Gelatin nanofibers (GNs) prepared by electrospinning were cross-linked with glutaraldehyde vapor to improve their water-resistant ability. After cross-linking treatment, the form of the fibers expressed no substantial change, but the average diameter of the fibers increased with increasing cross-linking time. The swelling induced by the moisture during the cross-linking process was moderated when the cross-linking time reached 45 min. The contact angle measurements confirmed that the electrospun gelatin fibers were more hydrophilic than the gelatin film (GF). Increasing the cross-linking time did not alter the hydrophilic properties of the gelatin fibers. The cell compatibility was evaluated based on 3-(4,5-dimethylthiazolyl)-2,5-diphenyltetrazolium bromide (MTT) assay, scanning electron microscope and confocal microscope observations, and Western blot analysis by culturing MG-63 cells on the GFs and GNs. The nanofibrous structure fabricated by an electrospinning technique was found to enhance cell adhesion and proliferation. This process is a cost-effective simulation of GN structures’ promising applications on scaffold preparation for tissue engineering.

The issue of micro-plastics is becoming more and more important due to their ubiquity and the harm they cause to the human body. Therefore, evaluating the biological–physical interaction of micro-plastics with health cells has become the focus of many research efforts. This study focuses on the movement mode and low concentration detection development for micro-plastics in surface plasmon resonance (SPR). Firstly, 20-micrometer micro-plastics were prepared by grinding and filtering, and the movement mode was explored; then, the characteristics were investigated by SPR. Chromatographic analysis showed that the surface charge of micro-plastics dominated the elution time, and estrogen receptors (ERs) played a supporting role. A difference of micro-plastics in SPR sensorgram was observed, inferring the micro-plastics’ movement in rolling mode on the ERs. Characteristics analysis indicated that the low particle number of micro-plastics on SPR showed a linear relationship with the response unit (RU). When ERs were immobilized on the biosensor, the force of the binding of micro-plastics to ERs under an ultra-low background was equivalent to the dissociation rate constant shown as follows: PS (0.05 nM) > PVC (0.09 nM) > PE (0.14 nM). The ELISA-like magnetic beads experiment verified the specificity between ERs and micro-plastics. Therefore, by using the SPR technique, a biological-derived over-occupation of PS was found via higher binding force with ERs and longer retention time. In the future, there will be considerable potential for micro-plastics issues, such as identification in natural samples, biomarking, real-time detection in specific environments/regions and human health subject.