2. Different Nanomaterials as Nanosensors for Detecting AAs, Proteins, and Peptides
Nanomaterials are promising materials with at least one size in the range of 1–100 nm. Outstandingly high surface areas can be attained via the intelligent design of nanomaterials. Furthermore, nanomaterials can be synthesized with outstanding electrical, optical, catalytic, and mechanical properties that are superior to those of their bulk counterparts. Nanomaterial properties can be adjusted as desired via controlling the synthesis conditions and adequate functionalization
[68][14].
Nanomaterials can be categorized into three classes according to their content: (i) organic-carbon-based nanomaterials-carbon nanotubes (CNTs), carbon nanofibers (CNFs), fullerenes (C60), and graphene (GR). Chemical vapor deposition (CVD)
[69][15], laser ablation
[70[16][17],
71], and arc discharge techniques
[72,73][18][19] are used for the production of organic-carbon-based nanomaterials; (ii) inorganic-based nanomaterials—quantum dots, gold NPs, and magnetic NPs. These nanomaterials can be synthesized into metals such as Au or AgNPs, metal oxides such as TiO
2 and ZnO NPs, and semiconductors such as silicon and ceramics; (iii) hybrid nanomaterials, which can be any combination of carbon-based, metal-based, or organic-based nanomaterials with any form of metal, ceramic, or polymer bulk materials
[74][20].
A sensor is an analytical device that can detect and quantify the presence of an analyte in a sample. It includes receptors, transducers, and reading systems. The biological receptor interacts specifically with the target analyte, and the transducer converts this information into a measurable signal
[75][21]. For example, piezoelectric transducers are involved in measuring the change in mass after the formation of analyte–bioreceptor complexes, while optical transducers and electrochemical transducers measure the changes in light intensity and conductivity, current, or potential, respectively. Finally, the magnitude of the change is measured by the reading system.
Figure 1 shows a schematic diagram of a typical biosensor.
Figure 1. Schematic diagram of a typical biosensor. Reprinted with permission from ref. [76]. Schematic diagram of a typical biosensor. Reprinted with permission from ref. [22].
Bio-based analysis systems have recently become the most used and desired devices for diagnosis in the clinical field because of their fast response times and reliable features. In biosensors, a biological element (the receptor) is immobilized on the transducer using different strategies
[77][23]. Analyte detection is performed using the high affinity between the receptor and its ligands, such as antigen-antibody, enzymatic (enzyme–substrate), or cellular (microorganisms, proteins) interactions. The ability to detect important biomarkers such as nucleic acids, AAs, and proteins associated with a disease is essential for the clinical field
[78][24]. The technique of immobilization of the biofunctional component on the working electrode dramatically affects the performance of biosensors. It is important to note that a biosensor’s stability is not lost while forming a close relationship between the biological component and the sensor surface (transducer). Therefore, the selection of immobilization matrices that support the performance of the sensor system is very critical.
Nanosensors are sensing devices with at least one sensing size smaller than 100 nm
[79][25]. The use of nanoscale materials as reinforcement increases the interface area of the resulting composites. For this reason, various reinforcement elements such as hydroxyapatite, gold NPs, GR, CNTs, and CNFs are used to increase the surface area and especially the conductivity in sensor applications
[80][26]. Carbon-based nanomaterials are widely used as reinforcements because of their stable, mechanically robust, flexible, electrical, and thermally conductive properties. Thus, these nanomaterials are promising in the development of high-performance devices
[81][27].
Macro- and microscale sensors such as electrochemical and optical sensors are currently being used in the clinical field. For example, electrochemical and optical sensors such as blood gas and pH are frequently used in intensive care. Likewise, disposable electrodes are used in the clinical field to record biopotentials such as electrocardiograms and electroencephalograms
[82][28]. Nevertheless, the use of nanosensors in the early-stage diagnosis of diseases and preclinical studies is increasing. In particular, whole-cell behaviors, adhesion processes of cells to the extracellular matrix, and cell-cell interactions can be easily monitored in vitro thanks to label-free electrochemical nanosensors
[83][29]. For example, in vitro studies can be performed in the presence of components (drug or toxic substance) that can affect cell adhesions to the biofunctional surface of a nanosensor developed on a cell-based platform under the electrochemical measurements. This sheds light on the studies carried out before the transition to in vivo applications, which is the next step of preclinical studies. This also reduces animal experiments by using these developed nanosensors. At the same time, nanosensors are attracting much attention as an alternative to the invasive methods currently used to diagnose diseases in the clinical field. Recently developed wearable nanosensors are promising for noninvasive monitoring of biomarkers. It is crucial that some compounds that serve as disease biomarkers can be determined from saliva, sweat, or tears. At the same time, electrochemical nanosensors with increased stability are being developed for real-time monitoring of small molecules in blood or drug-active substances in plasma in a continuous flow environment
[84][30].
3.1. Metal NP-Based Sensors
2.1. Metal NP-Based Sensors
With the development of nanoscience and nanotechnology, metal NPs are highly desirable in areas such as nanosensors, biomedicine, biological labeling, and microelectronics because of their unique properties such as sizeable surface-to-volume ratio and high electrical conductivity, biocompatibility, catalytic activity, etc.
[85][31]. Signal-generating molecules are usually used to bind bioreceptors to the biosensor recognition surface for labeling. Enzymes such as horseradish peroxidase are labeled agents and require an additional dye or substrate in affinity-based sensors. Enzyme labels are not stable, since they are affected by environmental conditions. Additionally, they are expensive. Nanoprobes have become quite popular as an alternative. Usage of electroactive NPs as nanolabels contributes to improving biosensor performance. Furthermore, electroactive NPs are inexpensive and stable
[86][32].
3.2. Carbon-Based Nanomaterials
2.2. Carbon-Based Nanomaterials
Carbon-based nanomaterials display outstanding properties such as high electrical conductivity, fast electron transfer capability, and high specific surface area, making them highly interesting for developing high-performance biosensors
[105][33]. Commonly used carbon nanomaterials are carbon nanotubes (CNTs) and graphene and its derivatives, in the forms of nanotubes and platelets, respectively.
.3. Electrospun Nanofibers (ESNFs)
2.3. Electrospun Nanofibers (ESNFs)
Electrospinning is defined as the production of nanofibers from polymer solutions under a high electric field (kV)
[123][34]. It is the only method for mass production of continuous long nanofibers
[124][35]. Among the numerous nanomaterials, ESNFs are building materials in drug delivery systems, biosensors, biomedicine, food textile, and environmental applications because of their large surface areas, controllable surface conformations, porous structures, and high concentrations adsorption capacity, and good biocompatibility
[125,126,127][36][37][38]. Because of these properties, electrospun nanofibers have better sensitivity than sensors formed with other materials. In addition, biomimetic coatings can prevent biofouling, thereby extending the life of biosensors
[128][39]. ESNFs are produced via electrospinning, which is a simple, effective, controlled, and economical method. Fibers can be obtained from various materials; solutions or melt forms of organic polymers are among the most common sources. In particular, the production of nanofibers is possible from composite materials obtained by the appropriate combination of components with different morphologies in the nano size (e.g., NPs, nanorods, nanowires, nanotubes, and nanosheets) with organic polymers.
Figure 52 shows a schematic representation of a conventional electrospinning setup.
3.4. Molecularly Imprinted Polymers
Figure 2. Representation of a conventional electrospinning setup.
2.4. Molecularly Imprinted Polymers
Molecular imprinting is a promising method for developing affinity-based nanomaterials with high specific recognition ability
[134,135][40][41]. Molecularly imprinted polymers (MIPs) provide many properties such as selectivity, stability, reusability, and low cost compared with biological recognition materials such as enzymes and antibodies. They have some drawbacks, such as a high diffusion barrier and low space accessibility, given that most of the imprinted areas are formed inside the MIP. To overcome these issues, the surface printing technique, which involves the production of a MIP layer on the surface of nanomaterials, has been developed in recent years. This method provides the advantages of higher bonding capacity and faster bonding kinetics on the material surface
[136][42]. The applications of MIPs combined with electrochemical studies have increased in the sensor field because of their ease of use and low cost
[137][43]. However, some problems still need to be overcome before MIP-based sensors can enter the sensor market. The most significant change is in the distance of the imprinted cavities to the sensor surface and, accordingly, low signal reception
[138][44]. Therefore, researchers have focused on improving the surface of nanosized support materials such as GR with ultrathin polymeric films. Through this method, higher selectivity is provided for thin MIP layers
[115][45].