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Modeling of supercritical extraction of mannitol from plane tree leaf.

The objective of this study was to investigate the theoretical feasibility of using supercritical fluid extraction of Mannitol from plane tree leaf as an alternative technology in the pharmaceutical industry. Simulation of an extraction column using dense liquid and supercritical carbon dioxide was modeled involving partial differential equations, using orthogonal collocation on finite elements. The important solvent extraction parameters such as the partition coefficient, mass transfer coefficient, dispersion coefficient, molecular diffusion and extraction efficiency (the amount of Mannitol extracted versus the amount of solvent used) were investigated as a function of the dimensionless Reynold's and Peclet numbers in order to optimize the extraction column geometry and the carbon dioxide operating conditions. The results of this study demonstrated that supercritical extraction is a viable technique for Mannitol production and that the process conditions for a large commercial extraction system do not require a high temperature in order to obtain a high extraction efficiency. However, at low pressures, the solubility of Mannitol in carbon dioxide would limit the success of the extraction process and at very high pressures the extraction technique may not be economically feasible. To investigate the authenticity of the mathematical model, the experimental data for the desorption of hexachlorobenzene from soil was compared with the theoretical results of this research. The model is able to predict the experimental data quite well without any adjustable parameters.

Chromatography↗

Evaluation of extraction procedures for removing lead from contaminated soil.

Soil extraction of lead contaminated soil collected from sites near an abandoned battery recycling and secondary lead-smelting factory was investigated for potential use in decontaminating soil at the sites. A fractionation study was conducted to elucidate soil retention mechanism for Pb at the site. Three soil pits were selected from an area surrounding the factory based on level of Pb contamination. Soil samples were collected from each pit in two layers: surface soil and subsoil (0-15 cm and 15-30 cm). Soil physical analysis showed that the soil texture was sandy loam and sandy clay loam with clay content between 11-21%. Soil pH was strongly acid to moderately acid (pH 4.8-5.9). Pb levels in the surface soil were 1620 and 153 mg kg(-1) (air-dried basis) respectively for heavily and slightly contaminated soil. A reference soil site contained 15 mg kg(-1) of Pb. Partitioning studies indicated that more than 90% of total Pb in the soil existed in three primary fractions: exchangeable, carbonate, and Fe-Mn oxide. This suggested that Pb sources entering the soil from the Pb factory remained in relatively weakly bound forms, which are mobile and have potentially biological availability. Mobility of Pb as in the soil assessed by mobility factor (MF) was as high as 75% indicating a high potential of Pb remobilization. Due to high mobility, the Pb would be amendable to remediation or removal by soil extraction procedures. To determine if such weekly bound Pb could be easily removed, both soil washing (ex situ) and soil flushing (in situ) techniques were evaluated for potential Pb remediation procedure. Particle size separation of soil into coarse (2.0-0.25 mm), medium (0.25-0.15 mm), and fine size (<0.15 mm) was conducted before initiating soil washing for comparing Pb removal efficiency in these fractions with the indigenous soil fraction. Using EDTA (2:1 mole to Pb) as a washing solution up to 85-95% of Pb was removed under the optimum conditions (retention time = 60 min), and liquid to solid ratio (L/S) at 5:1 for coarse fraction and 10:1 for smaller fraction. Pb could be removed from contaminated soil using EDTA extraction; however, the efficiency was higher in the coarse texture soil fraction. As a result particle size separation is recommended before application of the soil washing procedure. For smaller soil particle size fraction a series of extraction was needed for obtaining an adequate extraction efficiency. Three solvents tested as flushing solution showed 85, 84, and 74% of Pb was removed by EDTA (2:1 mole to Pb), 1M HNO3, and 0.2 M ammonium citrate, respectively after flushing with 20 pore volumes. The capacity of the three flushing solutions to remove Pb from the contaminated soil were ranked in the order: EDTA approximately 1 M HNO3 > 0.2 N ammonium citrate. However, in highly contaminated soil all solvent extract required several Pb leaching cycles. The flushing process using 1 M HNO3 increased soil acidity to extreme acid conditions (pH 2.0) resulting in adverse effects to physicochemical properties of the treated soil. In general, results showed three factors influenced Pb removal by the extraction techniques: (i) initial Pb concentrations, (ii) Pb partitioning within soil, and (iii) particle size of soil matrix.

Chelating Agents↗

Cancer mortality in the commune of Pargny sur Saulx in France.

Radioactive thorium wastes were found in April 1997 at the former industrial site of 'Orflam-Plast' in the commune of Pargny sur Saulx in the Northeast of France, where industrial activity began in 1934. On this site, between 1934 and 1970, cerium for lighter stones and thorium nitrate were extracted from imported monazite sand, a mineral containing elevated levels of natural radioactivity. We decided to study cancer mortality in the surrounding population. We found an excess of mortality due to lung and bladder cancer in the commune of Pargny sur Saulx and its neighbours, between 1968 and 1994. This excess did not seem to be linked to the river of Saulx which was a possible source of contamination. We conclude that a cancer incidence study of the former workers of this industrial site is necessary in order to investigate the role of natural radioactivity from monazite processing in the risk of cancer mortality among this workforce.

Adult↗

Biotransformation of cyanide to methane and ammonia by Klebsiella oxytoca.

Klebsiella oxytoca, isolated from cyanide-containing industrial wastewater, was shown to be able to biodegrade cyanide to non-toxic endproducts using cyanide as the sole nitrogen source. In this study, ammonia was one of the detected endproduct of cyanide biodegradation by the concentrated resting cells of K. oxytoca. Moreover, cyanide has been shown to be biotransformed to methane through the actions of concentrated resting cells. Biodegradation of cyanide by cell-free extracts was not observed, which might be due to the inactivation of nitrogenase (an oxygen-labial enzyme) caused by the oxygen exposure after cell disruption. Results show that the cyanide consumption by resting cells of K. oxytoca was induced when the pretreatment of these cells with cyanide was conducted. However, the cyanide-degrading capability of resting cells pretreated with ammonia was inhibited. The inhibition of cyanide degradation by resting cells of K. oxytoca was affected by the ammonia concentration. This might result from the suppression of nitrogenase activity of K. oxytoca by ammonia since nitrogenase was suggested to be the sole cyanide-degrading enzyme during the cyanide degradation process. Results from this study also show that the processes of cyanide biodegradation and ammonia production by resting cells occurred simultaneously. This suggests that the utilization of cyanide as nitrogen source by K. oxytoca might proceed using ammonia as an assimilatory substrate.

Ammonia↗

Initial proteome analysis of mature barley seeds and malt.

Several barley (Hordeum vulgare) cultivars are used in the production of malt for brewing. The malt quality depends on the cultivar, its growth and storage conditions, and the industrial process. To enhance studies on malt quality, we embarked on a proteome analysis approach for barley seeds and malt. The proteome analysis includes two-dimensional (2-D) gel electrophoresis, mass spectrometry, and bioinformatics for identification of selected proteins. This project initially focused on proteins in major spots in the neutral isoelectric point range (pI 4-7) including selected spots that differ between four barley cultivars. The excellent malting barley cultivar Barke was used as reference. Cultivar differences in the 2-D gel spot patterns are observed both at the seed and the malt level. In seed extracts one of the proteins causing variations has been identified as an alpha-amylase/trypsin inhibitor. In malt extracts multiple forms of the alpha-amylase isozyme 2 have been identified in varying cultivar characteristic spot patterns. The present identification of proteins in major spots from 2-D gels includes 27 different proteins from 42 spots from mature seed extract, while only three specific proteins were identified by analysing 13 different spots from the corresponding malt extract. It is suggested that post-translational processing causes the same protein to occur in different spots.

Computational Biology↗

Dynamic responses of photosystem II in the Namib Desert shrub, Zygophyllum prismatocarpum, during and after foliar deposition of limestone dust.

The effects of limestone dust deposition on vegetation in desert ecosystems have not yet been reported. We investigated these effects in a succulent shrub from the Namib Desert at a limestone quarry near Skorpion Zinc mine (Namibia). Effects of limestone dust were determined in Zygophyllum prismatocarpum (dollar bush) plants with heavy, moderate and no visible foliar dust cover by means of chlorophyll a fluorescence measurements. Limestone dust deposition decreased overall plant performance through loss of chlorophyll content, inhibition of CO(2) assimilation, uncoupling of the oxygen-evolving complex and decreased electron transport. Importantly, dynamic recovery occurred after termination of limestone extraction at the quarry. Recovery was accelerated by rainfall, mainly because of dust removal from leaves and stimulation of new growth. These results indicate that limestone dust has severe effects on photosynthesis in desert shrubs, but that recovery is possible and that, in arid environments, this process is modulated by rainfall.

Air Pollution↗

[Contribution of petroleum-processing plants to the total level of atmospheric air pollution].

On the basis of results of field studies the means to reveal the contribution of oil extracting and processing enterprises (the main components of discharges are similar to the common prevalent impurities in the air of residential areas) into the total level of ambient air pollution has been developed. The method takes into account the relationship between average annual concentrations of oil hydrocarbons and carbon oxide.

Air Pollutants↗

Downstream processing of enzymatically produced geranyl glucoside.

Geraniol plays an important role in the fragrance and flavor industry. The corresponding glucoside has interesting properties as a "slow release" aroma compound. Therefore, the enzymatic production and downstream processing of geranyl glucoside were investigated. Geranyl glucoside was produced in a spray column reactor with an initial production rate of 0.58 mg x U(-1) x h(-1). A pretreated hydrophobic microfiltration membrane was used to prevent migration of the aqueous, enzyme-containing phase to the downstream process. No retention of the glucoside, which accumulated in the geraniol phase, was found. On the basis of examples from the literature, four downstream processes were tested on their viability for this system. Extraction with water and foaming were not suitable to recover geranyl glucoside from geraniol. In the first case, the glucoside selectivity for the geraniol phase was found to be high, which made extraction with water unsuccessful. In the second case it was possible to obtain a stable foam, but significant enrichment of the foam with glucoside did not occur. Adsorption on alumina and distillation under reduced pressure were applied successfully and tested in-line with the bioreactor. A maximum glucoside adsorption of 7.86 mg x g(-1) was achieved on alumina. After desorption and evaporation of the extractant the pure glucoside was obtained quantitatively. A pure product could not be obtained after distillation because a small amount of glucose was present in the permeate as well, which accumulated in the bottom fraction. It was shown that with this reactor system a production of 1 kg of geranyl glucoside in 2 days is possible using an initial amount of 50,000 units of enzyme.

Acyclic Monoterpenes↗

Bleaching of bagasse pulp with enzyme pre-treatment.

The effluent from pulp bleaching processes containing chlorinated lignin and degraded polyphenolic intermediates remains as a major source of water pollution from the pulp and paper industries. Alternative elemental chlorine free bleaching methods based on the usage of chlorine dioxide, ozone and hydrogen peroxide are potential substitutes. Bio-bleaching methods, which involve pre-treatment of pulp with microbial enzymes such as xylanases, have emerged as viable options. Investigations reported in this paper aim at exploring the suitability of commercial bacterial xylanase enzyme preparations for bio-bleaching of bagasse pulps in conjunction with specific chemical bleach sequences employing hydrogen peroxide (P), alkali extraction (E), ozonation (Z), hypochlorite (H) and chelation (Q) stages. The effluent profiles and pulp qualities obtained for each of the bleach combinations (involving bio-bleaching and chemical bleaching sequences) were monitored. Analysis of the results clearly indicates that the inclusion of enzyme pre-treatment with the TCF (total chlorine free) and ECF (elemental chlorine free) sequences has a significant effect on the effluent (COD, lignin and colour) and pulp quality (kappa number, brightness) parameters. In conclusion, the findings of this investigation indicate the potential promise of enzyme pre-treatment in combination with chemical bleaching to enhance the quality of pulps and combined effluents.

Biodegradation, Environmental↗

Detection of antithyroid residues in meat and some organs of slaughtered animals.

A simple method is described for the routine detection of antithyroid residues in thyroid, liver, kidney and meat contaminated at levels as low as 10 ppb (10 parts per 10(9)). Tissue samples (2 g) are homogenized in methanol, contaminating lipids and amino acids are removed and the antithyroid residues are subjected to reaction with 7-chloro-4-nitrobenzo-2-oxa-1,3-diazole (NBD-Cl) in buffer. The NBD derivatives are extracted with diethyl ether and separated by thin-layer chromatography. After spraying with cysteine or mercaptoethylamine, the antithyroid residues appear as fluorescent spots. The detection limit of these compounds is of the order of 200 pg.

Animals↗

Improved fractionation of glycinin and beta-conglycinin and partitioning of phytochemicals.

Glycinin-rich and beta-conglycinin-rich products are prepared by soy protein fractionation. Physicochemical characteristics of these proteins affect their unique, important functionality in food systems and industrial applications. Soybean isoflavones and saponins are phytochemicals with potential health benefits. Objectives of this protein fractionation research were to (1) improve protein and phytochemical extraction from defatted soy flakes and recovery in product fractions and (2) evaluate phytochemical partitioning and profile changes during fractionation. Extraction environments (pH, ethanol concentration, temperature, and water-to-flake ratio) were each varied during bench-scale optimization. Optimized conditions of 45 degrees C and 10:1 water-to-flake ratio were compared with previous conditions of 20 degrees C and 15:1 water-to-flake ratio and a soy protein isolate process at pilot scale. Optimized conditions yielded more beta-conglycinin with higher isoflavone and saponin concentrations, but fraction purity was diminished by glycinin contamination. Bench-scale data demonstrated that increased phytochemical extraction did not translate into increased concentrations in product fractions.

Antigens, Plant↗

[Impact of different solvents on results of genotoxicity studies of airborne dust taken from work environments].

Mutagenicity and toxicity of extracts of airborne particulate matters, sampled during electrolysis of aluminium, cooking of coal and low-temperature carbonization processes, were determined by the Salmonella plate incorporation assay with strains TA98 and TA100. Organic materials were extracted with benzene, cyclohexane or toluene from airborne particles by sonication. The results showed that: a) the extracts were mutagenic only to strain TA98 (without and after metabolic activation); b) there was a similar efficiency of applied solvents in extraction of mutagenic substances detectable with TA98, and c) the toluene extracts were most toxic towards test bacteria TA98.

Air Pollutants, Occupational↗

The role of population pharmacokinetics in drug development in light of the Food and Drug Administration's 'Guidance for Industry: population pharmacokinetics'.

Population pharmacokinetics (PPK) has evolved from a discipline primarily applied to therapeutic drug monitoring to one that plays a significant role in clinical pharmacology in general and drug development in particular. In February 1999 the US Food and Drug Administration issued a 'Guidance for Industry: Population Pharmacokinetics' that sets out the mechanisms and philosophy of PPK and outlines its role in drug development. The application of PPK to the drug development process plays an important role in the efficient development of safe and effective drugs. PPK knowledge is essential for mapping the response surface, explaining subgroup differences, developing and evaluating competing dose administration strategies, and as an aid in designing future studies. The mapping of the response surface is done to maximise the benefit-risk ratio, so that the impact of the input profile and dose magnitude on beneficial and harmful pharmacological effects can be understood and applied to individual patients. PPK combined with simulation methods provides a tool for estimating the expected range of concentrations from competing dose administration strategies. Once extracted, this knowledge can be applied to labelling or used to assess various future study designs. PPK should be implemented across all phases of drug development. For preclinical studies, PPK can be applied to allometric scaling and toxicokinetic analyses, and is useful for determining 'first time in man' doses and explaining toxicological results. Phase I studies provide initial understanding of the structural model and the effect of possible covariates, and may later be used to evaluate PPK differences between patients and healthy individuals. Phase II studies provide the greatest opportunity to map the response surface. With these PPK models it is possible to gain an improved understanding of the role of the dose on the response surface and of the range of expected responses. In phase III and IV studies, PPK is implemented to further refine the PPK model and to explain unexpected responses. Planning for the implementation of PPK across all phases of drug development is necessary, as well as planning for individual PPK studies. Planning should include: defining important questions, identifying covariates and drug-drug interactions that need to be investigated, and identifying the applications and intended use of the model(s). The plan for each project must have a strategy for data management, data collection, data quality assurance, staff training for data collection, data analysis and model validation.

Animals↗

Efficacy of two cleaning and sanitizing combinations on Listeria monocytogenes biofilms formed at low temperature on a variety of materials in the presence of ready-to-eat meat residue.

Biofilms in the food-processing industry are a serious concern due to the potential for contamination of food products, which may lead to decreased food quality and safety. The effect of two detergent and sanitizer combinations on the inactivation of Listeria monocytogenes biofilms was studied. Combination A uses a chlorinated-alkaline, low-phosphate detergent, and dual peracid sanitizer. Combination B uses a solvated-alkaline environmental sanitation product and hypochlorite sanitizer. The survival of bacterial biofilms placed at 4 and 10 degrees C and held for up to 5 days was also addressed. To simulate conditions found in a ready-to-eat meat-processing environment, biofilms were developed in low-nutrient conditions at 10 degrees C (with and without meat and fat residue) on a variety of materials found in a plant setting. Included were two types of stainless steel, three materials for conveyor use, two rubber products, a wall, and floor material. Biofilms developed on all surfaces tested; numbers at day 2 ranged from 3.2 log on silicone rubber to 4.47 log CFU/cm2 on Delrin, an acetal copolymer. Biofilm survival during storage was higher at 4 degrees C (36.3 to 1,621%) than 10 degrees C (4.5 to 83.2%). Small amounts of meat extract, frankfurters, or pork fat reduced biofilm formation initially; with time, the biofilm cell number and survival percentage increased. Cleaning efficacy was surface dependent and decreased with residue-soiled surfaces; biofilms developed on the brick and conveyor material were most resistant. Both detergents significantly (P < 0.05) removed or inactivated biofilm bacteria. The sanitizers further reduced biofilm numbers; however, the reduction was not significant in most cases for the dual peracid. Using a benchmark efficacy of >3-log reduction, combination A was only effective on 50.0% of the samples, Combination B, at 86.1%, was more effective.

Biofilms↗

Solid-state fermentation of phytase from cassava dregs.

Phytases produced by numerous microorganisms and plants degrade phytic acid that has chelated with metal ions in food and feed. It is important to study phytase for the role of metal ions in nutrition of animals and humans as well as in the reduction of organic phosphate content of aqueous environment. This article reports on solid-state fermentation of phytase from a new substrate of cassava dregs. Large quantities of cassava dregs are produced in tropical areas as a byproduct of cassava starch processing. Protein and inorganic salts were found to be low in cassava dregs. Cassava dregs could be employed for phytase synthesis after the addition of a nitrogen source and mineral salts. Ammonium nitrate was the best nitrogen source among the nitrogen sources investigated, including beef extract, yeast extract, urea, ammonium nitrate, sodium nitrate, and ammonium sulfate. Sodium dodecyl sulfate promoted phytase production from cassava dregs. A maximum phytase yield of 6.73 U/g of dry mass was obtained. The obtained phytase was stable at feed-processing temperature, since 70% of initial enzyme activity was maintained after 30 min of treatment at 75 degrees C.

6-Phytase↗

Safety evaluation of food flavorings.

Food flavorings are an essential element in foods. Flavorings are a unique class of food ingredients and excluded from the legislative definition of a food additive because they are regulated by flavor legislation and not food additive legislation. Flavoring ingredients naturally present in foods, have simple chemical structures, low toxicity, and are used in very low levels in foods and beverages resulting in very low levels of human exposure or consumption. Today, the overwhelming regulatory trend is a positive list of flavoring substances, e.g. substances not listed are prohibited. Flavoring substances are added to the list following a safety evaluation based on the conditions of intended use by qualified experts. The basic principles for assessing the safety of flavoring ingredients will be discussed with emphasis on the safety evaluation of flavoring ingredients by the Food and Agriculture Organization (FAO) and World Health Organization (WHO) Joint Expert Committee on Food Additives (JECFA) and the US Flavor and Extract Manufacturers Expert Panel (FEXPAN). The main components of the JECFA evaluation process include chemical structure, human intake (exposure), metabolism to innocuous or harmless substances, and toxicity concerns consistent with JECFA principles. The Flavor and Extract Manufacturers Association (FEMA) evaluation is very similar to the JECFA procedure. Both the JECFA and FEMA evaluation procedures are widely recognized and the results are accepted by many countries. This implies that there is no need for developing countries to conduct their own toxicological assessment of flavoring ingredients unless it is an unique ingredient in one country, but it is helpful to survey intake or exposure assessment. The global safety program established by the International Organization of Flavor Industry (IOFI) resulting in one worldwide open positive list of flavoring substances will be reviewed.

Drug Evaluation↗

Extractive bioconversions in aqueous two-phase systems

Although extractive bioconversions in aqueous two-phase systems (ATPSs) have been studied for over a decade, this has not yet resulted in widespread industrial application. The main reasons are the cost of the phase-forming polymers and the complexity of ATPS behavior. A number of recent developments may give a new impetus to this technology. First of all, the use of extractive bioconversions in ATPSs has recently been extended to high-value protein products, while in the meantime the development of low-cost ATPSs is ongoing. Furthermore, novel chromatographic methods enable the analysis of polymer and metabolite compositions in complex ATPS mixtures, and recently employed statistical experimental designs provide a tool for efficient data gathering, while they also reveal synergistic effects between process parameters. Together, these developments open the way towards improved modeling of partitioning behavior in ATPSs.

Journal Article↗