s- and d-wave Symmetries in Nonadiabatic Theory of Superconductivity

High-$T_c$ superconductors have Fermi energies $E_F$ much smaller than conventional metals comparable to phonon frequencies. In such a situation nonadiabatic effects are important. A generalization of Eliashberg theory in the nonadiabatic regime has previously been shown to reproduce some anomalous features of the high-$T_c$ superconductors as for istance the enhancement of $T_c$ or the isotopic effects on $T_c$ and $m^*$. In this contribution we address the issue of the symmetry of the gap in the context of nonadiabatic superconductivity. We show that vertex corrections have a momentum structure which favours d-wave superconductivity when forward scattering is predominant. An additional increase of $T_c$ is also found.Comment: 6 pages, 3 eps figure, ijmpb-macros, proceeding of SATT10, to appear on Int. Journ. Mod. Phys.

Isotope effects in the Hubbard-Holstein model within dynamical mean-field theory

We study the isotope effects arising from the coupling of correlated electrons with dispersionless phonons by considering the Hubbard-Holstein model at half-filling within the dynamical mean-field theory. In particular we calculate the isotope effects on the quasi-particle spectral weight $Z$, the renormalized phonon frequency, and the static charge and spin susceptibilities. In the weakly correlated regime $U/t \lesssim 1.5$, where $U$ is the Hubbard repulsion and $t$ is the bare electron half-bandwidth, the physical properties are qualitatively similar to those characterizing the Holstein model in the absence of Coulomb repulsion, where the bipolaronic binding takes place at large electron-phonon coupling, and it reflects in divergent isotope responses. On the contrary in the strongly correlated regime $U/t \gtrsim 1.5$, where the bipolaronic metal-insulator transition becomes of first order, the isotope effects are bounded, suggesting that the first order transition is likely driven by an electronic mechanism, rather then by a lattice instability. These results point out how the isotope responses are extremely sensitive to phase boundaries and they may be used to characterize the competition between the electron-phonon coupling and the Hubbard repulsion.Comment: 10 pages, 8 figures. The paper has been already accepted on Phys. Rev.

Relevance of multiband Jahn-Teller effects on the electron-phonon interaction in A3A_3C60_{60}

Assessing the effective relevance of multiband effects in the fullerides is of fundamental importance to understand the complex superconducting and transport properties of these compounds. In this paper we investigate in particular the role of the multiband effects on the electron-phonon (el-ph) properties of the $t_{1u}$ bands coupled with the Jahn-Teller intra-molecular $H_g$ vibrational modes in the C$_{60}$ compounds. We show that, assuming perfect degeneracy of the electronic bands, vertex diagrams arising from the breakdown of the adiabatic hypothesis, are one order of magnitude smaller than the non-crossing terms usually retained in the Migdal-Eliashberg (ME) theory. These results permit to understand the robustness on ME theory found by numerical calculations. The effects of the non degeneracy of the $t_{1u}$ in realistic systems are also analyzed. Using a tight-binding model we show that the el-ph interaction is mainly dominated by interband scattering within a single electronic band. Our results question the reliability of a degenerate band modeling and show the importance of these combined effects in the $A_3$C$_{60}$ family.Comment: 5 pages, 3 eps figure

Characterization of DNA methylation as a function of biological complexity via dinucleotide inter-distances

We perform a statistical study of the distances between successive occurrencies of a given dinucleotide in the DNA sequence for a number of organisms of different complexity. Our analysis highlights peculiar features of the dinucleotide CG distribution in mammalian DNA, pointing towards a connection with the role of such dinucleotide in DNA methylation. While the CG distributions of mammals exhibit exponential tails with comparable parameters, the picture for the other organisms studied (e.g., fish, insects, bacteria and viruses) is more heterogeneous, possibly because in these organisms DNA methylation has different functional roles. Our analysis suggests that the distribution of the distances between dinucleotides CG provides useful insights in characterizing and classifying organisms in terms of methylation functionalities.Comment: 13 pages, 5 figures. To be published in the Philosophical Transactions A theme issue "DNA as information

Abstracts of the Giornate di Coniglicoltura ASIC 2007

(2008). Abstracts of the Giornate di Coniglicoltura ASIC 2007. World Rabbit Science. 16(2). doi:10.4995/wrs.2008.634SWORD16

Cataract and optic disk drusen in a patient with glycogenosis and di George syndrome: clinical and molecular report

Background We report the ophthalmic findings of a patient with type Ia glycogen storage disease (GSD Ia), DiGeorge syndrome (DGS), cataract and optic nerve head drusen (ONHD). Case presentation A 26-year-old white woman, born at term by natural delivery presented with a post-natal diagnosis of GSD Ia. Genetic testing by array-comparative genomic hybridization (CGH) for DGS was required because of her low levels of serum calcium. The patient has been followed from birth, attending the day-hospital every six months at the San Paolo Hospital, Milan, outpatient clinic for metabolic diseases and previously at another eye center. During the last day-hospital visit, a complete eye examination showed ONHD and cataract in both eyes. Next Generation Sequencing (NGS) was subsequently done to check for any association between the eye problems and metabolic aspects. Conclusions This is the first description of ocular changes in a patient with GSD Ia and DGS. Mutations explaining GSD Ia and DGS were found but no specific causative mutation for cataract and ONHD. The metabolic etiology of her lens changes is known, whereas the pathogenesis of ONHD is not clear. Although the presence of cataract and ONHD could be a coincidence; the case reported could suggest that hypocalcemia due to DGS could be the common biochemical pathway

O(^3P) +CO_2 Collisions at Hyperthermal Energies: Dynamics of Nonreactive Scattering, Oxygen Isotope Exchange, and Oxygen-Atom Abstraction

The dynamics of O(^3P) + CO_2 collisions at hyperthermal energies were investigated experimentally and theoretically. Crossed-molecular-beams experiments at Ecoll = 98.8 kcal mol^(–1) were performed with isotopically labeled ^(12)C^(18)O_2 to distinguish products of nonreactive scattering from those of reactive scattering. The following product channels were observed: elastic and inelastic scattering (^(16)O(^3P) + ^(12)C^(18)O^2), isotope exchange (^(18)O + ^(16)O^(12)C^(18)O), and oxygen-atom abstraction (^(18)O^(16)O + ^(12)C^(18)O). Stationary points on the two lowest triplet potential energy surfaces of the O(^3P) + CO_2 system were characterized at the CCSD(T)/aug-cc-pVTZ level of theory and by means of W4 theory, which represents an approximation to the relativistic basis set limit, full-configuration-interaction (FCI) energy. The calculations predict a planar CO_3(C_(2v),^3A″) intermediate that lies 16.3 kcal mol^(–1) (W4 FCI excluding zero point energy) above reactants and is approached by a C_(2v) transition state with energy 24.08 kcal mol^(–1). Quasi-classical trajectory (QCT) calculations with collision energies in the range 23–150 kcal mol^(–1) were performed at the B3LYP/6-311G(d) and BMK/6-311G(d) levels. Both reactive channels observed in the experiment were predicted by these calculations. In the isotope exchange reaction, the experimental center-of-mass (c.m.) angular distribution, T(θ_(c.m.)), of the ^(16)O^(12)C^(18)O products peaked along the initial CO_2 direction (backward relative to the direction of the reagent O atoms), with a smaller isotropic component. The product translational energy distribution, P(E_T), had a relatively low average of E_T = 35 kcal mol^(–1), indicating that the ^(16)O^(12)C^(18)O products were formed with substantial internal energy. The QCT calculations give c.m. P(E_T) and T(θ_(c.m.)) distributions and a relative product yield that agree qualitatively with the experimental results, and the trajectories indicate that exchange occurs through a short-lived CO_3^* intermediate. A low yield for the abstraction reaction was seen in both the experiment and the theory. Experimentally, a fast and weak ^(16)O^(18)O product signal from an abstraction reaction was observed, which could only be detected in the forward direction. A small number of QCT trajectories leading to abstraction were observed to occur primarily via a transient CO_3 intermediate, albeit only at high collision energies (149 kcal mol^(–1)). The oxygen isotope exchange mechanism for CO_2 in collisions with ground state O atoms is a newly discovered pathway through which oxygen isotopes may be cycled in the upper atmosphere, where O(^3P) atoms with hyperthermal translational energies can be generated by photodissociation of O_3 and O_2

Formulation and evaluation of new oxazaphosphorine prodrugs-loaded lipid nanocapsules for cancer treatment

Oxazaphosphorines (cyclophosphamide (CPA) and ifosfamide (IFO)) represent an important group of therapeutic molecules due to their substantial antitumor and immunomodulating activities. Unfortunately, despite the benefits brought by these molecules, their clinical use shows limitations, notably in chemotherapy, due to the development of resistance, interpatients variation and toxicities (urinary toxicity, neurotoxicity and nephrotoxicity). To circumvent these problems, new oxazaphosphorine analogs have been synthetized and present an interesting anti-tumor activity alone with reduced toxicity [1]. Pentanoxy moiety has been grafted on C4 position of ifosfamide (P-IFO). Nevertheless, these new analogs are lipophilic and unstable in aqueous medium. To administer it, this paper proposes to formulate this analog into nanocarriers. Lipid nanocapsules form a new generation of nanovector that can encapsulate a number of anticancer agents [2]. In the present research, P-IFO-loaded LNCs were formulated and characterized. A new formulation based on glycerol monooleate (Peceol®) was developed, optimized and then characterized. Batches of P-IFO-LNCs were obtained with a size of 47.2±0.7nm with a narrow size distribution and a drug payload of 8.42±1.05mg/g. The suspension remained stable at 4°C for 14 days in terms of mean particle size, polydispersity index and pH. The drug payload decreased after 7 days but a high rate was still found (5.88±1.01mg/g) up to 14 days. The stealth properties of these nanoparticles were examined in vitro using the complement activation (CH50) test. This test revealed a low consumption of plasma protein in the presence of such P-IFO-LNCs. In vitro cytotoxicity of P-IFO-LNCs was determined in two human cell lines; i.e. rhabdomyosarcoma (RMS-1) and Ewing sarcoma (A673) and showed a similar activity compared to the free form. Finally, in vivo activity testing of P-IFO-LNCs is in progress in a murine model bearing a RMS-1 xenograft after intravenous administration. References [1] Skarbek C, et al., Preactivated Oxazaphosphorines Designed for Isophosphoramide Mustard Delivery as Bulk Form or Nanoassemblies: Synthesis and Proof of Concept. Journal of Medicinal Chemistry. 22;58(2):105-17, 2015. [2] Huynh NT, et al., Lipid nanocapsules: A new platform for nanomedicine. International Journal of Pharmaceutics. 379(2):201–9, 2009. Acknowledgments: The authors are very grateful to the Ligue contre le Cancer, Comité du Maine et Loire and Comité d’Ille et Vilaine which founded this work

NEPA (netupitant/palonosetron) for the antiemetic prophylaxis of nausea and vomiting induced by chemotherapy (CINV) with Folfirinox and Folfoxiri even during the COVID-19 pandemic: A real-life study

OBJECTIVE: The outbreak of coronavirus disease 2019 (COVID-19) has affected the treatment of cancer patients, with particular regard to the management of both chemotherapy and side effects. Chemotherapy-induced nausea and vomiting (CINV) are amongst the most troublesome side effects that impair patients’ adherence to treatments and their quality of life (QoL). NEPA (Akynzeo®), is an oral fixed-dose combination of netupitant [a neurokinin-1 receptor antagonist (NK1RA), 300 mg] and palonosetron [(5-hydroxytryptamine (serotonin or 5HT) type3 receptor antagonist (5HT3RA), 0.5 mg] which has been shown to be effective in preventing CINV. PATIENTS AND METHODS: This prospective study started before the outbreak of COVID-19 and was carried out during the pandemic period. The aim was to evaluate the efficacy and safety of a single oral dose NEPA plus 12 mg of dexamethasone (DEX) in patients treated with Folfoxiri plus Bevacizumab and Folfirinox. The patients were diagnosed with advanced colorectal cancer (CRC) or advanced pancreatic ductal adenocarcinoma (PDAC). They were divided into two groups: naïve patients and patients previously treated with serotonin receptor antagonists (5HT3-RA) and neurokin-1 receptor antagonists (NK1-RA). RESULTS: During the overall phase, the complete response (CR) rate was 96.8% in naïve patients treated with Folfoxiri plus Bevacizumab, and 94.6% in patients treated with Folfirinox. During the acute and delayed phases, the CR rate was 92.8% and 94.2%, with Folfoxiri and Bevacizumab, as well as 96.2% and 94.6%, with Folfirinox. There was no adequate control of CINV events in patients on antiemetic prophylaxis with 5HT3-RA or NK1-RA associated with cortisone. During the overall phase, the CR rate was 74.6% with Folfoxiri plus Bevacizumab and 75.8% with Folfirinox. During the acute and delayed phases, the CR rate was 72.5% and 74.8% with Folfoxiri plus Bevacizumab, as well as 75.2% and 74.6% with Folfirinox. CONCLUSIONS: This study has shown the therapeutic benefits of NEPA in the management and prophylaxis of CINV events, both in naive patients and patients previously treated with 5HT3-RA and NK1-RA. In addition, NEPA has been shown to be safe, both before and during the COVID-19 pandemic