonas aeruginosa/drug effects , Staphylococcus aureus/drug effectsABSTRACT
In this study, the effects of gravitational settling time, temperature, speed and time of centrifugation, flocculant type and dosage, bubble size and gas amount were investigated. The results show that the simple increase in settling time and temperature is of no use for oil-water separation of the three wastewater samples. As far as oil-water separation efficiency is concerned, increasing centrifugal speed and centrifugal time is highly effective for L sample, and has a certain effect on J sample, but is not valid for S sample. The flocculants are highly effective for S and L samples, and the oil-water separation efficiency increases with an increase in the concentration of inorganic cationic flocculants. There exist critical reagent concentrations for the organic cationic and the nonionic flocculants, wherein a higher or lower concentration of flocculant would cause a decrease in the treatment efficiency. Flotation is an effective approach for oil-water separation of polymer-contained wastewater from the three oilfields. The oil-water separation efficiency can be enhanced by increasing floatation agent concentration, flotation time and gas amount, and by decreasing bubble size.
Subject(s)
Oils/isolation & purification , Petroleum , Polymers/chemistry , Waste Disposal, Fluid/methods , Wastewater/chemistry , Centrifugation , China , Flocculation , Hot Temperature , Petroleum Pollution/prevention & controlABSTRACT
CONTEXT: Animals are used for the treatment of diseases caused by inflammatory processes, although few studies evaluate their potential for these purposes. OBJECTIVES: To evaluate the anti-inflammatory potential of zootherapeutic products derived from vertebrates used in Brazilian traditional medicine. MATERIAL AND METHODS: The species analyzed were Tupinambis merianae, Iguana iguana, Crotalus durissus, Boa constrictor, and Euphractus sexcinctus. The methods used in anti-inflammatory assays were ear edema (topical) and paw (systemic). RESULTS: With regard to topical anti-inflammatory activity, the fat from T. merianae, C. durissus, I. iguana, B. constrictor, and E. sexcinctus reduced inflammation, while for systemic anti-inflammatory activity, only the fat and the skin of C. durissus, the skin of I. iguana and the fat from B. constrictor reduced inflammation. CONCLUSIONS: Studies should be conducted to evaluate the mechanisms of action for each product that demonstrated anti-inflammatory activity as well as against other inflammatory processes.
Subject(s)
Anti-Inflammatory Agents/isolation & purification , Anti-Inflammatory Agents/therapeutic use , Medicine, Traditional/methods , Skin/chemistry , Subcutaneous Fat/chemistry , Animals , Boidae , Brazil , Crotalus , Edema/drug therapy , Edema/pathology , Iguanas , Male , Mice , Oils/isolation & purification , Oils/therapeutic use , Rats , Rats, Wistar , Tissue Extracts/isolation & purification , Tissue Extracts/therapeutic useABSTRACT
This study evaluates the production of biodiesel and ethanol from spent coffee grounds (SCG). The extraction of oil from SCG, biodiesel production and ethanol production processes were studied. The liquid-to-solid ratio and temperature were evaluated in the ultrasound-assisted extraction of the oil from SCG. The highest yield (12%) was obtained using 4 mL g(-1) liquid-to-solid ratio at 60°C for 45 min. The process to produce biodiesel showed a yield of 97% into fatty acid methyl esters (FAME). The highest glucose yield (192 mg g SCG(-1)) was obtained by hydrolysis with 0.4 mol L(-1) sulfuric acid at 121°C for 15 min. The hydrolysate was used as fermentation medium for ethanol production by Saccharomyces cerevisiae obtaining 19.0 g L(-1) at 10h of process of ethanol with a yield of ethanol and productivity of 0.50 g g(-1) and 1.90 g L(-1)h(-1), respectively. Spent coffee grounds were considered a potential feedstock for biodiesel and ethanol production.
Subject(s)
Biofuels , Coffee/chemistry , Ethanol/metabolism , Ultrasonics/methods , Waste Products , Hydrolysis , Oils/isolation & purification , Saccharomyces cerevisiae/metabolism , ThermodynamicsABSTRACT
Oil products are the one out of major pollutants in soil. For reduction of the technogenic load on human beings and performing preventive measures in the Republic of Belarus differentiated hygienic rate setting for oil products in the soil have been scientifically substantiated for follows different categories of Lands: agricultural lands, defense lands, lands for recreation, historical and cultural purpose, forest lands, lands of water fund, reserve lands--50 mg/kg; settlements sand, garden housing and dacha cooperatives,--100 mg/kg; industrial, transport, communication, energy, defense and other appointments lands--500 mg/kg.
Subject(s)
Oils/chemistry , Soil Pollutants/chemistry , Soil/chemistry , Humans , Hygiene , Maximum Allowable Concentration , Oils/isolation & purification , Petroleum/analysis , Republic of BelarusABSTRACT
Water contaminated by oil and gas production poses challenges to the management of America's water resources. Here we report the design, fabrication, and laboratory evaluation of multi-walled carbon nanotubes decorated with superparamagnetic iron-oxide nanoparticles (SPIONs) for oil-water separation. As revealed by confocal laser-scanning fluorescence microscopy, the magnetic carbon nanotubes (MCNTs) remove oil droplets through a two-step mechanism, in which MCNTs are first dispersed at the oil-water interface and then drag the droplets with them out of water by a magnet. Measurements of removal efficiency with different initial oil concentration, MCNT dose, and mixing time show that kinetics and equilibrium of the separation process can be described by the Langmuir model. Separation capacity qt is a function of MCNT dose m, mixing time t, and residual oil concentration Ce at equilibrium: [Formula in text] where qmax, kw, and K are maximum separation capacity, wrapping rate constant, and equilibrium constant, respectively. Least-square regressions using experimental data estimate qmax = 6.6(± 0.6) g-diesel g-MCNT(-1), kw = 3.36(± 0.03) L g-diesel(-1) min(-1), and K = 2.4(± 0.2) L g-diesel(-1). For used MCNTs, we further show that over 80% of the separation capacity can be restored by a 10 min wash with 1 mL ethanol for every 6 mg MCNTs. The separation by reusable MCNTs provides a promising alternative strategy for water treatment design complementary to existing ones such as coagulation, adsorption, filtration, and membrane processes.
Subject(s)
Magnetic Phenomena , Nanotubes, Carbon/chemistry , Oils/isolation & purification , Water Pollutants, Chemical/isolation & purification , Water Purification/methods , Dextrans/chemistry , Magnetite Nanoparticles/chemistry , Nanotubes, Carbon/ultrastructure , Water/chemistryABSTRACT
Microbial enhanced oil recovery (MEOR) process utilizes microorganisms or their metabolites to mobilize the trapped oil in the oil formation after primary and secondary oil recovery stages. MEOR technique is considered as more environmentally friendly and low cost process. There are several identified mechanisms for more oil recovery using MEOR processes however; wettability alteration and interfacial tension (IFT) reduction are the important ones. Enterobacter Cloacae, a facultative bio-surfactant producer bacterium, was selected as a bacterial formulation due to its known performance on IFT reduction and wettability alteration. To quantify the effects of these two mechanisms, different tests including oil spreading, in situ and ex situ core flooding, wettability measurement (Amott), IFT, viscosity and pH measurements were performed. The obtained results revealed that the experimental procedure used in this study was able to quantitatively identify the individual effects of both mechanisms on the ultimate microbial oil recovery. The results demonstrated considerable effects of both mechanisms on the tertiary oil recovery; however after a proper shut in time period, more tertiary oil was recovered because of wettability alteration mechanism. Finally, SEM images taken from the treated cores showed biofilm formation on the rock pore surfaces, which is responsible for rock surface wettability alteration.
Subject(s)
Enterobacter cloacae/physiology , Oils/isolation & purification , Petroleum/microbiology , Surface-Active Agents/metabolism , Biofilms/growth & development , Hydrogen-Ion Concentration , Microscopy, Electron, Scanning , Surface Tension , Surface-Active Agents/chemistry , Viscosity , WettabilityABSTRACT
OBJECTIVE: To study the rudimentary immunoregulatory mechanisms of Ganoderma spore oil on immunocompromized mice model. METHODS: Thrity KM mice were randomly selected and assigned into three groups (ten animals per group): the model control group, Ganoderma Lucidum spores oil group and the normal control group. The model control group and Ganoderma Lucidum spores oil group were injected intraperitoneally with cyclophosphamide at 40 mg x kg(-1) d to generate a immunocompromized mice model. The normal control group were administered with 0.9% NaCl solution 0.1 ml/10 g BW as placebo. All agents were given orally once a day, given for consecutive 30 days, Ganoderma Lucidum spores oil group 150 mg/kg, the others given maize 0.1 ml/10 g BW. The serum TNF-alpha , IFN-gamma content of the mice through ELISA kit and the expression levels of IL-2, IL-10, IL-12, IL-4, IFN-gamma, TNF-alpha mRNA in mouse spleen and thymus were examined by RT-PCR to rudimentary study its immunoregulatory mechanisms. RESULTS: Ganoderma spore oil can significantly increased the content of TNF-alpha and IFN-gamma in the serum and the expression levels of IL-2, IL-10, IL-12, IL-4, IFN-gamma, TNF-alpha mRNA in spleen and thymus, with obvious difference from the model control (P < or = 0.05). CONCLUSION: Ganoderma spore oil can be able to improve the above cytokine ion expression to immunoregulate the immunocompromized mice.