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1.
Poly(2‐ethyl‐2‐oxazoline) and acrylic acid were copolymerized in different compositions using γ‐rays‐induced polymerization and cross‐linking to obtain a series of pH‐sensitive hydrogels. The preparation parameters that may affect the copolymerization process such as the feed solution composition and irradiation dose were optimized. Swelling characteristics of the obtained polymeric hydrogels were evaluated. The results show the significant effects of the hydrogel composition, soaking time, and pH on the swelling equilibrium. The diffusion parameters obtained at pH 1 and 7 show the possibility of using the prepared hydrogels in the field of colon‐specific drug delivery systems. Ibuprofen as a model drug was loaded into (poly(2‐ethyl‐2‐oxazoline)/acrylic acid) copolymer hydrogel to investigate their drug release behavior at different pH values. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
2.
Orally administrable hydrogel was prepared by crosslinking chitosan (CS) with γ‐poly(glutamic acid) (γ‐PGA) for an excellent pH‐responsive colon‐targeted drug delivery system. The stable crosslinked amide bond appeared in the shifted region of FTIR spectroscopy, and the tensile strength and elastic modulus were also reduced by crosslinking of CS and γ‐PGA. The surfaces of crosslinked hydrogel have a homogeneous pore array with pore size corresponding to the varied blending ratio. The swelling ratio was dramatically changed by increasing the pH from 3 to 6, and the responsiveness of swelling ratio to the reversible pH changes between 3 and 10 was reliable for 72 h. The drug diffusion rate was mainly dependent on the pH, and a water‐soluble tetrazolium (WST‐1) assay indicated that cytocompatibility of the hydrogel was in an acceptable range. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci. 2013 相似文献
3.
Novel acrylic monomers (β‐CD‐A and β‐CD‐6‐EA) containing β‐cyclodextrin (β‐CD) with different extent of substitution were prepared by using dicyclohexylcarbodiimide (DCC) as a condensation agent at room temperature. Two kinds of functional hydrogels were also synthesized by copolymerization of β‐CD‐A and β‐CD‐6‐EA with acrylic acid (AAc) using a redox initiator system in aqueous solution. The nuclear magnetic resonance (1H NMR), infrared spectroscopy (IR), thermogravimetric analysis (TGA) were employed to character the molecular structures of β‐CD modified monomers and their copolymers. The swelling experiments indicate that the hydrogels with different equilibrium swelling ratio (ESR) possess obvious pH‐sensitivity and distinct dynamic swelling behavior. Using an anti‐cancer drug, chlorambucil (CHL), able to form complexes with β‐CD in water, as a model compound, the controlled drug release behaviors of these hydrogels were investigated. The release behavior of CHL from two kinds of hydrogels synthesized reveals that the release rate of CHL can be effectively controlled by pH values, cross‐linking density, and β‐CD content. In addition, it is found that the β‐CD with the proper frame and concentration can increase release efficiency of CHL from the hydrogels. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
4.
The thermosensitive material that could be transformed into gel at 37°C was prepared from chitosan (dissolved in acetic acid/sodium acetate buffer solution) and a mixture of α‐ and β‐glycerophosphate (αβ‐GP). The thermosensitive characteristics, appearance, and structure of the hydrogel were all affected by the pH, ionic strength, and CS/αβ‐GP ratio. The optimal conditions for the preparation of a transparent CS‐αβ‐GP thermosensitive hydrogel were pH 4.6, ionic strength 0.15 mol/L, and a CS/αβ‐GP ratio of 8.8/1.2 (v/v). The hydrogel was stable for at least 3 months at 4°C. We believe that hydrogen bonding interactions between the N? H (and C?O) groups of chitosan and the O? H groups of αβ‐GP play an important role during the process of sol‐to‐gel transition. The cumulative release of adriamycin from the CS‐αβ‐GP hydrogel, measured in PBS at pH 7.4, reached only 60 to 70% over 24 h, indicating that this material could be potentially used in a sustained drug delivery system. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
5.
Hydrogel composed of β‐cyclodextrin (β‐CD) and poly(vinyl alcohol) was prepared in a strong alkaline condition using epichlorohydrin as a crosslinker. Phenylpropionic acid (PPA) and naphthylamine (NA) were loaded in the cavities of β‐CD residues to endow the hydrogel with a dual pH‐sensitive characteristic. In release experiments using fluorescein isothiocyanate‐dextran (FITC‐dextran) as a dye, PPA/NA‐loaded hydrogel exhibited an extensive release not only in acidic conditions (e.g. pH 3.0) but also in alkaline conditions (e.g. pH 9.0). PPA and NA will be highly ionized at the alkaline and the acidic pH and they could promote swelling of the hydrogel, causing an extensive release at those pH values. However, the release was suppressed at mid pH values (e.g. pH 5.0 and pH 7.4), possibly due to the formation of salt bridges between PPA? and NA+. In fact, the degree of swelling at mid pH was lower than that observed at strong acidic pH and alkaline pH. According to SEM images, the pore size and the texture compactness of hydrogels which had been subjected to swelling at different pH values could also account for the dual pH‐sensitive releases. The hydrogels exhibited dual pH sensitivities in terms of FITC‐dextran release and swelling. These hydrogels might be used as a pH‐sensitive vehicle for water‐soluble drugs. © 2013 Society of Chemical Industry 相似文献
6.
The pH‐sensitive swelling and release behaviors of the anionic P(MAA‐co‐EGMA) hydrogels were investigated as a biological on–off switch for the design of an intelligent drug delivery system triggered by external pH changes. There was a drastic change of the equilibrium weight swelling ratio of P(MAA‐co‐EGMA) hydrogels at a pH of around 5, which is the pKa of poly (methacrylic acid) (PMAA). At a pH below 5, the hydrogels were in a relatively collapsed state but at a pH higher than 5, the hydrogels swelled to a high degree. When the molecular weight of the pendent poly(ethylene glycol) (PEG) of the P(MAA‐co‐EGMA) increased, the swelling ratio decreased at a pH higher than 5. The pKa values of the P(MAA‐co‐EGMA) hydrogels moved to a higher pH range as the pendent PEG molecular weight increased. When the feed concentration of the crosslinker of the hydrogel increased the swelling ratio of the P(MAA‐co‐EGMA) hydrogels decreased at a pH higher than 5. In release experiments using Rhodamine B (Rh‐B) as a model solute, the P(MAA‐co‐EGMA) hydrogels showed a pH‐sensitive release behavior. At low pH (pH 4.0) a small amount of Rh‐B was released while at high pH (pH 6.0) a relatively large amount of Rh‐B was released from the hydrogels. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 相似文献
7.
Juseung Yang Geundo Cho Tai‐Gyu Lee Bumsang Kim 《American Institute of Chemical Engineers》2011,57(7):1919-1925
For a first step in the development of an intelligent delivery system for a nonapeptide as an α‐MSH antagonist, pH‐responsive P(MAA‐co‐EGMA) hydrogel microparticles were prepared and their feasibility as intelligent delivery carriers was evaluated. There was a drastic change in the swelling ratio of P(MAA‐co‐EGMA) microparticles at a pH of around 5 and as the MAA amount in the hydrogel increased, the swelling ratio increased at a pH above 5. The loading efficiency of the nonapeptide at pH 7 increased with the amount of Methacrylic acid (MAA) in the hydrogel and at pH 2, where the electrostatic attraction was greatest, a high loading efficiency was not obtained because of the low swelling ratio of the hydrogel. The P(MAA‐co‐EGMA) microparticles demonstrated a pH‐sensitive release behavior for the nonapeptide. In addition, the P(MAA‐co‐EGMA) microparticles showed a protective ability for the nonapeptide and preserved the stability of the nonapeptide. © 2010 American Institute of Chemical Engineers AIChE J, 2010 相似文献
8.
A new hydrogel that contains sulfur is prepared by radiation polymerization and its application for recovery of Hg2+, Pb2+, Cd2+, and Cu2+ ions is discussed. The metal hydrogel complexes are isolated and characterized by using different spectroscopic techniques (UV‐visible, IR, NMR, and mass), thermal analysis (TGA and DSC) measurements, and SEM. Also, the mode of complexation is determined using IR and NMR spectroscopy. The scanning electron micrographs show that the hydrogel has a great ability to recover the metal ions in the following order: Hg2+ > Cd2+ > Pb2+ > Cu2+. TGA thermograms are used to investigate the mechanism of thermal decomposition. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 955–966, 2000 相似文献
9.
Crosslinked polyacrylamide beads were irradiated in air with a Co60 γ‐radiation source. The preirradiated beads were graft‐copolymerized through heating with 4‐vinylpyridine in the presence of benzoyl peroxide. Grafting was studied as a function of various reaction parameters and was determined from the increase in the weight of the original polymer and the estimation of pyridine pendants in the homopolymer‐free graft copolymer. Although making the polymer basic in character, this modification retained the hydrophilic nature of polyacrylamide. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2613–2620, 2002 相似文献
10.
BACKGROUND: Polyacrylonitrile (PAN) artificial muscles have attracted considerable attention for their fast responses. This research work is based on the preparation of novel pH‐sensitive hydrogel fibers derived from hydrolyzed PAN and gelatin by wet spinning and chemical modification. RESULTS: Through characterization of the fiber dynamic and static pH‐sensitive behavior, pH response times were found to improve greatly with increasing gelatin content. At a weight ratio of 3 to 7 (PAN:gelatin), the best response times were obtained at 0.59 s for elongation and 1.14 s for contraction. Study of the chemical structures of hydrolyzed PAN and gelatin, as well as the surface morphology of the hydrogel fibers, indicated that the mechanism of formation of hydrogel fibers is closely interconnected with their pH‐sensitive behavior. From the standpoint of the mechanism we also found that the addition of urea gave rise to hydrogel fibers with a controllable morphology, influenced by the pH‐sensitive behavior. CONCLUSION: The hydrogel system reported here is simple in preparation, but quite complex in chemical structure. The strong response of the fibers to pH provides some idea on the development of new artificial muscle systems. Copyright © 2008 Society of Chemical Industry 相似文献
11.
Because of low aqueous solubility and slow dissolution rate, cantharidin has a low oral bioavailability. Our research aims to prepare the inclusion complex of cantharidin and β‐cyclodextrin (β‐CD) and accomplish characterization, in vitro and in vivo evaluation. CA‐β‐CD inclusion complex was prepared by saturated solution method. The CA was demonstrated by HPLC in vitro experiment and by GC‐MS in vivo experiment. CA‐β‐CD inclusion complex was characterized by differential scanning calorimetry (DSC), X‐ray diffractometry (XRD), and nuclear magnetic resonance (NMR). Through complexation with β‐CD, the solubility of CA in neutral aqueous solution was improved significantly. CA‐β‐CD inclusion complex also shows a significantly improved dissolution rate in comparison with free CA. Comparison of the pharmacokinetics between CA‐β‐CD inclusion complex and free CA was performed in rats. The in vivo results show that CA‐β‐CD inclusion complex has earlier tmax, higher Cmax, and higher bioavailability than free CA after oral dosing. By comparing the AUC0–t of CA and CA‐β‐CD inclusion complex, the relative bioavailability of CA‐β‐CD inclusion complex to free CA was 506.3%, which highlighted the evidence of significantly improved bioavailability of formulation of CA with β‐CD. Thus, this β‐CD‐based drug delivery system should be an effective oral dosage form to improve oral bioavailability of CA. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012 相似文献
12.
Umile Gianfranco Spizzirri Giuseppe Cirillo Francesca Iemma Francesco Puoci Manuela Curcio Ortensia Ilaria Parisi Nevio Picci 《应用聚合物科学杂志》2011,121(1):342-351
This paper deals with the synthesis of thermoresponsive microspheres with proteic structure exhibiting a transition temperature close to the body temperature. The hydrogels were synthesized by free radical polymerization of methacrylate Bovine Serum Albumin (BSA‐MA) as crosslinker, and 2‐hydroxyethyl methacrylate (HEMA) and/or N‐isopropylacrylamide (NIPAAm), as hydrophilic and thermoresponsive monomers, respectively. The modification of the hydrophilic/hydrophobic balance in the polymerization feed allows to modulate the volume phase transition temperature of the macromolecular network. The hydrogels were characterized by infrared spectroscopy and thermal analyses, which showed negative thermoresponsive behavior for all compositions and, by increasing the content of the hydrophilic moieties in the network, the transition temperature was ranged from 34.2 to 36.8°C. To test the preformed materials as drug carriers, diclofenac diethyl ammonium salt was chosen and drug entrapment percent was determined. Drug release profiles, in media at different temperature, depend on the crosslinking degree and on the composition of the hydrogels. By using semiempirical equations, the release mechanism was extensively studied and the diffusional contribute evaluated. The physic‐chemical characteristics of thermoresponsive materials confirm the applicability of the microspheres as drug delivery device. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
13.
The waste problem of the rebar inhibitors is very serious due to that it is a long time before they can exert their best effect in the concrete and they are kept losing all the time. However, there is still no effective solution to alleviate such situation. Meanwhile, drug delivery control technology based on environmental sensitive polymers has been successfully applied in biomedical fields. Thus, poly(acrylic acid)–acrylamide was synthesized as smart carrier for controlling rebar inhibitors delivery in concrete. Dipotassium hydrogen phosphate as model drug was encapsulated inside the polymeric particles via a self‐assembly process. The pH‐responsive activities of the polymeric particles were estimated by monitoring their swelling performances in solutions of different pH values and the drug delivery control characteristics were studied in simulated concrete pore solutions. The results indicate the polymeric particles deserve network structures with high porosity and exhibit excellent pH‐responsive activities, which can perform as perfect intelligent carriers whereas the releasing of the inhibitors follows the first‐order kinetic law. The work suggests a new application field of drug delivery control technology. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45886. 相似文献
14.
Poly‐α,β‐(3‐hydroxypropyl)‐DL ‐aspartamide (PHPA) was synthesized by the ring‐open reaction of polysuccinimide (PSI) and 3‐hydroxypropylamine. The polymer was characterized by 1H‐NMR, 13C‐NMR, FTIR, and GPC. Mark–Houwink coefficients were obtained from viscometry and GPC measurements, K = 5.53 × 10−3 and α = 0.78 in water. The acute toxicity of PHPA was examined and it revealed no death in ICR mice up to the dose treated of 15.3 kg/kg, and hematological parameters showed no significant difference between treated and control animals. The potential use of PHPA as a drug carrier was also investigated. In a typical case, a contraceptive drug, norethindrone (NET), was bonded to PHPA, and the drug sustained released as long as 120 days an in vitro test. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 2411–2417, 2000 相似文献
15.
Chetna Verma Poonam Negi Deepak Pathania Vipula Sethi Bhuvanesh Gupta 《Polymer International》2019,68(3):344-350
Graft polymerization of itaconic acid on tragacanth gum (TG) was carried out using potassium persulfate as initiator to develop smart hydrogels for drug delivery systems. The effect of the grafting parameters on the degree of grafting was investigated. The grafting was significantly influenced by the reaction medium, the reaction temperature and the monomer concentration. The monomer dependency of the system was found to be 1.52. The hydrogels were characterized using Fourier transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry and X‐ray diffraction. The grafted TG had an amorphous nature and exhibited excellent swelling in water and strong dependence on the pH of the medium. The grafted TG showed pH‐dependent release of ciprofloxacin which offers the possibility of using these materials in colon‐specific drug targeting for human healthcare systems. © 2018 Society of Chemical Industry 相似文献
16.
γ‐Ray initiated reversible addition–fragmentation chain transfer (RAFT) polymerizations of methyl acrylate (MA) were investigated in bulk using five different dithiocarbamate structures, 2‐phenyl‐benzoimidazole‐1‐carbodithioic acid benzyl ester ( 1b ), 2‐methyl‐benzoimidazole‐1‐carbodithioic acid benzyl ester ( 1c ), 2‐pheny‐indole‐1‐cardithioic acid benzyl ester ( 1d ), 2‐(carbazole‐9‐carbothioylsulfanyl)‐2‐methyl‐propionic acid ester ( 1e ), and carbazole‐9‐carbodithioic acid naphthalene‐1‐ylmethyl ester ( 1f ), as RAFT agents. The experiment results showed that MA polymerized in a controlled way under a low irradiation dose rate, i.e., first‐order kinetic plots, the experimental molecular weights increased linearly with monomer conversions. The polydispersity indices of polymers generally remained at a relatively low value (lower than 1.4). The effect of irradiation dose on the polymerization results was investigated. The obtained polymers were characterized with 1H NMR and GPC. Chain‐extension reaction was also successfully carried out using the obtained polymer as the macro‐RAFT agent and styrene as the second monomer. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1769–1775, 2007 相似文献
17.
Pulverization and degradation are important pretreatment procedures in producing bio‐ethanol from cellulose. In this study, microcrystalline cellulose (MCC), a pure α‐cellulose, was degraded by γ‐irradiation. The average degree of polymerization, content of reducing sugar, crystalline structure, and molecular structure were investigated to elucidate the radiation effect on the degradation of MCC. The results manifested that γ‐ray destroyed part of the chemical bond and hydrogen bond, leading to the degradation of cellulose and increasing of the reducing sugar content. According to the Fourier transform infrared result, radiation degradation led to the formation of reductive carbonyl group. Meanwhile, radiation had slight influence on the crystalline structures of MCC. Therefore, the radiation degradation procedure is expected to benefit the further proceedings such as ultrafine treatment and enzyme hydrolysis of cellulose. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013 相似文献
18.
The combustion performance of polyamide‐6,6 (PA‐6,6) can be improved by the addition of red phosphorus provided it is intermolecularly cross‐linked upon irradiation with 60Co‐γ‐rays in the presence of triallyl cyanurate (TAC). At a content of 5 wt.‐% the latter promotes cross‐linking, both in the presence and absence of O2, by a factor of about 100. From a variety of combustion tests with samples containing red phosphorus and having been γ‐irradiated in the presence of TAC it turned out that an improved fire resistance of PA‐6,6 is achieved if the red phosphorus content is at least 7 wt.‐%. In this case test samples were self‐extinguishing and the UL 94 rating corresponded to V‐0. IR analysis of the solid residue brought about evidence for the reaction of red phosphorus with the polymer. 相似文献
19.
Preparation and characterization of a series of ion‐exchange membranes for the purpose of separation and extraction of some heavy and toxic metal ions from their wastes were studied. Such ion‐exchange membranes were prepared by γ‐radiation grafting of acrylonitrile (AN) and vinyl acetate (VAc) in a binary monomer mixture onto low‐density polyethylene (LDPE) using the direct technique of grafting. The reaction conditions at which the grafting process proceeds successfully were determined. Many modification treatments were attempted for the prepared membranes to improve their ion‐exchange properties. The possibility of their practical use in waste‐water treatment to remove some heavy and toxic metal ions such as Pb2+, Cd 2+, Cu2+, Fe3+, Sr2+, and Li+ were investigated. These grafted membranes showed great promise for possible use in the field of extraction and removal of some heavy and toxic metals from their wastes. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 849–860, 2001 相似文献
20.
Biodegradable and biocompatible copolymeric hydrogels based on sucrose acrylate, N‐vinyl‐2‐pyrrolidinone, and acrylic acid were designed and synthesized. Because of the growing importance of sugar‐based hydrogels as drug delivery systems, these new pH‐responsive sucrose‐containing copolymeric hydrogels were investigated for oral drug delivery. The sucrose acrylate monomer was synthesized and characterized. The copolymeric hydrogel was synthesized by free‐radical polymerization. Azobisisobutyronitrile (AIBN) was the free‐radical initiator employed and bismethyleneacrylamide (BIS) was the crosslinking agent used for hydrogel preparations. Homopolymeric vinyl pyrrolidone hydrogels were also prepared by the same technique. The hydrogels were characterized by differential scanning calorimetry, thermogravimetric analysis, and scanning electron microscopy. Equilibrium swelling studies were carried out in enzyme‐free simulated gastric and intestinal fluids (SGF and SIF, respectively). These results indicate the pH‐responsive nature of the hydrogels. The gels swelled more in SIF than in SGF. A model drug, propranolol hydrochloride (PPH), was entrapped in these gels and the in vitro release profiles were established separately in both enzyme‐free SGF and enzyme‐free SIF. The drug release was found to be faster in SIF. About 93 and 99% of the entrapped drug was released over a period of 24 h in SGF and SIF, respectively. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2597–2604, 2002 相似文献