Molecular imprinting is a powerful, generic, and cost-effective technique; however, challenges still remain related to the fabrication and development of these systems involving nonhomogeneous binding sites, insufficient template removing, incompatibility with aqueous media, low rebinding capacity, and slow mass transfer. The vapor-phase deposition of polymers is a unique technique because of the conformal nature of coating and offers new possibilities in a number of applications including sensors, microfluidics, coating, and bioaffinity platforms. Herein, we demonstrated a simple but versatile concept to generate one-dimensional surface-imprinted polymeric nanotubes within anodic aluminum oxide (AAO) membranes based on initiated chemical vapor deposition (iCVD) technique for biorecognition of immunoglobulin G (IgG). It is reported that the fabricated surface-imprinted nanotubes showed high binding capacity and significant specific recognition ability toward target molecules compared with the nonimprinted forms. Given its simplicity and universality, the iCVD method can offer new possibilities in the field of molecular imprinting.

Monitoring of ammonia in the human breath is of paramount importance to monitor diseases link to liver and kidney mulfunctioning. The present paper describes a solid-state optical ammonia sensor based on Förster resonance energy transfer (FRET) between narrowly dispersed blue-emitting carbon nanodots (CNDs) as FRET donor and fluorescein as FRET acceptor. The fluorophores were physically entrapped in a close to superhydrophobic sol-gel matrix, in turn deposited on a PVDF-HFP electrospun fiber membrane. The sensor shows a linear calibration with a remarkably low limit of detection, i.e., 110 ppb, and adequate reproducibility up to six N2/NH3 cycles.

The first vapor-phase deposition of poly(vinyl cinnamate) (PVCin) is reported. Initiated chemical vapor deposition (iCVD) is used to synthesize PVCin thin films with an average thickness of 100 nm. Free radical polymerization and cyclization reactions compete during the deposition process, with approximately 45% of the repeat units undergoing cyclization. Exposure to UV light (λ = 254 nm) induces dimerization (cross-linking) of the PVCin, which is quantified using spectroscopic techniques. Approximately 90% of the free cinnamate moieties are dimerized at a UV dose of 300 mJ cm(-2) . PVCin is also incorporated into a copolymer with N-isopropylacrylamide, which exhibits a characteristic change in hydrophilicity with temperature. The copolymer is selectively cross-linked through a mask, and reversible swelling of patterns with 30 μm resolution is demonstrated by submerging the film in water.

Dental implant failure remains a prevalent problem around the globe. The integration of implants at the interface of soft and hard tissues is complex and susceptible to instability and infections. Modifications to the surface of titanium implants have been developed to improve the performance, yet insufficient integration and biofilm formation remain major problems. Introducing nanostructures on the surface to augment the implant–tissue contact holds promise for facilitated implant integration; however, current coating processes are limited in their versatility or costs. We present a highly modular single-step approach to produce multicomponent porous bioactive nanostructured coatings on implants. Inorganic nanoparticle building blocks with complex compositions and architectures are synthesized in situ and deposited on the implants in a single step using scalable liquid-feed flame spray pyrolysis. We present hybrid coatings based on ceria and bioglass, which render the implant surfaces superhydrophilic, promote cell adhesion, and exhibit antimicrobial properties. By modifications to the bioglass/ceria nanohybrid composition and architecture that prevent biomineralization, the coating can instead be tailored toward soft tissue healing. The one-step synthesis of nano-architected tissue-specific coatings has great potential in dental implantology and beyond.

In this experimental study, flow boiling in mini/microtubes was investigated with surface enhancements provided by polyhydroxyethylmethacrylate (pHEMA) coatings (of ∼30 nm thickness) on inner microtube walls. Flow boiling heat transfer experiments were conducted on microtubes (with inner diameters of 249, 507 and 998 µm) having inner surfaces of pHEMA coatings, which increase heat transfer surface area, enable liquid replenishment upon bubble departure, provide additional nucleation sites, and serve for extending critical heat flux (CHF) enhancing boiling heat transfer. The de-ionized water was utilized as the working fluid in this study. pHEMA nanofilms of thickness ∼30 nm on the microtube walls were coated through an initiated chemical vapor deposition technique. Experimental results obtained from the coated microtubes were compared to their plain surface counterparts at two mass flux values (10 000 and 13 000 kg m−2 s−1). In comparison to the plain surface microtubes, the coated surfaces demonstrated an increase up to 24% and 109% in CHF and heat transfer coefficients, respectively. These promising results support the use of pHEMA coated microtubes/channels as a surface enhancement technique for microscale cooling applications.