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1.
Clin Pharmacol Drug Dev ; 10(3): 260-271, 2021 03.
Artículo en Inglés | MEDLINE | ID: mdl-32748570

RESUMEN

Two open-label, single-dose, randomized crossover studies were conducted in healthy Japanesemen to (1) assess dose proportionality of 5 doses (1.38, 2.75, 5.5, 8.25, and 11.0 mg) of Lafenta, a novel matrix-type transdermal fentanyl patch with a rate-controlling membrane; and (2) compare patch bioequivalence (11.0 mg) with a commercially available reference patch (Durotep MT Patch [16.8 mg]). Pharmacokinetics, adhesion performance, residual fentanyl, and safety parameters were assessed. Increases in mean AUC0-t and Cmax after application of the test patch were dose proportional. The test patch (11.0 mg) was bioequivalent to the 16.8-mg reference patch in terms of mean AUC0-inf , AUC0-t , and Cmax . Residual fentanyl levels 72 hours postapplication were lower in the test than in the reference patch. Differences in adhesion performance between the test and the reference patch did not affect delivery efficacy and reliability of the novel matrix patch. Safety findings were in line with previous experiences with fentanyl. Both studies showed low variation in fentanyl exposure and delivery via the test patch. The test patch provided equivalent fentanyl exposure at a lower dose than the reference patch formulation with lower variability and the potential to lower medicinal waste.


Asunto(s)
Analgésicos Opioides/farmacocinética , Tolerancia a Medicamentos/etnología , Fentanilo/farmacocinética , Administración Cutánea , Adulto , Analgésicos Opioides/administración & dosificación , Analgésicos Opioides/efectos adversos , Área Bajo la Curva , Disponibilidad Biológica , Estudios Cruzados , Relación Dosis-Respuesta a Droga , Composición de Medicamentos/métodos , Sistemas de Liberación de Medicamentos , Fentanilo/administración & dosificación , Fentanilo/efectos adversos , Voluntarios Sanos/estadística & datos numéricos , Humanos , Japón/epidemiología , Naltrexona/administración & dosificación , Antagonistas de Narcóticos/administración & dosificación , Reproducibilidad de los Resultados , Seguridad , Equivalencia Terapéutica , Parche Transdérmico/efectos adversos
2.
Skin Res Technol ; 26(3): 329-337, 2020 May.
Artículo en Inglés | MEDLINE | ID: mdl-31785045

RESUMEN

BACKGROUND/AIMS: During dermatological forms development, one of the simplest non-invasive techniques used to evaluate cutaneous tolerance of formulations is to monitor the color changes using a tristimulus chromameter. Most published tolerance studies involving chromametric measurements are performed on Caucasian subjects. However, in the context of drug formulation for African-type populations, it is not always relevant to transpose tolerance results obtained on Caucasians populations to African-type ones due to histological ethnic differences of the skin. The goal of this work was to assess whether tristimulus chromameter can be used to highlight color variations following the application of dermatological topics on black skin in order to validate skin tolerance studies made on African-type subjects. MATERIALS AND METHODS: After application of two commercial creams with opposite side effects (skin irritation and skin blanching) in both Africans and Caucasians populations, color variations were evaluated using a tristimulus chromameter in L* a* b* color system and compared between both populations. L* indicating color brightness, a* represents green and red directions and b* represents blue and yellow directions. RESULTS: While skin irritation resulted in a significant increase of a* parameter in both studied populations, the skin blanching resulted in a decrease of a* associated with an increase of L* . CONCLUSION: We established that tristimulus chromameter can be used to achieve in vivo skin tolerance study of dermatologic formulations in Africans despite their dark skin even though it appeared less sensitive. This study can speed up the development of dermatological forms dedicated to Africans and/or Caucasians subjects.


Asunto(s)
Fármacos Dermatológicos/efectos adversos , Tolerancia a Medicamentos/etnología , Pigmentación de la Piel/efectos de los fármacos , Piel/efectos de los fármacos , Administración Cutánea , Adulto , Bélgica/etnología , Población Negra/estadística & datos numéricos , Color , Colorimetría/métodos , Fármacos Dermatológicos/administración & dosificación , Eritema/inducido químicamente , Eritema/etnología , Femenino , Humanos , Masculino , Preparaciones Farmacéuticas , Piel/patología , Pruebas de Irritación de la Piel/métodos , Población Blanca/estadística & datos numéricos
3.
Chem Senses ; 35(9): 813-22, 2010 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-20739429

RESUMEN

Preference determines behavioral choices such as choosing among food sources and mates. One preference-affecting chemical is ethanol, which guides insects to fermenting fruits or leaves. Here, we show that adult Drosophila melanogaster prefer food containing up to 5% ethanol over food without ethanol and avoid food with high levels (23%) of ethanol. Although female and male flies behaved differently at ethanol-containing food sources, there was no sexual dimorphism in the preference for food containing modest ethanol levels. We also investigated whether Drosophila preference, sensitivity and tolerance to ethanol was related to the activity of alcohol dehydrogenase (Adh), the primary ethanol-metabolizing enzyme in D. melanogaster. Impaired Adh function reduced ethanol preference in both D. melanogaster and a related species, D. sechellia. Adh-impaired flies also displayed reduced aversion to high ethanol concentrations, increased sensitivity to the effects of ethanol on postural control, and negative tolerance/sensitization (i.e., a reduction of the increased resistance to ethanol's effects that normally occurs upon repeated exposure). These data strongly indicate a linkage between ethanol-induced behavior and ethanol metabolism in adult fruit flies: Adh deficiency resulted in reduced preference to low ethanol concentrations and reduced aversion to high ones, despite recovery from ethanol being strongly impaired.


Asunto(s)
Alcohol Deshidrogenasa/fisiología , Drosophila melanogaster/efectos de los fármacos , Tolerancia a Medicamentos/etnología , Etanol/farmacología , Tolerancia Inmunológica/fisiología , Alcohol Deshidrogenasa/deficiencia , Alcohol Deshidrogenasa/metabolismo , Alcoholes/farmacología , Animales , Drosophila melanogaster/fisiología , Tolerancia a Medicamentos/fisiología , Femenino , Preferencias Alimentarias/efectos de los fármacos , Preferencias Alimentarias/fisiología , Masculino
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