Multiorgan-on-a-chip for cancer drug pharmacokinetics-pharmacodynamics (PK-PD) modeling and simulations

被引:0
作者
Mohammed, Abdurehman Eshete [1 ,3 ]
Kurucaovali, Filiz [2 ]
Okvur, Devrim Pesen [1 ]
机构
[1] Izmir Inst Technol, Dept Mol Biol & Genet, Izmir, Turkiye
[2] Izmir Inst Technol, Environm Dev Applicat & Res Ctr, Izmir, Turkiye
[3] Wollo Univ, Sch Med Lab Sci, Dessie, Ethiopia
关键词
Multiorgan-on-a-chip; Breast cancer; Pharmacometrics; Pharmacokinetics; Pharmacodynamics; Safety; Efficacy; CLINICAL-TRIALS; VALIDATED ASSAY; CELL-CULTURE; HPLC METHOD; DOXORUBICIN; PLASMA; METABOLITES; TISSUES; RAT;
D O I
10.1007/s10928-024-09955-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cancer is one of the most common and fatal diseases worldwide and kills millions of people every year. Cancer drug resistance, lack of efficacy, and safety are significant problems in cancer patients. A multiorgan-on-a-chip (MOC) device consisting of breast and liver compartments was designed with AutoCAD software. The MOC molds were printed by a Formlabs Form 2 3D printer. MDA-MB-231, HepG2, and MCF-10 A cells were used for the MOC experiments. The cell lines were cultured at 37 degrees C with 5% CO2, and cell viability was assessed via Alamar blue dye to generate pharmacodynamics (PD) data. Drug concentrations from the cell culture media were analyzed via Agilent 1260 Infinity II HPLC with a Waters Symmetry C18 column and used to generate pharmacokinetics (PK) data. The PK and PD data were modeled and simulated by Monolix and Simulix software, respectively. The safety and efficacy of drug dosing regimens were compared, and the best dosing regimens were selected. This research designed and fabricated a unique MOC consisting of liver and breast compartments that overcomes the need for sealing or assembling. It was used for PK-PD modeling and simulations, and its functionality was proven experimentally. The new MOC will be helpful in preclinical trials to evaluate the efficacy and safety of drugs.
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页数:13
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