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Buffer solution

About: Buffer solution is a research topic. Over the lifetime, 6948 publications have been published within this topic receiving 112440 citations. The topic is also known as: pH buffer & buffer.


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Journal ArticleDOI
TL;DR: Effects show that CO32− decreases the regularity of the atomic arrangement when incorporated in HA, and it is probable that the poor resolution of the X-ray and IR patterns is due, in large part, to small crystal size and internal disorder caused byCO32−.
Abstract: Amorphous calcium phosphate (ACP) was transformed at 25 degrees to hydroxyapatite (HA) in horse and bovine serum; solutions of serum-protein fractions in tris-HC1 buffer (pH 7.4), and pH 7.4 buffers containing from 0.1 to 10 times physiological CO3(2-) concentration. The ACP-to-HA transformation was slower in whole serum and serum fractions than in control buffer solution. The observed adsorption of serum proteins on ACP and HA probably inhibits both the dissolution of the ACP particles and the growth of HA crystals. After 72 h all transformations were complete as determined by X-ray diffraction. The HA crystal dimensions decreased with increasing C03(2-) but the shape, as shown by X-ray linewidths, was relatively constant up to about 4% CO3(2-). At 15% CO3(2-) the crystals were more equiaxial and less needle-like in habit. The radial distribution function (RDF) of HA with 3.7% CO3(2-) is less well resolved than the RDF of HA with ambient CO3(2-) (1.1%). The peaks are less sharp and their amplitude falls more rapidly with increasing atomic separation than for low CO3(2-)-HA. These effects show that CO3(2-) decreases the regularity of the atomic arrangement when incorporated in HA. The rapid decrease, with increasing CO3(2-) content, of the IR splitting of the P-O bending mode of CO3(2-)-HA is attributed to reduced crystal size and possibly to a perturbation of the crystal field due to CO3(2-)-induced lattice distortion. Finally, for bone mineral, it is probable that the poor resolution of the X-ray and IR patterns is due, in large part, to small crystal size and internal disorder caused by CO3(2-).

142 citations

Journal ArticleDOI
TL;DR: In this article, the effects of morphology, wall composition of mesoporous materials and different buffer solutions on drug delivery profiles were reported and used as drug carriers which exhibited higher loading capacity and slower release rate compared to the conventional periodic mesoporus silica (PMS) spheres and solid spheres of PMO.

142 citations

Journal ArticleDOI
TL;DR: In this paper, the possibility of horseradish peroxidase (HRP) modified solid graphite and carbon paste electrodes to perform as biosensors for the determination of phenol and related compounds was studied.

141 citations

Journal ArticleDOI
TL;DR: The presence of several contaminants was identified in the mass spectrum of the HEPES matrix, including a prominent contaminant present in levels similar to those obtained from the modeling of the copper titration data.
Abstract: Copper binding properties were investigated for several popular zwitterionic buffers. The two buffers 4-morpholinoethanesulfonic acid (MES) and 3-N-morpholinopropanesulfonic acid (MOPS) did not bind copper and would be good choices for metal speciation studies within their operational pH range. Conversely, 3-(N-morpholino)-2-hydroxypropanesulfonic acid (MOPSO) was observed to weakly bind copper directly (log Kc 2.02). Moreover, strong copper binding was observed for 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), 4-(2-hydroxyethyl)piperazine-1-propanesulfonic acid (HEPPS), and N-(2-hydroxyethyl)piperazine-N‘-(2-hydroxypropanesulfonic acid) (HEPPSO). Log Kc values range from 7.04 to 7.68 and are indicative of strong copper binding ligands. The latter buffer also exhibited weak binding characteristics with a log Kc of 2.05. The strong Cu binding ligands were present in HEPES, HEPPS, and HEPPSO at much lower concentrations than the total buffer concentration. MES, HEPES, MOPSO, and HEPPSO were an...

141 citations

Journal ArticleDOI
30 Mar 2001-Talanta
TL;DR: A new method for the determination of 4-nitrophenol(4-NP) by differential pulse voltammetry (DPV) based on adsorptive stripping technique was described, and the interference of organic and inorganic species on the voltammetric response have been studied.

140 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202317
202232
202185
2020151
2019220
2018245