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DOI: 10.1002/wnan.1347
OpenAccess: Closed
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Near‐infrared light‐responsive nanomaterials for cancer theranostics

Heejung Kim,Kyungwha Chung,Seungjin Lee,Dong Ha Kim,Hyukjin Lee

Photothermal therapy
Nanotechnology
Cancer
2015
Abstract Early diagnosis and effective cancer therapy are required, to properly treat cancer, which causes more than 8.2 million deaths in a year worldwide. Among various cancer treatments, nanoparticle‐based cancer therapies and molecular imaging techniques have been widely exploited over the past decades to overcome current drawbacks of existing cancer treatments. In particular, gold nanoparticles ( AuNPs ), carbon nanotubes ( CNTs ), graphene oxide ( GO ), and upconversion nanocrystals ( UNCs ) have attracted tremendous attention from researchers due to their near‐infrared ( NIR ) light‐responsive behaviors. These nanomaterials are considered new multifunctional platforms for cancer theranostics. They would enable on‐demand control of drug release or molecular imaging in response to a remote trigger by NIR light exposure. This approach allows the patient or physician to adjust therapy precisely to a target site, thus greatly improving the efficacy of cancer treatments, while reducing undesirable side effects. In this review, we have summarized the advantages of NIR light‐responsive nanomaterials for in vivo cancer treatments, which includes NIR triggered photothermal therapy ( PTT ) and photodynamic therapy ( PDT ). Furthermore, recent developments, perspectives, and new challenges of NIR light‐responsive nanomaterials are discussed for cancer theranostic applications. WIREs Nanomed Nanobiotechnol 2015, 8:23–45. doi: 10.1002/wnan.1347 This article is categorized under: Diagnostic Tools > In Vivo Nanodiagnostics and Imaging
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    Near‐infrared light‐responsive nanomaterials for cancer theranostics” is a paper by Heejung Kim Kyungwha Chung Seungjin Lee Dong Ha Kim Hyukjin Lee published in 2015. It has an Open Access status of “closed”. You can read and download a PDF Full Text of this paper here.