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Development of theranostic dual-layered Au-liposome for effective tumor targeting and photothermal therapy.
Jeon, Miyeon; Kim, Gaeun; Lee, Wooseung; Baek, Seungki; Jung, Han Na; Im, Hyung-Jun.
Afiliação
  • Jeon M; Department of Applied Bioengineering, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, 08826, Republic of Korea.
  • Kim G; Department of Applied Bioengineering, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, 08826, Republic of Korea.
  • Lee W; Department of Applied Bioengineering, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, 08826, Republic of Korea.
  • Baek S; Department of Applied Bioengineering, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, 08826, Republic of Korea.
  • Jung HN; Department of Applied Bioengineering, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, 08826, Republic of Korea.
  • Im HJ; Department of Applied Bioengineering, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, 08826, Republic of Korea. iiihjjj@gmail.com.
J Nanobiotechnology ; 19(1): 262, 2021 Sep 04.
Article em En | MEDLINE | ID: mdl-34481489
ABSTRACT

BACKGROUND:

Photothermal therapy (PTT) is an emerging anti-cancer therapeutic strategy that generates hyperthermia to ablate cancer cells under laser irradiation. Gold (Au) coated liposome (AL) was reported as an effective PTT agent with good biocompatibility and excretory property. However, exposed Au components on liposomes can cause instability in vivo and difficulty in further functionalization.

RESULTS:

Herein, we developed a theranostic dual-layered nanomaterial by adding liposomal layer to AL (LAL), followed by attaching polyethylene glycol (PEG) and radiolabeling. Functionalization with PEG improves the in vivo stability of LAL, and radioisotope labeling enables in vivo imaging of LAL. Functionalized LAL is stable in physiological conditions, and 64Cu labeled LAL (64Cu-LAL) shows a sufficient blood circulation property and an effective tumor targeting ability of 16.4%ID g-1 from in vivo positron emission tomography (PET) imaging. Also, intravenously injected LAL shows higher tumor targeting, temperature elevation in vivo, and better PTT effect in orthotopic breast cancer mouse model compared to AL. The tumor growth inhibition rate of LAL was 3.9-fold higher than AL.

CONCLUSION:

Based on these high stability, in vivo imaging ability, and tumor targeting efficiency, LAL could be a promising theranostic PTT agent.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistemas de Liberação de Medicamentos / Nanoestruturas / Medicina de Precisão / Terapia Fototérmica / Lipossomos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Nanobiotechnology Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistemas de Liberação de Medicamentos / Nanoestruturas / Medicina de Precisão / Terapia Fototérmica / Lipossomos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Nanobiotechnology Ano de publicação: 2021 Tipo de documento: Article