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Molecular Tuning of IR-786 for Improved Tumor Imaging and Photothermal Therapy.
Lim, Wonbong; Byun, Jae Yong; Jo, Gayoung; Kim, Eun Jeong; Park, Min Ho; Hyun, Hoon.
Afiliación
  • Lim W; Department of Premedical Program, School of Medicine, Chosun University, Gwangju 61452, Korea.
  • Byun JY; Madisarang Hospital, Cheongju 61469, Korea.
  • Jo G; Department of Biomedical Sciences, Chonnam National University Medical School, Hwasun 58128, Korea.
  • Kim EJ; Department of Surgery, Chonnam National University Medical School and Hwasun Hospital, Hwasun 58128, Korea.
  • Park MH; Department of Surgery, Chonnam National University Medical School and Hwasun Hospital, Hwasun 58128, Korea.
  • Hyun H; Department of Biomedical Sciences, Chonnam National University Medical School, Hwasun 58128, Korea.
Pharmaceutics ; 14(3)2022 Mar 19.
Article en En | MEDLINE | ID: mdl-35336050
ABSTRACT
A tumor-targeted near-infrared (NIR) fluorophore CA800Cl was developed based on commercially available IR-786 by modulating its physicochemical properties. IR-786, a hydrophobic cationic heptamethine cyanine fluorophore, was previously recognized as a mitochondria-targeting NIR agent with excellent optical properties. Owing to the poor tumor specificity of IR-786 itself, in vivo studies on tumor-targeted imaging have not yet been investigated. A chloro-cyclohexene ring and indolium side groups on the heptamethine chain are key structural features that improve tumor targetability, owing to better biodistribution and clearance. Thus, IR-786 should be designed to be more soluble in aqueous solutions so that it can preferentially accumulate in the tumor based on the structure-inherent targeting strategy. In this study, we developed a bifunctional NIR fluorophore CA800Cl by incorporating carboxylate moieties in the basic structure of IR-786. This improved its tumor targetability and water solubility, thereby enabling the use of CA800Cl for enhanced photothermal cancer therapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmaceutics Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmaceutics Año: 2022 Tipo del documento: Article
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