Logarithmic intertwining operators and vertex operators

This is the first in a series of papers where we study logarithmic intertwining operators for various vertex subalgebras of Heisenberg vertex operator algebras. In this paper we examine logarithmic intertwining operators associated with rank one Heisenberg vertex operator algebra $M(1)_a$, of central charge $1-12a^2$. We classify these operators in terms of {\em depth} and provide explicit constructions in all cases. Furthermore, for $a=0$ we focus on the vertex operator subalgebra L(1,0) of $M(1)_0$ and obtain logarithmic intertwining operators among indecomposable Virasoro algebra modules. In particular, we construct explicitly a family of {\em hidden} logarithmic intertwining operators, i.e., those that operate among two ordinary and one genuine logarithmic L(1,0)-module.Comment: 32 pages. To appear in CM

The N=1 triplet vertex operator superalgebras

We introduce a new family of C_2-cofinite N=1 vertex operator superalgebras SW(m), $m \geq 1$, which are natural super analogs of the triplet vertex algebra family W(p), $p \geq 2$, important in logarithmic conformal field theory. We classify irreducible SW(m)-modules and discuss logarithmic modules. We also compute bosonic and fermionic formulas of irreducible SW(m) characters. Finally, we contemplate possible connections between the category of SW(m)-modules and the category of modules for the quantum group U^{small}_q(sl_2), q=e^{\frac{2 \pi i}{2m+1}}, by focusing primarily on properties of characters and the Zhu's algebra A(SW(m)). This paper is a continuation of arXiv:0707.1857.Comment: 53 pages; v2: references added; v3: a few changes; v4: final version, to appear in CM

Viscoelastic gels of guar and xanthan gum mixtures provide long-term stabilization of iron micro- and nanoparticles

Iron micro- and nanoparticles used for groundwater remediation and medical applications are prone to fast aggregation and sedimentation. Diluted single biopolymer water solutions of guar gum (GG) or xanthan gum (XG) can stabilize these particles for few hours providing steric repulsion and by increasing the viscosity of the suspension. The goal of the study is to demonstrate that amending GG solutions with small amounts of XG (XG/GG weight ratio 1:19; 3 g/L of total biopolymer concentration) can significantly improve the capability of the biopolymer to stabilize highly concentrated iron micro- and nanoparticle suspensions. The synergistic effect between GG and XG generates a viscoelastic gel that can maintain 20 g/L iron particles suspended for over 24 h. This is attributed to (i) an increase in the static viscosity, (ii) a combined polymer structure the yield stress of which contrasts the downward stress exerted by the iron particles, and (iii) the adsorption of the polymers to the iron surface having an anchoring effect on the particles. The XG/GG viscoelastic gel is characterized by a marked shear thinning behavior. This property, coupled with the low biopolymer concentration, determines small viscosity values at high shear rates, facilitating the injection in porous media. Furthermore, the thermosensitivity of the soft elastic polymeric network promotes higher stability and longer storage times at low temperatures and rapid decrease of viscosity at higher temperatures. This feature can be exploited in order to improve the flowability and the delivery of the suspensions to the target as well as to effectively tune and control the release of the iron particle

Fusion rules and boundary conditions in the c=0 triplet model

The logarithmic triplet model W_2,3 at c=0 is studied. In particular, we determine the fusion rules of the irreducible representations from first principles, and show that there exists a finite set of representations, including all irreducible representations, that closes under fusion. With the help of these results we then investigate the possible boundary conditions of the W_2,3 theory. Unlike the familiar Cardy case where there is a consistent boundary condition for every representation of the chiral algebra, we find that for W_2,3 only a subset of representations gives rise to consistent boundary conditions. These then have boundary spectra with non-degenerate two-point correlators.Comment: 50 pages; v2: changed formulation in section 1.2.1 and corrected typos, version to appear in J. Phys.

Phase II study of induction chemotherapy with TPF followed by radioimmunotherapy with Cetuximab and intensity-modulated radiotherapy (IMRT) in combination with a carbon ion boost for locally advanced tumours of the oro-, hypopharynx and larynx - TPF-C-HIT

<p>Abstract</p> <p>Background</p> <p>Long-term locoregional control in locally advanced squamous cell carcinoma of the head and neck (SCCHN) remains challenging. While recent years have seen various approaches to improve outcome by intensification of treatment schedules through introduction of novel induction and combination chemotherapy regimen and altered fractionation regimen, patient tolerance to higher treatment intensities is limited by accompanying side-effects. Combined radioimmunotherapy with cetuximab as well as modern radiotherapy techniques such as intensity-modulated radiotherapy (IMRT) and carbon ion therapy (C12) are able to limit toxicity while maintaining treatment effects. In order to achieve maximum efficacy with yet acceptable toxicity, this sequential phase II trial combines induction chemotherapy with docetaxel, cisplatin, and 5-FU (TPF) followed by radioimmunotherapy with cetuximab as IMRT plus carbon ion boost. We expect this approach to result in increased cure rates with yet manageable accompanying toxicity.</p> <p>Methods/design</p> <p>The TPF-C-HIT trial is a prospective, mono-centric, open-label, non-randomized phase II trial evaluating efficacy and toxicity of the combined treatment with IMRT/carbon ion boost and weekly cetuximab in 50 patients with histologically proven locally advanced SCCHN following TPF induction chemotherapy. Patients receive 24 GyE carbon ions (8 fractions) and 50 Gy IMRT (2.0 Gy/fraction) in combination with weekly cetuximab throughout radiotherapy. Primary endpoint is locoregional control at 12 months, secondary endpoints are disease-free survival, progression-free survival, overall survival, acute and late radiation effects as well as any adverse events of the treatment as well as quality of life (QoL) analyses.</p> <p>Discussion</p> <p>The primary objective of TPF-C-HIT is to evaluate efficacy and toxicity of cetuximab in combination with combined IMRT/carbon ion therapy following TPF induction in locally advanced SCCHN.</p> <p>Trial Registration</p> <p>Clinical Trial Identifier: <a href="http://www.clinicaltrials.gov/ct2/show/NCT01245985">NCT01245985</a> (clinicaltrials.gov)</p> <p>EudraCT number: 2009 - 016489- 10</p

W-extended Kac representations and integrable boundary conditions in the logarithmic minimal models WLM(1,p)

We construct new Yang-Baxter integrable boundary conditions in the lattice approach to the logarithmic minimal model WLM(1,p) giving rise to reducible yet indecomposable representations of rank 1 in the continuum scaling limit. We interpret these W-extended Kac representations as finitely-generated W-extended Feigin-Fuchs modules over the triplet W-algebra W(p). The W-extended fusion rules of these representations are inferred from the recently conjectured Virasoro fusion rules of the Kac representations in the underlying logarithmic minimal model LM(1,p). We also introduce the modules contragredient to the W-extended Kac modules and work out the correspondingly-extended fusion algebra. Our results are in accordance with the Kazhdan-Lusztig dual of tensor products of modules over the restricted quantum universal enveloping algebra $\bar{U}_q(sl_2)$ at $q=e^{\pi i/p}$. Finally, polynomial fusion rings isomorphic with the various fusion algebras are determined, and the corresponding Grothendieck ring of characters is identified.Comment: 28 page

The global distribution of leaf chlorophyll content

Leaf chlorophyll is central to the exchange of carbon, water and energy between the biosphere and the atmosphere, and to the functioning of terrestrial ecosystems. This paper presents the first spatially-continuous view of terrestrial leaf chlorophyll content (ChlLeaf) at the global scale. Weekly maps of ChlLeaf were produced from ENVISAT MERIS full resolution (300 m) satellite data using a two-stage physically-based radiative transfer modelling approach. Firstly, leaf-level reflectance was derived from top-of-canopy satellite reflectance observations using 4-Scale and SAIL canopy radiative transfer models for woody and non-woody vegetation, respectively. Secondly, the modelled leaf-level reflectance was input into the PROSPECT leaf-level radiative transfer model to derive ChlLeaf. The ChlLeaf retrieval algorithm was validated using measured ChlLeaf data from 248 sample measurements at 28 field locations, and covering six plant functional types (PFTs). Modelled results show strong relationships with field measurements, particularly for deciduous broadleaf forests (R2 = 0.67; RMSE = 9.25 μg cm-2; p < 0.001), croplands (R2 = 0.41; RMSE = 13.18 μg cm-2; p < 0.001) and evergreen needleleaf forests (R2 = 0.47; RMSE = 10.63 μg cm-2; p < 0.001). When the modelled results from all PFTs were considered together, the overall relationship with measured ChlLeaf remained good (R2 = 0.47, RMSE = 10.79 μg cm-2; p < 0.001). This result is an improvement on the relationship between measured ChlLeaf and a commonly used chlorophyll-sensitive spectral vegetation index; the MERIS Terrestrial Chlorophyll Index (MTCI; R2 = 0.27, p < 0.001). The global maps show large temporal and spatial variability in ChlLeaf, with evergreen broadleaf forests presenting the highest leaf chlorophyll values, with global annual median values of 54.4 μg cm-2. Distinct seasonal ChlLeaf phenologies are also visible, particularly in deciduous plant forms, associated with budburst and crop growth, and leaf senescence. It is anticipated that this global ChlLeaf product will make an important step towards the explicit consideration of leaf-level biochemistry in terrestrial water, energy and carbon cycle modelling

Cytostatic potential of novel agents that inhibit the regulation of intracellular pH

Cells within the acidic extracellular environment of solid tumours maintain their intracellular pH (pHi) through the activity of membrane-based ion exchange mechanisms including the Na+/H+ antiport and the Na+-dependent Cl−/HCO3− exchanger. Inhibition of these regulatory mechanisms has been proposed as an approach to tumour therapy. Previously available inhibitors of these exchangers were toxic (e.g. 4,4-diisothiocyanstilbene-2,2-disulphonic acid), and/or non-specific (e.g. 5-N-ethyl-N-isopropyl amiloride). Using two human (MCF7, MDA-MB231) and one murine (EMT6) breast cancer cell lines, we evaluated the influence of two new agents, cariporide (an inhibitor of the Na+/H+ antiport) and S3705 (an inhibitor of the Na+-dependent Cl−/HCO3− exchanger) on the regulation of intracellular pH (pHi). The cytotoxicity of the two agents was assessed by using clonogenic assays. Our results suggest that cariporide has similar efficacy and potency to 5-N-ethyl-N-isopropyl amiloride for inhibition of Na+/H+ exchange while S3705 is more potent and efficient than 4,4-diisothiocyanstilbene-2,2-disulphonic acid in inhibiting Na+-dependent Cl−/HCO3− exchange. The agents inhibited the growth of tumour cells when they were incubated at low pHe (7.0–6.8), but were non-toxic to cells grown at doses that inhibited the regulation of pHi. Our results indicate that cariporide and S3705 are selective cytostatic agents under in vitro conditions that reflect the slightly acidic microenvironment found in solid tumours

The influence of P-glycoprotein expression and its inhibitors on the distribution of doxorubicin in breast tumors

Abstract Background Anti-cancer drugs access solid tumors via blood vessels, and must penetrate tumor tissue to reach all cancer cells. Previous studies have demonstrated steep gradients of decreasing doxorubicin fluorescence with increasing distance from blood vessels, such that many tumor cells are not exposed to drug. Studies using multilayered cell cultures show that increased P-glycoprotein (PgP) is associated with better penetration of doxorubicin, while PgP inhibitors decrease drug penetration in tumor tissue. Here we evaluate the effect of PgP expression on doxorubicin distribution in vivo. Methods Mice bearing tumor sublines with either high or low expression of PgP were treated with doxorubicin, with or without pre-treatment with the PgP inhibitors verapamil or PSC 833. The distribution of doxorubicin in relation to tumor blood vessels was quantified using immunofluorescence. Results Our results indicate greater uptake of doxorubicin by cells near blood vessels in wild type as compared to PgP-overexpressing tumors, and pre-treatment with verapamil or PSC 833 increased uptake in PgP-overexpressing tumors. However, there were steeper gradients of decreasing doxorubicin fluorescence in wild-type tumors compared to PgP overexpressing tumors, and treatment of PgP overexpressing tumors with PgP inhibitors led to steeper gradients and greater heterogeneity in the distribution of doxorubicin. Conclusion PgP inhibitors increase uptake of doxorubicin in cells close to blood vessels, have little effect on drug uptake into cells at intermediate distances, and might have a paradoxical effect to decrease doxorubicin uptake into distal cells. This effect probably contributes to the limited success of PgP inhibitors in clinical trials