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At least 541 records · Page 30Linked to original sources

PubMed1966

A new flavan-3,4-diol from Acacia auriculiformis by paper ionophoresis.

1. The heartwood of A. auriculiformis contains a typical mixture of analogues consisting of three isomeric flavan-3,4-diols, a dihydroflavonol, flavanone, flavonol and chalcone based on the 4',7,8-trihydroxyl pattern. These were resolved by preparative paper chromatography and preparative paper ionophoresis. 2. Crystalline (-)-teracacidin [(2R,3R,4R)-4',7,8-trihydroxy-2,3-cis-flavan-3,4-cis-diol] was obtained in high (10%) yield, and a new crystalline derivative of (-)-isoteracacidin [(-)-2,3-cis-3,4-trans isomer] was isolated. The crystalline methyl ether of a new (+)-2,3-trans-3,4-cis isomer was isolated. 3. The absolute configurations of (-)-isoteracacidin (2R,3R,4S) and of the (+)-2,3-trans-3,4-cis isomer (2R,3S,4S) were tentatively assigned on the basis of nuclear-magnetic-resonance spectroscopy, paper ionophoresis and paper-chromatographic comparison with the epimerization products of (-)-teracacidin. 4. Possible reasons for the absence of polymeric leuco-anthocyanidin tannins are discussed. 5. (+/-)-4',7,8-Trihydroxydihydroflavonol and (+/-)-4',7,8-trihydroxyflavanone were isolated for the first time. 6. The bark polyphenols consist mainly of polymeric leuco-delphinidins and leuco-cyanidins which redden exceptionally rapidly to light. The mechanism of this phenomenon is discussed.

Acacia↗

PubMed2002

[Image quality of paper prints compared to film copies in CT investigations].

PURPOSE: Evaluation of image quality of paper prints in routine CT investigations. METHOD: The image quality of paper prints from 104 CT scans of daily routine investigations was analysed by three observer three observers according to a five-point ranking scale for contrast, grey level, spatial resolution, and subjective confidence in correct evaluation. Each study was rated "acceptable" or "not acceptable for documentation". RESULTS: In 312 ratings the mean grade for contrast was 2.7, for grey levels 3.2, and for spatial resolution 3.3. Grades ranged from 1 = very good to 5 = insufficient. Subjective confidence in correct evaluation was rated as "certain" in 77.4 %, "likely" in 18.4 % and "impossible to evaluate" in 4.2 % of cases. 93.7 % of printed CT images were rated "acceptable for documentation". CONCLUSION: Image quality of paper prints does not reach the quality of laser films concerning its contrast, grey levels, and spatial resolution. Nevertheless, paper prints are acceptable for documentation of findings in most CT investigations. A high confidence in correct evaluation was found. Limitations are found in documentation of small coin lesions of the lung and ischemic lesions of the neurocranium.

Humans↗

PubMed2006

Contamination of dry foods with trimethyldiphenylmethanes by migration from recycled paper and board packaging.

Contamination of foods with trimethyldiphenylmethanes is reported and the origin is shown to be migration from food packaging materials of which the use of recycled carbonless copy paper was found to be the major source. This chemical is one of the solvents used in the carbonless copy paper and its presence in food and the environment has not been previously identified. In this paper we have pursued previous studies on diisopropylnaphthalenes and hydrogenated terphenyls contamination from packaging and now report the identification of this new food contaminant and present evidence of its source. Solid foods such as egg pasta, barley coffee and rice were analysed by GC/MS and a mean concentration of 18 microg/kg of trimethyldiphenylmethanes was found. Extracts from carbonless copy paper were analysed by proton NMR to characterize the trimethyldiphenylmethanes. Since trimethyldiphenylmethanes are found in solid food together with diisopropylnaphthalenes, and considering their similar chemical character, they may follow the same migration pathway as one another.

Chromatography, High Pressure Liquid↗

PubMedDate not supplied

Cytotoxicological safety assessment of papers and boards used for food packaging.

Because of the lack of information about the possible transfer of toxic compounds from papers and boards to food, the overall cytotoxicity induced by six papers and 15 boards was investigated from water extracts prepared according to the European prestandard. Cytotoxicity measurements were based on RNA synthesis rate of human HeLa S3 cells. The tested virgin and recycled papers and boards were differentiated and classified according to their cytotoxicological quality, which ranged from absence of any cytotoxic effect to severe inhibition of RNA synthesis rate. The cytotoxicity level also varied according to the total amount of compounds detected by gas chromatography. No correlation was found between cytotoxicity and endotoxins contained in the samples. No significant difference in cytotoxicity was observed between the papers and boards produced from virgin fibres and from recycled fibres. Moreover, the products obtained from chemical pulp showed lower cytotoxicity than the products based on mechanical pulp. More generally, the cytotoxicological approach is promising for monitoring paper/board treatment-induced problems. Further work is required to assess a modified standard procedure for the preparation of water extracts specifically adapted to paper/board.

Chromatography, Gas↗

PubMed2001

Comparison of two biocides--carbamate and glutaraldehyde--in the control of fouling in pulp and paper industry.

Formation of fouling deposits is a serious problem facing paper mills. Despite the search for alternative methods, chemical biocides still represent the chief countermeasure to control microbial growth and general fouling buid-up in pulp and paper mills. The purpose of this work was to determine the effect of two biocides (carbamate and glutaraldehyde) on both planktonic cells and fouling layers of a paper machine system. A flow system was used for the study of fouling accumulation in an industrial white water circuit. Both biocides proved to be more effective in reducing the microbial loading of the white water circuit than the deposit accumulated on the stainless steel surfaces. Carbamate, in contrast to glutaraldehyde, had the ability of promoting cell agglomeration since the microbial loading decreased much more when the white water, treated with carbamate, was filtered through a filter-linen. The retention of suspended cells in the cellulose fibres acquires major importance since it is obtained by using an already existing physical process (filtration), which strongly enhances the overall microbial reduction obtained with the addition of the carbamate, without increasing the economic costs. These results also suggest that the use of conventional retention agents in pulp and paper processes can be efficient in controlling unwanted microbial effects.

Carbamates↗

PubMed2006

Multi functional uptake behaviour of materials prepared by calcining waste paper sludge.

This study concerns with the utilization of waste paper sludge, which contains mainly cellulose fibers and inorganic fillers together with coating materials such as calcite, kaolinite and talc. Paper sludge was fired at 500-900 degrees C for 6 h. The crystalline phases originally present decomposed at increasing temperatures (up to 800 degrees C) in the order kaolinite < calcite < talc. Gehlenite was formed at 800 degrees C in increasing amounts above this temperature together with small amounts of magnesium aluminum silicate and anorthite. The uptake of these fired samples of Ni2+, PO3 and NH+ was investigated at room temperature. Paper sludge fired at 700 degrees C showed the highest uptake of Ni2+, PO4(3-) and NH4+ (3.93, 1.28 and 0.49 mmol/g, respectively). The main process responsible for the sorption of these ions is the ion change along with precipitation with higher solution pH. From an economic point of view, paper sludge is the cheapest raw material for preparing adsorbents with high uptake ability for heavy metal, phosphate and ammonium ions.

Adsorption↗

PubMedDate not supplied

Emissions of chemical compounds and bioaerosols during the secondary treatment of paper mill effluents.

This study identified and quantified the main chemical compounds--the substances responsible for the disagreeable odors--and the bioaerosols emitted during the biological treatment of paper mill effluents. It also identified the characteristics of the process that effects the generation or diffusion of these substances. All treatment stages were evaluated. Measuring sites were located as closely as possible to the potential emission sources. Measurements were taken in the summer in 11 paper mills during a 2- to 3-day period in each mill. Chemical compounds were evaluated by direct-reading instruments; bioaerosols were sampled by impaction and counted. Sulfur compounds, emitted into the air when the effluent or the sludge is stirred, had the highest concentrations; their presence was attributable to such things as kraft-type paper pulp. Next in concentration were the carbon and nitrogen oxides, ammonia, and some organic acids, produced by the action of microorganisms. These acids are found mainly in the sludge environment. Terpenes, which come from wood, are present at various locations in paper mills. Odor perception thresholds for most of these substances are much lower than those established to protect the health of workers. Significant concentrations of total bacteria, total molds, and endotoxins were measured at several sites. Gram-negative bacteria were high at only one site, whereas the mold Aspergillus fumigatus was occasionally present at low concentration. No actinomycetes bacteria were detected. The highest concentrations were measured where there was water or dust aerosolization. Emissions are therefore controlled by controlling the operations that lead to the dispersion of water and particles into the air.

Air Pollutants, Occupational↗

PubMedDate not supplied

An improved capillary blood-filter paper-graphite furnace atomic absorption spectrometric method for lead screening.

A revised procedure for processing a capillary blood sample collected on filter paper (FP) for analysis by graphite furnace atomic absorption spectrometry (GFAAS) is described. A 1/4-in. diameter disk of the dried FP sample was used, and a correlation of 0.975 with a false-positive rate of 0.8% and a false-negative rate of 1.7% was found when the results from the FP sample and its corresponding venous sample were compared. Several analytical variables were investigated, and the following was found: blood samples with hematocrit values of 30-39% did not show any significant differences between the paired FP and venous lead results; filter paper blank values were < 2 micrograms/dl with the use of aqueous standards without correction and 0.1 microgram/dl with paper blank correction; and during the collection of 163 samples from 6 different urban sites over a period of 1 year, no environmental lead contamination was encountered based upon the good agreement between all of the paired FP and venous lead results. The method described is easier to perform than an earlier version. All indications suggest that a fingerstick capillary blood sample collected on filter paper is suitable for lead screening. Proper precautions must always be taken to guard against contamination.

Blood Specimen Collection↗

PubMed2005

Filter paper for preservation, storage, and distribution of insect and pathogen DNA samples.

Proper DNA storage is critical for studies involving genetic analysis of insects and for molecular diagnostics of pathogens carried by them. Molecular surveillance of pathogens carried by insects can involve screening of thousands of insect DNA samples. Problems with storage and degradation of these samples can arise. In this study, a simple filter paper-based method for storage and preservation of insect DNA was evaluated using polymerase chain reaction (PCR). DNA was isolated from individual house fly, Musca domestica L., adults by using a cell lysis technique. From 50 house flies known to carry Campylobacter spp., a portion of the DNA sample was stored frozen and another portion was pipetted onto filter paper. At monthly intervals for 7 mo, PCR was conducted using 1 microl of the frozen DNA sample and a 2.0-mm disk from the filter paper samples as the PCR template. Two markers were used, a 450-bp region of the insect mitochondrial DNA (mtDNA) ND5 gene and a 857-bp region of the Campylobacter spp. mtDNA 16S rDNA gene. PCR amplification was successful for all of the samples regardless of the storage method. The filter paper method is a simple and economical way to store, preserve, and distribute DNA samples for PCR analysis.

Animals↗

PubMed1979

Quantitative analysis of specific labelled RNA'S using DNA covalently linked to diazobenzyloxymethyl-paper.

Substantial amounts of DNA (at least 25 microgram per cm2) can be stably bound to diazobenzyloxymethyl (DBM)-paper. Complementary RNA will hybridize to the DNA paper almost completely in 24 hours. Using several different conditions of hybridization and washing, the background of RNA bound non-specifically is very low (between 0.01 and 0.02%) and the efficiency of hybridization is very high (75 to 50% of complementary RNA is bound and retained through the washing procedure). Because the DNA is bound to the paper convalently, it is retained through all the washing and elution steps, and the DNA papers can be re-used many times.

Chromatography, Affinity↗

PubMed1984

Comparison of X-ray film and photographic paper in recording CT images.

Because of a potential film cost savings of approximately 35% using photographic print paper instead of X-ray film in recording CT images, a comparison was undertaken of these hard copy recording methods. One hundred consecutive CT examinations were reviewed on the scanner display console and recorded on X-ray film and photographic print paper using a multi-imager camera. Hard copy images were compared for diagnostic adequacy. X-ray film adequately recorded the pathology in all cases. Photographic paper adequately recorded the pathology in 97% of cases. In 26% of cases X-ray film was felt to better display the CT diagnosis whereas in 2% of cases photographic paper better displayed the CT diagnosis. Test phantom scans recorded on both media showed no observable difference in spatial or contrast resolution.

Humans↗

PubMed1998

Rose bengal dye concentration and volume delivered via dye-impregnated paper strips.

PURPOSE: The technique of administration and the resulting volume and concentration of the dye delivered to the eye via dye-impregnated paper strips are not standardized or known. The purpose of this study was to use a standard technique for preparation of rose bengal dye from commercially available paper strips to determine the variability in concentration based upon soak time, and to determine the volume delivered by such a technique to a model eye. METHODS: Rose bengal filter paper strips were wetted for either 15, 30, or 45 s, and the resulting concentration of dye eluted was determined by spectrophotometry. With the same preparation technique and a 15-s soak time, the strip was applied to wetted filter paper, as a model for the moist surface of the eye. The volume of solution delivered was calculated by weight. RESULTS: Concentrations of rose bengal for the various soak times were: 15 s: 7.64 (+/- 1.11) by 10(-6) g/ml; 30 s: 9.70 (+/- 1.79) by 10(-6) g/ml; and 45 s: 10.27 (+/- 0.66) by 10(-6) g/ml. The volume delivered to the eye model with this technique was 17.43 microliters (+/- 3.09). CONCLUSIONS: The concentration of rose bengal dye delivered to the ocular surface by means of a wetted strip is relatively low and soak time/technique-dependent. This suggests a possibility that results in clinical studies with rose bengal strip application may be different than if controlled volume applications of commercially available 1% liquid rose bengal dye are used.

Cornea↗

PubMed1986

Microfilter paper method for antipyrine determination in whole blood by high pressure liquid chromatography.

A method for measuring antipyrine in whole blood collected on filter paper is described. A 6.2-mm diameter disc (1/4 in) is punched out, eluted with distilled water, and then extracted with 5 ml of dichloromethane/pentane (50:50, vol/vol). After reconstitution of the dried residue, reverse-phase high pressure liquid chromatography is used to quantitate antipyrine using an internal standard. A mixture of 15% acetonitrile in 0.006 M phosphate buffer pH 7.2 was used as the mobile phase. Chromatography was carried out under isocratic conditions for 15 min. The retention time of antipyrine was 3.6 min. Intra- and interassay coefficients of variation were 3.1% and 7.2%, respectively. The limit of sensitivity was 6 ng/injection. The amount of blood in a 6.2-mm filter paper disc was calculated to be 8.4 +/- 0.8 (SD) microliter. Antipyrine half-lives, apparent volumes of distribution, and metabolic clearance rates measured from the filter paper concentrations or directly from plasma were virtually identical. Antipyrine was stable on filter paper for less than or equal to 6 weeks at room temperature. The method reported is convenient; requires a small amount of blood, which can be easily obtained by fingerstick; and readily permits the measurement of antipyrine clearance in the pediatric as well as adult populations.

Adult↗

PubMed1983

Factors regulating the density of bacteria in process waters of a paper mill.

Variations in the numbers of total colonies of Klebsiella pneumoniae, Acinetobacter spp. and pseudomonads were investigated in process waters of a paper mill in southern Finland. Variations were related to independent parameters, namely temperature, pH, redox potential and production of offset paper, by using multiple regression analysis. Temperature was the most significant regressor variable and was negatively correlated with bacterial counts. It accounted for up to about 80% of the variance in bacterial counts in various parts of the process. The significance of temperature was due to its fluctuations in a critical range, above and below the maxima for bacterial growth. The pH level was also significant for total colony count and for K. pneumoniae. Redox potential and the production of offset paper were of significance for Acinetobacter spp. Washing the paper machine with water and lye decreased the numbers of bacteria in process waters.

Acinetobacter↗

PubMed1991

Bacteria in food packaging paper and board.

The bacteria of food packaging paper and board were studied. Most of the aerobic strains were spore-formers; members of the genus Bacillus with B. cereus group (B. cereus, B. mycoides, B. thuringiensis), B. polymyxa group (B. polymyxa, B. circulans, B. macerans, B. pabuli), B. brevis and B. licheniformis predominated. The main source of spore-forming bacteria in paper and board was the broke (rejected paper or board, which is repulped and recycled into the process). Gram-negative bacteria were rare in paper and board in spite of their abundance in the stock. A strain of B. pumilus forming clumping, hairy spores may be of significance in aseptic packaging.

Bacillus↗

PubMed1991

Health aspects of carbonless copy paper.

In the past 20 years, there have been numerous reports of skin and mucous membrane disorders allegedly caused by the use of carbonless copy paper, to such an extent that some people in Europe were refusing to work with it and concern was expressed in the European Parliament. In view of its undoubted convenience and superiority over carbon paper, the author was asked by the Commission of the European Communities for a report. Based on visits to manufacturers and users and the investigation of complaints, the conclusion is that, as exposure to the constituents of the paper during its manufacture is considerably greater than in its use and no cases have arisen in his experience in the industry, the complaints are more likely to be attributable to "sick building syndrome" than to the specific effect of any component of the paper.

Dermatitis, Occupational↗

PubMed1993

Long-term retention of a paper point in the periapical tissues: a case report.

A case is reported of a 15 mm paper point found in the periapical area of a maxillary right central incisor during endodontic surgery for an unresolved periapical radiolucency. The paper point had been present for between five and nine years. Histopathological examination showed the presence of chronically inflamed fibrous connective tissue with a number of foreign body giant cells and focal collections of chronic inflammatory cells. SEM comparison of the specimen with a similarly treated fresh paper point showed no indication of degradation of the paper point by host defense cells.

Adult↗

PubMed2000

Coliform bacteria and nitrogen fixation in pulp and paper mill effluent treatment systems.

The majority of pulp and paper mills now biotreat their combined effluents using activated sludge. On the assumption that their wood-based effluents have negligible fixed N, and that activated-sludge microorganisms will not fix significant N, these mills routinely spend large amounts adding ammonia or urea to their aeration tanks (bioreactors) to permit normal biomass growth. N(2) fixation in seven Eastern Canadian pulp and paper mill effluent treatment systems was analyzed using acetylene reduction assays, quantitative nitrogenase (nifH) gene probing, and bacterial isolations. In situ N(2) fixation was undetectable in all seven bioreactors but was present in six associated primary clarifiers. One primary clarifier was studied in greater detail. Approximately 50% of all culturable cells in the clarifier contained nifH, of which >90% were Klebsiella strains. All primary-clarifier coliform bacteria growing on MacConkey agar were identified as klebsiellas, and all those probed contained nifH. In contrast, analysis of 48 random coliform isolates from other mill water system locations showed that only 24 (50%) possessed the nifH gene, and only 13 (27%) showed inducible N(2)-fixing activity. Thus, all the pulp and paper mill primary clarifiers tested appeared to be sites of active N(2) fixation (0.87 to 4.90 mg of N liter(-1) day(-1)) and a microbial community strongly biased toward this activity. This may also explain why coliform bacteria, especially klebsiellas, are indigenous in pulp and paper mill water systems.

Base Sequence↗