2017
DOI: 10.1016/j.jcrysgro.2016.09.066
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Rapid and label-free bioanalytical method of alpha fetoprotein detection using LSPR chip

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Cited by 17 publications
(3 citation statements)
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“…Research is also being conducted on other types of nanoparticle-based sensing devices for bacterial pathogens, virus particles, hazardous chemicals, toxic proteins, peptides, and other entities ( Kim et al, 2016a , b ). Figure 3 represents the evolution of various kinds of liposome nanoparticles for their potential commercial usage.…”
Section: Liposome Nanoparticles As Detection Sensor In Food Sectormentioning
confidence: 99%
“…Research is also being conducted on other types of nanoparticle-based sensing devices for bacterial pathogens, virus particles, hazardous chemicals, toxic proteins, peptides, and other entities ( Kim et al, 2016a , b ). Figure 3 represents the evolution of various kinds of liposome nanoparticles for their potential commercial usage.…”
Section: Liposome Nanoparticles As Detection Sensor In Food Sectormentioning
confidence: 99%
“…This characteristic can be used to prepare LSPR sensors for biological and chemical detection. LSPR biosensors can detect low-concentration cancer markers and provide a reference for auxiliary diagnosis, condition monitoring, and efficacy evaluation. The LSPR sensor based on Au NPs has been used to realize the rapid detection of low-concentration AFP, CEA, and other cancer markers. Recently, Lee et al developed a multiplex cancer marker biosensor by immobilizing chemically synthesized plasmonic nanoparticles . Aćimović et al demonstrated a nanoplasmonic biosensor of Au nanorods with eight independent microfluidic channels by the standard electron beam lithography (EBL)–reactive ion etching (RIE) process to achieve 50% human serum cancer marker detection .…”
Section: Introductionmentioning
confidence: 99%
“…A conventional universal strategy for enhancing the detection sensitivity is to amplify output signals by introducing as many enzyme molecules as possible . Currently, immunoassays that measure protein biomarkers by means of specific recognition include enzyme-linked immunosorbent assays (ELISA), , colorimetric methods, electrochemiluminescence assays, fluoroimmunoassays, , electrochemical immunosensor-based assays, , surface plasmon resonance-based assays , and photoelectrochemical-based immunoassays. , Despite ongoing efforts, the detection sensitivity of enzymes has been low due to their inferior stability and vulnerable catalytic activity, and consequently so has their limitation . The need for an effective enzyme-free signal amplification immunoassay has become increasingly urgent since this type of method enables ultrasensitive detection with rapid response and long-term stability, which are highly desirable for clinical diagnosis.…”
mentioning
confidence: 99%