656 research outputs found
Quantization of the open string on plane-wave limits of dS_n x S^n and non-commutativity outside branes
The open string on the plane-wave limit of with constant
and dilaton background fields is canonically quantized. This entails
solving the classical equations of motion for the string, computing the
symplectic form, and defining from its inverse the canonical commutation
relations. Canonical quantization is proved to be perfectly suited for this
task, since the symplectic form is unambiguously defined and non-singular. The
string position and the string momentum operators are shown to satisfy
equal-time canonical commutation relations. Noticeably the string position
operators define non-commutative spaces for all values of the string
world-sheet parameter \sig, thus extending non-commutativity outside the
branes on which the string endpoints may be assumed to move. The Minkowski
spacetime limit is smooth and reproduces the results in the literature, in
particular non-commutativity gets confined to the endpoints.Comment: 31 pages, 12p
D-branes with Lorentzian signature in the Nappi-Witten model
Lorentzian signature D-branes of all dimensions for the Nappi-Witten string
are constructed. This is done by rewriting the gluing condition for
the model chiral currents on the brane as a well posed first order differential
problem and by solving it for Lie algebra isometries other than Lie algebra
automorphisms. By construction, these D-branes are not twined conjugacy
classes. Metrically degenerate D-branes are also obtained.Comment: 22 page
Geometric construction of D-branes in WZW models
The geometric description of D-branes in WZW models is pushed forward. Our
starting point is a gluing condition\, that matches the model's
chiral currents at the worldsheet boundary through a linear map acting on
the WZW Lie algebra. The equivalence of boundary and gluing conditions of this
type is studied in detail. The analysis involves a thorough discussion of
Frobenius integrability, shows that must be an isometry, and applies to
both metrically degenerate and nondegenerate D-branes. The isometry need
not be a Lie algebra automorphism nor constantly defined over the brane. This
approach, when applied to isometries of the form with a constant Lie
algebra automorphism, validates metrically degenerate -twined conjugacy
classes as D-branes. It also shows that no D-branes exist in semisimple WZW
models for constant\, .Comment: 23 pages, discussion of limitations of the gluing condition approach
adde
Critical revision of some Myxomycetes deposited in the Buenos Aires HerbariaBAFC, BA and the Tucuman Herbarium LIL. IV
Fifty-seven collections preserved in herbaria BAFC, BA; LIL and Ah representing 26 different species of Myxomycetes are included in this paper. Five species, Comatricha ellae, Didymium megalosporum, Lycogala exiguum, Physarum flavicomum and P. stellatum, are new records from Argentina. Microphotograhs using both optical (LM) and scanning electron microscopy (SEM) are included. these photographs illustrate the most representative characteristics of those species which are rare or not mentioned in Argentina before this work.Cincuenta y siete colecciones conservadas en los herbarios BAFC, BA LIL y AH se incluyen en este trabajo que representan 26 especies diferentes de Myxomycetes. Cinco especies, Comatricha ellae, Didymium megalosporum, Lycogala exiguum, Physarum flavicomum y P. stellatum, son nuevas citas para Argentina. Microfotografias de microscopĂa Ăłptica y microscopĂa electrĂłnica de barrido son incluidas. Estas fotografĂas ilustran las caracterĂsticas mĂĄs representativas de las especies que son raras o no citadas en Argentina
Chitosan-coated mesoporous MIL-100(Fe) nanoparticles as improved bio-compatible oral nanocarriers
Nanometric biocompatible Metal-Organic Frameworks (nanoMOFs) are promising candidates for drug delivery. Up to now, most studies have targeted the intravenous route, related to pain and severe complications; whereas nanoMOFs for oral administration, a commonly used non-invasive and simpler route, remains however unexplored. We propose here the biofriendly preparation of a suitable oral nanocarrier based on the benchmarked biocompatible mesoporous iron(III) trimesate nanoparticles coated with the bioadhesive polysaccharide chitosan (CS). This method does not hamper the textural/ structural properties and the sorption/release abilities of the nanoMOFs upon surface engineering. The interaction between the CS and the nanoparticles has been characterized through a combination of high resolution soft X-ray absorption and computing simulation, while the positive impact of the coating on the colloidal and chemical stability under oral simulated conditions is here demonstrated. Finally, the intestinal barrier bypass capability and biocompatibility of CS-coated nanoMOF have been assessed in vitro, leading to an increased intestinal permeability with respect to the noncoated material, maintaining an optimal biocompatibility. In conclusion, the preservation of the interesting physicochemical features of the CS-coated nanoMOF and their adapted colloidal stability and progressive biodegradation, together with their improved intestinal barrier bypass, make these nanoparticles a promising oral nanocarrier
Economic evaluation of the treatment of Acute Bacterial Skin and Skin Structure Infections (ABSSSIs) from the national payer perspective : introduction of a new treatment to the patient journey. A simulation of three European countries
The aim of this study was to develop a spending predictor model to evaluate the direct costs associated with the management of ABSSSIs from the National health-care provider's perspective of Italy, Romania, and Spain.
METHODOLOGY:
A decision-analytic model was developed to evaluate the diagnostic and clinical pathways of hospitalized ABSSSI patients based on scientific guidelines and real-world data. A Standard of Care (SoC) scenario was compared with a dalbavancin scenario in which the patients could be discharged early. The epidemiological and cost parameters were extrapolated from national administrative databases (i.e., hospital information system). A probabilistic sensitivity analysis (PSA) and one-way sensitivity analysis (OWA) were performed.
RESULTS:
Overall, the model estimated an average annual number of patients with ABSSSIs of approximately 50,000 in Italy, Spain, and Romania. On average, the introduction of dalbavancin reduced the length of stay by 3.3 days per ABSSSI patient. From an economic perspective, dalbavancin did not incur any additional cost from the National Healthcare perspective, and the results were consistent among the countries. The PSA and OWA demonstrated the robustness of these results.
CONCLUSION:
This model represents a useful tool for policymakers by providing information regarding the economic and organizational consequences of an early discharge approach in ABSSSI management
MOFs as multifunctional catalysts: One-pot synthesis of menthol from citronellal over a bifunctional MIL-101 catalyst
A bifunctional MOF catalyst containing coordinatively unsaturated Cr3+ sites and palladium nanoparticles (Pd@MIL-101) has been used for the cyclization of citronellal to isopulegol and for the one-pot tandem isomerization/hydrogenation of citronellal to menthol. The MOF was found to be stable under the reaction conditions used, and the results obtained indicate that the performance of this bifunctional solid catalyst is comparable with other state-of-the-art materials for the tandem reaction: Full citronellal conversion was attained over Pd@MIL-101 in 18 h, with 86% selectivity to menthols and a diastereoselectivity of 81% to the desired (-)-menthol, while up to 30 h were necessary for attaining similar values over Ir/H-beta under analogous reaction conditions.Financial support by Ministerio de Educacion y Ciencia e Innovacion (Project MIYCIN, CSD2009-00050; PROGRAMA CONSOLIDER. INGENIO 2009), Generalidad Valenciana (GV PROMETEO/2008/130) and the CSIC (Proyectos Intramurales Especiales 201080I020) is gratefully acknowledged.GarcĂa Cirujano, F.; LlabrĂ©s I Xamena, FX.; Corma CanĂłs, A. (2012). MOFs as multifunctional catalysts: One-pot synthesis of menthol from citronellal over a bifunctional MIL-101 catalyst. Dalton Transactions. 41:4249-4254. https://doi.org/10.1039/c2dt12480gS4249425441Corma, A., GarciÌa, H., & LlabreÌs i Xamena, F. X. (2010). Engineering Metal Organic Frameworks for Heterogeneous Catalysis. Chemical Reviews, 110(8), 4606-4655. doi:10.1021/cr9003924Farrusseng, D., Aguado, S., & Pinel, C. (2009). Metal-Organic Frameworks: Opportunities for Catalysis. Angewandte Chemie International Edition, 48(41), 7502-7513. doi:10.1002/anie.200806063Lee, J., Farha, O. K., Roberts, J., Scheidt, K. A., Nguyen, S. T., & Hupp, J. T. (2009). Metalâorganic framework materials as catalysts. Chemical Society Reviews, 38(5), 1450. doi:10.1039/b807080fWang, Z., & Cohen, S. M. (2009). Postsynthetic modification of metalâorganic frameworks. Chemical Society Reviews, 38(5), 1315. doi:10.1039/b802258pBanerjee, M., Das, S., Yoon, M., Choi, H. J., Hyun, M. H., Park, S. M., ⊠Kim, K. (2009). Postsynthetic Modification Switches an Achiral Framework to Catalytically Active Homochiral MetalâOrganic Porous Materials. Journal of the American Chemical Society, 131(22), 7524-7525. doi:10.1021/ja901440gGASCON, J., AKTAY, U., HERNANDEZALONSO, M., VANKLINK, G., & KAPTEIJN, F. (2009). Amino-based metal-organic frameworks as stable, highly active basic catalysts. Journal of Catalysis, 261(1), 75-87. doi:10.1016/j.jcat.2008.11.010Hasegawa, S., Horike, S., Matsuda, R., Furukawa, S., Mochizuki, K., Kinoshita, Y., & Kitagawa, S. (2007). Three-Dimensional Porous Coordination Polymer Functionalized with Amide Groups Based on Tridentate Ligand: Selective Sorption and Catalysis. Journal of the American Chemical Society, 129(9), 2607-2614. doi:10.1021/ja067374yCho, S.-H., Ma, B., Nguyen, S. T., Hupp, J. T., & Albrecht-Schmitt, T. E. (2006). A metalâorganic framework material that functions as an enantioselective catalyst for olefin epoxidation. Chem. Commun., (24), 2563-2565. doi:10.1039/b600408cZhang, X., LlabrĂ©s i Xamena, F. X., & Corma, A. (2009). Gold(III) â metal organic framework bridges the gap between homogeneous and heterogeneous gold catalysts. Journal of Catalysis, 265(2), 155-160. doi:10.1016/j.jcat.2009.04.021Meilikhov, M., Yusenko, K., Esken, D., Turner, S., Van Tendeloo, G., & Fischer, R. A. (2010). Metals@MOFs - Loading MOFs with Metal Nanoparticles for Hybrid Functions. European Journal of Inorganic Chemistry, 2010(24), 3701-3714. doi:10.1002/ejic.201000473Henschel, A., Gedrich, K., Kraehnert, R., & Kaskel, S. (2008). Catalytic properties of MIL-101. Chemical Communications, (35), 4192. doi:10.1039/b718371bVermoortele, F., Ameloot, R., Vimont, A., Serre, C., & De Vos, D. (2011). An amino-modified Zr-terephthalate metalâorganic framework as an acidâbase catalyst for cross-aldol condensation. Chem. Commun., 47(5), 1521-1523. doi:10.1039/c0cc03038dWu, P., Wang, J., Li, Y., He, C., Xie, Z., & Duan, C. (2011). Luminescent Sensing and Catalytic Performances of a Multifunctional Lanthanide-Organic Framework Comprising a Triphenylamine Moiety. Advanced Functional Materials, 21(14), 2788-2794. doi:10.1002/adfm.201100115Pan, Y., Yuan, B., Li, Y., & He, D. (2010). Multifunctional catalysis by Pd@MIL-101: one-step synthesis of methyl isobutyl ketone over palladium nanoparticles deposited on a metalâorganic framework. Chemical Communications, 46(13), 2280. doi:10.1039/b922061eCliment, M. J., Corma, A., Guil-LĂłpez, R., Iborra, S., & Primo, J. (1998). Use of Mesoporous MCM-41 Aluminosilicates as Catalysts in the Preparation of Fine Chemicals. Journal of Catalysis, 175(1), 70-79. doi:10.1006/jcat.1998.1970Climent, M. J., Corma, A., Iborra, S., & Velty, A. (2002). Designing the adequate base solid catalyst with Lewis or Bronsted basic sites or with acidâbase pairs. Journal of Molecular Catalysis A: Chemical, 182-183, 327-342. doi:10.1016/s1381-1169(01)00501-5Boronat, M., Climent, M. J., Corma, A., Iborra, S., MontĂłn, R., & Sabater, M. J. (2010). Bifunctional Acid-Base Ionic Liquid Organocatalysts with a Controlled Distance Between Acid and Base Sites. Chemistry - A European Journal, 16(4), 1221-1231. doi:10.1002/chem.200901519Corma, A., DiÌaz, U., GarciÌa, T., Sastre, G., & Velty, A. (2010). Multifunctional Hybrid OrganicâInorganic Catalytic Materials with a Hierarchical System of Well-Defined Micro- and Mesopores. Journal of the American Chemical Society, 132(42), 15011-15021. doi:10.1021/ja106272zFerey, G. (2005). A Chromium Terephthalate-Based Solid with Unusually Large Pore Volumes and Surface Area. Science, 309(5743), 2040-2042. doi:10.1126/science.1116275Corma, A., & Renz, M. (2004). Sn-Beta zeolite as diastereoselective water-resistant heterogeneous Lewis-acid catalyst for carbonâcarbon bond formation in the intramolecular carbonylâene reaction. Chem. Commun., (5), 550-551. doi:10.1039/b313738dIosif, F., Coman, S., PĂąrvulescu, V., Grange, P., Delsarte, S., Vos, D. D., & Jacobs, P. (2004). Ir-Beta zeolite as a heterogeneous catalyst for the one-pot transformation of citronellal to menthol. Chem. Commun., (11), 1292-1293. doi:10.1039/b403692aNeaĆŁu, F., Coman, S., PĂąrvulescu, V. I., Poncelet, G., De Vos, D., & Jacobs, P. (2009). Heterogeneous Catalytic Transformation of Citronellal to Menthol in a Single Step on Ir-Beta Zeolite Catalysts. Topics in Catalysis, 52(9), 1292-1300. doi:10.1007/s11244-009-9270-9MERTENS, P., VERPOORT, F., PARVULESCU, A., & DEVOS, D. (2006). Pt/H-beta zeolites as productive bifunctional catalysts for the one-step citronellal-to-menthol conversion. Journal of Catalysis, 243(1), 7-13. doi:10.1016/j.jcat.2006.06.017Da Silva Rocha, K. A., Robles-Dutenhefner, P. A., Sousa, E. M. B., Kozhevnikova, E. F., Kozhevnikov, I. V., & Gusevskaya, E. V. (2007). Pdâheteropoly acid as a bifunctional heterogeneous catalyst for one-pot conversion of citronellal to menthol. Applied Catalysis A: General, 317(2), 171-174. doi:10.1016/j.apcata.2006.10.019Trasarti, A. F., Marchi, A. J., & ApesteguıÌa, C. R. (2004). Highly selective synthesis of menthols from citral in a one-step process. Journal of Catalysis, 224(2), 484-488. doi:10.1016/j.jcat.2004.03.016TRASARTI, A., MARCHI, A., & APESTEGUIA, C. (2007). Design of catalyst systems for the one-pot synthesis of menthols from citral. Journal of Catalysis, 247(2), 155-165. doi:10.1016/j.jcat.2007.01.016Alaerts, L., SĂ©guin, E., Poelman, H., Thibault-Starzyk, F., Jacobs, P. A., & De Vos, D. E. (2006). Probing the Lewis Acidity and Catalytic Activity of the MetalâOrganic Framework [Cu3(btc)2] (BTC=Benzene-1,3,5-tricarboxylate). Chemistry - A European Journal, 12(28), 7353-7363. doi:10.1002/chem.200600220Horcajada, P., SurblĂ©, S., Serre, C., Hong, D.-Y., Seo, Y.-K., Chang, J.-S., ⊠FĂ©rey, G. (2007). Synthesis and catalytic properties of MIL-100(Fe), an iron(iii) carboxylate with large pores. Chem. Commun., (27), 2820-2822. doi:10.1039/b704325bRavon, U., Chaplais, G., Chizallet, C., Seyyedi, B., Bonino, F., Bordiga, S., ⊠Farrusseng, D. (2010). Investigation of Acid Centers in MIL-53(Al, Ga) for BrĂžnsted-Type Catalysis: Inâ
Situ FTIR and Abâ
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Erratum to: 36th International Symposium on Intensive Care and Emergency Medicine: Brussels, Belgium. 15-18 March 2016.
[This corrects the article DOI: 10.1186/s13054-016-1208-6.]
Aqueous Stable Gold Nanostar/ZIFâ8 Nanocomposites for LightâTriggered Release of Active Cargo Inside Living Cells
This is the peer reviewed version of the following article: C. Carrillo-CarriĂłn, R. MartĂnez, M. F.
Navarro Poupard, B. Pelaz, E. Polo, A. Arenas-Vivo, A. Olgiati, P. Taboada, M. G. Soliman, Ă. CatalĂĄn,
S. FernĂĄndez-Castillejo, R. SolĂ , W. J. Parak, P. Horcajada, R. A. Alvarez-Puebla, P. del Pino, Angew.
Chem. Int. Ed. 2019, 58, 7078, which has been published in final form at https://
doi.org/10.1002/anie.201902817. This article may be used for non-commercial purposes in
accordance with Wiley Terms and Conditions for Use of Self-Archived VersionsA plasmonic coreâshell gold nanostar/zeoliticâimidazolateâframeworkâ8 (ZIFâ8) nanocomposite was developed for the thermoplasmonicâdriven release of encapsulated active molecules inside living cells. The nanocomposites were loaded, as a proof of concept, with bisbenzimide molecules as functional cargo and wrapped with an amphiphilic polymer that prevents ZIFâ8 degradation and bisbenzimide leaking in aqueous media or inside living cells. The demonstrated moleculeârelease mechanism relies on the use of nearâIR light coupled to the plasmonic absorption of the core gold nanostars, which creates local temperature gradients and thus, bisbenzimide thermodiffusion. Confocal microscopy and surfaceâenhanced Raman spectroscopy (SERS) were used to demonstrate bisbenzimide loading/leaking and nearâIRâtriggered cargo release inside cells, thereby leading to DNA stainingThis work has received financial support from the MINECOâSpain (MAT2016â80266âR, MAT2015â74381âJIN, CTQ2017â88648R, ENE2016â79608âC2â1âR, CTQ2017â89588âR, RYCâ2014â15039, RYCâ2014â16962), the Xunta de Galicia, Centro singular de investigaciĂłn de Galicia accreditation 2016â2019 (ED431G/09), the AgrupaciĂłn EstratĂ©gica de Materiales Action (ED431E 2018/08), the Generalitat de Cataluña (2017SGR522, 2017SGR883, SLT002/16/00239), the URV (2017PFRâURVâB2â02), the German Research Society (DFG PA 794â21â1), and the European Union (European Regional Development FundâERDF, H2020âMSCAâIFâ2016, project 749667). M.F.N.P acknowledges the CONACYT PhD fellowship programS
Designed Single-Step Synthesis, Structure, and Derivative Textural Properties of Well-Ordered Layered Penta-coordinate Silicon Alcoholate Complexes
The controllable synthesis of well-ordered layered materials with specific nanoarchitecture poses a grand challenge in materials chemistry. Here the solvothermal synthesis of two structurally analogous 5-coordinate organosilicate complexes through a novel transesterification mechanism is reported. Since the polycrystalline nature of the intrinsic hypervalent Si complex thwarts the endeavor in determining its structure, a novel strategy concerning the elegant addition of a small fraction of B species as an effective crystal growth mediator and a sacrificial agent is proposed to directly prepare diffraction-quality single crystals without disrupting the intrinsic elemental type. In the determined crystal structure, two monomeric primary building units (PBUs) self-assemble into a dimeric asymmetric secondary BU via strong Na+[BOND]O2â ionic bonds. The designed one-pot synthesis is straightforward, robust, and efficient, leading to a well-ordered (10Ä«)-parallel layered Si complex with its principal interlayers intercalated with extensive van der Waals gaps in spite of the presence of substantial Na+ counter-ions as a result of unique atomic arrangement in its structure. However, upon fast pyrolysis, followed by acid leaching, both complexes are converted into two SiO2 composites bearing BET surface areas of 163.3 and 254.7â
m2âgâ1 for the pyrolyzed intrinsic and B-assisted Si complexes, respectively. The transesterification methodology merely involving alcoholysis but without any hydrolysis side reaction is designed to have generalized applicability for use in synthesizing new layered metalâorganic compounds with tailored PBUs and corresponding metal oxide particles with hierarchical porosity.United States. Defense Advanced Research Projects Agency (control No. 0471-1627)National Institute for Biomedical Imaging and Bioengineering (U.S.) (award No. EB-001960)National Institutes of Health (U.S.) (NIBIB award No. EB-002026)National Science Foundation (U.S.) (Grant No. CHE-0946721
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