Thrombose du sinus lateral et de la veine jugulaire apres un traumatisme cranien ferme

Introduction Les traumatismes crâniens fermés représentent une étiologie exceptionnelle des thromboses veineuses cérébrales (TVC). Seule une trentaine de cas sont rapportés, contrastant avec la grande fréquence des traumatismes crâniens. Cette situation pose des difficultés diagnostiques pouvant expliquer le pronostic relativement mauvais des TVC post traumatiques.Objectif Rapporter un cas de thrombose veineuse après un traumatisme crânien fermé.Observation Un patient de 23 ans suivi pour une schizophrénie, a présenté suite à une tentative de suicide, un traumatisme crânien fermé sans anomalie clinique ou à la TDM cérébrale initiale. Après un intervalle de 48 heures, un syndrome d’hypertension intracrânienne est apparu de façon rapide. Une thrombose du sinus latéral droit, étendue à la veine jugulaire a été découverte fortuitement sur la TDM cérébrale et confirmée par l’angio-IRM. Le reste du bilan étiologique de cette TVC est resté négatif et les anticoagulants ont permis une amélioration rapide des symptômes.Conclusion Dans les suites d’un traumatisme crânien, l’apparition de symptômes neurologiques, en particulier d’une HTIC doit faire rechercher une TVC après avoir éliminé des causes plus classiques à ce contexte (hématomes intracrâniens).Mots clés : Thrombose veineuse cérébrale; traumatisme crânien; anticoagulants

Crystal structure of (1E, 1'E)-N, N'-(ethane-1,2-diyl) bis(pyridin-2-yl)methanimine]

The whole molecule of the title compound, C14H14N4, is generated by twofold rotation symmetry. The twofold axis bisects the central -CH2-CH2-bond and the planes of the pyridine rings are inclined to one another by 65.60 (7)degrees. In the crystal, there are no significant intermolecular interactions present

1H-Indole-3-carbaldehyde

In the title compound, C9H7NO, the benzene ring forms a dihedral angle of 3.98 (12)° with the pyrrole ring. In the crystal, N–H⋯O hydrogen bonds links the mol­ecules into chains which run parallel to [02-1]

Stabilnost amlodipin besilata i atenolola u jednoslojnim i dvoslojnim tabletama

Multi-drug tablets of amlodipine besylate and atenolol were prepared as either mono-layer (mixed matrix) or bi-layer tablets containing each drug in a separate layer by using similar excipients and processing. Each tablet batch was packed in strip and blister packs and kept under accelerated temperature and humidity conditions. The stability of two tablet and packaging types was compared by HPLC analysis after 0, 1, 3 and 4.5 months and expressed as the content of intact amlodipine and atenolol. The content of atenolol did not decline regardless of tablet and packaging type. Amlodipine content in bi-layer tablets decreased to about 95 and 88% when packed in strips and blisters, respectively. When prepared as mono-layer tablets, the content decreased to 72 and 32%, respectively. The study revealed that the bi-layer tablet formulation was more stable than the mono-layer type. Further, the stability was increased when the tablets were packed in aluminium strips as compared to PVC blisters.Tablete s amlodipinom i atenololom pripremljene su ili u obliku jednoslojne tablete (miješani matriks) ili kao dvoslojne tablete (lijekovi u zasebnim slojevima) koristeći slične pomoćne tvari i uvjete tabletiranja. Tablete su pakirane u dvije vrste pakiranja, aluminijske folije (strip) ili PVC (blister) i čuvane u uvjetima ubrzanog starenja. Stabilnost je određivana pomoću HPLC metode nakon 0, 1, 2, 3 i 4,5 mjeseci i izražena kao sadržaj intaktnog lijeka. Sadržaj atenolola nije se značajno promijenio bez obzira na tip tablete ili pakiranje. Sadržaj amlodipina u dvoslojnim tabletama smanjio se na 95 % (tablete u strip pakiranju) i 88 % (tablete u blister pakiranju). Istodobno, u jednoslojnom tipu kombiniranih tableta sadržaj se smanjio na 72 % (strip pakiranje) i 32 % (blister pakiranje). Rezultati pokazuju da su dvoslojne tablete s amlodipinom i atenololom stabilnije od jednoslojnih. Štoviše, pakiranje tableta u aluminijsku foliju u obliku strip pakiranja povećava njihovu stabilnost u usporedbi s PVC pakirnim materijalom (blister)

Measurements of 220Rn and 222Rn and CO2 emissions in soil and fumarole gases on Mt. Etna volcano (Italy) : implications for gas transport and shallow ground fracture

Author Posting. © American Geophysical Union, 2007. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry Geophysics Geosystems 8 (2007): Q10001, doi:10.1029/2007GC001644.Measurements of 220Rn and 222Rn activity and of CO2 flux in soil and fumaroles were carried out on Mount Etna volcano in 2005–2006, both in its summit area and along active faults on its flanks. We observe an empirical relationship between (220Rn/222Rn) and CO2 efflux. The higher the flux of CO2, the lower the ratio between 220Rn and 222Rn. Deep sources of gas are characterized by high 222Rn activity and high CO2 efflux, whereas shallow sources are indicated by high 220Rn activity and relatively low CO2 efflux. Excess 220Rn highlights sites of ongoing shallow rock fracturing that could be affected by collapse, as in the case of the rim of an active vent. Depletion both in 220Rn and in CO2 seems to be representative of residual degassing along recently active eruptive vents.This work was funded by the Istituto Nazionale di Geofisica e Vulcanologia (S.G., M.N.) and by the Dipartimento per la Protezione Civile (Italy), projects V3_6/28-Etna (M.N.) and V5/08-Diffuse degassing in Italy (S.G.), and NSF EAR 063824101 (K.W.W.S.)

Large-scale interaction profiling of PDZ domains through proteomic peptide-phage display using human and viral phage peptidomes

The human proteome contains a plethora of short linear motifs (SLiMs) that serve as binding interfaces for modular protein domains. Such interactions are crucial for signaling and other cellular processes, but are difficult to detect because of their low to moderate affinities. Here we developed a dedicated approach, proteomic peptide-phage display (ProP-PD), to identify domain-SLiM interactions. Specifically, we generated phage libraries containing all human and viral C-terminal peptides using custom oligonucleotide microarrays. With these libraries we screened the nine PSD-95/ Dlg/ZO-1 (PDZ) domains of human Densin-180, Erbin, Scribble, and Disks large homolog 1 for peptide ligands. We identified several known and putative interactions potentially relevant to cellular signaling pathways and confirmed interactions between fulllength Scribble and the target proteins β-PIX, plakophilin-4, and guanylate cyclase soluble subunit a-2 using colocalization and coimmunoprecipitation experiments. The affinities of recombinant Scribble PDZ domains and the synthetic peptides representing the C termini of these proteins were in the 1- to 40-μM range. Furthermore, we identified several well-established host-virus protein- protein interactions, and confirmed that PDZ domains of Scribble interact with the C terminus of Tax-1 of human T-cell leukemia virus with micromolar affinity. Previously unknown putative viral protein ligands for the PDZ domains of Scribble and Erbin were also identified. Thus, we demonstrate that our ProP-PD libraries are useful tools for probing PDZ domain interactions. The method can be extended to interrogate all potential eukaryotic, bacterial, and viral SLiMs and we suggest it will be a highly valuable approach for studying cellular and pathogen-host protein-protein interactions

Epitope-specific antibody responses differentiate COVID-19 outcomes and variants of concern

BACKGROUND. The role of humoral immunity in COVID-19 is not fully understood, owing, in large part, to the complexity of antibodies produced in response to the SARS-CoV-2 infection. There is a pressing need for serology tests to assess patient-specific antibody response and predict clinical outcome. METHODS. Using SARS-CoV-2 proteome and peptide microarrays, we screened 146 COVID-19 patients’ plasma samples to identify antigens and epitopes. This enabled us to develop a master epitope array and an epitope-specific agglutination assay to gauge antibody responses systematically and with high resolution. RESULTS. We identified linear epitopes from the spike (S) and nucleocapsid (N) proteins and showed that the epitopes enabled higher resolution antibody profiling than the S or N protein antigen. Specifically, we found that antibody responses to the S-811–825, S-881–895, and N-156–170 epitopes negatively or positively correlated with clinical severity or patient survival. Moreover, we found that the P681H and S235F mutations associated with the coronavirus variant of concern B.1.1.7 altered the specificity of the corresponding epitopes. CONCLUSION. Epitope-resolved antibody testing not only affords a high-resolution alternative to conventional immunoassays to delineate the complex humoral immunity to SARS-CoV-2 and differentiate between neutralizing and non-neutralizing antibodies, but it also may potentially be used to predict clinical outcome. The epitope peptides can be readily modified to detect antibodies against variants of concern in both the peptide array and latex agglutination formats. FUNDING. Ontario Research Fund (ORF) COVID-19 Rapid Research Fund, Toronto COVID-19 Action Fund, Western University, Lawson Health Research Institute, London Health Sciences Foundation, and Academic Medical Organization of Southwestern Ontario (AMOSO) Innovation Fund

Razvoj i vrednovanje lako topljivih tableta kompleksa meloksikama s β-ciklodekstrinom pripravljenih izravnom kompresijom

The aim of this study was to prepare fast-dissolving tablets of meloxicam after its complexation with β-cyclodextrin (β-CD) and to investigate the effect of using different superdisintegrants on the disintegration and release of meloxicam from the tablets. A complex of meloxicam with β-CD was prepared by spray drying and then compressed in the form of tablets utilizing the direct compression technique. Three superdisintegrants were employed at various levels sodium starch glycolate, croscarmellose sodium, and crospovidone. Co-spray dried micro-crystalline cellulose and mannitol (Avicel HFE-102) were used as diluents in the tablets. Prior to compression, the pre-compression parameters showed satisfactory flow properties. Post-compression parameters showed that all tablet formulations had acceptable mechanical properties. Wetting and disintegration times were prolonged by increasing the level of sodium starch glycolate in the tablets. This was attributed to the formation of a viscous gel layer around the tablets by sodium starch glycolate whereas this effect was not observed with croscarmellose sodium and crospovidone. Dissolution studies showed fast release of meloxicam except in tablets containing a high level of sodium starch glycolate. Complexation of meloxicam with β-CD significantly improved the solubility of the drug and improved the mechanical properties of tablets produced by direct compression.Cilj rada bio je priprava lako topljivih tableta kompleksa meloksikama s β-ciklodekstrinom (β-CD) te ispitati utjecaj različitih superdezintegratora na raspadljivost tableta i oslobađanje meloksikama. Kompleks meloksikama s β-CD pripravljen je metodom sušenja sprejem, a komprimiran je u tablete metodom izravne kompresije. U pripravi tableta korištene su tri različite količine triju superdezintegratora: natrijev škrobni glikolat, natrijeva sol kroskarmeloze i krospovidon, dok su mikrokristalinična celuloza i manitol (Avicel HFE-102) upotrijebljeni kao punila. Predkompresijski parametri ukazivali su na zadovoljavajuću tečnost. Postkompresijski parametri pokazali su da sve tablete imaju prihvatljiva mehanička svojstva. Vlaženje i vrijeme raspadanja bilo je produljeno kada se povećao udio natrijevog škrobnog glikolata u tabletama. To je pripisano stvaranju viskoznog sloja gela oko tableta, što nije primijećeno u pripravi tableta s natrijevom soli kroskarmeloze i krospovidonom. Oslobađanje meloksikama bilo je brzo iz svih tableta, osim iz tableta s visokim udjelom natrijeve soli škrobnog glikolata. Kompleksiranje meloksikama s β-CD značajno je povećalo topljivost lijeka i poboljšalo mehanička svojstva tableta