Enhanced Ehrlich tumor inhibition using DOX-NP and gold nanoparticles loaded liposomes

被引:0
|
作者
Mady, Mohsen Mahmoud [1 ,2 ]
Al-Shaikh, Fatima Hasan [1 ]
Al-Farhan, Faridah Farhan [1 ]
Aly, Amany Abdullah [1 ,2 ]
Al-Mohanna, Mai Abdullah [3 ]
Ghannam, Magdy Mohammed [1 ,2 ]
机构
[1] King Saud Univ, Coll Sci, Dept Phys & Astron, Riyadh 11451, Saudi Arabia
[2] Cairo Univ, Fac Sci, Dept Biophys, Giza, Egypt
[3] King Faisal Specialist Hosp & Res Ctr, Riyadh 11211, Saudi Arabia
关键词
Liposomes; doxorubicin; Ehrlich carcinoma; cytotoxicity; gold nanoparticles; VASCULAR-PERMEABILITY; DOXORUBICIN; DRUG; MECHANISMS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Treatment with doxorubicin (DOX) is a common treatment for different types of cancer. DOX-NP is one of a well established marketed liposomal formulation for DOX. It has advantages over free DOX in reducing the cardiac toxicity and increasing the efficacy. Gold nanoparticles (GNPs), have been widely used in biomedical applications such as medical imaging and biosensors. Mice bearing Ehrlich tumor were injected with saline, free doxorubicin (DOX) in solution, gold nanoparticles loaded liposomes and commercial liposomal encapsulated doxorubicin (DOX-NP). The results showed that GNPs loaded liposomes could enhance the antitumor activity of commercial liposomal formulation (DOX-NP) and displayed significantly decreased systemic toxicity compared with free DOX and commercial liposomal formulation (DOX-NP) at the equivalent dose. So the injection of GNPs and DOX-NP is expected to increase the cell killing and make it a promising approach to cancer treatment.
引用
收藏
页码:2321 / 2325
页数:5
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