Use Of Compounds Research Articles

Testing of acetaminophen in support of the international multilaboratory in vivo rat Pig-a assay validation trial.

Acetaminophen, a nonmutagenic compound as previously concluded from bacteria, in vitro mammalian cell, and in vivo transgenic rat assays, presented a good profile as a nonmutagenic reference compound for use in the international multilaboratory Pig‐a assay validation. Acetaminophen was administered at 250, 500, 1,000, and 2,000 mg·kg−1·day−1 to male Sprague Dawley rats once daily in 3 studies (3 days, 2 weeks, and 1 month with a 1‐month recovery group). The 3‐Day and 1‐Month Studies included assessments of the micronucleus endpoint in peripheral blood erythrocytes and the comet endpoint in liver cells and peripheral blood cells in addition to the Pig‐a assay; appropriate positive controls were included for each assay. Within these studies, potential toxicity of acetaminophen was evaluated and confirmed by inclusion of liver damage biomarkers and histopathology. Blood was sampled pre‐treatment and at multiple time points up to Day 57. Pig‐a mutant frequencies were determined in total red blood cells (RBCs) and reticulocytes (RETs) as CD59‐negative RBC and CD59‐negative RET frequencies, respectively. No increases in DNA damage as indicated through Pig‐a, micronucleus, or comet endpoints were seen in treated rats. All positive controls responded as appropriate. Data from this series of studies demonstrate that acetaminophen is not mutagenic in the rat Pig‐a model. These data are consistent with multiple studies in other nonclinical models, which have shown that acetaminophen is not mutagenic. At 1,000 mg·kg−1·day−1, Cmax values of acetaminophen on Day 28 were 153,600 ng/ml and 131,500 ng/ml after single and repeat dosing, respectively, which were multiples over that of clinical therapeutic exposures (2.6–6.1 fold for single doses of 4,000 mg and 1,000 mg, respectively, and 11.5 fold for multiple dose of 4,000 mg) (FDA 2002). Data generated were of high quality and valid for contribution to the international multilaboratory validation of the in vivo Rat Pig‐a Mutation Assay.

Formulations Based on Natural Ingredients for the Treatment of Nail Diseases.

Nail is a strong and resistant structure, characterized by a low permeability to foreign molecules. Nails can be subjected to many diseases, among which fungal infections (e.g. onchomycosis) are the most common and responsible for nail structure alteration. Many formulations have been produced for the delivery of active ingredients to treat nail disorders, based on newly synthesized active molecules or containing chemical enhancers or chemically-modified polymers able to improve the drug transungual penetration. To avoid permanent alterations of the nail structure due to the use of chemical compounds or organic solvent-based formulation, researchers have developed novel formulations focusing on the use of new natural-based compounds. The purpose of this review is to provide information on the outcoming of natural ingredients-based formulations that have been developed in the last years as potential alternative to chemical-based formulations.

Biological Effects of Propolis on Cancer

Propolis is a special resin and wax material collected from the leaves and shells of trees, buds and shoots of plants by honey bees (Apis mellifera L.). In recent years, many researchers have studied the chemical composition, biological activity and pharmacological properties of propolis. The colour, odour and pharmacological properties of the propolis composition also vary as the composition changes depending on the plant, region, season and bee colony. Flavonoids, aromatic acids, phenolic acids and esters are the main compounds responsible for the biological activity of propolis. A number of studies have been conducted on the use of propolis or its active ingredients in the treatment of cancer. It has been observed that the use of propolis did not cause side effects according to in-vitro and in-vivo studies. Propolis should be extracted with different compounds for use in biological assays. The most commonly used compounds for extraction are ethanol, methanol, oil and water. A number of studies have been carried out showing the antitumor effect of propolis in cell culture and animal tests. The search for new drugs derived from natural products, which may function as chemotherapeutic agents and have low side effects, has increased in recent years. Combination with antioxidant therapy may improve the side effects of chemotherapy on leukocytes, liver and kidney, thus increasing the effect of chemotherapy with dose increase.

Polyphenol-Rich Purple Corn Pericarp Extract Adversely Impacts Herbivore Growth and Development.

Plant secondary metabolites such as terpenes, phenolics, glycosides, and alkaloids play various functional roles including pigmentation, foliar and floral volatile synthesis, hormonal regulation, and direct and indirect defenses. Among these, phenolic compounds are commonly found in plants, but vary in the distribution of their specific compounds among plant families. Polyphenols, including anthocyanins and tannins, are widely distributed and have been well documented for their roles- primarily in plant pigmentation and also in plant defenses. However, commercialization of such compounds for use in insect pest management is severely hampered by expensive, inefficient, and time-consuming extraction protocols. Using a recently developed inexpensive and easy extraction method using the byproducts of pigmented (purple) corn processing, we examined whether the crude pericarp extract rich in polyphenols can affect the growth and development of tobacco hornworm (Manduca sexta L.) caterpillars. Our findings show that purple corn pericarp extract negatively affected M. sexta egg hatching and larval mass gain and prolonged developmental time compared to regular yellow corn extract or an artificial control diet. We also found that these effects were more severe during the early stages of caterpillar development. These results conclusively demonstrate that purple corn pericarp, an inexpensive by-product of the corn milling industry, is a valuable product with excellent potential as an insect antifeedant.

Preparation, characterization of some transition metal complexes of hydrazone derivatives and their antibacterial and antioxidant activities

A new series of metal complexes of Pd(II), Cd(II) and Cu(II, I) of polydentate Schiff base ligand (H2L), namely ((Z)-2-(phenylamino)-N'-(thiophen-2-ylmethylene) acetohydrazide) have been prepared. The ligand and its metal complexes have been characterized based on various physicochemical studies as elemental analyses, molar conductance, spectral (UV–Vis, MS, IR, 1H NMR, 13C NMR and XRD), magnetic moment measurements and thermal studies (TG, DTG). In the view of previous studies, the ligand (H2L) acts as polydentate one and coordinates with metal ions to form all metal complexes. The kinetic and thermodynamic parameters of decomposition process (ΔG, ΔH, ΔS) were calculated. The possible structures of the metal complexes have been computed using the molecular mechanic calculations using the hyper chem. 8.03 molecular modeling program. The calculations are performed to obtain the optimized molecular geometry. The antibacterial study of the selected compounds was assayed against two pathogenic bacteria. Moreover, the complexes (Cu II, I), Cd(II), Pd(II)) and the ligand revealed excellent antioxidant properties and could be useful in fighting the free radicals which occur in close connection with cancerous cells. It was remarkable that the two complexes (Cu II, I) demonstrated stronger antioxidant effects than their parent compounds. It is clear that the new complexes are good active compounds for use in a variety of applications.

FeCl3-catalyzed oxidative decarboxylation of aryl/heteroaryl acetic acids: preparation of selected API impurities.

There is an ever-increasing demand for impurity compounds for use in impurity profiling as regulatory agencies seek information during registration. Herein, we report the FeCl3-catalyzed oxidative decarboxylation of aryl- and heteroaryl acetic acids to the corresponding carbonyl compounds. A variety of useful aldehydes and ketones were prepared in a simple one-pot transformation by employing an environmentally benign, low-cost, and readily available iron salt. The utility of this method has been demonstrated by preparing five valuable API impurities including a multi-gram-scale synthesis of ketorolac impurity B for the first time.

Microwave Assisted Ultra-Fast Method to Synthesize Carbonate-Phosphates, Na3MCO3PO4 (M = Mn, Fe, Co, Ni) - Relevant Materials Applied in Sodium-Ion Batteries

Although largely used in mobiles and electric vehicles applications, insertion batteries based on Li-ion technology are high-cost devices. These applications require high-performance energy storage systems with high-energy and high-power densities, which are better attained by Li-ion technology. However, stationary applications such as power plants and uninterruptible power supplies (UPS) mainly require low-cost energy storage devices. In this scenario Na-ion insertion batteries feature as a cheaper option for such applications. Among the several compounds for use as cathode in Na-batteries, a largely studied class of compounds are the sodium-carbonate-phosphates, Na3MCO3PO4 (M = Mn, Fe, Co or Ni), with structure analogue to the mineral sidorenkite. In this work, it was developed a new microwave-assisted hydrothermal method as an ultra-fast way to prepare sodium-carbonate-phosphate compounds. This methodology results in high-quality materials with general formula Na3MCO3PO4 (M = Mn, Fe, Co or Ni) upon only 5 min processing time. Characterization techniques indicate highly ordered materials with sidorenkite-like phase and different morphologies or crystal habits, including plates, rods, and a ‘starfruit’ shape. As a proof-of-application the Mn-based material was evaluated from electrochemical tests for Na+ insertion reactions. The obtained results evidence initial discharge capacity of 107 mA h g-1 with good reversible capacity (65 mA h g-1) after several charge/discharge cycles.

A green deposition method of silver nanoparticles on textiles and their antifungal activity

This study aims to propose a new green method for the deposition of silver nanoparticles (AgNPs) on textiles without the use of chemical compounds as binders. The deposition of AgNPs on textiles was achieved by immersing textiles in silver nitrate solution before adding with a natural reducing agent obtained from the extraction of Mikania micrantha. Plasmonic properties of the synthesized AgNPs were characterized using Ultraviolet-visible (UV–vis) spectroscopy and surface morphology of textiles was identified using the field-emission scanning electron microscopy (FESEM). In addition, energy-dispersive X-ray spectroscopy was also employed for the characterization. Inhibition zone measurement was performed for evaluating the antifungal capability of textiles attached with AgNPs. This study showed that the attachment of AgNPs to several textile types (cotton, cotton-polyester, silk, and fiber) without the use of binders or other chemical compounds had been successfully achieved. Moreover, all textiles attached with AgNP exhibited effective antifungal activity.

Ability Test of Acacia Nilotica Leaves and Extract As Water Disinfectants

The fulfillment of clean water that meets bacteriological requirements for urban areas is increasingly difficult due to the high contamination of groundwater by microbes. The use of chemical compounds as disinfectants always produces long-term side effects, it is necessary to develop plants that can be used as disinfectants. Acacia nilotica has the ability to kill aerobic and coliform bacteria so that it has the potential to disinfect water. The study aimed to examine the ability of leaves and extracts of A. nilotica leaves that grow in the Baluran National Park in East Java in reducing the number of aerobic and coliform bacteria in clean water used by the community. Water samples were taken from the residents of Rt 006/011 Kebayoran lama with bacteriological quality criteria Total Plate Number (TPC) above 4.0 x 10 [2]CFU and MPN Coliform> 2400 cells/100ml. The leaves of A. nilotica are used at concentrations of 30%, 40%, and 50%, and ethanol extract of leaves of A. nilotica 5%, 7.5%, and 10% after 1 hour, 3 hours, 6 hours and 24 hours of contact. A coliform examination was performed on TPC and MPN. The yield of A. nilotica leaves was effective in reducing aerobic bacteria to 99.6% at a concentration of 50% after 24-hour contact, while leaf extract reduced the number of aerobic germs to 99.7% at a concentration of 10%. While MPN Coliform is reduced to 99.5% in the application of 50% of leaves of A. nilotica, the extract of A. nilotica can reduce coliform MPN to 100% at a concentration of 10%.

Antidiabetic and Hypolipidemic Effects of 5,7-Dimethoxyflavone in Streptozotocin-Induced Diabetic Rats.

BackgroundThe flavones are considered as competent antidiabetic molecules due to their strong antioxidant activities and higher in vivo stability. The present study evaluated the antidiabetic and hypolipidemic effects of 5,7-dimethoxyflavone in streptozotocin (STZ)-induced diabetic rat models.Material/MethodsThe antidiabetic potential of 5,7-dimethoxyflavone was evaluated in streptozotocin-induced diabetic rats. The serum levels of triglyceride, total cholesterol, and high-density lipoprotein cholesterol were measured using the Randox assay kit. Histopathological examination was carried out by hematoxylin and eosin (HE) staining.ResultsOral administration of 5,7-dimethoxyflavone significantly reduced STZ-induced enhancement in blood sugar and glycosylated hemoglobin, as well as significant increases in C-peptide, insulin, hemoglobin, and total protein content (p<0.05). Additionally, treatment with 5,7-dimethoxyflavone resulted in a remarkable increase in non-enzymic antioxidants. Administration of 5,7-dimethoxyflavone had a hypolipidemic effect by significantly reducing levels of serum triglycerides, total cholesterol, and low-density lipoproteins. The histopathological examination of rat pancreases revealed the beneficial effect of 5,7-dimethoxyflavone and protection of β cell integrity in STZ-induced diabetic rats.ConclusionsThese findings reflect the antidiabetic and hypolipidemic effects of 5,7-dimethoxyflavone, suggesting that 5,7-dimethoxyflavone may be a promising compound for use in development of new antidiabetic drugs.

Development and preclinical pharmacology of a novel dCK inhibitor, DI-87

BackgroundDeoxycytidine kinase (dCK) is an essential enzyme for production of nucleotides via the salvage pathway; DI-87 is a novel dCK inhibitor in preclinical development for use in anticancer therapy. The current study utilizes PET imaging to evaluate PK-PD relationships and to determine optimal dosing of the drug. MethodsNSG mice bearing CEM tumors had plasma and tumor PK assessed using mass spectrometry following oral administration of DI-87. dCK inhibition was assessed after a single dose of oral DI-87 followed by a [18F]CFA PET probe and PET imaging. Tumor growth inhibition was assessed by orally administering DI-87 with concurrent intraperitoneal thymidine. ResultsDI-87 had an in vitro EC50 of 10.2 nM with low protein binding. Peak DI-87 concentrations were observed between 1–3 h and 3–9 h in plasma and tumor, respectively, with tumor concentrations less than one third of plasma. Full dCK inhibition, as evaluated by PET imaging, was observed as early as 3 h following 25 mg/kg dosing and was maintained for 12 h, with full recovery of enzyme activity after 36 h. When DI-87 was administered as repeated doses in combination with thymidine, full dCK inhibition was maintained at 12 h (25 mg/kg twice daily dose) and led to maximal tumor growth inhibition. ConclusionsDI-87 is a promising new compound for use in combination therapy against tumors expressing dCK. Utilizing a [18F]CFA PET probe targeting the pathway of interest allowed for efficient and accurate identification of the optimal dose for growth inhibition.

Dependence of Fractional Structure of River Sediments on Chemical Composition

The article investigates the mechanical and chemical composition of river sediments and analyzes studies on changes in the chemical composition of sediments by changing their mechanical composition. Given scientific investigations about efficient use of chemical compounds in sediments. The connections between mechanical and chemical composition of the sediments are based on correlation coefficients. The results are based on the fact that small fractional sediments less than 0.05 mm can be used effectively in agriculture.

Extract of spray‐dried Malay apple (Syzygium malaccense L.) skin

AbstractThe Malay apple is a fruit tree found in northeastern Brazil; little is known about the composition and properties of its fruit, which motivated the present study. Among natural antioxidants, anthocyanins are pigments responsible for the red and blue coloring of a wide range of food plants. There is a growing interest in their use by the pharmaceutical industry; however, their sensitivity to environmental factors means processing is required to ensure their stability. Spray‐drying has proved to be effective in this regard. The aim of this study was to dry Malay apple skin extract by two different methods (spray‐ and freeze‐drying) and analyze the physical and chemical properties, morphology, and bioactive compounds of the products obtained, in order to assess the preservation of the antioxidants and conduct a preliminary study on their possible encapsulation. The results indicated that it is possible to obtain a powder with low humidity and preserved biocharacteristics using freeze‐ and spray‐drying, with high yield. When compared to the freeze‐dried product, the spray‐drying conserved the bioactive compounds and provided smaller size distribution than that obtained by freeze‐drying. The results obtained by spray‐drying showed favorable for use in controlled release systems.Practical applicationsThis work had as practical applications the use of a local and almost industrially unexplored fruit, the Malay apple, as a product rich in anthocyanins and other bioactive compounds for use as food additive and with potential use in cosmetics, since the compounds obtained, anthocyanins, have proven antioxidant capacity. Bioactive compounds from the peel of the Malay apple were determined for the first time. The spray‐drying process maintains much of the bioactive characteristics of the Malay apple skin. The freeze‐drying process is more effective in preserving the properties of the skin of the Malay apple. The zeta potential of the Malay apple was determined for the first time.

DDIS-01. NEW DRUG DISCOVERY WITH DRUG RE-POSITIONING SYSTEM TOWARD GBM TREATMENT

Abstract INTRODUCTION Invasion of Glioblastoma (GBM) cells into normal brain is the major cause of poor prognosis and requires dynamic reorganization of the actin cytoskeleton, which includes lamellipodial protrusions, focal adhesions, and stress fibers at the leading edge of GBM cells. Therefore, we hypothesized that the inhibition of actin polymerization with existing medication could lead to clinical GBM treatment directly in short time. The Drug Repositioning system is also known as drug repurposing or drug reprofiling and understood as the process of redeveloping a compound for use in a different disease. In this time, we would show the new direction of drug development with drug repositioning. MATERIALS AND METHODS We adopted a drug repositioning system for screening with a pyrene-actin-based actin polymerization assay and identified fluvoxamine, a clinically used antidepressant. Fluvoxamine, selective serotonin reuptake inhibitor, was a potent inhibitor of actin polymerization and confirmed as drug penetration through the blood–brain barrier (BBB) and accumulation of whole brain including brain tumor with no drug toxicity. RESULTS Fluvoxamine inhibited serum-induced ruffle formation, cell migration, and invasion of human GBM and glioma stem cells in vitro by suppressing FAK signaling. Fluvoxamine showed no drug toxicity. Daily treatment of athymic mice bearing human glioma-initiating cells with fluvoxamine blocked tumor cell invasion and prolonged the survival with almost same doze of anti-depressant effect. CONCLUSIONS The SSRI group has big potential for clinical GBM treatment with low cost, short time and low side effect.

Polyacrylates of Metals Are a New Class of the Potential Antitumor Drugs

The results of preclinical study of the original antitumor drug aurumacryl (gold polyacrylate), which belongs to polyacrylates of metals (PAMs), a new class of compounds for use in oncology, are presented. PAMs have been studied as cytostatics for the first time in the N.M. Emanuel Institute of Biochemical Physics at the Russian Academy of Sciences. The strong antitumor and cytotoxic activity of aurumacryl has been revealed. Aurumacryl induced in vivo the inhibition of growth of the murine solid tumors, as well as the death of the human tumor cells in vitro. The proliferation kinetics of the surviving fraction of tumor cells also changed after drug treatment. These alterations were expressed as the accumulation of the main part of cells in the phase of the proliferative rest and in the strong decrease of the number of proliferative cells. These data may be evaluated as the evidence of the loss of the reproductive activity by the tumor cells after aurumacryl treatment. The distribution of the aurumacryl between the tumor and some organs (blood, kidneys, liver, lungs, spleen and brain) of mice with the solid tumor has been also studied. The results of our own investigations of aurumacryl are discussed in the context of the contemporary concepts about the gold complexes antitumor effect and mechanism of action of these compounds.

Assessment of 2H–SiC based intercalation compound for use as anode in lithium ion batteries

The improvement in electrode materials to upgrade lithium ion battery (LIB) is at heart of research related to energy devices. Herein, we report on the prospects of using 2H–SiC as an anode material in LIB on the basis of first principles based theoretical predictions. The energy profiling of high symmetry structural sites pointed out that the site TC related to tetrahedral configuration with carbon is favorable intercalation site in the host. The reaction of Li with stoichiometric as well as non-stoichiometric 2H–SiC are found endothermic which points to their unsuitability for lithiation process in LIBs. However, Li intercalation into the host in presence of Si monovacancy appeared an exothermic process which motivated us to study this system in detail. The Li atom after intercalation into the host is found ionized thereby donating its 2s electron to carbon atoms. The average value of the lithium insertion voltage and theoretical capacity are calculated as 1.87 V and 85 mA h/g respectively for the host simulated in the form of supercell LixSi15C16. The diffusion barrier faced by lithium atom while moving along crystalline a-axis is minimum (among all the paths considered here) when it follows a path that links hexagonal rings while passing carbon atoms. On the other hand, in case of motion along c-axis, similar results are found for minimum energy path that is along Tc site. The low diffusion barrier will facilitate the lithium ion to move quickly that points to fast charging capability of the battery.

Bile acid-binding capacity of lobster shell-derived chitin, chitosan and chitooligosaccharides

The extraction of chitin and its derivatives, chitosan and chitooligosaccharides (COS) from lobster shell by-products and their hypocholesterolemic property through bile acid sequestration were studied. Chitin was extracted from lobster shells using chemical methods. The purity and recovery rate of extracted chitin were 96.4 and ~94%, respectively, from tail shells. Chitosan was derived from chitin with a high degree of deacetylation and a molecular weight >500 kDa. Pepsin and papain were used as a combined enzymatic system for hydrolysis of chitosan, which yielded 13% COS. The enzymatically prepared COS had net positive zeta (ζ) potential of +37.6 mV, bimodal molecular weight distribution, and showed the highest bile acid-binding capacity with sodium deoxycholate at 50 mg/mL. Results indicated that COS may have different binding reactions with multiple mechanisms with the bile acids compared to chitin and chitosan. The results suggested that the lobster shell-derived chitin, chitosan and COS could be promising compounds for use in the management of hypercholesterolaemia through binding with bile acids.

Structure design and property adjustment of new cage rich-nitrogen pentazolyltetraazacubanes as potential high energy density compounds

In this study, based on two attractive energetic compounds pentazole (PZ) and tetraazacubane (TAC), a new family of high energy and high nitrogen compounds pentazolyltetraazacubanes were designed. Then, a different number of NH2 or NO2 groups were introduced into the system to further adjust the property. The structures, properties, and the structure-property relationship of designed molecules were investigated theoretically. The results showed that all nine designed compounds have extremely high heat of formation (HOF, 1226-2734 kJ/mol), good density (1.73–1.88 g/cm3), high detonation velocity (8.30–9.35 km/s), high detonation pressure (29.8–39.7 GPa) and acceptable sensitivity (ΔV: 41-87 Å3). These properties could be effectively positive adjusted by replacing one or two PZ rings by NH2 or/and NO2 groups, especially for the energy and sensitivity performance, which were increased and decreased obviously, respectively. As a result, two designed pentazolyltetraazacubanes were predicted to have higher energy and lower sensitivity than the famous high energy compound in use 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane, while two others have better combination property than 1,3,5-Trinitro-1,3,5-triazacyclohexane. In all, four new pentazolyltetraazacubanes with good combination performance were successfully designed by combining PZ with TAC, and the further property adjustment strategy of introducing a suitable amount of NH2/NO2 groups into the system. This work may help develop new cage energetic compounds.

Buckwheat Hull Extracts Inhibit Aspergillus flavus Growth and AFB1 Biosynthesis.

Fungal contamination poses at risk the whole food production chain - from farm to fork - with potential negative impact on human health. So far, the insurgence of pathogens has been restrained by the use of chemical compounds, whose residues have gradually accumulated determining toxic effects in the environment. Modern innovative techniques imply the use of natural and eco-sustainable bioactive plant molecules as pathogens and pests-control agents. These may be profitably recovered in large amounts at the end of industrial milling processes. This is the case of the non-digestible hull of common buckwheat (Fagopyrum esculentum Moench), a natural source of polyphenols, tocopherols, phytosterols and fatty acids. We extract these compounds from the hull of buckwheat; apply them to Aspergillus flavus - aflatoxin producer - under in vitro conditions, checking their ability to inhibit fungal growth and aflatoxin biosynthesis. Moreover, a solvent free method implying the adoption of supercritical CO2 as solvent was set up to extract lipophilic molecules from the buckwheat’ hulls. Positive results in controlling fungal growth and aflatoxin biosynthesis let infer that the extracts could be further tested also under in vivo conditions.

Biotoxicity and life cycle assessment of two commercial antifouling coatings in marine systems

Two commercial coating systems, each one consisting of both a primer and an antifouling (“System 1” based on Copper Oxide and “System 2” based on Zinc Oxide), have been analyzed in order to investigate their environmental impacts through Life Cycle Assessment (LCA) and laboratory tests.A cradle-to-grave analysis has been performed in order to quantify the environmental footprint of each coating solution and to define which element, material, or process mainly affect the environmental impact of such products. Moreover, it was performed a comparison between the different products to determine the most environmentally sustainable choice.In addition to LCA, several incubations of coated metal samples, by means of an innovative incubation system developed by the authors, have also been performed in marine water (Gulf of Naples, Mediterranean Sea, Italy), as critical environment favoring metal corrosion and biofouling generation.The life cycle analysis has showed that the production phase presents the highest environmental impact in almost all categories, mainly due to the use of chemical compounds. Moreover, after the laboratory tests, strong biotoxicity and contaminant diffusion, contributing to the marine toxicity potential, have been observed for both the commercial paints.As a final remark, there are straightforward indications of a strong need for anti-Microbial-Induced-Corrosion commercial coatings to substitute the toxic compounds with others in order to develop a greener solution.