Unique Spectrum Research Articles

Spectroscopic Identification of Bacteria Resistance to Antibiotics by Means of Absorption of Specific Biochemical Groups and Special Machine Learning Algorithm.

FTIR (Fourier transform infrared spectroscopy) is one analytical technique of the absorption of infrared radiation. FTIR can also be used as a tool to characterize profiles of biomolecules in bacterial cells, which can be useful in differentiating different bacteria. Considering that different bacterial species have different molecular compositions, it will then result in unique FTIR spectra for each species and even bacterial strains. Having this important tool, here, we have developed a methodology aimed at refining the analysis and classification of the FTIR absorption spectra obtained from samples of Staphylococcus aureus, with the implementation of machine learning algorithms. In the first stage, the system conforming to four specified species groups, Control, Amoxicillin induced (AMO), Gentamicin induced (GEN), and Erythromycin induced (ERY), was analyzed. Then, in the second stage, five hidden samples were identified and correctly classified as with/without resistance to induced antibiotics. The total analyses were performed in three windows, Carbohydrates, Fatty Acids, and Proteins, of five hundred spectra. The protocol for acquiring the spectral data from the antibiotic-resistant bacteria via FTIR spectroscopy developed by Soares et al. was implemented here due to demonstrating high accuracy and sensitivity. The present study focuses on the prediction of antibiotic-induced samples through the implementation of the hierarchical cluster analysis (HCA), principal component analysis (PCA) algorithm, and calculation of confusion matrices (CMs) applied to the FTIR absorption spectra data. The data analysis process developed here has the main objective of obtaining knowledge about the intrinsic behavior of S. aureus samples within the analysis regions of the FTIR absorption spectra. The results yielded values with 0.7 to 1 accuracy and high values of sensitivity and specificity for the species identification in the CM calculations. Such results provide important information on antibiotic resistance in samples of S. aureus bacteria for potential application in the detection of antibiotic resistance in clinical use.

Critical Review on Broad Spectrum Action of Vasti Karma - A Literary Study

Ayurveda views a person's Tridosha balance as indicative of their overall health, and Pancakarma treatment aims to restore harmony and normality by purging the vitiated Dosha. One of the five Pancakarma procedures, Vasti karma is a unique and broad spectrum therapeutic and preventive strategy. The objective of this study was to determine why Vasti karma has emerged as a key Panchakarma therapeutic strategy. The study's data sources included primary Ayurvedic texts, secondary Ayurvedic medical literature, and scientific publications that were published online. Vasti is said to purge or calm vitiated Vata and further normalize its activities. Vasti is alleged to have a multifaceted activity that possesses preventative, curative, and promotional effects. As a result, it is recognized as the best course of therapy and a viable alternative to small surgeries. In contemporary medicine, enema is primarily used to remove feces from the large intestine, whereas in Ayurveda, Vasti is a route of drug administration for multiple actions, acting both locally in the large intestine and systemically on the body tissues, which is why it is considered to be a "Ardha chikitsa" as well as a "complete Chikitsa" due to its wider applicability and greater disease-curing ability. It ultimately comes to the conclusion that Vasti is the supreme and primary Panchakarma therapy method since it demonstrates broad spectrum action that may be used on a huge variety of disorders.

Progress on Hybrids and Mixed Alloys of Boron Subphthalocyanines (BsubPc) and Boron Subnaphthalocyanines (BsubNc); Tuning the Electrochemical Properties Towards Organic Electronic Applications

Our research and development focus has been on the molecular design, synthetic methodology and in-depth characterization of boron subphthalocyanines (BsubPcs) and subnaphthalocyanines (BsubNcs) to apply them to organic electronic applications. BsubPcs, BsubNcs and their hybrids are macrocycles with a chelated central boron atom via nitrogen bonding, and is a p-conjugated macrocyclic material. Our focal point balances between the basic and applied chemistry, chemical engineering, their in-depth physical properties (electrochemistry included). We also do computational modelling. Once materials are developed, we merge them into organic electronics to function as light emitting, light absorbing and electronic conducting materials within organic light emitting diodes (OLEDs) and organic photovoltaics (OPVs)/organic solar cells (OSCs). The basic electrochemical and photophysical properties, developing and evaluating the properties is critical to move onto such applications.For this presentation, I will focus on our progress on the development of hybrids and mixed alloys of BsubPcs and BsubNcs.Regarding hybrids, they are a mixture of BsubPcs and BsubNcs, and are formed via a reaction of a statistical distribution of phthalonitrile and 2,3-dicyanonaphthalene intermediates on reaction with BCl3; we have named them X-RnBsub(Pcx-Ncy); X the axial substituent, Rn the number of peripheral substitutions, Pcx being the number of 6 p-conjugated bonds, Ncy being the number of 10 p-conjugated bonds (Figure). On first study, we found that X-RnBsub(Pc1-Nc2) have low photostability. Therefore, we moved onto developing a ‘statistical’ synthetic methodology to target highest yields of X-RnBsub(Pc2-Nc1)s, and we did achieve relatively high yields. X-RnBsub(Pc2-Nc1)s therefore could be purified to enable physical characterization. Within a couple past publications, the unique absorption spectra was noted and we have confirmed its uniqueness. The X-RnBsub(Pc2-Nc1)s absorption spectra is as wide as if BsubPc and BsubNc were mixed together. This therefore has good potential to harvest a larger scope of photons from solar or to achieved FRET transfer from a host to emit via an OLED. We then did in-depth first electrochemical characterization, confirmed their electrochemical oxidation and reduction stability and also did in-depth photoluminescence characterization. Therefore, merging X-RnBsub(Pc2-Nc1)s into organic electronic devices as well as other chemistry to synthesis the hybrids is ongoing.Regarding mixed alloys, in the past as we have shown that BsubNcs ended up being a mixed alloyed composition with random bay-position halogenation, that is formed during the reaction of BCl3 with 2,3-dicyanonaphthalene at temperature, which is the process to form the BsubNcs. The random bay-position halogenation has been shown to be impactful in a positive way within OPV devices, negative within OLED devices and also has electrochemical variations and good reversibility. Ongoing, given it is random halogenation, and some of the positive outcomes, this justifies considering additional mixed alloyed compositions.We have also recently shown that mixed alloyed BsubPcs can be formed with three peripheral halogens in the alpha (a) or beta (b) positions, named as Cl-αCl3BsubPc, Cl-βCl3BsubPc, Cl-αF3BsubPc, and Cl-βF3BsubPc. The alloyed mixtures consisted of C1 and C3 isomers of trihalogenated BsubPcs. The physical properties characterization including photophysics, electrochemistry, and thermal characterization, were studied and were also positive and then were engineered into OSCs as electron donors and electrons acceptors to clarify their impact on device performance which had positivity aspects. Therefore, we moved onto developing a set of additional BsubPc mixtures. To be outlined for this presentation, we considered sets of phthalonitrile mixtures to form peripherally halogenated BsubPc mixtures during the formation of BsubPcs from these intermediates. For example, 4,5-dichlorophthalonitrile (Cl2-pn), 4,5-difluorophthalonitrile (F2-pn), tetrachlorophthalonitrile (Cl4-pn), and tetrafluorophthalonitrile (F4-pn) are commercially available compounds that were mixed together and yields a mixture of BsubPc which we named: X-Cl2nF2mBsubPc and X-Cl4nF4mBsubPc (X = Cl or F being a variant, Figure). We then did physical characterization and found positive aspects including electrochemical oxidation and reduction stability. Merging them into organic electronic devices is ongoing and might be present during this presentation time.We did also recently develop additional chemistry methodology to develop additional mixed alloyed BsubPcs. The methodology was to develop phthalonitrile intermediates that have numbers of hydrogen, chlorine and fluorine substitutions and to take them onto the formation of the BsubPc mixed alloys. This is ongoing and may have some aspects to outline during this presentation.We also do computational modelling to look into other relative impacts of the materials being developed, for example the HOMO and LUMO orbital distributions, the local ionization etc. This will also be outlined during this presentation. Figure 1

Color Centers in Hexagonal Boron Nitride.

Atomically thin two-dimensional (2D) hexagonal boron nitride (hBN) has emerged as an essential material for the encapsulation layer in van der Waals heterostructures and efficient deep ultraviolet optoelectronics. This is primarily due to its remarkable physical properties and ultrawide bandgap (close to 6 eV, and even larger in some cases) properties. Color centers in hBN refer to intrinsic vacancies and extrinsic impurities within the 2D crystal lattice, which result in distinct optical properties in the ultraviolet (UV) to near-infrared (IR) range. Furthermore, each color center in hBN exhibits a unique emission spectrum and possesses various spin properties. These characteristics open up possibilities for the development of next-generation optoelectronics and quantum information applications, including room-temperature single-photon sources and quantum sensors. Here, we provide a comprehensive overview of the atomic configuration, optical and quantum properties, and different techniques employed for the formation of color centers in hBN. A deep understanding of color centers in hBN allows for advances in the development of next-generation UV optoelectronic applications, solid-state quantum technologies, and nanophotonics by harnessing the exceptional capabilities offered by hBN color centers.

Interaction Study of Energetic Protons and Electrons with the Vacuum Ultra Violet Source used in the Complex Irradiation Facility

Context: One important factor to be considered for space missions is the radiation environment. It is composed of energetic particles, such as protons, electrons and ions, and electromagnetic radiation, photons ranging from Vacuum Ultra Violet (VUV) to Far Infrared (FIR). Each of these radiation sources have an unique energy spectrum that further depends on the location inside the solar system, e. g. Earth orbits or interplanetary space.For material qualification and material engineering, individual irradiation is considered and their effects are superimposed. However, effects occurring when two and more radiation types simultaneously are present have barely been investigated yet. Further complexity is added, when additional interactions take place due to laboratory hardware. Aims: This publication reports on the efforts made to analyse and measure the interaction of a VUV and corpuscular radiation sources. The aim is to quantify the deviations due to interactions and conclude consequences for the simultaneous operation of these radiation sources. Methods: In order to quantify the effects, the Complex Irradiation Facility (CIF), located at the DLR Bremen has been used. It connects proton and electron accelerators together with VUV and UV light sources to an ultra high vacuum chamber. The corpuscular and VUV radiation sources have been operated simultaneously. The reaction of the operation parameters, such as current measured with Faraday Cups (FC) has been tracked and post-processed. Results: It has been discovered, that protons considerably interact with the gas mixture used to operate the VUV source. This interaction decreases for higher beam intensities of the corpuscular irradiation. It was found, that this is likely due to protons ionizing gas atoms which are then measured by the FC as current. For electrons, this phenomena was not observed due to their smaller stopping power. The discovery restricts the acceleration factor of the CIF for proton together with VUV irradiation, but does not necessarily limit the range of application of the CIF depending on the requirements of the material and/or qualification test. Energy range of electrons stays unrestricted.

T-cell receptor beta variable gene polymorphism predicts immune-related adverse events during checkpoint blockade immunotherapy

BackgroundImmune checkpoint inhibitors have revolutionized cancer treatment. However, they are associated with a unique spectrum of side effects, called immune-related adverse events (irAEs), which can cause significant morbidity and quickly...

Nanoadjuvants: Promising Bioinspired and Biomimetic Approaches in Vaccine Innovation.

Adjuvants are the important part of vaccine manufacturing as they elicit the vaccination effect and enhance the durability of the immune response through controlled release. In light of this, nanoadjuvants have shown unique broad spectrum advantages. As nanoparticles (NPs) based vaccines are fast-acting and better in terms of safety and usability parameters as compared to traditional vaccines, they have attracted the attention of researchers. A vaccine nanocarrier is another interesting and promising area for the development of next-generation vaccines for prophylaxis. This review looks at the various nanoadjuvants and their structure-function relationships. It compiles the state-of-art literature on numerous nanoadjuvants to help domain researchers orient their understanding and extend their endeavors in vaccines research and development.

Angular correlations on causally-coherent inflationary horizons

We develop a model for correlations of cosmic microwave background (CMB) anisotropy on the largest angular scales, based on standard causal geometrical relationships in slow-roll inflation. Unlike standard models based on quantized field modes, it describes perturbations with nonlocal directional coherence on spherical boundaries of causal diamonds. Causal constraints reduce the number of independent degrees of freedom, impose new angular symmetries, and eliminate cosmic variance for purely angular 2-point correlations. Distortions of causal structure from vacuum fluctuations are modeled as gravitational memory from randomly oriented outgoing and incoming gravitational null shocks, with nonlocally coherent directional displacements on curved surfaces of causal diamonds formed by standard inflationary horizons. The angular distribution is determined by axially symmetric shock displacements on circular intersections of the comoving sphere that represents the CMB photosphere with other inflationary horizons—those centered on it, and those that pass through an observer’s world line. Displacements on thin spheres at the end of inflation have a unique angular power spectrum that approximates the standard expectation on small angular scales, but differs substantially at large angular scales due to horizon curvature. For a thin sphere, the model predicts a universal angular correlation function with an exact ‘causal shadow’ symmetry, , and significant large-angle parity violation. We apply a rank statistic to compare models with WMAP and Planck satellite data, and find that a causally-coherent model with no shape parameters or cosmic variance agrees with the measured better than a large fraction () of standard model realizations. Model-independent tests of holographic causal symmetries are proposed.

Unique Spectrum of Activating BRAF Alterations in Prostate Cancer.

Alterations in BRAF have been reported in 3% to 5% of prostate cancer, although further characterization is lacking. Here, we describe the nature of BRAF alterations in prostate cancer using a large cohort from commercially available tissue and liquid biopsies subjected to comprehensive genomic profiling (CGP). Tissue and liquid biopsies from patients with prostate cancer were profiled using FoundationOne CDx and FoundationOne Liquid CDx CGP assays, respectively. Tissue biopsies from non-prostate cancer types were used for comparison (n = 275,151). Genetic ancestry was predicted using a single-nucleotide polymorphism (SNP) based approach. Among 15,864 tissue biopsies, BRAF-activating alterations were detected in 520 cases (3.3%). The majority (463 samples, 2.9%) harbored class II alterations, including BRAF rearrangements (243 samples, 1.5%), K601E (101 samples, 0.6%), and G469A (58 samples, 0.4%). BRAF-altered prostate cancers were enriched for CDK12 mutations (OR, 1.87; 9.2% vs. 5.2%; P = 0.018), but depleted in TMPRSS2 fusions (OR, 0.25; 11% vs. 32%; P < 0.0001), PTEN alterations (OR, 0.47; 17% vs. 31%; P < 0.0001), and APC alterations (OR, 0.48; 4.4% vs. 8.9%; P = 0.018) relative to BRAF wild-type (WT) disease. Compared with patients of European ancestry, BRAF alterations were more common in tumors from patients of African ancestry (5.1% vs. 2.9%, P < 0.0001) and Asian ancestry (6.0% vs. 2.9%, P < 0.001). Activating BRAF alterations were detected in approximately 3% of prostate cancers, and most were class II mutations and rearrangements; BRAF V600 mutations were exceedingly rare. These findings suggest that BRAF activation in prostate cancer is unique from other cancers and supports further clinical investigation of therapeutics targeting the mitogen-activated protein kinase (MAPK) pathway.

Validating MALDI-IMS Feasibility in Ex Vivo Brain Slices.

Matrix-assisted laser desorption ionization imaging mass spectrometry (MALDI-IMS) generates unique mass spectra in X/Y coordinates across a tissue sample, thus allowing for the spatial detection and relative quantification of biologic compounds in situ. The soft ionization of MALDI-IMS makes it an ideal technique for high-resolution imaging of complex lipid species. Lipid-based spatial chemical maps derived from MALDI-IMS provide critical insight into the unique molecular profiles of a variety of neurologic diseases. Ex vivo brain slice preparations are a prominent alternative to in vivo animal models for studying many different neurologic conditions. For the first time, we present a feasible protocol for achieving reproducible lipidomic MALDI-IMS data from ex vivo rat brain slices and provide evidence that ex vivo brain slices maintain spatiochemical lipidomic profiles representative of an intact whole brain. We conducted a methods comparison assessing the lipid profiles within the neocortex, striatum, and corpus callosum between coronal sections taken from ex vivo brain slices and the current gold standard tissue preparation method, fresh frozen whole brains. For the first time we demonstrate a technique by which 400 μm ex vivo brain slices can be extracted from an imaging chamber and prepared for MALDI-IMS in a way that preserves their lipidomic integrity. We demonstrate the feasibility of MALDI-IMS in ex vivo brain slices and provide a roadmap for MALDI-IMS utilization in uncharted neuroscience fields.

Highly Luminescent Lanthanide Metal‐Organic Frameworks with Tunable Color for Nanomolar Detection of Iron(III), Ofloxacin and Gossypol and Anti‐counterfeiting Applications

AbstractSolvothermal reaction of 5,5′‐(pyridine‐2,6‐diylbis(oxy))diisophthalic acid (H4L) with europium(III) or terbium(III) nitrates in acetonitrile‐water (1 : 1) at 120 °C gave rise to isostructural 2D coordination polymers, [Ln(HL)(H2O)3]∞ (NIIC‐1‐Eu and NIIC‐1‐Tb), the layers of which are composed by eight‐coordinated lanthanide(III) ions interconnected by triply deprotonated ligands HL3−. The layers are packed in the crystal without any specific intermolecular interactions between them, allowing the facile preparation of stable water suspensions, in which NIIC‐1‐Tb exhibited top‐performing sensing properties through luminescence quenching effect with exceptionally low detection limits towards Fe3+ (LOD 8.62 nM), ofloxacin (OFX) antibiotic (LOD 3.91 nM) and cotton phytotoxicant gossypol (LOD 2.27 nM). In addition to low detection limit and high selectivity, NIIC‐1‐Tb features fast sensing response (within 60–90 seconds), making it superior to other MOF‐based sensors for metal cations and organic toxicants. The photoluminescence quantum yield of NIIC‐1‐Tb was 93 %, one of the highest among lanthanide MOFs. Mixed‐metal coordination polymers NIIC‐1‐EuxTb1−x demonstrated efficient photoluminescence, the color of which could be modulated by the excitation wavelength and time delay for emission monitoring (within 1 millisecond). Furthermore, an original 2D QR‐coding scheme was designed for anti‐counterfeiting labeling of goods based on unique and tunable emission spectra of NIIC‐1‐Ln coordination polymers.

Highly Luminescent Lanthanide Metal-Organic Frameworks with Tunable Color for Nanomolar Detection of Iron(III), Ofloxacin and Gossypol and Anti-counterfeiting Applications.

Solvothermal reaction of 5,5'-(pyridine-2,6-diylbis(oxy))diisophthalic acid (H4 L) with europium(III) or terbium(III) nitrates in acetonitrile-water (1 : 1) at 120 °C gave rise to isostructural 2D coordination polymers, [Ln(HL)(H2 O)3 ]∞ (NIIC-1-Eu and NIIC-1-Tb), the layers of which are composed by eight-coordinated lanthanide(III) ions interconnected by triply deprotonated ligands HL3- . The layers are packed in the crystal without any specific intermolecular interactions between them, allowing the facile preparation of stable water suspensions, in which NIIC-1-Tb exhibited top-performing sensing properties through luminescence quenching effect with exceptionally low detection limits towards Fe3+ (LOD 8.62 nM), ofloxacin (OFX) antibiotic (LOD 3.91 nM) and cotton phytotoxicant gossypol (LOD 2.27 nM). In addition to low detection limit and high selectivity, NIIC-1-Tb features fast sensing response (within 60-90 seconds), making it superior to other MOF-based sensors for metal cations and organic toxicants. The photoluminescence quantum yield of NIIC-1-Tb was 93 %, one of the highest among lanthanide MOFs. Mixed-metal coordination polymers NIIC-1-Eux Tb1-x demonstrated efficient photoluminescence, the color of which could be modulated by the excitation wavelength and time delay for emission monitoring (within 1 millisecond). Furthermore, an original 2D QR-coding scheme was designed for anti-counterfeiting labeling of goods based on unique and tunable emission spectra of NIIC-1-Ln coordination polymers.

Sampling local ant diversities and the importance of trait analyses

AbstractAnts are an incredibly diverse and ubiquitous group of invertebrates in most terrestrial ecosystems. Although extensively sampled, the majority of ant inventories do not evaluate the effect of different sampling techniques in capturing nontraditional metrics of diversity. We aimed to quantify TD (taxonomic) and FD (functional) diversities for a local ant assemblage by integrating metrics and evaluating complementarity of pitfall traps and Winkler extractors for the leaf litter versus epigeic ant faunas and to determine the effect of sampling techniques on functional composition (community‐weighted means of 11 morphological traits) and functional diversity (multi‐trait morphospace measured with three different metrics). We sampled the local community in an Atlantic Forest fragment using week‐long pitfall traps and 1m2 leaf litter samples submitted to Winkler extractors and quantified the contribution on the technique to uniquely capture the ant morphospace by applying a new index (PWindex). Although ant TD overlapped, FD was significantly affected by the sampling technique. By controlling for TD effects, the community collected by each technique was differentially structured. Higher TD did not translate into wider morphospace for Winklers. Pitfalls recovered more functionally overdispersed assemblages. Pitfalls and Winklers overlapped in the sampling of the overall community, but each sampling method contributed with a unique spectrum to the ant morphospace. Our results suggest the importance of incorporating FD metrics in local ant inventories and the importance of sampling techniques when measuring the magnitude of FD and community structure. Our PWindex further illuminates sampling effects for ant assemblages.Abstract in Portuguese &amp; Spanish is available with online material.

Probing the origin of primordial black holes through novel gravitational wave spectrum

In this article we investigate the cumulative stochastic gravitational wave spectra as a tool to gain insight on the creation mechanism of primordial black holes. We consider gravitational waves from the production mechanism of primordial black holes and from the gravitational interactions of those primordial black holes among themselves and other astrophysical black holes. We specifically focus on asynchronous bubble nucleation during a first order phase transition as the creation mechanism. We have used two benchmark phase transitions through which the primordial black holes and the primary gravitational wave spectra have been generated. We have considered binary systems and close hyperbolic interactions of primordial black holes with other primordial and astrophysical black holes as the source of the secondary part of the spectra. We have shown that this unique cumulative spectra have features which directly and indirectly depend on the specifics of the production mechanism.

Luminescence of undoped and Eu3+ activated zinc gallate phosphor: Synthesis, unusual intense 5D0 → 7F4 red emission

A series of Eu3+-doped ZnGa2O4 samples were synthesized via the urea-glycine combustion route. Powder X-ray diffraction (XRD) was used to investigate the crystallinity of the samples, energy dispersive spectroscopy (EDS) to explore the elemental composition, Fourier transform infrared (FTIR), to observe the vibrational modes of the samples, photoluminescence (PL) to determine the luminescence properties. The XRD data prove that the samples remain single cubic structure even at high concentrations of Eu³⁺, enabling the formation of a unique emission spectrum. The active ion concentration was varied to examine the influence of concentration on luminescent properties. This study revealed a 5D0 →7F4 transition located at 700 nm with unusual intensity that has not been documented in the literature, which suggests that the active ion concentration can influence the luminescent characteristics of the phosphors. The increasing Eu3+ content increases the number of Eu3+ ions in ZnGa2O4 host lattice, which enhances the luminescence efficiency of the phosphor. However, beyond a certain level of Eu3+content (i.e., 3 wt% Eu3+), the number of Eu3+ ions becomes excessive, resulting in a reduction in luminescence efficiency due to concentration quenching. The dipole dipole interaction is elucidated to play a prominent role in the mechanism of Eu3+ quenching in the ZnGa2O4. An assessment of color coordinates based on emission spectra reveals that the coordinates shift from blue to the white light region, and then to red as Eu3+ content increases. This suggests that there is a substantial relationship between the Eu3+ concentration and the measured color coordinates.

Reduced graphene oxide-functionalized zinc oxide nanorods as promising nanocomposites for white light emitting diodes and reliable UV photodetection devices

We present a breakthrough in the development of novel nanocomposites based on reduced graphene oxide (RGO)-functionalized zinc oxide (ZnO) nanorods that hold exceptional promise for their use in white light emitting diodes (LEDs) and reliable UV photodetection. The nanorods had a pristine hexagonal wurtzite structure, as confirmed by XRD analysis. SEM images revealed sandwich-like nanocomposites with ZnO nanorods coated in reduced graphene oxide and embedded between two layers of RGO. The study also confirmed the hybridization and interactions between the layers using Raman measurements. The resulting nanocomposites displayed a lower band gap energy than ZnO and exhibited unique photoluminescence spectra with a white PL light. The photodetector based on RGO/ZnO/RGO sandwich structures demonstrated exceptional photoresponse, with higher photocurrent under UV illumination, making it highly promising for a wide range of optoelectronic applications. Overall, this study offers a novel and powerful approach to create nanocomposite structures with enhanced optical characteristics.

Spectral and tiling properties for a class of planar self-affine sets

It is well known that Fuglede’s conjecture gives a connection between the spectrality and geometrical tiling property. In this paper, we consider a class of planar self-affine sets T, where T is generated by an expanding matrix M∈M2(Z) with |det(M)|=4 and D={(0,0)t,(1,0)t,(0,1)t,(−1,−1)t}. We show that T is a spectral set if and only if T is a translational tile. In particular, if T is a spectral set, then Z2 is the unique spectrum of T that contains 0, so it is a tiling set of T by dual criteria.

Perioperative Care Models for Neonates With Congenital Heart Disease: Evolving Role of Neonatology Within the Cardiac Intensive Care Unit.

A multidisciplinary team is needed to optimally care for infants with congenital heart disease (CHD). Different compositions of teams trained in cardiology, critical care, cardiothoracic surgery, anesthesia, and neonatology have been identified as being primarily responsible for perioperative care of this high-risk population in dedicated cardiac intensive care units (CICUs). Although the specific role of cardiac intensivists has become more well defined over the past two decades, the responsibilities of neonatologists remain highly variable in the CICU with neonatologists providing care along with a unique spectrum of primary, shared, or consultative care. The neonatologist can function as the primary physician and assume all or share responsibility with the cardiac intensivists for the management of infants with CHD. A neonatologist can provide care as a secondary consultant physician in a supportive role for the primary CICU team. Additionally, neonates with CHD can be mixed with older children in a CICU, cohorted in a dedicated space within the CICU or placed in a stand-alone infant CICU without older children. Although variations exist between centers on which model of care is deployed and the location within a CICU, characterization of current practice patterns represents the initial step required to determine optimal best practices to improve the quality of care for neonates with cardiac disease. In this manuscript, we present four models utilized in the United States in which the neonatologist provides neonatal-cardiac-focused care in a dedicated CICU. We also outline the different permutations of location where neonates can be cared for in dedicated pediatric/infant CICUs.

MDB-12. TRANS-SPECIES ANALYSIS OF REPLICATION-REPAIR DEFICIENT (RRD) MEDULLOBLASTOMA AND RESPONSE TO IMMUNE-CHECKPOINT INHIBITION: AN IRRDC REPORT

Abstract BACKGROUND Replication-repair deficiency (RRD) stemming from mismatch repair and polymerase-proofreading gene defects (MMRD/PPD) lead to hypermutant childhood cancers, most frequently brain tumors. While medulloblastoma is reported, the clinical, genomic and immune landscape remains unknown. METHODS We analysed the genome, methylome, transcriptome (bulk, single-nuclei) and immune-microenvironment of the largest cohort of RRD-medulloblastoma patients enrolled by the International RRD Consortium, and correlated these to clinical outcomes. RRD mice-models were used to preclinically assess response to immunotherapy. RESULTS RRD-medulloblastoma (n=40) were enriched for anaplasia (55%) and localised disease (85%). Methylation/nano-string-based subgrouping failed to classify 40%, while the remaining clustered with the SHH-subgroup. Copy-number changes were notably infrequent (&amp;lt;20%). All tumors harboured hypermutation and microsatellite instability in contrast to non-RRD controls (p&amp;lt;0.0001). Pathogenic variants were frequent in POLE/POLD1 (80%), TP53 (48%) and SHH-pathway genes (PTCH1, SUFU, SMO: 56%). Interestingly, some tumors additionally had glioma-driver alterations (ATRX, NF1: ~50%), similar to RRD cerebellar glioblastoma, but distinct from both non-RRD medulloblastoma (n=791) and hemispheric glioblastoma (n=733) controls. Moreover, although bulk-transcriptome matched non-RRD SHH-medulloblastoma, single-nuclei analyses suggested an earlier cell-of-origin potentially explaining the heterogenous phenotypes resulting from the driver mutations. Uniquely, immune analyses (gene expression and immunohistochemistry) demonstrated high intra-tumoral CD8 T-cell infiltration. Three-year progression-free survival was 60%. Outcome was worse for RRD-medulloblastoma harbouring TP53-mutation (p=0.04) and failing subgroup-classification (p=0.004). Nestin/Cre MSH2-/- POLE;p.S459F mice developing medulloblastoma recapitulated human disease and demonstrated response to anti-PD1 monotherapy. Recurrent/progressive human tumors including those harbouring TP53-mutations exhibited radiological responses to anti-PD1 monotherapy, which was associated with prolonged ongoing survival in comparison to those not treated with checkpoint-inhibitors (p=0.02). CONCLUSIONS Hypermutant RRD-medulloblastoma reveal heterogenous phenotypes due to unique spectrum of driver mutations and an early cell of origin. Their immune-hot microenvironment allows successful salvage treatment with checkpoint-inhibitors for those failing chemo-radiation, including the high-risk SHH/TP53-mutant and unclassified subgroups.

Limits of identification using VUV spectroscopy applied to C8H18 isomers isolated by GC×GC.

The vacuum ultraviolet detector for gas chromatography can be used to identify structural differences between isomers with similar chromatographic elution times, which adds detail to characterization, valuable for prescreening of sustainable aviation fuel candidates. Although this capability has been introduced elsewhere, vacuum ultraviolet spectroscopy for saturated hydrocarbons has been examined minimally, as the similarities between their spectra are much less significant than their aromatic counterparts. The fidelity with which structural differences can be identified has been unclear. In this work, all possible structural isomers of C8H18 are measured and determined to have unambiguously unique vacuum ultraviolet spectra. Using a statistically based residual comparison approach, the concentration limits at which the spectral differences are interpretable are tested in both a controlled study and a real fuel application. The concentration limit at which the spectral differences between C8H18 isomers are unambiguous is below 0.40% by mass and less than 0.20% with human discretion in our experimental configuration.