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1.
Trials ; 24(1): 724, 2023 Nov 13.
Artículo en Inglés | MEDLINE | ID: mdl-37957769

RESUMEN

BACKGROUND: Preoperative anxiety management is gaining particular attention in paediatric anaesthesia. Pharmacological and non-pharmacological resorts can be implemented to address this special issue. Despite the various approaches currently used for preoperative sedation in children, the different sedative and anti-anxiety effects between the newly marketed anaesthetic, S-ketamine, and the traditional sedative, midazolam, are still unclear. METHODS: This is a patient- and assessor-blinded randomized controlled clinical trial. Participants (n = 110) will receive S-ketamine (0.5 mg/kg) or midazolam (0.08 mg/kg) intravenously administrated at a ratio of 1:1 in the anaesthesia holding area. The primary outcome of this study is the sedative effect evaluated via the change in the modified Yale preoperative anxiety scale. It will be performed at two timepoints: in the pre-anaesthetic holding area before premedication (baseline, marked as T0) and about 5 min after premedication in the operating room without the existence of their guardians (marked as T1). Our secondary objectives include the parent separation anxiety score, postoperative agitation, caregivers' and anaesthesia care providers' satisfaction, and mask compliance. DISCUSSION: This randomized controlled trial is the first study to compare the anti-anxiety effect of intravenous S-ketamine and midazolam. We will provide a new approach for the clinical management of preoperative anxiety in preschool children posted for elective surgery. TRIAL REGISTRATION: ChiCTR2300069998. Registered on 30 March 2023.


Asunto(s)
Anestésicos , Ansiolíticos , Preescolar , Humanos , Hipnóticos y Sedantes/efectos adversos , Midazolam/efectos adversos , Ansiolíticos/efectos adversos , Método Doble Ciego , Ensayos Clínicos Controlados Aleatorios como Asunto
2.
Front Chem ; 8: 619307, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33585401

RESUMEN

In this study, two isomeric impurities were identified in cefotiam hydrochloride injection preparation and were characterized. Column-switching HPLC-MS and NMR techniques were used to identify the impurity 1 as the Δ3(4) isomers of cefotiam. Using software-based calculations, it was predicted that neither of the isomeric impurities was embryotoxic. This study provides a reference for the production, storage, and quality control of cefotiam and related cephalosporin antibiotics.

3.
J Chromatogr A ; 1608: 460418, 2019 Dec 20.
Artículo en Inglés | MEDLINE | ID: mdl-31420179

RESUMEN

High performance liquid chromatography coupled with quadrupole-time-of-flight mass spectrometry (HPLC-QTOF-MS) is widely used to qualitatively characterize the chemical profiles of herbal medicines, in which the generated adducts and fragments are crucial for confirming molecular ion (deprotonated/protonated ion) and deducing structure of detected components. However, how chromatographic and mass spectrometric (LC-MS) conditions/parameters affect the quantity and intensity of adducts and fragments of detected components is scarcely concerned. In present study, three types of triterpene saponins from the root of Ilex asprella (RIA) were selected as a case study to systematically investigate the effects of LC/MS conditions/parameters on their ionization and fragmentation, so as to obtain higher intensity (higher detection sensitivity) and quantity (rich information) of adducts and fragments for the characterization of components in RIA. It was found that for LC conditions, methanol as organic phase was more benefit for generating more adducts with higher intensity; formic acid as a modifier suppressed the formation of [M-2H]2-, thus promoted the generation of other types of adducts at lower concentration but inhibited the generation when the concentration exceeded 0.1%. MS parameters affect scarcely the quantity but mainly intensity of adducts, cone voltage, source temperature and desolvation gas flow have relatively higher impacts when compared with other parameters. Collision energy affected both quantity and intensity of fragments. MS parameters at the medium value largely increased the quantity and intensity of adducts and fragments. Three-types of triterpene saponins presented structurally specific ionization and fragmentation due to their amounts of acidic substitutes. A total of 55 components were detected and definitely or tentatively identified in RIA under the optimized LC-MS conditions, among which 35 triterpene saponins were firstly discovered. This is the first report that proposes and validates a systematic approach for assessing the effects of LC/MS conditions/parameters on the ionization and fragmentation of analytes, which could be helpful for the optimization of LC-MS conditions for effective chemical profiling analysis of herbal medicines.


Asunto(s)
Cromatografía Líquida de Alta Presión/métodos , Ilex/química , Extractos Vegetales/química , Saponinas/química , Espectrometría de Masa por Ionización de Electrospray/métodos , Triterpenos/química , Estructura Molecular , Plantas Medicinales/química
4.
J Chromatogr A ; 1581-1582: 33-42, 2018 Dec 21.
Artículo en Inglés | MEDLINE | ID: mdl-30389211

RESUMEN

In this study, a time segment scanning-based quasi-multiple reaction monitoring (quasi-MRM) mode was proposed to improve the quantitative performance of UPLC-QTOF-MS/MS. To achieve the quasi-MRM mode, a strategy to select the ion pair (precursor and product ions) of each analyte was adopted as follows. First, a stable and abundant ion by quadrupole was set as precursor ion in MS scan mode. Second, the fragment ions of the precursor ion formed via collision-induced dissociation were measured by time-of-flight (TOF) in MS/MS scan mode; a characteristic, stable and abundant fragment ion (or precursor ion in case of fragment ion unavailable) was designated as the product ion. Third, the detection specificity and sensitivity of the product ion by TOF were strengthened through time segment scanning over a narrowed mass scan range. The proposed quasi-MRM mode achieved simultaneous quantification of fifteen major components in Moutan Cortex, a widely used medicinal herb, as well as its sulfur-fumigated samples. The quasi-MRM mode was methodologically compared with the other two quantitative modes commonly used in the UPLC-PDA-QTOF-MS/MS apparatus, namely UPLC-PDA and extracted ion analysis. The results demonstrated that the quasi-MRM mode performed better in specificity, sensitivity and linearity. The quasi-MRM mode was further validated with regard to precision, accuracy and stability. The research deliverables indicate that the proposed mode improved the quantitative capability of UPLC-QTOF-MS/MS, and therefore could serve as a potential mode for QTOF-MS/MS-based quantification of herbal medicines.


Asunto(s)
Técnicas de Química Analítica/métodos , Cromatografía Líquida de Alta Presión , Medicamentos Herbarios Chinos/química , Medicina de Hierbas , Paeonia/química , Espectrometría de Masas en Tándem , Plantas Medicinales/química
5.
Yao Xue Xue Bao ; 43(5): 518-22, 2008 May.
Artículo en Chino | MEDLINE | ID: mdl-18717341

RESUMEN

The residual protein mixture (the content is 4%, approximately), called Salvia miltiorrhiza antigen, was extracted from the Salvia miltiorrhiza cruel materials by mimicking the alcohol-deposit extracts process. Both rabbits and guinea pigs sensitized by Salvia miltiorrhiza could produce specified antibodies. Large molecular antigenic impurities were extracted from the Danshen injection and Xiangdan injection using the centrifugal filtering method. The test results of active systemic anaphylaxis (ASA) and passive cutaneous anaphylaxis (PCA) in guinea pigs confirmed that the extracted antigenic impurities could induce the anaphylaxis reaction in the animals which were sensitized by the Salvia miltiorrhiza antigen. Using the specified antibody produced from rabbits which were sensitiyed by Salvia miltiorrhiza, ELISA test method was developed to test the residual Salvia miltiorrhiza antigenic materials contained in the parenteral Chinese traditional medicines. Calculated as residual protein, the linear range was 0.08-5.12 microg x mL(-1) (r2 = 0.9906), the detection limit and quantization limit are 0.08 microg x mL(-1) and 0.4 microg x mL(-1), respectively. 308 batches of parenteral Chinese traditional medicines containing water-soluable components of Salvia miltiorrhiza were tested, and the Salvia miltiorrhiza antigenic impurities were spotted in 35 (11.4%) batches of samples. The test results show that the extracting process currently used can not remove the Salvia miltiorrhiza antigenic impurities completely, and this may be one of the reasons for anaphylactic reaction in clinics. The proposed ELISA method can be used for improving the manufacture process and for routine quality control of drug products.


Asunto(s)
Anafilaxia/inducido químicamente , Antígenos de Plantas/análisis , Medicamentos Herbarios Chinos/química , Fenantrolinas/química , Salvia miltiorrhiza/química , Animales , Antígenos de Plantas/toxicidad , Combinación de Medicamentos , Ensayo de Inmunoadsorción Enzimática/métodos , Femenino , Cobayas , Masculino , Anafilaxis Cutánea Pasiva/efectos de los fármacos , Control de Calidad , Conejos
6.
Bioorg Med Chem ; 14(23): 7826-34, 2006 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-16919462

RESUMEN

A known N-acetyldopamine dimer, (2R,3S)-2-(3',4'-dihydroxyphenyl)-3-acetylamino-7-(N-acetyl-2''-aminoethyl)-1,4-benzodioxane (1) and a new N-acetyldopamine dimer, (2R,3S)-2-(3',4'-dihydroxyphenyl)-3-acetylamino-7-(N-acetyl-2''-aminoethylene)-1,4-benzodioxane (2) were isolated from the methanolic extracts of Periostracum Cicadae. Compounds 1 and 2 inhibited the Cu2+ -mediated, 2,2'-azobis(2-amidinopropane) hydrochloride (AAPH)-mediated, and 3-morpholinosydnonimine (SIN)-1-mediated LDL oxidation in the thiobarbituric acid-reactive substances (TBARS) assay. The antioxidant activities of 1 and 2 were tested with respect to other parameters, such as lag time of conjugated diene formation, relative electrophoretic mobility (REM), and apoB-100 fragmentation on copper-mediated LDL-oxidation. Compounds 1 and 2 also showed 1,1-diphenyl-2-picrylhydrasyl (DPPH) radical scavenging activity. Compound 2 was more efficient than compound 1 at inhibiting the reactive oxygen species (ROS) generation, nitric oxide (NO) production, and nuclear factor-kappaB (NF-kappaB) activity as well as the expression of pro-inflammatory molecules such as inducible nitric oxide synthase (iNOS), interleukin (IL)-6, tumor necrosis factor (TNF)-alpha, and cyclooxygenase (COX)-2 in LPS-induced RAW264.7 cells.


Asunto(s)
Antiinflamatorios no Esteroideos/farmacología , Antioxidantes/farmacología , Dopamina/análogos & derivados , Medicamentos Herbarios Chinos/farmacología , Plantas Medicinales/química , Animales , Antiinflamatorios no Esteroideos/aislamiento & purificación , Antioxidantes/aislamiento & purificación , Línea Celular , Dimerización , Dopamina/aislamiento & purificación , Dopamina/farmacología , Medicamentos Herbarios Chinos/aislamiento & purificación , Depuradores de Radicales Libres , Peroxidación de Lípido/efectos de los fármacos , Lipoproteínas LDL/metabolismo , Macrófagos/efectos de los fármacos , Macrófagos/metabolismo , Ratones , Oxidación-Reducción/efectos de los fármacos , Extractos Vegetales/farmacología , Sustancias Reactivas al Ácido Tiobarbitúrico
7.
Biol Pharm Bull ; 29(4): 735-9, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16595909

RESUMEN

The oxidized low-density lipoprotein (ox-LDL) plays a critical role at the early stages of atherosclerosis. Thus, the prevention of LDL-oxidation by antioxidants may arrest the progression of atherosclerosis. Two quinoline alkaloids, 3,8-dihydroxyquinoline (1) and 2,8-dihydroxy-3,4-dimethoxyquinoline (3), and 2,4-di-tert-butylphenol (2) were isolated from the dried body of Scolopendra subspinipes. Compounds 1-3 exhibited antioxidant activities on copper-mediated (1: IC50=2.6 microM, 2: IC50=8.2 microM, 3: IC50=63.0 microM), AAPH-mediated oxidation (1: IC50=3.9 microM, 2: IC50=9.9 microM, 3: IC50=71.8 microM), and SIN-1-mediated oxidation (1: 70%, 2: 52%, 3: 29% at 5.0 microM) in the TBARS assay. The antioxidant activities of compounds 1-3 were tested with respect to other parameters, such as the lag time of conjugated diene fromation, relative electrophoretic mobility (REM) of ox-LDL, and apoB-100 fragmentation on copper-mediated LDL-oxidation. In addition, compounds 1-3 showed 1,1-diphenyl-2-picrylhydrasyl (DPPH) radical scavenging activity and compound 1 also exhibited metal chelating activity.


Asunto(s)
Alcaloides/farmacología , Antioxidantes/farmacología , Artrópodos/química , Quinolinas/farmacología , Amidinas/química , Animales , Apolipoproteína B-100 , Apolipoproteínas B/metabolismo , Compuestos de Bifenilo , Quelantes/farmacología , Cobre/química , Ensayo de Cambio de Movilidad Electroforética , Depuradores de Radicales Libres/farmacología , Lipoproteínas LDL/sangre , Molsidomina/análogos & derivados , Molsidomina/farmacología , Oxidación-Reducción , Oxiquinolina/análogos & derivados , Oxiquinolina/química , Oxiquinolina/farmacología , Picratos/química , Espectrofotometría Infrarroja , Espectroscopía Infrarroja por Transformada de Fourier , Sustancias Reactivas al Ácido Tiobarbitúrico
8.
Bioorg Med Chem Lett ; 14(16): 4277-80, 2004 Aug 16.
Artículo en Inglés | MEDLINE | ID: mdl-15261286

RESUMEN

Unsaturated fatty acid amides, 9(Z)-octadecenamide (2) and 9(Z),12(Z)-octadecadienamide (4) as inhibitors of acyl-CoA: cholesterol acyltransferase (ACAT) were isolated from the ethyl acetate extracts of the insect, Mylabris phalerate Pallas, and elucidated by their spectroscopic data analysis. Compounds 2 and 4 inhibited rat liver microsomal ACAT, hACAT-1, and hACAT-2 with IC(50) values of 170, 85, and 63 microM for 2 and of 151, 53, and 45 microM for 4, respectively.


Asunto(s)
Amidas/farmacología , Ácidos Grasos/farmacología , Esterol O-Aciltransferasa/antagonistas & inhibidores , Tenebrio/química , Amidas/química , Amidas/aislamiento & purificación , Animales , Ácidos Grasos/química , Ácidos Grasos/aislamiento & purificación , Microsomas Hepáticos/enzimología , Ratas , Espectrometría de Masa por Ionización de Electrospray , Esterol O-Aciltransferasa/metabolismo
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