2017
DOI: 10.1007/s11426-016-0491-7
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The aptamers generated from HepG2 cells

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Cited by 28 publications
(13 citation statements)
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“…Compared with antibodies, aptamers possess some distinct advantages: in vitro screening of aptamers avoids ethical problems associated with animal experiments arising in antibody preparation. This further excludes the negative influences of immunogenicity and toxicity, and extends the range of targets to include metal ions, small molecules, biomacromolecules, , and even cells. , The obtained aptamer sequence can be rapidly produced by chemical synthesis with high purity, at low cost, and with minor batch-to-batch variations. , They can also be easily modified to enhance their chemical and thermal stability for long-term storage, and are labeled with various signal molecules to facilitate detection. The antibody-based immunosensors have already been made commercially available, such as enzyme-linked immunosorbent assay (ELISA) kits and immunochromatographic strips. , Because of the numerous advantages of aptamers, they have been promising alternative molecular recognition elements to antibodies in analytics, medical diagnosis, and food safety inspection. So it is of great significance to screen aptamers with high affinity and specificity.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Compared with antibodies, aptamers possess some distinct advantages: in vitro screening of aptamers avoids ethical problems associated with animal experiments arising in antibody preparation. This further excludes the negative influences of immunogenicity and toxicity, and extends the range of targets to include metal ions, small molecules, biomacromolecules, , and even cells. , The obtained aptamer sequence can be rapidly produced by chemical synthesis with high purity, at low cost, and with minor batch-to-batch variations. , They can also be easily modified to enhance their chemical and thermal stability for long-term storage, and are labeled with various signal molecules to facilitate detection. The antibody-based immunosensors have already been made commercially available, such as enzyme-linked immunosorbent assay (ELISA) kits and immunochromatographic strips. , Because of the numerous advantages of aptamers, they have been promising alternative molecular recognition elements to antibodies in analytics, medical diagnosis, and food safety inspection. So it is of great significance to screen aptamers with high affinity and specificity.…”
Section: Introductionmentioning
confidence: 99%
“…This further excludes the negative influences of immunogenicity and toxicity, and extends the range of targets to include metal ions, 16 small molecules, 17 biomacromolecules, 18,19 and even cells. 20,21 The obtained aptamer sequence can be rapidly produced by chemical synthesis with high purity, at low cost, and with minor batch-to-batch variations. 22,23 They can also be easily modified to enhance their chemical and thermal stability for long-term storage, and are labeled with various signal molecules to facilitate detection.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Poly (N-vinylpyrrolidone) (PVP) was then used to stabilize PLGA nanoparticles. To improve the specificity of DOX-PLGA-PVP NPs, aptamer AS1411 was modified on the surface of DOX-PLGA-PVP NPs, to enable it to target lung cancer cells [ 148 , 149 ]. When the aptamer reacted with a receptor on the cancer surface, APT-DOX-PLGA-PVP NPs could enter the cell by endocytosis.…”
Section: Commonly Used Nanomaterials Modified With Aptamers In Cancer Therapymentioning
confidence: 99%
“…Furthermore, tissue imaging indicated that XL-33-1 could distinguish between metastatic tumor tissues or lymph nodes and benign tissues with a detection rate of 81.7%. In our laboratory, we have recently successfully applied Cell-SELEX to develop a series of DNA aptamers specifically binding to cultured human hepatocellular carcinoma HepG2 cells [ 74 ]. The selected aptamers showed high binding affinity to HepG2 cells with K d values ranging from 46.3 to 199.4 nM and could distinguish HepG2 cells from normal human liver cells.…”
Section: Selection Of Specific Aptamers Using Selexmentioning
confidence: 99%