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1.
Rapid Commun Mass Spectrom ; 25(11): 1552-8, 2011 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-21594929

RESUMO

Recently, electrospray ionization mass spectroscopy (ESI-MS) has been widely used for the identification of drugs of abuse and their metabolites in biological samples. However, the sensitivity and selectivity of this technique are commonly inadequate for the analysis of tetrahydrocannabinol (THC) and its metabolites at very low levels, such as those sometimes required in forensic and clinical-legal applications. We coupled electrospray ionization and surface-activated chemical ionization (ESI-SACI) to various types of mass analyzers (ion trap, triple quadrupole and orbitrap) (ESI-SACI-MS) to improve the detection of 11-nor-9-carboxy-tetrahydrocannabinol (THC-COOH), the most common marker of THC abuse. The benefits of this approach in terms of sensitivity and selectivity compared with a common ESI-MS approach are clearly demonstrated.


Assuntos
Dronabinol/análogos & derivados , Cabelo/química , Espectrometria de Massas por Ionização por Electrospray/métodos , Dronabinol/análise , Dronabinol/química , Dronabinol/urina , Humanos , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
2.
J Mass Spectrom ; 52(1): 16-21, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27776380

RESUMO

Electrospray Ionization and collision induced dissociation tandem mass spectrometry are usually employed to obtain compound identification through a mass spectra match. Different algorithms have been developed for this purpose (for example the nist match algorithm). These approaches compare the tandem mass spectra of the unknown analyte with the tandem mass spectra spectra of known compounds inserted in a database. The compounds are usually identified on the basis of spectral match value associated with a probability of recognition. However, this approach is not usually applied to multiple reaction monitoring transition spectra achieved by means of triple quadrupole apparatus, mainly due to the lack of a transition spectra database. The Surface Activated Chemical Ionization-Electrospray-NIST Bayesian model database search (SANIST) platform has been recently developed for new potential metabolite biomarker discovery, to confirm their identity and to use them for clinical and diagnostic applications. Here, we present an improved version of the SANIST platform that extends its application to forensic, pharmaceutical, and food analysis studies, where the compound identification rules are strict. The European Union (EU) has set directives for compound identification (EU directive 2002/657/EC). We have applied the SANIST method to identification of 11-nor-9-carboxytetrahydro-cannabinol in urine samples (an example of a forensic application), circulating levels of the immunosuppressive drug tacrolimus in blood (an example of a pharmaceutical application) and glyphosate in fruit juice (an example of a food analysis application) that meet the EU directive requirements. Copyright © 2016 John Wiley & Sons, Ltd.


Assuntos
Biomarcadores/análise , Espectrometria de Massas em Tandem/instrumentação , Espectrometria de Massas em Tandem/métodos , Algoritmos , Teorema de Bayes , Química Farmacêutica , Cromatografia Líquida de Alta Pressão/métodos , Bases de Dados Factuais , União Europeia , Análise de Alimentos , Ciências Forenses , Humanos
3.
In Vivo ; 20(6A): 697-701, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17203748

RESUMO

Nanotechnology provides a variety of nanoscale tools for medicine. Among them nanoparticles are revolutionizing the field of drug delivery. These drug nanocarriers have the potential to enhance the therapeutic efficacy of a drug, since they can be engineered to modulate the release and the stability and to prolong the circulation time of a drug, protecting it from elimination by phagocytic cells or premature degradation. Moreover, nanoscale carriers can be tailored to accumulate in tumour cells and tissues, due to enhanced permeability and a retention effect or by active targeting using ligands designed to recognize tumour-associated antigens. Could these nanomedicine tools mark an end to the necessity for loco-regional drug delivery?


Assuntos
Antineoplásicos/administração & dosagem , Sistemas de Liberação de Medicamentos/métodos , Nanomedicina/métodos , Nanopartículas/administração & dosagem , Antineoplásicos/efeitos adversos , Portadores de Fármacos , Humanos , Nanopartículas/efeitos adversos
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