Titanium-Based Superlattice with Fe(III)-Regulable Bandgap and Performance for Optimal and Synergistic Sonodynamic–Chemotherapy Guided by Magnetic Resonance Imaging

Superlattices have considerable potential as sonosensitizers for cancer therapy because of their flexible and tunable band gaps, although they have not yet been reported. In this study, a Ti-based organic–inorganic superlattice with good electron–hole separation was synthesized, which consisted of orderly layered superlattices of 2,2′-bipyridine-5,5′-dicarboxylic acid (BPDC) and Ti−O layers. In addition, the superlattice was coordinated with Fe(III) and encapsulated doxorubicin (DOX) to prepare Ti-BPDC@Fe@DOX@PEG (TFDP) after biocompatibility modification. TFDP can realize the simultaneous generation of reactive oxygen species and release of DOX under ultrasound irradiation. Moreover, adjusting the Fe(III) content can effectively modulate the band gap of the superlattice and increase the efficiency of sonodynamic therapy (SDT). The mechanisms underlying this modulation were explored. TFDP with Fe(III) can also be used as a contrast agent for magnetic resonance imaging (MRI). Both in vitro and in vivo experiments demonstrated the ability of TFDP to precisely treat cancer using MRI-guided SDT/chemotherapy. This study expands the applications of superlattices as sonosensitizers with flexible and tailored modifications and indicates that superlattices are promising for precise and customized treatments.     

An Ultrasound Activated Vesicle of Janus Au‐MnO Nanoparticles for Promoted Tumor Penetration and Sono‐Chemodynamic Therapy of Orthotopic Liver Cancer

Sonodynamic therapy (SDT) has the advantages of high penetration, non‐invasiveness, and controllability, and it is suitable for deep‐seated tumors. However, there is still a lack of effective sonosensitizers with high sensitivity, safety, and penetration. Now, ultrasound (US) and glutathione (GSH) dual responsive vesicles of Janus Au‐MnO nanoparticles (JNPs) were coated with PEG and a ROS‐sensitive polymer. Upon US irradiation, the vesicles were disassembled into small Janus Au‐MnO nanoparticles (NPs) with promoted penetration ability. Subsequently, GSH‐triggered MnO degradation simultaneously released smaller Au NPs as numerous cavitation nucleation sites and Mn²⁺ for chemodynamic therapy (CDT), resulting in enhanced reactive oxygen species (ROS) generation. This also allowed dual‐modality photoacoustic imaging in the second near‐infrared (NIR) window and T₁‐MR imaging due to the released Mn²⁺, and inhibited orthotopic liver tumor growth via synergistic SDT/CDT.     

A MXene-derived redox homeostasis regulator perturbs the Nrf2 antioxidant program for reinforced sonodynamic therapy

Ultrasound (US)-mediated sonodynamic therapy (SDT) has emerged as a spatiotemporally controllable therapeutic modality in combating cancer because of its high tissue-penetration depth and minimal invasiveness. However, the elevated nuclear factor erythroid 2-related factor 2 (Nrf2) antioxidant program in cancer cells can serve as a chief reactive oxygen species (ROS) detoxification system to alleviate oxidative injury and promote tumorigenesis, and thus greatly antagonize the therapeutic efficacy of ROS-mediated anticancer therapies. Herein, we report that vanadium carbide MXene-derived carbon dots (PMQDs) can act as high-efficacy sonosensitizers to efficiently generate ROS upon US irradiation and simultaneously hinder the Nrf2 antioxidant program for enhanced sonodynamic therapy of cancer. These PMQDs show superior US-triggered ROS generating ability because of their efficient migration/separation of electron–hole pairs and narrow bandgap. Importantly, these PMQDs can serve as efficient redox homeostasis regulators to perturb the Nrf2 antioxidant mechanism and thus reduce its effects on ROS neutralization for enhanced SDT efficacy. Overall, the present study will not only provide a new paradigm to augment SDT by perturbing the Nrf2 antioxidant program, but also give valuable insights into developing high-efficacy MXene-derived nanoagents for cancer therapy.

A redox homeostasis regulator has been developed as a high-efficacy sonosensitizer to efficiently generate reactive oxygen species upon ultrasound irradiation and simultaneously hinder the Nrf2 antioxidant program for enhanced sonodynamic therapy.     

Investigation on Interaction and Sonodynamic Activity of Chlorophyll-Magnesium-Metronidazole (Chl-Mg-MTZ) with Bovine Serum Albumin (BSA) in Aqueous Solution

Sonodynamic therapy (SDT) is an innovative cancer treatment involving a tumor-localizing sonosensitizer. The synthesis, modification and activity of novel sonosensitizers have attracted more and more researchers’ attention. In the present study, chlorophyll-magnesium (Chl-Mg) and metronidazole (MTZ) were used as reactants and the chlorophyll-magnesium linked metronidazole complex (chlorophyll-magnesium-metronidazole, Chl-Mg-MTZ) was synthesized and characterized. Bovine serum albumin (BSA) was selected as the target protein; the biomolecule affinity and sonodynamic activity of Chl-Mg-MTZ were assessed by their UV–vis and fluorescence spectra. The results indicate that the interaction of Chl-Mg-MTZ to BSA is comparable with that of chlorophyll-magnesium (Chl-Mg). However, during damage of BSA, Chl-Mg-MTZ shows a higher sonodynamic activity than chlorophyll-magnesium (Chl-Mg). Moreover, synchronous fluorescence spectroscopy indicates that Chl-Mg-MTZ has similar binding ability with the tyrosine (Tyr) and tryptophan (Trp) residues of BSA molecules. However, the damage is mainly focused on the Trp residues. In addition, the production of reactive oxygen species (ROS) in the sonodynamic process was detected through the oxidation-extraction of 1,5-diphenylcarbazide (DPCI). The results promote the potential of Chl-Mg-MTZ as a new sonosensitive drug for use in SDT, encouraging further study on tumor treatment.     

An Ultrasound Activated Vesicle of Janus Au-MnO Nanoparticles for Promoted Tumor Penetration and Sono-Chemodynamic Therapy of Orthotopic Liver Cancer

Sonodynamic therapy (SDT) has the advantages of high penetration, non-invasiveness, and controllability, and it is suitable for deep-seated tumors. However, there is still a lack of effective sonosensitizers with high sensitivity, safety, and penetration. Now, ultrasound (US) and glutathione (GSH) dual responsive vesicles of Janus Au-MnO nanoparticles (JNPs) were coated with PEG and a ROS-sensitive polymer. Upon US irradiation, the vesicles were disassembled into small Janus Au-MnO nanoparticles (NPs) with promoted penetration ability. Subsequently, GSH-triggered MnO degradation simultaneously released smaller Au NPs as numerous cavitation nucleation sites and Mn²⁺ for chemodynamic therapy (CDT), resulting in enhanced reactive oxygen species (ROS) generation. This also allowed dual-modality photoacoustic imaging in the second near-infrared (NIR) window and T₁-MR imaging due to the released Mn²⁺, and inhibited orthotopic liver tumor growth via synergistic SDT/CDT.     

Current Advances in Quantum‐Dots‐Based Photoelectrochemical Immunoassays

As a newly developed technique, photoelectrochemical (PEC) immunoassays have attracted great attention in recent years because of their low cost and desirable sensitivity. Because the detection signal originates from the photoelectric conversion of photoelectric materials, the appearance and application of quantum dots (QDs), which possess unique photophysical properties and regulated optoelectronic characteristics, has taken the development of PEC immunoassays to new heights. This review concisely introduces the general mechanism of QDs‐based photoelectric conversion for immunoassays and summarizes the current advances in QD applications in immunoassays. Given that signal strategies and photoactive materials are the key elements in PEC biosensor systems, we comprehensively highlight the state‐of‐the‐art signaling strategies and various applications of QDs in PEC immunoassays to introduce advances in QDs‐based PEC immunoassays. Finally, challenges and future developmental trends are briefly discussed     

Progress in Polydiacetylene Nanowires by Self‐Assembly and SelfPolymerization

In recent years, there has been immense interest in studying nanoscale aggregate structures derived from various polydiacetylenes (PDAs). The motivation for this is not only to understand the fundamental aggregate structures at different scales, but also to explore their potential for future technological applications. PDAs have been made sensitive to external stimuli such as light and chemical entities by incorporating a spectroscopically active moiety or a receptor unit as the head group of the PDA molecule. This makes them suitable for applications such as sensing and actuating. Furthermore, owing to the delocalization of π‐conjugated electrons, PDAs have been exploited as good candidates for organic nonlinear optical materials. This Focus Review highlights some of the instructive work done by various groups to develop well‐defined one‐dimensional assembly systems with a highly structural aspect ratio, which can be directly imaged by microscopic techniques.     

Aligned Nanotubes

Since the discovery of carbon nanotubes by Iijima in 1991, various carbon nanotubes with either a single‐ or multilayered graphene cylinder(s) have been produced, along with their noncarbon counterparts (for example, inorganic and polymer nanotubes). These nanostructured materials often possess size‐dependent properties and show new phenomena related to the nanosize confinement of the charge carriers inside, which leads to the possibility of developing new materials with useful properties and advanced devices with desirable features for a wide range of applications. In particular, carbon nanotubes have been shown to exhibit superior properties attractive for various potential applications, ranging from their use as novel electron emitters in flat‐panel displays to electrodes in electrochemical sensors. For many of the applications, it is highly desirable to have aligned/patterned forms of carbon nanotubes so that their structure/property can be easily assessed and so that they can be effectively incorporated into devices. In this Review, we present an overview on the development of aligned and micropatterned nanotubes, with an emphasis on carbon nanotubes.     

Polymer blends: materials with versatile properties

During the last fifty years blending of dissimilar polymers has been a major path to tailor materials with new properties in industry. Especially in the area of engineering thermoplastic materials this approach has led to a significant number of large volume products, like Polyphenyleneether/High Impact Polystyrene‐blends (PPE/HIPS), Polycarbonate/Styrenics‐blends (PC/ABS), Polycarbonate/Polybutyleneterephthalate‐blends (PC/PBT) and Polyamide/Polyphenyleneether‐alloys (PA/PPE). The commercial success of these materials is mainly related to their unique combinations of properties, which enables their use in a multitude of applications.     

MOF‐Derived Double‐Layer Hollow Nanoparticles with Oxygen Generation Ability for Multimodal Imaging‐Guided Sonodynamic Therapy

The high reactive oxygen species (ROS) generation ability and simple construction of sonosensitizer systems remain challenging in sonodynamic therapy against the hypoxic tumor. In this work, we rationally prepared MOF‐derived double‐layer hollow manganese silicate nanoparticle (DHMS) with highly effective ROS yield under ultrasound irradiation for multimodal imaging‐guided sonodynamic therapy (SDT). The presence of Mn in DHMS increased ROS generation efficiency because it could be oxidized by holes to improve the electron–hole separation. Moreover, DHMS could produce oxygen in the tumor microenvironment, which helps overcome the hypoxia of the solid tumor and thus enhance the treatment efficiency. In vivo experiments demonstrated efficient tumor inhibition in DHMS‐mediated SDT guided by ultrasound and magnetic resonance imaging. This work presents a MOF‐derived nanoparticle with sonosensitive and oxygen generating ability, which provides a promising strategy for tumor hypoxia in SDT.     

Sonodynamic Therapeutic Effects of Sonosensitizers with Different Intracellular Distribution Delivered by Hollow Nanocapsules Exhibiting Cytosol Specific Release

Sonodynamic therapy (SDT) is a novel promising noninvasive therapy involving utilization of low‐intensity ultrasound and sonosensitizer, which can generate reactive oxygen species (ROS) by sonication. In SDT, a high therapeutic effect is achieved by intracellular delivery and accumulation at the target sites of sonosensitizer followed by oxidative damage of produced ROS by sonication. Here, pH‐ and redox‐responsive hollow nanocapsules are prepared through the introduction of disulfide cross‐linkages to self‐assembled polymer vesicles formed from polyamidoamine dendron‐poly(l‐ lysine) for the efficient delivery of sonosensitizer. As sonosensitizer, doxorubicin (DOX), an anticancer drug accumulating into cell nucleus, is selected. Also, the conjugate of DOX and triphenylphosphonium (TPP‐DOX) is synthesized as sonosensitizer with mitochondrial targeting ability. DOX and TPP‐DOX are delivered to nucleus and mitochondria by nanocapsules. Furthermore, DOX‐ or TPP‐DOX‐loaded nanocapsules exhibit in vitro sonodynamic therapeutic effect to HeLa cells with sonication, which might be through oxidative damage to nucleus and mitochondria.     

Stimulus‐Responsive Metal–Organic Frameworks

Materials that can recognize the changes in their local environment and respond by altering their inherent physical and/or chemical properties are strong candidates for future “smart” technology materials. Metal–organic frameworks (MOFs) have attracted a great deal of attention in recent years owing to their designable architecture, host–guest chemistry, and softness as porous materials. Despite this fact, studies on the tuning of the properties of MOFs by external stimuli are still rare. This review highlights the recent developments in the field of stimulus‐responsive MOFs or so‐called smart MOFs. In particular, the various stimuli used and the utility of stimulus‐responsive smart MOFs for various applications such as gas storage and separation, sensing, clean energy, catalysis, molecular motors, and biomedical applications are highlighted by using representative examples. Future directions in the developments of stimulus‐responsive smart MOFs and their applications are proposed from a personal perspective.     

Stimuli‐Responsive NO Release for On‐Demand Gas‐Sensitized Synergistic Cancer Therapy

Featuring high biocompatibility, the emerging field of gas therapy has attracted extensive attention in the medical and scientific communities. Currently, considerable research has focused on the gasotransmitter nitric oxide (NO) owing to its unparalleled dual roles in directly killing cancer cells at high concentrations and cooperatively sensitizing cancer cells to other treatments for synergistic therapy. Of particular note, recent state‐of‐the‐art studies have turned our attention to the chemical design of various endogenous/exogenous stimuli‐responsive NO‐releasing nanomedicines and their biomedical applications for on‐demand NO‐sensitized synergistic cancer therapy, which are discussed in this Minireview. Moreover, the potential challenges regarding NO gas therapy are also described, aiming to advance the development of NO nanomedicines as well as usher in new frontiers in this fertile research area.     

Self‐Assembly of Aggregation‐Induced‐Emission Molecules

The last decade has witnessed rapid developments in aggregation‐induced emission (AIE). In contrast to traditional aggregation, which causes luminescence quenching (ACQ), AIE is a reverse phenomenon that allows robust luminescence to be retained in aggregated and solid states. This makes it possible to fabricate various highly efficient luminescent materials, which opens new paradigms in a number of fields, such as imaging, sensing, medical therapy, light harvesting, light‐emitting devices, and organic electronic devices. Of the various important features of AIE molecules, their self‐assembly behavior is very attractive because the formation of a well‐defined emissive nanostructure may lead to advanced applications in diverse fields. However, due to the nonplanar topology of AIEgens, it is not easy for them to self‐assemble into well‐defined structures. To date, some strategies have been proposed to achieve the self‐assembly of AIEgens. Herein, we summarize the most recent approaches for the self‐assembly of AIE molecules. These approaches can be sorted into two classes: 1) covalent molecular design and 2) noncovalent supramolecular interactions. We hope this will inspire more excellent work in the field of AIE.     

2D Materials in Light: Excited‐State Dynamics and Applications

The development of two‐dimensional (2D) materials have attracted increasing interest due to their unique structure and various potential applications such as opto‐electronic devices and photocatalysis. Our group have contributed to this exciting field by creating novel preparation methods for a various of 2D materials including transition metal dichalcogenides (TMDs), carbon nitrides and single elemental 2D materials from Group 15. Particularly, employing powerful time‐resolved spectroscopic techniques such as femtosecond transient absorption spectroscopy, we elucidated the excited‐state dynamics of 2D materials behind their outstanding performance in photocatalytic and photonic devices. Therefore in this account, we focus on the effective fabrication methods of 2D materials and their photoinduced excited‐state dynamics. Following the introduction in Part 1 , we will summarize our novel strategies for fabricating 2D materials ( Part 2 ). Then in Part 3 we will introduce the instrumentation for exploring the photoinduced excited‐state dynamics of the 2D materials spanning a wide time scale from ultrafast fs to slow ms. Part 4 details the applications of the 2D materials in photocatalysis and nonlinear optics determined by their excited‐state physics and chemistry. Part 5 of perspectives summarizes a few future trends of 2D materials on a series of issues like fabrications, dynamic investigations and photonic optoelectronic applications. Collective efforts through researchers from interdisciplinary fields are expected to further push the exciting territory towards a new horizon.     

Periodic Mesoporous Organosilica with Molecular‐Scale Ordering Self‐Assembled by Hydrogen Bonds

Nanoporous materials with functional frameworks have attracted attention because of their potential for various applications. Silica‐based mesoporous materials generally consist of amorphous frameworks, whereas a molecular‐scale lamellar ordering within the pore wall has been found for periodic mesoporous organosilicas (PMOs) prepared from bridged organosilane precursors. Formation of a “crystal‐like” framework has been expected to significantly change the physical and chemical properties of PMOs. However, until now, there has been no report on other crystal‐like arrangements. Here, we report a new molecular‐scale ordering induced for a PMO. Our strategy is to form pore walls from precursors exhibiting directional H‐bonding interaction. We demonstrate that the H‐bonded organosilica columns are hexagonally packed within the pore walls. We also show that the H‐bonded pore walls can stably accommodate H‐bonding guest molecules, which represents a new method of modifying the PMO framework.     

Advances in Metal‐Free Heterocycle‐Based Columnar Liquid Crystals

Liquid crystals are ordered soft materials formed by self‐organized molecules and can potentially be used as new functional materials for electron‐, ion‐ or molecular‐transport; optical; and bio‐active materials. In particular, the columnar liquid crystals are promising candidates used in various optical and electronic devices. For this purpose, design and synthesis of unconventional materials are essential. In this review, we have summarized several approaches for the synthesis of columnar liquid crystals composed of various heterocyclic systems. We also outline their liquid crystalline and other relevant properties, and their suitability for applications in diverse fields.     

Polymeric STING Pro-agonists for Tumor-Specific Sonodynamic Immunotherapy

The efficacy of combination immunotherapy has been limited by tumor specificity and immune-related adverse events (irAEs). Herein, we report the development of polymeric STING pro-agonists (PSPA), whose sono-immunotherapeutic efficacy is activated by sono-irradiation and elevated glutathione (GSH) within the tumor microenvironment (TME). PSPA is composed of sonosensitizers (semiconducting polymer) and STING agonists (MSA-2) via the GSH-activatable linkers. Under sono-irradiation, PSPA serves as a sonosensitizer to generate ¹O₂ and induce immunogenic cell death (ICD) of malignant tumor cells. Furthermore, MSA-2 is released specifically in tumor microenvironment with highly expressed GSH, minimizing off-target side effects. The activation of the STING pathway elevates the interferon-β level and synergizes with SDT to enhance the anti-tumor response. Therefore, this work proposes a universal approach for spatiotemporal regulation of cancer sono-immunotherapy.     

Carbon Dots: Bottom‐Up Syntheses,Properties, and Light‐Harvesting Applications

The development of cost‐effective and environmentally friendly photocatalysts and photosensitizers has received tremendous attention because of their potential utilization in solar‐light‐harvesting applications. In this respect, carbon dots (CDs) prepared by bottom‐up methods have been considered to be promising light‐harvesting materials. Through their preparation from various molecular precursors and synthetic methods, CDs exhibit excellent optical and charge‐transfer properties. Furthermore, their photophysical properties can be readily optimized and enhanced by means of doping, functionalization, and post‐synthetic treatment. In this review, we summarize the recent progress in CDs synthesized using bottom‐up approaches. These CDs exhibit strong light absorption and unique electron donor/acceptor capabilities for light‐harvesting applications. We anticipate that this review will provide new insights into novel types of photosensitizers and photocatalysts for a wide range of applications.     

An Extra‐Large‐Pore Zeolite with 24×8×8‐Ring Channels Using a Structure‐Directing Agent Derived from Traditional Chinese Medicine

Extra‐large‐pore zeolites have attracted much interest because of their important applications for processing larger molecules. Although great progress has been made in academic science and industry, it is challenging to synthesize these materials. A new extra‐large‐pore zeolite SYSU‐3 (Sun Yat‐sen University no. 3) has been synthesized by using a novel sophoridine derivative as an organic structure‐directing agent (OSDA). The framework structure was solved and refined using continuous rotation electron diffraction (cRED) data from nanosized crystals. SYSU‐3 exhibits a new zeolite framework topology, which has the first 24×8×8‐ring extra‐large‐pore system and a framework density (FD) as low as 11.4 T/1000 ų. The unique skeleton of the OSDA plays an essential role in the formation of the distinctive zeolite structure. This work provides a new perspective for developing new zeolitic materials by using alkaloids as cost‐effective OSDAs.