Preparation and evaluation of biological activity of ZSM-5 nanoparticles loaded with gefitinib for the treatment of non-small cell lung carcinoma

被引:2
作者
Al-Sahlawi, Farah [1 ,2 ]
Al-Ani, Israa [1 ]
El-Tanani, Mohamed [1 ]
Farooq, Hafiz Aadil [3 ]
机构
[1] Al Ahliyya Amman Univ, Fac Pharm, Pharmacol & Diagnost Res Ctr, Amman, Jordan
[2] UCSI Univ, Fac Pharmaceut Sci, Kuala Lumpur 56000, Malaysia
[3] Bahauddin Zakariya Univ, Inst Chem Sci, Multan 60800, Pakistan
关键词
ZSM-5; Gefitinib; Non-small lung cell carcinoma; IN-VITRO; DELIVERY; DISSOLUTION; ZEOLITES; FORMULATION; DOXORUBICIN; SOLUBILITY; FRAMEWORKS; VIVO;
D O I
10.3897/pharmacia.71.e112449
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Gefitinib (GEF) is a tyrosine kinase inhibitor that has proven good efficacy against Non -small cell Lung Carcinoma (NSCLC). It has low solubility and dissolution rate and low oral bioavailability. This work aimed to improve efficacy by loading on ZSM-5 silica nanoparticles and testing the prepared delivery system on A-549 lung cancer cells. Methods: ZSM-5 was synthesized in the laboratory and different methods of loading GEF on the nanoparticles were used, then the system was characterized by X-ray diffraction, Fourier Transport Infra -Red (FTIR), and drug release and dissolution. Results and conclusion: GEF-loaded nanoparticles (NPs) showed prolonged release of GEF over 12 hours with an improved biological efficacy expressed by the decrease in IC50 compared to free GEF (P < 0.001) using 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay. Also, there was a significant decrease in migration and colony formation ability of the GEF-loaded NPs on A-549 lung cancer cells. In conclusion, loading GEF onto ZSM-5 NPs resulted in a lower IC50 and improved biological action toward A-549 cells.
引用
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页码:1 / 12
页数:12
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