The development of cost-effective cellulose fibers by utilizing agricultural residues have been attracted by the scientific community in the past few years; however, a facile production route along with minimal processing steps and a significant reduction in harsh chemical use is still lacking. Here, we report a straightforward ultrasound-assisted method to extract cellulose nanofiber (CNF) from fibrous waste sugarcane bagasse. X-ray diffraction-based crystallinity calculation showed 25% increase in the crystallinity of the extracted CNF (61.1%) as compared to raw sugarcane bagasse (35.1%), which is coherent with Raman studies. Field emission scanning electron microscopy (FE-SEM) images revealed thread-like CNF structures. Furthermore, we prepared thin films of the CNF using hot press and solution casting method and compared their mechanical properties. Our experiments demonstrated that hot press is a more effective way to produce high strength CNF films; Young’s modulus of the thin films prepared from the hot press was ten times higher than the solution casting method. Our results suggest that a combination of ultrasound-based extraction and hot press-based film preparation is an efficient route of producing high strength CNF films.

Oral drug delivery systems provide the most convenient, noninvasive, readily acceptable alternatives to parenteral systems. In the current work, eggshell-derived calcium carbonate (CaCO₃) nanoparticles were used to develop enteric drug delivery system in the form of tablets. CaCO₃nanoparticles were manufactured using top-down ball-milling method and characterized by X-ray diffractometry (XRD) and transmission electron microscopy (TEM) and loaded with 5-fluorouracil as a model drug. Tablets with varying CaCO₃core and binder compositions were fabricated and coated with Eudragit S100 or Eudragit L100. Suitability for enteric delivery of the tablets was tested by oral administration to rabbits and radiography. Radiograph images showed that the tablet remained in the stomach of the rabbit for up to 3 hours. Further modifications of these biomaterial-derived nanoparticles and the coatings will enable manufacturing of stable formulations for slow or controlled release of pharmaceuticals for enteric delivery.