Folin reaction

The protein concentrations were determined either by the biuret method, using serum albumin as standard (Gornall et al., 1949), or with the Folin reaction (Lowry et al., 1951). 

From Habeeb and Atassi (1977). Values are given in percent precipitation at equivalence relative to reaction of fragment 377-571 with the respective antiserum as 100%. Res te represent the average of three to six replicate determinations which varied 1.2% or less. The percent cross-reaction is based on mg of antibody precipitated at equivalence by e h antigen as determined by the Folin reaction and comparison with a standard curve of rabbit IgG run simultaneously. Single bleedings of these antisera, at the indicated periods after the first injections, were studied. 

A iridine traces in aqueous solution can be determined by reaction with 4-(p-nitroben25l)pyridine [1083-48-3] and potassium carbonate [584-08-7]. Quantitative determination is carried out by photometric measurement of the absorption of the blue dye formed (367,368). Alkylating reagents interfere in the determination. A iridine traces in the air can be detected discontinuously by absorption in Folin s reagent (l,2-naphthoquinone-4-sulfonate) [2066-93-5] (369,370) with subsequent chloroform extraction and hplc analysis of the red dye formed (371,372). The detection limit is ca 0.1 ppm. Nitrogen-specific thermal ionisation detectors can be used for continuous monitoring of the ambient air. 

The express method of phenolic compounds determination was designed. It is based on heterogeneous azo-coupling reaction of phenols, which different extracts of fresh raw material contain, with aryldiazonium salts grafted on the silica surface. We can carry out phenols analysis on-site, as formation of immobilized azocompounds leads to a drastic change in the sorbent s color. Thus, we pui pose a new method, that allows to indicate herb phenols in aqueous and non-aqueous medias and to compare it with a well-known Folin-Ciocalteau method. 

A method that has been the standard of choice for many years is the Lowry procedure. This method uses Cn ions along with Folin-Ciocalteau reagent, a combination of phosphomolybdic and phosphotnngstic acid complexes that react with Cn. Cn is generated from Cn by readily oxidizable protein components, such as cysteine or the phenols and indoles of tyrosine and tryptophan. Although the precise chemistry of the Lowry method remains uncertain, the Cn reaction with the Folin reagent gives intensely colored products measurable spectrophotometrically. 

Trimethoprim (Trimpex) interferes with the ability of bacteria to metabolize folinic acid, thereby exerting bacteriostatic activity. Trimethoprim is used for UTIs that are caused by susceptible microorganisms. Trimethoprim administration may result in rash, pruritus, epigastric distress, nausea, and vomiting. When trimethoprim is combined with sulfamethoxazole (Septra), the adverse effects associated with a sulfonamide may also occur. The adverse reactions seen with other anti-infectives, such as ampicillin, the sulfonamides, and cephalosporins, are given in their appropriate chapters. 

Leucovorin (folinic acid) - enzyme cofactor for thymidylate synthase rescues from methotrexate toxicity potentiates cytotoxicity of fluoro— pyrimidines -occasional nausea -skin rash -headache -rare allergic reactions... 

A relatively large number of agents have been utilized to treat this intractable disorder folinic acid (5-formyl-tetrahydrofolic acid), folic acid, methyltetrahydrofolic acid, betaine, methionine, pyridoxine, cobalamin and carnitine. Betaine, which provides methyl groups to the beta i ne ho mocystei ne methyltransferase reaction, is a safe treatment that lowers blood homocysteine and increases methionine. 

In living systems, folinic acid can be synthesized ultimately from folic acid by reduction to tetrahydrofolic acid followed by addition of a 1-carbon fragment to the molecule (N5.N1°-methylenetetrahydrofolate, V). After a 2-step oxidation, the formyl group resides either at the N5 or N10 position or as an equilibrium mixture. The essential reactions are summarized below 32... 

In Goiffon s method (G3) peptides are precipitated with phospho-tungstic acid from a trichloroacetic acid filtrate. The precipitate is dissolved and color is developed by a reaction with Folins phenol reagent. This method, however, is not only specific for peptides and a separate assay of uric acid has to be made since this substance also reacts with Folin s reagent. 

Recently, Choy et al. also reported that LDHs are an efficient drug reservoir for folate derivatives [187]. Folic acid derivatives, folinic acid and methotrexate (MTX), have been successfully hybridized with Mg/Al LDHs by ion-exchange reactions. Cellular uptake tests with the MTX-LDH hybrids were carried out in the fibroblast (human tendon) and osteosarcoma (SaOS-2) cell lines by in vitro assay. They found that the LDH not only plays a role as a biocompatible delivery matrix for drugs but also facilitates a significant increase in the delivery efficiency. 

Methods used for the detection of PAs in cmde or partially purified extracts can also be adapted for post-column analysis after fractionation (see below). Direct quantitative analysis of PAs in crude grape phenolic extracts is often impossible due to the complex sample matrix. Thus, fractionation or purification is often necessary before analysis. The Folin-Ciocalteu and Pmssian Blue assays are widely used for the quantification of total polyphenols in plants [27,28]. These methods are not specific for PAs due to the reaction of other phenolic compounds with these reagents. 

For a number of years, phenolic substances were dosed by colorimetric techniques, based on redox reactions usually known as Folin Ciocalteau methods, even if a number of adjustments were developed to fit different matrix characteristics. The Folin Cioalteau reagent is a mixture of phosphomolybdic and phosphotingstic acids, with molybdenum in the 6+ oxidation state and, when the reaction takes place, it is reduced to form a complex called molybdenum blue and tungsten blue. In this complex, the mean oxidation state is between 5 and 6 and the formed complex is blue so it can be read spectrophotometrically at 750 nm. 

In vitro tests, used in evaluation of antioxidant properties make use of the ability of antioxidants to quench free radicals. Based on this mechanism, the methods are divided into two groups SET - single electron transfer, and HAT - hydrogen atom transfer. Reactions with antioxidants in assays with the DPPH radical, ABTS and the Folin-Ciocalteu reagent both operate according to the SET and HAT mechanism. Due to the kinetics of the reaction, they are included in the... 

The Falin-Ciocalteu reagent (FCR) is a complex formed in a reaction between sodium tungstate and sodium molybdenate in hydrochloric add and phosphoric acid, which turns yellow after lithium sulphate is added. The reagent reads in an alkaline environment with reducing compounds. Such a reaction gives a blue chromophore which is observed by colorimetry. The Folin-Ciocalteu method is highly sensitive - both to phenolic and non-phenolic compounds, e.g. proteins, vitamin C, vitamin Bj, folic acid, Cu(I). The method is applied most frequently to determine the total content of phenolic compounds [34,35]. If that is the case, a sample for determination should be prepared in a proper manner to minimise the effect of non-phenolic... 

Performing the assay is reduced to putting an alcoholic solution of the analysed sample, Folin-Ciocalteu reagent and solution of sodium carbonate into a reaction tube, which brings the pH of the reaction environment to approx. 10. According to various literature reports, the reaction runs in the darkness for 10 to 120 minutes. After that time, the blue colour of the solution is observed colorimetrically at 725 nm - 760 nm [34, 35, 36, 37, 38]. The results are expressed based on calibration curves prepared for catechol and gallic acid. 

The reduced phosphomolybdic/phospho-lungstic acid complex produced by this reaction is intensely blue in color. The Folin phenol reagent loses its reactivity almost immediately... 

ALTERNATE PROTOCOL MICROSCALE PROTOCOL FOR FOLIN-CIOCALTEAU COLORIMETRY This protocol is adapted for small sample volumes. The reaction is performed directly in a 2-ml cuvette. For a list of materials needed, see Basic Protocol 1. 

In the Biuret reaction, a purple colour develops when the protein is treated with alkaline copper sulphate. This reaction is dependent on peptide bonds and not on the side chains of individual amino-acids present. In the Folin-Ciocalteu reaction, the protein is treated with tungstate and molybdate under alkaline conditions and the formation of a complex such phenylalanine and tyrosine gives rise to a blue colour. Lowry developed one of the most widely used protein assays in which a combination of the above reactions is involved07, l8). 

The oxidation reaction of phenolic compounds can be used for the purpose of detection. While the phenolic compound is oxidized, a reagent is reduced, and the reduction can be monitored by a change in color. Two common reagents are ammoniacal silver nitrate and the Folin-Denis reagent. 

The biuret reaction (M16), the Folin and Ciocalteu reagent (K22), ultraviolet adsorption (H2) and polarographic determinations (Fig. 25) have also been proposed (B2, H16). 

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