Ozonized oils: a qualitative and quantitative analysis

Most of the problems of endodontic origin have a bacterial etiological agent. Thus, there is a continued interest in seeking more effective chemical substances that can replace the camphorated paramonochiorophenol or antibiotics as intracanal medicaments. Among the possible substances, ozone has some interesting biological characteristics: bactericidal action, debriding effect, angiogenesis stimulation capacity and high oxidizing power. The purpose of this study was to chemically evaluate the presence of ozone in sunflower, castor, olive and almond oil, as well as in propylene glycol and byproducts of ozonation, such as formaldehyde. These compounds were ozonized, inserted into empty and sterile vials, and analyzed by testing the reaction between ozone and indigo, for determining the presence of ozone, and subjected to the chromotropic acid test for determining the presence of formaldehyde. It was observed complete absence of ozone in all samples tested and presence of formaldehyde. The bactericidal and healing action of ozonized oils could be attributed to products formed by the ozonation of mineral oils, such as formaldehyde, not to the ozone itself.

A maioria dos problemas de origem endodôntica tem um agente etiológico bacteriano. Assim, existe um interesse permanente em se buscar substâncias químicas mais efetivas e que possam substituir o PMCC ou os antibióticos como curativos de demora. Dentre as possíveis substâncias, o ozônio apresenta algumas características biológicas interessantes: ação bactericida, efeito debridante, estímulo a angiogênese, além do efeito oxidante. O propósito do presente estudo foi avaliar quimicamente a presença de ozônio nos óleos de girassol, rícino, oliva e amêndoas, além do propilenoglicol, bem como subproputos da ozonização, como formaldeído. Essas substâncias foram ozonizadas, inseridas em tubetes anestésicos vazios e esterilizados, e analisadas por meio do teste da reação entre ozônio e índigo, para determinação da presença de ozônio; e teste do ácido cromotrópico, para determinação da presença de formaldeído. Foi observado ausência total de ozônio em todas as amostras testadas, além da presença de formaldeído. A ação bactericida e curativa dos óleos ozonizados poderia ser atribuída aos produtos formados pela ozonização de óleos minerais, como o formaldeído, e não ao ozônio propriamente dito.

Production of leather fat liquoring agents from local sources as alternative for imported liquors

Local animal bone fat extracted from animal bone by-product was chemically treated with chlorosulfonic acid [15% chlorosulfonic acid based on weight of fat] to produce local leather fat liquoring agent. Different conditions include stirring time, reaction temperature, and presences of different solvents were investigated to obtain the optimum conditions of fat liquor preparation. The prepared fat liquor was found to possess a great emulsion stability and effective resistance towards different factors as pH and metallic ions. The prepared fat liquor was applied as fat liquoring agent for chrome tanned leather. The improvement of the quality of the fat liquored leather was manifested through the enhancement of chemical and physical parameters such as free and bounded fatty matter, tensile strength, and elongation at break, and through better visual properties and good general appearance of leather. The prepared fat liquor was used as an alternative for the imported fat liquors showing great performance and saving hard currency

Measurement of antioxidant activity with trifluoperazine dihydrochloride radical cation

A novel, rapid and cost-effective trifluoperazine dihydrochloride (TFPH) decolorization assay is described for the screening of antioxidant activity. A chromogenic reaction between TFPH and potassium persulfate at low pH produces an orange-red radical cation with maximum absorption at 502 nm in its first-order derivative spectrum. TFPH was dissolved in distilled water to give a 100 mM solution. The TFPH radical cation solution was made by reacting 0.5 mL of the solution with K2S2O8 (final concentration: 0.1 mM) and diluting to 100 mL with 4 M H2SO4 solution. A linear inhibition of color production was observed with linearly increasing amounts of antioxidants, with correlation coefficients (R²) ranging from 0.999 to 0.983. The antioxidant capacity of standard solutions of an antioxidant was evaluated by comparing with the inhibition curve using Trolox as the standard. Comparison of antioxidant capacity determined with this newly developed TFPH assay and with the well-known 2,2'-azinobis-[3-ethylbenzthiazoline-6-sulfonic acid] (ABTS)-persulfate decolorization assay indicated the efficacy and sensitivity of the procedure. The proposed assay is less expensive (costs about US$4 per 100 assays) and requires only 20 min for preparation of radical cation solution in comparison with ABTS assay, in which almost 12-16 h are required for preparation of a stable ABTS radical cation solution. The present assay has the advantage over ABTS assay that it can be used to measure the antioxidant activity of the samples, which are naturally found at a pH as low as 1, because the radical cation itself has been stabilized at low pH.

Antioxidant and antiulcer activity of aqueous extract of a polyherbal formulation.

The aqueous extract of Hingwashtak churna was evaluated for gastroprotection in rats using the ibuprofen and ethanol induced ulcer models. Efficacy was assessed by determination of mean ulcer size, ulcer number and ulcer index. Oral administration of the aqueous extract (750 mg/kg) significantly protected against gastric lesions by 84.96% and 91.12% as compared to ranititidine (95.54 and 95.2%) in the ibuprofen and alcohol induced ulcer models respectively. The findings suggest that the significant gastroprotective activity could be mediated by its antioxidant activity which was evaluated by using different antioxidant models of screening.

Coordinate compounds of trivalent lanthanides with 7-Phenylazo-8-Hydroxy-quinoline-5-Sulphonic acid and its halo derivatives

Trivalent Pr, Nd, Sm, Gd, Ho, Er, Yb and Y form MLn [n= 1-3] complexes in solution with 7-phenylazo-[I], 7[p-chlorophenylazo]-[II], 7 [p- bromophenylazo]-[III] and 7 [p-iodophenylazo]-8-hydroxyquinoline-5- sulphonic acid [IV]. The stability constants of the complexes were determined potentiometrically and correlated to the ionic potential, atomic number, ionization potential and electronegativity of the central metal ion. Solid complexes of [I] with the lanthanide ions have been prepared and their structure is studied by elemental and thermogravimetric analyses, IR spectroscopy and conductance measurements