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Effect of Noscapine Hydrochloride on the Near-Infrared Optical Properties of Indocyanine Green.

Created on 06 Aug 2026

Authors

Bhawana, Ankita Borah, Tanya Goel, Anamika Brahma, Aarushi Singh, Jayant Sindhu, Ramesh Chandra, Snigdha Singh

Published in

ACS omega. Volume 11. Issue 29. Pages 43052-43063. Jul 28, 2026. Epub Jul 16, 2026.

Abstract

Indocyanine Green (ICG) is a widely used near-infrared fluorophore in biomedical imaging and therapy due to its strong light absorption and effective heat conversion abilities. Recently, combination of chemotherapy with PTT (chemo-PTT) has emerged as a promising approach to improve cancer treatment effectiveness. This study investigates the interaction between Noscapine Hydrochloride (Np.HCl), a benzyl isoquinoline alkaloid with potential anticancer effects, and ICG, with a specific focus on its influence on ICG's optical properties. The findings indicate that Np.HCl promotes J-aggregation even at low concentrations, with aggregation intensity increasing proportionally to Np.HCl concentrations. A simple and reproducible method has been developed to synthesize these J-aggregates (IJAs) using FDA-approved agents, Np.HCl and ICG, highlighting their potential applications in improving chemotherapy outcomes. Spectral analysis revealed the presence of both blue and red shifts, depending on the dye concentration, indicating molecular interactions between Np.HCl and IGs, which were quantitatively assessed through Gaussian fitting. Additionally, Stern-Volmer plots were used to analyze the quenching dynamics and interaction mechanism. Further, cytotoxicity studies have been performed on H1299 cells, which revealed IC50 values of 354.4 and 165.8 μM for ICG and Np.HCl, respectively. Notably, the combination treatment (ICG:Np.HCl) exhibited the highest cytotoxic effect, suggesting a potential synergistic interaction. This is the first demonstration of noscapine-driven ICG J-aggregation, creating a new scope for designing dye-drug assemblies with optical and therapeutic functions.

PMID:
42555480
Bibliographic data and abstract were imported from PubMed on 06 Aug 2026.

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