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PubMed1986

Cytochemical evaluation of sperm and lymphocyte DNA content after treatment with 5 N HCl.

In situ as well as extra situm cytochemical methods were used to investigate why the observed Feulgen-DNA value of sperm versus lymphocyte cells is lower than expected. After treatment with 5 N HCl, in situ experiments involving the GCA reaction and the UV cytophotometry showed the loss of DNA in sperm nuclei to be 12% more than that in lymphocyte nuclei. Extra situm study of sperm and lymphocytes treated with 5 N HCl showed the phosphate and DABA contents of sperm to be 35% and 23%, respectively, less than those of lymphocytes. The data suggest that sperm chromatin is much more sensitive than somatic chromatin to HCl depolymerization during the Feulgen reaction, and this can tentatively be attributed to the protein complement of sperm chromatin.

Animals↗
PubMed1992

Factors affecting the rate of disappearance of sevoflurane in Baralyme.

The effects of temperature, water and Baralyme exhaustion on the rate of disappearance of sevoflurane in Baralyme were studied in an in vitro model. We found that the rate of disappearance of sevoflurane in Baralyme increased as the temperature increased and decreased as the concentration of water increased. The disappearance of sevoflurane also decreased in the presence of exhausted Baralyme compared with fresh Baralyme. The slower rate of disappearance of sevoflurane in Baralyme in the presence of water and Baralyme exhaustion suggests that the disappearance of sevoflurane may be self-limiting in the clinical setting.

Adsorption↗
PubMed2005

SiO2-CaO-K2O coatings on alumina and Ti6Al4V substrates for biomedical applications.

Alumina and Ti6Al4V alloys are widely used for orthopedics and dental applications due to their good mechanical properties and biocompatibility. Unfortunately they can not provide a satisfactory osteointegration when implanted. In fact, both alumina and Ti6Al4V are not bioactive and thus they can only guarantee a morphological fixation with the surrounding tissues without a suitable chemical anchorage. Aiming to impart bioactive properties to these materials a coating can be proposed. At this purpose, a bioactive glass belonging to the SiO2-CaO-K2O system was selected and prepared. This glass, named SCK, possess a thermal expansion coefficient matching with the alumina (8.5x 10(- 6)/ degrees C) and Ti6Al4V (9 x 10(- 6)/ degrees C) ones and thus is a good candidate to produce coatings on both of them. Simple and low-cost enameling and glazing techniques were used to realize the coatings. Structural, morphological and compositional characterizations of the coatings were carried out by means of X-ray diffraction, optical and scanning microscopy and compositional analyses. The in vitro properties of the coatings were investigated by soaking them in a simulated body fluid (SBF) in order to study the precipitation, on their surfaces, of a biologically active layer of hydroxylapatite (HAp).

Alloys↗
PubMed2000

Effect of etching and sandblasting on bond strength to sintered porcelain of unfilled resin.

This study determined the bond strength of an unfilled resin joined to a feldspathic porcelain for the purpose of evaluating the retentive performance of the prepared material surfaces. Porcelain disks (VMK 68 dentin) were either air abraded with alumina (AAA) or etched with one of the following five etchants: (1) ammonium hydrogen bifluoride (AHB); (2) acidulated phosphate fluoride (APF); (3) hydrofluoric acid (HFA); (4) phosphoric acid (PHA); and (5) sulfuric acid-hydrofluoric acid (SHF). Specimens ground with abrasive paper were also used as controls. After surface preparation, the two different sized porcelain disks were bonded together with a methyl methacrylate-based resin initiated with tri-n-butylborane (MMA-TBB resin). Shear bond strengths were determined both before and after thermocycling. Before the thermocycling, the greatest bond strengths (21.3 and 23.7 MPa) were generated with the use of the SHF and HFA agents, followed by the AHB agent (18.4 MPa). Reduction in bond strength after thermocycling was significant for all groups, although the SHF- and HFA-treated groups exhibited bond strengths greater than 15 MPa even after the thermocycling. The results indicated the effectiveness of the SHF- or HFA-etching for retaining the acrylic resin to the porcelain. However, ageing testing also revealed insufficient retentive characteristics of the acrylic resin by etching alone.

Acid Etching, Dental↗
PubMed2001

Compound A production from sevoflurane is not less when KOH-free absorbent is used in a closed-circuit lung model system.

In an in vitro study, less compound A was formed when a KOH-free carbon dioxide absorbent was used. To confirm this observation we used a lung model in which carbon dioxide was fed in at 160 ml min(-1) and sampling gas was taken out for analysis at 200 ml min(-1); ventilation aimed for a PE'CO2 of 5.4 kPa. The soda lime canister temperatures in the inflow and outflow ports (Tin and Tout) were recorded. In six runs of 240 min each, a standard soda lime, Sodasorb (Grace, Epernon, France) was used and in eight runs KOH-free Sofnolime (Molecular Products, Thaxted, UK) was used. Liquid sevoflurane was injected using a syringe pump to obtain 2.1% E'. Compound A was measured by capillary gas chromatography combined with mass spectrometry. Median (range) compound Ainsp increased to a maximum of 22.7 (7.9) ppm for Sodasorb and 33.1 (20) for Sofnolime at 60 min and decreased thereafter; the difference between groups was significant (P<0.05) at each time of analysis up to 240 min. The canister temperatures were similar in both groups and increased to approximately 40 degrees C at 240 min. Contrary to expectation, compound A concentrations were greater with the KOH-free absorbent despite similar canister temperatures with both absorbents.

Absorption↗
PubMed2006

The effect of ionic strength on the UV-vis spectrum of congo red in aqueous solution.

The major peak near 498 nm in the ultraviolet-visible spectrum of congo red in aqueous solution shifts toward the blue while the molar absorptivity of this peak decreases predictably with increasing ionic strength. The shift was observed for solutions in which ionic strength was varied from 0.0 to 1.8M using the uni-univalent ionic compounds, NaCl, NaClO(4), KNO(3) and KBr separately. A plot of the log of the absorbance at the peak versus ionic strength was linear as well as a plot of the log of the wavelength of the major peak (shifted from 498 nm) versus the ionic strength. The slopes of each of these plots were somewhat different depending on the ionic compound.

Bromides↗
PubMed2005

Effects of humic substances on the oxidation of pentachlorophenol by peroxosulfate catalyzed by iron(III)-phthalocyanine-tetrasulfonic acid.

In an attempt to enhance the oxidation of pentachlorophenol (PCP) in the Fe(III)-PcTS/KHSO5 system, the presence of added humic substances (HSs) was studied, investigating the chemical properties of HSs related to the enhancement in PCP oxidation by correlations with the degree of enhancement in PCP oxidation (%delta(PCP)60). The %delta(PCP)60 value increased with a decrease in the content of oxygen-containing functional groups, such as carboxylic acids. This indicated that HSs with a lower content of oxygen-containing functional groups would be useful for enhancing the oxidation of PCP. A negative correlation between %delta(PCP)60 and the kinetic constants of Fe(III)-PcTS self-oxidation indicated that the enhancement by added HSs could be attributed to the suppression of Fe(III)-PcTS deactivation by self-oxidation. Such a stabilization of Fe(III)-PcTS could be attributed to hydrophobic interactions between the catalyst and HSs.

Biodegradation, Environmental↗
PubMed2006

beta-carotene encapsulation in a mannitol matrix as affected by divalent cations and phosphate anion.

The effects of addition of divalent cations and phosphate buffer on the degree of beta-carotene encapsulation in a mannitol matrix during freeze-drying were analyzed. The degradation rate of encapsulated beta-carotene as a function of % RH and its relationship with the physical state of the matrix during storage at 25 degrees C was also studied. The presence of phosphate salts significantly delayed mannitol crystallization at a highly satisfactory degree during freeze-drying and, consequently, the degree of beta-carotene encapsulation increased. This effect was maintained over quite long time during storage of the freeze-dried samples at 25 degrees C. Unavoidable local variations in water content during 3 years storage caused the decrease of T(g) values and made the crystallization degree to increase. The divalent cations showed a synergistic effect and also modified the kinetics of beta-carotene degradation during storage, increasing its stability. The mechanism of crystallization inhibition likely includes a change in hydrogen bond network or/and change in molecular mobility in the presence of divalent cations and phosphate anions. The degradation rate of beta-carotene in a mannitol/KH(2)PO(4) matrix increased as increasing % RH until a value at which the samples collapsed (75% RH), and then the degradation rate decreased. Collapse phenomena may affect diffusion of oxygen from the surface to the inside of the matrix and increase retention of beta-carotene. Surface color was not an appropriate indicator for beta-carotene degradation, because it was mostly dependent on the optical properties of the matrix, which changed with the degree of matrix hydration and collapse.

Anions↗
PubMed2003

Improved synthesis of pure [18F]fluoro-compounds for PET studies from bromo-compounds.

For preparing [18F]labeled compounds free from bromo-compounds for PET (positron emission tomography) studies, we propose the following two processes in which no separation is needed between the fluoro-compound and bromo-compound : (1). the bromo-compound is first converted into O-tosylate, which is then [18F]fluorinated; and (2). after [18F]fluorination of the bromo-compound, its excess is converted into an easily separable compound, e.g., phthalimide-compound. Direct tosylation with silver tosylate was effected in 65-85% yield for most commercial bromo-compounds, and with potassium phthalimide, the bromo-compounds in cold run were converted easily into phthalimide-compounds in 84-90% yield.

Chemistry, Organic↗
PubMed2001

Iron coordination in photosystem II: interaction between bicarbonate and the QB pocket studied by Fourier transform infrared spectroscopy.

The non heme iron environment of photosystem II is studied by light-induced infrared spectroscopy. A conclusion of previous work [Hienerwadel, R., and Berthomieu, C. (1995) Biochemistry 34, 16288-16297] is that bicarbonate is a bidendate ligand of the reduced iron and a monodentate ligand in the Fe(3+) state. In this work, the effects of bicarbonate replacement with lactate, glycolate, and glyoxylate, and of o-phenanthroline binding are investigated to determine the specific interactions of bicarbonate with the protein. Fe(2+)/Fe(3+) FTIR spectra recorded with (12)C- and (13)C(1)-labeled lactate indicate that lactate displaces bicarbonate by direct binding to the iron through one carboxylate oxygen and the hydroxyl group in both the Fe(2+) and Fe(3+) states. This different binding mode with respect to bicarbonate could explain the lower midpoint of the iron couple observed in the presence of this anion [Deligiannakis, Y., Petrouleas, V., and Diner, B. A. (1994) Biochim. Biophys. Acta 1188, 260-270]. In agreement with the -60 mV/pH unit dependence of the iron midpoint potential in the presence of bicarbonate, the proton release upon iron oxidation by photosystem II is directly measured to 0.95 +/- 0.05 by the comparison of infrared signals of phosphate buffer and ferrocyanide modes. This accurate method may be applied to the study of other redox reactions in proteins. The pH dependence of the iron couple is proposed to reflect the deprotonation of D1His215, a putative iron ligand located at the Q(B) pocket, since the signal at 1094 cm(-1) assigned to the nu(C-N) mode of a histidinate ligand in the Fe(3+) state is not observed in the presence of o-phenanthroline. Specific regulation of the pK(a) of D1His215 by bicarbonate is inferred from the absence of the band at 1094 cm(-1) in Fe(2+)/Fe(3+) spectra recorded with glycolate, glyoxylate, or lactate. A broad positive continuum, maximum at approximately 2550 cm(-1), observed in the presence of bicarbonate, but absent with o-phenanthroline or lactate, glycolate, and glyoxylate, indicates a hydrogen bond network from the non heme iron toward the Q(B) pocket involving bicarbonate and His D1-215. Proton release of about 1, measured upon iron oxidation at pH 6 with the latter anions, points to a proton release mechanism different from that involved in the presence of bicarbonate.

Benzoquinones↗
PubMed2005

[Clinical study of the effect of preventing dentine hypersensitiveness by using Fluor Protector and Green Or on the prepared vital pulp abutment teeth].

PURPOSE: To study and evaluate the effect preventing dentine hypersensitiveness by using Fluor Protector or Green Or on the prepared vital pulp abutment teeth of PFM bridges. METHODS: 118 cases, 246 prepared vital pulp abutment teeth, were randomly divided into three groups: Experimental Group A--treated with the Fluor Protector and temporary crown; Experimental Group B--treated with the Green Or and temporary crown, and Control Group--only using temporary crown. The results of desensitization in 3 groups were evaluated. F test was used for analysis (DSPV6.01). RESULTS: Significant differences were found between experimental Group A, B and the control group after 1 week (when cementing the PFM bridges); and also after 1 month (P<0.05). But no significant difference was found between experimental Group A and B (P>0.05). CONCLUSIONS: The effect of preventing dental hypersensitiveness by using Fluor Protector or Green Or on the prepared vital pulp abutment teeth of PFM bridges is ideal. It is easy to use and worth being widely applied.

Calcium Compounds↗