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Artykuły w czasopismach na temat "Médicaments – Administration par voie transcutanée – Évaluation"
Nouvel, M., S. Parat, A. Lepape i V. Piriou. "Administration des médicaments par voie parentérale en réanimation : évaluation des incompatibilités médicamenteuses". Annales Françaises d'Anesthésie et de Réanimation 33 (wrzesień 2014): A224—A225. http://dx.doi.org/10.1016/j.annfar.2014.07.378.
Pełny tekst źródłaRozprawy doktorskie na temat "Médicaments – Administration par voie transcutanée – Évaluation"
Collaveri, Jean-Pierre. "Etude des timbres transdermiques : évaluation d'une formulation adaptée à un principe actif x". Paris 5, 1990. http://www.theses.fr/1990PA05P051.
Pełny tekst źródłaTrichard, Laury. "Billes à base de cyclodextrines et d'huile : étude du mécanisme de formation et évaluation du potentiel en formulation et en thérapeutique". Paris 11, 2007. http://www.theses.fr/2007PA114810.
Pełny tekst źródłaA new dispersed system, consisting in semi-solid “beads”, is produced from a mixture of natural cyclodextrins, water and oil (vegetable, mineral or silicone oils) employing a soft, simple and innovative process. Beads were characterised and their formation mechanism was investigated by various physicochemical techniques. Thus, we identified some of the key points involved in bead formation: formation of inclusion complexes between oil components and cyclodextrins, formation of an o/w emulsion and cyclodextrin crystallisation. We took then benefits from the high oil content of beads to encapsulate two lipophilic model drugs, i. E. Isotretinoin and adapalene. Encapsulation yields reached 90-100%. Finally, our in vitro and in vivo assays showed that beads are well tolerated and are able to release active ingredients as well by oral than topical route
Pereira, de Santana Davi. "Évaluation biopharmaceutique de différentes formulations galéniques de l'isotrétinoine en gel". Université Joseph Fourier (Grenoble), 1992. http://www.theses.fr/1992GRE18013.
Pełny tekst źródłaPakpayat, Assavarat Natthilda. "Formulation et évaluation de l'acide ascorbique dans des microémulsions et nanoémulsions à base d'alkylpolyglucosides". Montpellier 1, 2008. http://www.theses.fr/2008MON13502.
Pełny tekst źródłaGrangier, Jean-Louis. "Mise au point et évaluation de l'association entre le GRF 1-29 et les nanoparticules de polyalkylcyanoacrylate". Paris 11, 1991. http://www.theses.fr/1991PA114817.
Pełny tekst źródłaCesaro, Umberto. "Advanced instrumentation for smart monitoring and automatic diagnostics in industrial and health applications". Electronic Thesis or Diss., Amiens, 2020. http://www.theses.fr/2020AMIE0040.
Pełny tekst źródłaIn this thesis, the feasibility of a method to measure the quantity of drug administered transdermally by impedance spectroscopy is demonstrated. The thesis proves the relevance of the impedance measurement to assess the quantity of drug penetrated into the skin after transdermal administration. In particular, the measured quantity of drug depends linearly on the variation in amplitude of impedance normalized to the pretreated value. In this thesis, the feasibility of a method to measure the quantity of drug administered transdermally by impedance spectroscopy is demonstrated.This thesis is made up of several parts, briefly described below. The first chapter presents an overview of electrical impedance spectroscopy and its applications. The second chapter talks about transdermal administration. This chapter also shows the feasibility of a method to measure the amount of drug transported transdermally. Next, the Drug Under Skin Meter (DUSM), a general purpose bioimpedance device capable of determining the amount of drug transmitted transdermally, is proposed. In the thesis, the concept and physical design of the instrument, as well as details on its production and operation, are illustrated. In addition, the experimental results obtained are illustrated The results indicate that the quantity of drug delivered can be evaluated by reasonable metrological performance by a single measurement of the amplitude of the impedance at a single frequency. The prototyped device has been shown to be able to identify the amount of drug (ml) delivered to a test tissue, by measuring the impedance spectrum before and after administration. The volume of drug (ml) transported through the skin is evaluated by locally measuring the bioimpedance before and after childbirth. In therapeutic applications, the instrument can provide an inexpensive and clinically portable solution. Then, the metrological characterization, using the injection as reference subcutaneous transfer of a known volume of drug, is reported, in laboratory, in vitro on eggplants and ex vivo, on ear pigs. The results of resolution, short-term stability, interindividual tissue reproducibility, sensitivity, repeatability and linearity indicate remarkable scenarios of clinical applications for such a bioimpedance device. Chapter three shows how the DUSM could also be used to monitor insulin absorption: a transducer on a chip, to monitor insulin that is actually bio-available after administration in clinical diabetology, is proposed. Bioavailability after administration is assessed by monitoring the amount of insulin under the skin using a bioimpedance measurement. An individual model, specific to each person during each insulin injection is identified, characterized and validated, to manage the individual inter and intra differences. Ideas of concept, architecture and operation of the transducer, as well as details on its prototype, are illustrated. Then, metrological characterization and validation are reported in the laboratory, as well as in vitro on eggplants, using injection as a reference subcutaneous transfer of a known volume of insulin. The results of significant intra-individual reproducibility in vitro on eggplants indicate significant scenarios for assessing the bioavailability of insulin in clinical diabetology. As an important branch of this research, the possibility of studying failure conditions in industrial plants was explored in Chapter 4. Finally two collateral works developed during this study period are presented
Nicoli, Sara. "Administration dermique et transdermique des médicaments : deux cas d'étude". Paris 11, 2002. http://www.theses.fr/2002PA114804.
Pełny tekst źródłaBlanchon, Sylvène. "Méthodologie d'étude pharmacotéchnique pour l'élaboration de systèmes transdermiques : application à la progestérone et à un progestatif de synthèse". Paris 11, 1991. http://www.theses.fr/1991PA114801.
Pełny tekst źródłaIllel, Brigitte. "Contribution à l'étude de la pénétration cutanée des particules : mise au point de deux méthodes d'étude quantitative des voies de pénétration transépidermiques et transfolliculaires". Paris 11, 1990. http://www.theses.fr/1990PA114804.
Pełny tekst źródłaDenoyer, Laurence. "L'analgésie par voie transdermique". Paris 5, 1998. http://www.theses.fr/1998PA05P030.
Pełny tekst źródłaKsiążki na temat "Médicaments – Administration par voie transcutanée – Évaluation"
F, Kydonieus Agis, i Berner Bret, red. Transdermal delivery of drugs. Boca Raton, Fla: CRC Press, 1987.
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