Requirements
of speed and simplicity in testing stimulate the development
of modern biosensors. Electrolyte-gated organic field-effect transistors
(EGOFETs) are a promising platform for ultrasensitive, fast, and reliable
detection of biological molecules for low-cost, point-of-care bioelectronic
sensing. Biosensitivity of the EGOFET devices can be achieved by modification
with receptors of one of the electronic active interfaces of the transistor
gate or organic semiconductor surface. Functionalization of the latter
gives the advantage in the creation of a planar architecture and compact
devices for lab-on-chip design. Herein, we propose a universal, fast,
and simple technique based on doctor blading and Langmuir–Schaefer
methods for functionalization of the semiconducting surface of C8-BTBT-C8, allowing the fabrication of a large-scale
biorecognition layer based on the novel functional derivative of BTBT-containing
biotin fragments as a foundation for further biomodification. The
fabricated devices are very efficient and operate stably in phosphate-buffered
saline solution with high reproducibility of electrical properties
in the EGOFET regime. The development of biorecognition properties
of the proposed biolayer is based on the streptavidin–biotin
interactions between the consecutive layers and can be used for a
wide variety of receptors. As a proof-of-concept, we demonstrate the
specific response of the BTBT-based biorecognition layer in EGOFETs
to influenza A virus (H7N1 strain). The elaborated approach to biorecognition
layer formation is appropriate but not limited to aptamer-based receptor
molecules and can be further applied for fabricating several biosensors
for various analytes on one substrate and paves the way for “electronic
tongue” creation.