Gotowe bibliografie tematyczne / Drug mixture

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Gotowa bibliografia na temat „Drug mixture”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Drug mixture"

Gauvin, David V., and Frank A. Holloway. "The discriminative stimulus properties of an ethanol-nicotine mixture in rats." Journal of Psychopharmacology 7, no. 1_suppl (1993): 52–62. http://dx.doi.org/10.1177/026988119300700109.

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Sprague-Dawley rats were trained to discriminate between saline (SAL) and an ethanol-nicotine mixture (0.5 g/kg ethanol plus 0.5 mg/kg nicotine) administered 15 min prior to a 15-min drug discrimination training session under a FR-10 schedule of reinforcement. The mixture dose ratio was adjusted after training to obtain a drug mixture with which both individual drugs contributed about equally to the stimulus control (1.0 g/kg ethanol plus 0.3 mg/kg nicotine). The animals were then retrained for 32 sessions using this new mixture. After training, neither nicotine nor ethanol, when tested singly

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Pieczyńska, Ochoa-Chavez, Wilczewska, Bielicka-Giełdoń, and Siedlecka. "Insights into Mechanisms of Electrochemical Drug Degradation in Their Mixtures in the Split-Flow Reactor." Molecules 24, no. 23 (2019): 4356. http://dx.doi.org/10.3390/molecules24234356.

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The recirculating split-flow batch reactor with a cell divided into anolyte and catholyte compartments for oxidation mixture of cytostatic drugs (CD) was tested. In this study, kinetics and mechanisms of electrochemical oxidization of two mixtures: 5-FU/CP and IF/CP were investigated. The order of the CD degradation rate in single drug solutions and in mixtures was found to be 5-FU < CP < IF. In the 5-FU/CP mixture, kapp of 5-FU increased, while kapp of CP decreased comparing to the single drug solutions. No effect on the degradation rate was found in the CP/IF mixture. The presence of a

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Mariathasan, E. A., I. P. Stolerman, and J. A. W. White. "AND and AND-OR drug mixture discriminations in rats: generalization to single drugs and drug mixtures." Psychopharmacology 143, no. 1 (1999): 54–63. http://dx.doi.org/10.1007/s002130050919.

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Stawny, M., R. Olijarczyk, E. Jaroszkiewicz, and A. Jelińska. "Pharmaceutical Point of View on Parenteral Nutrition." Scientific World Journal 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/415310.

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Parenteral nutrition—a form of administering nutrients, electrolytes, trace elements, vitamins, and water—is a widely used mode of therapy applied in many diseases, in patients of different ages both at home and in hospital. The success of nutritional therapy depends chiefly on proper determination of the patient’s energetic and electrolytic needs as well as preparation and administration of a safe nutritional mixture. As a parenterally administered drug, it is expected to be microbiologically and physicochemically stable, with all of the components compatible with each other. It is very diffi

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Ahmed, Abdulkareem, Ahmed Nihad, Ghaeeb Sabreen, Yasin Youssef, and Jumaa Azal. "Synergistic Antiproliferative Effect of Linagliptin-Metformin Combination on the Growth of Hela Cancer Cell Line." Journal of Cancer Research Updates 14 (February 18, 2025): 12–23. https://doi.org/10.30683/1929-2279.2025.14.02.

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This in-vitro study explores the cytotoxic properties of the linagliptin-metformin combination on cervical cancer cells and examines the synergistic interaction between the two drugs. An MTT assay was used to explore the anti-cancer effects of the linagliptin-metformin mixture on a cervical cancer cell line (HeLa cell line) across 24 and 72-hour incubation periods. The concentrations of metformin, linagliptin, and their combination ranged from 0.1 to 1000 µg/ml. while the concentrations in the mixture were kept at fifty percentage of the individually used drug. The study included an estimated

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Mishra, Anoop, Vivek Ranjan Sinha, Sumit Sharma, Alen T. Mathew, Rajnish Kumar, and Ashok Kumar Yadav. "Molecular and qualitative characterization of compatibility between valacyclovir hydrochloride and excipients as raw materials for the development of solid oral dosage formulation." American Journal of Biopharmacy and Pharmaceutical Sciences 3 (December 11, 2023): 8. http://dx.doi.org/10.25259/ajbps_12_2023.

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Objectives: The objective of this present study is to know the compatibility of valacyclovir hydrochloride (VCH) with common excipients that would be utilized to develop solid oral dosage forms. Several spectroscopy techniques were used to know the possible interactions of VCH with excipients. More, a molecular docking study was also carried out to see the interaction of VCH with excipients. In vitro study of a physical mixture of VCH with excipients was executed to know the release of a drug. Material and Methods: Several analytical techniques such as differential scanning calorimetry, nuclea

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Ouhaddouch, H., A. Cheikh, M. O. B. Idrissi, M. Draoui, and M. Bouatia. "FT-IR Spectroscopy Applied for Identification of a Mineral Drug Substance in Drug Products: Application to Bentonite." Journal of Spectroscopy 2019 (March 3, 2019): 1–6. http://dx.doi.org/10.1155/2019/2960845.

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The aim of this study is to prove the effectiveness of IR spectroscopy as an identification test able to discriminate between mineral compounds in mixtures. This work is concerned with the physical characterisation of purified bentonite, bentonite in organic mixtures and organic excipients, and mineralized organic mixture containing bentonite using FT-IR spectroscopy. The different spectra were compared with each other in order to determine fingerprints of bentonite represented by bands located at 3632 cm−1 and 3437 cm−1. The analysis of the spectra of the nonmineralized mixture demonstrates t

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Mishra, Anoop, Vivek Ranjan Sinha, Sumit Sharma, Alen T. Mathew, Rajnish Kumar, and Ashok Kumar Yadav. "A comprehensive compatibility study of ganciclovir with some common excipients." American Journal of Biopharmacy and Pharmaceutical Sciences 3 (November 20, 2023): 2. http://dx.doi.org/10.25259/ajbps_4_2023.

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Objectives: The aim of the present study is to illustrate compatibility testing of ganciclovir (GCV) with some common excipients that would be used to manufacture solid oral dosage forms. Different spectroscopy techniques were utilized to see the interaction of GCV with excipients such as lactose, microcrystalline cellulose (MCC), magnesium stearate, and talc, and dicalcium phosphate. Further, a molecular docking study was also done to know the interaction of GCV with excipients. In vitro study of a physical mixture of GCV with excipients was performed to get the release of drug. Material and

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Mantas, Athanasios, and Albert Mihranyan. "Dissolution Behavior of Flufenamic Acid in Heated Mixtures with Nanocellulose." Molecules 25, no. 6 (2020): 1277. http://dx.doi.org/10.3390/molecules25061277.

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Flufenamic acid (FFA) is a problem drug that has up to eight different polymorphs and shows poor solubility. Variability in bioavailability has been reported in the past resulting in limited use of FFA in the oral solid dosage form. The goal of this article was to investigate the polymorphism and amorphization behavior of FFA in non-heated and heated mixtures with high surface area nanocellulose, i.e., Cladophora cellulose (CLAD). As a benchmark, low surface area microcrystalline cellulose (MCC) was used. The solid-state properties of mixtures were characterized with X-ray diffraction, Fourier

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Sonpal, Rakshit N., Pragna Shelat, and Anita Lalwani. "Solubility Enhancement of Hydrochlorothiazide using a Novel Drug-Drug Solid Dispersion Technology." International Journal of Pharmaceutical Sciences and Nanotechnology 8, no. 3 (2015): 2924–36. http://dx.doi.org/10.37285/ijpsn.2015.8.3.6.

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Fixed dose combination (FDC) is commonly used in pharmaceuticals to reduce pill burden and optimize the drug therapy. The recent advancements in combinatorial chemistry often lead to drugs with low aqueous solubility. Many FDC’s contain at least one drug with suboptimal physicochemical properties like BCS class II drugs for which its poor aqueous solubility may often be a limiting factor to its bioavailability. Considering the above fact, a novel drug – drug solid dispersion has been developed in present study, wherein a poorly soluble drug hydrochlorothiazide has been solid dispersed in a hyd

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Rozprawy doktorskie na temat "Drug mixture"

Bello, Hussaini. "Physiochemical and drug release properties of liquisolid formulations in comparison to their physical mixture counterparts." Thesis, University of Wolverhampton, 2018. http://hdl.handle.net/2436/621794.

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Various techniques have been used for modifying the release properties of drugs over the past years. Techniques such as liquisolid technology have raised a lot of interest in many researchers which can be employed to enhance or sustain dissolution. Various liquisolid (LS) tablets of diltiazem containing Polysorbate 80 as a non-volatile solvent for sustained release were prepared. PolyoxTM is an attractive pharmaceutical polymer used in controlled release dosage forms mainly because of its insensitivity to the pH of the biological medium and ease of production. The aim of this study was to inve

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Fransén, Nelly. "Studies on a Novel Powder Formulation for Nasal Drug Delivery." Doctoral thesis, Uppsala universitet, Institutionen för farmaci, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-9292.

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Nasal administration has potential for the treatment of indications requiring a fast onset of effect or for drugs with low oral bioavailability. Liquid nasal sprays are relatively common, but can be associated with suboptimal absorption from the nasal cavity; this thesis shows that nasal absorption can be significantly enhanced with a dry powder formulation. It was shown that interactive mixtures, consisting of fine drug particles adhered to the surface of mucoadhesive carrier particles, could be created in a particle size suitable for nasal administration. Sodium starch glycolate (SSG), a com

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Lajhar, Fathi. "Electrospray for pulmonary drug delivery." Thesis, University of Manchester, 2018. https://www.research.manchester.ac.uk/portal/en/theses/electrospray-for-pulmonary-drug-delivery(b8aeaea9-9032-40f5-a8e0-b51c1ba8c8f8).html.

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Drug administration through the pulmonary route is an ancient technique that evolved from inhaling the smoke of certain leaves as a medicine. The optimum droplet diameter for the pulmonary system deposition has been identified to be in the range from 2 to 3.5 μm, with potential deposition rates of up to 80% of this size range. Currently, the most used aerosol generator methods are the pressurized metered dose inhalers. However, they generally exhibit low deposition efficiency with less than 20 % of the spray reaching the target area of the lungs as most of the drug deposited in the upper airwa

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Cahill, Paul. "Latest variable mixture modelling : an examination of the influences and profiles of treated drug misuse in the Republic of Ireland." Thesis, University of Ulster, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.421741.

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Yu, Li. "Tau-Path Test - A Nonparametric Test For Testing Unspecified Subpopulation Monotone Association." The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1255657068.

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Duque, Marcelo Dutra. "Otimização da liberação de difosfato de primaquina em comprimidos de liberação controlada." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/9/9139/tde-17122009-141558/.

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O presente trabalho teve como objetivo produzir comprimidos de liberação controlada de difosfato de primaquina baseados em polímeros hidrofílicos e otimizar a liberação do fármaco por meio do planejamento estatístico de mistura (DOE). Na seleção dos componentes da formulação foram realizados estudos de calorimetria exploratória diferencial (DSC) para verificar a compatibilidade entre o fármaco/excipientes e avaliação do fluxo dos pós das formulações por meio da determinação do ângulo de repouso. As 20 formulações obtidas no planejamento experimental continham misturas de hidroxipropilmetilcelu

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Bredenberg, Susanne. "New Concepts in Administration of Drugs in Tablet Form : Formulation and Evaluation of a Sublingual Tablet for Rapid Absorption, and Presentation of an Individualised Dose Administration System." Doctoral thesis, Uppsala University, Department of Pharmacy, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3433.

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<p>This thesis presents two new concepts in oral drug administration and the results of evaluation of some relevant formulation factors.</p><p>Investigation into improving the homogeneity of mixtures for tableting indicated that it may be possible to obtain interactive dry mixtures of micronised drugs containing drug proportions as low as 0.015% w/w. By studying the relationship between disintegration time and tensile strength, it was found that the microstructure surrounding the disintegrant particles may influence the disintegration process. Therefore, avoidance of excipients which are highl

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Paudel, Liladhar. "High Field ¹H Nuclear Magnetic Resonance (NMR) Spectroscopy Based Metabolomics and Complex Mixture Analysis by Multidimensional NMR and Liquid Chromatography-Mass Spectrometry (LC-MS)." University of Akron / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=akron1343403647.

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Bramer, Tobias. "Prolonged Drug Release from Gels, using Catanionic Mixtures." Doctoral thesis, Uppsala University, Department of Pharmacy, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-8303.

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<p>The use of catanionic drug-surfactant mixtures was proven to be an efficient novel method of obtaining prolonged drug release from gels. It was shown that various commonly used drug compounds are able to form catanionic mixtures together with oppositely charged surfactants. These mixtures exhibited interesting phase behaviour, where, among other structures, vesicles and large worm-like or branched micelles were found. The size of these aggregates makes them a potential means of prolonging the drug release from gels, as only monomer drugs in equilibrium with larger aggregates were readily ab

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Kassem, Nuha Mohammed. "Generation of deeply inspirable clouds from dry powder mixtures." Thesis, King's College London (University of London), 1990. https://kclpure.kcl.ac.uk/portal/en/theses/generation-of-deeply-inspirable-clouds-from-dry-powder-mixtures(b714bb92-b27a-4ff0-81fa-8a44d9c58d2d).html.

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Książki na temat "Drug mixture"

D, Waters Michael, and International Conference on Environmental Mutagens (5th : 1989 : Cleveland, Ohio), eds. Genetic toxicology of complex mixtures. Plenum Press, 1990.

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Pirilä-Honkanen, Päivi. Physicochemical properties of 2-pyrrolidinone and n-methylbenzenesulfonamide in binary solution mixtures. Oulun Yliopisto, 1996.

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D, George Patricia, and Hill Ronald H, eds. Environmental health and safety for hazardous waste sites. American Industrial Hygiene Association, 2002.

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Institute of Medicine (U.S.). Committee to Study Priorities for Vaccine Development. Vaccines for the 21st century: A tool for decisionmaking. Edited by Stratton Kathleen R, Durch Jane, and Lawrence Robert S. 1938-. National Academy Press, 2000.

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Sheila, Davey, World Health Organization, UNICEF, and World Bank, eds. State of the world's vaccines and immunization. 3rd ed. World Health Organization, 2009.

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Love Drug: Love is a drug that should be handled with extreme caution; may cause a mixture of emotions… Createspace Independent Publishing Platform, 2013.

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Wheatley, Michael, John R. Weekes, Andrea E. Moser, and Kathleen Thibault. Drugs and Prisons. Edited by John Wooldredge and Paula Smith. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199948154.013.14.

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This essay explores how illegal drugs are linked to imprisonment, especially in the United States. First, the chapter considers statistics that demonstrate how the high U.S. imprisonment rate is driven by the criminalization of substance misuse, despite the high incidence of drug use in the general population. Prison populations that include a mixture of drug users and drug dealers are virtually guaranteed to find ways of bringing drugs into prison, and the demand is increased by the desire to ease the pains of imprisonment. The illicit drug economy in prisons and the associated violence is a

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Guenther, Lisa. On Pain of Death: The ‘Grotesque Sovereignty’ of the US Death Penalty. Edinburgh University Press, 2018. http://dx.doi.org/10.3366/edinburgh/9781474400046.003.0022.

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On 16 January 2014, Ohio prisoner Dennis McGuire was put to death with an untested mixture of lethal injection drugs. According to witnesses, McGuire gasped, snorted and appeared to struggle for air for ten minutes before dying. The entire execution lasted up to twenty-six minutes – the longest since Ohio resumed executions in 1999. McGuire’s family is suing the state and the drug manufacturer Hospira for what they claim was ‘unnecessary and extreme pain and suffering during the execution process’, amounting to cruel and unusual punishment.

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Drag Reduction of Complex Mixtures. Elsevier, 2018. http://dx.doi.org/10.1016/c2015-0-07002-2.

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Watanabe, Keizo. Drag Reduction of Complex Mixtures. Elsevier Science & Technology Books, 2018.

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Części książek na temat "Drug mixture"

Houghten, Richard A., Colette T. Dooley, and Jon R. Appel. "In Vitro and Direct In Vivo Testing of Mixture-Based Combinatorial Libraries for the Identification of Highly Active and Specific Opiate Ligands." In Drug Addiction. Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-76678-2_26.

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Verma, Rinkee, Chanchal Deep Kaur, Vijendra Suryavanshi, and Ritika Singh. "A Brief Review on Quetiapine Drug Containing Eutectic Mixture." In Computational Optimization, Modeling, and Simulation for Engineering Applications. Apple Academic Press, 2024. http://dx.doi.org/10.1201/9781003454021-4.

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Nefzi, Adel, John M. Ostresh, and Richard A. Houghten. "Combinatorial chemistry: Mixture-based combinatorial libraries of acyclic and heterocyclic compounds from amino acids and short peptides." In Modern Methods of Drug Discovery. Birkhäuser Basel, 2003. http://dx.doi.org/10.1007/978-3-0348-7997-2_6.

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Zhang, Xiang, Chenliang Qian, Jie Xia, and Fan Yang. "MOL-MOE: Learning Drug Molecular Characterization Based on Mixture of Expert Mechanism." In Bioinformatics Research and Applications. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-5131-0_20.

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Paddock, Susan, Mike West, S. Stanley Young, and Merlise Clyde. "Mixture Models in the Exploration of Structure-Activity Relationships in Drug Design." In Case Studies in Bayesian Statistics. Springer New York, 1999. http://dx.doi.org/10.1007/978-1-4612-1502-8_9.

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Nachiappan, V., K. R. Shanmugasundaram, and S. I. Mufti. "Control of Alcoholism by Treatment with SKV, A Herbal Drug Mixture from India." In Alcohol, Cell Membranes, and Signal Transduction in Brain. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2470-0_17.

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Carson, Mathew C., Peng Xu, John J. Gildea, Collin F. Marino, and Robin A. Felder. "Drug Screening Using Normal Cell and Cancer Cell Mixture in an Automated 3D Cell Culture System." In Methods in Molecular Biology. Springer US, 2024. http://dx.doi.org/10.1007/978-1-0716-3922-1_7.

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Moitra, Agnij. "GraphChem: Using Soft Graph Mixture of Experts for de novo Drug Design and Molecular Property Prediction." In Lecture Notes in Computer Science. Springer Nature Singapore, 2025. https://doi.org/10.1007/978-981-96-0692-4_32.

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Stolerman, Ian P. "The Discrimination of Drug Mixtures." In Drug Discrimination. John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118023150.ch10.

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Meguro, Yasuhiro, Masaru Enomoto, and Shigefumi Kuwahara. "Total Synthesis of Amycolamicin." In Modern Natural Product Synthesis. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-1619-7_2.

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AbstractAmycolamicin (also called kibdelomycin) produced by two species of soil actinomycetes is a potent antibiotic against a broad range of drug-resistant bacteria with a novel binding mode to bacterial type II DNA topoisomerases and with no cross-resistance to existing antibacterial agents. The unique hybrid molecular architecture of amycolamicin attracted interest of many synthetic organic chemists and three total syntheses have been reported so far. In this chapter, we describe our total synthesis of amycolamicin in detail, which features a nucleophilic addition of a vinyllithiun reagent

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Streszczenia konferencji na temat "Drug mixture"

Batista, Daniel V., and Marco S. Reis. "Balancing modelling complexity and experimental effort for conducting QbD on lipid nanoparticles (LNPs) systems." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.163183.

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The promising properties of lipid nanoparticles (LNPs) as drug carriers have been attracting significant attention in the field of drug delivery. However, further research is still required for a better understanding of their integration in the pharmaceutical industry. The Quality by Design (QbD) approach aims at ensuring the safety and efficiency in the development of new drugs, through an holistic, risk-based approach that gathers all sources of knowledge available about the system under analysis. One key resource of the QbD framework is the rich toolkit of Design of Experiments (DOE), to de

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Hwang, Suntae, Seonghyeon Kang, Kyungsu Kim, Semin Ahn, and Kyogu Lee. "DOSE: Drum One-Shot Extraction from Music Mixture." In ICASSP 2025 - 2025 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP). IEEE, 2025. https://doi.org/10.1109/icassp49660.2025.10889237.

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Cheng, Yong, Qingna Duan, Junhan Wen, Renyao Zhang, Huai Wang, and Yonghua Guo. "Research on Flow Field Modeling of Drum Wheel Solid-Liquid-Gas Mixture Separation Device of Slim Hollow Filter Rod Making Machine." In 2024 43rd Chinese Control Conference (CCC). IEEE, 2024. http://dx.doi.org/10.23919/ccc63176.2024.10662591.

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Kang, Cheolho, William P. Jepson, and Madan Gopal. "The Effect of Drag Reducing Agents on Corrosion in Multiphase Flow." In CORROSION 1998. NACE International, 1998. https://doi.org/10.5006/c1998-98054.

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Abstract The effect of drag reducing agents (DRA) on corrosion and flow regime has been studied in a 10 cm diameter, 18 m long plexiglass flow loop in 50% oil/water mixtures with carbon dioxide gas. Superficial liquid velocities between 0.1 and 1 m/s and gas velocities between 1 and 10 m/s respectively were studied. The corrosion rate was measured for stratified, slug and annular flow. The height of liquid film, slug velocity, and slug frequency were obtained from the video image using a super-VHS camera. The DRA effectiveness was examined for DRA concentrations between 0 and 75 ppm. Flow regi

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Krstić, Danijela Z., Mirjana B. Čolović, Lela B. Korićanac, et al. "Fe(III)-CONTAINING WELLS-DAWSON POLYOXOTUNGSTATE AND ASCORBATE: EFFECT OF EQUIMOLAR MIXTURE ON HELA CELLS." In 8th Workshop Food and Drug Safety and Qualit. Vinča Institute of Nuclear Sciences - National Institute of the Republic of Serbia, 2024. http://dx.doi.org/10.46793/8fdsq.pc6dk.

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This study aims to explore in vitro anti-tumor action of the equimolar mixture of Fe(III)-substituted monolacunary Wells-Dawson POM (Fe-WD), K7[FeIII(α2-P2W17O61)(H2O)] and L(+)-ascorbic acid sodium salt (ascorbate) using cervical carcinoma HeLa cells as a model system. Exponentially growing HeLa cells were exposed in vitro to Fe-WD and ascorbate separately (0.005 – 0.5 mM) and the equimolar Fe-WD/ascorbate mixtures of the same concentrations for 48 and 72 h, at 37 °C. Single and simultaneous exposure to the studied compounds resulted in concentration- and time-dependent decrease of cell viabi

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Čolović, Mirjana B., Jelena J. Žakula, Lela B. Korićanac, et al. "IN VITRO ANTI-TUMOR EFFECT OF Fe(III)-CONTAINING WELLS-DAWSON POLYANION AND ASCORBATE." In 8th Workshop Food and Drug Safety and Qualit. Vinča Institute of Nuclear Sciences - National Institute of the Republic of Serbia, 2024. http://dx.doi.org/10.46793/8fdsq.pc4mc.

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The cytotoxic effect of the mixture of Fe(III)-substituted monolacunary Wells-Dawson polyoxometalate (Fe-WD), K7[FeIII(α2-P2W17O61)(H2O)] and L(+)-ascorbic acid sodium salt (ascorbate) on cervical carcinoma HeLa cells was evaluated in this study. Exponentially growing HeLa cells were treated in vitro with Fe-WD (0.001 – 1 mM), forty times higher concentrations of ascorbate (0.040 – 40 mM), and Fe-WD/ascorbate mixtures (concentration ratio 1 : 40) for 24 h, at 37 °C. Fe-WD and ascorbate inhibited cell viability in a concentration-dependent manner with different potencies. IC50 values were deter

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Lu, Xuan, Yanfang Huang, Bo Zhang, and Shao Li. "Application of Mixture Designs for Detection and Characterization of Multi-Drug Synergism." In 2007 1st International Conference on Bioinformatics and Biomedical Engineering. IEEE, 2007. http://dx.doi.org/10.1109/icbbe.2007.108.

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Sencanski, Jelena, Jelena Maksimović, Ferenc Pastor, et al. "UV/VIS DETERMINING TARTRAZINE (E 102) IN A COMMERCIAL FOOD DYE." In 8th Workshop Food and Drug Safety and Quality. Vinča Institute of Nuclear Sciences - National Institute of the Republic of Serbia, 2024. http://dx.doi.org/10.46793/8fdsq.pb12js.

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Our research presents an analytical curve applicable to accurately determining unknown concentrations of tartrazine in an aqueous solution of any sample. The analytical curve that this study develops may be used to determine the concentration of tartrazine in an aqueous solution of a typical commercially available food dye, which is a mixture of tartrazine and dextrose. The concentration determined in the sample of the food dye was c=7.76 g/ dm3. The examined food dye contained 0.27% of tartrazine. To characterize the presented analytical method, LOD (limit of detection) and LOQ (limit of quan

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Tambatkar, Ganesh D. "Ultrasonic studies of substituted drug doxycycline, chlorothalidon and dexamethasone in DMF-water mixture." In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON MATHEMATICAL SCIENCES AND TECHNOLOGY 2022 (MATHTECH 2022): Navigating the Everchanging Norm with Mathematics and Technology. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0183737.

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Musaev, M. B., and V. V. Zashchepkina. "METHODOLOGY FOR THE APPLICATION OF THE SUPRAMOLECULAR COMPLEX OF IVERMECTIN "ANIVERM-2.0%" AGAINST PARASITOSIS OF HERD HORSES." In THEORY AND PRACTICE OF PARASITIC DISEASE CONTROL. All-Russian Scientific Research Institute for Fundamental and Applied Parasitology of Animals and Plant – a branch of the Federal State Budget Scientific Institution “Federal Scientific Centre VIEV”, 2023. http://dx.doi.org/10.31016/978-5-6048555-6-0.2023.24.325-330.

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Deworming untamed herd horses is a difficult task. It is more convenient to use drugs by free feeding, individually or in groups in a mixture with concentrated feed. In this regard, we have developed a new dosage form for the treatment and prevention of parasitosis in herd horses by free feeding in a mixture with concentrated feed based on the substance ivermectin, which has a high antiparasitic activity and a wide spectrum of action. To obtain an antiparasitic supramolecular complex based on the substance ivermectin, an innovative mechanochemical technology

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Raporty organizacyjne na temat "Drug mixture"

Norsworthy, Sarah, Rebecca Shute, Crystal M. Daye, and Paige Presler-Jur. National Institute of Justice’s Forensic Technology Center of Excellence 2019 National Opioid and Emerging Drug Threats Policy and Practice Forum. Edited by Jeri D. Ropero-Miller and Hope Smiley-McDonald. RTI Press, 2020. http://dx.doi.org/10.3768/rtipress.2020.cp.0011.2007.

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The National Institute of Justice (NIJ) and its Forensic Technology Center of Excellence (FTCoE) hosted the National Opioid and Emerging Drug Threats Policy and Practice Forum on July 18–19, 2019, in Washington, DC. The forum explored ways in which government agencies and programs, law enforcement officials, forensic laboratory personnel, medical examiners and coroners, researchers, and other experts can cooperate to respond to problems associated with drug abuse and misuse. Panelists from these stakeholder groups discussed ways to address concerns such as rapidly expanding crime laboratory ca

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Orhan, Nilüfer. St. John’s wort (Hypericum perforatum) Laboratory Guidance Document. ABC-AHP-NCNPR Botanical Adulterants Prevention Program, 2021. http://dx.doi.org/10.59520/bapp.lgd/awbq3781.

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For centuries, St. John’s wort (SJW; Hypericum perforatum L., Hypericaceae) has been used as an herbal remedy for various medical conditions both externally and internally in many countries. Although it is a well-known and widely used traditional medicinal plant, concerns about its safety and herb-drug interactions caused a significant decrease in market sales starting in the early 2000s. The adulteration history of St. John’s wort (SJW) goes back to 1875 in the United States; the American Pharmaceutical Association mentioned Ascyrum stans and A. crux-andreae as the substitutes of SJW in its r

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Chutimaworapan, Suchada, Chaiyo Chaichantippayuth, and Areerat Laopaksa. Formulation of pharmaceutical products of Garcinia mangostana Linn. extracts. Chulalongkorn University, 2006. https://doi.org/10.58837/chula.res.2006.32.

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Part I: The purpose of the investigation was to develop the extraction process that was simple, practical and giving high yield. The maceration of dried powder of Garcinia mangostana fruit husk with ethyl acetate gave yellow crystalline powder of mangostin. The yield was calculated as 7.47%. The identification of the Garcinia mangostanahusk extract was carried out by thin-layer chromatography (TLC) and differential scanning calorimetry. The TLC of mangostin was done by using the alumina sheet and ethyl acetate: hexane (3:1) as mobile phase. The Rf value as compared with standard mangostin was

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Chutimaworapan, Suchada. Fast release solid dispersion system of nifedipine. Chulalongkorn University, 1999. https://doi.org/10.58837/chula.res.1999.28.

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Nifedupine solid dispersions in polyethylene glycols (PEG4000 and PEG6000), poloxamers (poloxamer188 poloxamer288 and poloxamer407), [beta]-cyclodextrin (BCD) and 2-hydroxypropyl-[beta]-cyclodextrin (HPBCD), at the drug:carrier ratio if 1:1, 1:3, 1:5, and 1:10 were investigated. The systems were prepared by melting, solvent and kneading method and compared to physical mixtures. It was found that the drug:carrier ratio of 1:10 and by melting and solvent methods showed most conspicuous dissolution rates in most systems (p<0.05). The most markedly improved rate was exhibited from the poloxamer

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Rahman, Shahedur, Rodrigo Salgado, Monica Prezzi, and Peter J. Becker. Improvement of Stiffness and Strength of Backfill Soils Through Optimization of Compaction Procedures and Specifications. Purdue University, 2020. http://dx.doi.org/10.5703/1288284317134.

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Vibration compaction is the most effective way of compacting coarse-grained materials. The effects of vibration frequency and amplitude on the compaction density of different backfill materials commonly used by INDOT (No. 4 natural sand, No. 24 stone sand, and No. 5, No. 8, No. 43 aggregates) were studied in this research. The test materials were characterized based on the particle sizes and morphology parameters using digital image analysis technique. Small-scale laboratory compaction tests were carried out with variable frequency and amplitude of vibrations using vibratory hammer and vibrato

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Nelson, Thomas, and Leonard Wood. The Effect of Baghouse Fines and Incomplete Combustion Products in a Drum Drier on the Characteristics of Asphalt Paving Mixtures - Phase I. Purdue University, 1990. http://dx.doi.org/10.5703/1288284313430.

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Lin, Jyh-Dong, and Leonard Wood. The Effects of Bag House Fines and Incomplete Combustion Products in a Drum Drier on the Characteristics of Asphalt Paving Mixtures, Phase II. Purdue University, 1990. http://dx.doi.org/10.5703/1288284313429.

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