This review is dedicated to the development of molecularly imprinted polymers (MIPs) and the application of MIPs in sensor design. MIP-based biological recognition parts can replace receptors or antibodies, which are rather expensive. Conducting polymers show unique properties that are applicable in sensor design. Therefore, MIP-based conducting polymers, including polypyrrole, polythiophene, poly(3,4-ethylenedioxythiophene), polyaniline and ortho-phenylenediamine are frequently applied in sensor design. Some other materials that can be molecularly imprinted are also overviewed in this review. Among many imprintable materials conducting polymer, polypyrrole is one of the most suitable for molecular imprinting of various targets ranging from small organics up to rather large proteins. Some attention in this review is dedicated to overview methods applied to design MIP-based sensing structures. Some attention is dedicated to the physicochemical methods applied for the transduction of analytical signals. Expected new trends and horizons in the application of MIP-based structures are also discussed.

Nanostructured materials formed from metal oxides offer a number of advantages, such as large surface area, improved mechanical and other physical properties, as well as adjustable electronic properties that are important in the development and application of chemical sensors and biosensor design. Nanostructures are classified using the dimensions of the nanostructure itself and their components. In this review, various types of nanostructures classified as 0D, 1D, 2D, and 3D that were successfully applied in chemical sensors and biosensors, and formed from metal oxides using different synthesis methods, are discussed. In particular, significant attention is paid to detailed analysis and future prospects of the synthesis methods of metal oxide nanostructures and their integration in chemical sensors and biosensor design.

Conjugated polymers (CPs) are attractive materials for use in different areas; nevertheless, the enhancement of electrochromic stability and switching time is still necessary to expand the commercialization of electrochromic devices. To our best knowledge, this is the first study demonstrating the employment of electrodeposited gold nanostructures (AuNS) for the enhancement of CPs’ electrochromic properties when a transparent electrode is used as a substrate. Polyaniline–poly(3,4-ethylenedioxythiophene) (PANI-PEDOT) films were electrodeposited on a transparent indium tin oxide glass electrode, which was pre-modified by two different methods. AuNS were electrodeposited at −0.2 V constant potential for 60 s using both the 1st method (synthesis solution consisted of 3 mM HAuCl₄ and 0.1 M H₂SO₄) and 2nd method (15 mM HAuCl₄ and 1 M KNO₃) resulting in an improvement of optical contrast by 3% and 22%, respectively. Additionally, when using the 1st method, the coloration efficiency was improved by 50% while the switching time was reduced by 17%. Furthermore, in both cases, the employment of AuNS resulted in an enhancement of the electrochromic stability of the CPs layer. A further selection of AuNS pre-modification conditions with the aim to control their morphology and size can be a possible stepping stone for the further improvement of CPs electrochromic properties.

In this research Al₂O₃/ZnO nanolaminates were evaluated for possible application in the design of optical immunosensors. Total internal reflection ellipsometry (TIRE) was utilized to study the optical response during the formation of a bovine serum albumin (BSA) based monolayer on the surface of Al₂O₃/ZnO nanolaminates, which were pre-modified with a N-(3-aminopropyl)triethoxysilane (APTES) layer. The influence of the thicknesses of Al₂O₃ and ZnO layers on the performance of Al₂O₃/ZnO nanolaminate based structures has been assessed. This research has shown the noticeable contribution of multiple reflections from the interfaces between Al₂O₃ and ZnO for the enhancement of the optical response in a total internal reflection configuration. Al₂O₃/ZnO nanolaminates of 200 nm total thickness based on four 50 nm thick alternating Al₂O₃ and ZnO layers have shown better sensitivity than the nanolaminate based on two 100 nm oxide-layers. Real-time monitoring of the ellipsometric parameters Ψ(λ) and Δ(λ) has shown that BSA was successfully covalently attached to the nanolaminate/APTES surface. The surface concentration of immobilized BSA was evaluated from the real-time data of the ellipsometric parameters Ψ(λ) and Δ(λ). The expected advantages and disadvantages of Al₂O₃/ZnO nanolaminates during expected application in optical immunosensors are discussed.

Polymers represent materials that are applied in almost all areas of modern life, therefore, the characterization of polymer layers using different methods is of great importance. In this review, the main attention is dedicated to the non-invasive and label-free optical and acoustic methods, namely spectroscopic ellipsometry (SE) and quartz crystal microbalance with dissipation (QCM-D). The specific advantages of these techniques applied for in situ monitoring of polymer layer formation and characterization, biomolecule immobilization, and registration of specific interactions were summarized and discussed. In addition, the exceptional benefits and future perspectives of combined spectroscopic ellipsometry and QCM-D (SE/QCM-D) in one measurement are overviewed. Recent advances in the discussed area allow us to conclude that especially significant breakthroughs are foreseen in the complementary application of both QCM-D and SE techniques for the investigation of polymer structure and assessment of the interaction between biomolecules such as antigens and antibodies, receptors and ligands, and complementary DNA strands.