Enzymes are excellent catalysts in many applications due to their biocompatibility, low energy consumption, unique selectivity, and mild reaction condition. However, some disadvantages limit the usage of enzymes in end uses, such as low stabilities and difficult recovery. In order to overcome these disadvantages, enzyme immobilization was developed. Among various kinds of substrates for attaching enzyme, cellulose and its derivatives are one of the ideal matrixes because they are low cost, nontoxic, renewable, biodegradable, and biocompatible. In this review, we summarize recent progress in the research of enzyme immobilization on cellulose matrixes.

To accelerate the high value-added usage of agricultural residue, cellulose and cellulose nanofibers (CNFs) were extracted from wheat straw and then formed into all-cellulose nanocomposite films. The acid–alkali method (AM) and the extraction method (EM) were respectively adopted to prepare wheat straw cellulose (WSC), and the TEMPO oxidation method was used to extract CNFs. The nanocomposite films were fabricated by dissolving WSC and adding different CNF contents of 0.0, 0.5, 1.5, and 3.0%. There was a better miscibility for the all-cellulose nanocomposite film prepared by EM (Composite-E) compared to that for the all-cellulose nanocomposite film prepared by AM (Composite-A). Composite-E also showed a better optical transparency than Composite-A. The thermal stability of the two RWSCs presented contrary results when the CNFs were added, indicating a higher thermal stability for Composite-E than for Composite-A. This should have determined the properties of the films in which Cellulose I and Cellulose II coexisted for the all-cellulose nanocomposite films, and the forming mechanism of Cellulose II and crystallinity were determined by the cellulose-extracting method. X-ray diffraction (XRD) and Fourier-transform infrared (FT-IR) spectroscopy also showed that there was more Cellulose I in Composite-E than in Composite-A. The results are expected to enrich the data for deep processing of agricultural residues.

Hemocompatibility remains a challenge for injectable and/or implantable medical devices, and thromboresistant coatings appear to be one of the most attractive methods to down-regulate the unwanted enzymatic reactions that promote the formation of blood clots. Among all polymeric materials, polyurethanes (PUs) are a class of biomaterials with excellent biocompatibility and bioinertness that are suitable for the use of thromboresistant coatings. In this work, we investigated the thermal and physico-mechanical behaviors of ester-based and ether-based PU films for potential uses in thromboresistant coatings. Our results show that poly(ester urethane) and poly(ether urethane) films exhibited characteristic peaks corresponding to their molecular configurations. Thermal characterizations suggest a two-step decomposition process for the poly(ether urethane) films. Physico-mechanical characterizations show that the surfaces of the PU films were hydrophobic with minimal weight changes in physiological conditions over 14 days. All PU films exhibited high tensile strength and large elongation to failure, attributed to their semi-crystalline structure. Finally, the in vitro clotting assays confirmed their thromboresistance with approximately 1000-fold increase in contact time with human blood plasma as compared to the glass control. Our work correlates the structure-property relationships of PU films with their excellent thromboresistant ability.