Biomineralization is a process in which specialized cells secrete and deliver inorganic ions into confined spaces limited by organic matrices or scaffolds. Chicken eggshell is the fastest biomineralization system on earth, and therefore, it is a good experimental model for the study of biomineralization. Eggshell mineralization starts on specialized dispersed sites of the soft fibrillar eggshell membranes referred to as negatively charged keratan sulfate mammillae. However, the rest of the fibrillar eggshell membranes never mineralizes, although 21% of their amino acids are acidic. We hypothesized that, relative to the mammillae, the negatively charged amino acids of the fibrillar eggshell membranes are not competitive enough to promote calcite nucleation and growth. To test this hypothesis, we experimentally increased the number of negatively charged carboxylate groups on the eggshell membrane fibers and compared it with in vitro calcite deposition of isolated intact eggshell membranes. We conclude that the addition of poly-carboxylated groups onto eggshell membranes increases the number of surface nucleation sites but not the crystal size.

A phosphorylated chitin (Chi-P) derivative was synthesized and its chemical structure was verified with Fourier-transform infrared spectroscopy (FTIR), elemental analysis, and thermogravimetric techniques (TGA). The influence of Chi-P used as a solid template through in vitro electrocrystallization (EC) supported on an indium zinc oxide (ITO) surface on the growth of calcium carbonate (CaCO₃) was studied. CaCO₃ crystals through EC essays were also compared with crystals obtained with the gas diffusion (GD) method. Scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDS), chronopotentiometry, Raman, and powder X-ray diffractometry (XRD) characterized all resultant inorganic particles. Our findings revealed that the EC method selectively controlled the coexistence of truncate calcite and the metastable phase of vaterite. The crystals’ morphology reflects the electrostatic interaction of phosphate moieties from Chi-P onto CaCO₃ crystals through both EC and GD crystallization methods. We believe that the EC method represents a viable electrochemical approach for studying different inorganic minerals and could be useful as an in vitro classical crystallization method for the design of advanced inorganic materials with desirable shapes and properties.

An electrospinning method was used for the preparation of an in situ composite based on Ni₂P nanoparticles and carbon fiber (FC). The material was tested for the first time against direct glucose oxidation reaction. The Ni₂P nanoparticles were distributed homogeneously throughout the carbon fibers with a composition determined by thermogravimetric analysis (TGA) of 40 wt% Ni₂P and 60 wt% carbon fiber without impurities in the sample. The electrochemical measurement results indicate that the GCE/FC/Ni₂P in situ sensor exhibits excellent catalytic activity compared to the GCE/Ni₂P and GCE/FC/Ni₂P ex situ electrodes. The GCE/FC/Ni₂P in situ sensor presents a sensitivity of 1050 µAmM⁻¹cm⁻² in the range of 5–208 µM and a detection limit of 0.25 µM. The sensor was applied for glucose detection in artificial saliva, with a low interference observed from normally coexisting electroactive species. In conclusion, our sensor represents a novel and analytical competitive alternative for the development of non-enzymatic glucose sensors in the future.

In our crystallization experiments, the influence of alginate from Chilean Lessonia nigrescens and functionalized multi-walled carbon nanotubes (MWCNTs) was tested through electrocrystallization (EC) and gas diffusion (GD) methods on the crystal growth of calcium carbonate (CaCO₃) and their possible stabilization of proto-structures in amorphous CaCO₃ (ACC) state through pre-nucleation clusters (PNC) essays with automatic potentiometric titrations were performed. CaCO₃ crystals obtained in the in vitro above-mentioned crystallization systems were characterized by scanning electron microscope (SEM), energy-dispersive X-ray spectrometry (EDS) and powder X-ray diffractometer (XRD). Our experimental findings showed that ALG and functionalized MWCNTs stabilized truncated and agglomerated vaterite-like particles through GD and EC methods. While, on the other hand, we obtained qualitative information about induction or inhibition of CaCO₃ nucleation that was provided by potentiometric titrations.

Potential drug-eluting scaffolds of electrospun poly(acrylic acid-co-styrene sulfonate) P(AA-co-SS) in clonogenic assays using tumorigenic gastric and ovarian cancer cells were tested in vitro. Electrospun polymer nanofiber (EPnF) meshes of PAA and PSSNa homo- and P(AA-co-SS) copolymer composed of 30:70, 50:50, 70:30 acrylic acid (AA) and sodium 4-styrene sulfonate (SSNa) units were performed by electrospinning (ES). The synthesis, structural and morphological characterization of all EPnF meshes were analyzed by optical and electron microscopy (SEM-EDS), infrared spectroscopy (FTIR), contact angle, and X-ray diffraction (XRD) measurements. This study shows that different ratio of AA and SSNa of monomers in P(AA-co-SS) EPnF play a crucial role in clonogenic in vitro assays. We found that 50:50 P(AA-co-SS) EPnF mesh loaded with antineoplastic drugs can be an excellent suppressor of growth-independent anchored capacities in vitro assays and a good subcutaneous drug delivery system for chemotherapeutic medication in vivo model for surgical resection procedures in cancer research.