Course Description
| Course | Code | Semester | T+P (Hour) | Credit | ECTS |
|---|---|---|---|---|---|
| PHARMACEUTICAL CHEMISTRY LAB. III | - | Fall Semester | 0+3 | 1,5 | 3 |
| Course Program |
| Prerequisites Courses | |
| Recommended Elective Courses |
| Language of Course | Turkish |
| Course Level | First Cycle (Bachelor's Degree) |
| Course Type | Required |
| Course Coordinator | Prof.Dr. Seda ÜNSALAN |
| Name of Lecturer(s) | |
| Assistant(s) | |
| Aim | This course aims to provide information on quantitative analysis of pharmaceutical active ingredients and to make the application, UV-Vis spectrophotometric methods, analyzing the IR and HPLC system. |
| Course Content | This course contains; 1. General description of the quantitative analysis.,2. Titrimetric analysis methods.,3. Titrimetric analysis application,4. Titrimetric analysis application,5. Titrimetric analysis application,6. Titrimetric analysis application,7. UV-Vis. spectrophotometric method,8. The quantification by the UV-Vis spectrophotometric method application,9. The quantification by the UV-Vis spectrophotometric method application,10. IR spectrophotometric method,11. Recognition of the HPLC system,12. known sample application in HPLC,13. known sample application in HPLC,14. unknown sample application in HPLC. |
| Dersin Öğrenme Kazanımları | Teaching Methods | Assessment Methods |
| 1.compare general quantitative analysis techniques of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| 1.4.use HPLC in quantative analysis of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| 2.will be able to analyse IR spectrophotometric methods. | 12, 14, 16, 17, 5, 9 | A |
| 2.1.describe the IR spectrophotometric methods. | 12, 14, 16, 17, 5, 9 | A |
| 2.2.use the IR spectrophotometric methods | 12, 14, 16, 17, 5, 9 | A |
| 1.1. use titrimetric analysis methods of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| 1.2. adapt UV-Vis. Spectrophotometric methods in quantitative analysis of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| 1.3. compare chromatographic methods in quantitative analysis of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| Teaching Methods: | 12: Problem Solving Method, 14: Self Study Method, 16: Question - Answer Technique, 17: Experimental Technique, 5: Cooperative Learning, 9: Lecture Method |
| Assessment Methods: | A: Traditional Written Exam |
Course Outline
| Order | Subjects | Preliminary Work |
|---|---|---|
| 1 | 1. General description of the quantitative analysis. | 1 |
| 2 | 2. Titrimetric analysis methods. | 1 |
| 3 | 3. Titrimetric analysis application | 1 |
| 4 | 4. Titrimetric analysis application | 1 |
| 5 | 5. Titrimetric analysis application | 1 |
| 6 | 6. Titrimetric analysis application | 1 |
| 7 | 7. UV-Vis. spectrophotometric method | 1 |
| 8 | 8. The quantification by the UV-Vis spectrophotometric method application | 1 |
| 9 | 9. The quantification by the UV-Vis spectrophotometric method application | 1 |
| 10 | 10. IR spectrophotometric method | 1 |
| 11 | 11. Recognition of the HPLC system | 1 |
| 12 | 12. known sample application in HPLC | 1 |
| 13 | 13. known sample application in HPLC | 1 |
| 14 | 14. unknown sample application in HPLC | 1 |
| Resources |
| 1. The laboratory notes will be given to the students. |
Course Contribution to Program Qualifications
| Course Contribution to Program Qualifications | |||||||
| No | Program Qualification | Contribution Level | |||||
| 1 | 2 | 3 | 4 | 5 | |||
| 1 | PQ-1. Skilfully use information technology to access, follow, evaluate and apply current knowledge in the field of Pharmaceutical Sciences. | X | |||||
| 2 | PQ-2. Have advanced knowledge in APIs and DPs. | X | |||||
| 3 | PQ-3. Collaborate with the experts for collection, interpretation, application and declaration of data in Pharmaceutical Sciences field. | X | |||||
| 4 | PQ-4. Provide best patient counseling services and medication therapy management using his/her knowledge and pharmaceutical information systems to improve the quality of life and safety of patient. | X | |||||
| 5 | PQ-5. Capable of organizing and administering a drugstore as per responsibilities prescribed under the Pharmacy Law, using skills, knowledge and advanced technology systems. | X | |||||
| 6 | PQ-6. Skilfully use computer programs and advanced technology related to the Pharmaceutical Sciences. | X | |||||
| 7 | PQ-7. Provide solutions to the professional issues using scientific knowledge and data. | X | |||||
| 8 | PQ-8. Perform identification, quality control and standardization of the drug products. | X | |||||
| 9 | PQ-9. Prepare and implement developmental plans for his/her subordinates, frequently evaluate their progress and make necessary adjustments. | X | |||||
| 10 | PQ-10. Capable of conducting independent studies with his/her advanced knowledge in pharmaceutical sciences, takes responsibilities in professional organizations and efficiently collaborates with the members of his/her own organization as well as other organizations. | X | |||||
| 11 | PQ-11. Clearly show signs of adoption of life-long learning and openness to further development. | X | |||||
| 12 | PQ-12. Critically evaluate their knowledge in pharmaceutical sciences. | X | |||||
| 13 | PQ-13. Closely follow and evaluate the national and international professional developments. | X | |||||
| 14 | PQ-14. Record and document all professional activities and applications. | X | |||||
| 15 | PQ-15. Communicate all necessary information about medicines to patient, medical personnel and public. | X | |||||
| 16 | PQ-16. Proficient in English to communicate and follow current knowledge in pharmaceutical sciences. | X | |||||
| 17 | PQ-17. Inform officials and organizations about the issues with the quality assurance of pharmaceutical products. | X | |||||
| 18 | PQ-18. Actively involve in the preparation of APIs, every stage of the formulation and production of DPs. | X | |||||
| 19 | PQ-19. Knowledgable in the regulatory rules of new drug application, data protection and patent issues and understand their interrelationship. | X | |||||
| 20 | PQ-20. Have awareness of his/her duties, rights and responsibilities and act based on Pharmacy Law and high professional ethical standards. | X | |||||
| 21 | PQ-21. Familiar with and actively pursue the personal and public health, environmental, and work safety issues. | X | |||||
Assessment Methods
| Contribution Level | Absolute Evaluation | |
| Rate of Midterm Exam to Success | 60 | |
| Rate of Final Exam to Success | 40 | |
| Total | 100 | |
| ECTS / Workload Table | ||||||
| Activities | Number of | Duration(Hour) | Total Workload(Hour) | |||
| Course Hours | 14 | 3 | 42 | |||
| Guided Problem Solving | 14 | 3 | 42 | |||
| Resolution of Homework Problems and Submission as a Report | 0 | 0 | 0 | |||
| Term Project | 0 | 0 | 0 | |||
| Presentation of Project / Seminar | 0 | 0 | 0 | |||
| Quiz | 0 | 0 | 0 | |||
| Midterm Exam | 1 | 3 | 3 | |||
| General Exam | 1 | 3 | 3 | |||
| Performance Task, Maintenance Plan | 0 | 0 | 0 | |||
| Total Workload(Hour) | 90 | |||||
| Dersin AKTS Kredisi = Toplam İş Yükü (Saat)/30*=(90/30) | 3 | |||||
| ECTS of the course: 30 hours of work is counted as 1 ECTS credit. | ||||||
Detail Informations of the Course
Course Description
| Course | Code | Semester | T+P (Hour) | Credit | ECTS |
|---|---|---|---|---|---|
| PHARMACEUTICAL CHEMISTRY LAB. III | - | Fall Semester | 0+3 | 1,5 | 3 |
| Course Program |
| Prerequisites Courses | |
| Recommended Elective Courses |
| Language of Course | Turkish |
| Course Level | First Cycle (Bachelor's Degree) |
| Course Type | Required |
| Course Coordinator | Prof.Dr. Seda ÜNSALAN |
| Name of Lecturer(s) | |
| Assistant(s) | |
| Aim | This course aims to provide information on quantitative analysis of pharmaceutical active ingredients and to make the application, UV-Vis spectrophotometric methods, analyzing the IR and HPLC system. |
| Course Content | This course contains; 1. General description of the quantitative analysis.,2. Titrimetric analysis methods.,3. Titrimetric analysis application,4. Titrimetric analysis application,5. Titrimetric analysis application,6. Titrimetric analysis application,7. UV-Vis. spectrophotometric method,8. The quantification by the UV-Vis spectrophotometric method application,9. The quantification by the UV-Vis spectrophotometric method application,10. IR spectrophotometric method,11. Recognition of the HPLC system,12. known sample application in HPLC,13. known sample application in HPLC,14. unknown sample application in HPLC. |
| Dersin Öğrenme Kazanımları | Teaching Methods | Assessment Methods |
| 1.compare general quantitative analysis techniques of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| 1.4.use HPLC in quantative analysis of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| 2.will be able to analyse IR spectrophotometric methods. | 12, 14, 16, 17, 5, 9 | A |
| 2.1.describe the IR spectrophotometric methods. | 12, 14, 16, 17, 5, 9 | A |
| 2.2.use the IR spectrophotometric methods | 12, 14, 16, 17, 5, 9 | A |
| 1.1. use titrimetric analysis methods of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| 1.2. adapt UV-Vis. Spectrophotometric methods in quantitative analysis of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| 1.3. compare chromatographic methods in quantitative analysis of the drugs. | 12, 14, 16, 17, 5, 9 | A |
| Teaching Methods: | 12: Problem Solving Method, 14: Self Study Method, 16: Question - Answer Technique, 17: Experimental Technique, 5: Cooperative Learning, 9: Lecture Method |
| Assessment Methods: | A: Traditional Written Exam |
Course Outline
| Order | Subjects | Preliminary Work |
|---|---|---|
| 1 | 1. General description of the quantitative analysis. | 1 |
| 2 | 2. Titrimetric analysis methods. | 1 |
| 3 | 3. Titrimetric analysis application | 1 |
| 4 | 4. Titrimetric analysis application | 1 |
| 5 | 5. Titrimetric analysis application | 1 |
| 6 | 6. Titrimetric analysis application | 1 |
| 7 | 7. UV-Vis. spectrophotometric method | 1 |
| 8 | 8. The quantification by the UV-Vis spectrophotometric method application | 1 |
| 9 | 9. The quantification by the UV-Vis spectrophotometric method application | 1 |
| 10 | 10. IR spectrophotometric method | 1 |
| 11 | 11. Recognition of the HPLC system | 1 |
| 12 | 12. known sample application in HPLC | 1 |
| 13 | 13. known sample application in HPLC | 1 |
| 14 | 14. unknown sample application in HPLC | 1 |
| Resources |
| 1. The laboratory notes will be given to the students. |
Course Contribution to Program Qualifications
| Course Contribution to Program Qualifications | |||||||
| No | Program Qualification | Contribution Level | |||||
| 1 | 2 | 3 | 4 | 5 | |||
| 1 | PQ-1. Skilfully use information technology to access, follow, evaluate and apply current knowledge in the field of Pharmaceutical Sciences. | X | |||||
| 2 | PQ-2. Have advanced knowledge in APIs and DPs. | X | |||||
| 3 | PQ-3. Collaborate with the experts for collection, interpretation, application and declaration of data in Pharmaceutical Sciences field. | X | |||||
| 4 | PQ-4. Provide best patient counseling services and medication therapy management using his/her knowledge and pharmaceutical information systems to improve the quality of life and safety of patient. | X | |||||
| 5 | PQ-5. Capable of organizing and administering a drugstore as per responsibilities prescribed under the Pharmacy Law, using skills, knowledge and advanced technology systems. | X | |||||
| 6 | PQ-6. Skilfully use computer programs and advanced technology related to the Pharmaceutical Sciences. | X | |||||
| 7 | PQ-7. Provide solutions to the professional issues using scientific knowledge and data. | X | |||||
| 8 | PQ-8. Perform identification, quality control and standardization of the drug products. | X | |||||
| 9 | PQ-9. Prepare and implement developmental plans for his/her subordinates, frequently evaluate their progress and make necessary adjustments. | X | |||||
| 10 | PQ-10. Capable of conducting independent studies with his/her advanced knowledge in pharmaceutical sciences, takes responsibilities in professional organizations and efficiently collaborates with the members of his/her own organization as well as other organizations. | X | |||||
| 11 | PQ-11. Clearly show signs of adoption of life-long learning and openness to further development. | X | |||||
| 12 | PQ-12. Critically evaluate their knowledge in pharmaceutical sciences. | X | |||||
| 13 | PQ-13. Closely follow and evaluate the national and international professional developments. | X | |||||
| 14 | PQ-14. Record and document all professional activities and applications. | X | |||||
| 15 | PQ-15. Communicate all necessary information about medicines to patient, medical personnel and public. | X | |||||
| 16 | PQ-16. Proficient in English to communicate and follow current knowledge in pharmaceutical sciences. | X | |||||
| 17 | PQ-17. Inform officials and organizations about the issues with the quality assurance of pharmaceutical products. | X | |||||
| 18 | PQ-18. Actively involve in the preparation of APIs, every stage of the formulation and production of DPs. | X | |||||
| 19 | PQ-19. Knowledgable in the regulatory rules of new drug application, data protection and patent issues and understand their interrelationship. | X | |||||
| 20 | PQ-20. Have awareness of his/her duties, rights and responsibilities and act based on Pharmacy Law and high professional ethical standards. | X | |||||
| 21 | PQ-21. Familiar with and actively pursue the personal and public health, environmental, and work safety issues. | X | |||||
Assessment Methods
| Contribution Level | Absolute Evaluation | |
| Rate of Midterm Exam to Success | 60 | |
| Rate of Final Exam to Success | 40 | |
| Total | 100 | |