Helicobacter pylori, a human pathogen with a high global prevalence, is the causative pathogen for multiple gastrointestinal diseases, especially chronic gastritis, peptic ulcers, gastric mucosa-associated lymphoid tissue lymphoma, and gastric malignancies. Antibiotic therapies remain the mainstay for H. pylori eradication; however, this strategy is hampered by the emergence and spread of H. pylori antibiotic resistance. Exploring the mechanistic basis of this resistance is becoming one of the major research questions in contemporary biomedical research, as such knowledge could be exploited to devise novel rational avenues for counteracting the existing resistance and devising strategies to avoid the development of a novel anti-H. pylori medication. Encouragingly, important progress in this field has been made recently. Here, we attempt to review the current state and progress with respect to the molecular mechanism of antibiotic resistance for H. pylori. A picture is emerging in which mutations of various genes in H. pylori, resulting in decreased membrane permeability, altered oxidation-reduction potential, and a more efficient efflux pump system. The increased knowledge on these mechanisms produces hope that antibiotic resistance in H. pylori can ultimately be countered.

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The combination of high strength, great toughness, and high heat resistance for polymeric materials is a vital factor for their practical applications. Unfortunately, until now it has remained a major challenge to achieve this performance portfolio because the mechanisms of strength and toughness are mutually exclusive. In the natural world, spider silk features the combination of high strength, great toughness, and excellent thermal stability, which are governed by the nanoconfinement of hydrogen-bonded β-sheets. Here, we report a facile bioinspired methodology for fabricating advanced polymer composite films with a high tensile strength of 152.8 MPa, a high stiffness of 4.35 GPa, and a tensile toughness of 30.3 MJ/m in addition to high thermal stability (69 °C higher than that of the polymer matrix) only by adding 2.0 wt % of artificial β-sheets. The mechanical and thermostable performance portfolio is superior to that of its counterparts developed to date because of the nanoconfinement and hydrogen-bond cross-linking effects of artificial β-sheets. Our study offers a facile biomimetic strategy for the design of integrated mechanically robust and thermostable polymer materials, which hold promise for many applications in electrical devices and tissue engineering fields.

Expanding the application range of flame-retardant polymer biocomposites remains a huge challenge for a sustainable society. Despite largely enhanced flame retardancy, until now the resultant poly(lactic acid) (PLA) composites still suffer reduced tensile strength and impact toughness due to improper material design strategies. We, herein, demonstrate the design of a green flame retardant additive (ammonium polyphosphate (APP)@cellulose nanofiber (CNF)) via using the cellulose nanofibers (CNFs) as the green multifunctional additives hybridized with ammonium polyphosphate (APP). The results show that PLA composite with 5 wt % loading of APP@CNF can pass the UL-94 V-0 rating, besides a high limited oxygen index of 27.5%, indicative of a significantly enhanced flame retardancy. Moreover, the 5 wt % of APP@CNF enables the impact strength (σ i ) of the PVA matrix to significantly improve from 7.63 to 11.8 kJ/m 2 (increase by 54%), in addition to a high tensile strength of 50.3 MPa for the resultant flame-retardant PLA composite. The enhanced flame retardancy and mechanical strength performances are attributed to the improved dispersion of APP@CNF and its smaller phase size within the PLA matrix along with their synergistic effect between APP and CNF. This work opens up a facile innovative methodology for the design of high-performance ecofriendly flame retardants and their advanced polymeric composites.

A new intumescent flame retardant (IFR) system consisting of ammonium polyphosphate (APP) and charing-foaming agent (CFA) and a little organic montmorillonite (OMMT) was used in low-density polyethylene (LLDPE)/ethylene-vinyl acetate (EVA) composite. According to limiting oxygen index (LOI) value and UL-94 rating obtained from this work, the reasonable mass ratio of APP to CFA was 3 : 1, and OMMT could obviously enhance the flame retardancy of the composites. Cone calorimeter (CONE) and thermogravimetric analysis (TGA) were applied to evaluate the burning behavior and thermal stability of IFR-LLDPE/EVA (LLDPE/EVA) composites. The results of cone calorimeter showed that heat release rate peak (HRR-peak) and smoke production rate peak (SPR-peak) and time to ignition (TTI) of IFR-LLDPE/EVA composites decreased clearly compared with the pure blend. TGA data showed that IFR could enhance the thermal stability of the composites at high temperature and effectively increase the char residue. The morphological structures of the composites observed by scanning electron microscopy (SEM) and X-ray diffraction (XRD) demonstrated that OMMT could well disperse in the composites without exfoliation, and obviously improve the compatibility of components of IFR in LLDPE/EVA blend. The morphological structures of char layer obtained from Cone indicated that OMMT make the char layer structure be more homogenous and more stable.