Page 132 - 《中国药房》2025年8期
P. 132
[17] LIU J,LIN S,HUYNH A,et al. Effects of H2-receptor an‐ modeling approach[J]. Front Pharmacol,2024,15:
tagonists on the exposure of dacomitinib[J]. Pharmaceu‐ 1363259.
tics,2024,16(1):118. [27] DARRÉ H,MASSON P,NATIVEL A,et al. Comparing
[18] DELIWALA S S,HAMID K,GOYAL H,et al. Proton the efficacy of two generations of EGFR-TKIs:an inte‐
pump inhibitors versus histamine-2-receptor antagonists grated drug-disease mechanistic model approach in EGFR-
for stress ulcer prophylaxis in critically ill patients:a meta- mutated lung adenocarcinoma[J]. Biomedicines,2024,12
analysis and trial sequential analysis[J]. J Clin Gastroen‐ (3):704.
terol,2022,56(3):204-217. [28] JAKUBIAK P,WAGNER B,GRIMM H P,et al. Develop‐
[19] 张露丹,左旭锐,刘凡琪,等. 应用定量药理学模型开展 ment of a unified dissolution and precipitation model and
中西药相互作用的研究进展[J]. 中草药,2024,55(6): its use for the prediction of oral drug absorption[J]. Mol
1799-1805. Pharm,2016,13(2):586-598.
[20] EL BIALI M,WÖLFL-DUCHEK M,JACKWERTH M, [29] NARITOMI Y,SANOH S,OHTA S. Utility of chimeric
et al. St. John’s wort extract with a high hyperforin con‐ mice with humanized liver for predicting human pharma‐
tent does not induce P-glycoprotein activity at the human cokinetics in drug discovery:comparison with in vitro-in
blood-brain barrier[J]. Clin Transl Sci,2024,17(5): vivo extrapolation and allometric scaling[J]. Biol Pharm
e13804. Bull,2019,42(3):327-336.
[21] MASHAYEKHI-SARDOO H,MASHAYEKHI-SARDOO [30] BI Y W,DENG J X,MURRY D J,et al. A whole-body
A,ROUFOGALIS B D,et al. Impact of curcumin on physiologically based pharmacokinetic model of gefitinib
microsomal enzyme activities:drug interaction and in mice and scale-up to humans[J]. AAPS J,2016,18(1):
chemopreventive studies[J]. Curr Med Chem,2021,28 228-238.
(34):7122-7140. [31] VAN DE STADT E A,YAQUB M,LAMMERTSMA A A,
[22] PILLA REDDY V,JO H,NEUHOFF S. Food constituent- et al. Identifying advanced stage NSCLC patients who
and herb-drug interactions in oncology:influence of quan‐ benefit from afatinib therapy using F-afatinib PET/CT
18
titative modelling on drug labelling[J]. Br J Clin Pharma‐ imaging[J]. Lung Cancer,2021,155:156-162.
col,2021,87(10):3988-4000. [32] BAHCE I,YAQUB M,SMIT E F,et al. Personalizing
[23] CHEN Y X,ZHOU D S,TANG W F,et al. Physiologi‐ NSCLC therapy by characterizing tumors using TKI-PET
cally based pharmacokinetic modeling to evaluate the sys‐ and immuno-PET[J]. Lung Cancer,2017,107:1-13.
temic exposure of gefitinib in CYP2D6 ultrarapid metabo‐ [33] YAQUB M,BAHCE I,VOORHOEVE C,et al. Quantita‐
lizers and extensive metabolizers[J]. J Clin Pharmacol, tive and simplified analysis of C-erlotinib studies[J]. J
11
2018,58(4):485-493. Nucl Med,2016,57(6):861-866.
[24] CHEONG E J Y,NG D Z W,CHIN S Y,et al. Applica‐ [34] BARTELINK I H,VAN DE STADT E A,LEEUWERIK
tion of a physiologically based pharmacokinetic model of A F,et al. Physiologically based pharmacokinetic(PBPK)
rivaroxaban to prospective simulations of drug-drug- modeling to predict PET image quality of three genera‐
disease interactions with protein kinase inhibitors in tions EGFR TKI in advanced-stage NSCLC patients[J].
cancer-associated venous thromboembolism[J]. Br J Clin Pharmaceuticals(Basel),2022,15(7):796.
Pharmacol,2022,88(5):2267-2283. [35] GRUBER A,CZEJKA M,BUCHNER P,et al. Monito-
[25] SHARMA J,LV H,GALLO J M. Intratumoral modeling ring of erlotinib in pancreatic cancer patients during long-
of gefitinib pharmacokinetics and pharmacodynamics in time administration and comparison to a physiologically
an orthotopic mouse model of glioblastoma[J]. Cancer based pharmacokinetic model[J]. Cancer Chemother Phar‐
Res,2013,73(16):5242-5252. macol,2018,81(4):763-771.
[26] LIANG F,ZHANG Y M,XUE Q,et al. Exploring inter- (收稿日期:2024-10-28 修回日期:2025-03-28)
ethnic and inter-patient variability and optimal dosing of (编辑:李 劲)
osimertinib:a physiologically based pharmacokinetic
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