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  4. Selective Photothermal Therapy for Mixed Cancer Cells Using Aptamer-Conjugated Nanorods
 
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Selective Photothermal Therapy for Mixed Cancer Cells Using Aptamer-Conjugated Nanorods

Resource
Langmuir 24 (20): 11860-11865
Journal
Langmuir
Journal Volume
24
Journal Issue
20
Pages
11860-11865
Date Issued
2008
Author(s)
Huang, Yu-Fen
Sefah, Kwame
Bamrungsap, Suwussa
HUAN-TSUNG CHANG  
Tan, Weihong
DOI
10.1021/la801969c
URI
http://scholars.lib.ntu.edu.tw/handle/123456789/338139
Abstract
Safe and effective photothermal therapy depends on efficient delivery of heat for killing cells and molecular specificity for targeting cells. To address these requirements, we have designed an aptamer-based nanostructure which combines the high absorption efficiency of Au-Ag nanorods with the target specificity of molecular aptamers, a combination resulting in the development of an efficient and selective therapeutic agent for targeted cancer cell photothermal destruction. Most nanotmaterials, such as gold nanoshells or nanorods (NRs), require a relatively high power of laser irradiation (1 × 105-1 × 1010 W/m2). In contrast, the high absorption characteristic of our Au-Ag NRs requires only 8.5 × 10 4 W/m2 laser exposure to induce 93 (±11)% cell death of NR-aptamer-labeled cells. Aptamers, the second component of the nanostructure, are generated from a cell-SELEX (systematic evolution of ligands by exponential enrichment) process and can be easily selected for specific recognition of individual tumor cell types without prior knowledge of the biomarkers for the cell. When tested with both cell suspensions and artificial solid tumor samples, these aptamer conjugates were shown to have excellent hyperthermia efficiency and selectivity. Under a specific laser intensity and duration of laser exposure, about 50 (±1)% of target (CEM) cells were severely damaged, while more than 87 (±1)% of control (NB-4) cells remained intact in a suspension cell mixture. These results indicate that the Au-Ag nanorod combination offers selective and efficient photothermal killing of targeted tumor cells, thus satisfying the two key challenges noted above. Consequently, for future in vivo application, it is fully anticipated that the tumor tissue will be selectively destroyed at laser energies which will not harm the surrounding normal tissue. ? 2008 American Chemical Society.
SDGs

[SDGs]SDG3

Other Subjects
Absorption efficiencies; Aptamer; Aptamers; Artificial solids; Cancer cells; Cell suspensions; Gold nanoshells; High powers; In-vivo; Labeled cells; LASER energies; Laser exposures; Laser intensities; Laser irradiations; Molecular specificities; Normal tissues; Photothermal therapies; Prior knowledges; Specific recognitions; Suspension cells; Systematic Evolution of Ligands by Exponential enrichments; Tumor cells; Tumor tissues; Absorption; Cell culture; Cell death; Cytology; Lasers; Nanorods; Nanostructures; Silver; Suspensions (components); Suspensions (fluids); Tumors; Cells; biological marker; gold; metal nanoparticle; nanotube; silver; animal; article; cattle; chemistry; combinatorial chemistry; equipment design; HeLa cell; human; instrumentation; laser; metabolism; methodology; neoplasm; phototherapy; transmission electron microscopy; Animals; Biological Markers; Cattle; Equipment Design; Gold; Hela Cells; Humans; Lasers; Metal Nanoparticles; Microscopy, Electron, Transmission; Nanotubes; Neoplasms; Phototherapy; SELEX Aptamer Technique; Silver
Type
journal article
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