DRUG ANALYSIS III AND FOOD ANALYSIS
ANALISI DEI FARMACI III E DEGLI ALIMENTI
A.Y. | Credits |
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2023/2024 | 6 |
Lecturer | Office hours for students | |
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Annalida Bedini | Every weekday, except on Saturdays, after appointment by email at the address given, or by telephone at +39 0722 303326. |
Teaching in foreign languages |
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Course with optional materials in a foreign language
English
This course is entirely taught in Italian. Study materials can be provided in the foreign language and the final exam can be taken in the foreign language. |
Assigned to the Degree Course
Date | Time | Classroom / Location |
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Date | Time | Classroom / Location |
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Learning Objectives
The course, intended to provide theoretical and practical knowledge on instrumental techniques used for the determination of the purity of a drug, for the qualitative detection and for the determination of the amount of the active ingredients in a more or less complex systems, for the determination of the stability of a drug and for checks aimed at the search and identification of metabolites.
Program
Teaching is organized into theoretical lessons and practical laboratory exercises.
Theoretical lessons
1) Control of the quality of analytical methods.
2) Recalls of chemical-physical properties of molecules of pharmaceutical interest: acidity and basicity, distribution coefficient, stability and stereochemistry.
3) UV/visible spectroscopy - Instrumentation and sample preparation. Qualitative analysis: correlation UV spectrum and chemical structure. Quantitative analysis: Lambert-Beer law, pKa determination and other applications of interest in quantitative pharmaceutical analysis.
4) Infrared Spectroscopy - Instrumentation, sample preparation, identification of polymorphs and other applications of pharmaceutical interest. Near infrared spectroscopy (NIR): principles and applications.
5) Differential Scanning Calorimerty (DSC): principles and and applications in pharmaceutical analysis.
6) Chromatographic techniques - Gaschromatography: columns, injectors and detectors (FID, thermal conductivity, electron capture and mass); parameters that regulate the performance of GC and applications of GC in analysis of pharmaceutical interest. HPLC: instrumetation, mobile and stationary phases, parameters that regulate the performance of HPLC and applications of the instrumental technique in analysis of pharmaceutical interest. Ultra-Performance Liquid Chromatography (UPLC). TLC: quantitative analytical applications.
7) Extraction methods in pharmaceutical analysis, solid-phase extraction (SPE) and solid-phase microextraction (SPME).
8) Qualitative analysis and quantitative techniques in chromatography.
9) Polarimetric analysis: instrumentation and applications in pharmaceutical and food fields.
10) Mass spectrometry - Ionization sources: EI, CI, FAB, ESI, APCI and MALDI. Analyzers: magnetic sector, single and triple quadrupole, ion trap, time of flight and Orbitrap. High resolution mass spectrometry. Tandem mass spectrometry. Applications to pharmaceutical and biological sciences.
11) Molecular Emission Spectroscopy - Fluorescence spectroscopy: principles, instrumentation applications of pharmaceutical interest.
12) High performance capillary electrophoresis: key points, instrumentation and applications.
Practical laboratory exercises
The practical exercises focus on the analysis of herbal, food, nutraceutical and pharmaceutical preparations.
Bridging Courses
In order to attend the laboratory practice and acquire the frequency signature, it is necessary to have passed the exam of Organic Chemistry I and attended the laboratory practice of Drug Analysis II.
In order to take the exam it is necessary to acquire the signature of attendance and have passed the examinations of Organic Chemistry I, Drug Analysis I and Drug Analysis II.
Learning Achievements (Dublin Descriptors)
D1 - Knowledge and understanding. The student should have acquired the theoretical and practical knowledge on instrumental techniques used for the determination of the purity of a drug, for the qualitative detection and for the determination of the amount of the active ingredients in a more or less complex systems, for the determination of the stability of a drug and for checks aimed at the search and identification od metabolites.
D2 - Applying knowledge and understanding. The student will be able to apply the knowledge acquired during the course, and then be able to conduct qualitative and quantitative instrumental analysis of substances of pharmaceutical interest in more or less complex systems obtaining valid results. The student must also be able to plan and implement an analytical method.
D3 - Making judgements. The student must be able to interpret the experimental data and the results obtained. These skills will be verified through targeted oral application questions.
D4 - Communication skills. After completing the course the student will be able to present what he has learned using appropriate terminology for the purpose of scientific communication regarding methodologies and issues concerning the analysis of compounds of pharmaceutical interest. The student will be able to organize and present clear and complete reports.
D5 - Learning skills. The student will have developed the learn ability useful to continuously update his knowledge and will be able to use it in order to face new analytical issues.
Teaching Material
The teaching material prepared by the lecturer in addition to recommended textbooks (such as for instance slides, lecture notes, exercises, bibliography) and communications from the lecturer specific to the course can be found inside the Moodle platform › blended.uniurb.it
Supporting Activities
There are no supporting activities.
Teaching, Attendance, Course Books and Assessment
- Teaching
Lectures (3 cfu) and laboratory practice (3 cfu) .
- Attendance
Attendance at laboratory practice is compulsory in order to acquire the attendance signature and be able to take the exam.
- Course books
D. G. Watson Pharmaceutical Analysis, 3rd Edition, Elsevier.
- Assessment
Subject to approval of the practical laboratory part, the assessment of learning involves an oral test lasting 30-40 minutes aimed at ascertaining the level of knowledge and understanding achieved by the student on the theoretical contents exposed in class and on the practical procedures used during laboratory exercises. The student will be required to have knowledge regarding the instrumental techniques used in determining the purity of drugs, in the qualitative identification and quantitative dosing of active ingredients in more or less complex systems, in drug stability checks and in the research and identification of metabolites. The presentation and connection skills of the topics covered during the lessons as well as the ability to resolve practical and application problems will also be tested. The oral test is judged with a mark out of thirty.
- Disability and Specific Learning Disorders (SLD)
Students who have registered their disability certification or SLD certification with the Inclusion and Right to Study Office can request to use conceptual maps (for keywords) during exams.
To this end, it is necessary to send the maps, two weeks before the exam date, to the course instructor, who will verify their compliance with the university guidelines and may request modifications.
Additional Information for Non-Attending Students
- Teaching
Regular attendance of frontal lessons favors the acquisition of the skills necessary to pass the exam.
Non-attending students are invited to contact the teacher and consult the Moodle platform to acquire the teaching material.
Video tutorials preparatory to practical exercises in the laboratory are available on the moodle platform.
- Attendance
Attendance at laboratory practice is compulsory in order to acquire the attendance signature and be able to take the exam.
- Course books
D. G. Watson Pharmaceutical Analysis, 3rd Edition, Elsevier.
- Assessment
Subject to approval of the practical laboratory part, the assessment of learning involves an oral test lasting 30-40 minutes aimed at ascertaining the level of knowledge and understanding achieved by the student on the theoretical contents exposed in class and on the practical procedures used during laboratory exercises. The student will be required to have knowledge regarding the instrumental techniques used in determining the purity of drugs, in the qualitative identification and quantitative dosing of active ingredients in more or less complex systems, in drug stability checks and in the research and identification of metabolites. The presentation and connection skills of the topics covered during the lessons as well as the ability to resolve practical and application problems will also be tested. The oral test is judged with a mark out of thirty.
- Disability and Specific Learning Disorders (SLD)
Students who have registered their disability certification or SLD certification with the Inclusion and Right to Study Office can request to use conceptual maps (for keywords) during exams.
To this end, it is necessary to send the maps, two weeks before the exam date, to the course instructor, who will verify their compliance with the university guidelines and may request modifications.
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