在基质辅助激光解吸/电离质谱法中使用沸石提高肿瘤细胞内多种药物的电离效率(细胞内多种药物使用沸石质谱法)。

Q3 Physics and Astronomy
Mass spectrometry Pub Date : 2020-01-01 Epub Date: 2020-12-04 DOI:10.5702/massspectrometry.A0091
Hiroki Kannen, Shusei Nomura, Hisanao Hazama, Yasufumi Kaneda, Tatsuya Fujino, Kunio Awazu
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引用次数: 1

摘要

光动力疗法(PDT)和化疗联合治疗已被提出用于抗癌耐药癌细胞。为了评估这种联合治疗的效果,必须评估癌细胞对抗癌药物和光敏剂的吸收情况。采用基质辅助激光解吸/电离的质谱法可以同时检测多种药物。将人前列腺癌细胞PC-3或多西他赛耐药癌细胞PC-3- dr培养在含有光敏剂原卟啉IX (PpIX)和抗癌药物多西他赛的无血清培养基中。将6-氮杂-2-硫胸胺与NaY5.6沸石混合制备沸石基质,用50%丙酮水溶液溶解。利用飞行时间质谱仪,利用波长为355nm的Nd:YAG激光器获得离子。给药后用乙酸铵洗涤细胞,真空干燥保存细胞形态。利用沸石基质同时从PC-3细胞中得到质子化PpIX (m/z 563.3)和多西紫杉醇钠加合离子(m/z 829.9)。另一方面,PC-3-DR细胞中检测到PpIX,但未检测到来自多西他赛的离子。结果表明PDT对多西他赛耐药的癌细胞有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhancement of Ionization Efficiency Using Zeolite in Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry of Multiple Drugs in Cancer Cells (Mass Spectrometry of Multiple Drugs in Cells Using Zeolite).

Enhancement of Ionization Efficiency Using Zeolite in Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry of Multiple Drugs in Cancer Cells (Mass Spectrometry of Multiple Drugs in Cells Using Zeolite).

Enhancement of Ionization Efficiency Using Zeolite in Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry of Multiple Drugs in Cancer Cells (Mass Spectrometry of Multiple Drugs in Cells Using Zeolite).

Enhancement of Ionization Efficiency Using Zeolite in Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry of Multiple Drugs in Cancer Cells (Mass Spectrometry of Multiple Drugs in Cells Using Zeolite).

Combined therapy using photodynamic therapy (PDT) and chemotherapy has been proposed for anticancer-drug-resistant cancer cells. To evaluate the efficacy of such a combined therapy, the uptakes of an anticancer drug and a photosensitizer in cancer cells must be assessed. Mass spectrometry using matrix-assisted laser desorption/ionization can detect multiple drugs simultaneously. Human prostate cancer cells PC-3 or docetaxel-resistant cancer cells PC-3-DR were incubated in a serum-free medium containing a photosensitizer, protoporphyrin IX (PpIX), and an anticancer drug, docetaxel. A zeolite matrix was created by mixing 6-aza-2-thiothymine and NaY5.6 zeolite, and dissolving in water with 50% acetone. Ions were obtained with a time-of-flight mass spectrometer using a Nd:YAG laser at a wavelength of 355 nm. The cell morphology was preserved by washing the cells with ammonium acetate and drying in a vacuum after drug administration. Protonated PpIX (m/z 563.3) and the sodium adduct ion of docetaxel (m/z 829.9) were obtained from PC-3 cells simultaneously using the zeolite matrix. On the other hand, PpIX was detected but ions originating from docetaxel were not detected from PC-3-DR cells. The result indicated the efficacy of PDT for docetaxel-resistant cancer cells.

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来源期刊
Mass spectrometry
Mass spectrometry Physics and Astronomy-Instrumentation
CiteScore
1.90
自引率
0.00%
发文量
3
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