The aim of studying and bibliography

The main aim of study: The purpose of the course is the introduction to the most important natural resources, their composition and importance for the pharmaceutical industry

The general information about the module: The module is implemented in the fourth semester and includes 15 hours of lectures and 15 hours of laboratory exercises. It ends with a final test.

Teaching materials: instrukcje do ćwiczń laboratoryjnych

Bibliography required to complete the module

Bibliography used during lectures

1	S. Kohlmünzer	Farmakognozja	PZWL, Warszawa.	2007
2	I. Matławska	Farmakognozja. Podręcznik dla studentów farmacji	Wydawnictwo AM w Poznaniu, Poznań.	2005
3	Z. Kowalewski,	Farmakognozja. Leki roślinne	Wydawnictwo AM w Poznaniu, Poznań.	1997

Bibliography used during classes/laboratories/others

1	K. Dzierzbicka, D. Witt	Chemia organicznych zwiazków naturalnych	Wydawnictwo PG, Gdańsk.	2000
2	H. Strzelecka, J. Kamińska, J. Kowalski, E. Walewska	Chemiczne metody badań roślinnych surowców leczniczych	PZWL, Warszawa.	1982
3	U. Wrzeciono, L. Zaprutko	Chemia związków naturalnych	Wydawnictwo AM w Poznaniu, Poznań.	2001
4	B. Klimek	Analiza fitochemiczna roślinnych substancji leczniczych	Wydawnictwo UM w Łodzi, Łódź .	2011

Bibliography to self-study

1

E. Lamer-Zarawska, B. Kowal-Gierczak, J. Niedworok

Fitoterapia i leki roślinne

PZWL, Warszawa.

2007

Basic requirements in category knowledge/skills/social competences

Formal requirements: registration for the fourth semester

Basic requirements in category knowledge: Knowledge of organic and analytical chemistry is required

Basic requirements in category skills: Practical and manual skills necessary to perform laboratory experiments and use of basic laboratory equipment with applicable OHS and fire protection rules

Basic requirements in category social competences: Ability to cooperate in a group

Module outcomes

MEK	The student who completed the module	Types of classes / teaching methods leading to achieving a given outcome of teaching	Methods of verifying every mentioned outcome of teaching	Relationships with KEK	Relationships with PRK
01	has basic knowledge about the structure and physicochemical properties of the discussed groups of biologically active compounds	lecture	written test	K_W08++	P6S_WG
02	has knowledge of the physiological effects of biologically active compounds on living organisms	lecture, laboratory	written test, colloquium	K_W01+++ K_K02++	P6S_KO P6S_KR P6S_WG
03	knows the basics of analytical methods used for the isolation and purification of therapeutic substances of natural origin	laboratory	colloquium	K_W08+++ K_U06+++ K_U08+++ K_K03++	P6S_KR P6S_UW P6S_WG

Attention: Depending on the epidemic situation, verification of the achieved learning outcomes specified in the study program, in particular credits and examinations at the end of specific classes, can be implemented remotely (real-time meetings).

The syllabus of the module

Sem.	TK	The content	realized in	MEK
4	TK01	The subject of the course includes information about the chemical composition, pharmacological action and therapeutic use of natural substances. During the lectures will be presented classification of substances of plant origin by groups of active compounds that determine their pharmacological activity. For each group will be discussed issues related to the composition and chemical structure, physicochemical and pharmacological properties, use and dosage, as well as side effects. furthermore, drugs (including dietary supplements), whose ingredients are natural compounds or their synthetic or semi-synthetic equivalents will be presented. In addition, the methods for the isolation of compounds from biological material and determining their purity will be presented.	W01-W15	MEK01 MEK02 MEK03
4	TK02	Elements of qualitative and quantitative analysis of plant material. Determination of the content of water and mineral substances in the plant material. Detecting and determining the content of pirogalolic tannins and pyrocatechol tannins. Analysis of the nettle leaves. Determination of vitamin C in plant raw materials. Measurement of the antioxidant capacity of infusions by reducing the DPPH radical.	-	MEK01 MEK02 MEK03

The student's effort

The type of classes	The work before classes	The participation in classes	The work after classes
Lecture (sem. 4)	The preparation for a test: 3.00 hours/sem.	contact hours: 15.00 hours/sem.	complementing/reading through notes: 2.00 hours/sem. Studying the recommended bibliography: 2.00 hours/sem.
Laboratory (sem. 4)	The preparation for a Laboratory: 4.00 hours/sem. The preparation for a test: 4.00 hours/sem.	contact hours: 15.00 hours/sem.	Finishing/Making the report: 6.00 hours/sem.
Advice (sem. 4)	The preparation for Advice: 1.00 hours/sem.	The participation in Advice: 1.00 hours/sem.
Credit (sem. 4)	The preparation for a Credit: 4.00 hours/sem.	The written credit: 2.00 hours/sem.

The way of giving the component module grades and the final grade

The type of classes	The way of giving the final grade
Lecture	A positive evaluation of the written test - OW. The note of the lecture depends on the number of obtained points from test: 3,0 (51,0 %-60,9%); 3,5 (61,0%-70,9%); 4,0 (71,0%-80,9%); 4,5 (81,0%-90,9%); 5,0 (91,0%-100%).
Laboratory	Performing all laboratory exercises, preparing reports and obtaining a positive mark from the test - OL The final mark from the laboratory depends on the number of points obtained from the test: 3.0 (51.0% -60.9%); 3.5 (61.0% -70.9%); 4.0 (71.0% -80.9%); 4.5 (81.0% -90.9%); 5.0 (91.0% -100%).
The final grade	Final evaluation of the module is calculated by the following formula: OK = w*60%OW + w*40% OL First term: w=1, second term: w=0,9, third term: w=0,8. The final note is rounded according to the rules given in the Paper Faculty Quality of Education.

Sample problems

Required during the exam/when receiving the credit
(-)

Realized during classes/laboratories/projects
(-)

Others
(-)

Can a student use any teaching aids during the exam/when receiving the credit : no

The contents of the module are associated with the research profile: yes

1	M. Kosińska-Pezda; U. Maciołek; L. Zapała	Synthesis, Spectral Characterization and Potential Fluorescent Properties of Three Lanthanide(III) Ions Complexes with Nalidixic Acid	2023
2	Ł. Byczyński; M. Kosińska-Pezda; E. Woźnicka; L. Zapała; W. Zapała	Synteza oraz badania składu i właściwości związków: 3-hydroksyflawonu, chryzyny oraz sulfonowych pochodnych chryzyny i kwercetyny z jonami Mn(II)	2023
3	Ł. Byczyński; M. Kosińska-Pezda; U. Maciołek; L. Zapała	Study of the thermal behavior, evolved gas analysis and temperature diffraction patterns of new light lanthanide complexes with niflumic acid	2023
4	E. Ciszkowicz; M. Kosińska-Pezda; K. Lecka-Szlachta; A. Miłoś; E. Woźnicka; L. Zapała	Analiza właściwości antybakteryjnych oraz cytotoksyczności kompleksów jonów Co(II), Mn(II) oraz Zn(II) z chryzyną oraz 3-hydroksyflawonem	2022
5	L. Zapała; W. Zapała; P. Ziobrowski	Studies on the retention behavior of quercetin, phenol and caffeine as test substances on selected neutral and charged Hydrophilic Interaction Liquid Chromatography stationary phases	2022
6	M. Drewniak; M. Kosińska-Pezda; U. Maciołek; A. Nowicka; L. Zapała	Synteza i charakterystyka spektroskopowa kompleksu kwasu nalidyksowego z jonami samaru(III)	2022
7	M. Kosińska-Pezda; E. Woźnicka; L. Zapała	Synteza i charakterystyka spektroskopowa kompleksów jonów lantanowców ciężkich z 3-hydroksyflawonem	2022
8	M. Kosińska-Pezda; U. Maciołek; E. Woźnicka; L. Zapała	Kompleksy 3-hydroksyflawonu z jonami Zn(II) - synteza i właściwości związków	2022
9	M. Kosińska-Pezda; U. Maciołek; E. Woźnicka; L. Zapała; W. Zapała	Synteza, badania składu i właściwości spektroskopowych kompleksów wybranych jonów metali przejściowych z kwasem niflumowym	2022
10	E. Ciszkowicz; M. Kosińska-Pezda; A. Kuźniar; K. Lecka-Szlachta; E. Pieniążek; E. Woźnicka; L. Zapała	Synteza, charakterystyka i właściwości biologiczne kompleksów jonów antanowców lekkich z 3-hydroksyflawonem	2021
11	J. Kalembkiewicz; M. Kosińska-Pezda; J. Pusz; E. Woźnicka; L. Zapała	Badania równowagi reakcji kompleksowania chryzyny z jonami Er(III) w układach: woda - metanol i woda - metanol - 1,4-dioksan	2021
12	M. Chutkowski; L. Zapała; W. Zapała; P. Ziobrowski	Analiza mechanizmu retencji kwercetyny w wybranych układach chromatografii oddziaływań hydrofilowych (HILIC)	2021
13	M. Chutkowski; M. Kosińska-Pezda; M. Przywara; L. Zapała; W. Zapała; P. Ziobrowski	Analysis of adsorption energy distribution in selected hydrophilic-interaction chromatography systems with amide, amine, and zwitterionic stationary phases	2021
14	Ł. Byczyński; E. Ciszkowicz; M. Kosińska-Pezda; K. Lecka-Szlachta; U. Maciołek; E. Woźnicka; L. Zapała; W. Zapała	Green synthesis of niflumic acid complexes with some transition metal ions (Mn(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II)). Spectroscopic, thermoanalytical and antibacterial studies	2021
15	Ł. Byczyński; M. Kosińska-Pezda; U. Maciołek; E. Woźnicka; L. Zapała; W. Zapała	Thermal study, temperature diffraction patterns and evolved gas analysis during pyrolysis and oxidative decomposition of novel ternary complexes of light lanthanides with mefenamic acid and 1,10-phenanthroline	2021
16	J. Kalembkiewicz; B. Papciak; E. Pieniążek; J. Pusz; P. Skitał; E. Sočo; L. Zapała	Podstawy chemii	2020
17	M. Chutkowski; L. Zapała; W. Zapała; P. Ziobrowski	Influence of Mobile Phase Composition and Temperature on the Retention Behavior of Selected Test Substances in Diol-type Column	2020
18	M. Kosińska-Pezda; E. Pieniążek; E. Woźnicka; L. Zapała	Badania stałych produktów reakcji jonów Ag(I) i Cu(II) z 3-hydroksyflawonem i moryną	2020
19	M. Kosińska; E. Woźnicka; L. Zapała; W. Zapała	Response of the DFT study to the calculations of selected microdissociation constants of anthranilic acid and its derivatives	2019
20	Ł. Byczyński; M. Chutkowski; E. Ciszkowicz; M. Kosińska; K. Lecka-Szlachta; E. Woźnicka; L. Zapała; W. Zapała	Comparison of spectral and thermal properties and antibacterial activity of new binary and ternary complexes of Sm(III), Eu(III) and Gd (III) ions with N-phenylanthranilic acid and 1,10-phenanthroline	2019