A lysosomes and mitochondria dual-targeting AIE-active NIR photosensitizer: Constructing amphiphilic structure for enhanced antitumor activity and two-photon imaging.

Development of lysosomes and mitochondria dual-targeting photosensitizer with the virtues of near-infrared (NIR) emission, highly efficient reactive oxygen generation, good phototoxicity and biocompatibility is highly desirable in the field of imaging-guided photodynamic therapy (PDT) for cancer. Herein, a new positively charged amphiphilic organic compound (2-(2-(5-(7-(4-(diphenylamino)phenyl)benzo[c][1,2,5]thiadiazol-4-yl)thiophen-2-yl)vinyl)-3-methylbenzo[d]thiazol-3-ium iodide) (ADB) based on a D-A-π-A structure is designed and comprehensively investigated. ADB demonstrates special lysosomes and mitochondria dual-organelles targeting, bright NIR aggregation-induced emission (AIE) at 736 â€‹nm, high singlet oxygen (1O2) quantum yield (0.442), as well as good biocompatibility and photostability. In addition, ADB can act as a two-photon imaging agent for the elaborate observation of living cells and blood vessel networks of tissues. Upon light irradiation, obvious decrease of mitochondrial membrane potential (MMP), abnormal mitochondria morphology, as well as phagocytotic vesicles and lysosomal disruption in cells are observed, which further induce cell apoptosis and resulting in enhanced antitumor activity for cancer treatment. In vivo experiments reveal that ADB can inhibit tumor growth efficiently upon light exposure. These findings demonstrate that this dual-organelles targeted ADB has great potential for clinical imaging-guided photodynamic therapy, and this work provides a new avenue for the development of multi-organelles targeted photosensitizers for highly efficient cancer treatment.

Dual functional antifouling and bactericidal proteinaceous coating.

Coatings with both anti-fouling and bactericidal functions are used in many fields. In this work, lysozyme (Lyso) and poly (2-Methylallyloxyethyl phosphorylcholine) (PMPC) conjugate (Lyso-PMPC) is successfully designed and synthesized for the first time. A new nanofilm (PTL-PMPC) is then obtained by phase transition of lysozyme via the reduction of disulfide bonds in Lyso-PMPC. Benefit from lysozyme amyloid-like aggregates as surface anchors, the nanofilm shows excellent stability, it remains unchanged after treatment under extreme conditions such as ultrasonic and 3 M tape peeling. Due to the presence of zwitterionic polymer (PMPC) brush, the PTL-PMPC film has excellent antifouling properties against cell, bacterium, fungi, proteins, biofluids, phosphatide, polyose, esters, and carbohydrates. Meanwhile, the PTL-PMPC film is colourless and transparent. Further, a new coating (PTL-PMPC/PHMB) is fabricated by hybridizing PTL-PMPC with poly (hexamethylene biguanide) (PHMB). This coating had excellent antibacterial properties, and the antibacterial rate against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) is more than 99.99%. In addition, the coating exhibit good hemocompatibility and low cytotoxicity.

Low-cost diatomite supported binary transition metal sulfates: an efficient reusable solid catalyst for biodiesel synthesis.

Using a simple method of impregnation and then calcination, diatomite supported binary transition metal sulfates (Fe and Zr, designated as Fe2(SO4)3&Zr(SO4)2@diatomite) were prepared and used as a catalyst in the preparation of renewable biofuels. The synthesised Fe2(SO4)3&Zr(SO4)2@diatomite catalyst (Fe2(SO4)3 : Zr(SO4)2 : diatomite = 1 : 2 : 6, mass ratio) was thoroughly characterised using transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, microbeam X-ray fluorescence (µ-XRF) spectroscopy and thermogravimetric analysis (TG). The results demonstrated that the sulfate was successfully loaded onto the diatomite with a uniform distribution. The N2 adsorption/desorption analysis indicated that the catalyst's specific surface area was 1.54 m2 g-1. The catalyst exhibited outstanding performance in the preparation of renewable biofuel (biodiesel) from waste fatty acids and the optimal parameters were methanol-to-oil 1.25 : 1, reaction temperature 70 °C, catalyst concentration 10 wt%, reaction time 4 h. The conversion was found to reach 98.90% under optimal parameters, which is better than that of Fe2(SO4)3·xH2O, Zr(SO4)2·4H2O, Fe2(SO4)3@diatomite and Zr(SO4)2@diatomite. Moreover, the catalyst can be recycled by simple filtration and reused for three cycles after regeneration without noticeable reduction in catalytic activity.

Preparation of a reusable and pore size controllable porous polymer monolith and its catalysis of biodiesel synthesis.

A sulfonated porous polymer monolith (PPM-SO3H) has been prepared via the polymerisation of styrene (St) and divinyl benzene (DVB) with organic microspheres as pore-forming agents, followed by sulfonation with concentrated sulfuric acid. It was characterized by acid-base titration in order to determine its acid density, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, mercury intrusion porosimetry (MIP) and thermogravimetric analysis (TG). The PPM-SO3H showed an acid density of 1.89 mmol g-1 and pore cavities with an average diameter of 870 nm. The catalytic activity of PPM-SO3H in practical biodiesel synthesis from waste fatty acids was investigated and the main reaction parameters were optimized through orthogonal experiment. The best reaction conditions obtained for the optimization of methanol to oil ratio, catalyst concentration, reaction temperature and reaction time were 1 : 1, 20%, 80 °C and 8 h, respectively. PPM-SO3H showed excellent catalytic activity. In biodiesel synthesis, the esterification rate of PPM-SO3H is 96.9%, which is much higher than that of commercial poly(sodium-p-styrenesulfonate) (esterification rate 29.0%). The PPM-SO3H can be reused several times without significant loss of catalytic activity; the esterification rate was still 90.8% after 6 cycles. The pore size of this porous polymer monolith can be controlled. The dimension and shape of this porous polymer monolith were also adjustable by choosing a suitable polymerisation container.