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Artykuły w czasopismach na temat "Drugs"
Khanapure, Amol, Pem Chuki i Avinash De Sousa. "Drug Repositioning : Old Drugs For New Indications". Indian Journal of Applied Research 4, nr 8 (1.10.2011): 462–66. http://dx.doi.org/10.15373/2249555x/august2014/119.
Pełny tekst źródłaBocharova, Inna Anatolevna, Vadim Agadzhanov i Vadim Sagalaev. "Drug addiction. Drugs and their effects on man". Vestnik Volgogradskogo Gosudarstvennogo Universiteta. Serija 11. Estestvennye nauki, nr 2 (1.12.2013): 22–27. http://dx.doi.org/10.15688/jvolsu11.2013.2.3.
Pełny tekst źródłaIsnenia, Isnenia. "Penggunaan Non-Steroid Antiinflamatory Drug dan Potensi Interaksi Obatnya Pada Pasien Muskuloskeletal". Pharmaceutical Journal of Indonesia 6, nr 1 (1.12.2020): 47–55. http://dx.doi.org/10.21776/ub.pji.2020.006.01.8.
Pełny tekst źródłaRenner, Rebecca. "Drams of Drugs and Dregs". Scientific American 286, nr 5 (maj 2002): 29. http://dx.doi.org/10.1038/scientificamerican0502-29.
Pełny tekst źródłaIsmatov, Farrukh Asliddinovich. "DRUG TREATMENT WITH NON-STEROIDAL ANTI-INFLAMMATORY DRUGS JAW ALVEOLITIS". Frontline Medical Sciences and Pharmaceutical Journal 02, nr 03 (1.03.2022): 88–94. http://dx.doi.org/10.37547/medical-fmspj-02-03-09.
Pełny tekst źródłaA. Amer, Sayed. "المخدرات الجديدة: العقاقير المصممة". Security Policy Paper 2, nr 2 (31.12.2021): 01–03. http://dx.doi.org/10.26735/ndan7653.
Pełny tekst źródłaD, Subba Reddy, Prasanthi G, Amruth Raj S, Hari Krishna T, Sowjanya K i Shantha Kumari K. "EVALUATION OF ANTICANCER GENERIC DRUGS AND BRANDED DRUGS". Indian Research Journal of Pharmacy and Science 5, nr 1 (marzec 2018): 1378–91. http://dx.doi.org/10.21276/irjps.2018.5.1.16.
Pełny tekst źródłaKhrypunova, Tetiana. "Relationships between the Ukrainian Public's Awareness of Psychotropic Drugs, Stigmatizing People Taking Psychotropic Drugs and Stopping Psychotropic Drug Medication without Consulting with a Doctor". Ukraïnsʹkij žurnal medicini, bìologìï ta sportu 6, nr 5 (27.10.2021): 370–75. http://dx.doi.org/10.26693/jmbs06.05.370.
Pełny tekst źródłaGillam, Tony. "Drugs or no drugs?" Nursing Standard 20, nr 23 (15.02.2006): 26–27. http://dx.doi.org/10.7748/ns.20.23.26.s30.
Pełny tekst źródłaChawra, Himmat Singh, Y. S. Tanwar, Ritu M. Gilhotra i S. K. Singh. "Gastroretentive drug delivery systems a potential approach for antihypertensive drugs: An updated review". Asian Pacific Journal of Health Sciences 5, nr 2 (czerwiec 2018): 217–23. http://dx.doi.org/10.21276/apjhs.2018.5.2.40.
Pełny tekst źródłaRozprawy doktorskie na temat "Drugs"
Keesling, James Richard. "An evaluation of the drugs crime nexus, legalization of drugs, drug enforcement, and drug treatment rehabilitation". CSUSB ScholarWorks, 2000. https://scholarworks.lib.csusb.edu/etd-project/1697.
Pełny tekst źródłaApps, MIchael Garry. "Platinum anticancer drugs and drug delivery systems". Thesis, The University of Sydney, 2015. http://hdl.handle.net/2123/14409.
Pełny tekst źródłaOsorio, Javier. "Hobbes on drugs| Understanding drug violence in Mexico". Thesis, University of Notre Dame, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3738644.
Pełny tekst źródłaThis dissertation analyzes the unprecedented eruption of organized criminal violence in Mexico. To understand the dynamics of drug violence, this dissertation addresses three questions. What explains the onset of the war on drugs in Mexico? Once the conflict starts, why does drug violence escalate so rapidly? And lastly, why is there subnational variation in the concentration of violence?
Based on a game theoretic model, the central argument indicates that democratization erodes the peaceful configurations between the state and criminal organizations and motivates authorities to fight crime, thus triggering a wave of violence between the state and organized criminals and among rival criminal groups fighting to control strategic territories. In this account, state action is not neutral: law enforcement against a criminal group generates the opportunity for a rival criminal organization to invade its territory, thus leading to violent interactions among rival criminal groups. These dynamics of violence tend to concentrate in territories favorable for the reception, production and distribution of drugs. In this way, the disrupting effect of law enforcement unleashes a massive wave of violence of all-against-all resembling a Hobbesian state of war.
To test the observable implications of the theory, the empirical assessment relies on a novel database of geo-referenced daily event data at municipal level providing detailed information on who did what to whom, when and where in the Mexican war on drugs. This database covers all municipalities of the country between 2000 and 2010, thus comprising about 9.8 million observations. The creation of this fine-grained database required the development of Eventus ID, a novel software for automated coding of event data from text in Spanish. The statistical assessment relies on quasi-experimental identification strategies and time-series analysis to overcome problems of causal inference associated with analyzing the distinct - yet overlapping - processes of violence between government authorities and organized criminals and among rival criminal groups. In addition, the statistical analysis is complemented with insights from fieldwork and historical process tracing. Results provide strong support for the empirical implications derived from the theoretical model.
Hernández, Yulán. "Drugs". Revista de Química, 2016. http://repositorio.pucp.edu.pe/index/handle/123456789/101299.
Pełny tekst źródłaDossou-Yovo, Flore. "Modification de la biodisponibilité orale des médicaments : interactions « Herb-Drugs » « Drugs- Drugs»". Thesis, Paris, CNAM, 2014. http://www.theses.fr/2014CNAM0936/document.
Pełny tekst źródłaOral dosing is still seen as the silver bullet of drug administration, as it is cheaper andbetter adapted to patient comfort. However, oral route is still inaccessible to many drugssuch as biologics and biosimilars respectively certain anticancer drugs and antiretrovirals(ARV).The aim of this present study was to find new drugs enhancers that improve the oralbioavailability of drugs and xenobiotics. All the studies were realized in vitro using Ussingchambers technic. To achieve the set objective we used the strategy to develop drugenhancer which can modulate at the same time transcellular and paracellular pathways.In the first part of this study (patent) we have shown that the use of a pharmaceutical and /or a dietetic formulation containing a plant extract (Hibiscus sabdariffa) could increase thebioavailability in vitro in rats not only of cisplatin (21 fold), oxaliplatin (11 fold) andFluorescein Isothiocyanate-Dextran 4000 (FD4, 3 fold). All that drugs were transportedthrough intestinal barrier using paracellular pathway. In addition the study showed thatthis formulated enhancer can increased the bioavailability of Efavirenz (7 fold) andAtazanavir (4 fold) which are active transported.In order to assess the effect of new drugs enhancer on mucus thickness that limits thetransport of xenobiotic through intestinal barrier, we decide to evaluate his effect on passiveand active transport of drugs.In the second part of this study we have shown that after a week of pre-treatment of ratswith Metronidazole (MTZ, publication 1) and Cotrimoxazole (CTX, publication 2), the twomost commonly used antibiotics in the prophylaxis against opportunistic infections in HIV /AIDS, both increase colonic mucus thickness that affect directly passive intestinalpermeability by reducing conductance an index of passive transport through intestinalepithelium. In addition those antibiotics also entail a change in the transepithelialconductance and ARV fluxes. After MTZ and CTX treatment the secretion of Atazanavir(ATZ) increases respectively in the proximal colon by 2 to 4 fold and in the distal colon by 3to 5 fold respectively. Ritonavir (RTV) is poorly absorbed in control, after a week of pretreatmentwith MTZ and CTX one rather notices a secretion of RTV 5 to 10 fold higher in theproximal and 2 to 5 fold higher in the distal colon. The next study will be conducted toevaluate the effect of new drugs enhancer on mucus thickness layer.In conclusion, oral bioavailability of drugs and xenobiotics can be enhanced bypharmaceutical composition that contains herbal extract which increase passive and activetransport of drugs through intestinal barrier
Mohiddin, Syed Basha. "Development of novel unsupervised and supervised informatics methods for drug discovery applications". Columbus, Ohio : Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1138385657.
Pełny tekst źródłaRosenbaum, Erik. "Optical characterization of potential drugs and drug delivery systems". Doctoral thesis, Umeå universitet, Kemiska institutionen, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-40177.
Pełny tekst źródłaAttardo, Giorgio G. (Giorgio Giovanni). "Drug design and synthesis of novel heteroanthracycline antitumor drugs". Thesis, McGill University, 1990. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=74641.
Pełny tekst źródłaAfter extensive studies, three methodologies were developed for the general synthetic plan. The first method involved photoenolisation of 2,5-dimethoxybenzaldehyde and SO$ sb2$ entrapment of the o-quinodimethane to give 4,7-dimethoxy-1-hydroxy-1,3-dihydrobenzo(2,3-c) thiophene-2,2-dioxide. This compound served as a general intermediate towards the synthesis of several heteroanthracyclinones. It could be reduced to the oxathiin-2-oxide derivative which thermally extruded SO$ sb2$ to yield the o-quinodimethane. Reentrapment of this latter intermediate with various glyoxalates gave key isochroman derivatives. The second method is an improvement over the first. Isochromandiones with a C-1 hydroxyl functionality were prepared from oxidative demethylation of 1-hydroxyisochromans. These were obtained after acid hydrolysis of the coupling products between epoxides and the cuprate of 2,5-dimethoxy-6-methylbenzaldehydedioxane acetal. The third method involved a sequential cycloaddition routine with two o-quinodimethanes.
By combining newly developed techniques with known methods, a general synthetic plan was developed. Consequently, the total synthesis of six tetracyclic structural hybrids of the naphthoquinone(2,3-c) pyranyl class of antibiotics was accomplished; along with the total synthesis of (R) and (S) 1-(4$ sp prime$-O-p-nitrobenzoyl-N-trifluoroacetyldaunosamine)-$ 1,3$-dihydrothioxantho(2,3-c) thiophene-2,2-dioxide, p-nitrobenzyl(5,12-dihydroxy-3,4-dihydrothioxantho(2,3-c) and (3,2-c) pyran-3-yl)formate, and eight novel heteroanthracyclines with the 5,12-dioxo-2,3,5,12-tetrahydroanthraceno(2,3-c) pyranyl backbone. The diastereomeric mixture of (1$ sp prime$S, 1R, 3S) and (1$ sp prime$S, 1S, 3R) methyl(11-hydroxy-1-$(2 sp prime,3 sp prime,6 sp prime $-trideoxy-3-trifluoroacetamido-L-lyxohexopyranose)-$5,12 $-dioxo-3,4,5,12-tetrahydroanthraceno(2,3-c) pyran-3-yl) formate was found to possess equipotent antileukemic activity to doxorubicin with no cross resistance.
Hill, John C. "DRUMMING AWAY DRUGS: AN INNOVATIVE ALTERNATIVE TOWARDS DRUG REHABILITATION". UKnowledge, 2014. http://uknowledge.uky.edu/cld_etds/14.
Pełny tekst źródłaHemingway, Judith Frances Mary. "Spatializing drugs discourses : cultural geographies of illicit drug-using". Thesis, University College London (University of London), 2003. http://discovery.ucl.ac.uk/10020432/.
Pełny tekst źródłaKsiążki na temat "Drugs"
Ward, Brian R. Drugs and drug abuse. London: F. Watts, 1987.
Znajdź pełny tekst źródłaWard, Brian. Drugs and drug abuse. London: Watts, 1987.
Znajdź pełny tekst źródła1946-, Stangeland Per, red. Drugs and drug control. Oslo: Norwegian University Press, 1987.
Znajdź pełny tekst źródłaOttenbrite, Raphael M., red. Polymeric Drugs and Drug Administration. Washington, DC: American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0545.
Pełny tekst źródłaM, Ottenbrite Raphael, i Kim Sung Wan, red. Polymeric drugs & drug delivery systems. Lancaster, Pa: Technomic Pub. Co., 2001.
Znajdź pełny tekst źródłaGroup, Publishers, red. Street drugs: Drug identification guide. Plymouth, MN: Publishers Group, 2007.
Znajdź pełny tekst źródłaGroup, Publishers, red. Street drugs: Drug identification guide. [Plymouth, MN]: Publishers Group, 2002.
Znajdź pełny tekst źródłaMassachusetts. Department of Public Health. Generic drugs (interchangeable drugs). Boston, MA: Massachusetts Dept. of Public Health, 1988.
Znajdź pełny tekst źródłaOwen, Claire. Drugs. Cambridge: Independence, 2009.
Znajdź pełny tekst źródłaPolice, Illinois State. Drugs. Springfield, Ill.]: Illinois State Troopers, Dept. of State Police, 1986.
Znajdź pełny tekst źródłaCzęści książek na temat "Drugs"
Eleonorasdotter, Emma. "Obtaining Drugs". W Women’s Drug Use in Everyday Life, 143–73. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-46057-9_5.
Pełny tekst źródłaFolkers, Gerd, Elvan Kut i Martin Boyer. "Drug Design: Designer Drugs". W X.media.publishing, 53–63. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-69002-3_5.
Pełny tekst źródłaBarber, James G. "Drugs and Drug Addiction". W Social Work with Addictions, 1–25. London: Macmillan Education UK, 1995. http://dx.doi.org/10.1007/978-1-349-23805-7_1.
Pełny tekst źródłaHarris, Howard A., i Henry C. Lee. "Drugs and drug analysis". W Introduction to Forensic Science and Criminalistics, 327–56. Second edition. | Boca Raton, FL : CRC Press, [2019] | Revised edition of : Introduction to forensics & criminalistics / Howard A. Harris, Henry Lee, c2008.: CRC Press, 2019. http://dx.doi.org/10.4324/9781315119175-13.
Pełny tekst źródłaMishra, Soni, i Abhishek Kumar Mishra. "Drugs, Drug–Biomolecule Interactions, and Drugs Delivery Systems". W Computational Studies, 53–67. Boca Raton: CRC Press, 2024. http://dx.doi.org/10.1201/9781003441328-4.
Pełny tekst źródłaHartman, David E. "Drugs". W Critical Issues in Neuropsychology, 267–325. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-1849-5_6.
Pełny tekst źródłaLaw, Simon K. "Drugs". W Risk Prevention in Ophthalmology, 131–47. New York, NY: Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-73341-8_13.
Pełny tekst źródłaDe Castro, J., J. Meynadier i M. Zenz. "Drugs". W Regional Opioid Analgesia, 131–209. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-009-2321-8_8.
Pełny tekst źródłaBroad, John. "Drugs". W Science and Criminal Detection, 15–32. London: Macmillan Education UK, 1988. http://dx.doi.org/10.1007/978-1-349-10604-2_2.
Pełny tekst źródłaMcMullin, Tami S. "Drugs". W Physiologically Based Pharmacokinetic Modeling, 271–96. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471478768.ch10.
Pełny tekst źródłaStreszczenia konferencji na temat "Drugs"
Amer, Samar A., i Sami I. Almudarra. "Assessment of Drug Use Pattern among Hajj Pilgrims Saudi Arabia, 1439h (2018)". W 2nd International Conference on Public Health and Well-being. iConferences (Pvt) Ltd, 2022. http://dx.doi.org/10.32789/publichealth.2021.1009.
Pełny tekst źródłaLi, Kun, Weiwei Liu, Yong Luo, Xiantao Cai, Jia Wu i Wenbin Hu. "Zero-shot Learning for Preclinical Drug Screening". W Thirty-Third International Joint Conference on Artificial Intelligence {IJCAI-24}. California: International Joint Conferences on Artificial Intelligence Organization, 2024. http://dx.doi.org/10.24963/ijcai.2024/234.
Pełny tekst źródłaSuryakrishna, S. S., K. Praveen, S. Tamilselvan i S. Srinath. "IoT Based Automation and Blockchain for Medical Drug Storage and Smart Drug Store". W Intelligent Computing and Technologies Conference. AIJR Publisher, 2021. http://dx.doi.org/10.21467/proceedings.115.8.
Pełny tekst źródłaKathawate, Jyoti, i Sumanta Acharya. "Computational Modeling of Intravitrael Drug Delivery in the Vitreous Chamber With Vitreous Substitutes". W ASME 2005 Summer Heat Transfer Conference collocated with the ASME 2005 Pacific Rim Technical Conference and Exhibition on Integration and Packaging of MEMS, NEMS, and Electronic Systems. ASMEDC, 2005. http://dx.doi.org/10.1115/ht2005-72783.
Pełny tekst źródłaKOMARAGIRI, RAJESH. "Recycling of Drugs from Expired Drug Products". W 1st International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecmc-1-a003.
Pełny tekst źródłaKOMARAGIRI, RAJESH. "Recycling of Drugs from Expired Drug Products". W 1st International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecmc-1-a005.
Pełny tekst źródłaKADHIM, Shafq, Osama Q. FADHIL, Zahraa SAAD i Dhafir QAHTAN. "SAFETY AND MISUSE OF PRESCRIBED MEDICATIONS DURING PREGNANCY". W VI.International Scientific Congress of Pure,Applied and Technological Sciences. Rimar Academy, 2022. http://dx.doi.org/10.47832/minarcongress6-15.
Pełny tekst źródłaKurtoğlu, Gazi Levent. "Anti-Drug Supply Policies: Inter-institutional Coordination and Action Plans". W Panel on "Effective Drug Control Strategies in Northern Cyprus: Challenges and Opportunities in 2024". Emanate Publishing House Ltd., 2024. http://dx.doi.org/10.70020/ehass.2024.7.6.
Pełny tekst źródłaKhamenehfar, Avid, Ji Liu, Jia Cai, Michael Wong, Paul C. H. Li, Patrick Ling i Pamela Russell. "Drug Accumulation Into Single Drug-Sensitive and Drug-Resistant Prostate Cancer Cells Conducted on the Single Cell Bioanalyzer". W ASME 2014 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/imece2014-36166.
Pełny tekst źródłaCelebi, Remzi, Vahab Mostafapour, Erkan Yasar, Ozgur Gumus i Oguz Dikenelli. "Prediction of Drug-Drug Interactions Using Pharmacological Similarities of Drugs". W 2015 26th International Workshop on Database and Expert Systems Applications (DEXA). IEEE, 2015. http://dx.doi.org/10.1109/dexa.2015.23.
Pełny tekst źródłaRaporty organizacyjne na temat "Drugs"
Ciapponi, Agustín. What are the effects of reference pricing and other pharmaceutical pricing and purchasing policies? SUPPORT, 2016. http://dx.doi.org/10.30846/1608143.
Pełny tekst źródłaFadlallah, Racha, Fadi El-Jardali i Elie Akl. Which interventions are effective in combatting or preventing drug counterfeiting? SUPPORT, 2017. http://dx.doi.org/10.30846/170517.
Pełny tekst źródłaLim, Peter. Analytical and Characterization Studies of Organic Chemicals, Drugs, and Drug Formulation. Fort Belvoir, VA: Defense Technical Information Center, listopad 2010. http://dx.doi.org/10.21236/ada536829.
Pełny tekst źródłaLim, Peter. Analytical and Characteristics Studies of Organic Chemicals, Drugs, and Drug Formulations. Fort Belvoir, VA: Defense Technical Information Center, listopad 2012. http://dx.doi.org/10.21236/ada567567.
Pełny tekst źródłaLim, Peter. Analytical and Characterization Studies of Organic Chemicals, Drugs and Drug Formulation. Fort Belvoir, VA: Defense Technical Information Center, luty 2004. http://dx.doi.org/10.21236/ada421361.
Pełny tekst źródłaLim, Peter, i Lori Olson. Analytical and Characterization Studies of Organic Chemicals, Drugs and Drug Formulation. Fort Belvoir, VA: Defense Technical Information Center, lipiec 1998. http://dx.doi.org/10.21236/ada352491.
Pełny tekst źródłaLim, Peter. Analytical and Characterization Studies of Organic Chemicals, Drugs and Drug Formulations. Fort Belvoir, VA: Defense Technical Information Center, październik 2006. http://dx.doi.org/10.21236/ada466154.
Pełny tekst źródłaLim, Peter. Analytical and Characterization Studies of Organic Chemicals, Drugs and Drug Formulations. Fort Belvoir, VA: Defense Technical Information Center, październik 2005. http://dx.doi.org/10.21236/ada466189.
Pełny tekst źródłaLim, Peter. Analytical and Characterization Studies of Organic Chemicals, Drugs, and Drug Formulation. Fort Belvoir, VA: Defense Technical Information Center, listopad 2011. http://dx.doi.org/10.21236/ada554000.
Pełny tekst źródłaLim, Peter. Analytical, Characterization, and Stability Studies of Organic Chemical, Drugs, and Drug Formulation. Fort Belvoir, VA: Defense Technical Information Center, maj 2014. http://dx.doi.org/10.21236/ada601351.
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