scholarly journals Discovery of 2-[5-(4-Fluorophenylcarbamoyl)pyridin-2-ylsulfanylmethyl]phenylboronic Acid (SX-517): Noncompetitive Boronic Acid Antagonist of CXCR1 and CXCR2

2014 ◽  
Vol 57 (20) ◽  
pp. 8378-8397 ◽  
Author(s):  
Dean Y. Maeda ◽  
Angela M. Peck ◽  
Aaron D. Schuler ◽  
Mark T. Quinn ◽  
Liliya N. Kirpotina ◽  
...  
Keyword(s):  
Boronic Acid ◽  
Phenylboronic Acid ◽  
Acid Antagonist

scholarly journals Adsorption and Release of Rose Bengal on Layer-by-Layer Films of Poly(Vinyl Alcohol) and Poly(Amidoamine) Dendrimers Bearing 4-Carboxyphenylboronic Acid

Polymers ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 1854 ◽  
Author(s):  
Kentaro Yoshida ◽  
Akane Yamaguchi ◽  
Hiroki Midorikawa ◽  
Toshio Kamijo ◽  
Tetsuya Ono ◽  
...  
Keyword(s):  
Rose Bengal ◽  
Boronic Acid ◽  
Vinyl Alcohol ◽  
Acidic Solution ◽  
Phenylboronic Acid ◽  
Poly Vinyl Alcohol ◽  
Basic Solution ◽  
Layer By Layer ◽  
Lbl Films ◽  
H2o2 Solution

Phenylboronic acid-bearing polyamidoamine dendrimer (PBA-PAMAM)/poly(vinyl alcohol) (PVA) multilayer films were prepared through the layer-by-layer (LbL) deposition of PBA-PAMAM solution and PVA solution. PBA-PAMAM/PVA films were constructed successfully through the formation of boronate ester bonds between the boronic acid moiety in PBA and 1,3-diol units in PVA. When the (PBA-PAMAM/PVA)5 films were immersed in rose bengal (RB) solution, RB was adsorbed onto the LbL films. The amount of RB adsorbed was higher in the LbL films immersed in acidic solution than in basic solution. The release of RB from the LbL films was also promoted in the basic solution, while it was suppressed in the acidic solution. The boronic acid ester is oxidized to phenol by hydrogen peroxide (H2O2) and the carbon-boron bond is cleaved, so that the (PBA-PAMAM/PVA)5 films can be decomposed by immersion in H2O2 solution. Therefore, when RB-adsorbed (PBA-PAMAM/PVA)5 films were immersed in H2O2 solution, the release of RB was moderately promoted when the solution was weakly acidic.

scholarly journals Recent Advances in Phenylboronic Acid-Based Gels with Potential for Self-Regulated Drug Delivery

Molecules ◽  
2019 ◽  
Vol 24 (6) ◽  
pp. 1089 ◽  
Author(s):  
Chenyu Wang ◽  
Bozhong Lin ◽  
Haopeng Zhu ◽  
Fei Bi ◽  
Shanshan Xiao ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Physicochemical Properties ◽  
Boronic Acid ◽  
Drug Delivery Systems ◽  
Phenylboronic Acid ◽  
3D Structure ◽  
Three Dimensional ◽  
Drug Carriers ◽  
Delivery Systems ◽  
Diabetes Therapy

Glucose-sensitive drug platforms are highly attractive in the field of self-regulated drug delivery. Drug carriers based on boronic acid (BA), especially phenylboronic acid (PBA), have been designed for glucose-sensitive self-regulated insulin delivery. The PBA-functionalized gels have attracted more interest in recent years. The cross-linked three-dimensional (3D) structure endows the glucose-sensitive gels with great physicochemical properties. The PBA-based platforms with cross-linked structures have found promising applications in self-regulated drug delivery systems. This article summarizes some recent attempts at the developments of PBA-mediated glucose-sensitive gels for self-regulated drug delivery. The PBA-based glucose-sensitive gels, including hydrogels, microgels, and nanogels, are expected to significantly promote the development of smart self-regulated drug delivery systems for diabetes therapy.

Phenylboronic acid-functionalized core–shell magnetic composite nanoparticles as a novel protocol for selective enrichment of fructose from a fructose–glucose aqueous solution

2017 ◽  
Vol 41 (22) ◽  
pp. 13399-13407 ◽  
Author(s):  
Lei Gu ◽  
Yun Wang ◽  
Juan Han ◽  
Lei Wang ◽  
Xu Tang ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Magnetic Nanoparticles ◽  
Boronic Acid ◽  
Phenylboronic Acid ◽  
Sample Solution ◽  
Core Shell ◽  
Magnetic Composite ◽  
Selective Enrichment ◽  
Functionalized Magnetic Nanoparticles ◽  
First Time

We developed an efficient and mild method for the preparation of boronic acid-functionalized magnetic nanoparticles (MNPs), and the selective separation of fructose from a sample solution was demonstrated for the first time.

The ortho-substituent on 2,4-bis(trifluoromethyl)phenylboronic acid catalyzed dehydrative condensation between carboxylic acids and amines

2018 ◽  
Vol 54 (43) ◽  
pp. 5410-5413 ◽  
Author(s):  
Ke Wang ◽  
Yanhui Lu ◽  
Kazuaki Ishihara
Keyword(s):  
Carboxylic Acids ◽  
Boron Atom ◽  
Boronic Acid ◽  
Phenylboronic Acid ◽  
Acid Catalyzed ◽  
Ortho Substituent

The ortho-substituent of boronic acid plays a key role in preventing the coordination of amines to the boron atom.

scholarly journals Biodegradable Polycaprolactone Metallopolymer-Antibiotic Bioconjugates Containing Phenylboronic Acid and Cobaltocenium for Antimicrobial Applications

2021 ◽  
Author(s):  
Peng Yang ◽  
Yuanyuan Luo ◽  
Leman Kurnaz ◽  
Marpe Bam ◽  
Xiaoming Yang ◽  
...  
Keyword(s):  
Boronic Acid ◽  
Phenylboronic Acid ◽  
Side Chain ◽  
Bacterial Cells

This paper reports antimicrobial metallopolymers containing biodegradable polycaprolactone as the backbone with boronic acid and cobaltocenium as the side chain. While boronic acid promotes interactions with bacterial cells via boronolectin...

Development of molecularly imprinted Acrylamide-Acrylamido phenylboronic acid copolymer microbeads for selective glycosaminoglycan separation in children urine

2019 ◽  
Vol 44 (6) ◽  
pp. 738-744 ◽  
Author(s):  
Zihni Onur Uygun ◽  
Burcu Okutucu ◽  
Şükriye Hacikara ◽  
Ferhan Sağın
Keyword(s):  
Liquid Chromatography ◽  
Chondroitin Sulfate ◽  
Matrix Effect ◽  
Boronic Acid ◽  
Dermatan Sulfate ◽  
Binding Capacity ◽  
Phenylboronic Acid ◽  
Molecularly Imprinted ◽  
Acid Copolymer ◽  
Chromatography Columns

Abstract Background In this study, we synthesized molecularly imprinted copolymers for liquid chromatography columns as a separator for glycosaminoglycan (dermatan sulfate; DS and chondroitin sulfate; CS) in urine. Materials and methods Acrylamide and acrylamido phenylboronic acid were used as monomers, acrylamide was used for as base monomer to attract negatively charged groups and acrylamido phenylboronic acid (AAPBA) residues used to form diol bonds between sugar and boronic acid residues to strengthen the attraction. These monomers were synthesized by using precipitation polymerization to form uniform spheres, which are more durable for the pressurized chromatographic systems. Trimethylolpropane trimethacrylate and AIBN were used as crosslinker and starter, respectively. Results These GAG selective polymers were filled by pressurized flow into the steel (4.6 mm × 1.6 mm) columns, then imprinted GAGs were extracted and analyzed to calculate binding capacity of each milligram polymer. Calibration curves of the GAG selective columns were obtained 62.5–1000 ng/mL less than 5% coefficient variation, and lower matrix effect. Conclusion Our imprinted columns separated different GAGs from urine specifically and sensitively. Matrix effect was at an ignorable level thus the challenging use.

Phenylboronic Acid−Salicylhydroxamic Acid Bioconjugates. 1. A Novel Boronic Acid Complex for Protein Immobilization

2001 ◽  
Vol 12 (2) ◽  
pp. 229-239 ◽  
Author(s):  
Mark L. Stolowitz ◽  
Clarence Ahlem ◽  
Karin A. Hughes ◽  
Robert J. Kaiser ◽  
Edward A. Kesicki ◽  
...  
Keyword(s):  
Boronic Acid ◽  
Phenylboronic Acid ◽  
Protein Immobilization ◽  
Acid Complex ◽  
Salicylhydroxamic Acid

scholarly journals Catabolism of Arylboronic Acids by Arthrobacter nicotinovorans Strain PBA

2003 ◽  
Vol 69 (7) ◽  
pp. 4263-4267 ◽  
Author(s):  
Ana C. Negrete-Raymond ◽  
Barbara Weder ◽  
Lawrence P. Wackett
Keyword(s):  
Carbon Atom ◽  
Oxygen Atom ◽  
Boronic Acid ◽  
Phenylboronic Acid ◽  
Boronic Acids ◽  
Ring Carbon ◽  
Arylboronic Acids ◽  
Arthrobacter Nicotinovorans ◽  
Ring Carbon Atom

ABSTRACT Arthrobacter sp. strain PBA metabolized phenylboronic acid to phenol. The oxygen atom in phenol was shown to be derived from the atmosphere using 18O2. 1-Naphthalene-, 2-naphthalene-, 3-cyanophenyl-, 2,5-fluorophenyl-, and 3-thiophene-boronic acids were also transformed to monooxygenated products. The oxygen atom in the product was bonded to the ring carbon atom originally bearing the boronic acid substituent with all the substrates tested.

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