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Title:Integrirani mikrofiziološki sistemi za napredne ADME modele: od absorpcijskih poti do večorganske farmakokinetike
Authors:ID Maver, Tina (Author)
ID Maver, Uroš (Author)
Files:.pdf RAZ_Maver_Tina_2026.pdf (4,82 MB)
MD5: F44F6C0F945626A90CB22D0D0BFA5B8E
 
URL https://journals.um.si/index.php/anali-pazu/article/view/6280
 
Language:Slovenian
Work type:Scientific work
Typology:1.01 - Original Scientific Article
Organization:FNM - Faculty of Natural Sciences and Mathematics
MF - Faculty of Medicine
UZUM - University of Maribor Press
Abstract:Staranje prebivalstva in vse pogostejša polifarmakoterapija pomembno povečujeta tveganje za farmakokinetične interakcije zdravil, zato je razumevanje procesov absorpcije, porazdelitve, metabolizma in izločanja (ADME) ključno za napovedovanje, preprečevanje in obvladovanje neželenih učinkov ter optimizacijo zdravljenja. Vendar pa tradicionalni predklinični pristopi, živalski modeli in klasični statični in vitro sistemi, pogosto niso ustrezni pri posnemanju človeške fiziologije bodisi zaradi medvrstnih razlik ali zaradi pomanjkanja kompleksnih medorganskih povezav. Posledica so visoke stopnje neuspeha v kliničnih fazah razvoja zdravil. Mikro-fiziološki sistemi (MPS), npr. organi na čipu predstavljajo obetavno rešitev, saj omogočajo bolj realistično posnemanje človeških tkiv in dinamičnih interakcij med organi. Za povečanje njihove relevantnosti so potrebne široko integrirane platforme, ki posnemajo poti absorpcije pri različnih poteh uporabe zdravil, na primer peroralna, dermalna/transdermalna, podkožna in intravenska, ter omogočajo funkcionalno povezavo z organi, vključenimi v metabolizem, porazdelitev in izločanje.
Keywords:mikro-fiziološki sistemi, absorpcija, transdermalna uporaba, interakcije zdravil
Publication status:Published
Publication version:Version of Record
Publication date:31.07.2026
Year of publishing:2026
Number of pages:str. 55-73
Numbering:Letn. 16, št. 1/2
PID:20.500.12556/DKUM-99471 New window
UDC:615
ISSN on article:2232-416X
COBISS.SI-ID:288021507 New window
DOI:10.18690/analipazu.16.1-2.55-73.2026 New window
Publication date in DKUM:18.08.2026
Views:199
Downloads:0
Metadata:XML DC-XML DC-RDF
Categories:Misc.
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Record is a part of a journal

Title:Anali PAZU
Publisher:Združenje Pomurska akademsko znanstvena unija, Združenje Pomurska akademsko znanstvena unija, Univerzitetna založba Univerze v Mariboru
ISSN:2232-416X
COBISS.SI-ID:257553152 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0036
Name:Bio-psiho-socialni model kvalitete življenja

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:N1-0305
Name:Nova platforma za razvoj ADME modelov v farmakologiji

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J3-50098
Name:Razvoj mikrofiziološkega sistema sluznice tankega črevesa za raziskovanje učinkov mikrobiote na transepitelijski transport in imunski odziv gostitelja

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J3-4524
Name:Razvoj naprednih večdimenzionalnih in vitro modelov ledvic

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:L7-4494
Name:Kompleksen in vitro model kože z vključeno plastjo kosti za testiranje ne-invazivnega glukoznega senzorja

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:31.07.2026

Secondary language

Language:English
Title:Integrated microphysiological systems for advanced ADME modeling: from absorption routes to multi-organ pharmacokinetics
Abstract:Despite significant advances in understanding diseases and developing new therapeutics, the translation of scientific knowledge into effective therapies remains slow and costly. A key challenge in drug development lies in the high failure rate during clinical phases, often due to the limited predictive value of preclinical models for absorption, distribution, metabolism, and excretion (ADME) properties. Traditional ADME assessment methods, including animal models and basic in vitro systems, show limited human relevance and face various limitations due to ethical, economic, and physiological considerations. The development of microphysiological systems (MPS), such as organ-on-a-chip platforms, offers a promising alternative by more accurately mimicking human tissues and organs. There is a growing need for broadly integrated platforms that simulate different absorption types related to all major application routes, including peroral (intestinal), dermal/transdermal, subcutaneous, and intravenous, while enabling functional coupling with metabolic (liver), distribution (vascular), and excretory (renal) systems. This review summarizes current trends and challenges in developing multi-organ models for MPS in ADME and drug–drug interaction studies.
Keywords:microphysiological systems, absorption, transdermal delivery, drug-drug interactions


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  1. Anali PAZU

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