Because this issue journal is dedicated to Gelatin, here we present a few applications of gelatin in the field of optics. Optics is the science that studies the production, propagation, interaction and detection of light. Various materials sensitive to light (photosensitive) are used for detection of light, such as photomultipliers, CCDs, crystals, two dimensional (2D) materials and more. Among the 2D materials, the most popular for several centuries has been gelatin based photographic emulsion, which records spatial distributions of light. More recently (1970), films made of Gelatin with Dichromate (DCG) and dyes have been used. We describe some characteristics and applications of these two photosensitive materials. We also describe examples where gelatin is used as a Relative Humidity (RH) sensor and in the fabrication of optical elements based on gelatin. This article is intended for researchers outside the optics community.

Polarimeters are useful instruments that measure concentrations of optically active substances in a given solution. The conventional polarimetric principle consists of measuring the rotation angle of linearly polarized light. Here, we present a novel polarimeter based on the study of interference patterns. A Mach–Zehnder interferometer with linearly polarized light at the input is used. One beam passes through the liquid sample and the other is a reference beam. As the linearly polarized sample beam propagates through the optically active solution the vibration plane of the electric field will rotate. As a result, the visibility of the interference pattern at the interferometer output will decrease. Fringe contrast will be maximum when both beams present a polarization perpendicular to the plane of incidence. However, minimum visibility is obtained when, after propagation through the sample the polarization of the sample beam is oriented parallel to the plane of incidence. By using different solute concentrations, a calibration plot is obtained showing the behavior of visibility.

We report a NVT molecular dynamic study of colloid-polymer mixtures under slit confinement. For this purpose, we are employing the Asakura-Oosawa model for studying colloidal particles, polymer coils, and hard walls as the external confining field. The colloid-polymer size ratio, q, is varied in the range $1⩾q⩾0.4$ and the confinement distance, H, in $10{\sigma }_c⩾H⩾3{\sigma }_c$ , ${\sigma }_c$ being the colloidal diameter. Vapor-liquid coexistence properties are assessed, from which phase diagrams are built. The obtained data fulfill the corresponding states law for a constant H when q is varied. The shift of the polymer and colloidal chemical potentials of coexistence follows a linear relationship with ${(H-{\sigma }_c)}^{-1}$ for $H\gtrsim 4{\sigma }_c$ . The confined vapor-liquid interfaces can be fitted with a semicircular line of curvature ${(H-{\sigma }_c)}^{-1}$ , from which the contact angle can be obtained. We observe complete wetting of the confining walls for reservoir polymer concentrations above and close to the critical value, and partial wetting for reservoir polymer concentrations above and far from it.

Aggregation of amyloid β peptides (AβP) forming fibrils and senile plaques is associated with numerous neurodegenerative disorders such as Alzheimer’s disease (AD). While there is no cure for AD, there is a possibility to retard and prevent the impairment. Inhibiting or interfering the aggregation of Aβ using fullerenes has shown to be a promising strategy to treat AD. The hydrophobic nature of fullerenes compromises its interaction with living cells inducing toxicity; thus, it is necessary to functionalize the molecule promoting its water solubility. In this study, we evaluate the structural and dynamical properties of six diethyl malonate C₆₀ fullerene adducts and its corresponding sodium salts in aqueous solution by molecular dynamics simulations. By means of radial distribution functions, hydrogen bond counting, density profiles, and solvent-accessible surface area, we demonstrate that the sodium malonate fullerene adducts have higher hydration ability while the corresponding diethyl malonate adducts show a hydrophobic tendency, forming self-aggregates. Additionally, we calculate the density profiles of ternary systems including amyloid β peptide 1–42 (AβP₄₂) monomers and found that bis-, tris-, tetra-, and pentaadducts of C₆₀ with disodium malonate addends interact with amyloid molecules, blocking partially their self-aggregation. These data support the understanding of previous reports that indicated the efficiency of sodium malonate fullerene as inhibitors of AβP aggregation. Additionally, we performe measurements in vitro by dynamic light scattering and found that fullerene aggregation is independent of incubation time.