Hollow Mesoporous Organosilica Research Articles

Hollow multi-shelled structure engineering of organosilica for efficient and selective uranium extraction from seawater

Uranium extraction from seawater is critical for the development of nuclear energy, but the progress is still seriously limited by the performance and cost of current adsorbents. Herein, a convenient and general co-condensation process is designed to prepare amidoximated multi-shelled hollow mesoporous organosilica adsorbent (AO-HMO), which exhibits a high uranium extraction capacity of 862.07 mg·g−1 in uranium-spiked simulated seawater and 9.67 mg·g−1 in natural seawater. The run-through mesoporous structure and multi-shelled surface provide fast diffusion channels and more active sites for uranium adsorption. Moreover, AO-HMO exhibits a long service life due to its robust structure, maintaining an ideal adsorption capacity over 10 adsorption-desorption cycles. Coupled with the synthesis-cost advantage, AO-HMO will surely show great application potential in uranium extraction form seawater in future.

Synergistic chemo-photodynamic therapy based on hollow mesoporous organosilica nanoparticles for reducing psoriasis-like inflammation

Psoriasis is a prevalent chronic inflammatory and proliferative skin condition characterized by its tendency for recurrence, prolonged duration, and challenging treatment. The most commonly employed treatment approach in clinical practice involves methotrexate (MTX)-based systemic therapy. However, long-term oral intake of MTX is associated with numerous side effects, ranging from induced liver and kidney toxicity to severe cases of bone marrow suppression. To reduce the incidence of adverse reactions, the topical application of nano-drug delivery systems by modifying MTX might potentially prove beneficial. This study introduces a novel chemo-photodynamic therapy approach utilizing hollow mesoporous silica nanoparticles (MTX@HMN-Ce6-HA) loaded with methotrexate (MTX) (loading: 78 %) and chlorine e6 (Ce6) (loading: 80 %). These nanoparticles generate reactive oxygen species (ROS) under light conditions, which aid in breaking the disulfide bond in the silica nanoparticles to release MTX and encapsulated hyaluronic acid (HA), thereby enhancing the permeability of the nanomaterials. The efficacy of this approach was evaluated at both cellular and animal levels. MTX@HMN-Ce6@HA demonstrated significant reductions in HaCaT cell viability, induction of cell apoptosis, and inflammation reduction by modulating the mitochondrial apoptosis pathway and STAT3-NF-κB p65 pathway. Importantly, this strategy synergistically treats psoriasis showing enhanced therapeutic efficacy by combining MTX chemotherapy with Ce6 phototherapy. In summary, MTX@HMN-Ce6@HA demonstrated powerful therapeutic efficacy against psoriasis-like skin inflammation without displaying any noticeable toxic effects. This finding could serve as a theoretical foundation and experimental validation for the topical treatment of psoriasis.

Engineered Multi-Shelled hollow mesoporous organosilica for efficient Pb(II) and Cr(VI) removal

Adsorbents with fast kinetics and high capacity have always been attractive for wastewater treatment. Herein, multi-shelled hollow mesoporous organosilica functionalized by hydroxyphosphatoethyl groups on dual-pore surfaces (P-HMO) is prepared by general one-pot co-condensation. The resulting P-HMO exhibits high hydrophilicity, large surface area and well-developed pore structure, providing P-HMO fast adsorption kinetics (C0 = 320 mg·L-1, equilibrium within 5 min) and ultrahigh adsorption efficiency for Pb(II) and Cr(VI), the adsorption capacity reaches 1056.53 and 869.56 mg·g−1, respectively. Furthermore, P-HMO displays outstanding reusability over 10 adsorption–desorption cycles thanks to the stable framework structure that can resist wear and tear during water treatment. The advantages of long service life, high efficiency and broad pH range make P-HMO promising in industrial water purification.

Cobalt and nitrogen co-modified hollow periodic mesoporous organosilica spheres for selective oxidation of aryl alkanes

Hollow periodic mesoporous organosilica spheres (HPMOs) have stimulated great research interest owing to its unique organic–inorganic hybrid skeleton. In this work, HPMOs were synthesized by hydrothermal method, and then cobalt and nitrogen co-doped carbon catalyst was prepared by using HPMOs as supports. The optimal catalyst (Co-Nx/HPMOs-D) performed excellent activity in the selective oxidation reaction of aryl alkanes, with the conversion of ethylbenzene up to 97.0% and the selectivity of acetophenone was 98.9%, which was attributed to the Co-Nx active species and the unique HPMOs supports. The unique amphiphilic property of Co-Nx/HPMOs-D could better facilitate the adsorption and diffusion of organic substrates in the aqueous phase. The addition of dicyandiamide not only enhanced the nitrogen content in the catalyst, but also promoted the conversion of pyrrolic-N to pyridinic-N during the pyrolysis process, thus strengthened the interaction between the substrate and cobalt and improved the stability of the catalyst. This work presented a green and environmentally friendly method for the preparation of HPMOs and a facile strategy to obtain high performance catalysts for selective oxidation of aryl alkanes.

Lactic acid responsive sequential production of hydrogen peroxide and consumption of glutathione for enhanced ferroptosis tumor therapy

Ferroptosis is characterized by the lethal accumulation of lipid reactive oxygen species (ROS), which has great potential for tumor therapy. However, developing new ferroptosis-inducing strategies by combining nanomaterials with small molecule inducers is important. In this study, an enzyme-gated biodegradable natural-product delivery system based on lactate oxidase (LOD)-gated biodegradable iridium (Ir)-doped hollow mesoporous organosilica nanoparticles (HMONs) loaded with honokiol (HNK) (HNK@Ir-HMONs-LOD, HIHL) is designed to enhance ferroptosis in colon tumor therapy. After reaching the tumor microenvironment, the outer LOD dissociates and releases the HNK to induce ferroptosis. Moreover, the released dopant Ir4+ and disulfide-bridged organosilica frameworks deplete intracellular glutathione (GSH), which is followed by GSH-mediated Ir(IV)/Ir(III) conversion. This leads to the repression of glutathione peroxidase 4 (GPX4) activity and decomposition of intratumoral hydrogen peroxide (H2O2) into hydroxyl radicals (•OH) by Ir3+-mediated Fenton-like reactions. Moreover, LOD efficiently depletes lactic acid to facilitate the generation of H2O2 and boost the Fenton reaction, which in turn enhances ROS generation. With the synergistic effects of these cascade reactions and the release of HNK, notable ferroptosis efficacy was observed both in vitro and in vivo. This combination of natural product-induced and lactic acid-responsive sequential production of H2O2 as well as the consumption of glutathione may provide a new paradigm for achieving effective ferroptosis-based cancer therapy.

A Biodegradable Nanosuspension Locally Used for Inhibiting Postoperative Recurrence and Brain Metastasis of Breast Cancer.

Addressing the urgent need to prevent breast cancer postoperative recurrence and brain metastasis, Fe-metal organic framework (MOF)-coated hollow mesoporous organosilica nanoparticles (HMON) with tumor microenvironment dual-responsive degradability were prepared to encapsulate doxorubicin (DOX), formulating a tissue-adhesive nanosuspension for perioperative topical medication. This nanosuspension can not only retain the sustainably released drug in the postoperative residual tumor sites but also enhance the intracellular oxidative stress of tumors for remarkable tumor ferroptosis. Interestingly, the nanosuspension can act as an immune amplifier, which could not only stimulate DC cells to secrete chemokines for T cell recruitment but also elevate antigen exposure to facilitate the antigen presentation in lymph nodes. Thus, this nanosuspension could significantly activate antitumor immune responses in both in situ tumors and metastatic encephaloma for enhanced immunotherapy. In conjunction with the clinical PD-1 antibody, the locally administered nanosuspension could achieve an advanced therapeutic outcome for inhibiting postoperative recurrence and metastasis.

Redox/Near-Infrared Dual-Responsive Hollow Mesoporous Organosilica Nanoparticles for Pesticide Smart Delivery.

Extremely inefficient utilization of pesticides has prompted a study of low-cost, sustainable, and smart application systems. Herein, as a promising pesticide nanocarrier, hollow mesoporous organosilica nanoparticles (HMONs) were first synthesized by using inexpensive CaCO3 nanoparticles as the hollow templates. A redox/near-infrared light dual-triggered pesticide release system was further achieved via loading avermectin (AVM) into the HMONs and coating a layer of polydopamine (PDA). The as-prepared AVM@HMONs@PDA displays a favorable pesticide load capability (24.8 wt %), outstanding photothermal performance, and high adhesion to leaves. In addition, with glutathione (GSH), the AVM cumulative release from AVM@HMONs@PDA was 3.5 times higher than that without GSH. Under ultraviolet light irradiation, the half-life of AVM@HMONs@PDA was prolonged by 17.0-fold compared to that of the AVM technical. At day 21 after treatment in the insecticidal activity, the median lethal concentrations (LC50) values displayed that the toxicity of AVM@HMONs@PDA for Panonychus citri (McGregor) was enhanced 4.0-fold compared with the commercial emulsifiable concentrate. In the field trial, at day 28 after spraying, AVM@HMONs@PDA was significantly more control effective than AVM-EC in controlling the P. citri (McGregor), even at a 50% reduced dosage. Moreover, HMONs@PDA was safe for crops. This research presents a novel preparation approach for HMONs, and it also offers a promising nanoplatform for the precise release of pesticides.

One-step synthesis of hollow and yolk-shell mesoporous organosilica nanospheres for efficient separation of lead ions

In this work, we demonstrate that monodispersed hollow mesoporous organosilica nanospheres (MONs) and yolk-shell MONs possessing controlled core cavity and mesoporous shell is successfully synthesized through a one-pot approach, which involves co-condensation of 3-aminopropyltriethoxysilane and 1,2-bis(triethoxysilyl)ethane templated by lauryl sulfonate betaine and sodium dodecyl benzenesulfonate. The MONs present an open mesoporosity, hollow cavity with a morphology tailored by the various core templates, and high surface area (328 m2/g). In addition, the composition of the hollow MONs could be further tuned through the same approach. The as-prepared hollow MONs as adsorbent deliver an enormous adsorption capacity (414 mg/g) towards the removal of Pb2+ from water solution. Importantly, the prepared hollow MONs present acceptable recycling and stability, since the performance in Pb2+ removal from water remains above 80 % even after 5 consecutive cycles. The adsorption of Pb2+ on hollow MONs follows the pseudo-second-order mechanics and Langmuir isotherm models. The results confirm hollow MONs exhibit considerable promise for the remarkably efficient separation of Pb2+ ions in water solution.

Hollow Mesoporous SilicaNanoparticles for Dual Chemo-starvation Therapy of Hepatocellular Carcinoma.

This study aims at chemotherapy and starvation therapy of HCC via starvation and apoptosis. Hollow mesoporous organosilica nanoparticles (HMONs) with the thioether-hybrid structure were developed using an organic/inorganic co-templating assembly approach. Hydrofluoric acid was used to remove the internal MSN core for yielding large radial mesopores for loading drug cargos. The morphology and structure of NPs were determined using TEM and SEM. HMONs were stepwise surface modified with glucose oxidase (GOx), oxygen (O2) and Doxorubicin (DOX), and cancer cell membrane (CCM) for yielding CCM-coated HMONs (targeted stealth biorobots; TSBRs) for starvation, apoptotic, and enhanced cell uptake properties, respectively. The surface area and pore size distribution were determined via BET and BJH assays. The catalytic ability of GOx-modified NPs was measured using in vitro glucose conversion approach authenticated by H2O2 and pH determination assays. MTT assay was used to determine the cytotoxicities of NPs. Cell uptake and apoptotic assay were used for the NPs internalization and apoptosis mechanisms. The subcutaneous HepG2 tumor model was established in mice. The long-term in vivo toxicity was determined using blood assays. The prepared NPs were spherical, hollow and mesoporous with excellent surface area and pore size distribution. The GOx-modified NPs exhibited excellent catalytic activity. The TSBRs showed better cytotoxicity and reduce the tumor size and weight. The NPs showed long-term safety in vivo. TSBRs destroyed cancer cells by starvation and chemotherapy in both in-vitro and in-vivo settings which demonstrates its anti-cancer potential.

Gas therapy potentiates aggregation-induced emission luminogen-based photoimmunotherapy of poorly immunogenic tumors through cGAS-STING pathway activation

The immunologically “cold” microenvironment of triple negative breast cancer results in resistance to current immunotherapy. Here, we reveal the immunoadjuvant property of gas therapy with cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway activation to augment aggregation-induced emission (AIE)-active luminogen (AIEgen)-based photoimmunotherapy. A virus-mimicking hollow mesoporous tetrasulfide-doped organosilica is developed for co-encapsulation of AIEgen and manganese carbonyl to fabricate gas nanoadjuvant. As tetra-sulfide bonds are responsive to intratumoral glutathione, the gas nanoadjuvant achieves tumor-specific drug release, promotes photodynamic therapy, and produces hydrogen sulfide (H2S). Upon near-infrared laser irradiation, the AIEgen-mediated phototherapy triggers the burst of carbon monoxide (CO)/Mn2+. Both H2S and CO can destroy mitochondrial integrity to induce leakage of mitochondrial DNA into the cytoplasm, serving as gas immunoadjuvants to activate cGAS-STING pathway. Meanwhile, Mn2+ can sensitize cGAS to augment STING-mediated type I interferon production. Consequently, the gas nanoadjuvant potentiates photoimmunotherapy of poorly immunogenic breast tumors in female mice.

Etched hollow periodic mesoporous organosilica with enlarged pore size for high-performance solid phase microextraction of polybrominated biphenyls

Hollow mesoporous silica has attracted increasing attention due to its outstanding characteristics such as low density, large void, mesoporous channel, and large specific surface area. Herein, a kind of etched hollow periodic mesoporous organosilica (EHPMOS) with enlarged mesopore size was successfully synthesized for high-performance solid phase microextraction (SPME). The etched silica material was prepared as a SPME fiber with uniform morphology, and the enrichment capacities for polybrominated biphenyls (PBBs) were systematically studied. In particular, the EHPMOS showed significant enrichment factors (158–9516) for PBBs. In addition, based on the home-made SPME fiber and gas chromatography-mass spectrometry (GC–MS), an ultra-sensitive analytical method was developed, with low limits of detection (0.11–0.32 ng·L-1), a wide linear range (1–1000 ng·L-1), and satisfactory reproducibility. And accurate quantifications of ultra-trace PBBs in environmental water sample were achieved.

Proton pump inhibitor-enhanced nanocatalytic ferroptosis induction for stimuli-responsive dual-modal molecular imaging guided cancer radiosensitization.

Although radiotherapeutic efficiency has been revealed to be positively correlated with ferroptosis, the neutral/alkaline cytoplasm pH value of tumor cells remains an intrinsic challenge for efficient Fenton/Fenton-like reaction-based ferroptosis induction. Herein, PEGylated hollow mesoporous organosilica nanotheranostics (HMON)-GOx@MnO2 nanoparticles (HGMP NPs) were designed as a ferroptosis inducer, which could specifically release Mn2+ in tumor cells to activate the Fenton-like reaction for ferroptosis induction. Proton pump inhibitors (PPIs) were synchronously administered for cytoplasm pH level regulation by inhibiting V-H+-ATPases activity, enhancing Fenton-like reaction-based ferroptosis induction. Moreover, reactive oxygen species production was facilitated via the glucose oxidase triggered cascade catalytic reaction by utilizing intracellular β-D-glucose for H2O2 self-supply and generation of additional cytoplasm H+. The PPI enhanced ferroptosis inducing nanosystem effectively inhibited tumor growth both in vitro and in vivo for tumor-specific ferroptosis induction and radiotherapy sensitization, suggesting that PPI administration could be an efficient adjuvant to reinforce Fenton/Fenton-like reaction-based ferroptosis induction for radiosensitization. STATEMENT OF SIGNIFICANCE: The cytoplasm pH value of tumor cells is typically neutral to alkaline, which is higher than that of the Fenton/Fenton-like reaction desired acidic environments, hindering its efficiency. In this study, PEGylated hollow mesoporous organosilica nanotheranostics (HMON)-GOx@MnO2 nanoparticles were synthesized as a ferroptosis inducer, which could specifically release Mn2+ via depleting glutathione and then activate the Fenton-like reaction in the tumor microenvironment. The glucose oxidase was applied for H2O2 self-supply and addition of cytoplasm H+ to further boost the Fenton-like reaction. We found that proton pump inhibitors (PPIs) increased intracellular acidification by inhibiting the activity of V-H+-ATPases to enhance the Fenton reaction-based ferroptosis induction, suggesting PPIs administration could be a feasible strategy to reinforce ferroptosis induction for radiosensitization.

Polyoxometalates Encapsulated into Hollow Periodic Mesoporous Organosilica as Nanoreactors for Extraction Oxidation Desulfurization

In this work, the highly active polyoxometalate (PW2Mo2) with Venturello structure and its corresponding catalyst were applied in catalytic desulfurization for the first time. PW2Mo2 as an active component was effectively encapsulated in hollow periodic mesoporous organosilica (HPMOS) to form the nanoreactor PW2Mo2@HPMOS, where the central cavity and mesoporous shell facilitate mass transfer and both provide a stable place to react with organic sulfides. Desulfurization test results show that the hollow nanoreactor PW2Mo2@HPMOS can almost remove four sulfides simultaneously from diesel in 2 h under mild conditions. Besides, the nanocatalyst PW2Mo2@HPMOS can be reused and recycled for at least seven consecutive tests without any noticeable loss in performance. With the rapid development of the economy, the massive use of sulfur-containing fuel has a huge impact on the global climate. After combustion of sulfur-containing fuel, the realized SOX is an important inducement of the formation of acid rain, and the realized sulfur particle is also a major source of haze. Therefore, removing sulfur compounds from fuel is an important issue that needs to be solved immediately.

Synthesis of Monodispersed Hollow Mesoporous Organosilica and Silica Nanoparticles with Controllable Shell Thickness Using Soft and Hard Templates

Hollow mesoporous nanoparticles with controllable size (less than 100 nm) are desired as drug-delivery carriers. Herein, we report the synthesis of monodispersed hollow mesoporous organosilica (HMOS) and hollow mesoporous silica (HMS) nanoparticles using soft and hard templating methods. HMOS shells, with 1,2-bis(triethoxysilyl)ethane (BTEE) as the precursor and hexadecyltrimethylammonium bromide and sodium dodecyl sulfate (SDS) as the soft templates, were formed on monodispersed silica nanoparticles (SNPs), which were used as the hard templates. HMOS and HMS nanoparticles were obtained by removing the SNPs after three rounds of ammonia dialysis. The hollow size of HMOS can be tuned by changing the size of the SNPs. By using SNPs with a size of 36.5 nm, hollow spaces of approximately 20 nm connected the surface through narrow pores (<5 nm). Mesopores of approximately 12 nm were formed by the surfactant micelles. Additionally, the interparticle space in HMOS and HMS was approximately 12 nm. The shell thicknesses of HMOS and HMS could be tuned in the range of 5-9 nm by changing the BTEE amount. Moreover, the amount of surfactant used varied the porous structure. The HMOS with a thickness of 5 nm exhibited a Brunauer-Emmett-Teller (BET) surface area of 268 m2/g and a total pore volume of 1.14 cm3/g. Meanwhile, HMS demonstrated a BET surface area of 553 m2/g and a total pore volume of 1.82 cm3/g while maintaining a hollow structure. HMOS displayed a high loading capacity for ibuprofen (3009 mg/g), and its drug release system showed a sustained-release property. Therefore, the HMOS preparation using hard and soft templates proposed herein can control the hollow size and shell thickness for drug-delivery applications.

Hollow mesoporous organosilica nanoparticles reduced graphene oxide based nanosystem for multimodal image-guided photothermal/photodynamic/chemo combinational therapy triggered by near-infrared.

Developing a nanosystem that can perform multimodal imaging-guided combination therapy is highly desirable but challenging. In this study, we introduced multifunctional nanoparticles (NPs) consisting of graphene oxide-grafted hollow mesoporous organosilica loaded with the drug doxorubicin (DOX) and photosensitizers tetraphenylporphyrin (TPP). These NPs were encapsulated by thermosensitive liposomes that release their contents once the temperature exceeds a certain threshold. Metal oxide NPs grown on the graphene oxide (GO) surface served multiple roles, including enhancing photothermal efficiency, acting as contrast agents to improve magnetic resonance imaging, increasing the sensitivity and specificity of photoacoustic imaging, and catalysing hydrogen peroxide for the generation of reactive oxygen species (ROS). When locally injected, the HMONs-rNGO@Fe3 O4 /MnOx@FA/DOX/TPP NPs effectively enriched in subcutaneous Hela cell tumour of mice. The photothermal/photodynamic/chemo combination therapy triggered by near-infrared (NIR) successfully suppressed the tumour without noticeable side effects. This study presented a unique approach to develop multimodal imaging-guided combination therapy for cancer.

Self-Homeostasis Immunoregulatory Strategy for Implant-Related Infections through Remodeling Redox Balance.

Implant-related infections (IRIs) are catastrophic complications after orthopedic surgery. Excess reactive oxygen species (ROS) accumulated in IRIs create a redox-imbalanced microenvironment around the implant, which severely limits the curing of IRIs by inducing biofilm formation and immune disorders. However, current therapeutic strategies commonly eliminate infection utilizing the explosive generation of ROS, which exacerbates the redox imbalance, aggravating immune disorders and promoting infection chronicity. Herein, a self-homeostasis immunoregulatory strategy based on a luteolin (Lut)-loaded copper (Cu2+)-doped hollow mesoporous organosilica nanoparticle system (Lut@Cu-HN) is designed to cure IRIs by remodeling the redox balance. In the acidic infection environment, Lut@Cu-HN is continuously degraded to release Lut and Cu2+. As both an antibacterial and immunomodulatory agent, Cu2+ kills bacteria directly and promotes macrophage pro-inflammatory phenotype polarization to activate the antibacterial immune response. Simultaneously, Lut scavenges excessive ROS to prevent the Cu2+-exacerbated redox imbalance from impairing macrophage activity and function, thus reducing Cu2+ immunotoxicity. The synergistic effect of Lut and Cu2+ confers excellent antibacterial and immunomodulatory properties to Lut@Cu-HN. As demonstrated in vitro and in vivo, Lut@Cu-HN self-regulates immune homeostasis through redox balance remodeling, ultimately facilitating IRI eradication and tissue regeneration.

3D-CEUS tracking of injectable chemo-sonodynamic therapy-enabled mop-up of residual renal cell carcinoma after thermal ablation.

Thermal ablation (TA), as a minimally invasive therapeutic technique, has been extensively used to the treatment of solid tumors, such as renal cell carcinoma (RCC), which, unfortunately, still fails to overcome the high risk of local recurrence and distant metastasis since the incomplete ablation cannot be ignored due to various factors such as the indistinguishable tumor margins and limited ablation zone. Herein, we report the injectable thermosensitive hydrogel by confining curcumin (Cur)-loaded hollow mesoporous organosilica nanoparticles (Cur@HMON@gel) which can locate in tumor site more than half a month and mop up the residual RCC under ultrasound (US) irradiation after transforming from colloidal sol status to elastic gel matrix at physiological temperature. Based on the US-triggered accelerated diffusion of the model chemotherapy drug with multi-pharmacologic functions, the sustained and controlled release of Cur has been demonstrated in vitro. Significantly, US is employed as an external energy to trigger Cur, as a sonosensitizer also, to generate reactive oxygen species (ROS) for sonodynamic tumor therapy (SDT) in parallel. Tracking by the three-dimensional contrast-enhanced ultrasound (3D-CEUS) imaging, the typical decreased blood perfusions have been observed since the residual xenograft tumor after incomplete TA were effectively suppressed during the chemo-sonodynamic therapy process. The high in vivo biocompatibility and biodegradability of the multifunctional nanoplatform confined by thermogel provide the potential of their further clinical translation for the solid tumor eradication under the guidance and monitoring of 3D-CEUS.

Three birds with one stone: Contemporaneously boosting passive, active and self-healing properties for long-term anticorrosion coatings

Stimuli-responsive coatings can self-repair their own anticorrosion function in response to environmental changes, but they do not exhibit ideal long-term protective effect due to the lack of ability to regulate corrosive media, while this is vital to practical metal protection. Inspired by catalytic oxygen reduction, Cu-N center doped graphene oxide grafted with hollow periodic mesoporous organosilica nanocontainer (MBT@HPMO/Cu-GO) is synthesized via facile adsorption-pyrolysis strategy. Herein, introduced MBT@HPMO/Cu-GO is to simultaneously endow coatings with corrosive media shielding, active oxygen consumption and stimuli-responsive functions, thus “three birds with one stone”. The target catalyst exhibits excellent oxygen depletion performance (half-wave potential of 0.85 V) and is uniformly dispersed in the coating to construct steric hindrance against corrosive media. This dual effect allows composite coating to maintain the excellent anticorrosion performance over 60 days under oxygen environment. In addition, MBT@HPMO/Cu-GO can release inhibitor at corrosion sites in response to environment change when coating is damaged, so as to restore the protective ability of coating, with impedance increased from 2.4 × 107 Ω·cm2 to 1.5 × 108 Ω·cm2. Such multifunctional coating exploration overcomes the protective limitation of current self-healing coatings and sheds light on the design of intelligent long-term anticorrosion coatings.

Swellable hollow periodic mesoporous organosilica capsules with ultrahigh loading capacity for hydrophobic drugs.

As a new kind of drug carrier, practical applications of hollow periodic mesoporous organosilica (HPMO) have been greatly limited by their low loading capacity for hydrophobic drugs. In this work, we demonstrated the preparation of HPMO capsules with tunable shell thickness by using 1,2-bis(triethoxysilyl)ethane as the precursor. The capsules with thin shells and thus low Young's modulus showed excellent swellability to organic solvents containing hydrophobic drugs. As a result, hydrophobic drugs, i.e., paclitaxel (PTX) could be loaded into the hollow interior of the HPMO capsules with 4nm shell at an efficiency of ca. 120%. The as-prepared PTX-loaded HPMO capsules were dispersible in aqueous media and showed improved performance in killing cancer cells compared to free PTX.

Lanthanide-grafted hollow bipyridine-based periodic mesoporous organosilicas as chemical sensors.

We have synthesized a co-condensed hollow ethane-bipyridine periodic mesoporous organosilica (HEt-bpy-PMO) as a host material to anchor lanthanides for the purpose of developing a multifunctional chemical sensor. The host material was grafted with lanthanide chloride salts or complexes. The luminescence properties of the developed series of hybrid materials were studied in detail in the solid-state and after dispersing in water. The Eu3+ or Tb3+ singly incorporated materials were investigated for their use as ion sensors, showing ions selectivity towards Cu2+, Co2+ and Fe3+. Additionally, the Eu3+ or Tb3+ incorporated materials showed obvious luminescence quenching behavior towards acetone compared to other organic solvents, indicating excellent acetone sensing selectivity.