Facile synthesis of plasmonic BP@Au nanomatrix for sensitive detection of irinotecan and its active SN-38 metabolite via laser desorption/ionization mass spectrometry

IF 5.3 2区 化学 Q1 CHEMISTRY, ANALYTICAL Microchimica Acta Pub Date : 2025-01-21 DOI:10.1007/s00604-024-06881-5
Govinda Mandal, Muhammad Umar, Rui Lv, Ruochen Guo, Tianjin Ge, Muhammad Awais, Shunli Yang, Muhammad Sajjad Ul Hasan, Jian Liu
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Abstract

A new methodology is presented for the rapid, specific, and sensitive detection of irinotecan (CPT-11), a chemotherapeutic agent utilized in the treatment of cancer, along with its metabolically active derivative, SN-38, via laser desorption/ionization mass spectrometry (LDI MS). The method includes the detection of camptothecin (CPT), which can be utilized as an internal standard for the quantitative assessment of both CPT-11 and SN-38 in mouse serum. The approach utilizes a plasmonic two-dimensional (2D) black phosphorus nanosheet (BPN)-gold nanomatrix (BP@Au) in LDI MS. The experimental results demonstrated that the BP@Au nanomatrix outperformed the standard organic matrices (SA, CHCA, and DHB) in detecting irinotecan and its active metabolite with improved specificity and sensitivity, crucial factors for applications in personalized medicine. Mass spectra obtained using organic matrices revealed interference from matrix peaks overlapping with analyte peaks. The coefficient of determination (R2) was 0.9806 for CPT-11 and 0.9932 for SN-38, indicating strong linearity suitable for quantification. Moreover, the method achieved a lower limit of detection (LOD) of 62.76 ng/mL for CPT-11 and 189.87 ng/mL for SN-38, significantly enhancing the detection sensitivity by approximately 2–8 times compared with previous matrix-assisted laser desorption/ionization (MALDI) methodologies. This method was subsequently applied to the quantitative determination of analytes in mouse serum. The analyte recoveries for CPT-11 and SN-38 were 95.40% and 92.95%, respectively. Overall, this study offers potential insights and opens avenues for developing new nanomaterials as a MALDI nanomatrix, demonstrating enhanced capabilities for the rapid, specific, and sensitive detection of small biomolecules within the realms of analytical chemistry and personalized medicine.

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激光解吸/电离质谱法灵敏检测伊立替康及其活性SN-38代谢物的等离子体纳米基质BP@Au的快速合成
本文提出了一种新的方法,通过激光解吸/电离质谱(LDI MS)快速、特异、灵敏地检测伊立替康(CPT-11)及其代谢活性衍生物SN-38。伊立替康是一种用于治疗癌症的化疗药物。该方法包括喜树碱(CPT)的检测,可作为小鼠血清中CPT-11和SN-38定量评价的内标。该方法在LDI ms中利用等离子体二维(2D)黑磷纳米片(BPN)-金纳米基质(BP@Au)。实验结果表明,BP@Au纳米基质在检测伊立替康及其活性代谢物方面优于标准有机基质(SA, CHCA和DHB),具有更高的特异性和敏感性,这是个性化医疗应用的关键因素。利用有机基质获得的质谱揭示了基质峰与分析物峰重叠的干扰。CPT-11和SN-38的测定系数(R2)分别为0.9806和0.9932,线性较好,适合定量分析。此外,该方法对CPT-11和SN-38的检测下限(LOD)分别为62.76 ng/mL和189.87 ng/mL,与之前的基质辅助激光解吸/电离(MALDI)方法相比,检测灵敏度显著提高了约2-8倍。该方法随后应用于小鼠血清中分析物的定量测定。CPT-11和SN-38的加样回收率分别为95.40%和92.95%。总的来说,这项研究提供了潜在的见解,并为开发新的纳米材料作为MALDI纳米基质开辟了道路,展示了在分析化学和个性化医学领域快速、特异性和敏感性检测小生物分子的增强能力。图形抽象
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来源期刊
Microchimica Acta
Microchimica Acta 化学-分析化学
CiteScore
9.80
自引率
5.30%
发文量
410
审稿时长
2.7 months
期刊介绍: As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.
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