Using polyacrylic resin followed by the substitution reaction with 6-aminohexyl hydroxamic acid, poly(6-acryloylamino-hexyl hydroxamic acid) resin (PAMHA) was successfully synthesized. PAMHA, a spherical resin with the particle size of 0.4 mm, is a novel polyamide hydroxamic acid chelating resin containing acylamino and hydroxamic acid functional groups. A series of influences (pH, contact time, temperature, and the initial concentrations of rare earth ions) were investigated to determine the adsorption properties. The adsorption capacity for La(III), Ce(III), and Y(III) ions were 1.030, 0.962, and 1.450 mmol·g, respectively. Thermodynamic and kinetic studies were also carried out to show that the uptake of rare earth ions onto PAMHA fitted well the pseudo-second-order model and Langmuir isotherm, and the adsorption process was spontaneous endothermic. In addition, desorption of rare earth ions was achieved by using 2 mol·L HNO and desorption efficiencies for La(III), Ce(III), and Y(III) ions were 98.4, 99.1, and 98.8%, respectively. Properties of PAMHA resin were characterized by scanning electron microscope (SEM), Fourier transform infrared spectrometry (FTIR), and X-ray photoelectron spectrometer (XPS). The results showed that there was coordination between the rare earth ions with PAMHA and rare metal ions were chemically adsorbed on the surface of the PAMHA.
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http://dx.doi.org/10.3390/polym13010003 | DOI Listing |
Eur J Med Chem
January 2025
Department of Radiation Medicine, School of Public Health and Management, Wenzhou Medical University, Wenzhou, 325035, China. Electronic address:
Bioorg Chem
January 2025
Department of In Vitro Carcinogenesis and Cellular Chemotherapy, Chittaranjan National Cancer Institute, 37, S. P. Mukherjee Road, Kolkata 700026, India. Electronic address:
Histone deacetylases (HDACs) play a critical role in chromatin remodelling and modulating the activity of various histone proteins. Aberrant HDAC functions has been related to the progression of breast cancer (BC), making HDAC inhibitors (HDACi) promising small-molecule therapeutics for its treatment. Hydroxamic acid (HA) is a significant pharmacophore due to its strong metal-chelating ability, HDAC inhibition properties, MMP inhibition abilities, and more.
View Article and Find Full Text PDFInt J Mol Sci
January 2025
Department of Drug and Health Sciences, University of Catania, Viale A. Doria 6, 95125 Catania, Italy.
Precise binding free-energy predictions for ligands targeting metalloproteins, especially zinc-containing histone deacetylase (HDAC) enzymes, require specialized computational approaches due to the unique interactions at metal-binding sites. This study evaluates a docking algorithm optimized for zinc coordination to determine whether it could accurately differentiate between protonated and deprotonated states of hydroxamic acid ligands, a key functional group in HDAC inhibitors (HDACi). By systematically analyzing both protonation states, we sought to identify which state produces docking poses and binding energy estimates most closely aligned with experimental values.
View Article and Find Full Text PDFInt J Mol Sci
January 2025
Department of Pathogen Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan 250012, China.
is a globally widespread pathogen of significant veterinary and medical importance, causing abortion or congenital disease in humans and other warm-blooded animals. Nevertheless, the current treatment options are restricted and sometimes result in toxic side effects. Hence, it is essential to discover drugs that demonstrate potent anti- activity.
View Article and Find Full Text PDFPhytochemistry
January 2025
School of Pharmaceutical Sciences, South-Central Minzu University, 182 Minzu Road, Wuhan 430074, China; School of Pharmacy, Anhui University of Chinese Medicine, 350 Longzihu Road, Hefei, 230012, China. Electronic address:
Cultivation of the endophytic fungus Robillarda sessilis XL-308 with SAHA resulted in the discovery of two previously undescribed cyclonerane sesquiterpenes (1 and 2), one previously unreported norcadinane type sesquiterpene (3), and seven suberanilohydroxamic acid (SAHA) derivatives (4-10). The identification of previously undescribed compounds was confirmed through NMR spectroscopic analyses, quantum chemistry calculations, and single-crystal X-ray crystallography. Among them, compounds 1 and 2 were products of the silenced genome in XL-308 that activated by SAHA.
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