| Pharmacy (English) | |||||
| Bachelor | TR-NQF-HE: Level 6 | QF-EHEA: First Cycle | EQF-LLL: Level 6 | ||
| Course Code: | PHA324 | ||||
| Course Name: | Pharmaceutical Chemistry Laboratory-II | ||||
| Course Semester: | Spring | ||||
| Course Credits: |
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| Language of instruction: | EN | ||||
| Course Requirement: | |||||
| Does the Course Require Work Experience?: | No | ||||
| Type of course: | Necessary | ||||
| Course Level: |
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| Mode of Delivery: | Face to face | ||||
| Course Coordinator : | Ar.Gör. TUĞÇE CİNEK | ||||
| Course Lecturer(s): | Prof. Dr. Şeref Demirayak, Prof. Dr. İlkay Küçükgüzel | ||||
| Course Assistants: |
| Course Objectives: | The objective of this course is to teach the students the basics and application of the quantitative analysis techniques on active pharmaceutical ingredients using titration, UV-Vis spectrophotometry and high pressure liquid chromatography methods. |
| Course Content: | This course includes provide basic information on the quantitative analysis of pharmaceutical active ingredients in pharmaceutical formulations by titration, UV-Vis spectroscopy, and high pressure liquid chromatography. |
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The students who have succeeded in this course;
1) Access, evaluate and apply up-to-date scientific knowledge in the field of pharmacy 2) It conveys information to patients, health personnel and society on all matters related to drugs. 3) Has the necessary knowledge about the therapeutic effects, drug forms, pharmacokinetic properties, stability and incompatibilities of drug active substances and can use this information. 4) Recognizes, controls and standardizes quality assurance issues and processes of all pharmaceutical-related products. 5) Has knowledge and equipment about the administration and use of the drug to the patient, advises on rational and safe drug use, and supports pharmacovigilance practices. 6) Has knowledge about the production and production technologies of natural and synthetic pharmaceutical raw materials. 7) Have knowledge about the concepts related to the functioning, maintenance and pathology of biological systems that form the basis of human health. 8) Has sufficient knowledge and application skills on research, development and production of pharmaceutical and cosmetic products. 9) Plans and implements all subjects within the scope of pharmacy services in the hospital. 10) Has knowledge about licensing conditions, data protection, patent and pharmacoeconomics in pharmaceuticals. 11) She/He is administratively and technically equipped in every field where the pharmacy profession is responsible by law, and produces solutions to problems in line with scientific data / evidence. 12) Combines basic and applied sciences with pharmacy profession practices and uses them in the field of pharmacy. 13) Has sufficient knowledge and application skills on physical, chemical, biological and toxicological analyzes of pharmaceutical, biotechnological and radiopharmaceutical products. 14) Acts in accordance with ethical and legal principles in the field of pharmacy. 15) Has the necessary competencies to work with colleagues and other health professionals in terms of communicative, managerial and social skills. 16) Provides consultancy on medicinal plants, herbal supplements and food supplements. 17) Knows pharmaceutical care practices, understands and evaluates drug interactions. 18) Knows the risks associated with the use of drugs and other chemical substances and laboratory practice. |
| Week | Subject | Related Preparation |
| 1) | Theoretical basis of laboratory studies | |
| 2) | Theoretical basis of laboratory studies | |
| 3) | Principles of safety rules in laboratory | |
| 4) | Principals of UV spectrophotometric determination | |
| 5) | Alkalimetric aspirin determination | |
| 6) | Fundamentals of high-pressure liquid chromatography | |
| 7) | Quantitative analysis using high-pressure liquid chromatography | |
| 8) | Midterm exam | |
| 9) | Quantitative analysis of Vitamin E in tablets and capsules | |
| 10) | Derivatization methods in quantitative analysis | |
| 11) | Quantitative analysis with spectrophotometric methods in visible range | |
| 12) | Determination of Vitamin B6 by UV spectrophotometry | |
| 13) | Determination of paracetamol in formulations by UV spectrophotometry | |
| 14) | Assessment of experimental results in MS Excel software. | |
| 15) | Compensation laboratory |
| Course Notes / Textbooks: | İlaçların Tanınması ve Kantitatif Tayini. Nedime Ergenç, Aysel Gürsoy,Öznur Ateş (1999).İstanbul Üniversitesi Yayınları 1.Quantitative Analysis of Drugs in Pharmaceutical Formulations. P.D. Sethi .(2015)CBS Publishers 2. Pharmaceutical Drug Analysis. A.Kar. (2008) New Age International Publishers |
| References: | İlaçların Tanınması ve Kantitatif Tayini. Nedime Ergenç, Aysel Gürsoy,Öznur Ateş (1999).İstanbul Üniversitesi Yayınları 1.Quantitative Analysis of Drugs in Pharmaceutical Formulations. P.D. Sethi .(2015)CBS Publishers 2. Pharmaceutical Drug Analysis. A.Kar. (2008) New Age International Publishers |
| No Effect | 1 Lowest | 2 Medium | 3 Highest |
| Program Outcomes | Level of Contribution |
| Anlatım | |
| Course | |
| Labs | |
| Rapor Yazma | |
| Soru cevap/ Tartışma | |
| Uygulama (Modelleme, Tasarım, Maket, Simülasyon, Deney vs.) |
| Yazılı Sınav (Açık uçlu sorular, çoktan seçmeli, doğru yanlış, eşleştirme, boşluk doldurma, sıralama) | |
| Raporlama |
| Semester Requirements | Number of Activities | Level of Contribution |
| Midterms | 1 | % 40 |
| Final | 1 | % 60 |
| total | % 100 | |
| PERCENTAGE OF SEMESTER WORK | % 40 | |
| PERCENTAGE OF FINAL WORK | % 60 | |
| total | % 100 | |
| Activities | Number of Activities | Aktiviteye Hazırlık | Aktivitede Harçanan Süre | Aktivite Gereksinimi İçin Süre | Workload | ||
| Laboratory | 14 | 3 | 42 | ||||
| Study Hours Out of Class | 14 | 3 | 42 | ||||
| Quizzes | 6 | 1 | 6 | ||||
| Midterms | 1 | 1 | 1 | ||||
| Final | 1 | 1 | 1 | ||||
| Total Workload | 92 | ||||||