Development of LED Based Enzyme-Linked Immunosorbent Assay Reader

A. R. Ananda, D. Danudirdjo, A. W. Setiawan, T. Mengko
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Abstract

Enzyme-linked immunosorbent assay or better known as ELISA is a method commonly used for detecting antigen / antibody in the blood sample taken from the patient. The presence of antigen / antibody is detected for diagnosing viral infection such as Hepatitis, HIV or malaria. Although this method is gold standard for viral detection, this method is rarely use due to additional equipment need for the test. The ELISA reader that being designed use wavelength of 450 nm for the measurement and measured the optical density using 8 silicone photodiode. To guarantee that every photodiode have the same wavelength, the light source are split into 8 individual channel using fiber optic. Verification method is done by comparing the measurement result from the ELISA that been designed and compare it with commercial ELISA reader. The result show that ELISA reader that been designed have measurement range from 0.03 OD to 1.62 OD with correlation coefficient (R2) of 0.962. The error from the ELISA reader that been designed is $0.091 \pm 0.096$ OD
基于LED的酶联免疫吸附测定仪的研制
酶联免疫吸附测定法(ELISA)是一种通常用于检测患者血液样本中抗原/抗体的方法。检测抗原/抗体的存在是为了诊断病毒性感染,如肝炎、艾滋病毒或疟疾。虽然这种方法是病毒检测的金标准,但由于需要额外的设备,这种方法很少被使用。所设计的酶联免疫吸附仪测量波长为450 nm,光密度测量采用8硅光电二极管。为了保证每个光电二极管具有相同的波长,光源使用光纤分成8个单独的通道。验证方法是将所设计的酶联免疫吸附测定结果与市售酶联免疫吸附测定仪进行比较。结果表明,所设计的酶联免疫吸附测定试剂盒的测定范围为0.03 ~ 1.62 OD,相关系数(R2)为0.962。所设计的ELISA阅读器的误差为0.091美元/ pm 0.096美元OD
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