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Query: UMLS:C0847097 (acidity)
 15,165 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The design and development of novel pH-sensitive liposomes were investigated to improve the release of liposome-encapsulated chemicals. Stable liposomes comprising of L-alpha-dipalmitoylphosphatidylcholine (DPPC) and poly(carboxylic acid) were prepared and characterized. Poly(malic acid) (PMLA) was chosen as a fusogen, because of its excellent biodegradability in physiological regions. Octyl groups introduced in the poly(malic acid) worked as anchors at the surface of the liposomes and made a remarkable contribution to complexing. The interaction between the liposomes and the polyacids was studied in terms of the change in size of the liposomes. The influences of molecular weight and amounts of polymer upon their characteristics, especially fusion, were discussed. The influences of pH change with respect to the association behavior of the liposomes such as aggregation and fusion were estimated by the particle size of the liposomes, turbidimetry of the solution and resonance energy transfer assay. From the results of these studies, it was shown that more tightly complexed liposomes aggregated and fused more positively with increasing acidity of the solution. The leakage of calcein entrapped in the inner aqueous phase of the liposomes increased with decreasing pH. The effect of pH on the liposome aggregation in a solution qualitatively paralleled that found in the leakage behavior.
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PMID:Effects of complexation between liposome and poly(malic acid) on aggregation and leakage behaviour. 1073 63

Acid-initiated ring-opening polymerization (ROP) of epsilon-caprolactone (epsilon-CL) was conducted under microwave irradiation (MI) at 2.45 GHz. At this frequency, metallic catalysts were no longer necessary. The effects of microwave power, irradiation time, epsilon-CL: acid molar ratio and acidity of acid on the polymerization were investigated. Both the rate of polymerization and the molar mass of polymer obtained were enhanced in comparison with conventional thermal method. Poly(epsilon-caprolactone) (PCL) with weight-average molar mass (Mw) over 12000 g/mol and Mw/Mn below 1.6 was synthesized in the presence of carboxylic acids such as maleic acid (MA), succinic acid (SA) and adipic acid (AA). The polymerization was also carried out when the monomer contained a certain amount of ibuprofen (IBU), by which, the IBU-PCL controlled release system was prepared directly. The release of IBU from the system was sustained from 12 h to 9 days with IBU content in weight increasing from 5 to 20%. It seems that this is a promising method to prepare drug controlled release systems.
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PMID:Acid-initiated polymerization of epsilon-caprolactone under microwave irradiation and its application in the preparation of drug controlled release system. 1271 97

Poly(acryl p-aminobenzenesulfonamideamidine- p-aminobenzenesulfonylamide) chelating fiber containing "S", "N", and "O" elements was synthesized from polyacrylonitrile fiber and p-aminobenzene sulfonamide and used to enrich and separate trace Bi(III), Hg(III), Au(III), and Pd(IV) ions from wastewater and ore sample solution. The enrichment acidity, flow rate, elution conditions, reuse, interference ions, saturated adsorption capacity, constant of adsorption rate, analytical accuracy, and actual samples on chelating fiber were investigated by means of inductively coupled plasma optical emission spectrometry (ICP-OES) with satisfactory results. Solutions of 100 ng mL(-1) of Bi(III), Hg(III), Au(III), and Pd(IV) ions can be enriched quantitatively by this chelating fiber at a rate of 1.0 mL min(-1) at pH 4 and desorbed quantitatively with 20 mL of 0.25 M HCl and 2% CS(NH(2))(2) solution at 50 degrees C (with recovery >/=97%). When the chelating fiber was reused for 20 times, the recoveries of the analyzed ions enriched by the fiber were still over 95% (except for Hg(III)). One thousand-fold excesses of Mn(2+), Ca(2+), Zn(2+), Mg(2+), Fe(3+), Cu(2+), Ni(2+), Al(3+), and Ba(2+) ions and thousands-fold excesses of Na(+ )and K(+) cause little interference in the pre-concentration and determination of the analyzed ions. The saturated adsorption capacity of Bi(III), Hg(III), Au(III), and Pd(IV) was 4.850 x 10(-4), 3.235 x 10(-4), 2.807 x 10(-4), and 3.386 x 10(-4) mol g(-1), respectively. The constants of adsorption rate were 0.409 min(-1) for Bi, 0.122 min(-1) for Hg, 0.039 min(-1) for Au, and 0.080 min(-1 )for Pd. The relative standard deviations (RSDs) for the enrichment and determination of 10 ng mL(-1) Bi(III), Hg(III), Au(III), and Pd(IV) were lower than 2.3%. The results obtained for these ions in actual samples by this method were basically in agreement with the given values with average errors of less than 1.0%. FT-IR spectra shows that the existence of -SO(2)-Ar, -H(2)N-Ar, O=C-NH-, HN=C-NH-, and -HN-SO(2) functional groups are verified in the chelating fiber. From the FT-IR spectroscopy, we can see that Hg(III), Au(III), and Pd(IV) are mainly combined with nitrogen and sulfur (or oxygen), and Bi(III) is mainly combined with nitrogen (or oxygen) of the groups to form a chelating complex.
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PMID:Synthesis and applications of poly(acryl p-aminobenzenesulfonamideamidine- p-aminobenzenesulfonylamide) chelating fiber for pre-concentrating and separating trace Bi(III), Hg(III), Au(III) and Pd(IV) from solution samples. 1292 Apr 99

Poly(acrylamide-co-acrylic acid) (poly(AM-co-AA)) superporous hydrogels (SPHs) were synthesized and the acidification effects on the swelling and mechanical properties were studied. Gelation exotherms were measured to determine the optimum introduction time for adding a blowing agent. The gelation kinetics decreased with increasing the AA concentration. The maximum equilibrium swelling was observed around an AA weight fraction of 0.4, but the compressive strength decreased monotonically with increasing the AA concentration. Poly(AM-co-AA) SPHs were much less swollen in acidic solution than in distilled water of pH 6.7. The swelling ratio decreased with increasing acidity (decreasing pH). Reduction of water absorption content by acidification led to considerable increase in the mechanical strength.
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PMID:Polymer composition and acidification effects on the swelling and mechanical properties of poly(acrylamide-co-acrylic acid) superporous hydrogels. 1510 97

The aim of this study was to examine the stability of bovine serum albumin (BSA) in poly(DL-lactic acid-co-glycolic acid) (PLGA) microspheres upon addition of a new excipient, poly(ethylene glycol)-poly(L-histidine) diblock copolymer (PEG-PH). Poly(L-histidine) component can form an ionic complex with BSA under acidic conditions within a narrow pH range. To optimize the ionic complexation conditions for BSA with PEG-PH, the resulting complex sizes were monitored using the Zetasizer. PLGA microspheres containing BSA as a model protein were prepared by w/o/w double emulsion method. BSA stability in aqueous solutions and after release from PLGA microspheres was determined using circular dichroism (CD) spectroscopy for secondary structure analyses and fluorescence measurements for tertiary structure analyses. The release profile of BSA from the microspheres was monitored using UV spectrophotometry. The rate of PLGA degradation was monitored by gel permeation chromatography. The pH profile within microspheres was further evaluated by confocal microscopy using a pH-sensitive dye. Approximately 19 PEG-PH molecules and one BSA molecule coalesced to form an ionic complex around a pH range of 5.0-6.0. Plain BSA/PLGA and BSA/PEG-PH/PLGA microspheres had a mean size of 27-35 microm. PLGA microspheres with a BSA loading efficiency >80% were prepared using the double emulsion method. PEG-PH significantly improved the stability of BSA both in aqueous solutions and in PLGA microspheres. The release profiles of BSA from different formulations of PLGA microspheres were significantly different. PEG-PH effectively buffered the local acidity inside the microspheres and improved BSA release kinetics by reducing initial burst release and extending continuous release over a period of time, when encapsulated as an ionic complex. PLGA degradation rate was found to be delayed by PEG-PH. There was clear evidence that PEG-PH played multiple roles when complexed with BSA and incorporated into PLGA microspheres. PEG-PH is an effective excipient for preserving the structural stability of BSA in aqueous solution and BSA/PLGA microspheres formulation.
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PMID:Stability of bovine serum albumin complexed with PEG-poly(L-histidine) diblock copolymer in PLGA microspheres. 1626 69

Poly(acryldinitrophenylamidrazone-dinitroacrylphenylhydrazine) chelating fiber was synthesized from polyacrylonitrile fiber and used for enrichment and separation for traces of Au(III), Ru(III), In(III), Bi(III), Zr(IV), V(V), Ga(III) and Ti(IV) ions from solution samples. The acidity, rate, re-use, capacity and interference on the adsorption of ions on the chelating fiber as well as the conditions of desorption of these ions from the chelating fiber were investigated by means of inductively coupled plasma optical emission spectrometry. The results show that 10-100 ngml(-1) of Au(III), Ru(III), In(III), Bi(III), Zr(IV), V(V), Ga(III) and Ti(IV) ions can be quantitatively enriched by the chelating fiber at a 2 mlmin(-1) of flow rate in the range pH 4-5, and desorbed quantitatively with 20 ml of 5 M HCl for In(III), Bi(III), Zr(IV), V(V), Ga(III), Ti(IV) and 20 ml of 4 M HCl+2% CS(NH(2))(2) solution for Au(III), Ru(III) (with recovery>95%). 50- to 500- fold excesses of Fe(III), Al(III), Mg(II), Mn(II), Ca(II), Cu(II), Ni(II) ions cause little interference in the concentration and determination of analyzed ions. When the fiber was reused for 8 times, the recoveries of the above ions enriched by the fiber were still over 87%. The relative standard deviations (RSDs) for the enrichment and determination of 10 ngml(-1) Au, Ru, In, Bi, Ga and 1 ngml(-1) Zr, V, Ti were lower than 3.0%. The results obtained for these ions in real solution samples by this method were basically in agreement with the given values with average errors of less than 6.3%. FT-IR spectra show that existence of NNCNHNH, OCNHNH and NO(2) functional groups are verified in chelating fiber, and Au(III) or Ru(III) is mainly combined with nitrogen (or oxygen) of the groups to form a chelate complex.
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PMID:Efficiency and application of poly(acryldinitrophenylamidrazone-dinitroacrylphenylhydrazine) chelating fiber for pre-concentrating and separating trace Au(III), Ru(III), In(III), Bi(III), Zr(IV), V(V), Ga(III) and Ti(IV) from solution samples. 1896 25

Poly(malic acid) is water-soluble, functionalizable, and biodegradable, making it attractive as a precursor of hydrogels for biomedical applications. However, homopoly(malic acid), with pK(1/2) of 4.3, is too acidic for biocompatibility. To overcome the acidity, we have synthesized beta-malic acid-containing poly(ethylene glycol) dimethacrylate (PEGMAc) with pK(a) of 5.02. Solutions of methacrylated O-carboxymethylchitosan (OCMCS), PEGMAc, and poly(ethylene glycol) diacrylate (PEGDA; 7:7:86 and 6:20:74 (w/w/w)) in water (80%) have near neutral pHs (6.8-6.9). These solutions form firm hydrogels when photopolymerized. These are referred to as O7-PEGMAc7-B86 and O6-PEGMAc20-B74 (where the numerals refer to the weight content of each component, O is OCMCS and B is PEGDA added to make blend). The carboxyl groups in PEGMAc permit the surface grafting of hydrogels with Arg-Gly-Asp (RGD). The cytocompatibilities of smooth muscle cells (SMCs) on RGD-grafted hydrogels were studied. From the tetrazolium salt reduction assay, O6-PEGMAc20-B74 was found to have significantly better 10th day cytocompatibility compared to hydrogels containing lower or no PEGMAc. These gels degrade upon hydrolysis releasing malic acid, PEG and OCMCS. The increased cell compatibility of O6-PEGMAc20-B74 is possibly due to increased surface RGD content and near neutral pH even during biodegradation. Our novel PEGMAc-modified blends are a promising functionalizable biodegradable hydrogel precursor providing improved cell proliferation.
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PMID:Addition of beta-malic acid-containing poly(ethylene glycol) dimethacrylate to form biodegradable and biocompatible hydrogels. 1960 95

Poly(p-phenylene) (PPP) was chemically synthesized via oxidative polymerization using benzene and doped with FeCl(3). The electrical conductivity response of the doped PPP (dPPP) towards CO, H(2) and NH(3) is investigated. dPPP shows no electrical conductivity response towards the first two gases (CO and H(2)), but it shows a definite negative response towards NH(3). The electrical conductivity sensitivity of dPPP increases linearly with increasing NH(3) concentration. To improve the sensitivity of the sensor towards NH(3), ZSM-5 zeolite is added into the conductive polymer matrix. The electrical sensitivity of the sensor increases with increasing zeolite content up to 30%. The effect of the type of cation in the zeolite pores is investigated: namely, Na(+), K(+), NH(4) (+) and H(+). The electrical conductivity sensitivity of the composites with different cations in the zeolite can be arranged in this order: K(+) < no zeolite < Na(+) < NH(4) (+) < H(+). The variation in electrical sensitivity with cation type can be described in terms of the acid-base interaction, the zeolite pore size and surface area. The PPP/Zeolite composite with H(+) possesses the highest electrical sensitivity of -0.36 since H(+) has the highest acidity, the highest pore volume and surface area, which combine to induce a more favorable NH(3) adsorption and interaction with the conductive polymer.
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PMID:Fabrication of Poly(p-Phenylene)/Zeolite Composites and Their Responses Towards Ammonia. 2240 92

Poly(sodium 10-undecenyl sulfate) (poly-SUS), poly(sodium N-undecenyl leucinate) (poly-SUL) and their five molecular binary mixed micelles with varied SUS:SUL composition were prepared and used as pseudostationary phases in micellar electrokinetic chromatography (MEKC). Linear solvation energy relationships (LSERs) model and free energy of transfer studies were used to characterize the retention behavior and the selectivity differences among the seven surfactant systems. System constant differences and regression models for varied benzene derivative compounds are used to establish the selectivity differences of the seven pseudostationary phases. The cavity formation and dispersion interaction (the v system constant) and the hydrogen-bonding acidity (the b system constant) of the surfactant systems were found to have the most significant influence on selectivity and MEKC retention. The molecular micelle with sulfate head group, poly-SUS, was found to be more hydrogen-bond acidic than the molecular micelle with leucinate head group, poly-SUL. The other system constants (a, s and e) have modest effect on the retention and selectivity of the benzene derivatives. The model intercept coefficients (c system constants), which are negative for all surfactant systems have unusually large values. The free energy changes of transfer for the functional groups studied have all negative values except phenol and benzyl alcohol. Selectivity differences between pseudostationary phases were also compared by plotting the log k values against each other and were found to agree well with LSER results.
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PMID:Study of chemical selectivity of molecular binary mixed micelles of sodium 10-undecenyl sulfate and sodium N-undecenyl leucinate using linear solvation energy relationships model. 2244 78

New transparent conductive materials are urgently needed for optoelectronic devices. Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) will be a promising next-generation transparent electrode material if its conductivity is comparable to that of indium tin oxide (ITO). To enhance significantly the conductivity of PEDOT:PSS with mild compounds has practical significance. In this work, significant conductivity enhancements are achieved on PEDOT:PSS films after treatment with mild and weak organic acids. The treated PEDOT:PSS films exibit metallic behavior at room temperature. Their conductivity increases to about 3300 S cm(-1) after they are treated with 8 M methanesulfonic acid. The conductivity enhancement depends on the acidity and physical properties of the organic acids. The mechanism for the conductivity enhancement is ascribed to proton transfer from the mild or weak organic acids to PSS(-) of PEDOT:PSS. There are two factors for the proton transfer from mild or weak organic acids to PSS. One factor is the high acid concentration during the treatment, particularly after the vaporization of the water solvent. Another factor is the phase segregation of PSSH from PEDOT:PSS, because PSSH is hydrophilic, whereas PEDOT is hydrophobic. This method is better than that using very strong and corrosive acids like sulfuric acid. These highly conductive and highly transparent PEDOT:PSS films are promising for use as next-generation transparent electrodes.
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PMID:Solution-processed PEDOT:PSS films with conductivities as indium tin oxide through a treatment with mild and weak organic acids. 2430 24


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