Citric acid

About: Citric acid is a research topic. Over the lifetime, 17745 publications have been published within this topic receiving 277125 citations. The topic is also known as: citrate & H3cit.

A biodegradable thermoset polymer made by esterification of citric acid and glycerol.

Abstract: A new biomaterial, a degradable thermoset polymer, was made from simple, economical, biocompatable monomers without the need for a catalyst. Glycerol and citric acid, nontoxic and renewable reagents, were crosslinked by a melt polymerization reaction at temperatures from 90 to 150°C. Consistent with a condensation reaction, water was determined to be the primary byproduct. The amount of crosslinking was controlled by the reaction conditions, including temperature, reaction time, and ratio between glycerol and citric acid. Also, the amount of crosslinking was inversely proportional to the rate of degradation. As a proof-of-principle for drug delivery applications, gentamicin, an antibiotic, was incorporated into the polymer with preliminary evaluations of antimicrobial activity. The polymers incorporating gentamicin had significantly better bacteria clearing of Staphylococcus aureus compared to non-gentamicin gels for up to 9 days.

Carbon dots prepared from citric acid and urea as fluorescent probes for hypochlorite and peroxynitrite

Abstract: Carbon dots (CDs) were prepared from citric acid and urea, and their fluorescence was found to be quenched by hypochlorite and peroxynitrite. Microwave based synthesis gives CDs with excitation/emission wavelength-dependent quantum yields (8 % at 400/520 nm; 10 % at 360/451 nm; 12 % at 350/420 nm). Quenching of fluorescence depends on pH values, and response is most selective and sensitive to hypochlorite at pH 4, and to peroxynitrite at pH 9. The lower detection limits are 0.5 and 1.5 μM, respectively. The method was successfully applied to quantify hypochlorite and peroxynitrite in standard solutions and in spiked dilute serum samples.

Water-insoluble β-cyclodextrin polymer crosslinked by citric acid: synthesis and adsorption properties toward phenol and methylene blue

Abstract: Water-insoluble β-cyclodextrin polymer (β-CDP) crosslinked by citric acid was obtained with a yield of 65% through an environment friendly synthesis procedure. FT-IR spectra disclosed that the hydroxyl groups of β-CD had reacted and condensated with the carboxyl groups of citric acid, and at the same time the structural characteristics of β-CD were essentially maintained in β-CDP. The β-CDP exhibited notable adsorption capability toward phenol (q max = 13.8 mg g−1) and especially large adsorption capability toward methylene blue (q max = 105 mg g−1). The concentration of methylene blue in water could be reduced to 0.11 mg L−1 by the β-CDP, indicating the excellent adsorption sensitivity of β-CDP toward methylene blue. The adsorption results disclosed that the interior cavity and inclusion property of β-CD were maintained in the synthesized β-CDP.

Chiral separation of β-amino alcohols by capillary electrophoresis using cyclodextrins as buffer additives. I. Effect of varying operating parameters

Abstract: Capillary electrophoresis has been used for the chiral analysis of two β-amino alcohol pharmaceutical compounds. Capillary zone electrophoresis conditions were used with β-cyclodextrin as a chiral mobile phase additive. The effects of variation of β-cyclodextrin concentration, temperature, pH, background electrolyte composition and concentration have been investigated. Optimum separations were achieved for clenbuterol using β-cyclodextrin at its solubility limit (16mM), the lowest practicable temperature (19°C), pH 4.0 and an electrolyte solution with a high ionic strength prepared from 0.1 M citric acid and 0.3 M Na2HPO4. For the development compound picumeterol and its (S)-enationmer, the optimum pH 4.0 buffer was prepared from 0.1 M citric acid and 0.2 M sodium acetate. Baseline separation with resolution greater than 2 was achieved for both compounds.

Salt Antagonism of Glyphosate

Abstract: Glyphosate is often applied with diammonium sulfate to increase weed control. However, many other salts in the spray carrier have antagonized glyphosate phytotoxicity. Research was conducted with wheat as a bioassay species to further determine the influence of various salts on glyphosate phytotoxicity. Cation antagonism of glyphosate occurred with iron > zinc > calcium ≥ magnesium > sodium > potassium. Ammonium cation with hydroxide or most other anions was not antagonistic. Anions of ammonium compounds were of primary importance in overcoming glyphosate antagonistic salts, while the ammonium cation was neutral or slightly stimulatory with certain anions. Sulfate, phosphate, citrate, and acetate anions were not antagonistic, but nitrate and chloride anions were slightly antagonistic when applied as ammonium salts or acids. Antagonism of glyphosate action by sodium bicarbonate and calcium chloride was overcome by phosphoric, sulfuric, and citric acid and phosphate, sulfate, and citrate ammonium salts. Acid and ammonium salts of nitrate and chloride were more effective in overcoming sodium bicarbonate than calcium chloride antagonists of glyphosate. Ferric sulfate antagonism was overcome only by citric, partly by phosphoric and sulfuric but not by nitric and hydrochloric acids or their ammonium salts. Acetic acid, ammonium acetate, and ammonium hydroxide did not overcome any salt antagonism of glyphosate. Glyphosate response to salts was independent of spray carrier pH.