吲哚菁绿负载 N 掺杂碳量子点纳米粒子用于黑色素瘤的有效光动力治疗和细胞成像:体外、体内和体外研究。

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Drug Targeting Pub Date : 2024-05-23 DOI:10.1080/1061186X.2024.2358511
Hadiseh Mehravanfar, Nafiseh Farhadian, Khalil Abnous
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引用次数: 0

摘要

制备了掺杂 N 的碳量子点(CQD)纳米粒子,作为一种新型纳米载体,它具有优异的溶解性、稳定性和高量子产率,可克服吲哚菁绿(ICG)在光动力疗法(PDT)中的障碍,并同时具有细胞成像特性。研究人员对含有黑色素瘤癌细胞的 C57BL/6 小鼠进行了细胞培养研究和体内评估。结果表明,装入 ICG 后,CQD 的尺寸从 24.55 nm 微增至 42.67 nm。活性氧(ROS)检测表明,CQD提高了ICG在激光照射下的光稳定性和ROS生成能力。细胞培养研究表明,ICG@CQD 可降低 B16F10 细胞系黑色素瘤癌细胞的存活率,从纯 ICG 药物的 48% 降至 ICG@CQD 的 28%。共聚焦显微镜捕获的图像表明,ICG@CQD 的细胞吸收率更高,纳米载体的细胞成像能力更强。对含有黑色素瘤癌细胞的 C57BL/6 小鼠进行的体内评估显示,与游离 ICG 相比,ICG@CQD 对肿瘤生长有明显的抑制作用。体内荧光图像证实,ICG@CQD 在肿瘤区域的累积量明显高于游离 ICG。总之,ICG@CQD被认为是一种创新的纳米载体,在PDT和诊断方面具有巨大潜力。
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Indocyanine green-loaded N-doped carbon quantum dot nanoparticles for effective photodynamic therapy and cell imaging of melanoma cancer: In vitro, ex vivo and in vivo study.

N-doped carbon quantum dot (CQD) nanoparticle was prepared as a novel nanocarrier with excellent solubility, stability, and high quantum yield to overcome Indocyanine Green (ICG) obstacle in photodynamic therapy (PDT) with simultaneous cell imaging property. Cell culture study and In vivo assessments on the C57BL/6 mice containing melanoma cancer cells was performed. Results showed that CQD size after ICG loading slightly enhanced from 24.55 nm to 42.67 nm. Detection of reactive oxygen species (ROS) test demonstrated that CQD improved ICG photo-stability and ROS generation capacity upon laser irradiation. Cell culture study illustrated that ICG@CQD could decrease the survival rate of melanoma cancer cells of B16F10 cell line from 48% for pure ICG drug to 28% for ICG@CQD. Captured images by confocal microscopy approved more cellular uptake of ICG@CQD and more qualified cell imaging ability of the nanocarrier. In vivo assessments on the C57BL/6 mice containing melanoma cancer cells displayed the obvious inhibitory effect of the tumor growth for ICG@CQD in comparison to free ICG. In vivo fluorescence images confirmed that ICG@CQD accumulates remarkably more than free ICG in the tumor region. In conclusion, ICG@CQD is proposed as an innovative nanocarrier with great potential for PDT and diagnosis.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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