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用于化疗药物卡巴他赛的等离子体传感器的研发。

Development of a Plasmonic Sensor for a Chemotherapeutic Agent Cabazitaxel.

作者信息

Aşır Süleyman, Uğur Buse, Jalilzadeh Mitra, Göktürk Ilgım, Türkmen Deniz

机构信息

Department of Materials Science and Nanotechnology Engineering, Near East University, Mersin 10, Nicosia99138, North Cyprus, Turkey.

Department of Biomedical Engineering, Near East University, Mersin 10, Nicosia99138, North Cyprus, Turkey.

出版信息

ACS Omega. 2022 Dec 26;8(1):492-501. doi: 10.1021/acsomega.2c05327. eCollection 2023 Jan 10.

Abstract

Drug dosage is a crucial subject in both human and animal treatment. Administering less drug dosage may prevent treatment or make it less effective, and high drug dosage may cause a heightened risk of adverse effects, or in some cases, cost a patient's life. Also, even when the dosage is administered carefully, metabolic differences may cause different effects on different patients. Because of these considerations, monitoring drug dosage in the body is a critical and significant requirement in the health industry. Within the scope of this study, a reusable surface plasmon resonance (SPR) chip with fast response, high selectivity, and no pretreatment is produced for the chemotherapeutic agent cabazitaxel. A cabazitaxel-imprinted nanofilm was synthesized on the sensor chip surface and characterized by atomic force microscopy, ellipsometry, and contact angle measurements. Standard cabazitaxel solution and an artificial plasma sample were used for the kinetic analysis. Docetaxel, methylprednisolone, and dexamethasone were analyzed for their selectivity experiment. In addition, the repeatability and storage durability of the sensor were also evaluated. As a result of the adsorption studies, the limit of detection and limit of quantitation values were found to be 0.012 and 0.036 μg/mL, respectively. High-performance liquid chromatography analysis was used to validate the response of the cabazitaxel-imprinted sensor.

摘要

药物剂量在人类和动物治疗中都是一个关键问题。给予较低的药物剂量可能会妨碍治疗或使其效果降低,而高剂量药物可能会增加不良反应的风险,在某些情况下,甚至会危及患者生命。此外,即使谨慎给药,代谢差异也可能对不同患者产生不同影响。出于这些考虑,监测体内药物剂量是医疗行业一项至关重要的要求。在本研究范围内,制备了一种用于化疗药物卡巴他赛的具有快速响应、高选择性且无需预处理的可重复使用表面等离子体共振(SPR)芯片。在传感器芯片表面合成了卡巴他赛印迹纳米膜,并通过原子力显微镜、椭偏仪和接触角测量对其进行了表征。使用标准卡巴他赛溶液和人工血浆样本进行动力学分析。对多西他赛、甲泼尼龙和地塞米松进行了选择性实验分析。此外,还评估了传感器的重复性和储存耐久性。吸附研究结果表明,检测限和定量限分别为0.012和0.036μg/mL。使用高效液相色谱分析来验证卡巴他赛印迹传感器的响应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/9835620/d14ae0dc29f2/ao2c05327_0002.jpg

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