TY - JOUR
T1 - Antibiotic coordination frameworks against antibiotic resistance
T2 - how to involve students through experimental practices in the search for solutions to public health problems
AU - Domínguez-Martín, Eva María
AU - Ntungwe, Epole
AU - Isca, Vera M.S.
AU - Princiotto, Salvatore
AU - Díaz-Lanza, Ana María
AU - André, Vânia
AU - Ríjo, Patrícia
N1 - © 2024 The Authors. Published by American Chemical Society and Division of Chemical Education, Inc.
PY - 2024/3/6
Y1 - 2024/3/6
N2 - For decades, multiple varieties of antibiotics have been successfully used for therapeutic purposes. Nevertheless, antibiotic resistance is currently one of the major threats to global health. This work presents an innovative laboratory practice carried out in an inorganic medicinal chemistry course within the Degrees of Pharmacy and Biochemistry for undergraduate students. This experiment includes three classes of 2 h each. The first class consisted of the mechanochemical synthesis of an antibiotic coordination framework (ACF) using a known antibiotic (nalidixic acid) and zinc as the ligand. The prepared Zn-nalidixic acid ACF (Zn-ACF) was obtained in up to 82% yield with high purity. On the second day, the synthesized Zn-ACF was characterized by Fourier-transform infrared spectroscopy (FTIR) and powder X-ray diffraction (PXRD). Finally, during the last class, the antimicrobial activity was tested against Escherichia coli by the well diffusion method. The students verified the higher antimicrobial activity of Zn-ACF compared to nalidixic acid, proving that small changes in the chemical structure can result in great biological differences. In the end, the students presented their results in a poster format, encouraging the development of their soft skills and scientific results communication and dissemination. In the future, it is expected that such a laboratory experiment at the interface between medicinal chemistry, microbiology, analytical techniques, public health, and pharmacology will lead to the development and implementation of some service-learning practices and will serve as a model to look at for other courses and institutions.
AB - For decades, multiple varieties of antibiotics have been successfully used for therapeutic purposes. Nevertheless, antibiotic resistance is currently one of the major threats to global health. This work presents an innovative laboratory practice carried out in an inorganic medicinal chemistry course within the Degrees of Pharmacy and Biochemistry for undergraduate students. This experiment includes three classes of 2 h each. The first class consisted of the mechanochemical synthesis of an antibiotic coordination framework (ACF) using a known antibiotic (nalidixic acid) and zinc as the ligand. The prepared Zn-nalidixic acid ACF (Zn-ACF) was obtained in up to 82% yield with high purity. On the second day, the synthesized Zn-ACF was characterized by Fourier-transform infrared spectroscopy (FTIR) and powder X-ray diffraction (PXRD). Finally, during the last class, the antimicrobial activity was tested against Escherichia coli by the well diffusion method. The students verified the higher antimicrobial activity of Zn-ACF compared to nalidixic acid, proving that small changes in the chemical structure can result in great biological differences. In the end, the students presented their results in a poster format, encouraging the development of their soft skills and scientific results communication and dissemination. In the future, it is expected that such a laboratory experiment at the interface between medicinal chemistry, microbiology, analytical techniques, public health, and pharmacology will lead to the development and implementation of some service-learning practices and will serve as a model to look at for other courses and institutions.
KW - Antibiotic Coordination Framework (ACF)
KW - Hands-On Learning
KW - Inorganic Chemistry
KW - Laboratory Experiment
KW - Medicinal Chemistry
KW - Second Year/Upper-Division Undergraduate
UR - http://www.scopus.com/inward/record.url?scp=85187118055&partnerID=8YFLogxK
U2 - 10.1021/acs.jchemed.3c01125
DO - 10.1021/acs.jchemed.3c01125
M3 - Article
C2 - 38764939
AN - SCOPUS:85187118055
SN - 0021-9584
VL - 101
SP - 2045
EP - 2051
JO - Journal of Chemical Education
JF - Journal of Chemical Education
IS - 5
ER -