ABSTRACT
Personal Care Products (PCPs) have been one of the most studied chemicals in the last twenty years since they were identified as pseudo-persistent pollutants by the European Union in the early 2000s. The accumulation of PCPs in the aquatic environment and their effects on non-target species make it necessary to find new, less harmful, substances. Polyethylene glycol (PEGs) and polyvinyl alcohol (PVAs) are two polymers that have increased their presence in the composition of PCPs in recent years, but little is known about the effect of their accumulation in the environment on non-target species. Through embryotoxicity tests on two common models of aquatic organisms (Danio rerio and Xenopus laevis), this work aims to increase the knowledge of PEGs and PVAs' effects on non-target species. Animals were exposed to the pollutant for 96 h. The main embryotoxicity endpoint (mortality, hatching, malformations, heartbeat rate) was recorded every 24 h. The most significant results were hatching delay in Danio rerio exposed to both chemicals, in malformations (oedema, body malformations, changes in pigmentation and deformations of spine and tail) in D. rerio and X. laevis and significant change in the heartbeat rate (decrease or increase in the rate) in both animals for all chemicals tested.
Subject(s)
Embryo, Nonmammalian , Polyethylene Glycols , Polyvinyl Alcohol , Water Pollutants, Chemical , Zebrafish , Animals , Water Pollutants, Chemical/toxicity , Embryo, Nonmammalian/drug effects , Polyvinyl Alcohol/toxicity , Polyvinyl Alcohol/chemistry , Polyethylene Glycols/toxicity , Xenopus laevis , Toxicity TestsABSTRACT
The purpose of this research was to use polyvinyl alcohol (PVOH) 18-88 as a case study to evaluate the environmental fate, ecotoxicity, and overall safety profile of water-soluble, nonmodified PVOH polymers used in detergent films. An OECD 303A Wastewater Treatment Plant Simulation Study was conducted with dissolved organic carbon as the analytical endpoint to evaluate the removal of PVOH 18-88 during wastewater treatment. During the plateau phase, high levels of removal due to biodegradation were observed (average 97.4 ± 7.1, range: 88%-116%). The OECD 303A study quantitatively verified that surface water is the dominant receiving compartment for PVOH 18-88 post wastewater treatment. Acute algae, invertebrate, and fish embryo (fish embryo acute toxicity test [FET]) ecotoxicity studies quanitified the 50% lethal/effect concentration (L/EC50) for PVOH 18-88. Due to the potential for the chorion to impact PVOH 18-88 bioavailability, both chorionated and dechorionated FET tests were conducted. L/EC50 > 1000 mg/L for FET (chorionated and dechorionated), invertebrate, and algae were observed. The Sustainable Futures (US) and REACH (EU) frameworks were used to evaluate environmental risk. For the US assessment, the Exposure and Fate Assessment Screening Tool was used to predict the single day lowest flow over a 10-year period (1Q10) surface water concentration and the seven consecutive days of lowest flow over a 10-year period (7Q10) surface water concentration and compared with acute and chronic concentrations of concern. For the EU assessment, the European Union System for the Evaluation of Substances was used to predict local and regional exposure concentrations and compared to the predicted no effect concentration. For both regulatory assessments, the exposure concentrations were >2 orders of magnitude below the effect concentrations. Integr Environ Assess Manag 2024;20:1693-1705. © 2024 The Authors. Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC).
Subject(s)
Polyvinyl Alcohol , Water Pollutants, Chemical , Water Pollutants, Chemical/analysis , Water Pollutants, Chemical/toxicity , Polyvinyl Alcohol/toxicity , Polyvinyl Alcohol/chemistry , Animals , Waste Disposal, Fluid/methods , Environmental Monitoring/methods , Wastewater/toxicity , Wastewater/chemistry , Toxicity Tests, Acute , FishesABSTRACT
Plastics are widely used in industry and households, but improper disposal has caused their accumulation in aquatic systems worldwide. As a result, mechanical and photochemical processes break down these plastics into microplastics or nano plastics, posing a severe threat to marine organisms and humans as they enter the food chain. This study investigates the effect of Polyvinyl chloride (PVC) and Polyvinyl alcohol (PVA) microplastics in zebrafish by using multi-spectral imaging (MSI), Optical Coherence Tomography (OCT), and Biospeckle OCT (bOCT). These techniques allow for long-term studies in the fish without invasive procedures in real-time. Zebrafish were exposed to Nile red labeled PVC and PVA for 21 days with 500mg/L concentration. Image acquisition and analysis were performed every five days till the end of the study. MSI images revealed deposition of microplastics in the gills region of the fish; some diffused deposition was seen throughout the body in the PVA group towards the end of the experiment. The effect of these MPs on the structure of the gills and their exact location was determined by capturing OCT images. bOCT was used to determine the average speckle contrast for all the OCT images to determine the change in biological activity within the gills region. An increase in bioscpeckle contrast was observed for the MPs treated groups compared to the control group. PVC appeared to cause a more considerable rise in activity compared to PVA. The results indicated that the MPs exert stress on the gills and increase activity within the gills, possibly due to the blockage of the gills and disruption of the water filtration process, which could be monitored non-invasively only by using bOCT. Overall, our study demonstrates the usefulness of non-invasive, robust techniques like MSI, bOCT, and biospeckle for long-term zebrafish studies and real-time analyses.
Subject(s)
Microplastics , Water Pollutants, Chemical , Animals , Humans , Microplastics/toxicity , Plastics , Zebrafish , Polyvinyl Alcohol/toxicity , Tomography, Optical Coherence , Water Pollutants, Chemical/toxicity , Polyvinyl Chloride/toxicityABSTRACT
Despite the pollution induced by plastics become a well-known and documented problem, bringing many countries to adopt restrictions about their production, commercialization and use, the impact of another emerging category of synthetic polymers, represented by the Water-Soluble Polymers (WSPs), also known as "liquid plastics", is overlooked by scientific community. WSPs are produced in large quantities and used in a wide plethora of applications such as food packaging, pharmaceuticals and personal care products, cosmetics and detergents, with a consequent continuous release in the environment. The aim of this study was the investigation of the possible toxicity induced by polyvinyl alcohol (PVA), one of the main produced and used WSPs, on two freshwater model organisms, the crustacean Daphnia magna and the teleost Danio rerio (zebrafish). We evaluated the effects of solubilized standard PVA powder and PVA-based commercial bags for carp-fishing, at 3 different concentrations (1 µg/L, 0.5 mg/L and 1 mg/L), through the exposures for 14 days of D. magna (daphnids; age < 24 h) and for 5 days of zebrafish embryos (up to 120 h post fertilization - hpf). As acute effects we evaluated the immobilization/mortality of specimens, while for chronic toxicity we selected several endpoints with a high ecological relevance, as the behavioural alteration on swimming performance, in real-time readout, and the activity of monoamine oxidase (MAO), a neuro-enzyme with a potential implication in the organism movement. The results showed the lack of significant effects induced by the selected substances, at all tested concentrations and in both model organisms. However, considering the wide plethora of available WSPs, other investigations are needed to provide the initial knowledge of risk assessment of these compounds contained in some consumer products.
Subject(s)
Plastics , Water Pollutants, Chemical , Animals , Aquatic Organisms , Daphnia , Plastics/toxicity , Polymers/pharmacology , Polyvinyl Alcohol/toxicity , Water/pharmacology , Water Pollutants, Chemical/toxicity , ZebrafishABSTRACT
Globally, the production of zinc oxide nanoparticles (ZnO NPs) increased due to its wide applications including cosmetics, paints etc., and gets accumulated in the environment during their production, use or end-of-life. The toxic effects of the NPs vary with the presence of various surface modification agents. In the current report, toxic effect of bare and capped ZnO NPs with polymeric surface modifying agent including polyvinyl alcohol (PVA), polyethylene glycol (PEG) and polyvinylpyrrolidone (PVP) is studied against adult as well as embryonic zebra fish. The surface capped NPs showed great variation in toxicity levels. It was observed that ZnO-PVA showed highly reduced toxic effects relative to ZnO-PEG and ZnO-PVP. Further, various environmental agents including humic acid can also have an impact on NPs toxicity. ZnO particles showed increased toxic effect in humic acid presence. The uptake of ZnO particles by D. rerio was high in the order of PVP-, PEG- and PVA- followed by bare-ZnO. The current investigation found that ZnO NPs dissolution and uptake are the major factors which cause the toxicity against adult as well as embryonic zebra fishes respectively.
Subject(s)
Metal Nanoparticles , Nanoparticles , Zinc Oxide , Animals , Environmental Monitoring , Metal Nanoparticles/toxicity , Nanoparticles/toxicity , Polyethylene Glycols/toxicity , Polyvinyl Alcohol/toxicity , Povidone/toxicity , Zebrafish , Zinc Oxide/toxicityABSTRACT
To develop an effective and mechanically robust wound dressing, a poly (vinyl alcohol) (PVA)/methacrylate kappa-carrageenan (κ-CaMA) composite hydrogel encapsulated with a chitooligosaccharide (COS) was prepared in a cassette via repeated freeze/thaw cycles, photo-crosslinking, and chemical cross-linking. The chemical, physical, mechanical, in vitro biocompatibility, in vivo wound-healing properties, and antibacterial activity of triple-crosslinked hydrogel were subsequently characterized. The results showed that the PVA/κ-CaMA/COS (Pκ-CaC) hydrogel had a uniformly thick, highly porous three-dimensional architecture with uniformly distributed pores, a high fluid absorption, and retention capacity without disturbing its mechanical stability, and good in vitro biocompatibility. Macroscopic images from the full-thickness skin wound model revealed that the wounds dressed with the proposed Pκ-CaC hydrogel were completely healed by day 14, while the histomorphological results confirmed full re-epithelization and rapid skin-tissue remodeling. This study thus indicates that the composite Pκ-CaC hydrogel has significant potential for use as a wound dressing.
Subject(s)
Anti-Bacterial Agents/pharmacology , Bandages , Hydrogels/pharmacology , Wound Healing/drug effects , Animals , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/toxicity , Carrageenan/chemistry , Carrageenan/pharmacology , Carrageenan/toxicity , Cell Line , Chitosan/chemistry , Chitosan/pharmacology , Chitosan/toxicity , Compressive Strength , Humans , Hydrogels/chemistry , Hydrogels/toxicity , Male , Methacrylates/chemistry , Methacrylates/pharmacology , Methacrylates/toxicity , Mice, Inbred ICR , Oligosaccharides/chemistry , Oligosaccharides/pharmacology , Oligosaccharides/toxicity , Polyvinyl Alcohol/analogs & derivatives , Polyvinyl Alcohol/pharmacology , Polyvinyl Alcohol/toxicity , Porosity , Staphylococcus aureus/drug effects , Staphylococcus epidermidis/drug effectsABSTRACT
Administration of drugs via the buccal route has attracted much attention in recent years. However, developing systems with satisfactory adhesion under wet conditions and adequate drug bioavailability still remains a challenge. Here, we propose a mussel-inspired mucoadhesive film. Ex vivo models show that this film can achieve strong adhesion to wet buccal tissues (up to 38.72 ± 10.94 kPa). We also demonstrate that the adhesion mechanism of this film relies on both physical association and covalent bonding between the film and mucus. Additionally, the film with incorporated polydopamine nanoparticles shows superior advantages for transport across the mucosal barrier, with improved drug bioavailability (~3.5-fold greater than observed with oral delivery) and therapeutic efficacy in oral mucositis models (~6.0-fold improvement in wound closure at day 5 compared with that observed with no treatment). We anticipate that this platform might aid the development of tissue adhesives and inspire the design of nanoparticle-based buccal delivery systems.
Subject(s)
Biomimetics , Bivalvia/chemistry , Drug Delivery Systems , Mouth Mucosa/physiology , Adhesiveness , Administration, Buccal , Animals , Cell Line , Dexamethasone/pharmacology , Dihydroxyphenylalanine/chemistry , Drug Liberation , Humans , Indoles/toxicity , Male , Mucins/chemistry , Mucus/chemistry , Nanoparticles/chemistry , Nanoparticles/ultrastructure , Particle Size , Polylactic Acid-Polyglycolic Acid Copolymer/chemistry , Polylactic Acid-Polyglycolic Acid Copolymer/toxicity , Polymers/toxicity , Polyvinyl Alcohol/chemistry , Polyvinyl Alcohol/toxicity , Rats, Sprague-Dawley , Spectrophotometry, Ultraviolet , Swine , Tissue DistributionABSTRACT
This study targets to develop curcumin-loaded polyvinyl alcohol/cellulose nanocrystals (PVA/CNCs) membrane as localized delivery system for breast/liver cancer. A novel strategy was developed for enhancing encapsulation capacity and maximizing therapeutic efficiency of curcumin-loaded PVA/CNCs membranes. Membranes were prepared by solution-casting method using citric acid as crosslinker. SEM revealed that PVA/CNCs ratio (80:20) was chosen as the optimum for loading curcumin. FT-IR indicated that, curcumin was incorporated into PVA/CNCs in amorphous-phase via intermolecular hydrogen bond between curcumin and membrane components. Curcumin showed biphasic-release through burst-release of 41% of curcumin during the first hour, followed by sustained-release of 70% and 94% during 24 h and 48 h, respectively. In vitro cytotoxicity of PVA/CNCs/Curcumin membrane exhibited a selective inhibition proliferation of breast and liver cancer cells in a concentration-dependent without any toxic effect on normal cells. At high concentration (8 mg/ml) of PVA/CNCs/Curcumin, reduced viability to 35% and 7% of MCF-7 and Huh-7 cells, respectively; meanwhile high HFB-4 normal cell viability ≥80% was investigated. Antimicrobial activity of PVA/CNCs/Curcumin was investigated by multi-drug-resistant strains, and MIC values. PVA/CNCs/Curcumin membranes with concentration (40 mg/ml) showed broad-spectrum antimicrobial activities, thus inhibited ~96-99% of microbial growth. PVA/CNCs/Curcumin membranes could be as promised anti-infective biomaterials for breast and liver cancer wound healing.
Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Biological Dressings , Cellulose/administration & dosage , Curcumin/pharmacology , Hydrogels/administration & dosage , Membranes, Artificial , Nanoparticles/administration & dosage , Polyvinyl Alcohol/administration & dosage , Antineoplastic Agents, Phytogenic/administration & dosage , Antineoplastic Agents, Phytogenic/toxicity , Breast Neoplasms/pathology , Carcinoma/pathology , Cell Cycle/drug effects , Cellulose/toxicity , Curcumin/administration & dosage , Curcumin/toxicity , Cyclin D1/drug effects , Drug Carriers/administration & dosage , Drug Carriers/toxicity , Drug Liberation , Drug Resistance, Neoplasm , Drug Screening Assays, Antitumor , Humans , Hydrogels/toxicity , MCF-7 Cells , Melanocytes/drug effects , Models, Molecular , Molecular Docking Simulation , Nanoparticles/toxicity , Polyvinyl Alcohol/toxicity , Protein Conformation , Spectroscopy, Fourier Transform Infrared , Wound Healing/drug effects , X-Ray DiffractionABSTRACT
Conductive hydrogel-based epidermal strain sensors can generate repeatable electrical changes upon mechanical deformations for indication of the skin's physiological condition. However, this remains challenging for many conductive hydrogel sensors due to biomechanical mismatch with skin tissues and an unstable resistance variation response, resulting in non-conformable deformations with the epidermis and dermis, and consequently generating inaccurate monitoring of human movements. Herein, a conductive hydrogel that highly matches the skin is fabricated from dynamically hydrogen-bonded nanocrystallites of polydopamine-modified reduced graphene oxide (PDA-rGO) nanosheets composited with polyvinyl alcohol, namely the PDA-rGO/PVA hydrogel. PDA-rGO provides a large number of dynamic hydrogen-bonding interactions in the hydrogel, resulting in a skin-matching modulus (78 kPa) and stretchability. Moreover, the resultant hydrogel possesses excellent cytocompatibility and conductivity (0.87 S m-1), high sensitivity (gauge factor of compression: 20) at low strain and outstanding linearity at high strain as well as a stable resistance variation response. These desirable properties enable the application of the PDA-rGO/PVA hydrogel as a skin-friendly wearable sensor for real-time and accurate detection of both large-scale joint movements and tiny physiological signals, including the bending and relaxing of fingers, the wrist, elbow and knee joints, and wrist pulse and swallowing. Moreover, this hydrogel is integrated into a 2D sensor array that monitors strains or pressures in two dimensions, which is promising for electronic skin, biosensors, human-machine interfaces, and wearable electronic devices.
Subject(s)
Graphite/chemistry , Hydrogels/chemistry , Monitoring, Physiologic/methods , Movement/physiology , Polyvinyl Alcohol/chemistry , Wearable Electronic Devices , Animals , Biomimetic Materials/chemical synthesis , Biomimetic Materials/chemistry , Biomimetic Materials/toxicity , Compressive Strength , Deglutition , Electric Conductivity , Graphite/chemical synthesis , Graphite/toxicity , Humans , Hydrogels/chemical synthesis , Hydrogels/toxicity , Indoles/chemical synthesis , Indoles/chemistry , Indoles/toxicity , Mesenchymal Stem Cells/drug effects , Monitoring, Physiologic/instrumentation , Polymers/chemical synthesis , Polymers/chemistry , Polymers/toxicity , Polyvinyl Alcohol/chemical synthesis , Polyvinyl Alcohol/toxicity , Rats , Stress, MechanicalABSTRACT
PURPOSE: Crosslinked poly(vinyl alcohol) (PVA) is a biomaterial that can be used for multiple cardiovascular applications. The success of implanted biomaterials is contingent on the properties of the material. A crucial consideration for blood-contacting devices is their potential to incite thrombus formation, which is dependent on the material surface properties. The goal of this study was to quantify the effect of different crosslinking methods of PVA hydrogels on in vitro thrombogenicity. METHODS: PVA was manufactured using three different crosslinking methods: 30% sodium trimetaphosphate (STMP), three 24 h freeze-thaw cycles (FT), and 2% glutaraldehyde-crosslinked (GA) to produce STMP-PVA, FT-PVA and GA-PVA, respectively. Expanded polytetrafluoroethylene (ePTFE) was used as a clinical control. As markers of thrombus formation, the degree of coagulation factor (F) XII activation, fibrin formation, and platelet adhesion were measured. RESULTS: The GA-PVA material increased FXII activation in the presence of cofactors compared to vehicle and increase platelet adhesion compared to other PVA surfaces. The STMP-PVA and FT-PVA materials had equivalent degrees of FXII activation, fibrin formation and platelet adhesion. CONCLUSION: This work supports crosslinker dependent thrombogenicity of PVA hydrogels and advances our understanding of how the manufacturing of a PVA hydrogel affects its hemocompatibility.
Subject(s)
Cross-Linking Reagents/chemistry , Freezing , Glutaral/chemistry , Polyphosphates/chemistry , Polyvinyl Alcohol/chemistry , Thrombosis/prevention & control , Biocompatible Materials , Blood Coagulation , Blood Vessel Prosthesis , Cross-Linking Reagents/toxicity , Factor XIIa/metabolism , Fibrinolysis , Freezing/adverse effects , Glutaral/toxicity , Graft Occlusion, Vascular/blood , Graft Occlusion, Vascular/etiology , Graft Occlusion, Vascular/prevention & control , Humans , Hydrogels , Materials Testing , Platelet Adhesiveness , Polyphosphates/toxicity , Polyvinyl Alcohol/toxicity , Prosthesis Design , Surface Properties , Thrombosis/blood , Thrombosis/etiologyABSTRACT
Owing to the characteristics of mimicking human skin's function and transmitting sensory signals, electronic skin (e-skin), as an emerging and exciting research field, has inspired tremendous efforts in the biomedical field. However, it is frustrating that most e-skins are prone to bacterial infections, resulting a serious threat to human health. Therefore, the construction of e-skin with an integrated perceptual signal and antibacterial properties is highly desirable. Herein, the dynamic supramolecular hydrogel was prepared through a freezing/thawing method by cross-linking the conductive graphene (G), biocompatible polyvinyl alcohol (PVA), self-adhesive polydopamine (PDA), and in situ formation antibacterial silver nanoparticles (AgNPs). Having fabricated the hierarchical network structure, the PVA-G-PDA-AgNPs composite hydrogel with a tensile strength of 1.174 MPa and an elongation of 331% paves way for flexible e-skins. Notably, the PVA-G-PDA-AgNPs hydrogel exhibits outstanding antibacterial activity to typical pathogenic microbes (e.g., Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus), which effectively prevents bacterial infections that harm human health. With self-adhesiveness to various surfaces and excellent conductivity, the PVA-G-PDA-AgNPs composite hydrogel was used as strain sensors to detect a variety of macroscale and microscale human motions successfully. Meanwhile, the excellent rehealing property allows the hydrogel to recycle as a new sensor to detect large-scale human activities or tiny movement. Based on these remarkable features, the antibacterial, self-adhesive, recyclable, and tough conductive composite hydrogels possess the great promising application in biomedical materials.
Subject(s)
Adhesives/chemistry , Anti-Bacterial Agents/pharmacology , Biocompatible Materials/chemistry , Hydrogels/chemistry , Metal Nanoparticles/chemistry , Wearable Electronic Devices , Adhesives/toxicity , Animals , Anti-Bacterial Agents/toxicity , Biocompatible Materials/toxicity , Cell Line , Electric Conductivity , Escherichia coli/drug effects , Graphite/chemistry , Graphite/toxicity , Humans , Hydrogels/toxicity , Indoles/chemistry , Indoles/toxicity , Metal Nanoparticles/toxicity , Mice, Inbred BALB C , Microbial Sensitivity Tests , Polymers/chemistry , Polymers/toxicity , Polyvinyl Alcohol/chemistry , Polyvinyl Alcohol/toxicity , Silver/chemistry , Silver/pharmacology , Silver/toxicity , Staphylococcus aureus/drug effects , Tensile StrengthABSTRACT
Few studies aiming to develop a glue with an underwater reusable adhesive property have been reported because combining the two properties of reusable adhesion and underwater adhesion into a single glue formulation is a challenging issue. Herein, preparation of a simple mixture of poly(vinyl alcohol) (PVA) and a well-known phenolic compound, namely, tannic acid (TA), results in an underwater glue exhibiting reusable adhesion. We named the adhesive VATA (PVA + TA). Using VATA, two stainless steel objects (0.77 kg each) are able to be instantly attached. In addition to the high adhesive strength, surface-applied VATA in water retains its adhesive capability even after 24 h. In contrast, cyanoacrylate applied under the same water condition rapidly loses its adhesive power. Another advantage is that VATA's adhesion is reusable. Bonded objects can be forcibly detached, and then the detached ones can be reattached by the residual VATA. VATA maintains nearly 100% of its initial adhesive force, even after 10 repetitions of attach-detach cycles. VATA bonds various materials ranging from metals and polymers to ceramics. Particularly, we first attempt to test the toxicity of the underwater adhesives using an invertebrate nematode, Caenorhabditis elegans and gold fish (vertebrate) due to potential release to the environment.
Subject(s)
Adhesives/chemistry , Polyvinyl Alcohol/chemistry , Tannins/chemistry , Adhesiveness , Adhesives/toxicity , Animals , Caenorhabditis elegans/drug effects , Goldfish , Materials Testing , Polyvinyl Alcohol/toxicity , Stress, Mechanical , Tannins/toxicity , Tensile Strength , Water/chemistryABSTRACT
A highly efficient flame-retardant and ultra-low-smoke-toxicity biodegradable material, poly(vinyl alcohol) (PVA)/alginate/montmorillonite (MMT) composite aerogel, was fabricated by a new environment-friendly two-step crosslinking strategy using borate and calcium ions. Compressive and specific moduli of the crosslinked PVA/alginate/MMT (P4A4M4/BA/Ca) aerogel increased to 7.2- and 1.9-folds those of the non-crosslinked aerogel, respectively, and the limited oxygen index value increased to 40.0%. Cone calorimeter tests revealed that the total heat release and peak heat release rate values of the P4A4M4/BA/Ca composite aerogel distinctly decreased. Remarkably, the total smoke release value of the P4A4M4/BA/Ca aerogel was considerably lower than those of non-crosslinked PVA composite aerogels, indicating its superior smoke suppression ability and high fire hazardous safety. The flame-retardancy mechanism of the crosslinked P4A4M4/BA/Ca composite aerogels involved a combination of the gaseous phase and condensed phase flame retardancy. The high-performance PVA/alginate/MMT biodegradable composite aerogels with good sustainability is a promising alternative to conventional flame-retardant foams.
Subject(s)
Alginates/chemistry , Bentonite/chemistry , Flame Retardants/chemical synthesis , Hydrogels/chemistry , Polyvinyl Alcohol/chemistry , Alginates/chemical synthesis , Alginates/toxicity , Bentonite/chemical synthesis , Bentonite/toxicity , Borates/chemistry , Cross-Linking Reagents/chemistry , Flame Retardants/toxicity , Hydrogels/chemical synthesis , Hydrogels/toxicity , Polyvinyl Alcohol/chemical synthesis , Polyvinyl Alcohol/toxicity , SmokeABSTRACT
Solubilized dialdehyde cellulose (DAC), an efficient crosslinking agent for poly(vinyl alcohol) (PVA), provides less toxic alternative to current synthetic crosslinking agents such as glutaraldehyde, while simultaneously allowing for the preparation of hydrogels with comparably better characteristics. PVA/DAC hydrogels prepared using 0.5, 1 and 1.5 wt% of DAC were analyzed in terms of mechanical, swelling and cytotoxicity characteristics. Materials properties of PVA/DAC hydrogels range from stiff substances to soft viscoelastic gels capable of holding large amounts of water. Superior mechanical properties, porosity and surface area in comparison with analogical PVA/glutaraldehyde hydrogels were observed. Biological studies showed low toxicity and good biocompatibility of PVA/DAC hydrogels. Potential of PVA/DAC in mesh-controlled release of biologically active compounds was investigated using ibuprofen, rutin and phenanthriplatin. Hydrogel loaded with anticancer drug phenantriplatin was found effective against alveolar cancer cell line A549 under in vitro conditions.
Subject(s)
Biocompatible Materials/chemistry , Cellulose/analogs & derivatives , Cross-Linking Reagents/chemistry , Hydrogels/chemistry , Polyvinyl Alcohol/chemistry , Animals , Biocompatible Materials/toxicity , Cell Line, Tumor , Cellulose/chemistry , Cellulose/toxicity , Cross-Linking Reagents/toxicity , Drug Carriers/chemistry , Drug Carriers/toxicity , Drug Liberation , Elastic Modulus , Humans , Hydrogels/toxicity , Ibuprofen/chemistry , Mice , Organoplatinum Compounds/chemistry , Phenanthridines/chemistry , Polyvinyl Alcohol/toxicity , Rutin/chemistry , Viscoelastic Substances/chemistry , Viscoelastic Substances/toxicityABSTRACT
The aim of this study is to investigate the biocompatibility of polyvinyl alcohol (PVA) embolic microspheres by in vivo and in vitro evaluations. Two specifications of PVA microspheres including colorless microspheres (1 g microspheres with 7 mL 0.9% sodium chloride (SC) per vial, size: 500-700 µm) and blue microspheres (2 g microspheres with 7 mL 0.9% SC per vial, size: 500-700 µm) were assessed for biocompatibility. The vitro cytotoxicity was evaluated in L929 cells by MTT assay. Acute systemic toxicity and 28-repeat dose intravenous subchronic toxicity were assessed in 20 ICR mice and 40 SD rates, respectively. Skin sensitization was conducted in 30 adult albino guinea pigs by maximization test, in addition, intracutaneous reaction test was performed in New Zealand white rabbits. Hemolysis ratio of PVA microspheres was evaluated with rabbit blood. Moreover, test for genotoxicity was assessed by bacterial reverse mutation test and mouse lymphoma mutagenesis assay. No cytotoxicity, hemolysis, or acute toxicity of PVA microspheres was found, and slight fluctuations of biochemical indexes were observed in test of 28-day repeat dose intravenous subchronic toxicity, while these changes remained within our historical permitted range. Maximization test and intracutaneous reactivity test disclosed no irritation to skin or tissues. According to bacterial reverse mutation test and mouse lymphoma mutagenesis assay, no genotoxicity of PVA microspheres was observed. PVA microspheres showed excellent biocompatibility both in vivo and in vitro, and they were promising embolic materials for drug-eluting beads transarterial chemoembolization (DEB-TACE) therapy.
Subject(s)
Biocompatible Materials/toxicity , Microspheres , Polyvinyl Alcohol/toxicity , Animals , Cell Line , Cell Survival/drug effects , Chemoembolization, Therapeutic , Female , Guinea Pigs , Male , Materials Testing , Mice , Mutagenicity Tests , Particle Size , RabbitsABSTRACT
This research reports on the cytotoxicity of materials present in a wound biosensor on human keratinocytes (HaCaT) to evaluate the biocompatibility of the sensor for continuous wound monitoring applications. Individual and collective effects of the sensor materials, gold (Au) and silver (Ag) nanoparticles (NPs), uricase enzyme (UOx), ferrocene carboxylic acid (FCA), multi-walled carbon nanotubes (MWCNTs) and poly vinyl alcohol-based polymer (PVA-SbQ) on HaCaT were studied. The toxicology profiles of these materials were derived from cell viability, mitochondrial activity retention and apoptotic behavior studies. At the concentrations present in the sensor, the cell viability studies showed minimal toxicity for Au and Ag NPs, UOx and FCA (cell viability >75%), while MWCNTs and PVA-SbQ exhibited excellent biocompatibility towards keratinocytes (cell viability >90%). Resazurin assay confirmed minimal impairment of mitochondrial activity at lower concentrations for all the materials (mitochondrial activity >0.7). The caspase-3/7 apoptotic assay showed no pronounced apoptotic behavior caused by the materials. The material mixtures studied were Au/UOx/FCA/PVA-SbQ, Ag/UOx/FCA/PVA-SbQ, and MWCNTs/UOx/FCA/PVA-SbQ. A higher toxicity profile was observed for the heterogeneous material mixtures as a result of the cumulative effect of the individual materials. However, the biosensor itself was seen to exhibit lower toxicity (~5%) compared to the material mixtures, due to the protective PVA-SbQ capping over the biosensor. This work establishes the biocompatibility of the reported wound sensor for human measurements with minimal toxic effects on human keratinocytes.
Subject(s)
Ferrous Compounds/toxicity , Gold/toxicity , Keratinocytes/drug effects , Metal Nanoparticles/toxicity , Nanotubes, Carbon/toxicity , Polyvinyl Alcohol/toxicity , Silver/toxicity , Urate Oxidase/toxicity , Biosensing Techniques , Catalysis , Cell Line , Cell Survival/drug effects , Humans , Metallocenes , Wounds and InjuriesABSTRACT
Hyaluronic acid (HA) is widely investigated due to its high potential for wound dressing applications. The fabrication of biomimetic HA-based scaffolds by electrospinning is thus extensively studied. However, HA is often dissolved in toxic organic solvents to allow the efficient production of electrospun nanofibers. Indeed, although HA is soluble in water, its ionic nature leading to long-range electrostatic interactions and the presence of counter ions induce a dramatic increase of the viscosity of aqueous HA solutions without insuring enough chain entanglements necessary for a stable and efficient electrospinning. In this study, biocompatible insoluble HA-based nanofibers were fabricated by electrospinning in pure water. To this end, poly(vinyl alcohol) (PVA) was added as a carrier polymer and it was found that the addition of hydroxypropyl-ßcyclodextrin (HPßCD) stabilized the process of electrospinning and led to the efficient formation of uniform nanofibrous scaffolds. An in situ crosslinking process of the scaffolds is also proposed, insuring a whole fabrication process without any toxicity. Furthermore, the beneficial presence of HPßCD in the HA-based scaffolds paves the way for wound dressing applications with controlled drug encapsulation-release properties. As a proof of concept, naproxen (NAP), a non-steroidal anti-inflammatory drug was chosen as a model drug. NAP was impregnated into the scaffolds either in aqueous solution or under supercritical CO2. The resulting functional scaffolds showed a regular drug release profile along several days without losing the fibrous structure. This study proposes a simple approach to form stable HA-based nanofibrous scaffolds embedding HPßCD using water as the only solvent, enabling the development of safe functional wound dressings.
Subject(s)
Bandages , Hyaluronic Acid/chemistry , Nanofibers/chemistry , Polyvinyl Alcohol/chemistry , beta-Cyclodextrins/chemistry , Animals , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Carbon Dioxide/chemistry , Cattle , Cross-Linking Reagents/chemistry , Drug Delivery Systems , Drug Liberation , Elastic Modulus , Ethyldimethylaminopropyl Carbodiimide/chemistry , Hyaluronic Acid/toxicity , Kinetics , Mice , NIH 3T3 Cells , Nanofibers/toxicity , Naproxen/administration & dosage , Naproxen/chemistry , Polyvinyl Alcohol/toxicity , Succinimides/chemistry , Water/chemistry , beta-Cyclodextrins/toxicityABSTRACT
Toward engineering approaches that are designed to optimize the particle size, morphology, and mucoadhesion behavior of the particulate component of inhaler formulations, this paper presents the preparation, physicochemical characterization, and preliminary in vitro evaluation of multicomponent polymer-lipid systems that are based on "spray-drying engineered" α-lactose monohydrate microparticles. The formulations combine an active (budesonide) with a lung surfactant (dipalmitoylphosphatidylcholine) and with materials that are known for their desirable effects on morphology (polyvinyl alcohol), aerosolization (l-leucine), and mucoadhesion (chitosan). The effect of the composition of formulations on the morphology, distribution, and in vitro mucoadhesion profiles is presented along with "Calu-3 cell monolayers" data that indicate good cytocompatibility and also with simulated-lung-fluid data that are consistent with the therapeutically useful release of budesonide.
Subject(s)
Budesonide/chemistry , Drug Carriers/chemistry , Excipients/chemistry , Lactose/chemistry , Polyvinyl Alcohol/chemistry , 1,2-Dipalmitoylphosphatidylcholine/chemistry , 1,2-Dipalmitoylphosphatidylcholine/toxicity , Administration, Inhalation , Cell Line, Tumor , Chitosan/chemistry , Chitosan/toxicity , Drug Carriers/toxicity , Drug Compounding , Drug Liberation , Excipients/toxicity , Female , Humans , Lactose/toxicity , Leucine/chemistry , Leucine/toxicity , Male , Mucus/chemistry , Particle Size , Polyvinyl Alcohol/toxicity , Pulmonary Surfactants/chemistry , Pulmonary Surfactants/toxicityABSTRACT
Nanoparticle-based theranostic agents have emerged as a new paradigm in nanomedicine field for integration of multimodal imaging and therapeutic functions within a single platform. However, the clinical translation of these agents is severely limited by the complexity of fabrication, long-term toxicity of the materials, and unfavorable biodistributions. Here we report an extremely simple and robust approach to develop highly versatile and biocompatible theranostic poly(vinyl alcohol)-porphyrin nanoparticles (PPNs). Through a "one-pot" fabrication process, including the chelation of metal ions and encapsulation of hydrophobic drugs, monodispersenanoparticle could be formed by self-assembly of a very simple and biocompatible building block (poly(vinyl alcohol)-porphyrin conjugate). Using this approach, we could conveniently produce multifunctional PPNs that integrate optical imaging, positron emission tomography (PET), photodynamic therapy (PDT), photothermal therapy (PTT) and drug delivery functions in one formulation. PPNs exhibited unique architecture-dependent fluorescence self-quenching, as well as photodynamic- and photothermal- properties. Near-infrared fluorescence could be amplified upon PPN dissociation, providing feasibility of low-background fluorescence imaging. Doxorubicin (DOX)-loaded PPNs achieved 53 times longer half-life in blood circulation than free DOX. Upon irradiation by near infrared light at a single excitation wavelength, PPNs could be activated to release reactive oxygen species, heat and drugs simultaneously at the tumor sites in mice bearing tumor xenograft, resulting in complete eradication of tumors. Due to their organic compositions, PPNs showed no obvious cytotoxicity in mice via intravenous administration during therapeutic studies. This highly versatile and multifunctional PPN theranostic nanoplatform showed great potential for the integration of multimodal imaging and therapeutic functions towards personalized nanomedicine against cancers.