Home About us Contact
|
Home About us Contact | ||
|
|
||
Lipid Extraction (lipid + extraction)
Selected AbstractsEffects of lipid extraction on stable carbon and nitrogen isotope analyses of fish tissues: potential consequences for food web studiesECOLOGY OF FRESHWATER FISH, Issue 3 2004M. A. Sotiropoulos Abstract,,, We examined whether solvent-based lipid extractions, commonly used for stable isotope analysis (SIA) of biota, alters ,15N or ,13C values of fish muscle tissue or whole juvenile fish. Lipid extraction from muscle tissue led to only small (<1,) isotope shifts in ,13C and ,15N values. By contrast, ecologically significant shifts (+3.4, for ,13C and +2.8, for ,15N) were observed for whole juvenile fish. Sample variance was not affected by lipid extraction. For tissue-specific SIA, two sample aliquots may be required: a lipid-extracted aliquot for stable carbon isotope analysis when differing lipid content among tissues is a concern, and a nonextracted aliquot for ,15N determination. Whole organism SIA is not recommended because of the mix of tissues having different turnover times; for very small fish, we recommend that fish be eviscerated, decapitated, and skinned to minimise differences with samples of muscle tissue. Resumen 1. Cada vez con mayor frecuencia, los ecólogos de peces utilizan análisis de isótopos estables. Por ello, se hace cada vez más importante comprender las fuentes de variación, - debido a diferencias inherentes entre muestreos biológicos o como resultado de técnicas de procesamiento de muestreo - tanto como identificar estrategias para tratar tales fuentes. Examinamos si la extracción de lípidos basada en disolventes, comúnmente utilizada en análisis de isótopos de carbono estable, altera negativamente los valores de ,15N y ,13C de tejido muscular de tres peces de tamaño pequeño y de peces juveniles completos. 2. La extracción de lípidos de músculo de pez llevó a pequeños cambios isotópicos de + +0.4 a +1.0, y de +0.3 a +0.5, para ,13C y ,15N, respectivamente. Por el contrario, la extracción de lípidos de peces juveniles completos varió marcadamente en +3.4, para ,13C y +2.8, para ,15N - ambos cambios ecológicamente importantes. La varianza de los valores de muestreos de ,13C y de ,15N tanto para tejido muscular como para los peces completos no difirieron entre los muestreos de lípidos extraídos y muestreos sin tratamiento. 3. Nuestros resultados recomiendan el análisis de isótopos estables de tejidos específicos. Cuando ello no es posible o deseable, dos alícuotas de muestreo pueden ser requeridas: una alícuota de lípidos extraídos para el análisis de isótopos de carbono estable cuando la varianza de ,13C, debida a diferencias en el contenido de lípidos de diferentes tejidos, y una alícuota de no-extracción para determinaciones de ,15N. 4. Dada la mezcla de tejidos, el análisis de isótopos de un organismo completo no es recomendable , en el caso de peces muy pequeños, recomendamos que los peces sean eviscerados, decapitados, y despellejados para minimizar las diferencias de muestreos de tejido muscular. [source] Fatty acid metabolism assessed by 125I-iodophenyl 9-methylpentadecanoic acid (9MPA) and expression of fatty acid utilization enzymes in volume-overloaded heartsEUROPEAN JOURNAL OF CLINICAL INVESTIGATION, Issue 3 2004T. Miyamoto Abstract Background, The peroxisome proliferator-activated receptor (PPAR) , is a member of the nuclear receptor superfamily and regulates gene expression of fatty acid utilization enzymes. In cardiac hypertrophy and heart failure by pressure-overload, myocardial energy utilization reverts to the fetal pattern, and metabolic substrate switches from fatty acid to glucose. However, myocardial metabolism in volume-overloaded hearts has not been rigorously studied. The aim of the present study was to examine fatty acid metabolism and protein expressions of PPAR, and fatty acid oxidation enzymes in volume-overloaded rabbit hearts. Methods, Volume-overload was induced by carotid-jugular shunt formation. Sham-operated rabbits were used as control. Chronic volume-overload increased left ventricular weight and ventricular cavity size, and relative wall thickness was decreased, indicating eccentric cardiac hypertrophy. 125I-iodophenyl 9-methylpentadecanoic acid (9MPA) was intravenously administered, and animals were sacrificed at 5 min after injection. The 9MPA was rapidly metabolized to iodophenyl-3-methylnonanoic acid (3MNA) by ,-oxidation. Lipid extraction from the myocardium was performed by the Folch method, and radioactivity distribution of metabolites was assayed by thin-layer chromatography. The protein was extracted from the left ventricular myocardium, and levels of PPAR, and fatty acid oxidation enzymes were examined by Western blotting. Results, Myocardial distribution of 9MPA tended to be more heterogeneous in shunt than in sham rabbits (P = 0·06). In volume-overloaded hearts by shunt, the conversion from 9MPA to 3MNA by ,-oxidation was faster than the sham-control hearts (P < 0·05). However, protein levels of PPAR, and fatty acid utilization enzymes were unchanged in shunt rabbits compared with sham rabbits. Conclusions, These data suggest that myocardial fatty acid metabolism is enhanced in eccentric cardiac hypertrophy by volume-overload without changes in protein expressions of PPAR, and fatty acid utilization enzymes. Our data may provide a novel insight into the subcellular mechanisms for the pathological process of cardiac remodelling in response to mechanical stimuli. [source] Skin permeability enhancement by low frequency sonophoresis: Lipid extraction and transport pathwaysJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 6 2003R. Alvarez-Román Abstract The objective of this study was to shed light on the mechanism(s) by which low-frequency ultrasound (20 KHz) enhances the permeability of the skin. The physical effects on the barrier and the transport pathway, in particular, were examined. The amount of lipid removed from the intercellular domains of the stratum corneum following sonophoresis was determined by infrared spectroscopy. Transport of the fluorescent probes nile red and calcein, under the influence of ultrasound, was evaluated by laser-scanning confocal microscopy. The results were compared with the appropriate passive control data and with data obtained from experiments in which the skin was exposed simply to the thermal effects induced by ultrasound treatment. A significant fraction (,30%) of the intercellular lipids of the stratum corneum, which are principally responsible for skin barrier function, were removed during the application of low-frequency sonophoresis. Although the confocal images from the nile red experiments were not particularly informative, ultrasound clearly and significantly (again, relative to the corresponding controls) facilitated transport of the hydrophilic calcein via discrete permeabilized regions, whereas other areas of the barrier were apparently unaffected. Lipid removal from the stratum corneum is implicated as a factor contributing the observed permeation enhancement effects of low-frequency ultrasound. However, microscopic observations imply that sonophoresis induces localized (aqueous?) permeation pathways at discrete sites. © 2003 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 92:1138,1146, 2003 [source] Effects of lipid extraction on stable carbon and nitrogen isotope analyses of fish tissues: potential consequences for food web studiesECOLOGY OF FRESHWATER FISH, Issue 3 2004M. A. Sotiropoulos Abstract,,, We examined whether solvent-based lipid extractions, commonly used for stable isotope analysis (SIA) of biota, alters ,15N or ,13C values of fish muscle tissue or whole juvenile fish. Lipid extraction from muscle tissue led to only small (<1,) isotope shifts in ,13C and ,15N values. By contrast, ecologically significant shifts (+3.4, for ,13C and +2.8, for ,15N) were observed for whole juvenile fish. Sample variance was not affected by lipid extraction. For tissue-specific SIA, two sample aliquots may be required: a lipid-extracted aliquot for stable carbon isotope analysis when differing lipid content among tissues is a concern, and a nonextracted aliquot for ,15N determination. Whole organism SIA is not recommended because of the mix of tissues having different turnover times; for very small fish, we recommend that fish be eviscerated, decapitated, and skinned to minimise differences with samples of muscle tissue. Resumen 1. Cada vez con mayor frecuencia, los ecólogos de peces utilizan análisis de isótopos estables. Por ello, se hace cada vez más importante comprender las fuentes de variación, - debido a diferencias inherentes entre muestreos biológicos o como resultado de técnicas de procesamiento de muestreo - tanto como identificar estrategias para tratar tales fuentes. Examinamos si la extracción de lípidos basada en disolventes, comúnmente utilizada en análisis de isótopos de carbono estable, altera negativamente los valores de ,15N y ,13C de tejido muscular de tres peces de tamaño pequeño y de peces juveniles completos. 2. La extracción de lípidos de músculo de pez llevó a pequeños cambios isotópicos de + +0.4 a +1.0, y de +0.3 a +0.5, para ,13C y ,15N, respectivamente. Por el contrario, la extracción de lípidos de peces juveniles completos varió marcadamente en +3.4, para ,13C y +2.8, para ,15N - ambos cambios ecológicamente importantes. La varianza de los valores de muestreos de ,13C y de ,15N tanto para tejido muscular como para los peces completos no difirieron entre los muestreos de lípidos extraídos y muestreos sin tratamiento. 3. Nuestros resultados recomiendan el análisis de isótopos estables de tejidos específicos. Cuando ello no es posible o deseable, dos alícuotas de muestreo pueden ser requeridas: una alícuota de lípidos extraídos para el análisis de isótopos de carbono estable cuando la varianza de ,13C, debida a diferencias en el contenido de lípidos de diferentes tejidos, y una alícuota de no-extracción para determinaciones de ,15N. 4. Dada la mezcla de tejidos, el análisis de isótopos de un organismo completo no es recomendable , en el caso de peces muy pequeños, recomendamos que los peces sean eviscerados, decapitados, y despellejados para minimizar las diferencias de muestreos de tejido muscular. [source] Thermal analysis of merino wool fibres without internal lipidsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007M. Martí Abstract Merino wool is made up of cuticle and cortical cells held together by the cell membrane complex (CMC), which contains a small amount of internal lipids (IWL) (1.5% by mass). IWL have been extracted from wool on account of their considerable dermatological interest owing to their proportion of ceramides. IWL have been extracted by different methods and solvents, methanol and acetone at laboratory and pilot plant levels. Thermal analysis of these extracted wool fibers is presented using thermogravimetry (TG) and differential scanning calorimetry (DSC). TG provides a measurement of the weight loss of the sample as a function of time and temperature. DSC gives information about possible structure modification of extracted wool fibers. Thermoporometry was applied to evaluate the pore size distribution of extracted wool fibers. The results showed that the extraction process increased the pore size distribution and the cumulated pore volume, which is consistent with some changes in the extracted wool CMC. Extracted fiber becomes more hydrophilic and absorbs a large amount of water. We can conclude that the lipid extraction of wool produced no relevant changes in the crystalline fraction when extracted with acetone. However, part of the amorphous keratin material was extracted with methanol, the rest of the crystalline material becoming more stable. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 545,551, 2007 [source] How to account for the lipid effect on carbon stable-isotope ratio (,13C): sample treatment effects and model biasJOURNAL OF FISH BIOLOGY, Issue 4 2008K. Mintenbeck This study investigated the impact of lipid extraction, CaCO3 removal and of both treatments combined on fish tissue ,13C, ,15N and C:N ratio. Furthermore, the suitability of empirical ,13C lipid normalization and correction models was examined. ,15N was affected by lipid extraction (increase of up to 1·65,) and by the combination of both treatments, while acidification alone showed no effect. The observed shift in ,15N represents a significant bias in trophic level estimates, i.e. lipid-extracted samples are not suitable for ,15N analysis. C:N and ,13C were significantly affected by lipid extraction, proportional to initial tissue lipid content. For both variables, rates of change with lipid content (,C:N and ,,13C) were species specific. All tested lipid normalization and correction models produced biased estimates of fish tissue ,13C, probably due to a non-representative database and incorrect assumptions and generalizations the models were based on. Improved models need a priori more extensive and detailed studies of the relationships between lipid content, C:N and ,13C, as well as of the underlying biochemical processes. [source] REMOVAL OF LIPID FROM SURFACES OF ROASTED PEANUTS BY SONICATION AS ASSESSED BY FLUORESCENCE AND SCANNING ELECTRON MICROSCOPYJOURNAL OF FOOD PROCESS ENGINEERING, Issue 5 2010PETER WAMBURA ABSTRACT Peanut oil migrates to the outer surface during roasting, where it comes into contact with oxygen, leading to the oxidation reactions. Because of its cleaning effect, power ultrasound (sonication) was used for removing surface lipid of roasted peanuts. Georgia green runner-type peanuts were roasted at 178C for 15 min. Roasted peanuts were subjected to lipid extraction in n-hexane by sonication. Fluorescent and electron scanning micrographs revealed that the surface of sonicated peanuts was free of oil stains, as opposed to that of freshly roasted peanuts. These results showed that power ultrasound could remove the lipids from peanut surfaces very effectively. Details of microstructure of sonicated peanuts as was observed using scanning electron microscope reveal that 10 min sonication was sufficient to extract most of the lipids on the roasted peanut surfaces. Fluorescence and scanning electron microscopy are useful in peanut analysis because they can detect lipids in low concentration. PRACTICAL APPLICATIONS There is increasing interest of quick procedures to examine the surfaces of roasted peanut samples after undergoing treatments, such as removal of lipids. This research demonstrated the significant use of fluorescent and scanning electron microscopes to quickly study the extent of lipid removal from the surface of roasted peanuts after power ultrasound treatment (sonication). [source] Effect of freeze-drying and gamma irradiation on the mechanical properties of human cancellous boneJOURNAL OF ORTHOPAEDIC RESEARCH, Issue 3 2000O. Cornu Freeze-drying and gamma irradiation are commonly used for preservation and sterilization in bone banking. The cumulative effects of preparation and sterilization of cancellous graft material have not been adequately studied, despite the clinical importance of graft material in orthopaedic surgery. Taking benefit from the symmetry of the left and right femoral heads, the influence of lipid extraction followed by freeze-drying of a femoral head and a final 25-kGy gamma irradiation was determined, with the nonirradiated, nonprocessed counterpart as the control. Five hundred and fifty-six compression tests were performed (137 pairs for the first treatment and 141 pairs for the second). Mechanical tests were performed after 30 minutes of rehydration in saline solution. Freeze-dried femoral heads that had undergone lipid extraction experienced reductions of 18.9 and 20.2% in ultimate strength and stiffness, respectively. Unexpectedly, the work to failure did not decrease after this treatment. The addition of gamma irradiation resulted in a mean drop of 42.5% in ultimate strength. Stiffness of the processed bone was not modified by the final irradiation, with an insignificant drop of 24%, whereas work to failure was reduced by a mean of 71.8%. Freeze-dried bone was a bit less strong and stiff than its frozen control. Its work to failure was not reduced, due to more deformation in the nonlinear domain, and it was not brittle after 30 minutes of rehydration. Final irradiation of the freeze-dried bone weakened its mechanical resistance, namely by the loss of its capacity to absorb the energy (in a plastic way) and a subsequent greater brittleness. [source] Determination of cholesterol oxides content in milk products by solid phase extraction and gas chromatography-mass spectrometryJOURNAL OF SEPARATION SCIENCE, JSS, Issue 9-10 2003María V. Calvo Abstract A method for quick and reliable analysis of cholesterol oxidation products (COPs) in dairy products has been developed. After lipid extraction, fat was transesterified under mild conditions to avoid degradation of the target compounds. Isolation of the COPs studied from other components in the lipid fraction was carried out on an aminopropyl SPE cartridge. Finally, analytes were analysed by GC-MS without derivatisation. The method developed provides high specificity and good sensitivity, allowing the direct and unambiguous determination of the underivatized COPs investigated. Application of the method to dairy food analysis revealed the presence of COPs in powder milks and milk-based infant formulas commercially available in Spain, showing that attention should be focused on reduction of cholesterol oxidation levels during both the processing and the storage of these types of foodstuffs. [source] Novel corrective equations for complete estimation of human tissue lipids after their partial destruction by perchloric acid pre-treatment: high-resolution 1H-NMR-based studyNMR IN BIOMEDICINE, Issue 2 2008Niraj Kumar Srivastava Abstract Owing to the small quantity of tissue available in human biopsy specimens, aqueous and lipid components often have to be determined in the same tissue sample. Perchloric acid (PCA) used for the extraction of aqueous metabolites has a deleterious effect on lipid components; the severity of the damage is not known. In this study, human muscle tissue was first treated with PCA to extract aqueous metabolites, and the residue was then used for lipid extraction by conventional methods, i.e. the methods of Folch and Bligh & Dyer and a standardised one using methanol/chloroform (1:3, v/v) used in our laboratory. A 1H-NMR spectrum was obtained for each lipid extract. Lipid was quantified by measuring the integral area of N+ -(CH3)3 signals of phospholipids (PLs). Triacylglycerol (TG) and cholesterol (CHOL) were quantified using the -CH2 - signals of glycerol and the C18 methyl signal, respectively. This study shows that prior use of PCA caused marked attenuation of TG, PL, and CHOL. This was confirmed by recovery experiments and observation of the direct effect of PCA on the standard lipid components. On the basis of the quantity of lipid lost in each case, three novel equations (with respect to TG, PL, and CHOL) were derived. Application of these equations to lipid quantities estimated in different pathological tissues after PCA pre-treatment produced values equivalent to those estimated without PCA use. This study conclusively shows that PCA pre-treatment damages all three lipid moieties, TG, PL, and CHOL. When PCA is used in a fixed ratio to the tissue, the lipid damage is also proportional and correctable by statistically derived equations. These equations will be useful in human biopsy specimens where aqueous and lipid components have to be studied using the same tissue sample because of the small quantity available. Copyright © 2007 John Wiley & Sons, Ltd. [source] Maximized PUFA measurements improve insight in changes in fatty acid composition in response to temperatureARCHIVES OF INSECT BIOCHEMISTRY AND PHYSIOLOGY (ELECTRONIC), Issue 2 2009Coby van Dooremalen Abstract A general mechanism underlying the response of ectotherms to environmental changes often involves changes in fatty acid composition. Theory predicts that a decrease in temperature causes an increase in unsaturation of fatty acids, with an important role for long-chain poly-unsaturated fatty acids (PUFAs). However, PUFAs are particularly unstable and susceptible to peroxidation, hence subtle differences in fatty acid composition can be challenging to detect. We determined the fatty acid composition in springtail (Collembola) in response to two temperatures (5°C and 25°C). First, we tested different sample preparation methods to maximize PUFAs. Treatments consisted of different solvents for primary lipid extraction, mixing with antioxidant, flushing with inert gas, and using different temperature exposures during saponification. Especially slow saponification at low temperature (90,min at 70°C) in combination with replacement of headspace air with nitrogen during saponification and methylation maximized PUFAs for GC analysis. Applying these methods to measure thermal responses in fatty acid composition, the data showed that the (maximized) proportion of C20 PUFAs increased at low acclimation temperature. However, C18 PUFAs increased at high acclimation temperature, which is contrary to expectations. Our study illustrates that PUFA levels in lipids may often be underestimated and this may hamper a correct interpretation of differential responses of fatty acid composition. © 2009 Wiley Periodicals, Inc. [source] Emollient molecule effects on the drying stresses in human stratum corneumBRITISH JOURNAL OF DERMATOLOGY, Issue 4 2010K. Levi Summary Background Emollient molecules are widely used in skin care formulations to improve skin sensory properties and to alleviate dry skin but little is understood regarding their effects on skin biomechanical properties. Objectives To investigate the effects of emollient molecules on drying stresses in human stratum corneum (SC) and how these stresses are related to SC components and moisture content. Methods The substrate curvature method was used to measure the drying stresses in isolated SC following exposure to selected emollient molecules. While SC stresses measured using this method have the same biaxial in vivo stress state and moisture exchange with the environment, a limitation of the method is that moisture cannot be replenished by the underlying skin layers. This provides an opportunity to study the direct effects of emollient treatments on the moisture content and the components of the SC. Attenuated total reflectance Fourier transform infrared spectroscopy was used to determine the effects of emollient molecules on SC lipid extraction and conformation. Results Emollient molecules resulted in a complex SC drying stress profile where stresses increased rapidly to peak values and then gradually decreased to significantly lower values compared with the control. The partially occlusive treatments also penetrated into the SC where they caused extraction and changes in lipid conformation. These effects together with their effects on SC moisture content are used to rationalize the drying stress profiles. Conclusions Emollient molecules have dramatic effects on SC drying stresses that are related to their effects on intercellular lipids and SC moisture content. [source] Effects of lipid extraction on stable carbon and nitrogen isotope analyses of fish tissues: potential consequences for food web studiesECOLOGY OF FRESHWATER FISH, Issue 3 2004M. A. Sotiropoulos Abstract,,, We examined whether solvent-based lipid extractions, commonly used for stable isotope analysis (SIA) of biota, alters ,15N or ,13C values of fish muscle tissue or whole juvenile fish. Lipid extraction from muscle tissue led to only small (<1,) isotope shifts in ,13C and ,15N values. By contrast, ecologically significant shifts (+3.4, for ,13C and +2.8, for ,15N) were observed for whole juvenile fish. Sample variance was not affected by lipid extraction. For tissue-specific SIA, two sample aliquots may be required: a lipid-extracted aliquot for stable carbon isotope analysis when differing lipid content among tissues is a concern, and a nonextracted aliquot for ,15N determination. Whole organism SIA is not recommended because of the mix of tissues having different turnover times; for very small fish, we recommend that fish be eviscerated, decapitated, and skinned to minimise differences with samples of muscle tissue. Resumen 1. Cada vez con mayor frecuencia, los ecólogos de peces utilizan análisis de isótopos estables. Por ello, se hace cada vez más importante comprender las fuentes de variación, - debido a diferencias inherentes entre muestreos biológicos o como resultado de técnicas de procesamiento de muestreo - tanto como identificar estrategias para tratar tales fuentes. Examinamos si la extracción de lípidos basada en disolventes, comúnmente utilizada en análisis de isótopos de carbono estable, altera negativamente los valores de ,15N y ,13C de tejido muscular de tres peces de tamaño pequeño y de peces juveniles completos. 2. La extracción de lípidos de músculo de pez llevó a pequeños cambios isotópicos de + +0.4 a +1.0, y de +0.3 a +0.5, para ,13C y ,15N, respectivamente. Por el contrario, la extracción de lípidos de peces juveniles completos varió marcadamente en +3.4, para ,13C y +2.8, para ,15N - ambos cambios ecológicamente importantes. La varianza de los valores de muestreos de ,13C y de ,15N tanto para tejido muscular como para los peces completos no difirieron entre los muestreos de lípidos extraídos y muestreos sin tratamiento. 3. Nuestros resultados recomiendan el análisis de isótopos estables de tejidos específicos. Cuando ello no es posible o deseable, dos alícuotas de muestreo pueden ser requeridas: una alícuota de lípidos extraídos para el análisis de isótopos de carbono estable cuando la varianza de ,13C, debida a diferencias en el contenido de lípidos de diferentes tejidos, y una alícuota de no-extracción para determinaciones de ,15N. 4. Dada la mezcla de tejidos, el análisis de isótopos de un organismo completo no es recomendable , en el caso de peces muy pequeños, recomendamos que los peces sean eviscerados, decapitados, y despellejados para minimizar las diferencias de muestreos de tejido muscular. [source] | ||||||||||||||||