RESUMEN
The ATP binding site located on the subunit B of DNA gyrase is an attractive target for the development of new antibacterial agents. In recent decades, several small-molecule inhibitor classes have been discovered but none has so far reached the market. We present here the discovery of a promising new series of N-phenylpyrrolamides with low nanomolar IC50 values against DNA gyrase, and submicromolar IC50 values against topoisomerase IV from Escherichia coli and Staphylococcus aureus. The most potent compound in the series has an IC50 value of 13â¯nM against E. coli gyrase. Minimum inhibitory concentrations (MICs) against Gram-positive bacteria are in the low micromolar range. The oxadiazolone derivative 11a, with an IC50 value of 85â¯nM against E. coli DNA gyrase displays the most potent antibacterial activity, with MIC values of 1.56⯵M against Enterococcus faecalis, and 3.13⯵M against wild type S. aureus, methicillin-resistant S. aureus (MRSA) and vancomycin-resistant Enterococcus (VRE). The activity against wild type E. coli in the presence of efflux pump inhibitor phenylalanine-arginine ß-naphthylamide (PAßN) is 4.6⯵M.
Asunto(s)
Amidas/farmacología , Antibacterianos/farmacología , Girasa de ADN/metabolismo , Enterococcus faecalis/efectos de los fármacos , Escherichia coli/efectos de los fármacos , Pirroles/farmacología , Staphylococcus aureus/efectos de los fármacos , Inhibidores de Topoisomerasa II/farmacología , Amidas/líquido cefalorraquídeo , Amidas/química , Antibacterianos/síntesis química , Antibacterianos/química , Relación Dosis-Respuesta a Droga , Escherichia coli/enzimología , Pruebas de Sensibilidad Microbiana , Estructura Molecular , Pirroles/líquido cefalorraquídeo , Pirroles/química , Staphylococcus aureus/enzimología , Relación Estructura-Actividad , Inhibidores de Topoisomerasa II/síntesis química , Inhibidores de Topoisomerasa II/químicaRESUMEN
BACKGROUND: Identify if glycorrhachia and cerebrospinal fluid protein could influence the time of sensory block to T10, the duration and the metameric block's level, after a standard dose of Ropivacaine. METHODS: 80 patients, ASA I - III undergoing to transurethral prostate resection with spinal anesthesia in a prospected open study were recruited. A 0.2 ml liquor's sample was taken; glycorrhachia, by glycemic stix and CSF protein, by urinary stix, were got, before Ropivacaine 0.5% 15 mg injection (0.10 - 0.15 mlsec). After anti-trendelemburg, with 30 ° tilting for 15 min, the onset of sensory block to T10, the maximum metameric level to 15' and the time of sensory block were reported. The data collection were analyzed using the software language R. RESULTS: A significant correlation liquor specific weigh preoperative glycemia (0.749), liquoral specific weigh glycorrhachia (rho = 0.751; R2 = 0.564; P 0.05) and specific weigh CSF protein (rho = 0.684; R2 = 0.468; P 0.05) were reported. Inverse relation CSF weightsensory block level (rho -0.789, P 0.05, R2 0.621) was evidenced. Inverse relation onset time to T10 glycorrhachia (84%) and cephalic block glycorrhachia (76%) were found. Inverse correlation onset time to T 10 CSF protein and cephalic block proteinorrachia was respectively 84% and 67%. A rho of 0.712 with R2 of 51% BMI onset to T10 and rho of 0.681 with R2 of 51% BMI maximum cephalic block with P 0.05 were reported. CONCLUSIONS: The predictability of a iso-hypobaric local anesthetic could reduce the risk of procedure failure and adverse events by further cephalic spread.
Asunto(s)
Amidas/líquido cefalorraquídeo , Anestésicos Locales/líquido cefalorraquídeo , Bupivacaína/líquido cefalorraquídeo , Proteínas del Líquido Cefalorraquídeo/líquido cefalorraquídeo , Glucosa/líquido cefalorraquídeo , Sensación/efectos de los fármacos , Amidas/administración & dosificación , Analgésicos Opioides/administración & dosificación , Anestesia Local/métodos , Anestesia Raquidea , Anestésicos Locales/administración & dosificación , Proteínas del Líquido Cefalorraquídeo/administración & dosificación , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , RopivacaínaRESUMEN
Following epidural administration, cerebrospinal fluid bioavailability of local anesthetics is low, one major limiting factor being diffusion across the arachnoid mater barrier. The aim of this study was to evaluate the influence of absorption enhancers on the meningeal permeability of epidurally administered ropivacaine. Five enhancers known for their ability to increase drug permeability via transcellular and/or paracellular pathways, i.e. palmitoyl carnitine, ethylenediaminetetraacetic acid, sodium caprate, dodecylphosphocholine and pentylglycerol, were tested ex vivo on fresh specimen of meninges removed from cervical to lumbar level of rabbit spine following laminectomy and placed in diffusion chambers. Among them, sodium caprate lead to the best permeability improvement for both marker and drug (440% and 112% for mannitol and ropivacaine, respectively) and was therefore selected for in vivo study in a sheep model using microdialysis technique to evaluate epidural and intrathecal ropivacaine concentrations following epidural administration. Resulting dialysate and plasma concentrations were used to calculate pharmacokinetic parameters. Following sodium caprate pre-treatment, ropivacaine intrathecal maximal concentration (Cmax) was 1.6 times higher (78 ± 16 µg ml(-1) vs 129 ± 26 µg ml(-1), p<0.05) but the influence of the absorption enhancer was only effective the first 30 min following ropivacaine injection, as seen with the significantly increase of intrathecal AUC(0-30 min) (1629 ± 437 µg min ml(-1) vs 2477 ± 559 µg min ml(-1), p<0.05) resulting in a bioavailable fraction 130% higher 30 min after ropivavaine administration. Co-administration of local anesthetics with sodium caprate seems to allow a transient and reversible improvement of transmeningeal passage into intrathecal space.
Asunto(s)
Amidas/farmacocinética , Anestésicos Locales/farmacocinética , Ácidos Decanoicos/farmacología , Meninges/efectos de los fármacos , Absorción , Amidas/administración & dosificación , Amidas/sangre , Amidas/líquido cefalorraquídeo , Amidas/química , Anestésicos Locales/administración & dosificación , Anestésicos Locales/sangre , Anestésicos Locales/líquido cefalorraquídeo , Anestésicos Locales/química , Animales , Disponibilidad Biológica , Química Farmacéutica , Ácidos Decanoicos/administración & dosificación , Difusión , Composición de Medicamentos , Ácido Edético/farmacología , Glicerol/análogos & derivados , Glicerol/farmacología , Inyecciones Epidurales , Meninges/metabolismo , Microdiálisis , Palmitoilcarnitina/farmacología , Permeabilidad , Fosforilcolina/análogos & derivados , Fosforilcolina/farmacología , Conejos , Ropivacaína , OvinosRESUMEN
BACKGROUND: Microparticulate local anesthetics-loaded delivery systems are known to provide a controlled release of drug and to reduce systemic toxicity resulting from transient high plasma concentrations. The aim of this study was to evaluate epidural, intrathecal and plasma pharmacokinetics of ropivacaine following epidural administrations of repeated boluses or infusions and to compare them with the epidural administration of polylactide-co-glycolide ropivacaine-loaded microspheres. METHODS: In the first step, the epidural and intrathecal pharmacokinetics was evaluated in 3 Lacaunes ewes, receiving epidural continuous infusion of ropivacaine with increasing doses (20, 50 and 100mg/h). Then, six animals received an epidural administration of ropivacaine-loaded microspheres (500 mg), three others received ropivacaine in epidural bolus (30 mg) followed by infusion (2mg/ml during 6h), and the last three animals received three successive epidural boluses of ropivacaine (50mg) at 2h interval. A simultaneous microdialysis technique was used to measure epidural and intrathecal concentrations of ropivacaine. RESULTS: After epidural administration of ropivacaine-loaded microspheres, Cmax in plasma was around 100 ng/ml while epidural and intrathecal Cmax of ropivacaine were close to 600 and 150 microg/ml, respectively. The ratios of intrathecal to epidural AUC (AUCit/AUCepi) for bolus administration, bolus+infusion administration, and for microspheres were 13.4+/-2.4; 14.1+/-6.1 and 33.9+/-22.6%, respectively. This suggested that administration of ropivacaine as microspheres increased the transmeningeal passage of ropivacaine in comparison to other administration regimens. CONCLUSIONS: Epidural administration of ropivacaine-loaded microspheres led to the sustained levels of ropivacaine in the intrathecal space compared to the boluses of ropivacaine solution. Moreover, epidural administration of microspheres resulted in the highest efficiency in intrathecal uptake of ropivacaine compared to administration in solution.
Asunto(s)
Amidas/administración & dosificación , Analgesia Epidural/métodos , Ácido Láctico/química , Microesferas , Ácido Poliglicólico/química , Amidas/líquido cefalorraquídeo , Anestésicos Locales/administración & dosificación , Animales , Área Bajo la Curva , Disponibilidad Biológica , Química Farmacéutica/métodos , Relación Dosis-Respuesta a Droga , Sistemas de Liberación de Medicamentos , Meninges/efectos de los fármacos , Microscopía Electrónica de Rastreo/métodos , Copolímero de Ácido Poliláctico-Ácido Poliglicólico , Polímeros/química , Ropivacaína , OvinosRESUMEN
BACKGROUND: Extension of sensory blockade after an epidural top-up in combined spinal epidural (CSE) anesthesia is partly attributed to compression of the dural sac by the injected volume. This study investigated whether a volume effect plays a significant role when administering an epidural top-up after an initial epidural loading dose and assessed the predictive value of different factors with respect to the increase in sensory blockade. METHODS: After an epidural loading dose of 75 mg ropivacaine, 0.75%, 30 patients were randomly assigned to one of three groups. After the maximum level of sensory blockade (MLSB) had been established, patients received either an epidural top-up with 10 ml ropivacaine, 0.75% (group 1, n = 10) or saline (group 2, n = 10), or no epidural top-up (group 3, n = 10). Subsequently, sensory blockade was assessed at 5-min intervals for a further 30 min by a blinded observer. RESULTS: The MLSB increased significantly in the patients receiving an epidural top-up with ropivacaine but not in the patients receiving normal saline. Sensory block extension was inversely related to the number of segments blocked at the time of the epidural top-up, and female gender was associated with a smaller increase in MLSB. CONCLUSIONS: When using epidural ropivacaine, the extension of sensory blockade after administering an epidural top-up is caused by a local anesthetic effect and not by a volume effect. Under the conditions of this study, predictors of the increase in sensory blockade are the presence of ropivacaine in the top-up injectate, the number of segments blocked at the time of epidural top-up, and gender.
Asunto(s)
Anestesia Epidural/métodos , Anestesia Raquidea/métodos , Adulto , Anciano , Anciano de 80 o más Años , Amidas/líquido cefalorraquídeo , Método Doble Ciego , Femenino , Humanos , Masculino , Persona de Mediana Edad , Pronóstico , Ropivacaína , SensaciónRESUMEN
Peptidyl-glycine alpha-amidation activity has been detected in human cerebrospinal fluid (CSF) and in several regions of the central nervous system. Activity was monitored by measuring conversion of mono-125I-D-Tyr-Val-Gly into mono-125I-D-Tyr-Val-NH2. The alpha-amidation activity in CSF is dependent on molecular oxygen, copper ions and ascorbic acid and appears to recognize a variety of peptide substrates which contain carboxyl terminal glycine residues. Kinetic analyses demonstrated Michaelis-Menten kinetics with a Km of 4.6 microM for D-Tyr-Val-Gly. The level of peptidyl-glycine alpha-amidation activity in 14 samples of CSF averaged 43 +/- 5 pmol/ml/h (mean +/- SEM; range 11-85 pmol/ml/h) or 1.9 +/- 0.2 pmol/Mg protein/h. No difference was noted between samples from male and female subjects. Extracts of central nervous system tissue contained alpha-amidation activity. The highest levels of enzyme activity were found in the hypothalamus with lower levels in the neurohypophysis and the cerebral cortex. Still lower but detectable activity was found in the cerebellum and pons. Human peptidyl-glycine alph-amidation activity is found in central nervous system tissues known to synthesize alpha-amidated neuropeptides and may be secreted from these tissues along with alpha-amidated peptides into CSF.
Asunto(s)
Amidas/metabolismo , Sistema Nervioso Central/metabolismo , Oxigenasas de Función Mixta/líquido cefalorraquídeo , Péptidos/metabolismo , Amidas/líquido cefalorraquídeo , Sistema Nervioso Central/enzimología , Humanos , Técnicas In Vitro , Oxigenasas de Función Mixta/metabolismoAsunto(s)
Ácidos Cetoglutáricos/líquido cefalorraquídeo , Pirrolidinonas/líquido cefalorraquídeo , Ácido Pirrolidona Carboxílico/líquido cefalorraquídeo , Amidas/líquido cefalorraquídeo , Cromatografía de Gases/métodos , Ionización de Llama , Encefalopatía Hepática/líquido cefalorraquídeo , Humanos , Espectrometría de Masas , Compuestos de Trimetilsililo/análisisAsunto(s)
Amidas/análisis , Amidohidrolasas/análisis , Química Encefálica , Ácidos Cetoglutáricos/análisis , Riñón/análisis , Hígado/análisis , Transaminasas/análisis , Amidas/líquido cefalorraquídeo , Animales , Encéfalo/enzimología , Radioisótopos de Carbono , Cromatografía por Intercambio Iónico , Glutamina , Humanos , Marcaje Isotópico , Ácidos Cetoglutáricos/líquido cefalorraquídeo , Riñón/enzimología , Hígado/enzimología , Hepatopatías/líquido cefalorraquídeo , Ratas , UltrafiltraciónAsunto(s)
Encéfalo/efectos de los fármacos , Manifestaciones Neurológicas , Primidona/envenenamiento , Amidas/sangre , Amidas/líquido cefalorraquídeo , Amidas/orina , Biotransformación , Encéfalo/fisiopatología , Cromatografía en Capa Delgada , Cristalización , Electroencefalografía , Potenciales Evocados , Semivida , Malonatos/sangre , Malonatos/líquido cefalorraquídeo , Malonatos/orina , Fenobarbital/sangre , Fenobarbital/líquido cefalorraquídeo , Fenobarbital/orina , Estimulación Luminosa , Intoxicación/fisiopatología , Primidona/sangre , Primidona/líquido cefalorraquídeo , Primidona/metabolismo , Primidona/orinaRESUMEN
alpha-Ketoglutaramate, a deaminated metabolite of glutamine not previously identified in biological tissues, was measured in the cerebrospinal fluid of human subjects and found to be increased three- to tenfold in patients with hepatic coma. When perfused into the cerebral lateral ventricles of rats, alpha-ketoglutaramate (10 mM) depressed the animals' nocturnal locomotor activity, and at higher doses induced circling behavior and myoclonus. The concentration of alpha-ketoglutaramate in cerebrospinal fluid appears to be a reliable diagnostic indicator of hepatic coma, and its accumulation may contribute to the pathogenesis of this disease.