Fast-reacting smart hydrogel-based sensor platform for biomedical applications (original) (raw)

A Sensor Platform for Smart Hydrogels in Biomedical Applications

Proceedings, 2018

Smart hydrogels are inherently biocompatible hydrophilic three-dimensional polymer networks able to undergo a volume-phase transition in the presence of an analyte. By molecular imprinting and/or aptamer-based approaches they can be tailored for a wide range of analytes with high selectivity. In combination with the biocompatibility, this makes hydrogels very promising candidates for biomedical sensor applications. However, to date hydrogels are rarely used for that purpose as the reliable detection of their swelling state remains a challenge. Here we report on a newly developed biocompatible bending sensor platform which can be equipped with almost any smart hydrogel, thereby paving the way for biomedical applications.

Free swelling and confined smart hydrogels for applications in chemomechanical sensors for physiological monitoring

Sensors and Actuators B: Chemical, 2009

We investigate thin films of "smart" polymer hydrogels used to convert miniature pressure sensors into novel chemomechanical sensors. In this versatile sensing approach, a smart hydrogel is confined between a porous membrane and the diaphragm of a piezoresistive pressure transducer. An increase in the environmental analyte concentration, as sensed through the pores of the membrane, is detected by measuring the change in pressure exerted by the hydrogel on the pressure transducer diaphragm. We compare the response of such a sensor with the response of a free-swelling hydrogel identical to the one used within the sensor. The sensor and the free hydrogel are observed to have comparable mean response times. However, the time-dependent response curve of the sensor, unlike that of the free hydrogel, is highly asymmetric between swelling and deswelling, with a smaller time constant for deswelling. We also investigate novel methods for increasing sensor sensitivity, such as use of a two-layer membrane with a nanoporous polymer inner layer, and pre-loading of the hydrogel under pressure. In ionic strength response tests, use of an inner membrane increases sensor sensitivity without increasing mean response time, an effect that varies with membrane water fraction.

B1.2 - Hydrogel-Based Biochemical Sensors

2011

With respect to diabetes management, there is a critical societal need for a sensor that can be used to continuously measure a patient's blood glucose concentration twenty four hours a day on a long-term basis. In this work, thin films of "stimuli-responsive" or "smart" hydrogels were combined with microfabricated piezoresistive pressure transducers to obtain "chemomechanical sensors" that can serve as selective and versatile wireless biomedical sensors. The sensitivity of hydrogels with regard to the concentration of glucose in solutions with physiological pH, ionic strength and temperature was investigated in vitro. The response of the glucose-sensitive hydrogel was studied at different regimes of the glucose concentration change and at different temperatures for two sensor design variants. Sensor response time and accuracy with which a sensor can track gradual changes in glucose was estimated and calibration curve has been obtained.

A precision structured smart hydrogel for sensing applications

Journal of Applied Physics, 2017

We report on a macroinitiator based smart hydrogel film applied on a microcantilever for sensing applications. The studied hydrogel features a comparatively wide dynamic range for changes in the electrolyte's ionic strength. Furthermore, it offers a simple spin coating process for thin film deposition as well as the capability to obtain high aspect ratio microstructures by reactive ion etching. This makes the hydrogel compatible to microelectromechanical system integration. As a proof of concept, we study the response of hydrogel functionalized cantilevers in aqueous sodium chloride solutions of varying ionic strength. In contrast to the majority of hydrogel materials reported in the literature, we found that our hydrogel still responds in high ionic strength environments. This may be of future interest for sensing e.g., in sea water or physiological environments like urine.

Hydrogels in sensing applications

Hydrogels are hydrophilic, highly water swellable polymer networks capable of converting chemical energy into mechanical energy and vice versa. They can be tailored regarding their chemical nature and physical structure, sensitiveness to external stimuli and biocompatibility; they can be formed in various structures and integrated into (micro-)systems. Accordingly, over the last decade, these materials have gained considerable recognition as valuable tool for sensors and in diagnostics. This article reviews the use of hydrogels in sensor development with focus on recent efforts in the application of stimuli responsive hydrogels as sensors, hydrogels as suitable matrices in which the sensing (bio-)molecules are embedded and hydrogels for modification and protection of sensor surfaces. In the first part of the review, both sensors and hydrogels are defined and a basic theoretical overview of hydrogels and their behavior is given. Subsequent chapters focus on hydrogels in physicochemical and biochemical sensing mechanisms with a primary emphasis on the hydrogels as such and the applied sensing mechanism. Finally, the review is concluded by a summary and discussion including an outlook on future perspectives for hydrogels in sensing applications.

Smart hydrogels as functional biomimetic systems

Biomater. Sci., 2014

This review discusses the principles underlying stimuli-responsive behavior of hydrogels and how these properties contribute to their biomimetic functions and applications.

Bio-smart hydrogels: co-joined molecular recognition and signal transduction in biosensor fabrication and drug delivery

Biosensors and Bioelectronics, 2002

Two classes of polymers that are currently receiving widespread attention in biosensor development are hydrogels and conducting electroactive polymers. The present study reports on the integration of these two materials to produce electroactive hydrogel composites that physically entrap enzymes within their matrices for biosensor construction and chemically stimulated controlled release. Enhanced biosensing capabilities of these membranes have been demonstrated in the fabrication of glucose, cholesterol and galactose amperometric biosensors. All biosensors displayed extended linear response ranges (10 (5 Á/10 (2 M), rapid response times ( B/60 s), retained storage stabilities of up to 1 year, and excellent screening of the physiological interferents ascorbic acid, uric acid, and acetaminophen. When the cross-linked hydrogel components of these composite membranes were prepared with the amine containing dimethylaminoethyl methacrylate monomer the result was polymeric devices that swelled in response to pH changes (neutral to acidic). Entrapment of glucose oxidase within these materials made them glucose-responsive through the formation of gluconic acid. When insulin was co-loaded with glucose oxidase into these 'bio-smart' devices, there was a twofold increase in insulin release rate when the devices were immersed in glucose solutions. This demonstrates the potential of such systems to function as a chemically-synthesized artificial pancreas. # (A. Guiseppi-Elie).

Constant-Volume Hydrogel Osmometer: A New Device Concept for Miniature Biosensors

Biomacromolecules, 2002

A new type of biosensor is proposed that combines the recognition properties of "intelligent" hydrogels with the sensitivity and reliability of microfabricated pressure transducers. In the proposed device, analyteinduced changes in the osmotic swelling pressure of an environmentally responsive hydrogel are measured by confining it within a small implantable enclosure between a rigid semipermeable membrane and the diaphragm of a miniature pressure transducer. Proof-of-principle tests of this device were performed in vitro using pH-sensitive hydrogels, with osmotic deswelling data for the same hydrogels used as a benchmark for comparison. The swelling pressure of the hydrogel was accurately determined from osmotic deswelling measurements against reservoirs of known osmotic stress. Values of swelling pressure vs salt concentration measured with a preliminary version of the sensor agree well with osmotic deswelling results. Through modification of the hydrogel with various enzymes or pendant binding moieties, the sensor has the potential to detect a wide range of biological analytes with good specificity.

Smart/stimuli-responsive hydrogels: Cutting-edge platforms for tissue engineering and other biomedical applications

Materials Today Bio, 2021

Recently, biomedicine and tissue regeneration have emerged as great advances that impacted the spectrum of healthcare. This left the door open for further improvement of their applications to revitalize the impaired tissues. Hence, restoring their functions. The implementation of therapeutic protocols that merge biomimetic scaffolds, bioactive molecules, and cells plays a pivotal role in this track. Smart/stimuli-responsive hydrogels are remarkable three-dimensional (3D) bioscaffolds intended for tissue engineering and other biomedical purposes. They can simulate the physicochemical, mechanical, and biological characters of the innate tissues. Also, they provide the aqueous conditions for cell growth, support 3D conformation, provide mechanical stability for the cells, and serve as potent delivery matrices for bioactive molecules. Many natural and artificial polymers were broadly utilized to design these intelligent platforms with novel advanced characteristics and tailored functionalities that fit such applications. In the present review, we highlighted the different types of smart/stimuli-responsive hydrogels with emphasis on their synthesis scheme. Besides, the mechanisms of their responsiveness to different stimuli were elaborated. Their potential for tissue engineering applications was discussed. Furthermore, their exploitation in other biomedical applications as targeted drug delivery, smart biosensors, actuators, 3D and 4D printing, and 3D cell culture were outlined. In addition, we threw light on smart self-healing hydrogels and their applications in biomedicine. Eventually, we presented their future perceptions in biomedical and tissue regeneration applications. Conclusively, current progress in the design of smart/stimuli-responsive hydrogels enhances their prospective to function as intelligent, and sophisticated systems in different biomedical applications.

Smart Hydrogels for Pharmaceutical Applications

Novel Approaches for Drug Delivery

The latest development in the field of smart hydrogels application as drugs carriers is shown in this chapter. Hydrogels are three-dimensional polymer network consisting of at least one hydrophilic monomer. They are insoluble in water, but in the excess presence of water or physiological fluids, swell to the equilibrium state. The amount of absorbed water depends on the chemical composition and the crosslinking degree of 3D hydrogel network and reaches over 1000% of the xerogel weight. Stimuli-responsive hydrogels exhibit significant change of their properties (swelling, color, transparency, conductivity, shape) due to small changes in the external environment conditions (pH, ionic strength, temperature, light wavelength, magnetic or electric fields, ultrasound, or a combination thereof). This smart hydrogels, with different physical and chemical properties, chemical structure and technology of obtaining, show great potential for application in the pharmaceutical industry. The application of smart hydrogels is very promising and at the beginning of the development and exploitation.