TY - GEN
T1 - Paper-Microfluidic Platform with Cloud-Based Capillary Flow Analysis for Detection of HPV 16 DNA Towards Oropharyngeal Cancer Screening
AU - Loeffler, Reid S.
AU - Song, Bofan
AU - Pershina, Darya
AU - Chan, Christian
AU - Liang, Rongguang
AU - Yoon, Jeong Yeol
N1 - Publisher Copyright:
© 2024 IEEE.
PY - 2024
Y1 - 2024
N2 - Human papillomavirus (HPV) is an oncogenic virus that can lead to the development of many different types of cancers, including oropharyngeal cancer (OPC). While HPV is not the sole cause of OPC, it does account for the majority of cases, and HPV-positive OPC cases are predicted to continue rising in the future. While several HPV-positive OPC detection methods have been developed, all have limitations in ease of use, portability, and assay time, often lacking specificity and/or sensitivity. This work showcases capillary flow analysis on paper microfluidic platforms, combined with smartphone- and cloud-based detection, to rapidly identify HPV 16 amplicons. HPV template DNA was amplified using recombinase polymerase amplification (RPA), an isothermal method that achieves exponential amplification in 20 minutes with a low reaction temperature of 39° C. A smartphone captured a video clip as the samples flowed through wax-printed paper microfluidic channels. Amine-functionalized microspheres with diameters of 0.5 μ ~m and 1.0 μ ~m were preloaded onto the chips to boost the flow velocity differences between the no-target control (NTC) and HPV samples. Capillary flow velocities were automatically analyzed in a cloud using custom Python code. The initial slopes of the flow velocity profiles and the 1.0 μ ~m microspheres showed the maximum differences between NTC and HPV samples and between the amplicons of varied lengths.
AB - Human papillomavirus (HPV) is an oncogenic virus that can lead to the development of many different types of cancers, including oropharyngeal cancer (OPC). While HPV is not the sole cause of OPC, it does account for the majority of cases, and HPV-positive OPC cases are predicted to continue rising in the future. While several HPV-positive OPC detection methods have been developed, all have limitations in ease of use, portability, and assay time, often lacking specificity and/or sensitivity. This work showcases capillary flow analysis on paper microfluidic platforms, combined with smartphone- and cloud-based detection, to rapidly identify HPV 16 amplicons. HPV template DNA was amplified using recombinase polymerase amplification (RPA), an isothermal method that achieves exponential amplification in 20 minutes with a low reaction temperature of 39° C. A smartphone captured a video clip as the samples flowed through wax-printed paper microfluidic channels. Amine-functionalized microspheres with diameters of 0.5 μ ~m and 1.0 μ ~m were preloaded onto the chips to boost the flow velocity differences between the no-target control (NTC) and HPV samples. Capillary flow velocities were automatically analyzed in a cloud using custom Python code. The initial slopes of the flow velocity profiles and the 1.0 μ ~m microspheres showed the maximum differences between NTC and HPV samples and between the amplicons of varied lengths.
KW - RPA
KW - capillary action
KW - human papillomavirus
KW - recombinase polymerase amplification
KW - smartphone
UR - https://www.scopus.com/pages/publications/105000186543
UR - https://www.scopus.com/pages/publications/105000186543#tab=citedBy
U2 - 10.1109/HI-POCT64255.2024.10876197
DO - 10.1109/HI-POCT64255.2024.10876197
M3 - Conference contribution
AN - SCOPUS:105000186543
T3 - 2024 IEEE Healthcare Innovations and Point of Care Technologies, HI-POCT 2024
SP - 61
EP - 64
BT - 2024 IEEE Healthcare Innovations and Point of Care Technologies, HI-POCT 2024
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2024 IEEE Healthcare Innovations and Point of Care Technologies, HI-POCT 2024
Y2 - 19 September 2024 through 20 September 2024
ER -