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Background Gastroretentive drug delivery system (GDDS) are novel systems that have been recently developed for treating stomach diseases. The key function of all GDDS systems is to control the retention time in the stomach. However, research into the bulk density or entanglement of polymers, especially regarding their effects on drug float and release times, is scarce. Methods In this research, we prepared the floating core-shell beads carrying tetracycline. The ratio of chitosan and xanthan gum in the shell layer was changed to modify polymer compactness. Tetracycline was encapsulated in the alginate core. Results Using scanning electron microscopy (SEM) techniques, we observed that the shell formulation did not change the bead morphology. The cross-sectional images showed that the beads were highly porous. The interaction between anionic xanthan gum and cationic chitosan made the shell layer dense, resisting to the mass transfer in the shell layer. Due to the high mass transfer resistance to water penetration, the longer float and delivery time were caused by the dense surface of the beads. The cell culture demonstrated that floating core-shell beads were biocompatible. Importantly, the beads with tetracycline showed a significant prolonged anti-bacterial effect. Conclusion Research results proved that the floating and releasing progress of core-shell beads can be well controlled by adjusting the shell layer formulation that could promote the function of gastroretentive drugs.

Three-dimensional (3D) printing technology is now widely used in biomedical developments. Especially, photo-curing systems provide high resolution and precision. The current goal of biomedical 3D printing technology is the printing of human organs, but the current commercial photo-curable materials generally have high mechanical strength that cannot meet the mechanical properties of the object to be printed. In this research, a gastric model was printed using a photo-curing 3D printing technique. To mimic the wrinkle pattern of human gastric tissue, cis-1,4 polyisoprene with different reactive diluents was mixed and identified a formulation that produced a print with human gastric softness. This research discussed the effect of the Young’s modulus of the material and elucidated the relationship between the degree of conversion rate and viscosity. After modifying the cis-1,4 polyisoprene surface from hydrophobic to hydrophilic, we then evaluated its adhesion efficiency for gastric mucin and the gastrointestinal-inhabiting bacterium Helicobacter pylori.

The present study focused on the development of electric stimuli drug release carrier based on transition metal dicgalcogenides. First, tungsten disulfide (WS2) was exfoliated and functionalized using thiol chemistry with various thiol-terminated ligands such as thioglycolic acid (TGA), mercaptosuccinic acid (MSA), and 2-ethanethiol (2ET). The exfoliated WS2 underwent non-covalent coating with an electrically conductive polypyrrole (PPy) for functionalization, of which MSA-WS2-PPy achieved the highest 5-FU (anticancer drug) loading. An electrically-stimulated drug release experiment showed that TGA-WS2-PPy achieved a higher drug release (90%) than MSA-WS2-PPy (70%) and 2ET-WS2-Ppy (35%). The TGA-WS2-PPy exhibited swelling/recombination between PPY and MSA-WS2 substrate under electrical stimulation, resulting in the highest 5-FU release. From the MTT assay result, there was no significant toxicity observed for TGA-WS2-PPy-FU on HaCaT cells, indicating the biocompatibility of TGA-WS2-PPy-FU in the absence of electrical stimulation. However, HaCaT cells died when incubated with TGA-WS2-PPy-FU under electrical stimulation. Finally, Raman mapping studies for TGA-WS2-PPy drug release in the skin of nude mice demonstrated that the carrier penetrated deeper into the skin of the mice while other systems failed to exhibit significant effects under electrical stimulation. The present study offers a novel approach in developing a non-invasive electrically-stimulated drug release system based on WS2 and an externally-controlled delivery model.

Iron/copper composite particles were synthesized by a chemical reduction method and then used as the anode material for a rechargeable alkaline battery. The particle size and structure of the samples were characterized by SEM and XRD. Their electrochemical performance was also studied. The results showed that the iron/copper composite prepared by this method is nanosized. Copper improves the electron transfer between particles, and the nanosized iron/copper composite not only has a high electrochemical capacity of up to 800 mAh g −1 (Fe to Fe(III)), but also has an excellent rate-capacity performance at a current density of 3200 mA g −1 . Compared with the iron nanoparticle without copper, the iron/copper composite sample maintains a smaller particle size during electrochemical cycling, and therefore improves the cycling stability of the iron electrode.

Iron/carbon-black composite nanoparticles were synthesized by chemically reducing the iron salt mixing with carbon black by adding NaBH4 in the aqueous solution. Carbon-black particles, with a mean particle size of approximately 40 nm, function as the nucleation cores for iron deposition. Additionally, core–shell iron composite particles are observed to be 30–100 nm with spherical sharp. At the first time discharge, the iron/carbon-black composite nanoparticle discharged 1200 mAh g−1(Fe) at plateau one and 400 mAh g −1 at plateau two at a high current density of 200 mA g −1 (Fe). The capacity is larger than the theoretical value, which is attributed to the formation of iron hydride (FeHx) while the iron was reduced by NaBH4, followed the hydrogen reaction as an active material while the battery discharge occurs. In further cycles, the iron/carbon-black composite iron electrode shows a good reversibility of about 600 mAh g −1 (Fe) when the nickel–iron battery operated between 1.65 and 0.8 V. XRD analysis results indicate that the carbon black in the core of the iron/carbon-black composite enhances the reduction/oxidation reactions of iron, as achieved by the carbon black forming an enhanced electronic conductive network while iron is discharged as the insulator species such as Fe(OH)2 and Fe3O4. SEM images reveal that the iron/carbon-black composite keeps particle sizes smaller than 300 nm during the electrode cycling, indicating that carbon black also acts as the nucleation cores for the dissolution–deposition of iron.

For the preparation of polymer particles by free radical, stabilizers are usually present in the reaction mixture to maintain the separation of particles from each other. Polyvinylpyrrolidone (PVP) is one the hydrophilic polymers that has been extensively used as the stabilizer in the polymerization system employing a polar solvent or solvent mixture as the continuous phase. As shown in the present study, the presence of PVP in the later steps could significantly influence the hydrophobic property of partially porous poly(styrene–divinylbenzene) (PS–DVB) particles, prepared by the method of multistep swelling and polymerization involving the use of polymeric porogens. The association of PVP molecules on the particle surface reduced the hydrophobicity and consequently the capability of particles for biological applications. For the reversed-phase liquid chromatography of penicillin G and its enzymatic hydrolysis product, particles prepared without PVP led to an enhancement in both retention and resolution, compared with particles resulting from the use of PVP. Results from lipase immobilization on these particles also showed that the presence of PVP could shield the hydrophobic groups on the particle surface and then reduce the efficiency of enzyme immobilization. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1818–1824, 2003

A TiO2 film was prepared on indium tin oxide (ITO)/glass by aqueous solution deposition (ASD) with precursors of ammonium hexafluoro-titanate and boric acid at 40 °C. The photocatalysis of annealed TiO2 film increases with increasing growth time and decreases with increasing growth times longer than 60 min. A ZnO nanotip array was prepared on ZnO seed layer/TiO2 film/glass by aqueous solution deposition with precursors of zinc nitrate and ammonium hydroxide at 70 °C. The photocatalysis of ASD-ZnO/ASD-TiO2 film/ITO glass can be better than that of P25.

Partially porous poly(styrene-divinylbenzene) (PS-DVB) particles in the micron size range were prepared by the method of multistep swelling and polymerization involving the use of polymeric porogens. Polystyrene (PS) seeds prepared by dispersion polymerization were expanded in particle size by absorbing styrene and initiator, and then polymerized to form polymeric porogen particles. The newly synthesized PS chains served as the porogens of the PS-DVB particles, resulting from the copolymerization of styrene and divinylbenzene in the swollen polymeric porogen particles. PS-DVB particles with a specific surface area of up to 34 m 2 /g and a pore volume of up to 0.15 cm 3 /g were obtained. The average pore diameter of PS-DVB particles was in the range of 15-24 nm. An increasing amount of toluene used in the copolymerization step increased the pore volume and specific surface area. Lipase from Candida rugosa was immobilized on the prepared PS-DVB by physical adsorption. The optimum temperature for enzymatic activity was increased and the thermal deactivation of enzyme in organic solvent was slowed down by the immobilization. However, compared with soluble enzyme, the immobilized lipase on PS-DVB retained a less activity after the first stage deactivation, suggesting a possible change in the conformation of enzyme molecule by immobilization.

Poly(2-methacryloyloxyethyl phosphorylcholine) (pMPC) was grafted onto the surface of a silicon rubber (SR) membrane (pMPC-SR) by plasma induced grafted copolymerization (PIP). Argon plasma was used to activate the SR surfaces. Determination was also made of the influences of grafted copolymerization reaction time, reaction temperature, and monomer concentration on polymerization yield. The surface properties of SR were characterized by ATR-FTIR, ESCA, and SEM. In those analyses the ATR-FTIR spectra indicated that the pMPC grafted onto the SR surface at 1720 and 3300 cm(-1). The elemental composition and different carbon bindings on the surface of the SR were examined by ESCA. An increasing P1s/C1s value g was obtained in the grafted polymerization yield with a concentration of 0.05-0.5M of MPC in the isolated ethanol solution. The surface morphologies of pMPC-SR differed more than those of control and Ar plasma treated surfaces. The difference could have been caused by the homogeneous graft polymerization of pMPC onto the SR membrane. In the biological analyses, protein adsorption on pMPC-SR surfaces was reduced. The reduced level increased with an increase in the pMPC grafted amount. The epithelial cell attachment and growth onto these samples were suppressed. The blood compatibility for a series of pMPC-SR surfaces was examined by platelet adhesion. Blood platelet morphologies in contact with the high ratio of pMPC-SR surfaces were maintained, meaning that in this case the release reaction for platelets never occurred. Consequently, the high amount of pMPC-SR surface had excellent blood compatibility, further suggesting that prevention of adhesion, activation of platelets, and adsorption of blood protein could be achieved.

A method for producing various surfaces of silicone rubber membrane (SR) was developed in this study by grafting various amounts of poly(2-hydroxy ethyl methacrylate) (pHEMA) onto SR by plasma-induced grafted polymerization (PIP) as a homobifunctional membrane. The elemental composition and different carbon bindings on the surface of SR were examined by electron spectroscopy for chemical analysis with the amount of O1s/C1s being approximately 0.7 at 1 min, 60 W, 200 mTorr of Ar-plasma treatment. The peroxide group introduced on SR was measured via 1,1-diphenyl-2-picrylhydrazyl (DPPH) and the amount of 6.85 x 10(-8) mol cm-2 reached optimum value at 1 min of Ar-plasma treatment. After Ar-plasma treated SR, the peroxide group (33D peak) was introduced on the surface of SR by negative spectra of secondary ion mass spectroscopy analysis, whereas ester groups (72D peak) were observed for pHEMA-grafted SR. For the in vitro test, the influence of various surfaces of SR on attachment and growth of rabbit corneal epithelial cells (CEC) was studied by cell culture assay. These results indicated that 56-150 micrograms cm-2 of pHEMA grafted onto SR were suitable values for attachment and growth of CEC. On the contrary, the large grafted amounts (500-1650 micrograms cm-2) of pHEMA on SR were insufficient for attachment and growth of CEC. For the in vivo test, the migration of CEC from host cornea to implant was investigated by slit lamp microscopy. The experimental results indicated that SRs grafted with pHEMA were completely covered with CEC 3 weeks after implantation of the membranes into the host cornea. These results provide a valuable reference for developing an artificial cornea.

Polyacrylic acid (pAA) was introduced onto Ar-plasma treatment silicone rubber (SR) membrane surfaces by plasma-induced grafted polymerization. Collagen (type III) was also linked with the carboxylic group of pAA grafted onto the SR surface via a carbodiimine agent to obtain a secondary structure of SR. The SR surface properties were characterized by ATR-FTIR, ESCA, contact angle, and SEM. The biocompatibility of the SR surface was evaluated by a culture of cornea epithelial (CE) cells. Subsequently, 75-450 micrograms cm-2 of pAA were obtained on the SR surfaces under different reactive conditions; 3-12 micrograms cm-2 of collagen were linked on modified surfaces of SR. Moreover, ATR-FTIR and ESCA were utilized to confirm the proceedings of these reactions. The hydrophility of the modified SR was measured by a contact angle meter. The values of contact angle for SR grafted with pAA were approximately 45-50 degrees; a 50-55 degrees contact angle on pAA-g-SR to be further linked with collagen was subsequently obtained. Moreover, the influence of surface properties toward migration, growth and attachment of CE cells on the modified surfaces was also examined. Here, untreated SR was used as a control. Experimental results indicated that the number of CE cells attached onto the controlled SR was negligible. The attachment of cells onto pAA-grafted surfaces was clearly observed and peusopoda occurred; however, cell growth was depressed. This depression may have been caused by the acid environment of the pAA-grafted membrane. Nevertheless, both cell attachment and growth onto collagen-linked surfaces were significant. In addition, the morphology of the cells attached onto this surface was considered normal for primary cells. Collagen introduced on the SR surface was not denatured, i.e the natural properties of collagen were maintained. The results obtained in this study will hopefully lead to the successful development of modified SR for clinical applications.

The deposition of amorphous InGaZnO4 (a-IGZO) semiconductor film, via a sputtering process, has been demonstrated in the literature. In this paper, we present a solution method as an alternative to obtain this semiconducting film. The dispersible IGZO colloids is formed first by co-precipitation of precursors, followed by hydrothermal treatment at 200°C for 1 hour and using CMC as the dispersion agent. The crystalline colloid would become amorphous when it was heated at above 250°C. The TFT structure was made by growing a dielectric silica layer using the CVD method, a metal layer using the sputtering method, and an active IGZO layer using the solution method. This device exhibits low operating voltage, the mobility is about 2cm2V−1s−1 and the Ion/Ioff ratio is 104. Further improvement in processing is needed.

The primary objective of this study is to prepare a highly biocompatible polymer membrane by surface modification and to further develop an artificial cornea. Novel heterobifunctional membranes prepared by grafting different functional polymers onto silicone rubber membranes were achieved. In this work, we report preparation and surface characterization of the heterobifunctional membranes, and their biological analysis (in vitro and in vivo studies). Based on the biological analysis, the heterobifunctional membrane exhibits high potential to be used as artificial cornea.

It was demonstrated that continuous copper films could be grown onto printed lines of nanosized silver colloids. These silver colloids, with an average size of ∼55 nm, were printed on alumina substrates by either an ink-jet printer or a felt-tip pen and then served as a seed layer for subsequent electroless copper plating. A complete copper film could be obtained in less than 10 min when the surface density of silver particles was greater than 1.5 × 10 9 cm -2 and an appropriate plating solution to produce a mean copper growth rate of 7.2 μm h -1 . After 30 min of growth and a resulting film thickness of ∼3.6 μm, the measured electric resistivity of the lines was about 1.8 X 10 -6 Ω cm, being very close to bulk copper. In addition, the measured peel adhesion strength between the deposited copper film and the Al 2 Ο 3 substrate was larger than 6 kg/cm.