Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0267964 (PAA)
 2,561 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

We studied the effects of a high molecular weight polymer (polyacrylic acid, PAA, M(w)=7.5 x 10(5)) on the coexistence curve of a binary liquid mixture (2,6-lutidine + water, LW). A high precision refractometer was built to measure the temperature dependence of the refractive indexes of the two coexisting phases of phase separated LW samples containing less than 1 mg/cc of PAA. From the refractive indexes we mapped out the coexistence curve and obtained the refractive index difference triangle upn between the two coexisting phases. At temperature T close to the critical temperature T(c), the critical exponent beta such that triangle n inversely proportional to (T-T(c))(beta) was found to be 0.41+/-0.02 which is higher than (0.31+/-0.01) that of pure LW.
 ...
PMID:Coexistence curve exponent of a binary mixture with a high molecular weight polymer. 1130 43

Adsorption of metals from aqueous solution onto oxide and other surfaces is known to affect trace metal transport in many natural and engineered systems. It is therefore important to understand whether dissolved metal inputs will be easily bound to particles or will be strongly complexed in solution and transported with the water phase. The effect of poly(acrylic acid) (PAA), representing a model compound for natural organic matter, on the adsorption of Cd(II) onto gamma-Al2O3 was determined using batch adsorption experiments over a pH range from 4 to 10. Initially, interactions among the individual components were evaluated. Cadmium adsorption onto alumina showed a typical S-shaped metal adsorption curve. PAA adsorption onto gamma-Al2O3 decreased with increase in pH. The affinity of PAA for Cd2+ increased strongly with pH. In ternary systems, the presence of PAA resulted in an enhancement of Cd(II) adsorption below pH 6, apparently due to ternary surface complex formation. Above pH 6, a decrease in cadmium adsorption onto gamma-Al2O3 was observed resulting from an increase in the concentration of soluble Cd-PAA complexes. Overall, results indicate that the presence of natural organic matter could have a significant impact on the distribution and mobility of cadmium in the environment. Simple surface complexation modeling was insufficient to describe behavior in the ternary systems due to the complexity of the PAA polymer.
 ...
PMID:Cadmium adsorption on aluminum oxide in the presence of polyacrylic acid. 1134 8

Poly(amidoamine)s (PAAs) are water-soluble polymers that display pH-dependent membrane activity. PAAs have the potential to act as a synthetic alternative to fusogenic peptides and thus promote endosomal escape. The purpose of this study was to investigate for the first time whether PAA have the ability to complex DNA, protect it from nuclease degradation and to promote transfection in vitro. PAAs ISA 1 (Mn 6900) and ISA 23 (Mn 10,500) and their 2-phenylethylamine containing analogues ISA 4 and ISA 22 (Mn approximately 8000) were studied. All PAAs retarded the electrophoretic mobility of lambda Hind III DNA demonstrating interpolyelectrolyte complex (IPEC) formation and toroids of 80-150 nm in diameter (10:1 polymer excess) were visible using TEM. DNase II inhibition was observed. At a polymer:DNA ratio of 10:1, this was ISA 1(89.6 +/- 6.1%), ISA 4 (92.2 +/- 11.2%), ISA 22 (69.4 +/- 3.7%), and ISA 23 (58.0 +/- 10.0%). PAAs demonstrated the ability to mediate pSV beta-galactosidase transfection of HepG2 cells. At a vector:DNA mass ratio of 5:1, ISA 23 showed equivalent transfection ability compared with polyethylenimine and LipofectIN and was more effective than LipofectACE. These properties suggest that PAAs warrant further development as endosomolytic vectors.
 ...
PMID:Poly(amidoamine)s as potential nonviral vectors: ability to form interpolyelectrolyte complexes and to mediate transfection in vitro. 1171 5

Microbial degradation of thermally synthesized poly(aspartic acid) (PAA) was investigated. A PAA-P1 sample (Mn, 7500; Mw, 20,000; number of branched units/100 monomer units, 3.1) was completely degraded in natural river water within 15 days at 25 degrees C. A new PAA-degrading bacterium (strain KP-2: JCM10638) was isolated together with Sphingomonas sp. KT-1 (JCM10459) from river water, and identified as a member of Pedobacter. A Pedobacter isolate was capable of degrading high-molecular-weight PAA polymers of 5000 to 150,000, and a small amount of low-molecular-weight products of 250 to 5000 was accumulated as residues during the growth of the isolate on PAA. In contrast, the other isolate Sphingomonas sp. KT-1 degraded only low-molecular-weight PAA below 5000. A mixed culturing of Pedobacter sp. KP-2 with Sphingomonas sp. KT-1 resulted in a complete degradation of PAA-P1 sample, but a small amount of low molecular weight components was accumulated during the degradation of highly branched PAA-P2 and PAA-P3 samples.
 ...
PMID:Microbial degradation of poly(aspartic acid) by two isolated strains of Pedobacter sp. and Sphingomonas sp. 1171 94

Poly(amidoamine)s (PAAs) are water-soluble synthetic polymers designed to be biodegradable and biocompatible. Moreover, they display membrane disruptive properties in response to a decrease in pH. This attribute confers PAAs with endosomolytic properties in vitro and in vivo. A model system was developed to quantify their ability to promote the endosomal escape of macromolecules that may be interesting as therapeutic agents. Here, two PAAs (ISA 1 and 4) were incubated with B16F10 cells in vitro together with two non-permeant toxins: either ricin A-chain (RTA) or gelonin. The relatively non-toxic PAAs ISA 1 and 4 (IC50>1.5 mg/ml) restored activity to the inherently inert toxins. The IC50 values for the ISA 1/RTA and ISA 1/gelonin combinations were 0.65+/-0.05 and 0.55+/-0.12 mg/ml, respectively. Similarly, when ISA 4 was incubated with a non-toxic combination of RTA and gelonin the IC50 value decreased to 0.57+/-0.03 and 0.43+/-0.26 mg/ml, respectively. In contrast, the neutral polymer dextran and the PAA ISA 22 were unable to mediate this effect. These observations suggest that specific PAA-toxin combinations warrant further development as novel therapeutics.
 ...
PMID:Poly(amidoamine)-mediated intracytoplasmic delivery of ricin A-chain and gelonin. 1173 90

Polyterephthalamide microcapsules containing a poly(acrylic acid) gel as a macromolecular ligand (PAA-CAPS) were prepared using an original two step polymerization process in a water-in-oil inverse emulsion system. A polyamide microcapsule containing acrylic acid, initiator and cross-linking agent, is formed by interfacial polycondensation of terephthaloyl dichloride with hexamethylenediamine. In situ radical polymerization of the microcapsule core acrylic acid is initiated to obtain encapsulated poly(acrylic acid) gel. Reference polyamide microcapsules, i.e. without ligand (CAPS), were also synthesized. The mean diameter of synthesized microcapsules was 210 microm, and the microcapsule wall thickness was evaluated by SEM and TEM observations of microcapsule cross-section cuts. The microcapsule water content was determined by thermogravimetric experiments. The extractabilities of Cu(II), Ni(II), Co(II) and Zn(II) into PAA-CAPS were examined. The stripping of the various cations can be promoted in diluted hydrochloric acid solutions.
 ...
PMID:Extraction of metal cations by polyterephthalamide microcapsules containing a poly(acrylic acid) gel. 1181 55

Polyelectrolyte multilayers of poly(acrylic acid) (PAA) and polyacrylamide (PAAm) were prepared via hydrogen-bonding interactions. These multilayers as assembled were stable at low pH but dissolved quickly in neutral pH water. We developed methods for stabilizing these multilayers to high pH through cross-linking by heating or UV-irradiation. Thermal treatment of the multilayers, which resulted in a partial imidization between carboxylic acid and amide groups, gave the multilayer good stability at high pH. In addition, we introduced photoreactive groups in the multilayer, which rendered the film insoluble after UV irradiation. Using these selective stabilization approaches, we have succeeded in micropatterning these films by ink-jet printing and photolithography to create subtractive patterns.
 ...
PMID:Micropatterning of polymer thin films with pH-sensitive and cross-linkable hydrogen-bonded polyelectrolyte multilayers. 1187 48

A surface plasmon resonance (SPR) sensor was applied to analyses of some amine compounds (n-butylamine, isobutylamine, aniline, and N,N-dimethylaniline) by using a polymer film and an acid-base reaction in it. Poly(acrylamide) (PAA) was adopted as the polymer film and was immobilized on an Au film to prepare a sensor chip. Pivalic acid was entered into the PAA film as an acid. The PAA film with a thickness of 50 nm gave the highest sensitivity to the SPR sensor. Although water was better concerning the sensitivity for the SPR sensor as the solvent, ethanol was adopted because it dissolves well all of the amine compounds used. The Au film coated with the PAA film gave higher sensitivity for analyses of n-butylamine and isobutylamine, and lower sensitivity for analyses of aniline and N,N-dimethylaniline than an Au film without the PAA film. The PAA film containing pivalic acid gave 4-5 orders of magnitude higher sensitivity to the SPR sensor for analyses of all the amine compounds due to the reaction between pivalic acid and these amine compounds.
 ...
PMID:Application of a surface plasmon resonance sensor to analyses of amine compounds with the use of a polymer film and an acid-base reaction. 1191 82

The mechanism of morphological phase transitions was studied for rod-shaped supramolecular assemblies comprised of a poly(acrylic acid)-block-poly(methyl acrylate)-block-polystyrene (PAA(90)-b-PMA(80)-b-PS(100)) triblock copolymer in 33% tetrahydrofuran/water after perturbation by reaction with a positively charged water-soluble carbodiimide. Tetrahydrofuran solvation of the hydrophobic core domain provided the dynamic nature required for the rod-to-sphere phase transition to be complete within 30 min. The intermediate morphologies such as fragmenting rods and pearl-necklace structures were trapped kinetically by the subsequent addition of a diamino crosslinking agent, which underwent covalent crosslinking of the shell layer. Alternatively, shell-crosslinked rod-shaped nanostructures with preserved morphology were obtained by the addition of the crosslinking agent before the addition of the carbodiimide, which allowed for the shell crosslinking to be performed at a faster rate than the morphological reorganization. The formation of robust shell-crosslinked nanostructures provides a methodology by which the morphological evolution processes can be observed, and it allows access to otherwise thermodynamically unstable nanostructures.
 ...
PMID:Chemically induced supramolecular reorganization of triblock copolymer assemblies: trapping of intermediate states via a shell-crosslinking methodology. 1192 63

A cellulose-based anion exchanger bearing water-soluble polycation was tested for separation of proteins. The exchanger was obtained by partial oxidation of cellulose gel by aq. NaIO4 followed by Schiff base formation with polyallylamine (PAA, molecular mass 5000). The retention behavior of proteins for three grades of PAA-cellulose gels, with amino group contents of 0.35, 0.59 and 0.96 mmol/g cellulose, was examined at several pH values and compared with that for conventional DEAE-cellulose gel with amino group content of 1.07 mmol/g cellulose. The retention of proteins by PAA-cellulose gels was remarkably greater than that for the DEAE-cellulose gel. Pairs of proteins having close isoelectric points and molecular masses (human and bovine serum albumins; beta-lactoglobulin A and B) could be separated by the PAA-cellulose gel columns. Such efficiency can be ascribed to high local density of grafted polyallylamine, in contrast to the random and sparse charge distribution in DEAE-cellulose.
 ...
PMID:Ion-exchange separation of proteins by polyallylamine-grafted cellulose gel. 1207 22


<< Previous 1 2 3 4 5 6 7 8 9 10 Next >>