Pharmaceutical Technology and Legislation of Biotechnological Medicinal Products
A.Y. 2024/2025
Learning objectives
The purpose of the course is to introduce the students to the principles required for the design, preparation and control of dosage forms with a principal interest in the formulation strategies and production processes of biotechnological medicinal products. The national and EU rules governing their production will be dealt with.
Expected learning outcomes
The student will acquire the knowledge enabling to study problems on medicines for human use with particular reference to biotechnological medicinal products. Training in the lab will allow to consolidate theoretical concepts.
Lesson period: Second semester
Assessment methods: Esame
Assessment result: voto verbalizzato in trentesimi
Single course
This course can be attended as a single course.
Course syllabus and organization
Single session
Responsible
Lesson period
Second semester
Course syllabus
Contents
General principles of biopharmaceutics and pharmacokinetics: L.A.D.M.E. Bioavailability and bioequivalence. Classification of dosage form.
Physicochemical principles: solution; interfacial phenomena; disperse systems: colloids, emulsions, and suspensions.
Preformulation. Formulation, preparation and quality control of conventional dosage forms: oral, cutaneous, transdermal, parenteral and ophthalmic.
Sterilization methods and application in the manufacturing of parenteral dosage forms. Principle of lyophilization.
The Pharmacopoeia with particular interest for Quality aspects of medicinal products.
Introduction to Italian and UE forms of law. The rules governing the production and the dispensing of the biotechnological medicinal products.
Laboratory course of Pharmaceutical Technology
Technological characterization of podwers: flowability, apparent volume and density, size and size distribution.
Preparation and quality controls on:
- oral dosage forms: powders, capsules, tablets;
- semisolid dosage forms: ointments, creams, gels and pastes;
- liquid dosage forms: solutions and suspensions.
General principles of biopharmaceutics and pharmacokinetics: L.A.D.M.E. Bioavailability and bioequivalence. Classification of dosage form.
Physicochemical principles: solution; interfacial phenomena; disperse systems: colloids, emulsions, and suspensions.
Preformulation. Formulation, preparation and quality control of conventional dosage forms: oral, cutaneous, transdermal, parenteral and ophthalmic.
Sterilization methods and application in the manufacturing of parenteral dosage forms. Principle of lyophilization.
The Pharmacopoeia with particular interest for Quality aspects of medicinal products.
Introduction to Italian and UE forms of law. The rules governing the production and the dispensing of the biotechnological medicinal products.
Laboratory course of Pharmaceutical Technology
Technological characterization of podwers: flowability, apparent volume and density, size and size distribution.
Preparation and quality controls on:
- oral dosage forms: powders, capsules, tablets;
- semisolid dosage forms: ointments, creams, gels and pastes;
- liquid dosage forms: solutions and suspensions.
Prerequisites for admission
Fundamentals on general and inorganic chemistry, organic chemistry, physics and physiological.
Due to the connection among subjects, the student should be able to link them in order to become familiar with the topics of this course.
Due to the connection among subjects, the student should be able to link them in order to become familiar with the topics of this course.
Teaching methods
Lectures in classes and practical laboratory session.
Some assays or quiz will be provided during the semester and the outputs will be discussed in class.
Some assays or quiz will be provided during the semester and the outputs will be discussed in class.
Teaching Resources
- Aulton's Pharmaceutics: The Design and Manufacture of Medicines (lastest edition)
- Lecture handouts will be available on the ARIEL website.
- Lecture handouts will be available on the ARIEL website.
Assessment methods and Criteria
Written exam: 22 multiple choice questions + 4 open questions. It is possible to take the oral part only if the mark of the written exam is equal or higher than 18/30.
Oral exams: 2 questions on Pharmaceutica Techologies + 1 question on Legislation. The exam will be finalized only if the answers are considered sufficient (18/30).
Oral exams: 2 questions on Pharmaceutica Techologies + 1 question on Legislation. The exam will be finalized only if the answers are considered sufficient (18/30).
CHIM/09 - PHARMACEUTICAL AND TECHNOLOGICAL APPLICATIONS OF CHEMISTRY - University credits: 6
Single bench laboratory practical: 16 hours
Lessons: 40 hours
Lessons: 40 hours
Shifts:
Turno 1
Professor:
Anderluzzi GiuliaTurno 2
Professor:
Anderluzzi GiuliaProfessor(s)
Reception:
by appointment
Dept. Pharmaceutica Sciences - via G. Colombo, 71