2016/2017

2019/2020

DM270

CHIM/08 (PHARMACEUTICAL CHEMISTRY)

DEPARTMENT OF DRUGS SCIENCES

MEDICINAL CHEMISTRY AND PHARMACEUTICAL TECHNOLOGY

PERCORSO COMUNE

4°

(02/03/2020 - 19/06/2020)

6

68 lesson hours

Italian

ORAL TEST

UBIALI DANIELA - 6 ECTS

To attend this course, knowledge of inorganic chemistry, organic chemistry and medicinal chemistry is required.

Learning the basic techniques of practical organic chemistry for the obtainment of biologically active molecules of pharmaceutical interest.
Learning the tools to carry out a literature search aimed at designing a chemical synthesis.
Learning the main safety standards to be adopted in chemical laboratories for the prevention of accidents.

Contents: lectures (3,5 CFU, 28 hours) and laboratory training (2,5 CFU, 40 hours), strictly interconnected.
Laboratory training: students will directly experiment the basic methods and techniques routinely used to synthesize active pharmaceutical ingredients (APIs) and to isolate bioactive compounds from vegetable sources.
Programme: synthesis of known small molecules (also by biocatalysis), use of separative techniques (liquid-liquid extraction, crystallization, distillation, chromatography, evaporation, filtration), use of equipments routinely found in organic chemistry laboratories.
Students are expected to work in groups (no more than 5 students/group). Students are required to register daily the experimental activities in a personal lab notebook according to the guidelines provided during the course.

Note: lectures and lab training about the use of enzymes (biocatalysis) in organic synthesis are scheduled. Biocatalysis mostly occurs in aqueous media and under mild reaction conditions (pH, temperature, pressure), thus answering most of the 12 Principles of Green Chemistry (replacement of hazardous processes and products), and being considered as a Sustainable Chemistry.
The concept of sustainability ("meeting the needs of the present without compromising the ability of future generations to meet their needs"), when applied to chemistry, results into a new paradigm of chemistry addressing the efficiency of the use of resources, raw materials and energy, through the design of reactions that produce less by-products. Several key concepts of sustainable development are comprised in the methodologies used for product and process design in the framework of the chemical industry. Biocatalysis is characterized by less waste and losses, as well as by a lower environmental and energy impact.
The contents of this module meet the goals #12, #13, #14 and #15 of the 2030 Agenda (https://asvis.it/agenda-2030/).

Lectures and lab training. One lecture (seminar) will be given by a researcher from pharmaceutical industry.

AA.VV. “Vogel, chimica organica pratica” Casa Editrice Ambrosiana Milano
D. L. Pavia, G. M. Lampman, G. S. Kriz “Il laboratorio di chimica organica” Edizioni Sorbona Milano
K. Faber “Biotransformations in Organic Chemistry – A textbook” Springer Ed.

One midterm exam is scheduled at the end of the course (lectures and laboratory training).

Final exam: 1) first option: passing the midterm exam and the laboratory training;
2) second option: if a student has not taken the midterm exam or has failed it, he/she must take the whole exam (Chimica e Analisi Farmaceutica 3, 12 CFU) on scheduled exam sessions. Also in this case, a positive evaluation in the laboratory training is mandatory to be admitted to the final exam.

Slides used during lectures can be downloaded from the website Kiro. Tutorial videos about the main techniques of organic synthesis and scientific papers (both in English) are also available in Kiro. Registration to the laboratory training is mandatory and must be done by signing up the form in Kiro by the reported deadline. Communications/notices to the students will be uploaded in Kiro, too.