scholarly journals Stabilization of Calcium Oxalate Precursors during the Pre- and Post-Nucleation Stages with Poly(acrylic acid)

Nanomaterials ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 235
Author(s):  
Felipe Díaz-Soler ◽  
Carlos Rodriguez-Navarro ◽  
Encarnación Ruiz-Agudo ◽  
Andrónico Neira-Carrillo

In this work, calcium oxalate (CaOx) precursors were stabilized by poly(acrylic acid) (PAA) as an additive under in vitro crystallization assays involving the formation of pre-nucleation clusters of CaOx via a non-classical crystallization (NCC) pathway. The in vitro crystallization of CaOx was carried out in the presence of 10, 50 and 100 mg/L PAA by using automatic calcium potentiometric titration experiments at a constant pH of 6.7 at 20 °C. The results confirmed the successful stabilization of amorphous calcium oxalate II and III (ACOII and ACO III) nanoparticles formed after PNC in the presence of PAA and suggest the participation and stabilization of polymer-induced liquid-precursor (PILP) in the presence of PAA. We demonstrated that PAA stabilizes CaOx precursors with size in the range of 20–400 nm. PAA additive plays a key role in the in vitro crystallization of CaOx stabilizing multi-ion complexes in the pre-nucleation stage, thereby delaying the nucleation of ACO nanoparticles. Indeed, PAA additive favors the formation of more hydrated and soluble phase of ACO nanoparticles that are bound by electrostatic interactions to carboxylic acid groups of PAA during the post-nucleation stage. These findings may help to a better understanding of the pathological mineralization resulting in urolithiasis in mammals.

2003 ◽  
Vol 91 (3) ◽  
pp. 2035-2041 ◽  
Author(s):  
W. O. S. Doherty ◽  
C. M. Fellows ◽  
S. Gorjian ◽  
E. Senogles ◽  
W. H. Cheung

2009 ◽  
Vol 24 (5) ◽  
pp. 1653-1661 ◽  
Author(s):  
Qunwei Tang ◽  
Jihuai Wu ◽  
Jianming Lin ◽  
Shijun Fan ◽  
De Hu

A poly(acrylic acid)/gelatin interpenetrating network hydrogel was synthesized by aqueous solution polymerization. The influences of preparation conditions including cross-linker, initiator, gelatin content, and neutralization degree on the swelling ratios of the hydrogels are investigated. The swelling, mechanical strength, biodegradability, and drug-release properties of poly(acrylic acid)/gelatin hydrogel are evaluated. The hydrogel has excellent mechanical properties; tensile strength is 1500 kPa, and elongation at break is 887%, respectively. The in vitro biodegradation shows that an interpenetrating network structure exists in the poly(acrylic acid)/gelatin hybrid hydrogel. A release study indicates that the theophylline release from the hydrogel depends on the cross-linking density of the hydrogel and pH of the medium, and the drug diffusion obeys an anomalous transport model.


2001 ◽  
Vol 218-220 ◽  
pp. 347-352 ◽  
Author(s):  
S. Kenny ◽  
Martin Buggy ◽  
T. Pembroke ◽  
R. Hill ◽  
P.V. Hatton

2010 ◽  
Vol 53 (3) ◽  
pp. 623-628 ◽  
Author(s):  
Hortensia Ortega-Ortiz ◽  
Baltazar Gutiérrez-Rodríguez ◽  
Gregorio Cadenas-Pliego ◽  
Luis Ibarra Jimenez

The antimicrobial activity of chitosan and water soluble interpolyelectrolyte complexes of poly(acrylic acid)-chitosan was studied. Chitosans of two different molecular weights were tested at different concentration for 0.5 to 5 g·L-1 as antimicrobial agents against P. aeruginosa and P. oleovorans. In both cases, the best microbial inhibition was obtained with the concentration of 5 g·L-1. However, the interpolyelectrolyte complexes of poly(acrylic acid)-chitosan with composition φ =2 produced higher antibacterial activity than the two chitosans at the concentration of 0.5 g·L-1. The NPEC2 complex was more effective than chitosans. This could be attributed to the number of moles of the amino groups of chitosan and the carboxylic acid groups of the interpolyelectrolyte complexes poly(acrylic acid).


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