Surface treatments can be used to enhance adhesion of native pollen in polymers, optimizing pollen performance as a reinforcing filler.

Aptamer and antibody mediated adhesion is central to biological function and valuable in the engineering of “lab on a chip” devices. Single molecule force spectroscopy using optical tweezers enables direct non-equilibrium measurement of these non-covalent interactions for three peptide aptamers selected for glass, polystyrene, and carbon nanotubes. A comprehensive examination of the strong attachment between anti-fluorescein 4-4-20 and fluorescein was also carried out using the same assay. Bond lifetime, barrier width, and free energy of activation are extracted from unbinding histogram data using three single molecule pulling models. The evaluated aptamers appear to adhere stronger than the fluorescein antibody under no- and low-load conditions, yet weaker than antibodies at loads above ~25pN. Comparison to force spectroscopy data of other biological linkages shows the diversity of load dependent binding and provides insight into linkages used in biological processes and those designed for engineered systems.

A simple solution processed layer-by-layer approach was used to immobilize metal nanoparticles (NPs) on the surface of ragweed pollen exine to obtain multifunctional particles with significant surface-enhanced Raman scattering (SERS), two-photon excited fluorescence, and enhanced adhesion properties. The rugged pollen exine was functionalized with an amine terminated silane and then treated with Ag or Ag@SiO NPs that were electrostatically attached to the exterior of the pollen by incubation in an NP solution of the appropriate pH. Nanoparticle agglomeration on the pollen gives rise to broadband near infrared (NIR) (785-1064 nm) plasmonic activity, and strong SERS signals from benzenedithiol deposited on NP-pollen composite particles were observed. In addition to SERS activity, the AgNP coating provides a twofold increase in the adhesive properties of the RW pollen exine on a silicon substrate, leading to a robust, adhesive, broadband NIR excitable SERS microparticle.

Pollen grains have the potential to be effective plant-based biorenewable fillers in polymer matrices due to their high modulus, strength, chemical stability, and unique nanoscale architectures. In this work, we present evidence for the effectiveness of pollen as a reinforcing filler in epoxy matrices, characterized as a function of pollen loading and surface treatment. Composites prepared with unmodified native defatted ragweed pollen (D) displayed decreased mechanical properties and increasing glass transition temperatures (T g ) with increasing pollen loading. A soft interphase was observed to form around native pollen that is likely due to incompletely cured epoxy, resulting in decreased mechanical properties. However, pollen treated via a common base-acid (BA) surface preparation was a load-bearing, toughening filler in epoxy composites, displaying simultaneously increased tensile strength (by 47%) and strain at break (by 70%), improving interfacial morphology (absence of soft interphase), and increasing T g at 10 wt% pollen loading. Elastic modulus improves by 14% with 10 wt% BA pollen loading, and fitting of the modulus with the Halpin-Tsai and Counto models results in an estimated pollen exine modulus of 8 GPa, the first reported pollen modulus measurement from composite studies. Improvements in mechanical properties in BA pollen versus D pollen likely result due to crosslinks with the epoxy matrix due to the presence of protic functional groups (hydroxyls or carboxyls) on the BA surface. BAtreated ragweed pollen shows promise as a toughening filler for imparting higher strength to polymers without increasing mass.