Abstract:Poly(N-vinylcaprolactam-co-itaconic acid), P(VC-co-IA), gels were synthesized in ethanol by using the free radical cross-linking polymerization method at 60 °C for 24 h in the presence of azobis(isobutyronitrile) (AIBN) and allyl methacrylate (AMA) as the initiator and the cross-linking agent, respectively. In order to determine the effect of the synthesis medium on the percentage of gelation (PG) and equilibrium swelling value (ESV), an ethanol/distilled water mixture (80:20, v/v) was also used as the synthes… Show more
“…TGA analyses were carried out in the temperature range of 25–800 °C under inert nitrogen atmosphere. SR‐g‐MAA copolymer showed three steps of weight loss: the first step that occurred in the 200–280 °C range corresponds to the anhydrization of PMAA; the second one from 370 to 470 °C can be attributed to the scission of the main chain of PMAA, while the third one starting at 470 °C is due to thermal decomposition of SR.…”
Silicone rubber (SR) was γ‐ray grafted with poly(methacrylic acid) (PMAA) to improve its ability to host antimicrobial drugs. Dependence of grafting yield on monomer concentration, pre‐irradiation dose, temperature and reaction time was evaluated. Modified SR films were characterized by means of FT‐IR, DSC, TGA, SEM, contact angle measurements, and swelling studies. SR‐g‐MAA showed pH sensitivity (critical pH ∼6) and good cytocompatibility. Soaking of SR‐g‐MAA in benzalkonium chloride and vancomycin aqueous solutions led to high loadings; up to 5.8 and 15.2 mg cm‐2, respectively. SR‐g‐MAA released 100% vancomycin after 24 h in buffer pH 7.4 at 37 °C, but only 20% benzalkonium chloride due to strong ionic interactions. Drug‐loaded SR‐g‐MAA prevented in vitro growth of Staphylococcus aureus. Overall, grafting of PMAA may improve the performance of SR for biomedical applications.
“…TGA analyses were carried out in the temperature range of 25–800 °C under inert nitrogen atmosphere. SR‐g‐MAA copolymer showed three steps of weight loss: the first step that occurred in the 200–280 °C range corresponds to the anhydrization of PMAA; the second one from 370 to 470 °C can be attributed to the scission of the main chain of PMAA, while the third one starting at 470 °C is due to thermal decomposition of SR.…”
Silicone rubber (SR) was γ‐ray grafted with poly(methacrylic acid) (PMAA) to improve its ability to host antimicrobial drugs. Dependence of grafting yield on monomer concentration, pre‐irradiation dose, temperature and reaction time was evaluated. Modified SR films were characterized by means of FT‐IR, DSC, TGA, SEM, contact angle measurements, and swelling studies. SR‐g‐MAA showed pH sensitivity (critical pH ∼6) and good cytocompatibility. Soaking of SR‐g‐MAA in benzalkonium chloride and vancomycin aqueous solutions led to high loadings; up to 5.8 and 15.2 mg cm‐2, respectively. SR‐g‐MAA released 100% vancomycin after 24 h in buffer pH 7.4 at 37 °C, but only 20% benzalkonium chloride due to strong ionic interactions. Drug‐loaded SR‐g‐MAA prevented in vitro growth of Staphylococcus aureus. Overall, grafting of PMAA may improve the performance of SR for biomedical applications.
“…The maximum weight loss (52%) occurred in the second stage. The thermal degradation of the SR‐ g ‐(VCL/MAA) 68% graft was shown by the two weight losses occurring in the 200–300°C region (due to the decarboxylation of PMAA) and 350–450°C region (due to the scission of the main chain of PMAA and PVCL) …”
Silicone rubber (SR), a material widely used in the biomedical field, was modified with stimuli-responsive poly(N-vinyl caprolactam) (PVCL) and poly(methacrylic acid) (PMAA) with the aim of improving its ability to host drug molecules. The grafting of PVCL and PMAA onto SR was carried out by means of a c-ray preirradiation method, and the dependence of the grafting yield on the comonomer concentration, preirradiation dose, temperature, and reaction time was evaluated. Modified SR films were characterized by Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, and swelling studies to confirm the grafting of the copolymer. The SR-g-[vinyl caprolactam (VCL)/methacrylic acid (MAA)] copolymers showed a sensitivity to the temperature and pH, high hemocompatibility, and low affinity to bovine serum albumin and fibrinogen proteins. Moreover, the SR-g-(VCL/MAA) copolymers were able to host some nonsteroidal anti-inflammatory drugs, such as diclofenac and ibuprofen, and the antifungal agent nystatin. The graft copolymer was shown to be useful for providing sustained release for several hours; this indicates that the modified SR is a promising material for drug-eluting medical devices. V C 2015 Wiley Periodicals, Inc. J. Appl.Polym. Sci. 2015, 132, 41855.
“…[1][2][3] Special attention has been paid to microgels based on N-vinylcaprolactam (VCL) during the last years, since these exhibit outstanding properties like a high biocompatibility and temperatureresponsive behavior. [4][5][6] PVCL microgels show a volume phase transition at a temperature of 32 °C, [7,8] being swollen at temperatures below while losing water and thus collapsing at temperatures above. Due to the unique properties of PVCL microgels, numerous applications in the biomedical field were developed in the last years, for example, the use of PVCL-based microgels for drug release [6,9,10] or as contrast agent in tumor magnetic resonance (MR) imaging after gadolinium loading.…”
Herein, the synthesis of amylose‐coated, temperature‐responsive poly(N‐vinylcaprolactam) (VCL)‐based copolymer microgels by enzyme‐catalyzed grafting‐from polymerization with phosphorylase b from rabbit muscle is reported. The phosphorylase is able to recognize the oligosaccharide maltoheptaose as primer and attach glucose units from the monomer glucose‐1‐phosphate to it, thereby forming amylose chains while releasing inorganic phosphate. Therefore, to enable the phosphorylase‐catalyzed grafting‐from polymerization of glucose‐1‐phosphate from the PVCL‐based microgels, the maltoheptaose primer is covalently attached to the microgel in the first synthesis step. This is realized by adding N‐(2‐aminoethyl)methacrylamide (AEMAA) as a comonomer to the PVCL microgel to integrate primary amino groups and subsequent coupling of maltoheptaonolactone. Both the PVCL/AEMAA microgel as well as the obtained microgel–maltoheptaose construct are characterized in detail by dynamic light scattering, electrophoretic mobility measurements, IR spectroscopy, and atomic force microscopy. From the microgel–maltoheptaose construct, the grafting‐from polymerization of glucose‐1‐phosphate is performed by the addition of phosphorylase b. Atomic force microscopy images clearly demonstrate the formation of an amylose shell around the microgels. The developed amylose‐coated microgels open up promising application possibilities, for example, as colloidal scavengers, since amylose helices can serve as host molecules for inclusion of hydrophobic guest molecules.
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