Smith Jerome P, Sammons Deborah L, Robertson Shirley A, Pretty Jack R, DeBord D Gayle, Connor Thomas H, Snawder John E
Division of Applied Research & Technology, National institute for Occupational Safety & Health, Cincinnati, OH, USA
Division of Applied Research & Technology, National institute for Occupational Safety & Health, Cincinnati, OH, USA.
J Oncol Pharm Pract. 2016 Feb;22(1):60-7. doi: 10.1177/1078155214554407. Epub 2014 Oct 6.
Contamination of workplace surfaces by antineoplastic drugs presents an exposure risk for healthcare workers. Traditional instrumental methods to detect contamination such as liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) are sensitive and accurate but expensive. Since immunochemical methods may be cheaper and faster than instrumental methods, we wanted to explore their use for routine drug residue detection for preventing worker exposure.
In this study we examined the feasibility of using fluorescence covalent microbead immunosorbent assay (FCMIA) for simultaneous detection and semi-quantitative measurement of three antineoplastic drugs (5-fluorouracil, paclitaxel, and doxorubicin). The concentration ranges for the assay were 0-1000 ng/ml for 5-fluorouracil, 0-100 ng/ml for paclitaxel, and 0-2 ng/ml for doxorubicin. The surface sampling technique involved wiping a loaded surface with a swab wetted with wash buffer, extracting the swab in storage/blocking buffer, and measuring drugs in the extract using FCMIA.
There was no significant cross-reactivity between these drugs at the ranges studied indicated by a lack of response in the assay to cross analytes. The limit of detection (LOD) for 5-fluorouracil on the surface studied was 0.93 ng/cm(2) with a limit of quantitation (LOQ) of 2.8 ng/cm(2), the LOD for paclitaxel was 0.57 ng/cm(2) with an LOQ of 2.06 ng/cm(2), and the LOD for doxorubicin was 0.0036 ng/cm(2) with an LOQ of 0.013 ng/cm(2).
The use of FCMIA with a simple sampling technique has potential for low cost simultaneous detection and semi-quantitative measurement of surface contamination from multiple antineoplastic drugs.
抗肿瘤药物对工作场所表面的污染会给医护人员带来暴露风险。传统的检测污染的仪器方法,如液相色谱 - 质谱/质谱联用(LC-MS/MS),灵敏且准确,但成本高昂。由于免疫化学方法可能比仪器方法更便宜、更快速,我们希望探索将其用于常规药物残留检测以预防工作人员暴露。
在本研究中,我们考察了使用荧光共价微珠免疫吸附测定法(FCMIA)同时检测和半定量测定三种抗肿瘤药物(5-氟尿嘧啶、紫杉醇和阿霉素)的可行性。该测定法的浓度范围为:5-氟尿嘧啶0 - 1000 ng/ml,紫杉醇0 - 100 ng/ml,阿霉素0 - 2 ng/ml。表面采样技术包括用经洗涤缓冲液浸湿的拭子擦拭负载表面,将拭子在储存/封闭缓冲液中提取,然后使用FCMIA测定提取物中的药物。
在所研究的浓度范围内,这些药物之间未观察到显著的交叉反应,这由测定法对交叉分析物无反应表明。在所研究的表面上,5-氟尿嘧啶的检测限(LOD)为0.93 ng/cm²,定量限(LOQ)为2.8 ng/cm²;紫杉醇的LOD为0.57 ng/cm²,LOQ为2.06 ng/cm²;阿霉素的LOD为0.0036 ng/cm²,LOQ为0.013 ng/cm²。
将FCMIA与简单采样技术结合使用,有潜力低成本地同时检测和半定量测定多种抗肿瘤药物造成的表面污染。