Tunable Size Research Articles

Review and Future Perspectives of Stimuli-Responsive Bridged Polysilsesquioxanes in Controlled Release Applications

Bridged polysilsesquioxanes (BPSs) are emerging biomaterials composed of synergistic inorganic and organic components. These materials have been investigated as ideal carriers for therapeutic and diagnostic systems for their favorable properties, including excellent biocompatibility, physiological inertia, tunable size and morphology, and their extensive design flexibility of functional organic groups to satisfy diverse application requirements. Stimuli-responsive BPSs can be activated by both endogenous and exogenous stimuli, offering a precise, safe, and effective platform for the controlled release of various targeted therapeutics. This review aims to provide a comprehensive overview of stimuli-responsive BPSs, focusing on their synthetic strategies, biocompatibility, and biodegradability, while critically assessing their capabilities for controlled release in response to specific stimuli. Furthermore, practical suggestions and future perspectives for the design and development of BPSs are presented. This review highlights the significant role of stimuli-responsive BPSs in advancing biomedical research.

Thickness and Doping Density Influence of a High-Voltage Inorganic Perovskite Solar Cell: A SCAPS 1-D Simulation Study

Recently, all inorganic perovskite solar cells have triggered great attention thanks to the rising performance during their development in solid state photovoltaics showing enhanced characteristics, such as: good stability, high photoluminescence quantum yield, tunable size, and morphology. In this work, a high open-circuit voltage solar cell based on all-inorganic perovskite through SCAPS simulator program is presented by analysing electron transport layer (ETL), perovskite layer, hole transport layer (HTL) thickness and doping density from a FTO/TiO2/CsPbBr3/Spiro-OMeTAD/Au structure were modified to observe its influence on solar cell performance. Therefore, simulation results show that a thicker ETL hinders carrier transport towards the FTO layer due to larger distance which leads to higher recombination rate, reducing carrier’s lifetime. Albeit high doping density values in ETL enhances the overall solar cell performance. As for the absorber layer, while its thickness increases, carrier collection rate decreases due to recombination impacting Voc, which results from thickness increase. Based on the results, solar cell efficiency improvement is attributed to the built-in electric field as absorber layer doping density increases. While HTL thickness has minimum impact on the solar cell output, doping density enhances device parameters significantly. Summarising the results obtained from thickness and doping density simulations, the optimal solar cell operation was obtained at 10 nm, 600 nm, and 100 nm layer thickness as well as 1020 cm-3, 1016 cm-3, and 1020 cm-3 doping density (TiO2, CsPbBr3 and Spiro-OMeTAD). Results from three different sources, collected from literature, were used to compare, and fitting them along with simulation results.

Inorganic-Based Nanoparticles and Biomaterials as Biocompatible Scaffolds for Regenerative Medicine and Tissue Engineering: Current Advances and Trends of Development

Regenerative medicine amalgamates stem cell technology and tissue engineering strategies to replace tissues and organs damaged by injury, aging, ailment, and/or chronic conditions by leveraging the innate self-healing mechanism of the body. The term ‘regenerative medicine’ was coined by William A. Haseltine during a 1999 conference on Lake Como. Since its inception in 1968, the field has offered clinical benefits for the regeneration, repair, and restoration of bones, skin, cartilage, neural tissue, and the heart, as well as scaffold fabrication. The field of tissue engineering and regenerative medicine can vastly benefit from advancements in nanoscience and technology, particularly in the fabrication and application of inorganic-based nanoparticles and bionanomaterials. Due to the tunable intrinsic properties, i.e., size, topography, surface charge, and chemical stability, inorganic-based nanoparticles and biomaterials have surpassed traditional synthetic materials. Given the wide gamut of near-future applications of inorganic nanoparticles and biomaterials, this article gives an overview of the emerging roles in stem cell regenerative research, tissue engineering, artificial skin and cartilage regeneration, neural nerve injuries, 3D bioprinting, and development of new inorganic bio-scaffolds. The review also addresses the challenges related to the clinical application and tissue compatibility of inorganic nanoparticles and biomaterials, utilizing current state-of-the-art techniques.

Exploring size-dependent optical property alterations in fine-tuning intermetallic PdCd nanocube sizes.

Tuning the size of intermetallic nanocrystals is challenging due to the conflicting effects of surface free energy and surface diffusion on the disorder-to-order phase transition during wet-chemistry growth. Herein, we synthesized intermetallic PdCd nanocubes with tunable sizes ranging from 8 to 15 nm by adjusting the Cd precursor concentrations using a wet-chemistry approach. This process shares a mechanism of size tuning similar to quantum dot synthesis, involving the regulation of monomer concentration determined by the precursor concentrations. The intermetallic PdCd nanocubes exhibit distinct size-dependent optical properties compared to platinum group metal nanocrystals of similar size ranges, with increased light-induced catalytic enhancement as size increases. The 15 nm-sized nanocubes exhibited the most significant light-induced catalytic enhancement, reaching 3.3 times, while the 8 nm-sized nanocubes showed only a 1.6-fold enhancement in 4-nitrophenol reduction. This study emphasizes the importance of tuning the size of intermetallic nanocrystals, providing valuable insights for future exploration of their size-dependent properties.

Selective ion transport through hydrated micropores in polymer membranes.

Ion-conducting polymer membranes are essential in manyseparation processes and electrochemical devices, including electrodialysis1, redox flow batteries2, fuel cells3 and electrolysers4,5. Controlling ion transport and selectivity in these membranes largely hinges on the manipulation of pore size. Although membrane pore structures can be designed in the dry state6, they are redefined upon hydration owing to swelling in electrolyte solutions. Strategies to control pore hydration and a deeper understanding of pore structure evolution are vital for accurate pore size tuning. Here we report polymer membranes containing pendant groups of varying hydrophobicity, strategically positioned near charged groups to regulate theirhydration capacity and pore swelling. Modulation of thehydrated micropore size (less thantwo nanometres) enables direct control over water and ion transport across broad length scales, as quantified by spectroscopic and computational methods. Ion selectivity improves in hydration-restrained pores created by more hydrophobic pendant groups. These highly interconnected ion transport channels, with tuned pore gate sizes, show higher ionic conductivity and orders-of-magnitude lower permeation rates of redox-active species compared with conventional membranes, enabling stable cycling of energy-dense aqueous organic redox flow batteries. This pore size tailoringapproach provides a promising avenue to membranes with precisely controlled ionic and molecular transportfunctions.

Tetraphenylethene-Containing Nanofilm via Interfacial Confinement Self-Assembly for Fluorescent Monitoring of SOCl2 Leakage in a Li-SOCl2 Battery Electrolyte.

Lithium thionyl chloride (Li-SOCl2) batteries are widely used due to their high energy density and long shelf life. However, the corrosive nature of SOCl2 poses a safety hazard, necessitating effective leak detection methods. We report an approach for real-time fluorescent detection of SOCl2 leakage in Li-SOCl2 batteries using a tetraphenylethene-based nanofilm. The nanofilms were prepared through the interfacial confined self-assembly method and exhibit excellent flexibility, homogeneity, tunable size and thickness, and adaptability to various substrates, enabling easy integration into sensor devices. They possess high photochemical stability and a photoluminescence quantum yield exceeding 25%, demonstrating their potential as high-performance fluorescent sensing material. The nanofilms also exhibit high sensitivity, good reproducibility, and selectivity toward SOCl2 detection. Upon exposure to SOCl2 vapor, the nanofilm shows a red-shifted and fluorescence quenching response, attributed to the protonation of the acylhydrazone bond in the nanofilm by the hydrolysis product of SOCl2, which disrupts the electronic structure of the nanofilm and leads to a decrease in the fluorescence intensity and a shift in the emission wavelength. A detection limit of ∼1.31 ppt and excellent repeatability over 300 cycles are demonstrated, highlighting their high sensitivity and reliability. This work paves the way for a highly sensitive and reliable leak detection system for Li-SOCl2 batteries, enhancing their safety and reliability in various applications.

Electrostatic Assembly of Gold Nanoclusters in Reverse Emulsion Enabling Nanoassemblies with Tunable Structure and Size for Enhanced NIR-II Fluorescence Imaging.

The precise control of the assembly structure and size of gold nanoclusters (AuNCs) can potentially amplify their near-infrared II (NIR-II) fluorescence imaging and targeting properties. However, the conventional electrostatic assembly of AuNCs and charged molecules faces challenges in balancing the inherent electrostatic repulsions among charged units and regulating the diffusion of assembly units. These difficulties limit precise control over assembly size and structure, along with limited options for coassembled molecules, thereby restricting imaging properties and targeting capability. To circumvent this challenge, we developed a reverse emulsion-confined electrostatic assembly method. This technique efficiently constructs AuNC nanoassemblies with diverse coassembled molecules, allowing for the fine-tuning of assembly size and structure, including both core-satellite and homogeneous AuNC nanoassemblies. The development of two distinct nanoassemblies can be partially attributed to the varying diffusive rates of AuNCs or the AuNCs/polymer complex within the fused emulsion droplets. This variance arises from steric hindrances encountered during the emulsion fusion process. Interestingly, core-satellite nanoassemblies exhibit the strongest NIR-II fluorescence enhancement. Finally, the introduction of a hyaluronic acid coating on the surfaces of nanoassemblies with varying sizes enables the nanoprobes to achieve enhanced lymph node imaging through size modulation and macrophage targeting, which are used for surgical navigation to remove lymph node metastases. We envision that this self-assembly strategy can be extended to a wide range of electrostatic assembly systems for the development of multicomponent functional materials.

Potential of a CO2-Responsive supramolecular drug-carrier system as a safer and more effective treatment for cancer

We combined carbon dioxide (CO2)-responsive cytosine-containing rhodamine 6G (Cy-R6G) as a hydrophobic anticancer agent with hydrogen-bonded cytosine-functionalized polyethylene glycol (Cy-PEG) as a hydrophilic supramolecular carrier to construct a CO2-responsive drug delivery system, with the aim of enhancing the responsiveness of the system to the tumor microenvironment and thus the overall effectiveness of anticancer therapy. Due to self-complementary hydrogen bonding interactions between cytosine units, Cy-R6G and Cy-PEG co-assemble in water to form spherical-like nanogels, with Cy-R6G effectively encapsulated within the nanogels. The nanogels exhibit several distinctive physical features, such as widely tunable nanogel size and drug loading capacity for Cy-R6G, intriguing fluorescence properties, high co-assembled structural stability in normal aqueous environments, enhanced anti-hemolytic characteristics, sensitive dual CO2/pH-responsive behavior, and precise and easily controllable CO2-induced release of Cy-R6G. Cytotoxicity assays clearly indicated that, due to the presence of cytosine receptors on the surface of cancer cells, Cy-R6G-loaded nanogels exert selective cytotoxicity against cancer cells in pristine culture medium, but do not affect the viability of normal cells. Surprisingly, in CO2-rich culture medium, Cy-R6G-loaded nanogels exhibit a further significant enhancement in cytotoxicity against cancer cells, and remain non-cytotoxic to normal cells. More importantly, a series of in vitro experiments demonstrated that compared to pristine culture medium, CO2-rich culture medium promotes more rapid selective internalization of Cy-R6G-loaded nanogels into cancer cells through cytosine-mediated macropinocytosis and thus accelerates the induction of apoptosis. Therefore, this newly developed system provides novel avenues for the development of highly effective CO2-responsive drug delivery systems with potent anticancer capabilities.

Nanocarrier-Based Transdermal Drug Delivery Systems for Dermatological Therapy

Dermatoses are among the most prevalent non-fatal conditions worldwide. Given this context, it is imperative to introduce safe and effective dermatological treatments to address the diverse needs and concerns of individuals. Transdermal delivery technology offers a promising alternative compared to traditional administration methods such as oral or injection routes. Therefore, this review focuses on the recent achievements of nanocarrier-based transdermal delivery technology for dermatological therapy, which summarizes diverse delivery strategies to enhance skin penetration using various nanocarriers including vesicular nanocarriers, lipid-based nanocarriers, emulsion-based nanocarriers, and polymeric nanocarrier according to the pathogenesis of common dermatoses. The fundamentals of transdermal delivery including skin physiology structure and routes of penetration are introduced. Moreover, mechanisms to enhance skin penetration due to the utilization of nanocarriers such as skin hydration, system deformability, disruption of the stratum corneum, surface charge, and tunable particle size are outlined as well.

High quality factor, monodisperse micron-sized random lasers based on porous PLGA spheres.

Miniature random lasers with high quality factor are crucial for applications in barcoding, bioimaging, and on-chip technologies. However, achieving monodisperse and size-tunable biocompatible random lasers has been a significant challenge. In this study, we employed poly(lactic-co-glycolic) acid (PLGA), a biocompatible material approved for medical use, as the base material for random lasers. By integrating a dye-doped PLGA solution with a microfluidic system, we successfully fabricated monodisperse and miniature dye-doped PLGA spheres with tunable sizes ranging from 25 to 52 µm. Upon optical pulse excitation, these spheres exhibited strong random lasing emission at 610-640 nm with a threshold of approximately 22 µJ·mm-2. The lasing modes demonstrated a spectral linewidth of 0.2 nm, corresponding to a quality factor of 3100. Fourier transform analysis of the lasing emission revealed fundamental cavity lengths, providing insights into the properties of the random lasers.

Tetrahydropyrimidine Ionizable Lipids for Efficient mRNA Delivery.

Lipid nanoparticles (LNPs) have emerged as an effective and promising technology for messenger RNA (mRNA) delivery, offering a potential solution to physiological barriers and providing an alternative approach to gene therapy without the drawbacks associated with viral delivery. However, efficiently delivering mRNA remains a significant challenge in nucleic acid-based therapies due to the limitations of current LNP platforms in achieving optimal endosomal escape and mRNA release, which largely relies on finding a suitable ionizable lipid. Additionally, the synthesis of these ionizable lipids involves multiple chemical reactions, often making the process time-consuming and difficult to translate. In this study, we employed a facile, catalyst-free, and versatile one-pot multicomponent reaction (MCR) to develop a library of ionizable lipids featuring a pharmacologically significant tetrahydropyrimidine (THP) backbone, tailored for enhanced mRNA delivery. A library of 26 THP ionizable lipids was systematically synthesized in just 3 h and formulated with luciferase mRNA for initial in vitro screening. The THP LNPs exhibited tunable particle sizes, favorable ζ-potentials, and high encapsulation efficiencies. Among them, THP1 demonstrated the highest transfection efficiency both in vitro and in vivo after intramuscular administration, comparable to DLin-MC3-DMA (MC3), a conventional benchmark. Further optimization of THP1 with phospholipids significantly enhanced intramuscular mRNA delivery and showed sustained protein expression in vivo for up to 5 days. More importantly, it demonstrated successful intravenous delivery in a dose-dependent manner with minimal toxicity, as indicated by hematological, histopathological, and proinflammatory cytokine assessments. Furthermore, THP1 LNPs also demonstrated the ability to edit genes in specific liver tissues in a tdTomato transgenic mouse model, highlighting their precision and utility in targeted therapeutic applications. These findings position THP1 LNPs as promising candidates for advancing mRNA-based therapies, with significant implications for clinical translation in vaccine delivery and CRISPR/Cas9-mediated gene editing in the liver.

Self-assembled nanostructured membranes with tunable pore size and shape from plant-derived materials.

Nanostructured materials derived from sustainable sources are of interest as viable alternatives to traditional petroleum-derived sources in membrane applications due to environmental concerns. Here, we present the development of pore size-tunable nanostructured polymer membranes based on a plant-derived material. The membranes were fabricated using a tri-functional amine as the templating core species and a cross-linkable ligand synthesized from rose oil-derived citronellol. The self-assembly of a supramolecular complex between the template core and the ligand forms a hexagonally packed columnar (Colh) mesophase, the dimensions of which can be precisely controlled by changing the stoichiometric ratio between these constituents. Within the hexagonal mesophase stoichiometric range, the pore size of the nanostructured membranes can be tuned from 1.0 to 1.3 nm, with a step size of approximately 0.1 nm. The membranes exhibited a clear distinction in molecular size selectivity, as demonstrated by dye adsorption experiments. The membrane fabricated with a ligand-to-core ratio of 3 to 1 demonstrated shape-based selectivity, exhibiting a higher permeability for propeller-shaped penetrants and highlighting its potential for shape-selective transport. We anticipate that this straightforward approach, using plant-derived materials, can contribute to important sustainability aspects while enhancing the performance of current state-of-the-art nanostructured membranes by enabling precise control over pore size.

Revealing the Mechanism of Ultrasound-Assisted Spherical Agglomeration for Achieving Millimeter-Sized Agglomerates of 3-Nitro-1,2,4-triazol-5-one with High Sphericity and Tunable Sizes

Revealing the Mechanism of Ultrasound-Assisted Spherical Agglomeration for Achieving Millimeter-Sized Agglomerates of 3-Nitro-1,2,4-triazol-5-one with High Sphericity and Tunable Sizes

Sodium Assists Controlled Synthesis of Cubic Rare-Earth Oxyfluorides Nanocrystals for Information Encryption and Near-Infrared-IIb Bioimaging.

Rare-earth oxyfluoride (REOF) colloidal nanocrystals (NCs) suffer from a low photoluminescence efficiency due to their small size with poor crystallinity and a detrimental surface quenching effect. Herein, we introduce an innovative approach that involves doping sodium ions into REOF NCs to produce monodisperse, size-controllable, well-crystallized, and highly luminescent colloidal REOF core/shell NCs. The Na+ doping allows for successfully synthesizing the cubic REOF NCs with a tunable size from 6 to 30 nm. Further fabrication of the core/shell NCs doped with Na+ results in enhancements up to 1062 (Ho3+), 1140 (Er3+), and 2212 (Tm3+) folds in upconversion luminescence and 17.7 folds (Er3+) in downconversion luminescence compared to that of core/shell NCs without doping Na+ ions. These NCs were subsequently developed into multicolor luminescent inks, demonstrating significant potential application for information security, and used for near-infrared-IIb (NIR-IIb) (1500-1700 nm) in vivo imaging, which exhibits a high-resolution in vivo dynamic imaging capability with a signal-to-noise ratio of 5.28. These results present the way to the controlled synthesis of efficient luminescent cubic LuOF: RE3+/LuOF core/shell NCs, expanding the toolkit of rare-earth doped NCs in diverse applications such as advanced encoding encryption, varied fluorescence imaging, and biomedicine.

Synthesis and Magnetic Properties of Spherical Maghemite Nanoparticles with Tunable Size and Surface Chemistry.

We report the synthesis of uniform populations of spherical maghemite nanoparticles by thermal decomposition of iron precursors with tunable diameters centered at 3.3, 7.5, and 12.0 nm and tunable surface chemistry. The three stabilizing ligands were fatty acids with three different alkyl chain lengths (18, 12, and 8 carbon atoms). The unprecedented accurate control of the surface chemistry is made possible by the use of three types of iron complexes, that is, iron oleate (C18), iron dodecanoate (C12), and iron octanoate (C8), associated with fatty acid ligands having the same alkyl chain length, that is, oleic acid (C18), dodecanoic acid (C12), and octanoic acid (C8). Since the thermal decomposition of the iron precursor varies with the chain length, no general rules can be applied to control the nanoparticle size, but optimal synthesis conditions have been investigated to induce the growth of nanoparticles with three different surface chemistries, keeping the diameters centered at 3.3, 7.5, and 12.0 nm. Finally, structural characterization of the nine populations of maghemite nanoparticles was performed by transmission electron microscopy and X-ray diffraction, and magnetic properties were determined by using SQUID magnetometry.

Flexible MOF@fabrics composites: The in-situ growth of metal-organic frameworks on cotton and selectively adsorption of gold(III) from aqueous solution

Metal-organic frameworks (MOFs) show great potential applications in dealing with heavy metal pollution due to their unique large specific surface area, tunable pore size, and diverse active groups. However, the powder form of MOFs has suffered from the disadvantages of difficult recycling and secondary contamination after adsorption of heavy metals, which seriously limits their practical application. Therefore, in this work, we prepared a series of bifunctional zirconium-based MOFs cotton fabric composites (MCFC) via in situ growth of MOFs on carboxylated cotton fabric, exhibiting large specific surface area, adjustable pore size, and effective adsorption ability. The prepared CF-UiO-66-(OH)2-FA shows an excellent adsorption efficiency of Au(III) more than 99.990 %, and the saturated adsorption amount is up to 190.98 mg·g−1 at 25 °C. Meanwhile, the kinetic experiment analysis demonstrated that the Au(III) adsorption behavior of MCFC follows pseudo-second-order (PSO) kinetic model. More importantly, it also exhibits great selectivity in adsorbing Au(III) from the mixture of multiple metal ions coexisted solution. The results of adsorption thermodynamics and adsorption isotherms indicate that adsorption is monolayer and a spontaneous, exothermic process. And the ideal adsorption and separation process could be finished by quickly filtrating with a single or multi-layer MCFC. Excellent adsorption performance even after four cycles of adsorption. Therefore, the fabricated MCFC shows great processability, flexibility, collectability and reusability in adsorbing and recycling precious metal ion from wastewater.

Formation of flake-like DAAF crystals with tunable size realized on a microfluidic platform for binder-free initiator explosives

Flake-like energetic crystal has a great potential to achieve initiator explosive with high reactivity, low initiation threshold, high safety, and facile post-processing, but it has been limited for 3,3′-diamino-4,4′-azoxyfurazan (DAAF) by the difficulties in controlling crystal morphology. Here reported is a microfluidic preparation of flake-like DAAF crystals (f-DAAF) with tunable size by combined effect of the adding of facet-controlling agent (nigrosin alcohol soluble) and tuning of the external crystallization conditions. The results show that the crystal system of f-DAAF belong to monoclinic system, the (−201) facet is the largest exposed face. The f-DAAF possess high crystallinity, tunable flake aspect ratio from 6.15 to 66.8 and specific surface area from 2.57 to 5.67 m2·g−1. Molecular dynamics simulations were performed to investigate the selective interactions between the two molecules (facet-controlling agent and solvent) and different crystal faces of DAAF in a real experiment environment. Combined with the experimental results, a possible growth mechanism of the flake-like morphology was discussed. It is found that the f-DAAF not only possess lower impact sensitivity itself, but also can reduce the impact sensitivity of other explosives with high impact sensitivity. The electric explosion derived flyer initiation experiments show that the initiation sensitivity of f-DAAF is much lower than that of raw DAAF in micron size, and comparable to that of ultrafine DAAF. This work demonstrates the promising application potential of f-DAAF as high-performance initiator explosives with low initiation threshold and high safety, and also provides an effective way for their preparation.

Novel post-heat treatment green biodegradable PLA@SiO2 nanocomposite membrane for water desalination

Membrane distillation (MD) has received significant attention because of its energy efficiency and ability to treat industrial wastewater and salty water. However, the synthetic nature of commonly used membranes raises environmental disposal concerns, requiring the development of alternative eco-membranes. To address this issue, a novel, eco-friendly membrane using polylactic acid (PLA) coated with green silica nanoparticles (SiO2 NPs), modified by post-heat treatment, was developed for effective direct contact membrane distillation (DCMD). Herein, two nanofibrous membranes were fabricated via electrospinning/electrospraying: one, PLA, with a 12.5 wt% PLA solution, and another, PLA@SiO2, with 2 % (w/v) SiO2 NPs coating. The PLA@SiO2 membrane demonstrated enhanced hydrophobicity. Various post-heat treatments were applied to optimize membrane properties, such as structure, pore size, hydrophobicity, liquid entry pressure (LEP), thickness, and thermal stability. In addition, the desalination performance of all membranes was evaluated using a DCMD unit for 6 h. Results showed that the heat-pressed then annealed PLA@SiO2 membrane (denoted M44) exhibited notable improvements, including an LEP of 128.7 kPa, a tunable pore size of 0.21 μm, and a contact angle of 135.9°. Furthermore, the M44 membrane demonstrated a porosity of 80.5 %, a stable permeate flux of 14.3 kg.m−2.h−1, and an exceptional salt rejection of 99.99 % over a 24 h DCMD test. This novel eco-membrane shows promising potential for efficient desalination and represents a significant advancement in sustainable MD applications.

Overview of Liquid Sample Preparation Techniques for Analysis, Using Metal-Organic Frameworks as Sorbents.

The preparation of samples for instrumental analysis is the most essential and time-consuming stage of the entire analytical process; it also has the greatest impact on the analysis results. Concentrating the sample, changing its matrix, and removing interferents are often necessary. Techniques for preparing samples for analysis are constantly being developed and modified to meet new challenges, facilitate work, and enable the determination of analytes in the most comprehensive concentration range possible. This paper focuses on using metal-organic frameworks (MOFs) as sorbents in the most popular techniques for preparing liquid samples for analysis, based on liquid-solid extraction. An increase in interest in MOFs-type materials has been observed for about 20 years, mainly due to their sorption properties, resulting, among others, from the high specific surface area, tunable pore size, and the theoretically wide possibility of their modification. This paper presents certain advantages and disadvantages of the most popular sample preparation techniques based on liquid-solid extraction, the newest trends in the application of MOFs as sorbents in those techniques, and, most importantly, presents the reader with a summary, which a specific technique and MOF for the desired application. To make a tailor-made and well-informed choice as to the extraction technique.

Optimized Fabrication of Dendritic Mesoporous Silica Nanoparticles as Efficient Delivery System for Cancer Immunotherapy.

In the past decade, cancer immunotherapy has revolutionized the field of oncology. Major immunotherapy approaches such as immune checkpoint inhibitors, cancer vaccines, adoptive cell therapy, cytokines, and immunomodulators have shown great promise in preclinical and clinical settings. Among them, immunomodulatory agents including cancer vaccines are particularly appealing; however, they face limitations, notably the absence of efficient and precise targeted delivery of immune-modulatory agents to specific immune cells and the potential for off-target toxicity. Nanomaterials can play a pivotal role in addressing targeting and other challenges in cancer immunotherapy. Dendritic mesoporous silica nanoparticles (DMSNs) can enhance the efficacy of cancer vaccines by enhancing the effective loading of immune modulatory agents owing to their tunable pore sizes. In this work, an emulsion-based method is optimized to customize the pore size of DMSNs and loaded DMSNs with ovalbumin (OVA) and cytosine-phosphate-guanine (CpG) oligodeoxynucleotides (CpG-OVA-DMSNs). The immunotherapeutic effect of DMSNs is achieved through controlled chemical release of OVA and CpG in antigen-presenting cells (APCs). The results demonstrated that CpG-OVA-DMSNs efficiently activated the immune response in APCs and reduced tumor growth in the murine B16-OVA tumor model.