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Structure-Inherent Tumor-Targeted IR-783 for Near-Infrared Fluorescence-Guided Photothermal Therapy
by
Park, Yoonbin
, Hyun, Hoon
, Park, Min Ho
in
Ablation
/ Animals
/ Biocompatibility
/ Brain cancer
/ Breast cancer
/ Cancer
/ Cancer therapies
/ Carbocyanines - chemistry
/ Cell death
/ Chemotherapy
/ Colorectal cancer
/ Colorectal Neoplasms - diagnostic imaging
/ Colorectal Neoplasms - drug therapy
/ Colorectal Neoplasms - pathology
/ Colorectal Neoplasms - therapy
/ Comparative analysis
/ Cytotoxicity
/ Dyes
/ Efficiency
/ Fluorescence
/ Fluorescent Dyes - chemistry
/ HT29 Cells
/ Humans
/ Infrared Rays
/ Lasers
/ Light therapy
/ Mice
/ Mice, Inbred BALB C
/ Mice, Nude
/ Nanomaterials
/ Photographic industry
/ Phototherapy
/ Photothermal Therapy - methods
/ Surface active agents
/ Xenograft Model Antitumor Assays
2024
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Structure-Inherent Tumor-Targeted IR-783 for Near-Infrared Fluorescence-Guided Photothermal Therapy
by
Park, Yoonbin
, Hyun, Hoon
, Park, Min Ho
in
Ablation
/ Animals
/ Biocompatibility
/ Brain cancer
/ Breast cancer
/ Cancer
/ Cancer therapies
/ Carbocyanines - chemistry
/ Cell death
/ Chemotherapy
/ Colorectal cancer
/ Colorectal Neoplasms - diagnostic imaging
/ Colorectal Neoplasms - drug therapy
/ Colorectal Neoplasms - pathology
/ Colorectal Neoplasms - therapy
/ Comparative analysis
/ Cytotoxicity
/ Dyes
/ Efficiency
/ Fluorescence
/ Fluorescent Dyes - chemistry
/ HT29 Cells
/ Humans
/ Infrared Rays
/ Lasers
/ Light therapy
/ Mice
/ Mice, Inbred BALB C
/ Mice, Nude
/ Nanomaterials
/ Photographic industry
/ Phototherapy
/ Photothermal Therapy - methods
/ Surface active agents
/ Xenograft Model Antitumor Assays
2024
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Structure-Inherent Tumor-Targeted IR-783 for Near-Infrared Fluorescence-Guided Photothermal Therapy
by
Park, Yoonbin
, Hyun, Hoon
, Park, Min Ho
in
Ablation
/ Animals
/ Biocompatibility
/ Brain cancer
/ Breast cancer
/ Cancer
/ Cancer therapies
/ Carbocyanines - chemistry
/ Cell death
/ Chemotherapy
/ Colorectal cancer
/ Colorectal Neoplasms - diagnostic imaging
/ Colorectal Neoplasms - drug therapy
/ Colorectal Neoplasms - pathology
/ Colorectal Neoplasms - therapy
/ Comparative analysis
/ Cytotoxicity
/ Dyes
/ Efficiency
/ Fluorescence
/ Fluorescent Dyes - chemistry
/ HT29 Cells
/ Humans
/ Infrared Rays
/ Lasers
/ Light therapy
/ Mice
/ Mice, Inbred BALB C
/ Mice, Nude
/ Nanomaterials
/ Photographic industry
/ Phototherapy
/ Photothermal Therapy - methods
/ Surface active agents
/ Xenograft Model Antitumor Assays
2024
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Structure-Inherent Tumor-Targeted IR-783 for Near-Infrared Fluorescence-Guided Photothermal Therapy
Journal Article
Structure-Inherent Tumor-Targeted IR-783 for Near-Infrared Fluorescence-Guided Photothermal Therapy
2024
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Overview
IR-783, a commercially available near-infrared (NIR) heptamethine cyanine dye, has been used for selective tumor imaging in breast, prostate, cervical, and brain cancers in vitro and in vivo. Although the molecular mechanism behind the structure-inherent tumor targeting of IR-783 has not been well-demonstrated, IR-783 has unique properties such as a good water solubility and low cytotoxicity compared with other commercial heptamethine cyanine dyes. The goal of this study is to evaluate the phototherapeutic efficacy of IR-783 as a tumor-targeted photothermal agent in human colorectal cancer xenografts. The results demonstrate that IR-783 shows both the subcellular localization in HT-29 cancer cells and preferential accumulation in HT-29 xenografted tumors 24 h after its intravenous administration. Furthermore, the IR-783 dye reveals the superior capability to convert NIR light into heat energy under 808 nm NIR laser irradiation in vitro and in vivo, thereby inducing cancer cell death. Taken together, these findings suggest that water-soluble anionic IR-783 can be used as a bifunctional phototherapeutic agent for the targeted imaging and photothermal therapy (PTT) of colorectal cancer. Therefore, this work provides a simple and effective approach to develop biocompatible, hydrophilic, and tumor-targetable PTT agents for targeted cancer phototherapy.
Publisher
MDPI AG
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