A Dual-Crosslinked Hydrogel Based on Gelatin Methacryloyl and Sulfhydrylated Chitosan for Promoting Wound Healing.

The skin is the largest organ of the human body. Skin injuries, especially full-thickness injuries, are a major treatment challenge in clinical practice. Therefore, wound dressing materials with therapeutic effects have great practical significance in healthcare. This study used photocrosslinkable gelatin methacryloyl (GelMA) and sulfhydrylated chitosan (CS-SH) to design a double-crosslinked hydrogel for wound dressing. When crosslinked together, the resulting hydrogels showed a highly porous inner structure, and enhanced mechanical properties and moisture retention capacity. The compression modulus of the GelMA/CS-SH hydrogel (GCH) reached up to about 40 kPa and was much higher than that of pure GelMA hydrogel, and the compression modulus was increased with the amount of CS-SH. In vitro study showed no cytotoxicity of obtained hydrogels. Interestingly, a higher concentration of CS-SH slightly promoted the proliferation of cells. Moreover, the double-crosslinked hydrogel exhibited antibacterial properties because of the presence of chitosan. In vivo study based on rats showed that full-thickness skin defects healed on the 15th day. Histological results indicate that the hydrogel accelerated the repair of hair follicles and encouraged the orderly growth of collagen fibers in the wound. Furthermore, better blood vessel formation and a higher expression of VEGFR were observed in the hydrogel group when compared with the untreated control group. Based on our findings, GCH could be a promising candidate for full-thickness wound dressing.

lncRNA AFAP1-AS1 Promotes Migration and Invasion of Non-Small Cell Lung Cancer via Up-Regulating IRF7 and the RIG-I-Like Receptor Signaling Pathway.

BACKGROUND/AIMS: Accumulating evidence has highlighted the importance of long non-coding RNAs (lncRNAs) as competing endogenous RNAs (ceRNAs) in tumor biology. Among others, actin filament-associated protein 1 antisense RNA 1 (AFAP1-AS1) has been associated with non-small cell lung cancer (NSCLC). However, it remains unclear how AFAP1-AS1 participates in the development and progression of NSCLC. METHODS: The peripheral blood samples were collected from patients with NSCLC. White blood cell subsets were classified and levels of interleukin (IL)-10, IL-12 and IFN-γ in serum were measured. We then identified its target gene of AFAP1-AS1 via bioinformatics methods. NSCLC cell line with the highest expression of AFAP1-AS1, i.e. H1975 was selected for in vitro experiments. A series of inhibitor, vector and siRNA were employed to validate the regulatory mechanisms of AFAP1-AS1 in the development and progression of NSCLC. Cell proliferation was detected by MTT assay and EdU staining. Cell migration and invasion, and cell cycle and apoptosis were measured by transwell assay and flow cytometry, respectively. RESULTS: A high expression of AFAP1-AS1 was identified in NSCLC, alongside with a reduced level of IL-12 and increased levels of IL-10 and interferon (IFN)-γ. Aberrant expressions of AFAP1-AS1 were associated with pathological grade, TNM staging and metastatic potential of NSCLC. AFAP1-AS1 could activate interferon regulatory factor (IRF)7, the retinoid-inducible protein (RIG)-I-like receptor signaling pathway and Bcl-2 in vitro. Over-expression of AFAP1-AS1 promoted NSCLC cell proliferation, invasion and migration while inhibiting cell apoptosis. CONCLUSION: lncRNA AFAP1-AS1 promotes migration and invasion of non-small cell lung cancer via up-regulating IRF7 and the RIG-I-like receptor signaling pathway.

Chondroitin Sulfate Improves Mechanical Properties of Gelatin Hydrogel for Cartilage Regeneration in Rats.

Cartilage injury is a common disease in daily life. Especially in aging populations, the incidence of osteoarthritis is increasing. However, due to the poor regeneration ability of cartilage, most cartilage injuries cannot be effectively repaired. Even cartilage tissue engineering still faces many problems such as complex composition and poor integration of scaffolds and host tissues. In this study, chondroitin sulfate, one of the main components of extracellular matrix (ECM), is chosen as the main natural component of the material, which can protect cartilage in a variety of ways. Moreover, the results show that the addition of chondroitin sulfate improves the mechanical properties of gelatin methacrylate (GelMA) hydrogel, making it able to effectively bear mechanical loads in vivo. Further, chondroitin sulfate is modified to obtain the oxidized chondroitin sulfate (OCS) containing aldehyde groups via sodium periodate. This special group improves the interface integration and adhesion ability of the hydrogel to host cartilage tissue through schiff base reactions. In summary, GelMA/OCS hydrogel is a promising candidate for cartilage regeneration with good biocompatibility, mechanical properties, tissue integration ability, and excellent cartilage repair ability.

Isolation and identification of a novel vardenafil analogue, propoxy-vardenafil, found as an adulterant in a health supplement.

Background: A novel vardenafil analogue was detected from a health wine claimed to be anti-impotence during a special inspection in an online store. Methods: The unknown compound was found by using ultra-high performance liquid chromatography coupled to quadrupole time of flight mass spectrometry (UHPLC/Q-TOF MS). The characteristic product ions were similar to those of vardenafil. The UV spectrum of the compound closely mirrored that of vardenafil. The analogue underwent purification by semi-preparative HPLC and structurally identified by FT-IR and NMR analysis. Results: Based on the data, The structure of the analogue was characterized as 2-[2-propyloxy-5-(4-ethylpiperazin-1-yl)sulfonylphenyl]-5-methyl-7-propyl-3H-imidazo [5,15,1-f] [1,2,4]triazin-4-one, simplified as propoxy-vardenafil. Conclusion: To the best of our knowledge, the analogue has not been reported and is even only ninth vardenafil analogue, which was confirmed that a n-propyloxy group had replaced the ethoxy group on the aromatic ring of vardenafil. Therefore, It is essential to pay more attention to vardenafil analogues in the routine inspection of health supplements.

Hydrogel Development for Rotator Cuff Repair.

Rotator cuff tears (RCTs) are common in shoulder disease and disability. Despite significant advances in surgical repair techniques, 20-70% of patients still have postoperative rotator cuff dysfunction. These functional defects may be related to retear or rotator cuff quality deterioration due to tendon retraction and scar tissue at the repair site. As an effective delivery system, hydrogel scaffolds may improve the healing of RCTs and be a useful treatment for irreparable rotator cuff injuries. Although many studies have tested this hypothesis, most are limited to laboratory animal experiments. This review summarizes differences in hydrogel scaffold construction, active ingredients, and application methods in recent research. Efforts to determine the indications of hydrogel scaffolds (with different constructions and cargos) for various types of RCTs, as well as the effectiveness and reliability of application methods and devices, are also discussed.

Xylan-Derived Light Conversion Nanocomposite Film.

A new type of sustainable light conversion nanocomposite film was fabricated by using carboxymethyl xylan as matrix and xylan-derived carbon dots (CDs) as both light conversion regents and nano reinforcements. The results demonstrate that CDs can not only significantly enhance the mechanical strength of the nanocomposite film because of chemical reaction between CDs and carboxymethyl xylan, but also impart the film with excellent optical properties. With 1.92 wt% CDs, the tensile strength and elastic modulus of the film are increased by 114.3% and 90.7%, respectively. Moreover, the film has typical excitation and emission spectra, enabling the efficient absorption of UV and the conversion of UV to blue light. This xylan-derived light conversion nanocomposite film is expected to be used in agricultural planting and food packaging.

Correlation between pyrolysis behaviors of the components and the overall pyrolysates from pulping spent liquor.

The pyrolysis behaviors of the three major organic components of eucalyptus alkaline peroxide mechanical pulping (APMP) spent liquor including alkali lignin (AL), lignin-carbohydrate complexes (LCC), and polysaccharide (PLS) were studied with emphasis on the effect and contributions of components on the overall pyrolysates of APMP spent liquor solid (ASLS). Profound differences on product properties from each component pyrolysis were illustrated. The results indicated that the bio-oil during ASLS pyrolysis was mainly attributed to AL, while the bio-gas and char were mostly affected by PLS. Small molecule hydrocarbons released during ASLS pyrolysis mainly came from AL and LCC, and CO and CO2 mainly produced from PLS. As for bio-oils, AL generated the largest proportion of monomeric phenols and aromatic hydrocarbons (AHs), while PLS and LCC mainly contributed to the production of ketones, furans and acids. The correlation shown here is of interest for further studies on pulping spent liquor grading utilization.

Energy transfer between rare earths in layered rare-earth hydroxides.

Energy transfer between rare earths in layered rare-earth hydroxides (LRHs) is worth the intensive study because the hydroxyls that act as the bridge connecting the neighbouring rare earths would generate non-radiative transitions. This study focuses on the energy transfer in the intralayer and the adjacent layers of LRHs. A series of LEu x Tb1-x Hs (x = 0, 0.05, 0.2, 0.5, 0.8, and 0.95) was synthesized, the basal spacing (d basal) was adjusted from 8.3 to 46 Å through ion-exchange process, and unilamellar nanosheets were prepared through a delamination process. The luminescence behaviours of the samples demonstrated the following: (1) for the delaminated nanosheets, the quenching effect of both Eu3+ and Tb3+ was hardly observed. This implies that in the intralayer, the efficiency of energy transfer is extremely low, so that highly-concentrated co-doping does not influence the luminescence and by controlling the Eu/Tb molar ratio, white light can be obtained. (2) For small d basal, e.g., 27 Å, the fluorescence quenching of Tb3+ and Eu3+ was remarkable, while for large d basal, e.g., 46 Å, the emission of Tb3+ emerged and the self-quenching between Eu3+ ions weakened. (3) The energy transfer efficiency deceased with an increase in the distance between adjacent layers. In other words, either the energy transfer between Eu3+ and Tb3+ or the energy migration between Eu3+ ions was more efficient when they were located in adjacent layers than in intralayers even when they were the nearest neighbours.

Structure and luminescence behaviour of as-synthesized, calcined, and restored MgAlEu-LDH with high crystallinity.

Highly crystalline Eu(3+)-incorporated MgAl layered double hydroxides (LDHs) were synthesized by the homogeneous precipitation method. For the crystals as-prepared, after their calcination from 200-1000 °C, and, further, after restoration in a Na(2)CO(3) solution, the structural and luminescent changes were investigated for the first time. Eu(3+) ions with a coordination number of, probably, 8, were incorporated into the hydrotalcite layer, which led to a basal spacing (d(basal)) increase, microstrain formation, and crystalline morphology imperfections, while retaining the original lattice symmetry, R3[combining macron]m. In the deconstruction process due to calcination, the Eu(3+) ions restrained the formation of the spinel phase from the layered double oxide (LDO), but did not significantly change the memory effect, by which LDOs can convert to LDHs during the hydration process. For the reversible phase transformation between LDH and LDO, the morphology observation revealed that, in addition to the formation of pores on the surface, nano-slabs were formed, especially for the restored crystals. A layered phase with a d(basal) of 5.8 Å, due to bridging bidentate carbonates with the hydrotalcite layer, was formed in the calcination process at low temperature (300 °C) before the formation of LDO, but could not be restored to a large spacing. Typical (5)D(0) → (7)F(J) (J = 0-4) transitions of Eu(3+) at 579, 593, 615, 653, and 698 nm were observed in the photoluminescence spectra and the intensity of the dominating 615 nm band decreased with the LDH deconstruction and the formation of free water, and then increased with the formation of LDOs in the calcination process, and vice versa in the reconstruction process. The Eu(3+) ions had a probable 9- or 10-coordination mode in addition to the probable 8-coordination mode as the spinel phase appeared.

Intercalation of organic sensitisers into layered europium hydroxide and enhanced luminescence property.

Two organic sensitisers 4-biphenylcarboxylate (BPC) and terephthalate (TA) were intercalated into the gallery of layered europium hydroxide (LEuH). PL spectra tests indicated that BPC markedly enhanced the red luminescence of Eu(3+) due to efficient energy transfer between BPC and Eu(3+), forming a contrast to intercalated TA and the starting NO(3)(-) anions in the gallery. The energy level matching of the organic guests and Eu(3+) was also discussed to explain the energy transfer from sensitiser to Eu(3+).