GAZI UNIVERSITY INFORMATION PACKAGE - 2019 ACADEMIC YEAR

COURSE DESCRIPTION
CONTROLLED RELEASE DRUG DELIVERY TECHNOLOGY -PRACTICE/FTE-2041
Course Title: CONTROLLED RELEASE DRUG DELIVERY TECHNOLOGY -PRACTICE
Credits 2 ECTS 7
Semester 1 Compulsory/Elective Elective
COURSE INFO
 -- LANGUAGE OF INSTRUCTION
  Turkish
 -- NAME OF LECTURER(S)
  Prof.Dr.F.Acartürk, Prof.Dr.F.Tırnaksız, Prof.Dr.S.Takka, Assoc.Prof.Dr.Z.Ş.Teksin, Assoc.Prof.Dr.T.İnceçayır, Assoc.Prof.Dr.S.İ.Tamer, Assoc.Prof.Dr.F.T.Demiröz
 -- WEB SITE(S) OF LECTURER(S)
  http://websitem.gazi.edu.tr/site/tfigen
 -- EMAIL(S) OF LECTURER(S)
  acarturk@gazi.edu.tr, tfigen@gazi.edu.tr, takka@gazi.edu.tr, zsteksin@gazi.edu.tr, tincecayir@gazi.edu.tr, ilbasmis@gazi.edu.tr, fatmanur@gazi.edu.tr
 -- LEARNING OUTCOMES OF THE COURSE UNIT
Understanding of the fundamentals and basic concepts of controlled release dosage forms.
Students learn designing oral controlled release dosage forms,designing of parenteral controlled release dosage forms.
Additionaly, students understand ocular and intrauterine controlled release dosage forms etc.
As a result of this course students learn the preparation and applications of sustained release drug delivery system, will discuss the results of know
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 -- MODE OF DELIVERY
  The mode of delivery of this course is Face to face
 -- PREREQUISITES AND CO-REQUISITES
  There is no prerequisite or co-requisite for this course.
 -- RECOMMENDED OPTIONAL PROGRAMME COMPONENTS
  There is no recommended optional programme component for this course.
 --COURSE CONTENT
1. Week  Controlled release dosage forms, descriptions and classsifications
2. Week  The preparation methods of controlled release dosage forms
3. Week  The calculation methods to design controlled release dosage forms
4. Week  Diffusion controlled systems
5. Week  Matrix controlled systems
6. Week  Membrane controlled systems
7. Week  Chemical controlled release systems
8. Week  The design of parenteral controlled release dosage forms
9. Week  Oral controlled release dosage forms
10. Week  Vaginal, cervical and rectal controlled release systems
11. Week  Buccal and nasal controlled release systems
12. Week  Bioadhesive controlled release systems
13. Week  Ocular and transdermal controlled release systems
14. Week  Implant systems, types and characteristics
15. Week  -
16. Week  -
 -- RECOMMENDED OR REQUIRED READING
  -Kontrollü salım sistemleri (Ed: Ayla GÜRSOY) Elam Bilgisayar Basım ve Ambalaj San. Tic. Ltd. Şti., İstanbul 2002 -Modified-Release Drug Delivery Tec
 -- PLANNED LEARNING ACTIVITIES AND TEACHING METHODS
  Lecture, Question & Answer, Demonstration, Drill - Practise
 -- WORK PLACEMENT(S)
  NA
 -- ASSESSMENT METHODS AND CRITERIA
 
Quantity
Percentage
 Mid-terms
0
0
 Assignment
1
10
 Exercises
0
0
 Projects
0
0
 Practice
1
60
 Quiz
0
0
 Contribution of In-term Studies to Overall Grade  
70
 Contribution of Final Examination to Overall Grade  
30
 -- WORKLOAD
 Efficiency  Total Week Count  Weekly Duration (in hour)  Total Workload in Semester
 Theoretical Study Hours of Course Per Week
0
 Practising Hours of Course Per Week
14
4
56
 Reading
10
2
20
 Searching in Internet and Library
10
2
20
 Designing and Applying Materials
14
2
28
 Preparing Reports
8
1
8
 Preparing Presentation
7
3
21
 Presentation
1
1
1
 Mid-Term and Studying for Mid-Term
3
3
9
 Final and Studying for Final
4
3
12
 Other
0
 TOTAL WORKLOAD: 
175
 TOTAL WORKLOAD / 25: 
7
 ECTS: 
7
 -- COURSE'S CONTRIBUTION TO PROGRAM
NO
PROGRAM LEARNING OUTCOMES
1
2
3
4
5
1Posesses extensive knowledge accumulation on the field of Pharmaceutical Technology, learns pre-formulations of all pharmaceutical dosage forms, formulation designs and in vitro/in vivo evaluations of formulations.X
2Gains the capability of following up novalities in technology, and posesses the capability of literature search, evaluation and interpretation on the fields of Pharmacy.X
3Gains the capability of patent search and evaluation and patenting regarding the formulations of active drug ingredient, dosage forms and preparation technologies.X
4Learns sufficient knowledge on the the field of laboratory, pilot batch and industrial scale productions, quality controls, quality assurance system, good manufacture practice (GMP) and stability assurance of all dosage forms.X
5Learns the knowledge satisfying the capability level for designing original and generic drugs, evaluating process validation and quality assurance.X
6Learns the interpretation, statistical evaluation and practical application of the research results.X
7Posesses the knowledge on new drug delivery systems and posesses the knowledge and capacity on targetting these systems at a level of an expert.X
8Learns designing, formulations, preparation techniques, physical and chemical stabilities of biotechnological products.X
9Gains the capability of finding solutions to the problems encountered during research. He/she gains the capability of analytical thinking. He/she gains the capability of publishing the experimental results in the national/international journals.X
10Gains the capability of following and interpretion of important wold health organizations (FDA, EMA, ICH and WHO) and official reference books (pharmacopoeia etc.). As a result, he/she transfers his/her knowledge to the field of Pharmaceutical Technology, and develops new approaches.X