Research and Educational Experience

Major: Pharmacy and Industrial Pharmacy
Code of subject: 7.226.00.O.025
Credits: 6.00
Department: Technology of Biologically Active Substances, Pharmacy and Biotechnology
Lecturer: Supervisor of Master`s Qualification Thesis
Semester: 4 семестр
Mode of study: денна
Learning outcomes: - ability to work with literary sources, scientific publications, to search for the necessary methods, to be able to analyze different methods of obtaining potential medicines; - ability to make material calculations, to model chemical processes - ability to work out and improve the methods of obtaining new substances - ability to use computer programs to calculate molecules of synthesized substances, to predict their biological activity - ability to process the results of scientific work - the ability to design a graphic part in the form of a presentation - the ability to demonstrate practical engineering skills and the ability to apply a systems approach to solving scientific problems - identification and investigation of the properties of the synthesized compounds and possible ways of their further practical application - knowledge of regulatory documents and rules for modeling chemical-pharmaceutical processes in accordance with international GMP requirements and principles
Required prior and related subjects: Prerequisites: Modeling and designing of chemical and pharmaceutical enterprises in the GMP system; Chemistry and technology of medicinal products, P. 1, P. 2; Scientific aspects of ecology of chemical and pharmaceutical industries; Industrial equipment of chemical and pharmaceutical enterprises; Fundamentals of Research and Intellectual Property; Economics of chemical and pharmaceutical enterprises. Corequisites: Practice on the topic of master's qualification work; Performance of master's qualification work.
Summary of the subject: Justification of the subject and purpose of master's qualification work. Review of literary data. The main part, which includes the justification for choosing methods for obtaining new compounds. Experimental part. Material calculations. Short technology. Principle technological scheme and creation of hardware-technological scheme. Economic part. Conclusions References. Attachments (presentation).
Assessment methods and criteria: Correct registration statement and objectives practices completeness of the material (20), processing and links to documents that regulate drug production in manufacturing (25 points), accuracy design, application diagrams, illustrations (5 points). - Oral defense of report on practice (50 points).
Recommended books: 1. Процеси і апарати хіміко-фармацевтичної промисловості. Навч посібник для фарм і хім спец. / Сидоров Ю.І., Чуєшов В.І., Новіков В.П. - Винница: Нова Книга, 2009. -816 с. 2. Технологічне обладнання біотехнологічної і фармацевтичної промисловості: підручник [для вищ. навч. закл.] / Стасевич М.В., Милянич., А.О., Стрельников Л.С., Крутських Т.В, Бучкевич І.Р., Зайцев О.І Гузьова., І.О., Стрілець О.П., Гладух Є.В., Новіков В.П. –Львів: «Новий Світ-2000», 2016. –410 с. 3. Технологія ліків промислового виробництва : підручник: у 2 ч. / В. І. Чуєшов, Є. В. Гладух, І. В. Сайко [та ін.]; – Харків: НФаУ; Оригінал, 2012. – Ч. 1 і 2. 4. Ол. Швайка Основи синтезу лікарських речовин та їх проміжних продуктів: Посібник. – Донецьк. 2004. – 552 с.