645 research outputs found

    Quantization of the open string on plane-wave limits of dS_n x S^n and non-commutativity outside branes

    Get PDF
    The open string on the plane-wave limit of dSn×SndS_n\times S^n with constant B2B_2 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

    Get PDF
    Lorentzian signature D-branes of all dimensions for the Nappi-Witten string are constructed. This is done by rewriting the gluing condition J+=FJ−J_+=FJ_- for the model chiral currents on the brane as a well posed first order differential problem and by solving it for Lie algebra isometries FF 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

    Get PDF
    The geometric description of D-branes in WZW models is pushed forward. Our starting point is a gluing condition\, J+=FJ−J_{+}=FJ_- that matches the model's chiral currents at the worldsheet boundary through a linear map FF 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 FF must be an isometry, and applies to both metrically degenerate and nondegenerate D-branes. The isometry FF need not be a Lie algebra automorphism nor constantly defined over the brane. This approach, when applied to isometries of the form F=RF=R with RR a constant Lie algebra automorphism, validates metrically degenerate RR-twined conjugacy classes as D-branes. It also shows that no D-branes exist in semisimple WZW models for constant\, F=−RF=-R.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

    Get PDF
    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

    Get PDF
    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

    Get PDF
    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

    Full text link
    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., García, H., & Llabrés 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). Metal–organic framework materials as catalysts. Chemical Society Reviews, 38(5), 1450. doi:10.1039/b807080fWang, Z., & Cohen, S. M. (2009). Postsynthetic modification of metal–organic 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 Metal−Organic 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 metal–organic 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) – 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 metal–organic framework as an acid–base 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 metal–organic 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 acid–base 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., Díaz, U., García, T., Sastre, G., & Velty, A. (2010). Multifunctional Hybrid Organic−Inorganic 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 carbon–carbon bond formation in the intramolecular carbonyl–ene 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). Pd–heteropoly 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., & Apesteguı́a, 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 Metal–Organic 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: In Situ FTIR and Ab Initio Molecular Modeling. ChemCatChem, 2(10), 1235-1238. doi:10.1002/cctc.201000055Vimont, A., Leclerc, H., MaugĂ©, F., Daturi, M., Lavalley, J.-C., SurblĂ©, S., 
 FĂ©rey, G. (2007). Creation of Controlled BrĂžnsted Acidity on a Zeotypic Mesoporous Chromium(III) Carboxylate by Grafting Water and Alcohol Molecules. The Journal of Physical Chemistry C, 111(1), 383-388. doi:10.1021/jp064686

    Aqueous Stable Gold Nanostar/ZIF‐8 Nanocomposites for Light‐Triggered Release of Active Cargo Inside Living Cells

    Get PDF
    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, Ú. 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 core–shell gold nanostar/zeolitic‐imidazolate‐framework‐8 (ZIF‐8) nanocomposite was developed for the thermoplasmonic‐driven 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 ZIF‐8 degradation and bisbenzimide leaking in aqueous media or inside living cells. The demonstrated molecule‐release mechanism relies on the use of near‐IR light coupled to the plasmonic absorption of the core gold nanostars, which creates local temperature gradients and thus, bisbenzimide thermodiffusion. Confocal microscopy and surface‐enhanced Raman spectroscopy (SERS) were used to demonstrate bisbenzimide loading/leaking and near‐IR‐triggered cargo release inside cells, thereby leading to DNA stainingThis work has received financial support from the MINECO‐Spain (MAT2016‐80266‐R, MAT2015‐74381‐JIN, CTQ2017‐88648R, ENE2016‐79608‐C2‐1‐R, CTQ2017‐89588‐R, RYC‐2014‐15039, RYC‐2014‐16962), the Xunta de Galicia, Centro singular de investigaciĂłn de Galicia accreditation 2016–2019 (ED431G/09), the AgrupaciĂłn EstratĂ©gica de Materiales Action (ED431E 2018/08), the Generalitat de Cataluña (2017SGR522, 2017SGR883, SLT002/16/00239), the URV (2017PFR‐URV‐B2‐02), the German Research Society (DFG PA 794‐21‐1), and the European Union (European Regional Development Fund—ERDF, H2020‐MSCA‐IF‐2016, 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

    Get PDF
    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]O2− ionic bonds. The designed one-pot synthesis is straightforward, robust, and efficient, leading to a well-ordered (10ī)-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 254.7 m2 g−1 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 metal–organic 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
    • 

    corecore