Hydrogel Spheres Research Articles

The short-term effect of contact lens wear on blink characteristics

PurposeThe aim of this pilot study was to investigate the initial effect of contact lens wear on spontaneous blink characteristics. MethodsThis was a randomised, crossover pilot study. Spontaneous blinking was recorded using a high-speed infrared camera in ten subjects with three different soft contact lenses (spherical hydrogel, spherical silicone hydrogel and toric hydrogel), one rigid contact lens and without contact lenses. Custom semi-automated software was used to determine palpebral aperture height, interblink interval (IBI), blink speed, blink completeness and blink duration. ResultsThe IBI was significantly greater for non-lens wear compared with the silicone hydrogel [ratio (95% CI): 1.34 (1.16, 1.55), p < 0.0001], toric hydrogel [1.28 (1.10, 1.48), p = 0.0001] and rigid corneal lenses [1.48 (1.27, 1.73), p < 0.0001]. The spherical silicone hydrogel lens showed greater closing-phase speed than non-lens wear [mean difference (95% CI): 27.4 (5.6, 49.1) mm/s, p = 0.006]. Shorter total blink duration was found for non-lens wear compared with any of the lens types [spherical hydrogel: ratio 0.89 (0.81, 0.98), p = 0.01; spherical silicone hydrogel: 0.87 (0.80, 0.95), p = 0.0001; toric hydrogel: 0.90 (0.83, 0.98), p = 0.004; and rigid corneal: 0.88 (0.82, 0.96), p = 0.0004]. Opening-phase speed (p = 0.12) and blink completeness metrics (all p > 0.5) were not influenced by wearing condition. ConclusionThis work showed that short-term contact lens wear influenced the palpebral aperture height, IBI, speed and duration of the blink, and the effect is dependent on the contact lens type. The completeness of the blink was not altered by contact lens wear. Future work should be conducted to assess the effect of long-term wear of different contact lens types on blink characteristics. The measurement of spontaneous blinking characteristics represents an immediate, sensitive and non-invasive evaluation of the impact of a contact lens on the ocular surface.

Controlling the volume fraction of glass-forming colloidal suspensions using thermosensitive host "mesogels".

The key parameter controlling the glass transition of colloidal suspensions is φ, the fraction of the sample volume occupied by the particles. Unfortunately, changing φ by varying an external parameter, e.g., temperature T as in molecular glass formers, is not possible, unless one uses thermosensitive colloidal particles, such as the popular poly(N-isopropylacrylamide) (PNiPAM) microgels. These, however, have several drawbacks, including high deformability, osmotic deswelling, and interpenetration, which complicate their use as a model system to study the colloidal glass transition. Here, we propose a new system consisting of a colloidal suspension of non-deformable spherical silica nanoparticles, in which PNiPAM hydrogel spheres of ∼100-200μm size are suspended. These non-colloidal "mesogels" allow for controlling the sample volume effectively available to the silica nanoparticles and hence their φ, thanks to the T-induced change in mesogels' volume. Using optical microscopy, we first show that the mesogels retain their ability to change size with T when suspended in Ludox suspensions, similarly as in water. We then show that their size is independent of the sample thermal history such that a well-defined, reversible relationship between T and φ may be established. Finally, we use space-resolved dynamic light scattering to demonstrate that, upon varying T, our system exhibits a broad range of dynamical behaviors across the glass transition and beyond, comparable with those exhibited by a series of distinct silica nanoparticle suspensions of various φ.

Mesogels control volume to explore the glass transition

Suspending colloidal particles in solution with thermosensitive hydrogel spheres allows for study of the liquid and solid conditions in glass-forming suspensions

Preparation of photocrosslinked spherical hydrogels bearing β-cyclodextrin and application in immobilizing microbes to decompose organic pollutants

Preparation of photocrosslinked spherical hydrogels bearing β-cyclodextrin and application in immobilizing microbes to decompose organic pollutants

Colorimetric photonic tongue for metal ions screening

<h2>Summary</h2> Screening of metal ions in body fluid is vital for monitoring human health. Here, inspired by taste-sensing functions of human tongue, we reported a novel colorimetric photonic tongue for multiple metal ions screening by using spherical structural color hydrogel particles (SCHPs) as sensory units. As SCHPs are composed of acrylic acid (AA)-based skeleton, the sensory units could respond to metal ions with color variations like receptors in taste buds. Thus, through analyzing all units' sensory information, a colorimetric "fingerprint" for each metal ion could be obtained in a database. Based on this, we constructed a portable, reusable, and biocompatible device by integrating SCHP arrays into a test-strip microchip for real-time monitoring of metal ions. The target ions could be distinguished by multivariate data analysis for pattern recognition. These features indicated that the proposed photonic tongue is valuable for metal ions screening in biological samples and promising for clinical disease diagnosis.

Wheat straw-core hydrogel spheres with polypyrrole nanotubes for the removal of organic dyes

Straw biomass is an underutilized raw material, the use of which could make a significant contribution to sustainable development. Herein, wheat straw waste was regenerated into novel porous core-shell wheat straw-polypyrrole hydrogel spheres for the removal of dyes from wastewater. Adsorption experiments demonstrated that the hydrogel spheres had long-term structural and functional stability, and a high performance for the removal of the water-soluble model anionic dye eosin Y (EY). The maximum adsorption capacity of the hybrid spheres (520.2 mg/g) was 12 times greater than that of the wheat straw hydrogel sphere. Recycling experiments showed that it the initial adsorption capacity of 75.0% could be maintained after seven adsorption-desorption cycles, and the material could be recovered by simple filtration. The results from spectroscopic (FTIR, XPS) analysis, adsorption experiments and computational quantum mechanical modelling suggested that hydrogen bonds, π-π stacking and electrostatic forces, were involved in the removal of EY from aqueous solution. Interestingly, the hydrogel sphere exhibited enhanced adsorption at elevated temperature, and this could be attributed to the dynamic breaking of crosslinked hydrogen bonds in the hydrogel sphere and release of activated –OH. The results from this study provide a basis for the development of sustainable high-performance adsorption materials from wheat straw biomass for the removal of organic dyes from wastewater. It also provides a strategy to design adsorbents that work efficiently at elevated temperatures.

Additive Soft Matter Design by UV-Induced Polymer Hydrogel Inter-Crosslinking.

In recent years, stimuli-responsive hydrogels have gained tremendous interest in designing complex smart 4D materials for applications ranging from biomedicine to soft electronics that can change their properties on demand over time. However, at present, a hydrogel’s response is often induced by merely a single stimulus, restricting its broader applicability. The controlled hierarchical assembly of various hydrogel building blocks, each with a tailored set of mechanical and physicochemical properties as well as programmed stimulus response, may potentially enable the design and fabrication of multi-responsive polymer parts that process complex operations, like signal routing dependent on different stimuli. Since inter-connection stability of such building blocks directly accompanies the transmission of information across building blocks and is as important as the building property itself to create complex 4D materials, we provide a study on the utility of an inter-crosslinking mechanism based on UV-induced 2,3-dimethylmaleimide (DMMI) dimerization to inter-connect acrylamide-based and N-isopropylacrylamide-based millimeter-sized cubic building blocks, respectively. The resulting dual-crosslinked assemblies are freestanding and stable against contraction–expansion cycles in solution. In addition, the approach is also applicable for connecting microfluidically fabricated, micrometer-sized hydrogel spheres, with the resulting assemblies being processable and mechanical stable, likewise resisting contraction–expansion in different solvents, for instance.

Self-Gelling Solid Lipid Nanoparticle Hydrogel Containing Simvastatin as Suitable Wound Dressing: An Investigative Study.

Hydrogels, an advanced interactive system, is finding use as wound dressings, however, they exhibit restricted mechanical properties, macroscopic nature, and may not manage high exudate wounds or incorporate lipophilic actives. In this study, we developed a self-gelling solid lipid nanoparticle (SLNs) dressing to incorporate simvastatin (SIM), a lipophilic, potential wound-healing agent, clinically limited due to poor solubility (0.03 mg/mL) and absorption. The study explores unconventional and novel application of SIM. The idea was to incorporate a significant amount of SIM in a soluble form and release it slowly over a prolonged time. Further, a suitable polymeric surfactant was selected that assigned a self-gelling property to SLNs (SLN-hydrogel) so as to be used as a novel wound dressing. SLNs assign porosity, elasticity, and occlusivity to the dressing to keep the wound area moist. It will also provide better tolerance and sensory properties to the hydrogel. SIM loaded SLN-hydrogel was prepared employing an industry amenable high-pressure homogenization technique. The unique hydrogel dressing was characterized for particle size, zeta potential, Fourier transform infra-red spectroscopy, powder X-ray diffraction, differential scanning calorimetry, rheology, and texture. Significant loading of SIM (10% w/w) was achieved in spherical nanoparticule hydrogel (0.3 nm (nanoparticles) to 2 µm (gelled-matrix)) that exhibited good spreadability and mechanical properties and slow release up to 72 h. SLN-hydrogel was safe as per the organization for economic co-operation and development (OECD-404) guidelines, with no signs of irritation. Complete healing of excision wound observed in rats within 11 days was 10 times better than marketed povidone-iodine product. The presented work is novel both in terms of classifying a per se SLN-hydrogel and employing SIM. Further, it was established to be a safe, effective, and industry amenable invention.

Dialysis Technology Supporting the Preparation of Acid-Resistant Picolylamine-Based Hydrogel Sphere for Selectively Recycling Copper, Nickel and Cobalt from Strongly Acidic Wastewaters

Dialysis Technology Supporting the Preparation of Acid-Resistant Picolylamine-Based Hydrogel Sphere for Selectively Recycling Copper, Nickel and Cobalt from Strongly Acidic Wastewaters

A template synthesized strategy on bentonite-doped lignin hydrogel spheres for organic dyes removal

A super-adsorbent bentonite-doped lignin hydrogel spheres (LHS-BT) were synthesized in 2 min via a simple template method to remove cationic dyes in wastewater. In this process, acrylic acid (AA) and 2-acrylamido-2-methyl-propanesulfonic acid (AMPS) are grafted onto lignosulfonate through free radical reaction to construct polymer cross-linking network and enhance the adsorption capacity of lignin. Moreover, polyethersulfone was designed as a template to protect the internal crosslinking and maintain the spherical shape. Then, the template shell was ingeniously removed through heat shrinkage. The shell separation and drying process was completed in one step, reducing the post-processing process. A series of characterization methods were used to evaluate the structural characteristics of LHS-BT. The influences of dye concentration, initial pH value, temperature and contact time on adsorption procedure were systematically studied. The adsorption kinetics and equilibrium adsorption isotherms are in accordance with the pseudo-second-order kinetic model and Langmuir isotherm model, respectively. Adsorption experiments showed that LHS-BT have ultra-high adsorption capacity (2541.76 mg/g for malachite green, 1284.46 mg/g for methylene blue and 1047.72 mg/g for rhodamine B) and faster adsorption rate within 85 min. Additionally, LHS-BT exhibited excellent recyclability without significant efficiency loss for at least five cycles. The mechanism of dyes molecular capture onto LHS-BT might be principally ascribed to electrostatic attraction, π-π interaction and hydrogen bonding. Thus, LHS-BT exhibits great potential for used in efficient, environmental, and economical wastewater remediation. Lastly, it is proved that LHS-BT is suitable for adsorption column to quickly purify wastewater containing dyes.

Carbon dots embedded hydrogel spheres for sensing and removing rifampicin

Although a plethora of carbon dots (CDs) based sensors continue to spring up, hardly any study on CDs acting as fluorescent probe for detecting rifampicin (RF) has been reported so far. Furthermore, no CDs hydrogel spheres (HSs) were fabricated and utilized as optical sensors as well as absorbent to recognize and remove pollutants. In this paper, bright blue luminescent CDs possess remarkable fluorescence sensing ability for the detection of RF, with high selectivity, outstanding sensitivity (LOD, 0.46 μM) and good anti-interference, which enabled CDs to successfully applied for the quantitative determination of RF in different real water samples. Furthermore, in order to integrate the advantages of hydrogel and CDs, fluorescent CDs HSs were fabricated, which could not only act as efficient optical sensors to recognize RF, but also conduct as absorbent to facilitate RF removal. The present work offers a new insight into taking advantage of CDs for the detection of RF in a convenient and efficient way.

Preparation and adsorption performance of cellulose nanofibrils/polyvinyl alcohol composite gel spheres with millimeter size

Wastewater treatment is a huge problem facing human beings. The development of recyclable and efficient adsorption materials is of great benefit to solve the problem. Based on the biodegradable cellulose nanofibers (CNFs) derived from biomass resources, the large sized CNFs/PVA composite hydrogel spheres (CV-HSs, 1–3 mm) were successfully prepared by the inverse suspension pellet-forming technology using the polymers as raw materials, and another hydrophobic CNFs/PVA composite aerogel spheres (HCV-ASs) were also obtained by lyophilization and followed silylation of as-prepared CV-HSs. The CV-HSs showed excellent adsorption properties for simulated pollutants, including Cu2+, phenol and aniline in water. The maximum absorption capacity of CV-HSs was 17.22 mmol/g for Cu2+, 176.72 mg/g for phenol and 341.93 mg/g for aniline respectively. The HCV-ASs exhibited good absorption properties for weak polar organic solvents, such as petroleum ether, ethyl acetate and toluene. In summary, two kinds of large-sized CNFs/PVA composite gel spheres were successfully fabricated, and exhibited good adsorption properties for organic pollutants and heavy metal ions, indicating their potential for wastewater treatment.

Hydrogel sphere impact cratering, spreading and bouncing on granular media

The impact of a hydrogel sphere onto a granular target results in both the deformation of the sphere and the formation of a prominent topographic feature known as an impact crater on the granular surface. We investigate the crater formation and scaling, together with the spreading diameter and post-impact dynamics of spheres by performing a series of experiments, varying the Young's modulus $Y$ and impact speed $U_{0}$ of the hydrogel spheres, and the packing fraction and grain size of the granular target. We determine how the crater diameter and depth depend on $Y$ and show the data to be consistent with those from earlier experiments using droplets and hard spheres. Most specifically, we find that the crater diameter data are consistent with a power law, where the power exponent changes more sharply when $Y$ becomes less than 200 Pa. Next, we introduce an estimate for the portion of the impact kinetic energy that is stored as elastic energy during impact, and thus correct the energy that remains available for crater formation. Subsequently, we determine the deformation of the hydrogel spheres and find that the normalized spreading diameter data are well collapsed introducing an equivalent velocity from an energy balance of the initial kinetic energy against surface and elastic energy. Finally, we observe that under certain intermediate values for the Young's modulus and impact velocities, the particles rebound from the impact crater. We determine the phase diagram and explain our findings from a comparison of the elastocapillary spreading time and the impact duration.

Evaluation of Microfluidic Approaches to Encapsulate Cells into PEGDA Microparticles

PurposePolyethylene glycol diacrylate (PEGDA) is increasingly used to microencapsulate cells via a vortex-induced water-in-oil emulsion process. Herein, we evaluated methods to encapsulate cells into microparticles using microfluidic methods.MethodsPEGDA prepolymer solution with or without cells was photopolymerized with white light under varying microfluidic parameters to form empty microspheres or cell-laden microparticles. Microparticles and entrapped cells were assessed for size and viability.ResultsPEGDA microparticles were easily formed when cells were absent; the introduction of cells resulted in aggregation that clogged microfluidic devices, resulting in a mix of empty polymer microparticles and cells that were not encapsulated. Cells that were successfully encapsulated had poor viability.ConclusionMicrofluidic methods may work for low density microencapsulation of mammalian cells; however, when the cell density within each microparticle must be relatively high, emulsion-based methods are superior to microfluidic methods.Lay SummaryThe synthetic polymer polyethylene glycol diacrylate (PEGDA) has been increasingly used to encapsulate cells into micrometer-sized hydrogel spheres (microspheres). One method to microencapsulate cells has been to form a water-in-oil emulsion with liquid polymer containing cells and then expose the suspended droplets to white light, polymerizing them into PEGDA hydrogel microspheres. Although successful, this method has poor control over the process, resulting in polydisperse microsphere sizes with varying cell density. We evaluated microfluidic methods to form both empty and cell-laden PEGDA microspheres. Although microfluidic methods resulted in monodisperse microsphere sizes, the introduction of cells resulted in clogging of microfluidic devices, non-spherical microparticles, and poor cell viability.Future WorkBecause the microfluidic approach successfully formed cell-free microspheres, the effect of reducing cell aggregation will be examined. Specifically, the use of anti-aggregation agents as well as a reduced cell density in the liquid polymer phase and their effects on polymer formation will be explored.

Feedback and Communication in Active Hydrogel Spheres with pH Fronts: Facile Approaches to Grow Soft Hydrogel Structures

AbstractCompartmentalized reaction networks regulating signal processing, communication and pattern formation are central to living systems. Towards achieving life‐like materials, we compartmentalized urea‐urease and more complex urea‐urease/ester‐esterase pH‐feedback reaction networks into hydrogel spheres and investigate how fuel‐driven pH fronts can be sent out from these spheres and regulated by internal reaction networks. Membrane characteristics are installed by covering urease spheres with responsive hydrogel shells. We then encapsulate the two networks (urea‐urease and ester‐esterase) separately into different hydrogel spheres to devise communication, pattern formation and attraction. Moreover, these pH fronts and patterns can be used for self‐growing hydrogels, and for developing complex geometries from non‐injectable hydrogels without 3D printing tools. This study opens possibilities for compartmentalized feedback reactions and their use in next generation materials fabrication.

Feedback and Communication in Active Hydrogel Spheres with pH Fronts: Facile Approaches to Grow Soft Hydrogel Structures.

Compartmentalized reaction networks regulating signal processing, communication and pattern formation are central to living systems. Towards achieving life‐like materials, we compartmentalized urea‐urease and more complex urea‐urease/ester‐esterase pH‐feedback reaction networks into hydrogel spheres and investigate how fuel‐driven pH fronts can be sent out from these spheres and regulated by internal reaction networks. Membrane characteristics are installed by covering urease spheres with responsive hydrogel shells. We then encapsulate the two networks (urea‐urease and ester‐esterase) separately into different hydrogel spheres to devise communication, pattern formation and attraction. Moreover, these pH fronts and patterns can be used for self‐growing hydrogels, and for developing complex geometries from non‐injectable hydrogels without 3D printing tools. This study opens possibilities for compartmentalized feedback reactions and their use in next generation materials fabrication.

CloneSeq: A highly sensitive analysis platform for the characterization of 3D-cultured single-cell-derived clones.

Single-cell assays have revealed the importance of heterogeneity in many biological systems. However, limited sensitivity is a major hurdle for uncovering cellular variation. To overcome it, we developed CloneSeq, combining clonal expansion inside 3D hydrogel spheres and droplet-based RNA sequencing (RNA-seq). We show that clonal cells maintain similar transcriptional profiles and cell states. CloneSeq of lung cancer cells revealed cancer-specific subpopulations, including cancer stem-like cells, that were not revealed by scRNA-seq. Clonal expansion within 3D soft microenvironments supported cellular stemness of embryonic stem cells (ESCs) even without pluripotent media, and it improved epigenetic reprogramming efficiency of mouse embryonic fibroblasts. CloneSeq of ESCs revealed that the differentiation decision is made early during Oct4 downregulation and is maintained during early clonal expansion. Together, we show CloneSeq can be adapted to different biological systems to discover rare subpopulations by leveraging the enhanced sensitivity within clones.

Facile preparation of sulfhydryl modified montmorillonite nanosheets hydrogel and its enhancement for Pb(II) adsorption

In the work, sulfhydryl functionalized montmorillonite nanosheets based hydrogel balls were firstly synthesized for Pb(II) adsorption, and then characterized by scanning electron microscope (SEM), fourier transform infrared spectroscopy (FTIR), surface area analyzer (BET), thermogravimetry (TG), and zeta potential. Effects of initial solution pH, adsorbent dosage, contact time, temperature on Pb(II) adsorption of the resulting hydrogel balls were investigated systematically. The experimental results showed that the increase amount of sulfhydryl functionalized montmorillonite nanosheets (MMTNs-SH) maintained the hydrogel balls a better porous structure and bigger specific surface area, endowing it a bigger adsorption capacity. The adsorption process was fitted well with pseudo-second-order kinetics model and Freundlich model, and more than 97% of Pb(II) could be removed under the optimum conditions. Moreover, hydrogel spheres have a certain cycle performance. In addition, the interactions between Pb(Ⅱ) ions and the oxygen atoms in the hydroxyl groups and the sulfur atoms in the sulfhydryl groups, and the ion exchange in MMTNs-SH dominated the adsorption.

Quarter of a century of contact lens prescribing trends in the United Kingdom (1996 – 2020)

PurposeTo document contact lens prescribing trends in the United Kingdom over the past quarter of a century. MethodsAn annual survey of contact lens prescribing was conducted each year from 1996 to 2020, inclusive, by asking a random selection of optometrists and contact lens opticians to provide information relating to 10 consecutive contact lens fits between January and March. ResultsOver the 25 year survey period, 2,671 practitioners returned survey forms, reporting a total of 25,575 contact lens fits. The mean (± standard deviation) age of lens wearers was 35 ± 15 years, of which 64 % were female. Over the survey period, rigid lens new fits decreased from 22 % to 2%. The prescribing of silicone hydrogel lenses has increased steadily since their introduction towards the end of the 1990s, and now represent 80 % of soft lens fits. Soft toric lens prescribing has gradually increased to 47 % – a value at which astigmatism ≥ 0.75DC is theoretically corrected in all contact lens wearers. Daily disposable prescribing increased steadily over the survey period and now represents 63 % of lenses prescribed. Extended wear fits remain at very low levels, except for some prescribing for overnight orthokeratology. Multi-purpose lens care solutions are ubiquitous; peroxide and other systems are now seldom prescribed. Rigid lenses and monthly replacement soft lenses are predominantly worn on a full time basis, whereas daily disposable soft lenses are mainly worn part time. ConclusionsThis report documents the evolution of contact lens fitting in the United Kingdom over the past 25 years. The most likely lens fit is a spherical design silicone hydrogel daily disposable contact lens prescribed for a 35 year old female and worn on a part-time basis.

Birth and Growth of Neuroimaging and Vascular Intervention at Sree Chitra Tirunal Institute for Medical Sciences &amp; Technology, Thiruvananthapuram—Part I

AbstractThis article is a historical narrative that traces the growth of neuroradiology and interventional radiology at the Sree Chitra Tirunal Institute of Medical Sciences and Technology, Thiruvananthapuram. From its humble origins in the pre-CT scan era of the mid and late 1970s, when invasive diagnostic procedures such as percutaneous carotid angiography, myelography, pneumoencephalography (PEG) and ventriculography were the mainstay of neuroimaging, the authors take the reader through their gradual foray into catheter four-vessel angiography and later free-flow embolization of arteriovenous malformations (AVMs), and finally to the use of microcatheters for selective embolization procedures. The equipment used in those early years—fluoroscopic tilting table, roll-film cameras, serial changers, PEG tables—provide an insight to an era with all its challenges before the advent of digital imaging. The authors’ efforts to indigenize some of the hardware such as metallic stents and embolization material such as hydrogel spheres and lyophilized dura are also highlighted. The development of peripheral vascular intervention alongside neuroradiology is also highlighted. The authors pay tribute to an early pioneer of neuroradiology in India, Prof. Mahadevan Pillai, who was a guiding light to them during those nascent years.