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Статті в журналах з теми "Administration contrôlée de médicaments":
Nkurunziza, Aimable, Geldine Chironda, Godfrey Katende, Lakshmi Rajeswaran, Emmanuel Munyaneza, and Madeleine Mukeshim. "Medication interruptions and associated factors among nurses working in pediatric unit at a selected referral hospital in Rwanda." Research Journal of Health Sciences 9, no. 4 (December 13, 2021): 320–29. http://dx.doi.org/10.4314/rejhs.v9i4.1.
Catros, Véronique. "Les CAR-T cells, des cellules tueuses spécifiques d’antigènes tumoraux." médecine/sciences 35, no. 4 (April 2019): 316–26. http://dx.doi.org/10.1051/medsci/2019067.
Tamai, Irene Y., Laurence Z. Rubenstein, Karen R. Josephson, Joyce A. Yamauchi, Brenda R. Morand, and Ina Lukosevicius. "Impact of Computerized Drug Profiles and a Consulting Pharmacist on Outpatient Prescribing Patterns: A Clinical Trial." Drug Intelligence & Clinical Pharmacy 21, no. 11 (November 1987): 890–95. http://dx.doi.org/10.1177/106002808702101109.
Trépanier, Eric F., and Guy W. Amsden. "Current Issues in Onychomycosis." Annals of Pharmacotherapy 32, no. 2 (February 1998): 204–14. http://dx.doi.org/10.1345/aph.17006.
Yang, Jiping, Bei Yang, Baoxin Xiu, Jinchong Qi, and Huaijun Liu. "Effect of Combination Therapy with Neuroprotective and Vasoprotective Agents on Cerebral Ischemia." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 45, no. 3 (May 2018): 325–31. http://dx.doi.org/10.1017/cjn.2018.8.
Le Floch-Meunier, Béatrice. "Administration des médicaments et événements indésirables." Soins 59, no. 784 (April 2014): 48–51. http://dx.doi.org/10.1016/j.soin.2014.02.009.
Brana, A., R. Getti, K. Mezaib, M. de Beauchene, and N. Simon. "182 - L’auto-administration contrôlée de morphine aux urgences." Journal Européen des Urgences 17 (March 2004): 74. http://dx.doi.org/10.1016/s0993-9857(04)97192-0.
Gordon, Richard L. "Prolonged Central Intravenous Ketorolac Continuous Infusion in a Cancer Patient with Intractable Bone Pain." Annals of Pharmacotherapy 32, no. 2 (February 1998): 193–96. http://dx.doi.org/10.1345/aph.17205.
Fourchard, Laurent. "Citoyens d’origine contrôlée au Nigeria." Genèses 112, no. 3 (2018): 58. http://dx.doi.org/10.3917/gen.112.0058.
Kwok, Jacqueline, Michael Kammermayer, Vincent H. Mabasa, Tiffany Winstone, and Darwin Chan. "Evaluating a Pharmacist-Initiated Care Bundle for Patients with Chronic Obstructive Pulmonary Disease." Canadian Journal of Hospital Pharmacy 75, no. 4 (October 3, 2022): 302–8. http://dx.doi.org/10.4212/cjhp.3226.
Дисертації з теми "Administration contrôlée de médicaments":
Yang, QiaoWen. "Systèmes polymériques à base de dispersion aqueuse administrés par voie orale pour la libération contrôlée du principe actif." Lille 2, 2009. http://www.theses.fr/2009LIL2S045.
Blanchemain, Nicolas. "Etude de la biocompatibilité et du greffage de cyclodextrines sur les prothèses vasculaires en PET pour la réalisation d'une prothèse à libération contrôlée de principe actif." Lille 1, 2005. http://www.theses.fr/2005LIL10146.
Prostheses used in vascular surgery (polyester) present a disadvantage: post-operative infections in up to 6 percent of the clinical cases. Based on the knowledge on inclusion properties and grafting of cyclodextrins (CDs), we established the concept of a vascular prosthesis modified with CDs that should be able to absorb antibiotics (ABs), and release them within a prolonged period. The study of the curing parameters allowed us to settle the optimal fixation temperature and time of curing for each four CD. We observed that the finishing reaction did not provoke any degradation of the mechanical properties of the prosthesis; moreover, it contributed to their blood tightness. Biological evaluation confirmed the non-toxicity of grafted surfaces, but proliferation tests revealed a low adaptation of epithelial and endothelial cells on prostheses. In vitro release assessments revealed the presence of all three ABs up to 30 days in water and up to 48 hours in plasma. Compared to virgin prostheses and on the market existing antibiotic impregnated prosthesis, this new prosthesis functionalised with CDs has a significantly prolonged bactericide effect
Abdul-Nour, Faraj. "Étude et conception des pompes implantables mécaniques pour l'administration de médicaments." Compiègne, 1988. http://www.theses.fr/1988COMPD149.
Vagnair, Virginie. "Les contrôles administratifs sur les médicaments." Bordeaux 4, 2003. http://www.theses.fr/2003BOR40042.
Drugs intended for human medicine are potentially dangerous products to public health and must be placed under the permanent control of public authorities. The main objective of the administration is to guarantee the safety of consumers, who must not be faced with mindless health risks. The controls exerted over that are a particular application of the famous precautionary principle. Two types of controls are distinguished. On the one hand, the controls in the sense of constraints weighing on the medicines are various examinations, verifications and appreciations focused on the pharmaceutical specialities throughout their chain, from their conception to their surveillance on the market, having passed through their manufacture, their authorization and their marketing. On the other hand, there are controls which are related to the various responsibilities incurred in the domain of medicines, those that could be harmful
Mimiague, Madeleine. "Les Drug Master Files type I et type II : application à une unité de fabrication d'injectables." Bordeaux 2, 1999. http://www.theses.fr/1999BOR2P072.
Darres, Céline. "Conservation des formes buvables multidoses pédiatriques." Paris 5, 1998. http://www.theses.fr/1998PA05P239.
Elkhoury, Kamil. "Nanofunctionalization and biofabrication of natural hydrogels for tissue engineering applications." Electronic Thesis or Diss., Université de Lorraine, 2021. http://www.theses.fr/2021LORR0020.
The main objective of this thesis is to develop a new natural material based on methacrylated gelatin (GelMA) nanofunctionalized by the incorporation of nanoliposomes or soft hybrid exosome-liposome nanoparticles. The physicochemical and biological properties of these hydrogel matrices were characterized in order to evaluate their potential use for tissue engineering applications. GelMA is prepared by the chemical modification of gelatin when methacrylate groups are attached to side groups containing amine functions. In a first part of this work, the influence of the gelatin source (pork or fish) and the degree of methacrylation on the physicochemical and biological properties of hydrogels was studied. In a second part of this work, the GelMA matrix was nanofunctionalized by the incorporation of nanoliposomes, which are soft and natural nanoparticles with remarkable self-assembly properties. These well-established drug delivery systems are formed of lipid bilayers and can transport and release hydrophobic, hydrophilic, and amphiphilic molecules. In this study, naringin, an active molecule that can guide the differentiation process of stem cells to the osteoblastic lineage, was encapsulated in nanoliposomes before their incorporation into the GelMA polymeric matrix in order to develop a system of interest for bone regeneration applications. This nanocomposite material was physicochemically and biologically characterized and the release profile of naringin was investigated. In a third and final part of this work, the GelMA matrix was nanofunctionalized by the incorporation of exosome-liposome soft hybrid nanoparticles. Exosomes, natural nanovesicles secreted by cells, are of increasing interest for targeted drug delivery applications due to the presence of cell specific receptors on their surface. The hybrid GelMA hydrogels were physicochemically and biologically characterized for applications in cardiac reprogramming and was successfully bioprinted and microfabricated. Biofabricated GelMA hydrogels nanofunctionalized with nanoliposomes or hybrid exosome-liposome nanoparticles are promising platforms for the controlled release of bioactive molecules and for tissue engineering applications
Padula, Cristina. "Patch-non-patch® : film polymérique pour la délivrance contrôlée des médicaments." Lyon 1, 2005. http://www.theses.fr/2005LYO10036.
Ongkasin, Kanjana. "Elaboration de dispositifs médicaux ophtalmiques à libération contrôlée de médicaments par imprégnation supercritique." Thesis, Aix-Marseille, 2019. http://www.theses.fr/2019AIXM0536.
Supercritical CO2 technologies are arisen as green and eco-responsible alternatives for drug formulation and medical device processing. The present PhD work aims to develop innovative ocular therapeutic medical devices to mitigate two post-operative complications of cataract surgery, endophthalmitis and posterior capsule opacification. Among other processes, supercritical impregnation was selected to load commercially available intraocular lenses (IOLs) commonly used in cataract surgery with ophthalmic drug components. A targeted action of drug molecules can be therefore achieved through a sustained release directly at the potential affected zones without requiring subsequent medical interventions. Supercritical impregnation of foldable hydrophobic acrylic IOLs was studied by varying the operating conditions of pressure (8 to 25 MPa), temperature (308 to 328 K) and impregnation duration (30 to 240 min). The influence of using ethanol as a co-solvent was also evaluated. In vitro drug release kinetics were studied and used to determine the impregnation yields. In order to rationalize the influence of the concomitant phenomena governing impregnation, thermodynamic behaviors of the involved systems, polymer/CO2 and drug/CO2 were studied. {Ex vivo} implantation of methotrexate impregnated IOLs on human donor capsular bags shown fibrosis reduction by inhibiting epithelial-mesenchymal transformation highlighting the potential of the innovative sustained-release drug-delivery IOLs to become of clinical relevance
Veaux, Adeline. "Zones à atmosphère contrôlée et eau purifiée dans l'application de la maîtrise de la contamination." Paris 5, 1998. http://www.theses.fr/1998PA05P021.
Книги з теми "Administration contrôlée de médicaments":
Curren, Anna M. Mathématiques et médicaments. 2nd ed. Laval, Qué: Beauchemin, 2001.
Curren, Anna M. Mathématiques et médicaments. Montréal, Qué: Études vivantes, 1991.
Curren, Anna M. Mathématiques et médicaments. 3rd ed. Montréal: Beauchemin Chenelière éducation, 2006.
Gaston, Labrecque, and Sirois-Labrecque Marcelle, eds. Chronopharmacologie: Rythmes biologiques et administration des médicaments. [Montréal]: Presses de l'Université de Montréal, 2003.
Dubois, Sylvie. Calcul, dosage, médicaments. 2nd ed. Montréal: Chenelière/McGraw-Hill, 2002.
Calop, Jean. La pharmacie clinique: Pourquoi?, comment? Paris: Ellipses, 1985.
Fortin, Marlène. Math et méd: Guide pour une administration sécuritaire des médicaments. 2nd ed. Montréal (Québec) Canada: Chenelière éducation, 2015.
Fortin, Marlène. Math et méd: Guide pour une administration sécuritaire des médicaments. Montréal: Chenelière-éducation, 2010.
Hilts, Philip J. Protecting America's health: The FDA, business, and one hundred years of regulation. New York: Alfred A. Knopf, 2003.
Boullata, Joseph I. Guidebook on enteral medication administration. Silver Spring, Md: American Society for Parenteral and Enteral Nutrition, 2019.
Частини книг з теми "Administration contrôlée de médicaments":
Mulot, A. "Administration des médicaments." In Réanimation et urgences, 405–19. Paris: Springer Paris, 2010. http://dx.doi.org/10.1007/978-2-287-99129-5_28.