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用于靶向检测MET抑制剂卡马替尼的低能量室温碳点

Low-energy room-temperature carbon dots for targeted sensing of MET inhibitor capmatinib.

作者信息

Goda Mohamed N, Alqarni Laila S, Ibrahim Hossieny, Ali Al-Montaser Bellah H, El-Wekil Mohamed M

机构信息

Department of Chemistry, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU) Riyadh 11623 Saudi Arabia.

Department of Chemistry, Faculty of Science, Assiut University Assiut 71516 Egypt.

出版信息

RSC Adv. 2025 Aug 11;15(35):28375-28383. doi: 10.1039/d5ra04346h.

Abstract

Capmatinib (CMB) monitoring in biological fluids is critical for evaluating its pharmacokinetics, optimizing dosing, and minimizing toxicity. Accurate measurement is essential for ensuring therapeutic efficacy, enabling personalized treatment, and preventing adverse effects. Given the variability in patient metabolism and excretion, regular monitoring helps maintain CMB levels within the therapeutic range, improving treatment outcomes and minimizing the risk of drug resistance. This work presents an economical and energy-efficient strategy for preparing highly luminescent nitrogen-doped carbon dots (NCDs), employing 2,5-dihydroxy-1,4-benzoquinone alongside triethylenetetramine. The synthesized NCDs demonstrated excellent photostability and a high fluorescence quantum yield of 38.72%. Upon the addition of CMB, concentration-dependent fluorescence quenching was observed at 515 nm, which was attributed to the inner filter effect (IFE), with LOD of 3.6 nM. The NCDs exhibited high selectivity in detecting CMB, with minimal cross-reactivity from simultaneously present compounds. Recovery studies in real biological samples yielded rates between 97.4% and 105.3%, and RSDs were consistently below 4.11%. These results demonstrate the method's precision, reproducibility, and potential for reliable CMB detection in complex biological matrices.

摘要

在生物流体中监测卡马替尼(CMB)对于评估其药代动力学、优化给药剂量以及将毒性降至最低至关重要。准确测量对于确保治疗效果、实现个性化治疗以及预防不良反应必不可少。鉴于患者新陈代谢和排泄的变异性,定期监测有助于将CMB水平维持在治疗范围内,改善治疗效果并降低耐药风险。这项工作提出了一种经济且节能的策略,用于制备高发光性的氮掺杂碳点(NCDs),该策略采用2,5 - 二羟基 - 1,4 - 苯醌和三亚乙基四胺。合成的NCDs表现出优异的光稳定性和38.72%的高荧光量子产率。加入CMB后,在515 nm处观察到浓度依赖性荧光猝灭,这归因于内滤效应(IFE),检测限为3.6 nM。NCDs在检测CMB时具有高选择性,与同时存在的化合物的交叉反应最小。在实际生物样品中的回收率研究得出的回收率在97.4%至105.3%之间,相对标准偏差始终低于4.11%。这些结果证明了该方法在复杂生物基质中可靠检测CMB的准确性、可重复性和潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96fe/12376873/f7d48ecfc100/d5ra04346h-f1.jpg

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