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51.
Megan Douglass Sean Hopkins Rashmi Pandey Priya Singha Megan Norman Hitesh Handa 《Macromolecular bioscience》2021,21(1)
The novel use of nanofibers as a physical barrier between blood and medical devices has allowed for modifiable, innovative surface coatings on devices ordinarily plagued by thrombosis, delayed healing, and chronic infection. In this study, the nitric oxide (NO) donor S‐nitrosoglutathione (GSNO) is blended with the biodegradable polymers polyhydroxybutyrate (PHB) and polylactic acid (PLA) for the fabrication of hemocompatible, antibacterial nanofibers tailored for blood‐contacting applications. Stress/strain behavior of different concentrations of PHB and PLA is recorded to optimize the mechanical properties of the nanofibers. Nanofibers incorporated with different concentrations of GSNO (10, 15, 20 wt%) are evaluated based on their NO‐releasing kinetics. PLA/PHB + 20 wt% GSNO nanofibers display the greatest NO release over 72 h (0.4–1.5 × 10?10 mol mg?1 min?1). NO‐releasing fibers successfully reduce viable adhered bacterial counts by ≈80% after 24 h of exposure to Staphylococcus aureus. NO‐releasing nanofibers exposed to porcine plasma reduce platelet adhesion by 64.6% compared to control nanofibers. The nanofibers are found noncytotoxic (>95% viability) toward NIH/3T3 mouse fibroblasts, and 4′,6‐diamidino‐2‐phenylindole and phalloidin staining shows that fibroblasts cultured on NO‐releasing fibers have improved cellular adhesion and functionality. Therefore, these novel NO‐releasing nanofibers provide a safe antimicrobial and hemocompatible coating for blood‐contacting medical devices. 相似文献
52.
53.
Vladislav Stroganov Jitendra Pant Georgi Stoychev Andreas Janke Dieter Jehnichen Andreas Fery Hitesh Handa Leonid Ionov 《Advanced functional materials》2018,28(11)
A novel approach for fabrication of 3D cellular structures using new thermosensitive shape‐changing polymer films with photolithographically patterned surface—4D biofabrication is reported. The surface of shape‐changing polymer films is patterned to selectively adsorb cells in specific regions. The 2D cell pattern is converted to the 3D cell structure after temperature‐induced folding of the polymer films. This approach has a great potential in the field of tissue engineering and bioscaffolds fabrication. 相似文献
54.
Foster SL Handa S Krafft M Rowling D 《Chemical communications (Cambridge, England)》2007,(45):4791-4793
The first reported intramolecular pinacol coupling of cyclopropyl ketones has been achieved, demonstrating that cyclisation competes favourably with ring-opening of the cyclopropyl ketyl radical. 相似文献
55.
Steed JW Goeta AE Lipkowski J Swierczynski D Panteleon V Handa S 《Chemical communications (Cambridge, England)》2007,(8):813-815
Templation of a daughter phase by a parent crystal results from an equilibrating mixture of two very different copper(ii) N,N',N'-trimethyltriazacyclononane complexes. 相似文献
56.
Three new compounds, Ru4(mu4-GePh)2(mu-GePh2)2(mu-CO)2(CO)8 (11), Ru4(mu4-GePh)2(mu-GePh2)3(mu-CO)(CO)8 (12), and Ru4(mu4-GePh)2(mu-GePh2)4(CO)8 (13), were obtained from the reaction of H(4)Ru(4)(CO)12 with excess Ph(3)GeH in octane (11 and 12) or decane (13) reflux. Compound 11 was converted to compound 13 by reaction with Ph(3)GeH by heating solutions in nonane solvent to reflux. Compounds 11-13 each contain a square-type arrangement of four Ru atoms capped on each side by a quadruply bridging GePh ligand to form an octahedral geometry for the Ru(4)Ge(2) group. Compound 11 also contains two edge-bridging GePh(2) groups on opposite sides of the cluster and two bridging carbonyl ligands. Compound 12 contains three edge-bridging GePh(2) groups and one bridging carbonyl ligand. Compound 13 contains four bridging GePh(2) groups, one on each edge of the Ru4 square. The reaction of H(4)Os(4)(CO)12 with excess Ph(3)GeH in decane at reflux yielded two new tetraosmium cluster complexes, Os4(mu4-GePh)2(mu-GePh2)3(mu-CO)(CO)8 (14) and Os4(mu4-GePh)2(mu-GePh(2))4(CO)8 (15). These compounds are structurally similar to compounds 12 and 13, respectively. 相似文献
57.
A stepwise temperature‐ and pressure‐scanning thermal analysis method was developed to measure glass‐transition temperature Tg in the two‐phase polymer–gas systems as a function of gas pressure p, and was used to confirm recent theoretical predictions that certain polymer–gas systems exhibit retrograde vitrification, that is, they undergo rubber‐to‐glass transition on heating. A complete Tg‐p profile delineating the glass–rubber phase envelope was established for the PMMA‐CO2 system. The retrograde vitrification behavior observed, where at certain gas pressures the polymer exists in the rubbery state at low and high temperatures and in the glassy state at intermediate temperatures, was similar to that reported previously based on the creep‐compliance measurements. The existence of the rubbery state at low temperatures was used to generate foams by saturating the polymer with CO2 at 34 atm and at temperatures in the range −0.2 to 24 °C followed by foaming at temperatures in the range 24 to 90 °C. Foams with very fine cell structure never reported before could be prepared by this technique. For example, PMMA foams with average cell size of 0.35 μm and cell density of 4.4 × 1013 cells/g were prepared by processing the low temperature rubbery phase. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 716–725, 2000 相似文献
58.
Rieko Ichikawa Masayuki Hata Noriaki Okimoto Setsuko OikawaHanda Minoru Tsuda 《Journal of polymer science. Part A, Polymer chemistry》1998,36(7):1035-1042
A mechanism of acid-catalyzed deprotection of poly(4-tert-butyloxycarbonyloxy-styrene), PBOCST, in chemically amplified resists has been elucidated in terms of elementary processes by means of semiempirical molecular orbital calculations. It is concluded that the overall deprotection of tert-butyloxycarbonyl (t-BOC) group proceeds stepwise; i.e., (a) the first products are an acid carbonate and a tert-butyl cation; (b) a phenolic compound is the secondary and final product from the acid carbonate, which is realized by assistance with a counter anion accompanied by acid; (c) the counter anion also assists acid regeneration from the tert-butyl cation to produce isobutylene. The yield rate of the phenol is proportional to the product of concentrations of the polymer, the catalytic acid, and the counter anion. The activation energy (21 kcal/mol) calculated for the rate-determining step (a) is in good agreement with an experiment. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1035–1042, 1998 相似文献
59.
In this work we present the results from studies on novel poly(arylene ether ketone)s, including gas permeability, wide-angle x-ray diffraction (WAXD), and dynamic mechanical analysis (DMA). Poly(arylene ether ketone)s containing 2,2′- and 3,3′-dibenzoylbiphenyl (DBBP) moieties were characterized to study the effect of biphenyl substitution on gas transport properties. Gas permeabilities of naphthalene-containing poly(arylene ether ketone)s were also measured. Higher permeabilities were observed for polymers prepared with 6F-BPA, compared to 9,9-bis(4-hydroxyphenyl)fluorene (HPF). The naphthalene-containing polymers exhibited higher permeabilities than the DBBP polymers, except for a polymer having the 2,2′-DBBP and tetramethylbiphenyl moieties. Based on our work, and results reported in the literature, the 3,3′-DBBP polymers showed the lowest permeabilities for DBBP-containing poly-(arylene ether ketone)s. The low permeabilities are due to more efficiently packed chains brought on by greater flexibility of the backbone, compared to the other polymers studied. DMA studies confirmed the higher barriers to rotation which are believed to be responsible for 2,2′-DBBP polymers having similar selectivities compared to 3,3′-DBBP polymers. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 425–431, 1998 相似文献
60.
Y. Paul Handa Jacques Roovers Pierre Moulini 《Journal of Polymer Science.Polymer Physics》1997,35(14):2355-2362
Tert-butyl and di-tert-butyl were added as pendant groups to the ether-ether phenyl ring of poly(ether ether ketone), PEEK. tert-butyl PEEK, TBPEEK, was amorphous and di-tert-butyl PEEK, DBPEEK, was semicrystalline. However, a 2 : 1 random copolymer of TBPEEK and DBPEEK, TBDBPEEK, was amorphous. Gas transport of N2, O2, CH4, and CO2 through amorphous films of PEEK, TBPEEK, TBDBPEEK, and tetramethylbiphenyl PEEK were determined at 35°C and at pressures to about 15 atm. The results support previous observations that tert-butyl and tetramethylbiphenyl groups are very effective in disrupting chain packing in the polymer. For the present polymers, these substitutions led to a 5–18-fold increase in permeability, and, in some cases, at no loss in permselectivity. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35 : 2355–2362, 1997 相似文献