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1.
Phys Rev Lett ; 128(6): 061101, 2022 Feb 11.
Artículo en Inglés | MEDLINE | ID: mdl-35213191

RESUMEN

We perform the first magnetohydrodynamic simulations in full general relativity of self-consistent rotating neutron stars (NSs) with ultrastrong mixed poloidal and toroidal magnetic fields. The initial uniformly rotating NS models are computed assuming perfect conductivity, stationarity, and axisymmetry. Although the specific geometry of the mixed field configuration can delay or accelerate the development of various instabilities known from analytic perturbative studies, all our models finally succumb to them. Differential rotation is developed spontaneously in the cores of our magnetars which, after sufficient time, is converted back to uniform rotation. The rapidly rotating magnetars show a significant amount of ejecta, which can be responsible for transient kilonova signatures. However, no highly collimated, helical magnetic fields or incipient jets, which are necessary for γ-ray bursts, arise at the poles of these magnetars by the time our simulations are terminated.

2.
Antimicrob Agents Chemother ; 65(8): e0092621, 2021 07 16.
Artículo en Inglés | MEDLINE | ID: mdl-34097479

RESUMEN

The use of carbapenem antibiotics to treat infections caused by Enterobacterales expressing increasingly aggressive extended-spectrum ß-lactamases (ESBLs) has contributed to the emergence of carbapenem resistance. Enmetazobactam is a novel ESBL inhibitor being developed in combination with cefepime as a carbapenem-sparing option for infections caused by ESBL-producing Enterobacterales. Cefepime-enmetazobactam checkerboard MIC profiles were obtained for a challenge panel of cefepime-resistant ESBL-producing clinical isolates of Klebsiella pneumoniae. Sigmoid maximum effect (Emax) modeling described cefepime MICs as a function of enmetazobactam concentration with no bias. A concentration of 8 µg/ml enmetazobactam proved sufficient to restore >95% of cefepime antibacterial activity in vitro against >95% of isolates tested. These results support a fixed concentration of 8 µg/ml of enmetazobactam for MIC testing.


Asunto(s)
Cefalosporinas , beta-Lactamasas , Antibacterianos/farmacología , Antibacterianos/uso terapéutico , Compuestos de Azabiciclo/farmacología , Cefepima , Cefalosporinas/farmacología , Humanos , Klebsiella pneumoniae , Pruebas de Sensibilidad Microbiana , Triazoles , beta-Lactamasas/genética
3.
Phys Rev Lett ; 124(7): 071101, 2020 Feb 21.
Artículo en Inglés | MEDLINE | ID: mdl-32142310

RESUMEN

Can one distinguish a binary black hole undergoing a merger from a binary neutron star if the individual compact companions have masses that fall inside the so-called mass gap of 3-5 M_{⊙}? For neutron stars, achieving such masses typically requires extreme compactness and in this work we present initial data and evolutions of binary neutron stars initially in quasiequilibrium circular orbits having a compactness C=0.336. These are the most compact, nonvacuum, quasiequilibrium binary objects that have been constructed and evolved to date, including boson stars. The compactness achieved is only slightly smaller than the maximum possible imposed by causality, C_{max}=0.355, which requires the sound speed to be less than the speed of light. By comparing the emitted gravitational waveforms from the late inspiral to merger and postmerger phases between such a binary neutron star vs a binary black hole of the same total mass we identify concrete measurements that serve to distinguish them. With that level of compactness, the binary neutron stars exhibit no tidal disruption up until merger, whereupon a prompt collapse is initiated even before a common core forms. Within the accuracy of our simulations the black hole remnants from both binaries exhibit ringdown radiation that is not distinguishable from a perturbed Kerr spacetime. However, their inspiral leads to phase differences of the order of ∼5 rad over an ∼81 km separation (1.7 orbits) while typical neutron stars exhibit phase differences of ≥20 rad. Although a difference of ∼5 rad can be measured by current gravitational wave laser interferometers (e.g., aLIGO/Virgo), uncertainties in the individual masses and spins will likely prevent distinguishing such compact, massive neutron stars from black holes.

4.
Artículo en Inglés | MEDLINE | ID: mdl-30988152

RESUMEN

Enmetazobactam, formerly AAI101, is a novel penicillanic acid sulfone extended-spectrum ß-lactamase (ESBL) inhibitor. The combination of enmetazobactam with cefepime has entered clinical trials to assess safety and efficacy in patients with complicated urinary tract infections. Here, the in vitro activity of cefepime-enmetazobactam was determined for 1,993 clinical isolates of Enterobacteriaceae and Pseudomonas aeruginosa collected in the United States and Europe during 2014 and 2015. Enmetazobactam at a fixed concentration of 8 µg/ml lowered the cefepime MIC90 from 16 to 0.12 µg/ml for Escherichia coli, from >64 to 0.5 µg/ml for Klebsiella pneumoniae, from 16 to 1 µg/ml for Enterobacter cloacae, and from 0.5 to 0.25 µg/ml for Enterobacter aerogenes Enmetazobactam did not enhance the potency of cefepime against P. aeruginosa Applying the Clinical and Laboratory Standards Institute susceptible-dose-dependent (SDD) breakpoint of 8 µg/ml to cefepime-enmetazobactam for comparative purposes resulted in cumulative inhibitions of 99.9% for E. coli, 96.4% for K. pneumoniae, 97.0% for E. cloacae, 100% for E. aerogenes, 98.1% for all Enterobacteriaceae assessed, and 82.8% for P. aeruginosa Comparator susceptibilities for all Enterobacteriaceae were 99.7% for ceftazidime-avibactam, 96.2% for meropenem, 90.7% for ceftolozane-tazobactam, 87% for cefepime (SDD breakpoint), 85.7% for piperacillin-tazobactam, and 81.2% for ceftazidime. For the subset of ESBL-producing K. pneumoniae isolates, the addition of 8 µg/ml enmetazobactam to cefepime lowered the MIC90 from >64 to 1 µg/ml, whereas the shift for 8 µg/ml tazobactam was from >64 to 8 µg/ml. Cefepime-enmetazobactam may represent a novel carbapenem-sparing option for empirical treatment of serious Gram-negative infections in settings where ESBL-producing Enterobacteriaceae are expected.


Asunto(s)
Antibacterianos/farmacología , Compuestos de Azabiciclo/farmacología , Cefepima/farmacología , Bacterias Gramnegativas/efectos de los fármacos , Triazoles/farmacología , Ceftazidima/farmacología , Cefalosporinas/farmacología , Infección Hospitalaria/microbiología , Combinación de Medicamentos , Farmacorresistencia Bacteriana/efectos de los fármacos , Enterobacteriaceae/efectos de los fármacos , Europa (Continente) , Bacterias Gramnegativas/aislamiento & purificación , Infecciones por Bacterias Gramnegativas/microbiología , Hospitales , Humanos , Pruebas de Sensibilidad Microbiana , Pseudomonas aeruginosa/efectos de los fármacos , Tazobactam/farmacología , Estados Unidos
5.
Artículo en Inglés | MEDLINE | ID: mdl-30858223

RESUMEN

Impeding, as well as reducing, the burden of antimicrobial resistance in Gram-negative pathogens is an urgent public health endeavor. Our current antibiotic armamentarium is dwindling, while major resistance determinants (e.g., extended-spectrum ß-lactamases [ESBLs]) continue to evolve and disseminate around the world. One approach to attack this problem is to develop novel therapies that will protect our current agents. AAI101 is a novel penicillanic acid sulfone ß-lactamase inhibitor similar in structure to tazobactam, with one important difference. AAI101 possesses a strategically placed methyl group that gives the inhibitor a net neutral charge, enhancing bacterial cell penetration. AAI101 paired with cefepime, also a zwitterion, is in phase III of clinical development for the treatment of serious Gram-negative infections. Here, AAI101 was found to restore the activity of cefepime against class A ESBLs (e.g., CTX-M-15) and demonstrated increased potency compared to that of piperacillin-tazobactam when tested against an established isogenic panel. The enzymological properties of AAI101 further revealed that AAI101 possessed a unique mechanism of ß-lactamase inhibition compared to that of tazobactam. Additionally, upon reaction with AAI101, CTX-M-15 was modified to an inactive state. Notably, the in vivo efficacy of cefepime-AAI101 was demonstrated using a mouse septicemia model, indicating the ability of AAI101 to bolster significantly the therapeutic efficacy of cefepime in vivo The combination of AAI101 with cefepime represents a potential carbapenem-sparing treatment regimen for infections suspected to be caused by Enterobacteriaceae expressing ESBLs.


Asunto(s)
Compuestos de Azabiciclo/farmacología , Cefepima/farmacología , Enterobacteriaceae/efectos de los fármacos , Enterobacteriaceae/metabolismo , Combinación Piperacilina y Tazobactam/farmacología , Sulbactam/farmacología , Triazoles/farmacología , Inhibidores de beta-Lactamasas/farmacología , Espectrometría de Masa por Ionización de Electrospray
6.
J Clin Microbiol ; 57(8)2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31167844

RESUMEN

Third-generation cephalosporin resistance among Enterobacteriaceae, mediated by the spread of extended-spectrum ß-lactamases (ESBLs), is a very serious medical concern with limited therapeutic options. Enmetazobactam (formerly AAI101) is a novel penicillanic sulfone ß-lactamase inhibitor active against a wide range of ESBLs. The combination of enmetazobactam and cefepime has entered phase 3 development in patients with complicated urinary tract infections. Using the Clinical and Laboratory Standards Institute (CLSI) M23 tier 2 study design, broth microdilution MIC and disk diffusion quality control (QC) ranges were determined for cefepime-enmetazobactam. Enmetazobactam was tested at a fixed concentration of 8 µg/ml in the MIC assay, and a cefepime-enmetazobactam disk mass of 30/20 µg was used in the disk diffusion assay. Escherichia coli ATCC 25922, E. coli ATCC 35218, E. coli NCTC 13353, Klebsiella pneumoniae ATCC 700603, and Pseudomonas aeruginosa ATCC 27853 were chosen as reference strains. The CTX-M-15-producing E. coli NCTC 13353 isolate is recommended for routine testing to control for inhibition of ESBL activity by enmetazobactam. Broth microdilution MIC QC ranges spanned 3 to 4 doubling dilutions and contained 99.6% to 100.0% of obtained MIC values for the five reference strains. Disk diffusion yielded inhibition zone diameter QC ranges that spanned 7 mm and encompassed 97.1% to 100.0% of the obtained values. Quality control ranges were approved by the CLSI in 2017 (broth microdilution MIC) and 2019 (disk diffusion). The established QC ranges will ensure that appropriate assay performance criteria are attained using CLSI reference methodology when determining the susceptibility of clinical isolates to cefepime-enmetazobactam.


Asunto(s)
Antibacterianos/farmacología , Compuestos de Azabiciclo/farmacología , Cefepima/farmacología , Pruebas Antimicrobianas de Difusión por Disco/métodos , Enterobacteriaceae/efectos de los fármacos , Control de Calidad , Triazoles/farmacología , Inhibidores de beta-Lactamasas/farmacología , Pruebas Antimicrobianas de Difusión por Disco/normas , Pruebas de Sensibilidad Microbiana/normas
7.
Phys Rev Lett ; 123(23): 231103, 2019 Dec 06.
Artículo en Inglés | MEDLINE | ID: mdl-31868499

RESUMEN

We construct the first dynamically stable ergostars (equilibrium neutron stars that contain an ergoregion) for a compressible, causal equation of state. We demonstrate their stability by evolving both strict and perturbed equilibrium configurations in full general relativity for over a hundred dynamical timescales (≳30 rotational periods) and observing their stationary behavior. This stability is in contrast to earlier models which prove radially unstable to collapse. Our solutions are highly differentially rotating hypermassive neutron stars with a corresponding spherical compaction of C=0.3. Such ergostars can provide new insights into the geometry of spacetimes around highly compact, rotating objects and on the equation of state at supranuclear densities. Ergostars may form as remnants of extreme binary neutron star mergers and possibly provide another mechanism for powering short gamma-ray bursts.

9.
Phys Rev Lett ; 115(23): 231302, 2015 Dec 04.
Artículo en Inglés | MEDLINE | ID: mdl-26684108

RESUMEN

We present a new method to measure or constrain p-wave-suppressed cross sections for dark matter (DM) annihilations inside the steep density spikes induced by supermassive black holes. We demonstrate that the high DM densities, together with the increased velocity dispersion, within such spikes combine to make thermal p-wave annihilation cross sections potentially visible in γ-ray observations of the Galactic center (GC). The resulting DM signal is a bright central point source with emission originating from DM annihilations in the absence of a detectable spatially extended signal from the halo. We define two simple reference theories of DM with a thermal p-wave annihilation cross section and establish new limits on the combined particle and astrophysical parameter space of these models, demonstrating that Fermi Large Area Telescope is currently sensitive to thermal p-wave DM over a wide range of possible scenarios for the DM distribution in the GC.

10.
Phys Rev Lett ; 113(15): 151302, 2014 Oct 10.
Artículo en Inglés | MEDLINE | ID: mdl-25375700

RESUMEN

If the supermassive black hole Sgr A* at the center of the Milky Way grew adiabatically from an initial seed embedded in a Navarro-Frenk-White dark matter (DM) halo, then the DM profile near the hole has steepened into a spike. We calculate the dramatic enhancement to the gamma-ray flux from the Galactic center (GC) from such a spike if the 1-3 GeV excess observed in Fermi data is due to DM annihilations. We find that for the parameter values favored in recent fits, the point-source-like flux from the spike is 35 times greater than the flux from the inner 1° of the halo, far exceeding all Fermi point source detections near the GC. We consider the dependence of the spike signal on astrophysical and particle parameters and conclude that if the GC excess is due to DM, then a canonical adiabatic spike is disfavored by the data. We discuss alternative Galactic histories that predict different spike signals, including (i) the nonadiabatic growth of the black hole, possibly associated with halo and/or black hole mergers, (ii) gravitational interaction of DM with baryons in the dense core, such as heating by stars, or (iii) DM self-interactions. We emphasize that the spike signal is sensitive to a different combination of particle parameters than the halo signal and that the inclusion of a spike component to any DM signal in future analyses would provide novel information about both the history of the GC and the particle physics of DM annihilations.

11.
Phys Rev Lett ; 109(22): 221102, 2012 Nov 30.
Artículo en Inglés | MEDLINE | ID: mdl-23368111

RESUMEN

We present results from the first fully general relativistic, magnetohydrodynamic (MHD) simulations of an equal-mass black-hole binary (BHBH) in a magnetized, circumbinary accretion disk. We simulate both the pre- and postdecoupling phases of a BHBH-disk system and both "cooling" and "no-cooling" gas flows. Prior to decoupling, the competition between the binary tidal torques and the effective viscous torques due to MHD turbulence depletes the disk interior to the binary orbit. However, it also induces a two-stream accretion flow and mildly relativistic polar outflows from the BHs. Following decoupling, but before gas fills the low-density "hollow" surrounding the remnant, the accretion rate is reduced, while there is a prompt electromagnetic luminosity enhancement following merger due to shock heating and accretion onto the spinning BH remnant. This investigation, though preliminary, previews more detailed general relativistic, MHD simulations we plan to perform in anticipation of future, simultaneous detections of gravitational and electromagnetic radiation from a merging BHBH-disk system.

12.
mBio ; 13(3): e0179321, 2022 06 28.
Artículo en Inglés | MEDLINE | ID: mdl-35612361

RESUMEN

ß-Lactamases hydrolyze ß-lactam antibiotics and are major determinants of antibiotic resistance in Gram-negative pathogens. Enmetazobactam (formerly AAI101) and tazobactam are penicillanic acid sulfone (PAS) ß-lactamase inhibitors that differ by an additional methyl group on the triazole ring of enmetazobactam, rendering it zwitterionic. In this study, ultrahigh-resolution X-ray crystal structures and mass spectrometry revealed the mechanism of PAS inhibition of CTX-M-15, an extended-spectrum ß-lactamase (ESBL) globally disseminated among Enterobacterales. CTX-M-15 crystals grown in the presence of enmetazobactam or tazobactam revealed loss of the Ser70 hydroxyl group and formation of a lysinoalanine cross-link between Lys73 and Ser70, two residues critical for catalysis. Moreover, the residue at position 70 undergoes epimerization, resulting in formation of a d-amino acid. Cocrystallization of enmetazobactam or tazobactam with CTX-M-15 with a Glu166Gln mutant revealed the same cross-link, indicating that this modification is not dependent on Glu166-catalyzed deacylation of the PAS-acylenzyme. A cocrystal structure of enmetazobactam with CTX-M-15 with a Lys73Ala mutation indicates that epimerization can occur without cross-link formation and positions the Ser70 Cß closer to Lys73, likely facilitating formation of the Ser70-Lys73 cross-link. A crystal structure of a tazobactam-derived imine intermediate covalently linked to Ser70, obtained after 30 min of exposure of CTX-M-15 crystals to tazobactam, supports formation of an initial acylenzyme by PAS inhibitors on reaction with CTX-M-15. These data rationalize earlier results showing CTX-M-15 deactivation by PAS inhibitors to involve loss of protein mass, and they identify a distinct mechanism of ß-lactamase inhibition by these agents. IMPORTANCE ß-Lactams are the most prescribed antibiotic class for treating bacterial diseases, but their continued efficacy is threatened by bacterial strains producing ß-lactamase enzymes that catalyze their inactivation. The CTX-M family of ESBLs are major contributors to ß-lactam resistance in Enterobacterales, preventing effective treatment with most penicillins and cephalosporins. Combining ß-lactams with ß-lactamase inhibitors (BLIs) is a validated route to overcome such resistance. Here, we describe how exposure to enmetazobactam and tazobactam, BLIs based on a penicillanic acid sulfone (PAS) scaffold, leads to a protein modification in CTX-M-15, resulting in irremediable inactivation of this most commonly encountered member of the CTX-M family. High-resolution X-ray crystal structures showed that PAS exposure induces formation of a cross-link between Ser70 and Lys73, two residues critical to ß-lactamase function. This previously undescribed mechanism of inhibition furthers our understanding of ß-lactamase inhibition by classical PAS inhibitors and provides a basis for further, rational inhibitor development.


Asunto(s)
Sulbactam , Inhibidores de beta-Lactamasas , Antibacterianos/farmacología , Lisina , Pruebas de Sensibilidad Microbiana , Serina , Sulbactam/farmacología , Tazobactam/farmacología , Inhibidores de beta-Lactamasas/farmacología , beta-Lactamasas/metabolismo
13.
Risk Anal ; 31(6): 893-901, 2011 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-21679219

RESUMEN

The regulatory process is often criticized for being cumbersome and slow, much like a computer whose hard drive is fragmented by files no longer used or useful. Like such a computer, the regulatory process contains many requirements of dubious utility. These include the Paperwork Reduction Act, the Regulatory Flexibility Act, and numerous executive orders. While other parts of the regulatory process such as notice and comment and cost-benefit analysis have received much more academic attention, these other parts of the process deserve examination as well. This article argues that such an examination will reveal that these statutes and executive orders add little of value to the regulatory process while consuming agency resources. An improved requirement for cost-benefit analysis with distributional analysis could easily replace virtually all of these requirements and improve regulations while reducing the time needed to promulgate regulations.

14.
Phys Rev D ; 103(8)2021 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-34589636

RESUMEN

We explore in general relativity the survival time of neutron stars that host an endoparasitic, possibly primordial, black hole at their center. Corresponding to the minimum steady-state Bondi accretion rate for adiabatic flow that we found earlier for stiff nuclear equations of state (EOSs), we derive analytically the maximum survival time after which the entire star will be consumed by the black hole. We also show that this maximum survival time depends only weakly on the stiffness for polytropic EOSs with Γ ≥ 5/3, so that this survival time assumes a nearly universal value that depends on the initial black-hole mass alone. Establishing such a value is important for constraining the contribution of primordial black holes in the mass range 10-16 M ⊙ ≲ M ≲ 10-10 M ⊙ to the dark-matter content of the Universe.

15.
Artículo en Inglés | MEDLINE | ID: mdl-34651021

RESUMEN

Neutron stars (NSs) are extraordinary not only because they are the densest form of matter in the visible Universe but also because they can generate magnetic fields ten orders of magnitude larger than those currently constructed on earth. The combination of extreme gravity with the enormous electromagnetic (EM) fields gives rise to spectacular phenomena like those observed on August 2017 with the merger of a binary neutron star system, an event that generated a gravitational wave (GW) signal, a short γ -ray burst (sGRB), and a kilonova. This event serves as the highlight so far of the era of multimessenger astronomy. In this review, we present the current state of our theoretical understanding of compact binary mergers containing NSs as gleaned from the latest general relativistic magnetohydrodynamic simulations. Such mergers can lead to events like the one on August 2017, GW170817, and its EM counterparts, GRB 170817 and AT 2017gfo. In addition to exploring the GW emission from binary black hole-neutron star and neutron star-neutron star mergers, we also focus on their counterpart EM signals. In particular, we are interested in identifying the conditions under which a relativistic jet can be launched following these mergers. Such a jet is an essential feature of most sGRB models and provides the main conduit of energy from the central object to the outer radiation regions. Jet properties, including their lifetimes and Poynting luminosities, the effects of the initial magnetic field geometries and spins of the coalescing NSs, as well as their governing equation of state, are discussed. Lastly, we present our current understanding of how the Blandford-Znajek mechanism arises from merger remnants as the trigger for launching jets, if, when and how a horizon is necessary for this mechanism, and the possibility that it can turn on in magnetized neutron ergostars, which contain ergoregions, but no horizons.

16.
Phys Rev D ; 103(10)2021 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-34651092

RESUMEN

We revisit the system consisting of a neutron star that harbors a small, possibly primordial, black hole at its center, focusing on a nonspinning black hole embedded in a nonrotating neutron star. Extending earlier treatments, we provide an analytical treatment describing the rate of secular accretion of the neutron star matter onto the black hole, adopting the relativistic Bondi accretion formalism for stiff equations of state that we presented elsewhere. We use these accretion rates to sketch the evolution of the system analytically until the neutron star is completely consumed. We also perform numerical simulations in full general relativity for black holes with masses up to nine orders of magnitude smaller than the neutron star mass, including a simulation of the entire evolution through collapse for the largest black hole mass. We construct relativistic initial data for these simulations by generalizing the black hole puncture method to allow for the presence of matter, and evolve these data with a code that is optimally designed to resolve the vastly different length scales present in this problem. We compare our analytic and numerical results, and provide expressions for the lifetime of neutron stars harboring such endoparasitic black holes.

17.
Mon Not R Astron Soc ; 502(2): 3003-3011, 2021 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-34594057

RESUMEN

We revisit Bondi accretion - steady-state, adiabatic, spherical gas flow on to a Schwarzschild black hole at rest in an asymptotically homogeneous medium - for stiff polytropic equations of state (EOSs) with adiabatic indices Γ > 5/3. A general relativistic treatment is required to determine their accretion rates, for which we provide exact expressions. We discuss several qualitative differences between results for soft and stiff EOSs - including the appearance of a minimum steady-state accretion rate for EOSs with Γ ≥ 5/3 - and explore limiting cases in order to examine these differences. As an example, we highlight results for Γ = 2, which is often used in numerical simulations to model the EOS of neutron stars. We also discuss a special case with this index, the ultrarelativistic 'causal' EOS, P = ρ. The latter serves as a useful limit for the still undetermined neutron star EOS above nuclear density. The results are useful, for example, to estimate the accretion rate on to a mini-black hole residing at the centre of a neutron star.

18.
Phys Rev D ; 103(4)2021 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-34595363

RESUMEN

We present fully general-relativistic numerical evolutions of self-gravitating tori around spinning black holes with dimensionless spin a/M = 0.7 parallel or antiparallel to the disk angular momentum. The initial disks are unstable to the hydrodynamic Papaloizou-Pringle instability which causes them to grow persistent orbiting matter clumps. The effect of black hole spin on the growth and saturation of the instability is assessed. We find that the instability behaves similarly to prior simulations with nonspinning black holes, with a shift in frequency due to spin-induced changes in disk orbital period. Copious gravitational waves are generated by these systems, and we analyze their detectability by current and future gravitational wave observatories for a large range of masses. We find that systems of 10 M ⊙-relevant for black hole-neutron star mergers-are detectable by Cosmic Explorer out to ~300 Mpc, while DECIGO (LISA) will be able to detect systems of 1000 M ⊙ (105 M ⊙)-relevant for disks forming in collapsing supermassive stars-out to cosmological redshift of z ~ 5 (z ~ 1). Computing the accretion rate of these systems we find that these systems may also be promising sources of coincident electromagnetic signals.

19.
Bioorg Med Chem Lett ; 20(15): 4635-8, 2010 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-20576430

RESUMEN

Novel C(3) propenylamide and propenylsulfonamide cephalosporins have been synthesized and tested for their ability to inhibit the penicillin-binding protein 2' (PBP2') from Staphylococcus epidermidis and the growth of a panel of clinically relevant bacterial species, including methicillin-resistant Staphylococcus aureus (MRSA). The most potent compounds inhibited the growth of MRSA strains with minimum inhibitory concentrations (MIC) as low as 1 microg/mL. The structure-activity relationship revealed the potential for further optimization of this new cephalosporin class.


Asunto(s)
Amidas/química , Antibacterianos/química , Cefalosporinas/química , Staphylococcus aureus Resistente a Meticilina/efectos de los fármacos , beta-Lactamas/antagonistas & inhibidores , Antibacterianos/síntesis química , Antibacterianos/farmacología , Cefalosporinas/síntesis química , Cefalosporinas/farmacología , Staphylococcus aureus Resistente a Meticilina/enzimología , Pruebas de Sensibilidad Microbiana , Relación Estructura-Actividad , beta-Lactamas/metabolismo
20.
Viruses ; 12(12)2020 12 19.
Artículo en Inglés | MEDLINE | ID: mdl-33352755

RESUMEN

Funding vaccine development research is more complicated than simply putting out an announcement of funds available. The funders must decide whether product development can be accomplished by purely applied research, or whether more fundamental knowledge is needed before product development can be started. If additional basic knowledge is needed, identifying the specific area of the knowledge gap can be a challenge. Additionally, when there appears to be a clear path of applied research sometimes obstacles are encountered that require a return to more basic work. After deciding on the work to be done, funders must attract the scientists with the broad range of needed skills to cover all the stages of development. Collaborations must be promoted and alliances with other funders and industry must be developed. Funders use multiple tools and strategies to accomplish these tasks with varying success.


Asunto(s)
Vacunas contra el SIDA/inmunología , Infecciones por VIH/prevención & control , VIH/inmunología , Investigación , Financiación del Capital , Infecciones por VIH/virología , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Investigación/economía , Investigación/historia , Investigación/tendencias
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