Εμφανίζονται 1 - 15 Αποτελέσματα από 15 για την αναζήτηση '"биотехнологические препараты"', χρόνος αναζήτησης: 0,73δλ Περιορισμός αποτελεσμάτων
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  8. 8
    Academic Journal

    Πηγή: Drug development & registration; № 2 (2017); 160-165 ; Разработка и регистрация лекарственных средств; № 2 (2017); 160-165 ; 2658-5049 ; 2305-2066

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.pharmjournal.ru/jour/article/view/424/419; M. Hu, M. Niculescu, X.M. Zhang, A. Hui. High-performance liquid chromatographic determination of polysorbate 80 in pharmaceutical suspensions // Journal of Chromatography A. 2003. V. 984. I. 2. P. 233-236.; S. Fekete, K. Ganzler, J. Fekete. Fast and sensitive determination of Polysorbate 80 in solutions containing proteins // Journal of Pharmaceutical and Biomedical Analysis, 2010. V. 52. I. 5. P. 672-679.; Evaluation Report of Food Additives «Polysorbate 20, Polysorbate 60, Polysorbate 65 and Polysorbate 80». Food Safety Commission. Office Location of the FSC: Japan. Tokyo. 2007.; R. Zhang, Y. Wang, L. Tan, H.Y. Zhang, M. Yang. Analysis of polysorbate 80 and its related compounds by RP-HPLC with ELSD and MS detection // Journal of Сhromatographic Science. 2012. V. 50(7) P. 598-607.; R.C. Rowe, P.J. Sheskey, M.E. Quinn. Handbook of Pharmaceutical Excipients. 6th Edition. - London; Chicago: Pharmaceutical Press and American Pharmacists Association, 2009. 888 p.; L.M. Nair, N.V. Stephens, S. Vincent, N. Raghavan, P.J. Sand. Determination of polysorbate 80 in parenteral formulations by high-performance liquid chromatography and evaporative light scattering detection // Journal of Chromatography A. 2003. V. 1012(1) P. 81-86.; A. Sparreboom, M. Zhao, J.R. Brahmer, J. Verweij, S.D. Baker. Determination of the docetaxel vehicle, polysorbate 80, in patient samples by liquid chromatography-tandem mass spectrometry // Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences. V. 773(2). P. 183-190.; T.H. Tani, J.M. Moore, T.W. Patapoff. Single step method for the accurate concentration determination of polysorbate 80 // Journal of Chromatography A. 1997. V. 786. I. 1. P. 99-106.; D.L. McKean, A.J. Pesce, W. Koo. Analysis of polysorbate and its polyoxyethylated metabolite // Analytical Biochemistry. 1987. V. 161. I. 2. P. 348-351.; R.A. Greff, E.A. Setzkorn, W.D. Leslie. A colorimetric method for the determination of parts million of nonionic surfactants // Journal of the American Oil Chemists’ Society. 1965. V. 42 (3). P. 180-185.; A. Nozawa, T. Ohnuma, T. Sekine. Re-examination of the microanalysis of non-ionic surfactants that contain polyoxyethylene chains by the method involving solvent extraction of the thiocyanatocobaltate(II) complex // Analyst. 1976. V. 101 (1204). P. 543-548.; N.H. Anderson, J. Girling. Determination of polyoxyethylene non-ionic surfactants at trace levels // Analyst. 1982. V.107 (1276). P. 836-838.; N.B. Cucakovich, N.B. Cucakovich. Determination of Tween 80 in tissue culture media, vaccines, and related products // Analytical Biochemistry. 1971. V. 40. I. 1. P. 183-186.; H.V. Dang, A.I. Gray, D. Watson, C.D. Bates, P. Scholes, G.M. Eccleston. Composition analysis of two batches of polysorbate 60 using MS and NMR techniques // Journal of Pharmaceutical and Biomedical Analysis. 2006. V. 40. I. 5. P. 1155-1165.; M. Khossravi, Y.H. Kao, R.J. Mrsny, T.D. Sweeney. Analysis methods of polysorbate 20: A new method to assess the stability of polysorbate 20 and established methods that may overlook degraded polysorbate 20 // Pharmaceutical research 2002. V. 19 (5). P. 634-9.; H.C. Mahle, S.K.K. Ravuri. Pharmaceutical formulation for proteins. November 22. 2012. US Patent App. 13/574,071.; M. Adamo, L.W. Jr. Dick, D. Qiu, A.H. Lee, J. Devincentis, K.C. Cheng. A simple reversed phase high-performance liquid chromatography method for polysorbate 80 quantitation in monoclonal antibody drug products // Journal of chromatography B. 2010. V. 878 (21). P. 1865-70.; Z. Őszi, G. Pethő, Quantitative determination of polysorbate 20 in nasal pharmaceutical preparations by high-performance liquid chromatography // Journal of Pharmaceutical and Biomedical Analysis. 1998. V. 18. I. 4-5. P. 715-720.; https://www.pharmjournal.ru/jour/article/view/424

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    Academic Journal

    Πηγή: Biological Products. Prevention, Diagnosis, Treatment; Том 16, № 1 (2016); 14-26 ; БИОпрепараты. Профилактика, диагностика, лечение; Том 16, № 1 (2016); 14-26 ; 2619-1156 ; 2221-996X ; undefined

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.biopreparations.ru/jour/article/view/37/86; Public Health Services Act 42 U. S. C. § 262(i).; Directive 2001/83/EC of the European parliament and of the council of 6 November 2001 on the Community code relating to medicinal products for human use (OJ L 311, 28.11.2001, p. 67).; Pichler WJ. Adverse side-effects to biological agents. Allergy; 2006; 61: 912-20.; Leader B, Baca QJ, Golan DE. Protein therapeutics: a summary and pharmacological classification. Nat Rev Drug Discov. 2008; 7(1): 21 - 39.; International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, Q5C: Quality of biotechnological products: Stability testing of biotechnological/biological products, Nov. 30, 1995.; Солдатов АА, Авдеева ЖИ, Алпатова НА, Медуницын НВ, Киселевский МВ, Лысикова СЛ. и др. Проблемы регистрации биологических неоригинальных препаратов. Биопрепараты 2014; (4): 24-36.; Wax PM. Elixirs, diluents, and the passage of the 1938 Federal Food, Drug and Cosmetic Act. Ann Intern Med. 1995; 122(6): 456-61.; Stephens T, Brynner R. Dark Remedy. The Impact of Thalidomide and its Revival as a Vital Medicine. Cambridge, Massachusetts: Perseus Publishing; 2001.; Dukes MNG. The seven pillars of foolishness. In: Dukes MNG, editor. Side Effects of Drugs. Annual 8. Amsterdam: Elsevier; 1984. P. xvii-xxiii.; Shah RR. Drug-induced prolongation of the QT interval: why the regulatory concern? Fundam Clin Pharmacol. 2002; 16(2): 119-24.; World Health Organization. The Importance of Pharmacovigilance. Safety Monitoring of Medicinal Products. Chapter 2. A Short History of Involvement in Drug Safety Monitoring by WHO. Available from: http://apps.who.int/medicinedocs/en/d/Js4893e/3.html.; Available from: evs.nci.gov/ftp1/CTCAE v 4.03.; Ferner RE, Butt TF. Adverse drug reactions. Med. 2012; 40: 366-70.; Rawlins M, Thompson W. Mechanisms of adverse drug reactions. In: Davies D, ed. Textbook of adverse drug reactions. New York: Oxford University Press; 1991. P. 18-45.; Ebbers HC, Al-Temimi E, Moors EHM, Mantel-Teeuwisse AK, Schellekens H, Leufkens HGM. Differences Between Post-Authorization Adverse Drug Reactions of Biopharmaceuticals and Small Molecules. BioDrugs 2013; 27(2): 167-74.; Giezen TJ, Mantel-Teeuwisse AK, Straus SMJM, et al. Safety-related regulatory actions for biologicals approved in the United States and the European Union. JAMA 2008; 300: 1887-96.; Pichler WJ. Delayed drug hypersensitivity reactions. Ann Intern Med. 2003; 139: 683-93.; Perez-Soler R, Saltz L. Cutaneous adverse effects with HER1/ EGFR-targeted agents: is there a silver lining? J Clin Oncol. 2005; 23: 5235-46.; Danese S, Fiocchi C. Platelet activation and the CD40 / CD40 ligand pathway: mechanisms and implications for human disease. Crit Rev Immunol 2005; 25: 103-21.; Kwon HJ, Cote TR, Cuffe MS, Kramer JM, Braun MM. Case reports of heart failure after therapy with a tumor necrosis factor antagonist. Ann Intern Med. 2003; 138: 807-11.; Kasahara A, Hiraide A, Tomita N, Iwahashi H, Imagawa A, Ohguro N, et al. Vogt-Koyanagi-Harada disease occurring during interferon alpha therapy for chronic hepatitis C. J Gastroenterol. 2004; 39: 1106-09.; Sherer K, Spoerl D, Bircher AJ. Adverse drug reactions to biologics. JDDG 2010; (8): 411-26.; Clarke JB. Mechanisms of adverse drug reactions to biologics. In: Uetrecht J, ed. Adverse Drug Reactions. Handbook of Experimental Pharmacology. New York: Springer; 2010. P. 453-74.; Aronson JK, Ferner RE. Joining the DoTS: new approach to classify adverse drug reactions. BMJ 2003; 327: 1222-25.; Napoleone E. Children and ADRs (Adverse Drug Reactions). Ital. J. Pediat. 2011; 36: e1-e5.; Horen B, Montastruc JL. Adverse drug reactions and off-label drug use in pediatric outpatients. Br J Clin Pharmacol. 2002; 5(4): 665-70.; Pichler WJ, Adam J, Daubner B, Gentinetta T, Keller M, Yerly D. Drug Hypersensitivity Reactions: Pathomechanism and Clinical Symptoms. Med Clin № Am. 2010; 94: 645-64.; Nassif A, Bensussan A, Dorothee G, et al. Drug specific cytotoxic T-cells in the skin lesions of a patient with toxic epidermal necrolysis. J Invest Dermatol. 2002; 118: 728-33.; Britschgi M, Steiner UC, Schmid S, et al. T-cell involvement in drug-induced acute generalized exanthematous pustulosis. J Clin Invest. 2001; 107: 1433-41.; Pichler WJ. Pharmacological interaction of drugs with antigen-specific immune receptors: the p-i concept. Curr Opin Allergy Clin Immunol. 2002; 2: 301-5.; National Cancer Institute. Common Terminology Criteria for Adverse Events v3.0 (CTCAE). 9 August, 2006. Available from: http://ctep.cancer.gov/protocolDevelopment/electronic_applications/docs/ctcaev3.pdf.; Barbaud A., Granel F., Waton J., Poreaux C. How to manage hypersensitivity reactions to biological agents? Eur J Dermatol. 2011; 21 (5): 667-74.; https://www.biopreparations.ru/jour/article/view/37; undefined

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    Academic Journal

    Πηγή: Biological Products. Prevention, Diagnosis, Treatment; Том 16, № 3 (2016); 145-150 ; БИОпрепараты. Профилактика, диагностика, лечение; Том 16, № 3 (2016); 145-150 ; 2619-1156 ; 2221-996X ; undefined

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.biopreparations.ru/jour/article/view/57/109; Волова ТГ. Биотехнология. Новосибирск: Изд-во Сибирского отделения Российской академии наук; 1999.; Бекер МЕ. Введение в биотехнологию. М.: Пищевая промышленность; 1978.; Елинов НП. Основы биотехнологии. СПб.: Наука; 1995.; Катлинский АВ, ред. Учебное пособие для студентов высших фармацевтических учебных заведений. 3-е изд. М.: Академия; 2008.; Егоров НС, Самуилов ВД, ред. Биотехнология. Учебное пособие для вузов в 8-ми книгах. Кн. 1. Проблемы и перспективы. М.: Высшая школа; 1987.; Евтушенков АН, Фомичев ЮК. Введение в биотехнологию. Курс лекций. Минск: БГУ; 2002.; Катлинский АВ. Курс лекций по биотехнологии. М.: ММА им. И. М. Сеченова; 2005.; Глик ИБ, Пастернак Дж. Молекулярная биотехнология. М.: Мир; 2002.; WHO Library Cataloguing-in-Publication Data. The world health report 2013: research for universal health coverage.; Прищеп ТП, Чучалин ВС. Основы фармацевтической биотехнологии. Ростов-на-Дону: Феникс; 2006.; Сартакова ОЮ. Основы микробиологии и биотехнологии. Ч. 1. Барнаул: АГТУ; 2001.; Хиггинс И, ред. Биотехнология: принципы и применение. М.: Мир; 1988.; Виестур УЭ, Шмите ИА, Жилевич АВ. Биотехнология. Биологические агенты, технология, аппаратура. Рига: Зинатне; 1987.; Сартакова ОЮ. Основы микробиологии и биотехнологии. Ч. 2. Барнаул: Азбука; 2005.; Егоров НС, Самуилов ВД, ред. Биотехнология. Учебное пособие для вузов в 8-ми книгах. Кн. 6. Микробиологическое производство биологически активных веществ и препаратов. М.: Высшая школа; 1987.; Егоров НС, Самуилов ВД, ред. Биотехнология. Учебное пособие для вузов в 8-ми книгах. Кн. 3. Клеточная инженерия. М.: Высшая школа; 1987.; Кузьмина НА. Основы биотехнологии. Учебное пособие. Омск; 2006.; Садченко ЛС. Современные достижения биотехнологии в медицинской промышленности. М.; 2008.; Грачева ИМ. Технология ферментных препаратов. 3-е изд. М.: Элевар; 2000.; Егорова ТА, Клунова СМ, Живухина ЕА. Основы биотехнологии. М.: Академия; 2003.; Дятлова ВИ, Богун АГ, Бикетов СФ. Оценка серодиагностического потенциала рекомбинантных антигенов Mycobacterium tuberculosis, полученных в разных экспрессионных системах. Биотехнология 2014; (1): 72-8.; Эршлер МА, Оловникова НИ. Продукция моноклональных антител класса IgM в клетках DG44. Биотехнология 2014; (2): 24-34.; Смирнов В, Красных Л, Меркулов В, Бунятян Н, Раменская Г, Ельцова Е, Смолярчук Е, Егоренков Е, Бушманова А. Мировая практика в оценке взаимозаменяемости биоинженерных препаратов. Врач 2015; (9): 12-4.; Бушманова АВ, Ельцова ЕА, Раменская ГВ, Смолярчук ЕА. Биосимиляры - препараты будущего. Фармакокинетика и фармакодинамика 2015; (1): 14-7.; https://www.biopreparations.ru/jour/article/view/57; undefined

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    Academic Journal

    Πηγή: Biological Products. Prevention, Diagnosis, Treatment; № 3 (2015); 21-24 ; БИОпрепараты. Профилактика, диагностика, лечение; № 3 (2015); 21-24 ; 2619-1156 ; 2221-996X ; undefined

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.biopreparations.ru/jour/article/view/18/519; The Commission of the European Communities (2003) Commission Directive 2003/63/EC of 25 June 2003 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use. Official J Eur Union 2004; 47(L159): 46-94.; Misra A. Are biosimilars really generics? Expert Opin. Biol. Ther. 2010; 10(4): 489-4, Goldsmith D., Kuhlmann M., Covic A. Through the looking glass: the protein science of biosimilars. Clin Exp Nephrol. 2007;11: 1915.; Дугин И. На мировом фармрынке доминируют препараты. ФВ. Фармвестник. Available from: http://www.pharmvestnik.ru/publs/lenta/obzory/na-mirovom-farmrynke-dominirujut-biopreparaty.html#.U0wwBFV_tc0 (дата обращения 15.01.2015); Сазыкин Ю.О., Орехов С.Н., Чакалева И.И. Биотехнология. Учебное пособие для студентов высших учебных заведений. 2008.; Jenkins N., Murphy L., Tyther R. Post-translational modifications of recombinant proteins: significance for biopharmaceuticals. Mol Biotechnol. 2008; 39: 113-8.; Annex to Guideline on Similar Biological Medicinal Products Containing Biotechnology derived Proteins as Drug Substance - Non Clinical and Clinical Issues containing Recombinant Human Erythropoietin, CHMP/94526/05, March 2006.; Guideline on Similar Biological Medicinal Products Containing Biotechnology-derived Proteins as Drug Substance - Non Clinical and Clinical Issues, EMEA/CHMP/BMWP/42832/05, February 2006.; Committee for medicinal products for human use (CHMP) Available from: http://www.triskel.com/2%20Guideline%20biotech%20derived%20proteins.pdf (дата обращения 15.01.2015); Guideline on Similar Biological Medicinal Products containing biotechnology-derived proteins as active substance: quality issues (revision 1). EMA., Committee for Medicinal Products for Human Use, 2012. Available from: http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2012/05/WC500127960.pdf (дата обращения 14.04.2014).; Guideline on similar biological medicinal products containing monoclonal antibodies - non-clinical and clinical issues, CHMP/BMWP/403543/2010, May 2012.; Guideline on similar biological medicinal products containing recombinant interferon alpha, CHMP/BMWP/102046/2006, October 2007.; IMS Health 2007 & 2009, Evaluate Pharma, Sandoz analysis. С! ПРЕПАРАТЫ; The European Parliament and the Council of the European Union (2004) Directive 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use. Official J Eur Union 2004; 47 (L136): 34-57.; European Medicines Agency. Guideline on Similar Biological Medicinal Products Containing Biotechnology-derived Proteins as Drug Substance -Non Clinical and Clinical Issues, EMEA/CHMP/BMWP/42832/05, February 2006. Available from: www.ema.europa.eu/pdfs/human/biosimilar/4283205en Accessed Sept 2, 2010.; Sahoo N., Choudhury, K., Manchikanti P. Manufacturing of biodrugs: need for harmonization in regulatory standards. Biodrugs 2009; 23: 217-29.; US Food and Drug Administration. Available from: www.fda.org. Accessed Sept 2, 2010.; Федерального закона от 24.12.2014 г. «О внесении изменений в Федеральный закон «Об обращении лекарственных средств» и в статью 333.32.1. части второй Налогового кодекса Российской Федерации».; Guideline on Immunogenicity Assessment of Biotechnology-derived Therapeutic Proteins. EMEA/CHMP/BMWP/14327/2006, December 2007.; Guideline on non-clinical and clinical development of similar biological medicinal products containing recombinant human insulin and insulin analogues EMEA/CHMP/BMWP/32775/2005_Rev., December 2012.; Об обращении лекарственных средств [Электронный ресурс]: Федеральный закон от 12.04.2010 N 61-ФЗ (ред. от 12.03.2014). Доступ из справ.-правовой системы «Консультант Плюс».; Guideline on Similar Biological Medicinal Products, CPMP/437/04, October 2005.; Солдатов А.А., Авдеева Ж.И., Алпатова Н.А., Медуницын Н.В., Киселевский М.В., Лысикова С.Л. и др. Проблемы регистрации биологических неоригинальных лекарственных препаратов. Биопрепараты 2014; (4); 25-36.; https://www.biopreparations.ru/jour/article/view/18; undefined

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    Academic Journal

    Πηγή: Regulatory Research and Medicine Evaluation; № 4 (2015); 32-38 ; Регуляторные исследования и экспертиза лекарственных средств; № 4 (2015); 32-38 ; 3034-3453 ; 3034-3062 ; undefined

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.vedomostincesmp.ru/jour/article/view/62/46; Guidelines on use of International Nonproprietary Names (INNs) for Pharmaceutical Substances. WHO/PHARM S/Nom 1570. Geneva: WHO; 1997.; International Nonproprietary Names: revised procedure. Procedure for the selection of recommended international nonproprietary names for pharmaceutical substances. EB115.R4. Geneva: WHO; 2005.; WHO/EMP/RHT/TSN/2013.1. The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances. 2013.; WHO International Nonproprietary Names (INN) for Biological and Biotechnological Substances. A Review. Programme on International Nonproprietary Names (INN). Quality Assurance and Safety: Medicines (QSM). Medicines Policy and Standards (PSM) Department.; Васильев АН, Гавришина ЕВ, Ниязов РР, Снегирева АА, Адонин ВК. Введение в европейское законодательство о лекарственных средствах. Биологические лекарственные средства. Ремедиум 2013; (9): 49-54.; Васильев АН, Ниязов РР, Енгалычева ГН, Гавришина ЕВ, Тутер ЕА, Бекерман АН. Подтверждение качества, доклинические и клинические исследования биологически аналогичных лекарственных препаратов. Общие принципы. Ремедиум 2013; (6): 22-26.; Ниязов Рр, Горячев ДВ, Гавришина ЕВ, Ромодановский ДП, Драницына МА. Обоснование границ признания эквивалентности показателей качества, безопасности и эффективности при разработке биоаналогов. Экспериментальная и клиническая фармакология 2015; 78(6): 37-44.; Романов БК, Глаголев СВ, Поливанов ВА, Леонова МВ. Мониторинг безопасности лекарственных средств. Безопасность и риск фармакотерапии 2014; 3(4): 11-14.; Purple Book: Lists of Licensed Biological Products with Reference Product Exclusivity and Biosimilarity or Interchangeability Evaluations. U.S. Food and Drug Administration. Available from: http://www.fda.gov/Drugs/Develop-mentApprovalProcess/ HowDrugsareDevelopedandApproved/ApprovalAp-plications/TherapeuticBiologicApplications/Biosimilars/ucm411418.htm.; Васильев АН, Гавришина ЕВ, Ниязов РР, Добровольский АВ, Тутер ЕА, Бекерман АН. Биологически аналогичные лекарственные препараты в Российской Федерации и перспективы их разработки. Ремедиум 2013; (7-8): 67-70; https://www.vedomostincesmp.ru/jour/article/view/62; undefined

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