Gold cluster encapsulated liposomes: theranostic agent with stimulus triggered release capability

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作者
Seyed Mohammad Amini
Seyed Mahdi Rezayat
Rassoul Dinarvand
Sharmin Kharrazi
Mahmoud Reza Jaafari
机构
[1] Iran University of Medical Sciences (IUMS),Radiation Biology Research Center
[2] Tehran University of Medical Sciences (TUMS),Department of Medical Nanotechnology, School of Advanced Technologies in Medicine (SATiM)
[3] Tehran University of Medical Sciences,Department of Pharmacology, School of Medicine
[4] Tehran University of Medical Sciences,Nanotechnology Research Centre, Novel Drug Delivery Department, Faculty of Pharmacy
[5] Nanotechnology Research Center,Pharmaceutical Technology Institute, School of Pharmacy
[6] Mashhad University of Medical Sciences,Department of Pharmaceutical Nanotechnology, School of Pharmacy
[7] Mashhad University of Medical Sciences,undefined
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Gold clusters; Liposomes; Theranostic agents; Trigger release; Radio frequency electric field; Radiation therapy; X-ray contrast agent;
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摘要
Cancer is a major cause of death worldwide. Cancer-resistant to chemo or radiotherapy treatment is a challenge that could be overcome by a nanotechnology approach. Providing a theranostic nano-platform for different cancer treatment strategies could be revolutionary. Here we introduce a multifunctional theranostic nanostructure which has the capacity for improving cancer diagnosis and treatment through better chemo and radiotherapy and current x-ray imaging systems through co-encapsulation of a small gold cluster and anticancer drug doxorubicin. 2 nm gold clusters represent good heating under radio frequency electric field (RF-EF) exposure and have been used for in vitro hyperthermia treatment of cancerous cells. Liposomal doxorubicin (169 ± 19.8 nm) with gold clusters encapsulation efficiency of 13.2 ± 3.0% and doxorubicin encapsulation efficiency of 64.7 ± 0.7% were prepared and studied as a theranostic agent with a high potential in different cancer treatment modalities. Exposure to a radiofrequency electric field on prepared formulation caused 20.2 ± 2.1% drug release and twice decreasing of IC50 on colorectal carcinoma cells. X-ray attenuation efficiency of the liposomal gold cluster was better than commercial iohexol and free gold clusters in different concentrations. Finally, treatment of gold clusters on cancerous cells results in a significant decrease in the viability of irradiated cells to cobalt-60 beam. Based on these experiments, we concluded that the conventional liposomal formulation of doxorubicin that has been co-encapsulated with small gold clusters could be a suitable theranostic nanostructure for cancer treatment and merits further investigation.
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