Search

Nano α-glycine crystals, γ-glycine crystals, and amorphous solid dispersion (ASD) of glycine were prepared through solvent-free ball milling of commercial α-glycine. The solid-state polymorph conversion of glycine from α to γ was completely realized by ball milling with 0.2 wt.% NaCl for 1 h or by ball milling with 0.02 wt.% NaCl for 1 h with subsequent storage for one week. The ASD of glycine was prepared by ball milling α-glycine with an equal amount of CaCl2 for 1 h. We studied the effect of inorganic salt types and their concentrations on the extent of polymorph conversion and amorphization of glycine in our experiments. This solvent-free ball milling method could be used for the synthesis of polymorphs and amorphous phase of drugs and other organic materials.

Guanosine (GR) dihydrate and inosine (IR) dihydrate have similar crystal structure, water molecules are almost at the same locations in them. GR dihydrate has the reversible dehydration/hydration property and is a good candidate for materials harvesting water from atmosphere. IR dihydrate is not stable and can be easily transformed to anhydrous IR α form. In this work, doping of IR in GR dihydrate in all the range was realized for the first time by using a solution method. The successful preparation of doped dihydrate of IR and GR by the solution method was attributed to the similar molecular conformations of IR and GR in solution. The doped dihydrates could maintain the reversible dehydration/hydration property similar to pure GR dihydrate even the ratio of IR was up to 71.1 ± 1.2 mol% under a mild drying treatment with freeze-dry. A pure amorphous GR was prepared by ball milling, and it showed a similar dehydration/hydration property to GR dihydrate with a lower dehydration temperature (about 84 °C). The implementation of doping IR in GR dihydrate would shed light on the design and fabrication of functional doped organic crystals. And study on the structural insights and the dehydration/hydration processes of the doped dihydrates and the pure amorphous GR would shed light on the design and fabrication of novel hydrogen-bonded organic frameworks (HOFs) materials for water harvesting.

In order to make the gastrointestinal microrobot (GMR) expand and anchor in the gastrointestinal tract reliably, a novel expanding mechanism of the GMR is proposed in this paper. The overlapping expanding arm is designed to be used to increase the variable diameter ratio (ratio of fully expanded diameter to fully folded diameter) to 3.3, which makes the robot more adaptable to the intestinal tract of different sections of the human body. The double-layer structure of the expanding arm increases the contact area with the intestine, reducing the risk of intestinal damage. The kinematics and mechanical model of the expanding arm are established, and the rigid velocity, rigid acceleration, and expanding force of the expanding arm are analyzed. The elastodynamics model of the expanding arm is established. Through the finite element analysis (FEA), the velocity, acceleration, and the value and distribution of the stress of the expanding arm under elastic deformation are obtained. Based on the elastodynamics analysis, the structure of the expanding arm is optimized. By the structure optimization, the thickness of the expanding mechanism is reduced by 0.4mm, the weight is reduced by 31%, and the stress distribution is more uniform. Through the mechanical test, the minimum expanding force of the expanding mechanism is 1.3 N and the maximum expanding force is 6.5 N. Finally, the robot is tested in the rigid pipeline and the isolated intestine to verify the reliability and safety of the expanding mechanism.

Cadmium (Cd) is a highly toxic heavy metal for both animals and plants. Rice consumption is a major source of Cd intake for human. Minimization of Cd accumulation in rice is key to reduce Cd hazard to human. Here we showed alleviating effects of boron (B), silicon (Si) and their mixture on Cd accumulation and toxicity in hydroponically-cultured rice plants. Cd treatment (100 μM) led to Cd accumulation in roots and shoots, as well as significant reduction in plant growth. However, amendment of either B or Si significantly alleviated Cd accumulation and toxicity. Moreover, simultaneous supply of B and Si showed better alleviating effect. However, addition of B and Si alleviated Cd-induced oxidative stress in Cd-treated plants as reflected by reduced MDA, H2O2 and O2-, as well as increased activities of major antioxidant enzymes. Cd exposure induced the expression of Cd transporter genes of OsHMA2, OsHMA3, OsNramp1 and OsNramp5. In contrast, simultaneous supplement of B and Si in Cd-treated plants compromised the gene expression. Our results show that both B and Si alleviate Cd accumulation and toxicity by improving oxidative stress and suppressing Cd uptake and transport, and the two elements display joint effect.

Printable hydrogels desired in bioengineering have extremely high demands on biocompatibility and mechanic strength, which can hardly be achieved in conventional hydrogels made with biopolymers. Here, we show that on employment of the strategy of coordination-triggered hierarchical self-assembly of naturally occurring small-molecule folic acid, supramolecular hydrogels with robust mechanical elastic modulus comparable to synthetic double-network polymer gels can be made at concentrations below 1%. A sequence of hierarchical steps are involved in the formation of this extraordinary hydrogel: petrin rings on folate form tetramers through hydrogen bonding, tetramers stack into nanofibers by π-π stacking, and zinc ions cross-link the nanofibers into larger-scale fibrils and further cross-link the fibril network to gel water. These supramolecular qualities endow the hydrogel with shear-thinning and instant healing ability, which makes the robust gel injectable and printable into various three-dimensional structures. Owing to the excellent biocompatibility, the gel can support cells three-dimensionally and can be used as an ideal carrier for imaging agent (Gd

Cis-to-trans transition of azobenzene compounds usually occurs under appropriate light irradiation or slow thermal relaxation, and one can hardly obtain complete cis-to-trans transition of azos due to the overlap of the n-π* transition of the trans and the cis isomers. We show that by viewing the photostationary state as a chemical equilibrium between the cis and trans isomers, triggered self-assembly of the trans isomers can promote the cis-to-trans transition, and trans azos with spectrum-grade purity can even be achieved using an elegantly designed coordinating azo. This work establishes a new paradigm for manipulating the cis-to-trans transition of azo compounds, which may inspire designs for various azo-based advanced materials.