Aromatherapy, an alternative treatment approach, is gaining popularity in Indonesia due to its ability to provide psychological and physiological relaxation. The use of Indonesian herbal plants, especially <em>Syzygium polyanthum</em> (bay leaf), <em>Camellia sinensis</em> (green tea), <em>Cymbopogon citratus</em> (lemongrass), <em>Lavandula angustifolia</em> (lavender), and <em>Citrus limon</em> (lemon) in aromatherapy has long been recognized for its distinctive, refreshing aroma and diverse secondary metabolites. This scientific literature review is presented to reveal the relationships between the presence and diversity of chemical composition of selected Indonesian herbal plants and various influencing factors, such as plant origin and the extraction method used. The aroma-defining properties of eugenol, geraniol, linalool, citral, and limonene in essential oils, when combined, can synergistically trigger bioactivities, including antioxidant, antibacterial, anti-inflammatory, and relaxing effects. Scientifically, the relaxing effects of aromatherapy are produced through stimulation of the olfactory system, which connects to the limbic system in the brain, including the amygdala and hypothalamus, which are responsible for improving mood and enhancing emotional regulation. Based on this review, the metabolite profile of essential oils plays a role in determining their potential bioactivity, especially in selected herbal plants as sources of natural relaxation therapy.
Ismael Lamas, Bhuvana L. Chandrashekar, Claudia C. Biguetti
et al.
Soft tissues exhibit remarkable stretchability, fracture toughness, and stress–relaxation ability. They possess a large water content to support cellular processes. Mimicking such a combination of mechanical and physical properties in hydrogels is important for tissue engineering applications but remains challenging. This work aims to develop a hydrogel that can combine excellent mechanical properties with cellular viability. The research focused on polyvinyl alcohol (PVA)/agar double-network (DN) hydrogels, fabricated by thermal gelation and freeze–thawing methods. Their mechanical properties were characterized through tension, compression, fracture, and stress–relaxation tests, and their cellular viability was measured through cytotoxicity tests. The results show that the PVA/agar DN gels are highly stretchable (>200%) and compressible (>30%) while containing high water content. The incorporation of agar by 6 wt% improved the fracture toughness of hydrogels from 1 to 1.76 kJ/m<sup>2</sup>. The degree of stress–relaxation, a key indicator of gel viscoelastic properties, improved by roughly 170% with an increase in agar content from 0 to 6 wt%. Cytotoxicity analysis showed that the gels, being physically cross-linked, were able to promote cellular proliferation. This work shows that tough and viscoelastic PVA/agar DN gels are suitable for soft tissue engineering applications, especially cartilage repair.
Soumya Narayana, B. H. Jaswanth Gowda, Umme Hani
et al.
Hydrogels are innovative materials characterized by a water-swollen, crosslinked polymeric network capable of retaining substantial amounts of water while maintaining structural integrity. Their unique ability to swell or contract in response to environmental stimuli makes them integral to biomedical applications, including drug delivery, tissue engineering, and wound healing. Among these, “smart” hydrogels, sensitive to stimuli such as pH, temperature, and light, showcase reversible transitions between liquid and semi-solid states. Thermoresponsive hydrogels, exemplified by poly(N-isopropylacrylamide) (PNIPAM), are particularly notable for their sensitivity to temperature changes, transitioning near their lower critical solution temperature (LCST) of approximately 32 °C in water. Structurally, PNIPAM-based hydrogels (PNIPAM-HYDs) are chemically versatile, allowing for modifications that enhance biocompatibility and functional adaptability. These properties enable their application in diverse therapeutic areas such as cancer therapy, phototherapy, wound healing, and tissue engineering. In this review, the unique properties and behavior of smart PNIPAM are explored, with an emphasis on diverse synthesis methods and a brief note on biocompatibility. Furthermore, the structural and functional modifications of PNIPAM-HYDs are detailed, along with their biomedical applications in cancer therapy, phototherapy, wound healing, tissue engineering, skin conditions, ocular diseases, etc. Various delivery routes and patents highlighting therapeutic advancements are also examined. Finally, the future prospects of PNIPAM-HYDs remain promising, with ongoing research focused on enhancing their stability, responsiveness, and clinical applicability. Their continued development is expected to revolutionize biomedical technologies, paving the way for more efficient and targeted therapeutic solutions.
Dehbiya Gherdaoui, Fatma Bouazza, Samira Ihadadene
et al.
The aim of this study was to quantify the total extraction yield (GEY) of polyphenols from pomegranate peels using a solid–liquid extraction process without evaporation but with UV-Vis spectrophotometry. Extraction kinetics models were tested to evaluate the extract yield (GEY), total phenolic compounds (TPCs), total flavonoids (TFCs), and condensed tannins (CTCs). The results showed maximum values of 45% for GEY, 97.560 mg EAG/g db for TPC, 4.416 mg EQ/g db for TFC, and 0.412 mg EC/g db for CTC, obtained with a methanol/water mixture (75/25, <i>v</i>/<i>v</i>) for 24 h. Spectrophotometry proved to be a reliable method for quantifying the total extraction yield, with a correlation of 99.79% compared to the conventional method. The second-order kinetic model accurately described the mass transfer mechanisms of the bioactive compounds studied. This study provides important insights into the mass transfer mechanisms during the extraction of bioactive compounds, facilitating the design, optimization, and control of large-scale processes for the recovery of pomegranate waste.
Edible hydrogels are the central material class in 3D food printing because they reconcile two competing needs: (i) low resistance to flow under nozzle shear and (ii) fast recovery of elastic structure after deposition to preserve geometry. This review consolidates the recent years of progress on hydrogel formulations—gelatin, alginate, pectin, carrageenan, agar, starch-based gels, gellan, and cellulose derivatives, xanthan/konjac blends, protein–polysaccharide composites, and emulsion gels alongside a critical analysis of printing technologies relevant to food: extrusion, inkjet, binder jetting, and laser-based approaches. For each material, this review connects gelation triggers and compositional variables to rheology signatures that govern printability and then maps these to process windows and post-processing routes. This review consolidates a decision-oriented workflow for edible-hydrogel printability that links formulation variables, process parameters, and geometric fidelity through standardized test constructs (single line, bridge, thin wall) and rheology-anchored gates (e.g., yield stress and recovery). Building on these elements, a “printability map/window” is formalized to position inks within actionable operating regions, enabling recipe screening and process transfer. Compared with prior reviews, the emphasis is on decisions: what to measure, how to interpret it, and how to adjust inks and post-set enablers to meet target fidelity and texture. Reporting minima and a stability checklist are identified to close the loop from design to shelf.
This paper investigates the flow performance and mechanical properties of underground gelled filling materials made from potash mine tailings, using lime as a gel. It demonstrates the feasibility of using lime as a gel, potash mine tailings as aggregate, and replacing water with potash mine tailings to create filling materials that meet design requirements for flow and compressive strength. The role of lime in the hardening process is explored through X-ray diffraction, scanning electron microscopy with energy-dispersive X-ray spectroscopy, thermogravimetric analysis, and infrared analysis. Results show that hydration products vary with lime dosage. With 9% lime (L9), the products are primarily ghiaraite (CaCl<sub>2</sub>·4H<sub>2</sub>O) and carnallite (KMgCl<sub>3</sub>·6H<sub>2</sub>O); with 5% lime (L5), tachyhydrite (CaMg<sub>2</sub>Cl<sub>6</sub>·12H<sub>2</sub>O) predominates, along with minor amounts of antarcticite (CaCl<sub>2</sub>·6H<sub>2</sub>O) and korshunovskite (Mg<sub>2</sub>Cl(OH)<sub>3</sub>·4H<sub>2</sub>O); and with 2.6% lime (L2.6), the products include tachyhydrite, ghiaraite, bischofite (MgCl<sub>2</sub>·6H<sub>2</sub>O), and korshunovskite. These hydration products form a dense, interwoven structure, enhancing the strength of the filling material. This study offers a theoretical foundation for using lime gel as a filling material in potash mining, with significant implications for sustainable mining practices.
Repairing damaged tissue caused by bacterial infection poses a significant challenge. Traditional antibacterial hydrogels typically incorporate various components such as metal antimicrobials, inorganic antimicrobials, organic antimicrobials, and more. However, drawbacks such as the emergence of multi-drug resistance to antibiotics, the low antibacterial efficacy of natural agents, and the potential cytotoxicity associated with metal antibacterial nanoparticles in hydrogels hindered their broader clinical application. In this study, we successfully developed imidazolium poly(ionic liquids) (PILs) polymer microspheres (APMs) through emulsion polymerization. These APMs exhibited notable antibacterial effectiveness and demonstrated minimal cell toxicity. Subsequently, we integrated the APMs into a gelatin methacryloyl (GelMA)—polyethylene glycol (PEG) hydrogel. This composite hydrogel not only showcased strong antibacterial and anti-inflammatory properties but also facilitated the migration of human skin fibroblasts (HSF) and human umbilical vein endothelial cells (HUVECs) and promoted osteogenic differentiation in vitro.
Konstantinos Loukelis, Zina A. Helal, Antonios G. Mikos
et al.
Bioprinting aims to provide new avenues for regenerating damaged human tissues through the controlled printing of live cells and biocompatible materials that can function therapeutically. Polymeric hydrogels are commonly investigated ink materials for 3D and 4D bioprinting applications, as they can contain intrinsic properties relative to those of the native tissue extracellular matrix and can be printed to produce scaffolds of hierarchical organization. The incorporation of nanoscale material additives, such as nanoparticles, to the bulk of inks, has allowed for significant tunability of the mechanical, biological, structural, and physicochemical material properties during and after printing. The modulatory and biological effects of nanoparticles as bioink additives can derive from their shape, size, surface chemistry, concentration, and/or material source, making many configurations of nanoparticle additives of high interest to be thoroughly investigated for the improved design of bioactive tissue engineering constructs. This paper aims to review the incorporation of nanoparticles, as well as other nanoscale additive materials, to printable bioinks for tissue engineering applications, specifically bone, cartilage, dental, and cardiovascular tissues. An overview of the various bioinks and their classifications will be discussed with emphasis on cellular and mechanical material interactions, as well the various bioink formulation methodologies for 3D and 4D bioprinting techniques. The current advances and limitations within the field will be highlighted.
Afzal Hussain, Mohammad A. Altamimi, Mohhammad Ramzan
et al.
Oral and parenteral delivery routes of valproic acid (VA) are associated with serious adverse effects, high hepatic metabolism, high clearance, and low bioavailability in the brain. A GastroPlus program was used to predict in vivo performance of immediate (IR) and sustained release (SR) products in humans. HSPiP software 5.4.08 predicted excipients with maximum possible miscibility of the drug. Based on the GastroPlus and HSPiP program, various excipients were screened for experimental solubility, nanoemulsions, and respective gel studies intended for nasal-to-brain delivery. These were characterized by size, size distribution, polydispersity index, zeta potential, morphology, pH, % transmittance, drug content, and viscosity. In vitro drug release, ex vivo permeation profile (goat nasal mucosa), and penetration studies were conducted. Results showed that in vivo oral drug dissolution and absorption were predicted as 98.6 mg and 18.8 mg, respectively, from both tablets (IR and SR) at 8 h using GastroPlus. The predicted drug access to the portal vein was substantially higher in IR (115 mg) compared to SR (82.6 mg). The plasma drug concentration–time profile predicted was in good agreement with published reports. The program predicted duodenum and jejunum as the prime sites of the drug absorption and no effect of nanonization on T<sub>max</sub> for sustained release formulation. Hansen parameters suggested a suitable selection of excipients. The program recommended nasal-to-brain delivery of the drug using a cationic mucoadhesive nanoemulsion. The optimized CVE6 was associated with the optimal size (113 nm), low PDI (polydispersity index) (0.26), high zeta potential (+34.7 mV), high transmittance (97.8%), and high strength (0.7% <i>w</i>/<i>w</i>). In vitro release and ex vivo permeation of CVE6 were found to be substantially high as compared to anionic AVE6 and respective gels. A penetration study using confocal laser scanning microscopy (CLSM) executed high fluorescence intensity with CVE6 and CVE6-gel as compared to suspension and ANE6. This might be attributed to the electrostatic interaction existing between the mucosal membrane and nanoglobules. Thus, cationic nanoemulsions and respective mucoadhesive gels are promising strategies for the delivery of VA to the brain through intransal administration for the treatment of seizures and convulsions.
Hydrogels containing renewable resources, such as hemicellulose, have received a lot of attention owing to their softness and electrical conductivity which could be applied in soft devices and wearable equipment. However, traditional hemicellulose-based hydrogels generally exhibit poor electrical conductivity and suffer from freezing at lower temperatures owing to the presence of a lot of water. In this study, we dissolved hemicellulose by employing deep eutectic solvents (DESs), which were prepared by mixing choline chloride and imidazole. In addition, hemicellulose-based DES hydrogels were fabricated via photo-initiated reactions of acrylamide and hemicellulose with <i>N</i>, <i>N</i>′-Methylenebisacrylamide as a crosslinking agent. The produced hydrogels demonstrated high electrical conductivity and anti-freezing properties. The conductivity of the hydrogels was 2.13 S/m at room temperature and 1.97 S/m at −29 °C. The hydrogel’s freezing point was measured by differential scanning calorimetry (DSC) to be −47.78 °C. Furthermore, the hemicellulose-based DES hydrogels can function as a dependable and sensitive strain sensor for monitoring a variety of human activities.
Maria Minodora Marin, Ioana Catalina Gifu, Gratiela Gradisteanu Pircalabioru
et al.
Natural polysaccharides are highly attractive biopolymers recommended for medical applications due to their low cytotoxicity and hydrophilicity. Polysaccharides and their derivatives are also suitable for additive manufacturing, a process in which various customized geometries of 3D structures/scaffolds can be achieved. Polysaccharide-based hydrogel materials are widely used in 3D hydrogel printing of tissue substitutes. In this context, our goal was to obtain printable hydrogel nanocomposites by adding silica nanoparticles to a microbial polysaccharide’s polymer network. Several amounts of silica nanoparticles were added to the biopolymer, and their effects on the morpho-structural characteristics of the resulting nanocomposite hydrogel inks and subsequent 3D printed constructs were studied. FTIR, TGA, and microscopy analysis were used to investigate the resulting crosslinked structures. Assessment of the swelling characteristics and mechanical stability of the nanocomposite materials in a wet state was also conducted. The salecan-based hydrogels displayed excellent biocompatibility and could be employed for biomedical purposes, according to the results of the MTT, LDH, and Live/Dead tests. The innovative, crosslinked, nanocomposite materials are recommended for use in regenerative medicine.
Linas Kudrevicius, Diana Adliene, Judita Puiso
et al.
Occupational radiation exposure monitoring is well-established in clinical or industrial environments with various different dosimeter systems. Despite the availability of many dosimetry methods and devices, a challenge with the occasional exposure registration, which may occur due to the spilling of radioactive materials or splitting of these materials in the environment, still exists, because not every individual will have an appropriate dosimeter at the time of the irradiation event. The aim of this work was to develop radiation-sensitive films—color-changing radiation indicators, which can be attached to or integrated in the textile. Polyvinyl alcohol (PVA)-based polymer hydrogels were used as a basis for fabrication of radiation indicator films. Several organic dyes (brilliant carmosine (BC), brilliant scarlet (BS), methylene red (MR), brilliant green (BG), brilliant blue (BB), methylene blue (MB) and xylenol orange (XiO)) were used as a coloring additives. Moreover, PVA films enriched with Ag nanoparticles (PVA-Ag) were investigated. In order to assess the radiation sensitivity of the produced films, experimental samples were irradiated in a linear accelerator with 6 MeV X-ray photons and the radiation sensitivity of irradiated films was evaluated using UV–Vis spectrophotometry method. The most sensitive were PVA-BB films indicating 0.4 Gy<sup>−1</sup> sensitivity in low-dose (0–1 or 2 Gy) range. The sensitivity at higher doses was modest. These PVA-dye films were sensitive enough to detect doses up to 10 Gy and PVA-MR film indicated stable 33.3% decolorization after irradiation at this dose. It was found that the dose sensitivity of all PVA-Ag gel films varied from 0.068 to 0.11 Gy<sup>−1</sup> and was dependent on the Ag additives concentration. Exchange of a small amount of water with ethanol or isopropanol caused the enhancement of radiation sensitivity in the films with the lowest AgNO<sub>3</sub> concentration. Radiation-induced color change of AgPVA films varied between 30 and 40%. Performed research demonstrated the potential of colored hydrogel films in their applications as indicators for the assessment of the occasional radiation exposure.
K. Thiankhaw, Kenneth Chattipakorn, S. Chattipakorn
et al.
BACKGROUND Alzheimer's disease (AD), Parkinson's disease (PD), and age-related macular degeneration (AMD) are common among neurodegenerative diseases, but investigations into novel therapeutic approaches are currently limited. Humanin (HN) is a mitochondrial-derived peptide found in brain tissues of patients with familial AD and has been increasingly investigated in AD and other neurodegenerative diseases. SCOPE OF REVIEW In this review, we summarize and discuss the effects of HN on the pathology of neurodegenerative diseases and cognition based on several studies from preclinical to clinical models. The association between cardiac ischemia-reperfusion (I/R) injury and brain are also included. Findings from in vitro studies and those involving mice provide the most fundamental information on the impact of HN and its potential association with clinical studies. MAJOR CONCLUSIONS HN plays a considerable role in countering the progression and neuropathology of AD. Inhibition and reduction of oxidative stress and neuroinflammation of the original amyloid hypothesis is the mainstay mechanism. Multiple intracellular mechanisms will be elucidated, including those involved in the anti-apoptotic signaling cascades, the insulin signaling pathway, and mitochondrial function, and especially autophagic activity. These beneficial roles are also found following cardiac I/R injury. Cognitive improvement was found to be related to maintenance of synaptic integrity and neurotransmitter modulation. Small humanin-like peptide 2 demonstrates the neuroprotective effects in PD and AMD via prevention of mitochondrial loss. GENERAL SIGNIFICANCE Comprehensive knowledge of HN effects on cognition and neurodegenerative diseases emphasizes its potential to treat a viable disease, as it ameliorates the pathogenesis of the disease.
Elisa Sturabotti, Silvia Consalvi, Luca Tucciarone
et al.
Here, we present a one-pot procedure for the preparation of hyaluronic acid (HA) sulfonated hydrogels in aqueous alkaline medium. The HA hydrogels were crosslinked using 1,4-butanedioldiglycidyl ether (BDDE) alone, or together with N-bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (Bes), as a safe sulfonating agent. Conditions for the simultaneous reaction of HA with BDDE and Bes were optimized and the resulting hydrogels were characterized under different reaction times (24, 72, and 96 h). The incorporation of sulfonic groups into the HA network was proven by elemental analysis and FTIR spectroscopy and its effect on water uptake was evaluated. Compared with the non-sulfonated sample, sulfonated gels showed improved mechanical properties, with their compressive modulus increased from 15 to 70 kPa, higher stability towards hyaluronidase, and better biocompatibility to 10T1/2 fibroblasts, especially after the absorption of collagen. As main advantages, the procedure described represents an easy and reproducible methodology for the fabrication of sulfonated hydrogels, which does not require toxic chemicals and/or solvents.
Colon cancer (CC) belongs to the three major malignancies with a high recurrence rate. Therefore, a novel drug delivery system that can prevent CC recurrence while minimizing side effects is needed. Tumor-necrosis-factor-related apoptosis-inducing ligand (TRAIL) has recently been spotlighted as a protein drug that can induce apoptosis of cancer cells specifically. However, its short in vivo half-life is still a challenge to overcome. Hence, in this study, a gel-like mPEGylated coacervate (mPEG-Coa) delivery platform was developed through electrostatic interaction of mPEG-poly(ethylene arginylaspartate diglyceride) (mPEG-PEAD) and heparin for effective protection of cargo TRAIL, subsequently preserving its bioactivity. mPEG-Coa could protect cargo TRAIL against protease. Sustained release was observed for a long-term (14 days). In addition, recurrence of HCT-116 cells was suppressed when cells were treated with TRAIL-loaded mPEG-Coa for 7 days through long-term continuous supply of active TRAIL, whereas re-proliferation occurred in the bolus TRAIL-treated group. Taken together, these results suggest that our gel-like mPEG-Coa could be utilized as a functional delivery platform to suppress CC recurrence by exogenously supplying TRAIL for a long time with a single administration.
Paulina Pisaniak, Aleksander Tarczon, Milena Konarska
et al.
Background and Objectives Despite the fact that vaccines save many lives worldwide, in many countries, including Poland, the percentage of unvaccinated children is constantly growing. The main reasons for low immunisation coverage include parents’ concerns about the safety of vaccines, their fears related to possible adverse events following vaccination, and the increasingly powerful activity of anti-vaccine movements. It is necessary to monitor the public’s attitudes to vaccination in order to implement appropriate solutions to prevent a resurgence of epidemics. The aim of the study was to assess Polish parents’ opinions about and awareness of immunisation-related issues. Methods The study, based on an online survey, investigated Polish mothers’ attitudes towards the use of vaccines, their opinions regarding the sanctions for a failure to vaccinate a child, and the correlations between the result and the socio-demographic characteristics. Results A total of 646 responses were collected, including 593 from mothers from general-interest groups and 53 from anti-vax groups. Differences were identified in vaccination coverage among children of respondents from general-interest groups and anti-vax groups. The findings show that the respondents from anti-vax groups stopped vaccinating more often due to vaccine adverse events and inadequate response from doctors. Conclusion Most of the respondents are aware of anti-vaccine movements and have a negative attitude to them, but these movements still influence the public. Also, the findings show a correlation between the level of education and a general attitude to immunisation – people with higher education more often have a negative opinion on this matter.
Abstract Background Metabolic Syndrome (MetS) is a clustering of abdominal obesity, hypertriglyceridaemia, low HDL cholesterol, hyperglycaemia and hypertension. Early identification of MetS is important for preventing cardiovascular disease (CVD). MetS has not been systematically explored in Greek primary care. Objectives To examine MetS frequency among primary care patients 40 years of age or older in Crete. Methods A descriptive study was conducted (July–December 2015). General practitioners, randomly selected from regional physician listings, recruited consecutive patients, 40 years of age or older, visiting their practice. Chart audits were completed for eligible patients using medical records, including demographics and cardiovascular risk factors (hypertension, dyslipidaemia, diabetes mellitus). MetS was defined using the revised NCEP ATP III criteria. Frequencies with 95% confidence intervals were calculated. Gender differences were explored using Chi-square and Mann–Whitney tests. Results Our sample consisted of 815 patients (55.7% female; mean age 65.2 years; range 40–98 years) from 44 GP practices. Overall, 73.6% (95% CI 70.4, 76.6) were identified with MetS, with a higher proportion of males (75.6%; 95% CI 71.0, 79.8) than females (72.0%; 95% CI 67.8, 76.0). Among the total sample, relatively high rates of hypertension (males: 64.5%; 95% CI 59.9, 70.0 and females: 61.1%; 95% CI 56.8, 65.8), dyslipidaemia (males: 69.3%; 95% CI 64.3, 74.1 and females: 63.5%; 95% CI 59.3, 68.0), diabetes mellitus (males: 46.9%; 95% CI 42.2, 52.4 and females: 36.5%; 95% CI 32.5, 41.6) and coronary heart disease (males: 21.2%; 95% CI 17.0, 25.2 and females: 6.2%; 95% CI 4.2, 8.6) were documented. Conclusion MetS and CVD risk factors were encountered at high frequencies in the studied population of primary care patients in Crete.