GAZI UNIVERSITY INFORMATION PACKAGE - 2019 ACADEMIC YEAR

COURSE DESCRIPTION
CONTROLLED RELEASE DRUG DELIVERY TECHNOLOGY I./FTE-2040
Course Title: CONTROLLED RELEASE DRUG DELIVERY TECHNOLOGY I.
Credits 3 ECTS 8
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 sustained release dosage forms.
Understanding of designing oral sustained release dosage forms.
Students learn designing of parenteral sustained release dosage forms, ocular and intrauterine sustained release dosage forms.
As a result of this course students learn the information in the field of desining of drug formulation will discuss the results of knowledge.
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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  Sustained release dosage forms, descriptions and classsifications
2. Week  Basic principles of sustained release dosage forms
3. Week  The preparation methods of sustained release dosage forms
4. Week  The calculation methods to design sustained release dosage forms
5. Week  Diffusion controlled systems, matrix and membrane systems
6. Week  Chemical controlled systems
7. Week  The excipients and polymers used in the formulations
8. Week  The design of parenteral sustained release dosage forms
9. Week  Oral sustained release dosage forms
10. Week  Vaginal, cervical and rectal sustained release systems
11. Week  Buccal and nasal sustained release systems
12. Week  Bioadhesive sustained release systems
13. Week  Ocular and transdermal sustained 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
1
30
 Practice
0
0
 Quiz
0
0
 Contribution of In-term Studies to Overall Grade  
40
 Contribution of Final Examination to Overall Grade  
60
 -- WORKLOAD
 Efficiency  Total Week Count  Weekly Duration (in hour)  Total Workload in Semester
 Theoretical Study Hours of Course Per Week
14
3
42
 Practising Hours of Course Per Week
0
 Reading
14
4
56
 Searching in Internet and Library
12
1
12
 Designing and Applying Materials
0
 Preparing Reports
10
3
30
 Preparing Presentation
8
2
16
 Presentation
2
2
4
 Mid-Term and Studying for Mid-Term
4
4
16
 Final and Studying for Final
6
4
24
 Other
0
 TOTAL WORKLOAD: 
200
 TOTAL WORKLOAD / 25: 
8
 ECTS: 
8
 -- 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