Protein polymers are repetitive polypeptides produced by ribosomal biosynthetic pathways; furthermore, they offer emerging opportunities in drug and biopharmaceutical delivery. As for any polymer, biodegradation is one of the most important determinants affecting how a protein polymer can be utilized in the body. This study was designed to characterize the proteolytic biodegradation for a library of protein polymers derived from the human tropoelastin, the Elastin‐like polypeptides (ELPs). ELPs are of particular interest for controlled drug delivery because they reversibly transition from soluble to insoluble above an inverse phase transition temperature (Tt). More recently, ELP block copolymers have been developed that can assemble into micelles; however, it remains unclear if proteases can act on these ELP nanoparticles. For the first time, we demonstrate that ELP nanoparticles can be degraded by two model proteases and that comparable proteolysis occurs after cell uptake into a transformed culture of murine hepatocytes. Both elastase and collagenase endopeptidases can proteolytically degrade soluble ELPs. To our surprise, the ELP phase transition was protective against collagenase but not to elastase activity. These findings enhance our ability to predict how ELPs will biodegrade in different physiological microenvironments and are essential to develop protein polymers into biopharmaceuticals.

Using the polymer blending method, conductive materials and waterborne polyurethane (WPU) were mixed to fabricate conductive composite films for application in electromagnetic shielding. First, nitric acid was used to purify the multi-walled carbon nanotubes (MWCNT). Second, sodium dodecyl sulfate (SDS) was utilized to disperse the carbon nanotubes, and then they were mixed with 8 microm diameter and 2 mm long stainless steel fibers (SSF) in the WPU by the polymer blending method. Finally, the thickness of 0.25 mm of conductive composite film was fabricated by means of coating. According to the ASTM D4935-99 standard, a coaxial transmission line was used to measure the electromagnetic shielding effectiveness (EMSE) of conductive composite film within the range of 50 MHz approximately 3.0 GHz. Moreover, the influence of the prior and posterior dispersion of carbon nanotubes dispersed on electromagnetic shielding was dealt with in the paper. Results demonstrated that the conductive composite film, within 50 MHz approximately 3.0 GHz, fabricated by the 15 wt% of the multi-walled carbon nanotubes and 30 wt% of the stainless steel fibers can achieve the maximum of the electromagnetic shielding effectiveness, 34.86 dB, and its shielding effect, 99.9%.

This study examined the photodecomposition of volatile organic compounds (VOCs) using TiO2 catalyst fabricated by the Submerged Arc Nanoparticle Synthesis System (SANSS). TiO2 catalyst was employed to decompose volatile organic compounds and compare with Degussa-P25 TiO2 in terms of decomposition efficiency. In the electric discharge manufacturing process, a Ti bar, applied as the electrode, was melted and vaporized under high temperature. The vaporized Ti powders were then rapidly quenched under low-temperature and low-pressure conditions in deionized water, thus nucleating and forming nanocrystalline powders uniformly dispersed in the base solvent. The average diameter of the TiO2 nanoparticles was 20 nm. X-ray diffraction analysis confirmed that the nanoparticles in the deionized water were Anatase type TiO2. It was found that gaseous toluene exposed to UV irradiation produced intermediates that were even harder to decompose. After 60-min photocomposition, Degussa-P25 TiO2 reduced the concentration of gaseous toluene to 8.18% while the concentration after decomposition by SANSS TiO2 catalyst dropped to 0.35%. Under UV irradiation at 253.7 +/- 184.9 nm, TiO2 prepared by SANSS can produce strong chemical debonding energy, thus showing great efficiency, superior to that of Degussa-P25 TiO2, in decomposing gaseous toluene and its intermediates.

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