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穿刺装置对化疗给药中 cyclophosphamide 剂量准确性的影响。

Influence of Puncture Devices on the Accuracy of Cyclophosphamide Dosing for Chemotherapy Administration.

作者信息

Carvalho Susana, Cardoso Andreia, Ferreira Débora, Dias da Silva Diana, Moreira Fernando

机构信息

REQUIMTE/LAQV, Escola Superior de Saúde, Instituto Politécnico do Porto, Rua Dr. António Bernardino de Almeida, 4200-072 Porto, Portugal.

Centro Hospitalar Universitário São João, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Portugal.

出版信息

Pharmaceuticals (Basel). 2025 Jun 12;18(6):879. doi: 10.3390/ph18060879.

DOI:10.3390/ph18060879
PMID:40573273
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12195922/
Abstract

Cyclophosphamide is one of the most commonly used cytotoxic drugs in chemotherapy protocols. Its preparation in the hospital setting involves handling concentrated solutions, which pose occupational exposure risks and potential variations in the final dose administered. The aim of this study was to evaluate the effect of aspiration devices on the concentration of cyclophosphamide in reconstituted solutions. : An analytical method was validated using high-performance liquid chromatography coupled to a diode-array detector (HPLC-DAD) for quality control. Cyclophosphamide solutions were prepared and aspirated using either a conventional needle or spike device with or without a filtration system. : The validated method demonstrated linearity (R = 0.9999), high precision (0.22-4.59%) and accuracy (88.9-99.4%), with a limit of quantification of 4.03 µg/mL. Significant differences ( < 0.001) were observed between samples aspirated with a needle and those aspirated with a spike fitted with a 5 µm filter, with the latter showing lower cyclophosphamide concentrations, suggesting partial retention of the drug. No significant differences were found between the needle and filterless spike preparations. : These results suggest that the choice of aspiration device influences the final drug concentration, potentially affecting therapeutic efficacy. Standardisation of preparation techniques and an awareness of device limitations are essential to ensure accurate chemotherapy dosing and patient safety.

摘要

环磷酰胺是化疗方案中最常用的细胞毒性药物之一。在医院环境中制备环磷酰胺涉及处理浓缩溶液,这存在职业暴露风险以及最终给药剂量的潜在差异。本研究的目的是评估抽吸装置对复溶溶液中环磷酰胺浓度的影响。采用高效液相色谱-二极管阵列检测器(HPLC-DAD)联用的分析方法进行质量控制验证。使用传统针头或带或不带过滤系统的穿刺装置制备并抽吸环磷酰胺溶液。验证后的方法显示出线性(R = 0.9999)、高精度(0.22 - 4.59%)和准确度(88.9 - 99.4%),定量限为4.03 µg/mL。用针头抽吸的样品与装有5 µm过滤器的穿刺装置抽吸的样品之间观察到显著差异(< 0.001),后者显示环磷酰胺浓度较低,表明药物有部分保留。在使用针头和无过滤穿刺装置制备的样品之间未发现显著差异。这些结果表明,抽吸装置的选择会影响最终药物浓度,可能影响治疗效果。制备技术的标准化以及对装置局限性的认识对于确保准确的化疗给药和患者安全至关重要。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4958/12195922/73a0c7c2b41e/pharmaceuticals-18-00879-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4958/12195922/1ad2214495b0/pharmaceuticals-18-00879-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4958/12195922/49b6bd3842f5/pharmaceuticals-18-00879-g003.jpg
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