Arrays of fully hydrogel-supported, artificial hair cell (AHC) sensors based on bilayer membrane mechanotransduction are designed and characterized to determine sensitivity to multiple stimuli. The work draws upon key engineering design principles inspired by the characteristics of biological hair cells, primarily the use of slender hair-like structures as flow measurement elements. Many hair cell microelectromechanical (MEMS) devices to sense fluid flow have already been built based on this principle. However, recent developments in lipid bilayer applications, namely physically encapsulated bilayers and hydrogel interface bilayers, have facilitated the development of AHCs made primarily from biomolecular materials. The most current research in this field of "membrane based AHCs," shows promise, yet still lacks the modularity to create large sensor arrays similar to those in nature. This paper presents a novel bilayer based AHC platform, developed for array implementation by applying some of the core design principles of biological hair cells. These principles are translated into key design, fabrication and material considerations toward improved sensor sensitivity and modularity. Single hair cell responses to base excitation and short air pulses are to investigate the dynamic coupling between hair and bilayer membrane transducer. In addition, a spectral analysis of the AHC system under varying voltages and air flow velocities helps to build simple, predictive models for the sensitivity properties of the AHC. And finally, based on these results, we implement a spatial sensing strategy that involves mapping frequency content to stimulus location by "tuning" linear, three-unit arrays of AHCs. Individual AHC sensors characterization results demonstrate peak current outputs in the nanoamp range and measure flow velocities as high as 72 m/s. Characterization of the AHC response to base excitation and air pulses show that membrane current oscillates with the first three bending modes of the hair. Output magnitudes reflect of vibrations near the base of the hair. A 2 degree-of-freedom Rayleigh-Ritz approximation of the system dynamics yields estimates of 19 N/m and 0.0011 Nm/rad for the equivalent linear and torsional stiffness of the hair's hydrogel base, although double modes suggest non-symmetry in the gel's linear stiffness. The sensor output scales linearly with applied voltage (1.79 pA/V), avoiding a higher-order dependence on electrowetting effects. The free vibration amplitude of the sensor also increases in a linear fashion with applied airflow pressure (3.39 pA/m s??). Array sensing tests show that the bilayers' consistent spectral responses allow for an accurate localization of the airflow source. However, temporal variations in bilayer size affect sensitivity properties and make airflow magnitude estimation difficult. The overall successful implementation of the array sensing method validates the sensory capability of the bilayer based AHC. / Master of Science

No description available.

In the last decade, there has been a growing interest in the use of differential sensing for molecular recognition. Inspired by the mammalian olfactory system, differential sensing employs an array of non-selective receptors, which through cross-reactive interactions, create a distinct pattern for each analyte tested. The unique fingerprints obtained for each analyte with differential sensing are studied with statistical analysis techniques, such as principal component analysis and linear discriminant analysis. It was postulated that serum albumin proteins would be applicable to differential sensing schemes due to significant differences in sequence identity between different serum albumin species, and due to the wide range of hydrophobic molecules which are known to bind to these proteins. Consequently, cross-reactive serum albumin arrays were developed, utilizing hydrophobic fluorescent indicators to detect hydrophobic molecules. As such, serum albumin cross-reactive arrays were employed to discriminate subtly different hydrophobic analytes, and mixtures of these analytes, in the form of terpenes and perfumes, plasticizers and plastic explosive mixtures, and glycerides and adipocyte extracts. In this doctoral work, a detailed review of the field of differential sensing, and a thorough study of principal component analysis and linear discriminant analysis in various differential sensing scenarios, are given. These introductory chapters aid in better understanding the methods and techniques applied in later experimental chapters. In chapter 3, serum albumins, a PRODAN indicator, and an additive are shown to discriminate five terpene analytes and terpene doped perfumes. Chapter 4 describes an array with serum albumins, two dansyl fluorophores, and an additive which successfully differentiate the plasticizers found within the plastic explosives C4 and Semtex and simulated C4 and Semtex mixtures. Discrimination of these simulated mixtures was also achieved with this array in the presence of soil contaminants, demonstrating the potential real-world applicability of this sensing ensemble. Finally, chapter 5 details an array consisting of serum albumins, several fluorescent indicators, and a Grubb's olefin metathesis reaction, to differentiate saturated and unsaturated triglycerides, diglycerides, and monoglycerides. Mixtures of glycerides in adipocyte extracts taken from rats with different health states were then successfully discriminated, showing promise for clinical applications in differentiating adipoctyes from pre-diabetic, type 2 diabetic, and non-diabetic individuals. / text