Harde Minal T, Lakade Sameer, Patokar Samiksha, More Mahesh P, Joshi Shrikant, Lodha Sandesh, Deshmukh Prashant K, Nangare Sopan
Department of Pharmaceutical Chemistry, PES's Modern College of Pharmacy, Sector No. 21, Yamuna Nagar, Nigdi, Pune, MH, 411 044, India.
Department of Pharmaceutics, RMD Institute of Pharmaceutical Education & Research, Pune, MH, 411 019, India.
J Fluoresc. 2025 Jun 7. doi: 10.1007/s10895-025-04388-7.
Designing of fluorescent materials in biomedical sciences is gaining attention due to unique characteristics like imaging driven by diagnosis and treatment. The exploration of fluorescent materials from green sources with highlights its application arena in cancer theranostic gained significant attention of oncology researchers. Outwards to the bioimaging techniques, fluorescent graphene quantum dots (fGQDs) grasp a potential place in biomedical research. Additionally, fGQDs have tuneable surface characteristics with high fluorescence, high loading and permeation capability. The present investigation explored the green synthesis of fGQDs using star anise fruit as precursor followed by surface decorated hyaluronic acid (HA) to form conjugated HA - GQD. The advance spectral characterization was used to confirm the synthesis of fGQDs and HA-GQD. The emission at 338 nm with excitation at 576 nm promise strong fluorescence with quantum yield of 16.52%. The conjugated HA-GQDs shows prominent bioimaging capability and lower cytotoxic potential at concentration less than 40 µg/ml. While cell inhibition against MCF-7 was dramatically increases at concentration above 100 µg/mL suitable to promote synergistic inhibition with other anticancer agents. This work demonstrates a sustainable route for developing multifunctional nanomaterials with promising application in cancer theranostics.
由于具有诊断和治疗驱动成像等独特特性,生物医学科学中荧光材料的设计正受到关注。对来自绿色来源的荧光材料的探索及其在癌症诊疗中的应用领域,引起了肿瘤学研究人员的极大关注。在生物成像技术方面,荧光石墨烯量子点(fGQDs)在生物医学研究中占据着重要地位。此外,fGQDs具有可调节的表面特性,具有高荧光、高负载和渗透能力。本研究探索了以八角茴香果实为前驱体绿色合成fGQDs,随后用透明质酸(HA)进行表面修饰,形成共轭HA - GQD。通过先进的光谱表征来确认fGQDs和HA - GQD的合成。在576 nm激发下338 nm处的发射表明具有强荧光,量子产率为16.52%。共轭HA - GQDs在浓度低于40 μg/ml时显示出显著的生物成像能力和较低的细胞毒性潜力。而在浓度高于100 μg/mL时,对MCF - 7的细胞抑制作用显著增加,适合与其他抗癌药物协同抑制。这项工作展示了一条开发多功能纳米材料的可持续途径,在癌症诊疗中具有广阔的应用前景。