Detailed Information on Publication Record
2023
Research in the Field of Drug Design and Development
BIALA, Grazyna, Ewa KEDZIERSKA, Marta KRUK-SLOMKA, Jolanta ORZELSKA-GORKA, Sara HMAIDAN et. al.Basic information
Original name
Research in the Field of Drug Design and Development
Authors
BIALA, Grazyna (guarantor), Ewa KEDZIERSKA, Marta KRUK-SLOMKA, Jolanta ORZELSKA-GORKA, Sara HMAIDAN, Aleksandra SKROK, Jakub KAMINSKI, Eva HAVRÁNKOVÁ (203 Czech Republic, belonging to the institution), Dominika NADASKA and Ivan MALIK
Edition
Pharmaceuticals, BASEL, MDPI, 2023, 1424-8247
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30104 Pharmacology and pharmacy
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 4.600 in 2022
RIV identification code
RIV/00216224:14160/23:00132055
Organization unit
Faculty of Pharmacy
UT WoS
001074283700001
Keywords in English
drug discovery; drug synthesis; in vivo studies; in vitro studies; clinical trials
Tags
International impact, Reviewed
Změněno: 27/10/2023 15:29, JUDr. Sabina Krejčiříková
Abstract
V originále
The processes used by academic and industrial scientists to discover new drugs have recently experienced a true renaissance, with many new and exciting techniques being developed over the past 5-10 years alone. Drug design and discovery, and the search for new safe and well-tolerated compounds, as well as the ineffectiveness of existing therapies, and society's insufficient knowledge concerning the prophylactics and pharmacotherapy of the most common diseases today, comprise a serious challenge. This can influence not only the quality of human life, but also the health of whole societies, which became evident during the COVID-19 pandemic. In general, the process of drug development consists of three main stages: drug discovery, preclinical development using cell-based and animal models/tests, clinical trials on humans and, finally, forward moving toward the step of obtaining regulatory approval, in order to market the potential drug. In this review, we will attempt to outline the first three most important consecutive phases in drug design and development, based on the experience of three cooperating and complementary academic centers of the Visegrad group; i.e., Medical University of Lublin, Poland, Masaryk University of Brno, Czech Republic, and Comenius University Bratislava, Slovak Republic.