Shrink wrap can boost fluorescent marker detection in biosensing 1000X
By depositing a combination of metals onto common shrink wrap, University of California, Irvine researchers were able to significantly boost the signal of fluorescent markers used in biosensing.
Researchers at the University of California, Irvine turned to plastic shrink wrap to help make highly sensitive, extremely low-cost diagnosis of infectious disease agents possible. By depositing a combination of metals onto the shrink wrap, they were able to significantly boost the signal of fluorescent markers used in biosensing.
"Using commodity shrink wrap and bulk manufacturing processes, we can make low-cost nanostructures to enable fluorescence enhancements greater than a thousand-fold, allowing for significantly lower limits of detection," says paper co-author Michelle Khine, a biomedical engineering professor at UC Irvine. “If you have a solution with very few molecules that you are trying to detect—as in the case of infectious diseases—this platform will help amplify the signal so that a single molecule can be detected.”
|Close-up images of the new shrink wrap nanostructures taken with a scanning electron microscope (SEM). Each image depicts the shrink wrap’s surface with a fixed amount of nickel (5 nm) and different thicknesses of gold in the metal coating. Top: 10 nm thick. Middle: 20 nm thick. Bottom: 30 nm thick. The black arrows in the top image indicate a nanogap. (All images courtesy of Optical Materials Express)|
In the new method developed by Khine and her graduate student Himanshu Sharma, along with their collaborators, Professors Enrico Gratton and Michelle Digman, also at UC Irvine, thin layers of gold and nickel are first deposited onto a thermoplastic polymer (a shrink wrap film). When heated, the shrink wrap contracts, causing the stiffer metal layers to buckle and wrinkle into flower-like structures that are significantly smaller than previously demonstrated. To the top of the wrinkled metal layer, the researchers add samples of biomarkers, antibodies generated by the immune system in response to infection with a certain pathogen. These biomarkers are tagged with fluorescent probes to allow their detection under near-infrared (NIR) light.
The team found that the shrink wrap’s wrinkles significantly enhanced the intensity of the signals emitted by the biomarkers. The enhanced emission, Khine says, is due to the excitation of localized surface plasmons—coherent oscillations of the free electrons in the metal. When researchers shined a light on their wrinkled creation, the electromagnetic field was amplified within the nanoscale gaps between the shrink wrap’s folds, Khine said. This produced “hotspots”—areas characterized by sudden bursts of intense fluorescence signals from the biomarkers.
In their study, the researchers used an immune system molecule known as immunoglobin G (IgG) as the biomarker. “IgG is one of the most common circulating antibodies in the immune system, making up about 80 percent of the all antibodies in the body, and is found in most bodily fluids,” Sharma says. In particular, IgG is a good biomarker for the detection of rotavirus, the virus that is the leading cause of severe diarrheal infection in infants and young children worldwide. IgG is also a biomarker for infection with the Epstein-Barr virus and Herpes simplex virus.
In the future, he says, additional antibodies, such as immunoglobulin A (IgA) and immunoglobulin M (IgM), might be used to detect other agents including cytomegalovirus and the pathogen that causes typhoid fever.
|Close-up images taken with a scanning electron microscope (SEM) showing the shrink wrap’s surface with a fixed amount of gold (10 nm) and different thicknesses of nickel in the metal coating. Left: 5 nm thick. Middle: 15 nm thick. Right: 25 nm thick.|
“The technique should work with measuring fluorescent markers in biological samples, but we have not yet tested bodily fluids,” says Khine, who cautions that the technique is far from ready for clinical use. For example, she notes, “We are currently working on trying to detect rotavirus, but one of the main challenges is that our surface is hydrophobic”—that is, water-repelling—“so diffusion of the biomarker onto our composite structures is limited.”
Though their current setup requires the use of expensive equipment, the researchers say, they believe their work will pave the way to creating an integrated, low-cost device to trap and identify biomarkers.
Full details of the work appear in the journal Optical Materials Express; for more information, please visit http://dx.doi.org/10.1364/OME.4.000753.
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