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Query: UMLS:C0267964 (PAA)
 2,561 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The heterogeneity of the surface energy of multiwalled carbon nanotubes (MWNTs) before and after the adsorption of poly(acrylic acid) (PAA) at 77 K was investigated by a nitrogen probe adsorption technique in a wide range of pressures. The adsorption energy distributions (AEDs) were calculated from the low-pressure data of isotherms (i.e., the data of submonolayer adsorption) using the regularization method. Based on the AED, two types of dominant energetic surfaces are identified and assigned to the graphite-like carbon and disordered carbon or defects in the pure MWNTs, respectively. While the adsorption amount of PAA is raised, a significant decrease in the contribution of higher-energy surface in AEDs is observed for those PAA-adsorbed MWNTs. It is thus demonstrated that PAA prefers interacting with higher-energy surfaces to lower-energy surfaces in MWNTs. Nitrogen probe adsorption measurements including low-pressure data are shown to be a feasible and effective tool to characterize the heterogeneity of structure and surface properties of porous materials.
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PMID:Study of influence on the surface energy heterogeneity of multiwalled carbon nanotubes after the adsorption of poly(acrylic acid). 1545 Apr 47

pH-Sensitive bipolar ion-permselective films of polyelectrolyte multilayers were prepared by layer-by-layer (LbL) assembly and photo-cross-linking of benzophenone-modified poly(acrylic acid) (PAA-BP) and poly(allylamine hydrochloride) (PAH-BP). The multilayer structure and ionizable group composition was finely tuned by changing the pH of the dipping solution. This structure and composition was in turn "preserved" by photo-cross-linking, forming highly stable membrane films. Since PAA-BP and PAH-BP are weak polyelectrolytes, it is possible to control the number of unbound, un-ionized -COOH or -NH2 groups in the multilayer by changing the pH. Moreover, the pH of the deposited film also plays an important role in determining selective latter permselectivity. For example, PAA-BP/PAH-BP multilayers deposited from two pH conditions, pH = 3 (PAA-BP) and pH = 6 (PAH-BP), showed pH-switchable permselectivity for both cationic (pH = 10) and anionic (pH = 3) probe molecules in a single film. The system offers advantages in film stability and introducing reversible selective ion permeability over previous multilayer film and cross-linking methods.
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PMID:pH-sensitive bipolar ion-permselective ultrathin films. 1549 31

Polyelectrolyte multilayer thin films were prepared by an alternate deposition of poly(allylamine hydrochloride) (PAH) and anionic polysaccharides {carboxymethylcellulose (CMC) and alginic acid (AGA)} on the surface of a gold (Au) disk electrode, and the binding of ferricyanide [Fe(CN)(6)](3)(-) and hexaammine ruthenium ions [Ru(NH(3))(6)](3+) to the films was evaluated. Poly(acrylic acid) (PAA) was also employed as a reference polyanion bearing carboxylate side chains. A quartz-crystal microbalance study showed that PAH-CMC and PAH-AGA multilayer films grow exponentially as the number of depositions increases. The thicknesses of five bilayers of (PAH-CMC)(5) and (PAH-AGA)(5) films were estimated to be 150 +/- 20 and 90 +/- 15 nm, respectively, in the dry state. The PAH/polysaccharide multilayer film-coated Au electrodes exhibited a redox response to the [Fe(CN)(6)](3)(-) ion dissolved in solution, irrespective of the sign of the surface charge of the film, suggesting the high permeability of the films to the [Fe(CN)(6)](3)(-) ion. In contrast, the PAH-PAA film-coated Au electrodes exhibited a redox response only when the outermost surface of the film was covered with a positively charged PAH layer. However, the permeation of the [Ru(NH(3))(6)](3+) cation was severely suppressed for all of the multilayer films. It was possible to confine the [Fe(CN)(6)](3)(-) ion in the films by immersing the film-coated electrodes in a 1 mM [Fe(CN)(6)](3)(-) solution for 15 min. Thus, the [Fe(CN)(6)](3)(-)-confined electrodes exhibited a cyclic voltammetric response in the [Fe(CN)(6)](3)(-) ion-free buffer solution. The loading of the [Fe(CN)(6)](3)(-) ion in the films was higher when the surface charge of the film was positive and increased with increasing film thickness. It was also found that the [Fe(CN)(6)](3)(-) ion confined in the films serves as an electrocatalyst that oxidizes ascorbic acid in solution.
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PMID:Redox properties of the ferricyanide ion on electrodes coated with layer-by-layer thin films composed of polysaccharide and poly(allylamine). 1651 97

A series of novel bioreducible poly(amido amine)s containing multiple disulfide linkages (SS-PAAs) were synthesized and evaluated as nonviral gene vectors. These linear SS-PAAs could be easily obtained by Michael-type polyaddition of various primary amines to the disulfide-containing cystamine bisacrylamide. The SS-PAA polymers are relatively stable in medium mimicking physiological conditions (pH 7.4, 150 mM PBS, 37 degrees C), but are rapidly degraded in the presence of 2.5 mM DTT, mimicking the intracellular reductive environment (pH 7.4, [R-SH] = 5 mM, 37 degrees C). The polymers efficiently condense DNA into nanoscaled (<200 nm) and positively charged (>+20 mV) polyplexes that are stable under neutral conditions but are rapidly destabilized in a reductive environment, as was revealed by both dynamic light scatting measurement and agarose gel assays. Moreover, most of the poly(amido amine)s possess buffer capacities in the pH range pH 7.4-5.1 that are even higher than polyethylenimine (pEI), a property that may favorably contribute to the endosomal escape of the polyplexes. Polyplexes of four of the seven SS-PAAs studied were able to transfect COS-7 cells in vitro with transfection efficiencies significantly higher than those of branched pEI, being one of the most effective polymeric gene carriers reported to date. Importantly, also in the presence of serum, a high level of gene expression could be observed when the incubation time was elongated from 1 h to 4 h. XTT assays showed that SS-PAAs and their polyplexes possess essentially no or only very low cytotoxicity at concentrations where the highest transfection activity is observed. The results indicate that bioreducible poly(amido amine)s have excellent properties for the development of highly potent and nontoxic polymeric gene carriers.
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PMID:Novel bioreducible poly(amido amine)s for highly efficient gene delivery. 1722 66

Amine-functionalized mesoporous SBA-15 silica loaded with bovine serum albumin (BSA) has been successfully encapsulated with a thin layer coating of poly(acrylic acid) PAA, with the entrapped BSA being released from the PAA-encapsulated SBA-15 at the higher pH value of 7.4 rather than at the lower pH value of 1.2. This novel drug delivery system has a potential application in the release of protein drug to the site of higher pH value, such as small intestine or colon.
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PMID:pH-Controllable drug release using hydrogel encapsulated mesoporous silica. 1795 98

Double-surface-silvered polyimide films have been successfully fabricated using silver ammonia complex cation ([Ag(NH3)2]+) as the silver precursor and 3,3',4,4'-benzophenonetetracarboxylic dianhydride/4,4'-oxidianile- (BTDA/ODA-) based poly(amic acid) (PAA) as the polyimide precursor via a direct ion-exchange self-metallization technique. The process has been clarified to involve the loading of silver(I) into PAA via ion exchange, the thermally induced reduction of silver(I) to silver(0) and the concomitant imidization of PAA to polyimide upon thermal treatment, the subsequent silver-catalyzed and oxygen-assisted decomposition of the polyimide overlayer, and the self-accelerated aggregation of silver clusters on the film surface to produce well-defined surface silver layers. By employing [Ag(NH3)2]+ solution with a concentration of only 0.01 M and an ion-exchange time of no more than 10 min, the controlled formation of highly reflective and conductive silver surfaces upon thermal treatment at 300 degrees C for less than 4.5 h indicates that the present work provides an efficient route and an effacious silver species for polyimide surface metallization. Although the alkaline characteristics of [Ag(NH3)2]+ have a strong hydrolysis effect on the polyimide precursor chains, the final metallized films retain the key mechanical and thermal properties of the pure polyimide. Films were characterized by ATR-FTIR, XPS, ICP-AES, SEM, TEM, DSC, TGA, reflectivity, conductivity, and mechanical measurements.
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PMID:Controlled formation of optically reflective and electrically conductive silvered surfaces on polyimide film via a direct ion-exchange self-metallization technique using silver ammonia complex cation as the precursor. 1840 10

Poly(amidoamine)s (PAAs) have received significant attention due to their good biocompatibility and fast biodegradation profile which gives these polymers high potential in biomedical applications. Conventional synthesis of PAAs via aza-type Michael addition reaction of primary amines to bis-acrylamides often proceeds slowly and takes several days, which does not allow fast and extensive screening of PAA libraries for their bioactivity. Current investigation was dedicated to the development of catalytic synthesis procedures in order to decrease the polymerization times. The salts of several transition metals, as well as earth alkali metals were studied for their catalytic activity in the polymerization reaction. It was found that the salts of earth alkali metals showed the highest potential in the catalysis of polymerization, whereas the salts of transition metals showed either no effect or even resulted in slowing down the reaction. In particular, the addition of CaCl(2) to the reaction mixtures resulted in remarkable increase of the reaction rate as compared to the system without catalyst. PAAs synthesized by the conventional procedure and those obtained by using CaCl(2) as a catalyst showed no difference in physico-chemical properties as well as in biological activity. The novel synthetic method for PAAs, using catalysts based on earth alkali metals, represents an attractive alternative to currently applied methods. Characteristics of earth alkali metals such as low toxicity and good biocompatibility make them especially useful in the preparation of these polymers for biomedical applications.
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PMID:Improved synthesis strategy of poly(amidoamine)s for biomedical applications: catalysis by "green" biocompatible earth alkaline metal salts. 2143 78

A series of novel granular chitosan-g-poly(acrylic acid)/attapulgite/sodium humate (CTS-g-PAA/APT/SH) composite hydrogels were successfully prepared by one-step free radical graft polymerization and applied as adsorbents for the removal of Pb(II) from aqueous solution. The effects of adsorbent composition (including the contents of APT, SH and CTS) on adsorption capacity and adsorption rate were investigated in detail. Results from kinetic experiments showed that the rate of Pb(II) adsorption on the composite hydrogels was quite fast, that more than 90% of the equilibrium adsorption capacity occurs within two minutes and that the adsorption equilibrium could be achieved within 10 minutes. The adsorption kinetics fit well with the pseudo-second order equation. The introduced SH is helpful for both adsorption capacity and adsorption rate. The -COOH and -COO of PAA, -NH2 of CTS, Ph-O and -COO- of SH, as well as cation exchange and Si-OH of APT, participate in adsorption of Pb(II). The synergistic effect of these groups is responsible for the high adsorption capacity and rate.
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PMID:Rapid removal of Pb(II) from aqueous solution by chitosan-g-poly(acrylic acid)/attapulgite/ sodium humate composite hydrogels. 2187 33

Polymers have attracted much attention as potential gene delivery vectors due to their chemical and structural versatility. However, several challenges associated with polymeric carriers, including low transfection efficiencies, insufficient cargo release, and high cytotoxicity levels have prevented clinical implementation. Strong electrostatic interactions between polymeric carriers and DNA cargo can prohibit complete cargo release within the cell. As a result, cargo DNA never reaches the cell's nucleus where gene expression takes place. In addition, highly charged cationic polymers have been correlated with high cytotoxicity levels, making them unsuitable carriers in vivo. Using poly(allylamine) (PAA) as a model, we investigated how pH-sensitive disulfide cross-linked polymer networks can improve the delivery potential of cationic polymer carriers. To accomplish this, we conjugated thiol-terminated pendant chains onto the primary amines of PAA using 2-iminothiolane, developing three new polymer vectors with 5, 13, or 20% thiol modification. Unmodified PAA and thiol-conjugated polymers were tested for their ability to bind and release plasmid DNA, their capacity to protect genetic cargo from enzymatic degradation, and their potential for endolysosomal escape. Our results demonstrate that polymer-plasmid complexes (polyplexes) formed by the 13% thiolated polymer demonstrate the greatest delivery potential. At high N/P ratios, all thiolated polymers (but not unmodified counterparts) were able to resist decomplexation in the presence of heparin, a negatively charged polysaccharide used to mimic in vivo polyplex-protein interactions. Further, all thiolated polymers exhibited higher buffering capacities than unmodified PAA and, therefore, have a greater potential for endolysosomal escape. However, 5 and 20% thiolated polymers exhibited poor DNA binding-release kinetics, making them unsuitable carriers for gene delivery. The 13% thiolated polymers, on the other hand, displayed high DNA binding efficiency and pH-sensitive release.
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PMID:Effect of thiol pendant conjugates on plasmid DNA binding, release, and stability of polymeric delivery vectors. 2251 94

This paper reports our works on the preparation of the silver-nanoparticle-incorporated ultrafine polyimide (PI) ultrafine fibers via a direct ion exchange self-metallization technique using silver ammonia complex cation ([Ag(NH(3))(2)](+)) as the silver precursor and pyromellitic dianhydride (PMDA)/4,4'-oxidianiline (4,4'-ODA) polyimide as the matrix. The polyimide precursor, poly(amic acid) (PAA), was synthesized and then electrospun into ultrafine fibers. By thermally treating the silver(I)-doped PAA ultrafine fibers, where the silver(I) ions were loaded through the ion exchange reactions of the carboxylic acid groups of the PAA macromolecules with the [Ag(NH(3))(2)](+) cations in an aqueous solution, ultrafine polyimide fibers embedded with silver nanoparticles with diameters less than 20 nm were successfully fabricated. The fiber-electrospinning process, the ion exchange process, and various factors influencing the hybrid ultrafine fibers preparation process such as the thermal treatment atmospheres and the thermal catalytic oxidative degradation effect of the reduced silver nanoparticles were discussed. The ultrafine fibers were characterized by attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), inductively coupled plasma atomic emission spectroscopy (ICP-AES), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA).
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PMID:Incorporation of silver nanoparticles into the bulk of the electrospun ultrafine polyimide nanofibers via a direct ion exchange self-metallization process. 2251 11


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