scholarly journals Antibacterial Effect on Enterococcus Faecalis and Physical Properties of Chitosan Added Calcium Hydroxide Canal Filling Material

2021 ◽  
Vol 48 (2) ◽  
pp. 198-208
Author(s):  
Sol Song ◽  
Yu-Jin Kim ◽  
Jung-Hwan Lee ◽  
Joonhaeng Lee ◽  
Jisun Shin ◽  
...  

The aim of this study was to evaluate the antibacterial effect on Enterococcus Faecalis and physical properties of chitosan added calcium hydroxide canal filling material.<br/>Low, medium, high molecular weights of chitosan powder were mixed with calcium hydroxide canal filling material. Also, for each molecular weight group, 1.0, 2.0, 5.0 wt% of chitosan powder were added. An overnight culture of <i>E. faecalis</i> was adjusted to 1 × 10<sup>6</sup> CFU/ml. For test of antibacterial effect, three different molecular weights of 2.0 wt% chitosan and three different concentrations of high molecular weight chitosan were mixed with calcium hydroxide canal filling material. The absorbance of plates was analyzed using spectrophotometer at 570 nm with a reference wavelength of 600 nm. Physical properties such as flow, film thickness and radiopacity were examined according to ISO 6876 : 2012.<br/>All molecular weight type of chitosan containing material showed inhibitory effect against E. faecalis growth compared to non-chitosan added calcium hydroxide canal filling material group (<i>p</i> < 0.05). High molecular weight chitosan containing material showed the most antibacterial effect. Also, the antibacterial effect decreased as the incorporated amount of chitosan decreased (<i>p</i> < 0.05). Every molecular weight group of material containing chitosan had a tendency for reduced flow and radiopacity, increased film thickness according to amount of chitosan. Low molecular weight of 1.0 wt% chitosan addition did not show any significant difference of physical properties compared to conventional calcium hydroxide canal filling material.<br/>In conclusion, for reinforcement of antibacterial effect against <i>E. faecalis</i> and for favorable physical properties, 2.0 wt% of chitosan adding is recommended. Considering its antibacterial effect of chitosan, further studies are required for clinical application of chitosan in endodontics and pediatric dentistry.

1941 ◽  
Vol 14 (3) ◽  
pp. 580-589 ◽  
Author(s):  
G. Gee ◽  
L. R. G. Treloar

Abstract As high elasticity is a property possessed only by substances of high molecular weight, it is of interest to enquire into the relation between the elastic properties of a highly elastic material such as rubber and its molecular weight. An investigation on these lines has been made possible through the work of Bloomfield and Farmer, who have succeeded in separating natural rubber into fractions having different average molecular weights. The more important physical properties of these fractions have been examined with the object of determining which of the properties are dependent on molecular weight and which are not. Fairly extensive observations were made on the fractions from latex rubber referred to as Nos. 2, 3 and 4 by Bloomfield and Farmer, and some less extensive observations were carried out on the less oxygenated portion of fraction No. 1 obtained from crepe rubber (called hereafter 1b) . Before considering these experimental results, and their relation to the molecular weights of the fractions, it will be necessary to refer briefly to the methods used for the molecular-weight determinations, and to discuss the significance of the figures obtained.


1976 ◽  
Vol 49 (2) ◽  
pp. 303-319 ◽  
Author(s):  
M. Morton ◽  
L. J. Fetters ◽  
J. Inomata ◽  
D. C. Rubio ◽  
R. N. Young

Abstract The results of this study are the first to show that high-1,4 linear α,ω-dihydroxypolydienes can be synthesized with (a) predictable molecular weights, (b) narrow molecular weight distributions, and (c) high functionalities. Using the functionalized polyisoprenes prepared in this work, a series of networks was prepared with a purified triisocyanate as the chain linking agent. The soluble fraction in these networks ranged from 4.6 to 1.6 per cent. The characteristics and physical properties of these networks will be the subject of a forthcoming publication.


1984 ◽  
Vol 11 (1) ◽  
pp. 1-3 ◽  
Author(s):  
Sheikh M. Basha ◽  
Sunil K. Pancholy

Abstract Methionine-rich proteins (MRP) from seeds of different species of the Genus Arachis were isolated and analyzed by gel electrophoresis to detect possible compositional differences. One-dimensional gel electrophoretic analysis showed presence of quantitative and qualitative variations among the MRP-fractions. Following two-dimensional gel electrophoresis, the MRP-fractions were found to contain three groups of polypeptides with apparent molecular weights of approximately 21,000; 19,000 and 16,000, and isoelectric points between 5.1 and 5.8. Within each molecular weight group the number of polypeptides varied between 1 and 3.


1942 ◽  
Vol 15 (3) ◽  
pp. 446-451
Author(s):  
G. Gee

Abstract The molecular weight data reported in Part II depend on the assumption that the values obtained by extrapolating osmotic pressure measurements to infinite dilution represent true molecular weights. This point of view has been strongly criticized, particularly by Pummerer and his coworkers, according to whom rubber normally exists in solution in the form of micelles comprising more or less well-defined aggregates containing a considerable number of chemical molecules. The- osmotic “molecular weight” is then regarded as the weight of an average micelle. If they exist, these micelles may be important in determining both the chemical and physical behavior of rubber, for we should clearly expect the bonds by which the chemical molecules are bound into micelles to be weaker than those within the molecules. It may be noted that it has been shown elsewhere that the physical properties of a series of rubber fractions are closely related to their osmotic and viscosity molecular weights. Since, according to the micellar theory, these fractions can differ only in micelle size, their mechanical behavior must, from this viewpoint, be determined by the size of the micelles, which must therefore remain intact during mechanical deformation of the rubber. It is the object of the present paper to examine in more detail the basis of the micellar theory, and especially to offer an interpretation of the results of the East method, on which Pummerer's arguments are mainly based.


HortScience ◽  
2005 ◽  
Vol 40 (5) ◽  
pp. 1333-1335 ◽  
Author(s):  
Young-Sang Lee ◽  
Yong-Ho Kim ◽  
Sung-Bae Kim

To study the effects of chitosan on the productivity and nutritional quality of soybean (Glycine max L.) sprouts, soybean seeds were soaked in solutions containing 1,000 ppm chitosan of low (<10 kDa), medium (50 to 100 kDa), or high (>1,000 kDa) molecular weight, and the respiration, growth, and vitamin C content of the sprouts were subsequently evaluated. Sprouts treated with high molecular weight chitosan exhibited a significant increase in respiration, 5%, within 1 day of treatment. Chitosan effectively increased the growth of the sprouts: sprouts treated with high molecular weight chitosan showed increases of 3%, 1%, 3%, 1%, and 12% in the total length, hypocotyl length, root length, hypocotyl thickness, and fresh weight, respectively, as compared to a control. The growth-improving effects of chitosan were proportional to the molecular weight of the molecule used in the treatment. Chitosan treatment did not result in any significant reduction in vitamin C content or postharvest chlorophyll formation, traits that determine the nutritional and marketing values of soybean sprouts. All these results suggest that soaking soybean seeds in a solution of chitosan, especially of high molecular weight, may effectively enhance the productivity of soybean sprouts without adverse effects on the nutritional and postharvest characteristics.


1986 ◽  
Vol 250 (3) ◽  
pp. C460-C467 ◽  
Author(s):  
R. J. King ◽  
H. M. Martin ◽  
J. B. Baseman ◽  
J. Morrison-Plummer

We have used monoclonal antibodies developed against the apolipoproteins associated with pulmonary surfactant purified from rabbit lavage fluid to study the expression of epitopes common to these proteins. The pulmonary surfactant contained nearly 20 proteins, of which at least 10 were not derived from serum. Electrophoresis, with sulfhydryl reduction of these proteins indicated apparent molecular weights of approximately 155, 135, 125, and 115 X 10(3) (high-molecular-weight group); 80, 70, and 60 X 10(3) (intermediate group); and 18 through 10 X 10(3) (low-molecular-weight group). Two-dimensional polyacrylamide gel electrophoresis, in which the proteins were electrophoresed without reduction in the first dimension, but with sulfhydryl reduction in the second dimension, revealed that the 80, 70, and 60 X 10(3) proteins dissociated into proteins of nominal molecular weights of 40, 35, and 30 X 10(3), respectively. In contrast, the 125 and 115 X 10(3) proteins of the high-molecular-weight group contained a protein which could only be reduced to a minimum molecular weight of 55 to 60 X 10(3). Monoclonal antibodies generally were of three types: those that reacted strongly with the high-molecular-weight group and weakly with the intermediate group; those that reacted conversely; and those that reacted only with the low-molecular-weight group. Our results indicate that at least two different surfactant apolipoproteins, with differing minimum molecular weights in SDS-polyacrylamide gel electrophoresis, have common epitopes. Although these results cannot certify a physiological relationship between these proteins, they suggest that the intracellular synthesis or extracellular processing of surfactant apolipoproteins may be more complicated than predicted by the findings of previous experiments, perhaps involving the posttranslational assembly of one surfactant protein into oligomers which resist dissociation under the conditions used for the analyses.


1983 ◽  
Vol 23 (04) ◽  
pp. 683-694 ◽  
Author(s):  
Curtis H. Whitson

Whitson, Curtis H., SPE, U. of Trondheim Abstract Methods are developed for characterizing the molar distribution (mole fraction/molecular weight relation) and physical properties of petroleum fractions such as heptanes-plus (C7 +). These methods should enhance equation-of-state (EOS) predictions when experimental data are lacking. predictions when experimental data are lacking. The three-parameter gamma probability function is used to characterize the molar distribution, as well as to fit experimental weight and molar distributions and to generate synthetic distributions of heptanes-plus fractions. Equations are provided for calculating physical properties such as critical pressure and temperature properties such as critical pressure and temperature of single-carbon-number (SCN) groups. A simple three-parameter equation is also presented for calculating the Watson characterization factor from molecular weight and specific gravity. Finally, a regrouping scheme is developed to reduce extended analyses to only a few multiple-carbon-number (MCN) groups. Two sets of mixing rules are considered, giving essentially the same results when used with the proposed regrouping procedure. Introduction During the development of the application of EOS's to naturally occurring hydrocarbon mixtures, it has become clear that insufficient description of heavier hydrocarbons (e.g., heptanes and heavier) reduces the accuracy of PVT predictions. Volatile oil and gas-condensate volumetric phase behavior is particularly sensitive to composition and properties of the heaviest components. properties of the heaviest components. Until recently there has not been published in technical journals a comprehensive method for characterizing compositional variation, which we call "molar distribution." Several authors have given lucid descriptions of petroleum fraction characterization, though they deal mainly with physical property estimation. Usually, only physical property estimation. Usually, only a single heptanes-plus (C7 + ) fraction lumps together thousands of compounds with a carbon number higher than six. Molecular weight and specific gravity (or density) of the C7 + fraction may be the only measured data available. Preferably, a complete true-boiling-point (TBP) analysis should be performed on fluids to be matched by an EOS. Distillation experiments yield boiling points, specific gravities, and molecular weights, from which molar distribution is found directly. Special analyses of TBP data can also provide estimates of the paraffin/napthene/ aromatic (PNA) content of SCN groups, which are useful in some property correlations. Unfortunately, such high-quality data are seldom available for fluids being matched or predicted by an EOS. If data other than lumped C7+ properties are available, they might include a partial component analysis (weight distribution) from chromatographic measurements. In this case. only weight fractions of SCN groups are reported; normal boiling points, specific gravities, and molecular weights (needed to convert to a molar basis) simply are not available. Compositional simulation based on an EOS involves two major problems:how to "split" a C7 + fraction into SCN groups with mole fractions. molecular weights, and specific gravities that match measured C7+ properties, andif a partial extended analysis (e.g., C 11 + ) is available, how to extend it to higher carbon numbers. The first step in addressing these problems is to find a versatile, easy-to-use probability function for describing molar distribution. The distribution function should allow consistent matching and reasonable extension of partial analyses. Also, it should not contain too many unknown or difficult-to-determine parameters. This paper presents such a probabilistic model and describes its application to several reservoir fluids under "Molar Distribution."The second step in characterizing plus fractions involves estimating SCN group specific gravities, which, together with estimated molecular weights (from the probabilistic model), could be used to estimate critical properties required by EOS's. We address this problem and suggest a simple method for specific gravity estimation under "Physical Properties Estimation." SPEJ p. 683


2020 ◽  
Vol 20 (12) ◽  
pp. 7464-7468
Author(s):  
Xiaobo Wang ◽  
Feng Ji

We assessed the effect of chitosan on Helicobacter pylori (HPY) in vitro to provide an experimental basis for the clinical application of chitosan in the treatment of gastric diseases. Here, the method of hole drilling was used to detect the bacteriostatic effect of different concentrations and pH values of chitosan on the standard bacterial strain Sydney strain I (SSI) and two strains of HPY isolated from patients. The bacteriostatic test was used to explore the effect of different molecular weights of chitosan and metal ions on the antibacterial effect of chitosan. The effect of chitosan showed no significant difference among three HPY strains (p < 0.05); moreover, in the range of pH 5.5–8.5, the antibacterial effect of chitosan increased with decrease in pH value (p < 0.01). A significant difference in the antibacterial effect of chitosan was observed at different concentrations (p < 0.01), reaching a peak at 40 g/mL. The molecular weight of chitosan was within 400 kb. With increasing molecular weight, the antibacterial activity of chitosan increased initially and then decreased. The molecular weight of 0.200 kb demonstrated the strongest anti-HPY effect, with the antibacterial effect observed for up to 134 h. Metal ions such as NaCl and MgCl2 affected the anti-HPY effect of chitosan; with increasing concentration, the antibacterial percentage decreased.


e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Yingzhi Guo ◽  
Changjiang Yu ◽  
Zhongwei Gu

Abstract By anionic ring opening polymerization initiated by cyclodextrin oxyanions generated from NaH and β-cyclodextrin(β-CD), novel biodegradable β- CD cored star-shaped poly(ε-caprolactone)s (s-PCLs) were synthesized and then characterized by means of FTIR, GPC, 1H-NMR. The effects of different feed molar ratios of NaH and β-CD on arm number and on the molecular weight of s-PCLs, and the relationship between the polymerization time and monomer conversion were investigated. Moreover, the physical properties of linear PCL (l-PCL) and s- PCLs with similar molecular weights but different arm number were studied and compared by DSC, SEM and intrinsic viscosity measurement, respectively. It was found that the feed molar ratio of NaH and β-CD is an important factor which influences both the molecular weight and arm number. The melting points and intrinsic viscosities of s-PCLs with similar molecular weights were lower than that of l-PCL, and were found to decrease with increasing arm number. Both SEM and AFM showed that the surface morphology of s-PCL films was different from that of l-PCL. These results indicated that s-PCL with different arms and physical properties could be synthesized using just a β-CD core by adjusting the feed molar ratio of NaH and β-CD


1946 ◽  
Vol 19 (3) ◽  
pp. 552-598 ◽  
Author(s):  
Paul J. Flory

Abstract The investigation was undertaken in an attempt to establish the fundamental connections between the physical properties of a typical vulcanized rubberlike polymer and its chemical structure. The structural variables to be considered are the molecular weight of the “primary molecules” entering the vulcanizate, their molecular-weight distribution, and the concentration (or frequency) of cross-linkages introduced during vulcanization. The molecular weights of Butyl rubbers were determined by previously established procedures ; the effects of molecular-weight heterogeneity were suppressed by careful fractionation from very dilute solution. An indirect method, based on the theory of gelation and on the observation of critical molecular weight for incipient gelation (partial insolubility) in “vulcanisates” formed when the cross-linking capacity is fixed, was employed to determine the frequency of occurrence of cross-linked units—a quantity not hitherto evaluated in a vulcanized rubber. In representative pure-gum vulcanizates of Butyl the molecular weight per cross-linked unit ranges from about 35,000 to 20,000, depending (inversely) on the diolefin content of the raw rubber. Micro compounding and testing procedures have been devised for evaluating the necessarily small samples ob- tained in fractionation. Complete evaluation of tensile strength, stress-strain characteristics, swelling in solvents, and creep rate can be obtained with as little as 3 grams of rubber. Results are no less reproducible than those obtained with conventional procedures requiring 50 grams or more. A number of rela- tionships between vulcanizate structure and physical properties have been established. The feasibility of a rational approach to the interpretation of properties of rubber vulcanizates in terms of molecular structure has been demonstrated.


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