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

Poly(acrylic acid) (PAA) was polymerized on both termini of Pluronic F87 copolymer using the atom transfer radical polymerization technique to produce a novel block copolymer, PAA-b-F87-b-PAA (F87PAA). The loading of a cationic anticancer drug, doxorubicin (DOX), to F87PAA at different pH values was investigated using isothermal titration calorimetry (ITC), laser light scattering techniques, and UV-vis spectroscopy. At pH of 4.3-7.1, the ITC profile exhibited a significant exothermic peak, which indicated that the drug loading is an enthalpically driven process. At a pH of 4.3, the enthalpy maximum was significantly reduced in the presence of 2 M urea, indicating the existence of hydrogen bonds between the DOX and F87PAA copolymer. At a pH of 7.1, the fraction of bound DOX was close to the stoichiometric proportion of 1:1 to the molar concentration of carboxyl groups in the copolymer, where the drug loading is governed by electrostatic and stacking interactions. The TEM image of the complex indicated the formation of large compound micelles induced by the binding of DOX to the PAA segments.
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PMID:Synthesis and aggregation behavior of pluronic F87/poly(acrylic acid) block copolymer in the presence of doxorubicin. 1726 98

Poly(styrene)-block-poly(4-vinylpyridine) (PS-b-P4VP) copolymers and poly(acrylic acid) (PAA) have been mixed in organic solvents. Complexation via hydrogen bonding occurs between the P4VP and PAA blocks. Those insoluble complexes aggregate to form the core of micelles surrounded by a corona of PS chains. Reorganization of these structures occurs upon addition of acidic or basic water, which results in the breaking of the hydrogen bonds between the P4VP and PAA blocks. After transfer of the initial complexes in acidic water, micelles consisting of a PS core and a protonated P4VP corona are observed. In basic water, well-defined nanoparticles formed by the PS-b-P4VP copolymers are obtained. It is demonstrated that these nanoparticles are stabilized by the negatively charged PAA chains. Finally, thermally induced disintegration of the micelles is investigated in organic solvents.
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PMID:Reorganization of hydrogen-bonded block copolymer complexes. 1731 7

We report a general click chemistry approach for the layer-by-layer assembly of ultrathin, polymer films on particles and the subsequent formation of polymer click capsules (CCs). Poly(acrylic acid) copolymers, synthesized with a minor component of either alkyne (PAA-Alk) or azide (PAA-Az) functionality, were alternately assembled on silica particles. The (PAA-Az/PAA-Alk)-coated particles were subsequently functionalized by exploiting the free alkyne click moieties present in the film upon exposure to an azide-modified rhodamine dye. Further, PAA CCs, obtained following removal of the silica particle template, were shown to exhibit pH-responsive behavior. This was demonstrated by reversible size changes of the CCs upon cycling between basic and acidic solutions. Polymer CCs are anticipated to find applications in various fields, including drug delivery and sensing.
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PMID:Ultrathin, responsive polymer click capsules. 1753 Aug 11

Poly(acrylic acid) (PAA) was attached on both termini of Pluronic P85 copolymer (EO27PO39EO27) via atom transfer radical polymerization (ATRP) to produce a novel block copolymer, PAA-b-P85-b-PAA (P85PAA). The P85PAA-DOX complex formation and drug loading were strongly dependent on the PAA segment length and pH, where the protonation of carboxyl groups in the PAA segment at pH < 7.2 reduced the binding sites of DOX onto P85PAA chains, resulting in a diminished DOX uptake at low pH. The composition of copolymer-DOX complexes at pH 7.2 was close to the stoichiometric 1:1 DOX:carboxyl molar ratio, confirming the dominance of electrostatic interactions between cationic DOX molecules and carboxyl groups. The stability study of the copolymer-DOX complex suggested that non-polyelectrolyte interactions may also participate in the complexation of drug and P85PAA block copolymer. DOX loading at pH 5.0 decreased to 60% of the total binding capacity, indicating that protonation of carboxyl groups reduced the DOX binding to P85PAA block copolymer. DOX release from the complex is a pH-responsive process, where the protonation of carboxyl groups at mildly acidic condition resulted in a faster dissociation of copolymer-DOX complex, leading to an accelerated release of DOX at pH 5.0. Thus, complexation of DOX with P85PAA yielded a drug delivery system affording a pH-triggered release of DOX in an acidic environment of pH 5.0.
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PMID:Complexation and release of doxorubicin from its complexes with pluronic P85-b-poly(acrylic acid) block copolymers. 1763 11

We have studied the melting of polymeric amphiphilic micelles induced by small-molecule surfactant and explained the results by experimental determination of the interfacial tension between the core of the micelles and the surfactant solutions. Poly(n-butyl acrylate-b-acrylic acid) (PBA-b-PAA) amphiphilic diblock copolymers form kinetically frozen micelles in aqueous solutions. Strong interactions with surfactants, either neutral or anionic [C12E6, C6E4, sodium dodecyl sulfate (SDS)], were revealed by critical micelle concentration (cmc) shifts in specific electrode and surface tension measurements. Since both polymer and surfactant are either neutral or bear negative charges, the attractive interactions are not due to electrostatic interactions. Light scattering, neutron scattering, and capillary electrophoresis experiments showed important structural changes in mixed PBA-b-PAA/surfactant systems. Kinetically frozen micelles of PBA-b-PAA, that are hardly perturbed by concentration, ionization, ionic strength, and temperature stresses, can be disintegrated by addition of small-molecule surfactants. The interfacial energy of the PBA in surfactant solutions was measured by drop shape analysis with h-PBA homopolymer drops immersed in small-molecule surfactant solutions. The PBA/water interfacial energy gammaPBA/H2O of 20 mN/m induces a high energy cost for the extraction of unimers from micelles so that PBA-b-PAA micelles are kinetically frozen. Small-molecule surfactants can reduce the interfacial energy gammaPBA/solution to 5 mN/m. This induces a shift of the micelle-unimer equilibrium toward unimers and leads, in some cases, to the apparent disintegration of PBA-b-PAA micelles. Before total disintegration, polymer/surfactant mixtures are dispersions of polydisperse mixed micelles. Based on core interfacial energy arguments, the disintegration of kinetically frozen polymeric micelles was interpreted by gradual fractionation of objects (polydisperse dispersion mechanism), whereas the disintegration of polymeric micelles in a thermodynamically stable state was interpreted by an exchange between a population of large polymer-rich micelles and a population of small surfactant-rich micelles (bidisperse dispersion mechanism). Finally, in our system and other systems from the literature, interfacial energy arguments could explain why the disintegration of polymer micelles is either partial or total as a function of the surfactant type and concentration and the hydrophobic block molar mass of the polymer.
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PMID:Controlling the melting of kinetically frozen poly(butyl acrylate-b-acrylic acid) micelles via addition of surfactant. 1771 79

Poly(amido amine) (SS-PAA) random and block copolymers having bioreducible disulfide bonds in the main chain and amino groups with distinctly different basicity in the side chain were designed and synthesized by Michael addition polymerization between N, N'-cystaminebisacrylamide (CBA) and two amine monomers, i.e., histamine (HIS) and 3-(dimethylamino)-1-propylamine (DMPA). Copolymers containing variable HIS/DMPA ratios show higher ability to bind DNA than p(CBA-HIS) homopolymer and condense DNA into the polyplexes with particle sizes (<150 nm) that are smaller than polyplexes of p(CBA-HIS) ( approximately 220 nm). The buffer capacities of the copolymers increase with increasing HIS/DMPA ratio. These copolymers are able to transfect COS-7 cells in vitro with efficiencies that increase with increasing HIS/DMPA ratio. The random and block copolymers at a HIS/DMPA ratio of 70/30 combines optimal DNA condensation capability and buffer capacity, thereby inducing higher transfection efficiency in the absence and presence of serum as compared to p(CBA-HIS) homopolymer. Moreover, random and block copolymers show a similar transfection capacity, but both have higher capacity than the physical mixtures of p(CBA-HIS) and p(CBA-DMPA) homopolymers. XTT assay reveals that the polyplexes of the SS-PAA copolymers have essentially low cytotoxicity when the highest transfection activity is observed.
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PMID:Random and block copolymers of bioreducible poly(amido amine)s with high- and low-basicity amino groups: study of DNA condensation and buffer capacity on gene transfection. 1772 1

Poly(divinylbenzene-co-acrylic acid) (poly(DVB-co-AA)) hollow microspheres with movable poly(DVB-co-AA) cores were prepared by a facile route. In this approach, poly(DVB-co-AA) microspheres were first used as templates to synthesize poly(DVB-co-AA)@PAA core-shell particles with a non-crosslinked PAA shell by distillation precipitation polymerization in acetonitrile. In situ polymerization to prepare poly(DVB-co-AA)@PAA@poly(DVB-co-AA) trilayer microspheres was then developed, in which the hydrogen-bonding interaction between the carboxylic acid groups played a key role as the driving force for the formation of monodisperse trilayer structure polymer microspheres. After removal of the non-crosslinked poly(acrylic acid) (PAA) midlayer of the poly(DVB-co-AA)@PAA@poly(DVB-co-AA) microspheres in ethanol under basic conditions, poly(DVB-co-AA) hollow microspheres with movable poly(DVB-co-AA) cores were obtained. Functional poly(DVB-co-AA) cores could be released successfully when the hollow structure was destroyed. The resultant core-shell, trilayer polymer microspheres and hollow polymer microspheres with movable cores were characterized by transmission electron microscopy (TEM), dynamic laser scattering (DLS), and Fourier transform infrared (FT-IR) spectra.
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PMID:Facile synthesis of hollow polymer microspheres with movable cores with the aid of hydrogen-bonding interaction. 1794 4

Polymer/Au nanoparticle multilayer ultrathin films are fabricated via hydrogen-bonding interaction by a layer-by-layer technique. The Au nanoparticles surface-modified with pyridine groups of poly(4-vinylpyridine) (PVP) are prepared in dimethyl formamide (DMF). Transmission electron microscopy (TEM) image shows that uniform nanoparticles are dispersed in the PVP chains. Poly(3-thiophene acetic acid) (PTAA) and poly(acrylic acid) (PAA) are utilized to form hydrogen bonds with PVP, respectively. Considering the pH-sensitive dissociation behavior of PTAA and PAA, we investigate the release behavior of the Au-containing multilayers at different pH values in this work. UV-vis spectroscopy and atomic force microscopy (AFM) are employed to monitor the buildup and the release of the multilayers. The results indicate that in the films assembled with gold nanoparticles, the polymers are difficult to be removed from the substrate. The interaction between the gold particles and the neighboring PVP chains is responsible for the phenomenon. Gold particles act as physical cross-link points in the multilayers. Due to the additional interaction caused by the gold nanoparticles in the films except the hydrogen-bonding interaction between PTAA (or PAA) and PVP, the stability of the Au-containing multilayer film is ensured even though the changes in pH values may result in the break of the hydrogen bonds.
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PMID:Self-assembly of multilayer films containing gold nanoparticles via hydrogen bonding. 1818 44

Poly(acrylic acid) (PAA) chains exhibit conformational change in response to pH, whereas bromate-sulfite-ferrocyanide (BSF) solution shows pH oscillation between 3.2 and 6.6. By use of quartz crystal microbalance with dissipation (QCM-D), we have investigated the pH induced conformational change of PAA brushes under a continuous flow of BSF solution in real time. The changes in frequency and dissipation clearly indicate the periodic swelling and collapse of brushes with pH oscillation. The changes in thickness, viscosity, and elastic modulus further indicate the oscillation of the interface.
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PMID:Periodic swelling and collapse of polyelectrolyte brushes driven by chemical oscillation. 1866 35

Poly(amidoamine) (PAA) networks that are obtained by the use of cystamine as a cross-linking agent in the reaction with 2,2'-dithiodipyridine turn into linear PAAs with dithiopyridyl side groups that easily undergo an exchange reaction with thiocholesterol. The resultant products represent the first examples of amphiphilic PAA-cholesterol conjugates in which lipophilic cholesterol moieties are linked to the hydrophilic PAA chain by S-S bonds that are stable in blood but cleavable inside cells. In aqueous media, these conjugates self-assemble into nanoaggregates whose inner cores consist of lipophilic cholesterol domains. A series of PAA-cholesterol conjugates that are derived from two different bis-acrylamides, namely 2,2-bis(acrylamido)acetic acid and 1,4-bis(acryloyl)piperazine, and that have different cholesterol contents were obtained. All products were characterized by (1)H and (13)C NMR spectroscopy, and the average molecular weights of the soluble polymers were determined by size exclusion chromatography. In all instances, the segregation of cholesterol residues from the aqueous medium was revealed by the comparison of their NMR spectra in CDCl3 and D2O, respectively. The TEM analysis of the PAA-cholesterol aggregates in aqueous buffers revealed homogeneous round nanospheres whose dimensions and dimension distributions were determined by DLS. Preliminary cytocompatibility tests demonstrated that all prepared PAA-cholesterol samples are cytocompatible and thus show potential for biotechnological applications.
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PMID:Poly(amidoamine) conjugates with disulfide-linked cholesterol pendants self-assembling into redox-sensitive nanoparticles. 1878 98


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