Identification and imaging of leukemia cells using dual-aptamer-functionalized graphene oxide complex

被引:17
作者
Bahreyni, Amirhossein [1 ,2 ]
Yazdian-Robati, Rezvan [3 ]
Ramezani, Mohammad [4 ]
Rasouli, Mehdi [1 ,2 ]
Nameghi, Morteza Alinezhad [5 ]
Alibolandi, Mona [6 ]
Abnous, Khalil [6 ,7 ]
Taghdisi, Seyed Mohammad [8 ]
机构
[1] Mazandaran Univ Med Sci, Dept Clin Biochem, Fac Med, Sari, Mazandaran, Iran
[2] Mazandaran Univ Med Sci, Immunogenet Res Ctr, Fac Med, Sari, Mazandaran, Iran
[3] Mashhad Univ Med Sci, Sch Pharm, Dept Pharmaceut Biotechnol, Mashhad, Iran
[4] Mashhad Univ Med Sci, Nanotechnol Res Ctr, Mashhad, Iran
[5] Mashhad Univ Med Sci, Sch Pharm, Mashhad, Iran
[6] Mashhad Univ Med Sci, Pharmaceut Res Ctr, Mashhad, Iran
[7] Mashhad Univ Med Sci, Sch Pharm, Dept Med Chem, Mashhad, Iran
[8] Mashhad Univ Med Sci, Targeted Drug Delivery Res Ctr, Mashhad, Iran
关键词
Aptamer; graphene oxide; leukemia; imaging; Sgc8c; ACUTE LYMPHOBLASTIC-LEUKEMIA; MODIFIED GOLD NANOPARTICLES; RESONANCE ENERGY-TRANSFER; QUANTUM DOTS; CONTROLLED-RELEASE; DRUG-DELIVERY; CANCER-CELLS; ATP; APTASENSOR; ADENOSINE;
D O I
10.1177/0885328217712111
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Acute lymphoblastic leukemia is the most common malignancy in children. Patient improvement completely depends on the diagnosis of acute lymphoblastic leukemia. So there is a great demand for diagnosis of acute lymphoblastic leukemia. In this study, a novel assay based on dual-aptamer (Sgc8c and ATP aptamers)-functionalized graphene oxide (DAFGO) complex was designed for the identification of Molt-4 cells (human acute lymphoblastic leukemia T-cell). This assay relies on the internalization of DAFGO complex into Molt-4 cells, but not into U266 cells, using Sgc8c aptamer as molecular recognition probe, and release of FAM-labeled ATP aptamer from the complex in the presence of high amounts of ATP in lysosome, leading to a strong fluorescence emission. Formation of DAFGO complex was analyzed by fluorometric analysis and gel retardation assay. The internalization of complex was monitored by flow cytometry and fluorescence microscopy in Molt-4 (target) and U266 cells (nontarget) with DAFGO complex. Our results showed that the developed complex was efficiently internalized into target cells and induced a strong fluorescence emission.
引用
收藏
页码:74 / 81
页数:8
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