본문으로 건너뛰기
← 뒤로

Metabolic Trojan Horse: Multivalent Glucose Ligand Modified Near-Infrared-Absorbing Gold Nanorods for Targeted Photothermal Therapy.

ACS applied materials & interfaces 2026 Nanoplatforms for cancer theranostic
OpenAlex 토픽 · Nanoplatforms for cancer theranostics Gold and Silver Nanoparticles Synthesis and Applications Nanocluster Synthesis and Applications

Jiang C, Bandyopadhyay S, Kincanon M, Wo A, Tedford EM, East AK, Marcellus M, Murphy CJ, Chan J

📝 환자 설명용 한 줄

Nanoparticle-based photothermal therapy (PTT) provides localized tumor ablation but remains limited by off-target accumulation and the need for high systemic doses.

이 논문을 인용하기

BibTeX ↓ RIS ↓
APA Jiang Chang, Suritra Bandyopadhyay, et al. (2026). Metabolic Trojan Horse: Multivalent Glucose Ligand Modified Near-Infrared-Absorbing Gold Nanorods for Targeted Photothermal Therapy.. ACS applied materials & interfaces. https://doi.org/10.1021/acsami.5c25469
MLA Jiang Chang, et al.. "Metabolic Trojan Horse: Multivalent Glucose Ligand Modified Near-Infrared-Absorbing Gold Nanorods for Targeted Photothermal Therapy.." ACS applied materials & interfaces, 2026.
PMID 42018460

Abstract

Nanoparticle-based photothermal therapy (PTT) provides localized tumor ablation but remains limited by off-target accumulation and the need for high systemic doses. To address these challenges, we developed gold nanorods (AuNRs) coated with a multivalent glucose ligand (mvGlu-AuNR) that engages glucose transporter type 1 (GLUT1) for selective tumor delivery. This design leverages the Warburg effect, using GLUT1 as a metabolic Trojan horse to enter glycolytic cancer cells. In 4T1 breast cancer models, mvGlu-AuNR showed an 8-fold increase in gold content and a 3-fold rise in photoacoustic signal compared to nontargeted controls. Notably, mvGlu-AuNRs converted light to heat more efficiently than mPEG-AuNRs under identical irradiation conditions. ICP-MS analysis confirmed tumor-to-liver ratios ranging from 1.56 to 4.88, which is consistent with strong tumor localization and minimal hepatic uptake. At a systemic dose of 1 mg/kg, mvGlu-AuNRs enabled efficient tumor heating and slowed tumor growth without signs of off-target toxicity. These findings establish metabolic targeting as an effective strategy to enhance PTT specificity, reduce off-target exposure, and enable markedly lower gold dosing.

같은 제1저자의 인용 많은 논문 (5)