This paper describes the fabrication of microfluidic cloth-based analytical devices (μCADs) using a simple wax patterning method on cotton cloth for performing colorimetric bioassays. Commercial cotton cloth fabric is proposed as a new inexpensive, lightweight, and flexible platform for fabricating two- (2D) and three-dimensional (3D) microfluidic systems. We demonstrated that the wicking property of the cotton microfluidic channel can be improved by scouring in soda ash (Na(2)CO(3)) solution which will remove the natural surface wax and expose the underlying texture of the cellulose fiber. After this treatment, we fabricated narrow hydrophilic channels with hydrophobic barriers made from patterned wax to define the 2D microfluidic devices. The designed pattern is carved on wax-impregnated paper, and subsequently transferred to attached cotton cloth by heat treatment. To further obtain 3D microfluidic devices having multiple layers of pattern, a single layer of wax patterned cloth can be folded along a predefined folding line and subsequently pressed using mechanical force. All the fabrication steps are simple and low cost since no special equipment is required. Diagnostic application of cloth-based devices is shown by the development of simple devices that wick and distribute microvolumes of simulated body fluids along the hydrophilic channels into reaction zones to react with analytical reagents. Colorimetric detection of bovine serum albumin (BSA) in artificial urine is carried out by direct visual observation of bromophenol blue (BPB) colour change in the reaction zones. Finally, we show the flexibility of the novel microfluidic platform by conducting a similar reaction in a bent pinned μCAD.

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Scaffolds have been utilized in tissue regeneration to facilitate the formation and maturation of new tissues or organs where a balance between temporary mechanical support and mass transport (degradation and cell growth) is ideally achieved. Polymers have been widely chosen as tissue scaffolding material having a good combination of biodegradability, biocompatibility, and porous structure. Metals that can degrade in physiological environment, namely, biodegradable metals, are proposed as potential materials for hard tissue scaffolding where biodegradable polymers are often considered as having poor mechanical properties. Biodegradable metal scaffolds have showed interesting mechanical property that was close to that of human bone with tailored degradation behaviour. The current promising fabrication technique for making scaffolds, such as computation-aided solid free-form method, can be easily applied to metals. With further optimization in topologically ordered porosity design exploiting material property and fabrication technique, porous biodegradable metals could be the potential materials for making hard tissue scaffolds.

Bioactive glasses (BGs) based on 50SiO2‐45CaO‐5P2O5 system doped with 1, 5, and 10 mol% CuO or Ag2O were separately synthesized using quick alkali sol‐gel method. Scanning electron microscope (SEM) analysis of the samples confirmed the formation of nano‐sized BGs, whereas Fourier transform infrared (FTIR) spectra showed characteristic peaks for silica and phosphate groups. X‐ray diffraction (XRD) pattern of the heat‐treated (700°C) samples revealed the presence of crystalline metallic silver phase in all Ag‐doped samples, while the XRD pattern of Cu‐doped and control sample (50Si‐45CaO‐5P2O5) also heat‐treated at 700°C confirmed their amorphous nature. Ultraviolet–visible (UV‐Vis) studies along with Energy‐dispersive X‐ray spectroscopy (EDX) analysis confirmed the successful incorporation of Cu and Ag in bioglass. Antibacterial properties of the synthesized BGs were investigated by quantitative viable count method, and the results were related to the ion release profiles of the samples studied by flame atomic absorption spectroscopy (FAAS). Fast initial release of Ag observed in this study makes Ag‐doped BG a better rapid bacteria‐killing agent than Cu‐doped BG, which exhibited a prolonged release of ions, suggesting that it may be a better candidate for long‐term antibacterial protection.

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