TY - JOUR
T1 - Bioplasmonic calligraphy for multiplexed label-free biodetection
AU - Tian, Limei
AU - Tadepalli, Sirimuvva
AU - Hyun Park, Sang
AU - Liu, Keng Ku
AU - Morrissey, Jeremiah J.
AU - Kharasch, Evan D.
AU - Naik, Rajesh R.
AU - Singamaneni, Srikanth
N1 - Funding Information:
We would like to thank Ms. Marilee Fisher for technical help in performing antibody conjugates affinity study. We acknowledge financial support from National Science Foundation under award number CBET-1254399 (CAREER), NCI R01CA141521, and Air Force Research Laboratories. We would like thank Nano Research Facility (NRF), a member of the National Nanotechnology Infrastructure Network (NNIN), for providing access to electron microscopy facilities.
PY - 2014/9/15
Y1 - 2014/9/15
N2 - Printable multi-marker biochips that enable simultaneous quantitative detection of multiple target biomarkers in point-of-care and resource-limited settings are a holy grail in the field of biodiagnostics. However, preserving the functionality of biomolecules, which are routinely employed as recognition elements, during conventional printing approaches remains challenging. In this article, we introduce a simple yet powerful approach, namely plasmonic calligraphy, for realizing multiplexed label-free bioassays. Plasmonic calligraphy involves a regular ballpoint pen filled with biofunctionalized gold nanorods as plasmonic ink for creating isolated test domains on paper substrates. Biofriendly plasmonic calligraphy approach serves as a facile method to miniaturize the test domain size to few mm2, which significantly improves the sensitivity of the plasmonic biosensor compared to bioplasmonic paper fabricated using immersion approach. Furthermore, plasmonic calligraphy also serves as a simple and efficient means to isolate multiple test domains on a single test strip, which facilitates multiplexed biodetection and multi-marker biochips. Plasmonic calligraphy, which can be potentially automated by implementing with a robotic arm, serves as an alternate path forward to overcome the limitations of conventional ink-jet printing.
AB - Printable multi-marker biochips that enable simultaneous quantitative detection of multiple target biomarkers in point-of-care and resource-limited settings are a holy grail in the field of biodiagnostics. However, preserving the functionality of biomolecules, which are routinely employed as recognition elements, during conventional printing approaches remains challenging. In this article, we introduce a simple yet powerful approach, namely plasmonic calligraphy, for realizing multiplexed label-free bioassays. Plasmonic calligraphy involves a regular ballpoint pen filled with biofunctionalized gold nanorods as plasmonic ink for creating isolated test domains on paper substrates. Biofriendly plasmonic calligraphy approach serves as a facile method to miniaturize the test domain size to few mm2, which significantly improves the sensitivity of the plasmonic biosensor compared to bioplasmonic paper fabricated using immersion approach. Furthermore, plasmonic calligraphy also serves as a simple and efficient means to isolate multiple test domains on a single test strip, which facilitates multiplexed biodetection and multi-marker biochips. Plasmonic calligraphy, which can be potentially automated by implementing with a robotic arm, serves as an alternate path forward to overcome the limitations of conventional ink-jet printing.
KW - Calligraphy
KW - Gold nanorods
KW - Localized surface plasmon resonance
KW - Plasmonic ink
UR - http://www.scopus.com/inward/record.url?scp=84898605209&partnerID=8YFLogxK
U2 - 10.1016/j.bios.2014.03.043
DO - 10.1016/j.bios.2014.03.043
M3 - Article
C2 - 24727607
AN - SCOPUS:84898605209
SN - 0956-5663
VL - 59
SP - 208
EP - 215
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
ER -