Candidates For Carriers Research Articles

Preparation and structure of titanium‐containing pyrophosphate glasses prepared using the liquid‐phase method

AbstractPhosphate invert glasses (PIGs) exhibit excellent biocompatibility because of their high chemical durability and controlled ion releasability. PIGs are composed of short phosphate units such as ortho‐ and pyrophosphate. This structure makes it difficult to obtain clear glass using the melt‐quenching method. Our previous work reported that intermediate oxides (such as TiO2 and Nb2O5)‐containing PIGs exhibit good glass‐forming ability and ion dissolution controllability. This work used a liquid‐phase method to prepare PIGs at room temperature and pressure. Furthermore, TiO2 was used to control ion releasability for biomedical applications. Titanium‐containing PIGs were successfully prepared using a liquid‐phase method. Pyrophosphate and titania formed P‐O‐Ti bonds with an increasing TiO2 content in the glass, forming chain‐like structural units such as (‐O‐P‐O‐P‐O‐Ti‐O‐)n. The number of chain‐like structures increased with an increasing TiO2 content in the glass, improving the chemical durability. Hence, the ion releasability of titanium‐containing PIGs prepared using the liquid‐phase method can be controlled by the glass structure. Additionally, the PIGs exhibited good cell viability. Therefore, the PIGs are candidates for carriers of therapeutic inorganic ions for biomedical applications.

Topological Magneto-optical Effect from Skyrmions in Two-Dimensional Ferromagnets.

Skyrmions in two-dimensional (2D) magnetic materials are considered as ideal candidates for information carriers in next-generation spintronic devices. However, conventional methods for elucidating the physical properties of skyrmions have limited the development of skyrmions in diverse 2D magnetic material systems due to their requirements for electrical conductivity. To overcome this limitation, we propose to utilize an optical method (magneto-optical Kerr technique) to detect the skyrmions in 2D magnetic materials. Herein, the graphene/Fe3GeTe2/graphene vertical van der Waals (vdW) heterostructure devices are fabricated to generate stabilized skyrmions by applying out-of-plane current. In combination with magnetic circular dichroism measurements, we observe topological-reflective magnetic circular dichroism (T-RMCD) effects in Fe3GeTe2 flakes and attribute the peak-shaped component in T-RMCD to the annihilation of skyrmion magnetic domains. Notably, the T-RMCD signal can maintain up to a temperature as high as the Curie temperature of Fe3GeTe2 flakes (∼200 K). Our work provides a universal, contactless, and nondestructive approach for studying the physical properties of skyrmions in 2D vdW magnetic materials while adding another degree of freedom to the modulation of skyrmions.

Non-volatile magnon transport in a single domain multiferroic

Antiferromagnets have attracted significant attention in the field of magnonics, as promising candidates for ultralow-energy carriers for information transfer for future computing. The role of crystalline orientation distribution on magnon transport has received very little attention. In multiferroics such as BiFeO3 the coupling between antiferromagnetic and polar order imposes yet another boundary condition on spin transport. Thus, understanding the fundamentals of spin transport in such systems requires a single domain, a single crystal. We show that through Lanthanum (La) substitution, a single ferroelectric domain can be engineered with a stable, single-variant spin cycloid, controllable by an electric field. The spin transport in such a single domain displays a strong anisotropy, arising from the underlying spin cycloid lattice. Our work shows a pathway to understanding the fundamental origins of magnon transport in such a single domain multiferroic.

Easily recyclable pd-decorated hierarchically porous nanofibers for the selective hydrogenation of phenol

The electrospun nanofibers are good candidates for the catalyst carriers, however the fabrication of electrospun nanofibers with well-developed porous structures is still a big challenge. Herein, the SiO2 nanofibers obtained by electrospinning and pyrolysis are functionalized with polydopamine (PDA) and UiO-66-NH2, and after Pd loading the hierarchically porous Pd/UiO-SiO2 nanofiber catalysts were developed. The surface properties and microstructures of the Pd/UiO-SiO2 nanofiber catalysts were regulated by adjusting the concentrations of dopamine (DA) and zirconium tetrachloride (ZrCl4), and the catalytic performance was tested in the selective hydrogenation of phenol to cyclohexanone. The as-prepared Pd/UiO-SiO2-3–21.44 has abundant hierarchical pores and amino groups, high Pd content with good dispersion, and rich Pd(0), thus exhibiting a superior specific activity of 47.3 h−1 higher than most Pd-based catalysts. Most importantly, the Pd/UiO-SiO2-3–21.44 nanofiber catalyst can be directly taken out from the reaction solution and used for the next run, and has good catalytic stability.

Graphene-Based Photodynamic Therapy and Overcoming Cancer Resistance Mechanisms: A Comprehensive Review.

Photodynamic therapy (PDT) is a non-invasive therapy that has made significant progress in treating different diseases, including cancer, by utilizing new nanotechnology products such as graphene and its derivatives. Graphene-based materials have large surface area and photothermal effects thereby making them suitable candidates for PDT or photo-active drug carriers. The remarkable photophysical properties of graphene derivates facilitate the efficient generation of reactive oxygen species (ROS) upon light irradiation, which destroys cancer cells. Surface functionalization of graphene and its materials can also enhance their biocompatibility and anticancer activity. The paper delves into the distinct roles played by graphene-based materials in PDT such as photosensitizers (PS) and drug carriers while at the same time considers how these materials could be used to circumvent cancer resistance. This will provide readers with an extensive discussion of various pathways contributing to PDT inefficiency. Consequently, this comprehensive review underscores the vital roles that graphene and its derivatives may play in emerging PDT strategies for cancer treatment and other medical purposes. With a better comprehension of the current state of research and the existing challenges, the integration of graphene-based materials in PDT holds great promise for developing targeted, effective, and personalized cancer treatments.

Preparation and characterization of AChE immobilized magnetic bio-nanocomposites (Fe3O4@Cht/Au) for pesticide detection

Free enzymes cause difficulties in many applications due to their insufficient stability, loss of activity in a short time, and most importantly, although they are costly, they are used only once in reactions, lose their effect and cannot be recovered from the environment. Magnetic nanoparticles coated with biocompatible polymeric material are potential candidates for promising enzyme carriers due to their multifunctional pore surfaces, easy removal from the environment provided by the magnetization, ability to main stability under various harsh conditions. This study prepared a biosensor candidate based on the inhibiting acetylcholinesterase enzyme by organophosphate pesticides from chitosan-coated magnetic nanoparticles doped with gold. Transmission electron microscopy, scanning electron microscopy, X-ray diffraction diffractometry, and Fourier transform infrared spectroscopy analysis confirmed the structure of synthesized nanocomposites. Magnetic characteristics of the nanocomposites were assessed using VSM. Bio-nanocomposite (Fe3O4@Cht/Au/AChE) was used to determine environmental pollutants qualitatively. Remediation of organophosphate-containing wastewater is an essential issue for environmental sustainability. In this work, Dichlorvos and Chlorpyrifos were selected as organic pollutants to assess the enzymatic activity of immobilized Fe3O4@Cht/Au/AChE. Optimum conditions for AChE enzyme were immobilized nanostructures (Fe3O4@Cht/Au/AChE) were determined. The optimum pH for the immobilized enzyme was found to be 8, and the optimum temperature was found to be 60 °C. Retained immobilized enzyme activity is found to be around 50% for the 20th reuse. In the presence of 150 µL pesticide, retained immobilized enzyme activity is found to be around 25%. Method validation was performed for pesticides. When using immobilized AChE, the LOD (limit of detection)-LOQ (limit of quantitation) values for Dichlorovos and Chlorpyrifos was obtained in the range of 0.0087–0.029 nM and 0.0014–0.0046 nM, respectively. The relative standard deviation (RSD%) values, which are indicators of precision, were found to be below 2%.

Temperature/GSH Dual Responsive Fluorinated Mesoporous Silica‐Coated Au NRs for Serum‐Resistant Gene Delivery**

AbstractMesoporous silica nanoparticles (MSN) are emerging as one of the most appealing candidates for gene carriers. Nevertheless, one major obstacle for their clinical application is the lack of efficient controlled release and gene delivery. In this study, a mesoporous silica‐modified gold nanorods (Au NRs) controlled release platform was synthesized. Then a thermosensitive copolymer was grafted to the surface of release platform, to impart the switching response of carrier under the photothermal of Au NRs. Fluorination were modified on the surface of MSN through a disulfide bond to achieve glutathione (GSH) response release and improve serum‐resistant ability. This gene carrier, with notable DNA condensation ability and negligible cytotoxicity, could be easily internalized into cells, enhanced green fluorescent protein expression in the presence of serum under laser irradiation. This work inspired us to solve the problem of traditional controllable sustained release and realize the performance of intracellular switch response to gene sustained release.

Carbon Dots an Integrative Nanostructure for Fluorescent Bio-imaging, Targeted Delivery of Medication and Phototherapy in Malignancy: A Review

Background: Silent onset and metastasis in tissues make cancer the most devastating illness globally. Monitoring the growth of the tumour and delivering drugs to specific tissues are some of the major issues associated with treatment. However, with an improved understanding of tumour microenvironments and advancements in nanocarriers of drugs, novel nano-targeting pathways that can be utilised by nanocarriers have been developed. Carbon Dots, with their tiny size and outstanding physicochemical features, are an emerging category of carbon nanostructures that have attracted a lot of curiosity. Objective: Multitudinous attempts and extensive studies have been undertaken by many researchers regarding the synthesis of Carbon Dots and their applications in various fields. These studies have explained that the synthesised Carbon Dots have versatile surface functionalities, high luminescence, and excellent biocompatibility. This article focuses on recent developments in synthesis approaches, carbon precursors used, and applications of Carbon Dots, specifically within the biomedical field, with a particular focus on cancer. Results: Carbon dots synthesised from a variety of precursors can act as prominent candidates for bioimaging and drug carriers and are used in cancer phototherapy. In this article, Carbon Dots are summarised based on their bright luminescent properties, distinct structure, drug loading capacity, and near-infrared (NIR) emission. Conclusion: Carbon dots, employed as tumour theranostics, can serve as an alternative to synthetic fluorescent dyes. They fulfil the role of bioimaging agents and facilitate the precise delivery of drugs to cancer cells. Additionally, they exhibit excellence as phototherapeutic agents, featuring high nearinfrared (NIR) emission and minimal side effects.

Transformable binary-prodrug nanoparticles harness heterogeneity of neutrophils to overcome multidrug resistance and promote pyroptosis in cancer

Neutrophils, the most abundant myeloid cells, exhibit diverse phenotypic and functional variants in both homeostatic and disease conditions. The inherent heterogeneity of neutrophils positions them as promising candidates for drug carriers, facilitating precise drug delivery to tumor tissues and enhancing treatment accuracy and effectiveness. However, challenges arise from drug toxicity hindering neutrophil migration and the imperative need for efficient drug release at tumor sites. In response to these challenges, we have developed transformable binary-prodrug nanoparticles known as DSST@PSA. These nanoparticles manifest in two distinct forms: U-shaped and I-shaped. The U-shaped DSST@PSA variant demonstrates reduced toxicity and can be effectively transported to tumor sites through a neutrophil-mediated drug delivery system. Within the tumor microenvironment, the elevated glutathione concentration triggers a transformation of DSST@PSA into I-shaped structures. The I-shaped DSST@PSA variant exhibits the capability to overcome doxorubicin-induced multidrug resistance and promote pyroptosis in tumor cells. Our innovative DSST@PSA treatment strategy has demonstrated remarkable therapeutic effects in both in situ breast and metastatic mouse models. This breakthrough in neutrophil-mediated drug delivery systems significantly enhances treatment precision and efficacy.

Iron Complexes as Potential Carriers of Diffuse Interstellar Bands: The Photodissociation Spectrum of Fe+(H2O) at Optical Wavelengths.

The fullerene ion C60+ is the only carrier of diffuse interstellar bands (DIBs) identified so far. Transition-metal compounds feature electronic transitions in the visible and near-infrared regions, making them potential DIB carriers. Since iron is the most abundant transition metal in the cosmos, we here test this idea with Fe+(H2O). Laboratory spectra were obtained by photodissociation spectroscopy at 80 K. Spectra were modeled with the reflection principle. A high-resolution spectrum of the DIB standard star HD 183143 served as an observational reference. Two broad bands were observed from 4120 to 6800 Å. The 4120-4800 Å band has sharp features emerging from the background, which have the width of DIBs but do not match the band positions of the reference spectrum. Calculations show that the spectrum arises from a d-d transition at the iron center. While no match was found for Fe+(H2O) with known DIBs, the observation of structured bands with line widths typical for DIBs shows that small molecules or molecular ions containing iron are promising candidates for DIB carriers.

Redox regulation of Ni hydroxides with controllable phase composition towards biomass-derived polyol electro-refinery.

Electrocatalytic refinery from biomass-derived glycerol (GLY) to formic acid (FA), one of the most promising candidates for green H2 carriers, has driven widespread attention for its sustainability. Herein, we fabricated a series of monolithic Ni hydroxide-based electrocatalysts by a facile and in situ electrochemical method through the manipulation of local pH near the electrode. The as-synthesized Ni(OH)2@NF-1.0 affords a low working potential of 1.36 VRHE to achieve 100% GLY conversion, 98.5% FA yield, 96.1% faradaic efficiency and ∼0.13 A cm-2 of current density. Its high efficiency on a wide range of polyol substrates further underscores the promise of sustainable electro-refinery. Through a combinatory analysis via H2 temperature-programmed reduction, cyclic voltammetry and in situ Raman spectroscopy, the precise regulation of synthetic potential was discovered to be highly essential to controlling the content, phase composition and redox properties of Ni hydroxides, which significantly determine the catalytic performance. Additionally, the 'adsorption-activation' mode of ortho-di-hydroxyl groups during the C-C bond cleavage of polyols was proposed based on a series of probe reactions. This work illuminates an advanced path for designing non-noble-metal-based catalysts to facilitate electrochemical biomass valorization.

Simultaneous Electrophysiology and Imaging Reveal Changes in Lipid Membrane Thickness and Tension upon Uptake of Amphiphilic Gold Nanoparticles.

Amphiphilic gold core nanoparticles (AmNPs) striped with hydrophilic 11-mercapto-1-undecanesulfonate (MUS) and hydrophobic 1-octanethiol (OT) ligands are promising candidates for drug carriers that passively and nondisruptively enter cells. Yet, how they interact with cellular membranes is still only partially understood. Herein, we use electrophysiology and imaging to carefully assess changes in droplet interface bilayer lipid membranes (DIBs) incurred by striped AmNPs added via microinjection. We find that AmNPs spontaneously reduce the steady-state specific capacitance and contact angle of phosphatidylcholine DIBs by amounts dependent on the final NP concentration. These reductions, which are greater for NPs with a higher % OT ligands and membranes containing unsaturated lipids but negligible for MUS-only-coated NPs, reveal that AmNPs passively embed in the interior of the bilayer where they increase membrane thickness and lateral tension through disruption of lipid packing. These results demonstrate the enhanced evaluation of nano-bio interactions possible via electrophysiology and imaging of DIBs.

Spatial control of skyrmion stabilization energy by low-energy Ga+ ion implantation

Magnetic skyrmions are candidates for information carriers in Brownian and stochastic computers. Developing a technique for fabricating a film with a suitable potential landscape, wherein the information carrier may diffuse freely, is essential for these probabilistic computers. In this study, to build the desired local potential into magnetic films, a 1.2 nm-thick Co-Fe-B film with a 5.2 nm-thick cap layer was irradiated by a focused ion beam (FIB) using Ga+ as the ion source under a low acceleration voltage of 5 keV. The fluences ranged from 0 to 25 × 1012 ions/cm2. Consequently, the critical temperature at which skyrmions appear or disappear is shifted by several 1–10 K depending on the ion fluence. The origin of this effect is discussed by observing the ion implantation profile and the surface sputtering depth using time-of-flight secondary ion mass spectrometry (TOF-SIMS) and atomic force microscopy (AFM). The results of TOF-SIMS measurements show that most of the Ga atoms exist in the Co–Fe–B layer. If all Ga atoms exist in the Co–Fe–B layer, the Ga concentration is 7 × 10−3 at. % after irradiation of 0.8 × 1012 ions/cm2. The AFM results show a sputtered pattern with 0.2 nm depth after irradiation of 16 × 1012 ions/cm2. Finally, the effect of irradiation on the diffusion coefficient was examined. It was determined that small fluences of 1.6 × 1012 and 0.8 × 1012 ions/cm2 can construct a potential barrier controlling skyrmions while maintaining diffusion coefficients as high as 10 μm2/s. The FIB process can be used to draw a circuit of probabilistic computers with skyrmions as information carriers.

Antiferromagnetic half-skyrmions electrically generated and controlled at room temperature.

Topologically protected magnetic textures are promising candidates for information carriers in future memory devices, as they can be efficiently propelled at very high velocities using current-induced spin torques. These textures-nanoscale whirls in the magnetic order-include skyrmions, half-skyrmions (merons) and their antiparticles. Antiferromagnets have been shown to host versions of these textures that have high potential for terahertz dynamics, deflection-free motion and improved size scaling due to the absence of stray field. Here we show that topological spin textures, merons and antimerons, can be generated at room temperature and reversibly moved using electrical pulses in thin-film CuMnAs, a semimetallic antiferromagnet that is a testbed system for spintronic applications. The merons and antimerons are localized on 180° domain walls, and move in the direction of the current pulses. The electrical generation and manipulation of antiferromagnetic merons is a crucial step towards realizing the full potential of antiferromagnetic thin films as active components in high-density, high-speed magnetic memory devices.

Electronic spectroscopy of heptacene ions in the search for carriers of diffuse interstellar bands

Context. The absorption bands of the interstellar medium (ISM) in the optical and near-infrared regions called the diffuse interstellar bands (DIBs) have been known for almost a century, yet their origins remain largely unknown. Knowledge of molecular carriers of DIBs would allow for a much better understanding of the chemistry and physics of the ISM. Polycyclic aromatic hydrocarbons (PAHs) and, among them, polyacenes have been suggested as promising candidates for carriers of DIBs. Aims. In this paper, we report on the spectroscopy of heptacene (Hep), the polyacene molecule consisting of seven aromatic rings in a linear arrangement, in its cationic and anionic forms (Hep+/−). The performed spectroscopic studies made it possible to accurately determine the Hep+/− absorption band positions and to conduct a direct comparison of laboratory and observational spectra. Methods. We utilized helium-tagging action spectroscopy to measure the spectra of Hep+/− in a wide spectral range of 3000–13 000 Å. In most cases, the spectra obtained by this method can be directly compared with the observational spectra. By analyzing the spectral shift as a function of the number of attached helium atoms, we obtained precise estimates of the gas-phase band positions. Quantum-chemical computations were used to support and interpret the findings. Matrix isolation spectroscopy provided information on the spectral properties of neutral Hep and extended the spectral range for Hep+. Results. We found several absorption bands characterized by a rather large full width at half maximum in the spectra of Hep+/−. The two most intense bands were found at 4714 ± 5 Å and 12 250 ± 12 Å for Hep+ and at 4673 ± 14 Å and 11326 ± 4 Å for Hep−. We did not find any good match between laboratory and observational spectra. In particular, the intrinsic width of the absorption bands of Hep+/− is much higher than that of most observed DIBs. Conclusions. The non-detection of Hep+/− in the observational spectra excludes the bottom-up formation route for polyacenes in the ISM. Larger polyacene molecules could still be considered as potential carriers of DIBs in the case of an efficient top-down formation route. All currently measured polyacene ions exhibit relatively broad absorption bands. Therefore, additional spectroscopy studies of neutral polyacenes and larger polyacene ions as well as the study of possible top-down formation routes are suggested.

Design of an Antibiotic-Releasing Polymer: Physicochemical Characterization and Drug Release Patterns.

Conventional drug delivery has its share of shortcomings, especially its rapid drug release with a relatively short duration of therapeutic drug concentrations, even in topical applications. Prolonged drug release can be effectively achieved by modifying the carrier in a drug delivery system. Among the several candidates for carriers studied over the years, poly (ether ether ketone), a biocompatible thermoplastic, was chosen as a suitable carrier. Its inherent hydrophobicity was overcome by controlled sulfonation, which introduced polar sulfonate groups onto the polymer backbone. Optimization of the sulfonation process was completed by the variation of the duration, temperature of the sulfonation, and concentration of sulfuric acid. The sulfonation was confirmed by EDS and the degree of sulfonation was determined by an NMR analysis (61.6% and 98.9%). Various physical properties such as morphology, mechanical strength, and thermal stability were studied using scanning electron microscopy, tensile testing, and thermogravimetric analysis. Cytotoxicity tests were performed on the SPEEK samples to study the variation in biocompatibility against a Vero cell line. The drug release kinetics of ciprofloxacin (CP) and nalidixic acid sodium salt (NA)-loaded membranes were studied in deionized water as well as SBF and compared against the absorbance of standardized solutions of the drug. The data were then used to determine the diffusion, distribution, and permeability coefficients. Various mathematical models were used to fit the obtained data to establish the order and mechanism of drug release. Studies revealed that drug release occurs by diffusion and follows zero-order kinetics.

Beyond Pristine Metal-Organic Frameworks: Preparation of Hollow MOFs and Their Composites for Catalysis, Sensing, and Adsorption Removal Applications.

Metal-organic frameworks (MOFs) have been broadly applied to numerous domains with a substantial surface area, tunable pore size, and multiple unsaturated metal sites. Recently, hollow MOFs have greatly attracted the scientific community due to their internal cavities and gradient pore structures. Hollow MOFs have a higher tunability, faster mass-transfer rates, and more accessible active sites when compared to traditional, solid MOFs. Hollow MOFs are also considered to be candidates for some functional material carriers. For example, composite materials such as hollow MOFs and metal nanoparticles, metal oxides, and enzymes have been prepared. These composite materials integrate the characteristics of hollow MOFs with functional materials and are broadly used in many aspects. This review describes the preparation strategies of hollow MOFs and their composites as well as their applications in organic catalysis, electrochemical sensing, and adsorption separation. Finally, we hope that this review provides meaningful knowledge about hollow-MOF composites and their derivatives and offers many valuable references to develop hollow-MOF-based applied materials.

Tracing PAH Emission in λ-Orionis Using COBE/DIRBE Data

We use archival COBE/DIRBE data to construct a map of polycyclic aromatic hydrocarbon (PAH) emission in the λ-Orionis region. The presence of the 3.3 μm PAH feature within the DIRBE 3.5 μm band and the corresponding lack of significant PAH spectral features in the adjacent DIRBE bands (1.25, 2.2, and 4.9 μm) enable estimation of the PAH contribution to the 3.5 μm data. Having the shortest wavelength of known PAH features, the 3.3 μm feature probes the smallest PAHs, which are also the leading candidates for carriers of anomalous microwave emission (AME). We use this map to investigate the association between the AME and the emission from PAH molecules. We find that the spatial correlation in λ-Orionis is higher between AME and far-infrared dust emission (as represented by the DIRBE 240 μm map) than it is between our PAH map and AME. This finding, in agreement with previous studies using PAH features at longer wavelengths, is in tension with the hypothesis that AME is due to spinning PAHs. However, the expected correlation between mid-infrared and microwave emission could potentially be degraded by different sensitivities of each emission mechanism to local environmental conditions even if PAHs are the carriers of both.

Supramolecular Biopharmaceutical Carriers Based on Host-Guest Interactions.

Traditional drugs have the disadvantages of poor permeability and low solubility, which makes the utilization of pesticides lower and brings many side effects. With the continuous development of supramolecular chemistry in recent years, it has also played an irreplaceable role in the field of pharmaceutical science. Supramolecular macrocycles, such as crown ethers, cyclodextrins, calixarenes, pillararenes and cucurbiturils, are potentially good candidates for drug carriers due to their biocompatibility, hydrophobic cavity and ease of derivatization. The encapsulation of drugs based on host-guest interaction has the advantage of being adjustable and reversible as well as improving the low availability of drugs. Here, the recent advances in methods and strategies for drug encapsulation and release based on supramolecular macrocycles with host-guest interactions have been systematically summarized, laying a bright foundation for the development of novel nanopesticide preparations in the future and pointing out future directions of novel biopesticide research.

Annihilation dynamics of magnetic skyrmion lattice state under in-plane magnetic field and spontaneous recovery after field removal

Nanoscale magnetic skyrmions are potential candidates for information carriers, for which the nonvolatility under external stimuli is critical to the stability of recorded bits. Here, we present a micromagnetic study on the annihilation dynamics of a two-dimensional skyrmion lattice under a transverse magnetic field and the recoverability of the topological charge after removing the field. The temporal and spatial correlation functions and their Fourier transforms of the spin system reveal position-dependent dynamics under the transverse field. The slow modes $(<10\phantom{\rule{0.16em}{0ex}}\mathrm{GHz})$ hosted by all spins determine the spin configurations, and the fast ones $(>10\phantom{\rule{4pt}{0ex}}\mathrm{GHz})$ around the skyrmion core region control the dynamics of topological properties. A dynamic critical time ${t}_{\mathrm{cri}}$, when the field-induced ferromagnetic nuclei begin to be long-range correlated, is proved by statistical analyses of their spatial distribution over time. If turning off the transverse field before ${t}_{\mathrm{cri}}$, the collective motion of the spin system can restore the previously lost topological charge. Our results guide the realization of nonvolatile information storage in skyrmion lattice, thus widening the possibility of skyrmion-based devices for future spintronics-based nanocomputing.