Literatura académica sobre el tema "In vitro standardization"
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Artículos de revistas sobre el tema "In vitro standardization"
Yman, Lars. "Standardization of in vitro methods". Allergy 56, s67 (abril de 2001): 70–74. http://dx.doi.org/10.1111/j.1398-9995.2001.00921.x.
Texto completoGoggs, Robert, Antonio Borrelli, Benjamin M. Brainard, Daniel L. Chan, Armelle de Laforcade, Isabelle Goy-Thollot, Karl E. Jandrey et al. "Multicenter in vitro thromboelastography and thromboelastometry standardization". Journal of Veterinary Emergency and Critical Care 28, n.º 3 (31 de marzo de 2018): 201–12. http://dx.doi.org/10.1111/vec.12710.
Texto completoChander, NGopi. "Standardization of in vitro studies". Journal of Indian Prosthodontic Society 16, n.º 3 (2016): 227. http://dx.doi.org/10.4103/0972-4052.186399.
Texto completoPooja, A., Sapna Panwar, A. K. Tiwari y Gunjeet Kumar. "Standardization of in vitro regeneration protocol in annual chrysanthemum". Indian Journal of Horticulture 78, n.º 1 (2021): 46–52. http://dx.doi.org/10.5958/0974-0112.2021.00007.4.
Texto completoAhmad, Sayeed, Mhaveer Singh, MohammadA Khan, MasoodS Khan y SH Ansari. "Standardization and in vitro antioxidant activity of jatamansi rhizome". Journal of Pharmacy and Bioallied Sciences 7, n.º 4 (2015): 275. http://dx.doi.org/10.4103/0975-7406.168025.
Texto completoMalvicini, R., D. Santa Cruz, C. Sanmartin, N. Pacienza y G. Yannarelli. "Bioassay standardization to assess exosomes antiinflammatory activity in vitro". Cytotherapy 22, n.º 5 (mayo de 2020): S24. http://dx.doi.org/10.1016/j.jcyt.2020.03.500.
Texto completoMorosato, Federico, Francesco Traina y Luca Cristofolini. "Standardization of hemipelvis alignment for in vitro biomechanical testing". Journal of Orthopaedic Research® 36, n.º 6 (19 de diciembre de 2017): 1645–52. http://dx.doi.org/10.1002/jor.23825.
Texto completoKaur, Harpreet, Jaismeen Kaur y Bhagwant Singh Chahil. "in vitro protocol standardization for growth and rooting in strawberry". Journal of Krishi Vigyan 9, n.º 1 (2020): 193–201. http://dx.doi.org/10.5958/2349-4433.2020.00158.0.
Texto completoSchendel, Dolores J., Rudolf Wank y Bo Dupont. "Standardization of the Human in vitro Cell-mediated Lympholysis Technique". Tissue Antigens 13, n.º 2 (11 de diciembre de 2008): 112–20. http://dx.doi.org/10.1111/j.1399-0039.1979.tb01146.x.
Texto completoSudha, V., K. L. Niraimathi, R. Lavanya, C. David Raj y P. Brindha. "Chemical Standardization and in vitro Cytotoxic Studies on Nellikai lehyam". Asian Journal of Chemistry 26, n.º 12 (2014): 3679–82. http://dx.doi.org/10.14233/ajchem.2014.17053.
Texto completoTesis sobre el tema "In vitro standardization"
NUNES, Cristina Freitas. "Atividade virucida de um extrato etanólico de própolis verde in vitro e in vivo". Universidade Federal de Pelotas, 2011. http://repositorio.ufpel.edu.br/handle/ri/2567.
Texto completoCurrently, the drug industry looks for new drugs based on natural products, for the production of drugs more efficient, for which the microorganisms did not show resistance to both humans and animals. A natural product that has been the subject of intense pharmacological and chemical studies by scientists for the control of diseases is propolis, a resinous substance produced by honeybees from exudates collected from different parts of the plant, which has been used for centuries in popular medicine due to its therapeutic properties. Chemical studies revealed the complex chemical composition, identifying in some cases more than 300 components including various bioactive phenolic compounds responsible for the virucidal action. This work initially describes the standardization of an ethanol extract of green propolis (EEPV), where the chemicals were identified by high performance liquid chromatography (HPLC), phytochemical characterization by thin layer chromatography (TLC), soluble solids, content of phenolics and flavonoids and antioxidant activity by 2.2 diphenil picryl hydrazyl (DPPH). The EEPV was also evaluated in vitro and in vivo for their capacity lentogenic virucidal against a strain of the virus of Newcastle disease (NDV) at two different temperatures (22 and 37 ° C), 5 incubation periods (0, 1, 2, 4 and 8 hours) of NDV in five different concentrations of EEPV (4000μg/dose, 400μg/dose, 40μg/dose, and 4μg/dose 0μg/dose). The EEPV standard is within the standards required by the MAP, with high levels of phenolics and flavonoids (12.93 and 6.05% respectively) as shown by HPLC, which identified high concentrations of phenolic acids (p-coumaric acid, hydroxycinnamic acid diprenyl , cinâmino acid derivatives), which are assigned the antibacterial, antioxidant, antiviral and virucidal. This extract showed dose-dependent virucidal activity (4000μg/dose e 400μg/dose) and time of incubation with the virus (2 hour). The inhibitory activity of EEPV against the strain of NDV lentogenic found in the present study suggests the use of this extract as an alternative to fight the infection by this virus.
Atualmente, a indústria farmacêutica busca novos medicamentos com base em produtos naturais, visando à produção de fármacos mais eficientes, para os quais os microrganismos não apresentem resistência, tanto para humanos quanto para animais. Um dos produtos naturais que tem sido objeto de intensos estudos farmacológicos e químicos por cientistas para o controle de enfermidades é a própolis, uma substância resinosa produzida por abelhas melíferas a partir de exsudatos coletados em diferentes partes das plantas, que tem sido utilizada durante séculos na medicina popular devido as suas propriedades terapêuticas. Estudos químicos revelaram a complexa composição da própolis, identificando em alguns casos mais de 300 componentes, incluindo vários compostos bioativos fenólicos responsáveis pela ação virucida. Este trabalho inicialmente descreve a padronização de um extrato etanólico de própolis verde (EEPV), onde foram identificados os compostos químicos por cromatografia liquida de alta eficiência (CLAE), caracterização fitoquímica por cromatografia em camada delgada (CCD), teor de sólidos solúveis, teor de fenóis e flavonóides totais e atividade antioxidante por 2,2 diphenil picril hidrazil(DPPH). O EEPV foi avaliado também in vitro e in vivo, quanto a sua capacidade virucida contra uma cepa lentogênica do vírus da doença de Newcastle (NDV) em duas temperaturas distintas (22 e 37°C), 5 períodos de incubação (0, 1, 2, 4 e 8 horas) do NDV em 5 concentrações de EEPV distintos (4000μg/dose, 400μg/dose, 40μg/dose, 4μg/dose e 0μg/dose). O EEPV padronizado está dentro dos padrões requisitados pelo MAPA, com altos níveis de fenóis e flavonóides totais (12.93 e 6,05% respectivamente), comprovado por CLAE, o qual identificou altas concentrações de ácidos fenólicos (ácido p-cumárico, ácido diprenil hidroxicinâmico, derivados do ácido cinâmino), os quais são atribuídos as propriedades antibacteriana, antioxidante, antiviral e virucida. Este extrato apresentou atividade virucida dependente da dose (4000μg/dose, 400μg/dose) e do tempo de incubação com o vírus (2 horas). A atividade inibitória do EEPV contra a cepa lentogênica de NDV, encontrada no presente estudo sugere a utilização deste extrato como uma alternativa no combate a infecções por este vírus.
LUCO, DAYANE P. "Padronização de técnicas de isolamento de células de Langerhans imaturas e desenvolvimento de um modelo tridimensional de pele humana para testes de sensibilidade in vitro". reponame:Repositório Institucional do IPEN, 2014. http://repositorio.ipen.br:8080/xmlui/handle/123456789/23179.
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Dissertação (Mestrado em Tecnologia Nuclear)
IPEN/D
Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP
STANCO, DEBORAH. "Toward personalized medicine: human adipose-derived stem cells (ASCs) and xenogenic-free media as enabling tools in tendon tissue engineering strategies". Doctoral thesis, Politecnico di Torino, 2020. http://hdl.handle.net/11583/2839845.
Texto completoLibros sobre el tema "In vitro standardization"
S, Ambesi-Impiombato F. y Perrild H, eds. FRTL-5 today: Proceedings of the First International Workshop on Characterization and Standardization of an In Vitro Thyroid Cell System, Udine, Italy, 26-28 October 1988. Amsterdam: Excerpta Medica, 1989.
Buscar texto completoCapítulos de libros sobre el tema "In vitro standardization"
Stacey, Glyn N. y Thomas Hartung. "Availability, Standardization and Safety of Human Cells and Tissues for Drug Screening and Testing". En Drug Testing in vitro, 229–50. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/9783527609611.ch9.
Texto completoRaja, Pavan M. V., Ghislaine Lacroix, Jacques-Aurélien Sergent, Frédéric Bois, Andrew R. Barron, Enrico Monbelli y Dan Elgrabli. "Nanotoxicology: Role of Physical and Chemical Characterization and RelatedIn Vitro,In Vivo, andIn SilicoMethods". En Metrology and Standardization of Nanotechnology, 363–80. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527800308.ch23.
Texto completoLima-Filho, José Vitor y Rossana de Aguiar Cordeiro. "In Vitro and In Vivo Antibacterial and Antifungal Screening of Natural Plant Products: Prospective Standardization of Basic Methods". En Springer Protocols Handbooks, 275–91. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-8636-7_17.
Texto completoSchmitt, K., S. Rosenkranz, F. Platzer, G. Jagarzewskj, M. Kästner, A. Schroda, R. Seitz y J. Dodt. "Standardization of the Thrombin-Fibrinogen Clotting Time (TFCT) — An In Vitro Test on Thrombogenicity of Prothrombin Complex Concentrates (PCCs)". En 28. Hämophilie-Symposion Hamburg 1997, 125–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-59915-6_17.
Texto completoEkwall, Bjorn y Frank A. Barile. "Standardization and Validation". En Introduction to In Vitro Cytotoxicology, 189–208. CRC Press, 2019. http://dx.doi.org/10.1201/9780429275487-11.
Texto completoBhatt, Deepa, M. K. Tripathi, M. Vidhya Sankar, Sushma Tiwari, Mohini Sharma, Niraj Tripathi y Sharad Tiwari. "Standardization of In-vitro Regeneration Protocol in Gerbera jamesonii Bolus Ex Hooker F." En Current Topics in Agricultural Sciences Vol. 7, 105–21. Book Publisher International (a part of SCIENCEDOMAIN International), 2022. http://dx.doi.org/10.9734/bpi/ctas/v7/2303b.
Texto completoBorziak, Kirill, Irena Parvanova y Joseph Finkelstein. "Introducing a Platform for Integrating and Sharing Stem Cell Research Data". En Studies in Health Technology and Informatics. IOS Press, 2021. http://dx.doi.org/10.3233/shti210186.
Texto completo"Good cell culture practice: good laboratory practice in the cell culture laboratory for the standardization and quality assurance of in vitro studies". En Cell Culture Models of Biological Barriers, 138–46. CRC Press, 2002. http://dx.doi.org/10.1201/9780203219935-14.
Texto completoOliver, Anthony R. "Laboratory Quality Control and Accreditation". En Tutorial Topics in Infection for the Combined Infection Training Programme. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198801740.003.0019.
Texto completoActas de conferencias sobre el tema "In vitro standardization"
Singhera, G. K., T. Guo, J. M. Leung y D. R. Dorscheid. "Standardization of Airway Epithelial 3D Culture for In Vitro Studies". En American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a1300.
Texto completoSilva, Andréa, Tamiris Azamor, Leonardo Batista-Silva, Nathalia Benigno, Thyago Calvo, Camilla Bayma, Denise Matos y Milton Moraes. "Standardization of an in vitro assay for the evaluation of a candidate yellow fever vaccine". En IV International Symposium on Immunobiologicals & VII Seminário Anual Científico e Tecnológico. Instituto de Tecnologia em Imunobiológicos, 2019. http://dx.doi.org/10.35259/isi.sact.2019_32551.
Texto completoHoppensteadt, D., J. Fareed, J. M. Walenga, R. M. Emnuele y A. Racanelli. "DIFFERENT LOW MOLECULAR WEIGHT HEPARINS (LMWHs) ARE NOT IDENTICAL IN THE IN VITRO SCREENING REGARDLESS OF POTENCY ADJUSTMENT". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643227.
Texto completoZwagerman, Ralph. "Development of ISO18363-4 / AOCS Cd29f-2021: A new standardized method to quantify MCPDE and GE in edible oils". En 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/dqcb6439.
Texto completoSuor-Cherer, S., H. Bui Thi Quynh y P. Caillis. "Standardization of an in vitro spectrophotometric method for the evaluation of the ammonia-binding properties of plant extracts rich in saponins". En 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399745.
Texto completoWehmeier, A. y W. Schneider. "FACTORS AFFECTING PLATELET VOLUME ANALYSIS". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643538.
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