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1.
Sci Total Environ ; 878: 162954, 2023 Jun 20.
Article in English | MEDLINE | ID: mdl-36948318

ABSTRACT

Polymeric wastes are among the current major environmental problems due to potential pollution and contamination. Within the spectrum of polymeric waste, microplastics (MPs) and nanoplastics (NPs) have gained ground in recent research since these particles can affect the local biota, inducing toxic effects on several organisms. Different outcomes have been reported depending on particle sizes, shape, types, and exposed organisms and conditions, among other variables. This review aimed to compile and discuss the current knowledge and possible literature gaps regarding the MPs and NPs generation and their toxicological effects as stressors, considering polymer type (as polyethylene, polypropylene, polyethylene terephthalate, polystyrene, polyvinyl chloride, or others), size (micro- or nano-scale), source (commercial, lab-synthesized, or environmental) and test organism group. In that sense, 615 publications were analyzed, among which 72 % discussed micro-sized plastics, while <28 % assayed the toxicity of NPs (<1 µm). For most polymers, MPs and NPs were commercially purchased and used without additional size reduction processes; except for polyethylene terephthalate studies that mostly used grinding and cutting methods to obtain MPs. Polystyrene (PS) was the main polymer studied, as both MPs and NPs. PS accounts for >90 % of NPs reports evaluated, reflecting a major literature gap if compared to its 35.3 % share on MPs studies. Among the main organisms, arthropods and fish combined accounted for nearly 40 % of toxicity testing. Overall, the different types of plastics showed a tendency to report toxic effects, except for the 'Survival/lethality' category, which might indicate that polymeric particles induce mostly sublethal toxic effects. Furthermore, despite differences in publication numbers, we observed greater toxicity reported for NPs than MPs with oxidative stress among the majorly investigated endpoints. This study allowed a hazard profile overview of micro/nanoplastics (MNPs) and the visualization of literature gaps, under a broad diversity of toxicological evidence.


Subject(s)
Plastics , Water Pollutants, Chemical , Animals , Plastics/toxicity , Microplastics , Polystyrenes , Polyethylene Terephthalates , Polyethylene , Polymers
2.
Enzyme Microb Technol ; 150: 109889, 2021 Oct.
Article in English | MEDLINE | ID: mdl-34489042

ABSTRACT

Hybrid nanoparticles composed of different biopolymers for delivery of enzyme/prodrug systems are of interest for cancer therapy. Hyaluronic acid-coated chitosan nanoparticles (CS/HA NP) were prepared to encapsulate individually an enzyme/pro-drug complex based on horseradish peroxidase (HRP) and indole-3-acetic acid (IAA). CS/HA NP showed size around 158 nm and increase to 170 and 200 nm after IAA and HRP encapsulation, respectively. Nanoparticles showed positive zeta potential values (between +20.36 mV and +24.40 mV) and higher encapsulation efficiencies for both nanoparticles (up to 90 %) were obtained. Electron microscopy indicated the formation of spherical particles with smooth surface characteristic. Physicochemical and thermal characterizations suggest the encapsulation of HRP and IAA. Kinetic parameters for encapsulated HRP were similar to those of the free enzyme. IAA-CS/HA NP showed a bimodal release profile of IAA with a high initial release (72 %) followed by a slow-release pattern. The combination of HRP-CS/HA NP and IAA- CS/HA NP reduced by 88 % the cell viability of human bladder carcinoma cell line (T24) in the concentrations 0.5 mM of pro-drug and 1.2 µg/mL of the enzyme after 24 h.


Subject(s)
Chitosan , Nanoparticles , Prodrugs , Urinary Bladder Neoplasms , Horseradish Peroxidase , Humans , Hyaluronic Acid , Indoleacetic Acids
3.
Mater Sci Eng C Mater Biol Appl ; 124: 112089, 2021 May.
Article in English | MEDLINE | ID: mdl-33947529

ABSTRACT

Indole-3-carbinol (I3C) is a plant molecule known to be active against several types of cancer, but some chemical characteristics limit its clinical applications. In order to overcome these limitations, polymeric nanoparticles can be used as carrier systems for targeted delivery of I3C. In this study, chitosan and chitosan/polyethylene glycol nanoparticles (CS NP and CS/PEG NP, respectively) were prepared to encapsulate I3C by ionic gelation method. The polymeric nanoparticles were characterized by Dynamic Scattering Light (DLS), Zeta Potential (ZP), Fourier Transform Infrared (FTIR) spetroscopy, X-Ray Diffraction (XRD), Thermogravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), and Field Emission Gun Scanning Electron Microscopy (FEG-SEM). I3C release testing was performed at an acidic media and the interactions between I3C and chitosan or PEG were evaluated by Density Functional Theory (DFT). Cytotoxicity of nanoparticles in bladder cancer T24 cell line was evaluated by the Methyl-thiazolyl-tetrazolium (MTT) colorimetric assay. The average size of the nanoparticles was observed to be in the range from 133.3 ± 3.7 nm to 180.4 ± 2.7 nm with a relatively homogeneous distribution. Samples had relatively high positive zeta potential values (between +20.3 ± 0.5 mV and + 24.3 ± 0.5 mV). Similar encapsulation efficiencies (about 80%) for both nanoparticles were obtained. Physicochemical and thermal characterizations pointed to the encapsulation of I3c. electron microscopy showed spherical particles with smooth or ragged surface characteristics, depending on the presence of PEG. The mathematical fitting of the release profile demonstrated that I3C-CS NP followed the Higuchi model whereas I3C-CS/PEG NP the Korsmeyer-Peppas model. Chemical differences between the nanoparticles as based on the I3C/CS or I3C/PEG interactions were demonstrate by computational characterization. The assessment of cell viability by the MTT test showed that the presence of both free I3C and I3C-loaded nanoparticles lead to statistically significant reduction in T24 cells viability in the concentrations from 500 to 2000 µM, when comparison to the control group after 24 h of exposure. Thus, CS and CS/PEG nanoparticles present as feasible I3C carrier systems for cancer therapy.


Subject(s)
Chitosan , Nanoparticles , Urinary Bladder Neoplasms , Drug Carriers , Humans , Indoles , Particle Size , Spectroscopy, Fourier Transform Infrared
4.
Rev. odontol. UNESP (Online) ; 44(4): 218-225, jul.-ago. 2015. ilus
Article in Portuguese | LILACS, BBO - Dentistry | ID: lil-755986

ABSTRACT

Objetivo: Incorporar o hormônio de crescimento recombinante humano em um polímero biodegradável (PLGA). Material e método: As matrizes foram confeccionadas através da técnica de evaporação de solventes. Foi feita uma mistura do polímero (poli ácido glicólico lático) e do hormônio do crescimento humano recombinante (Saizen® Merck Serono S.A. Aubonne, Suíça). Essa mistura foi vertida em moldes de silicone circulares de 1 cm de diâmetro e aproximadamente 2 mm de espessura, e levada para secagem em uma câmara de evaporação de solvente por 48 horas. Após esse período, as matrizes foram imersas em PBS e passaram por um banho termostatizado (ensaio de degradação hidrolítica), in vitro, à temperatura de 37°C. As amostras foram retiradas do banho no intervalo de 1, 2, 3, 4, 7, 10 e 14 dias. Foram aferidas a perda de massa, a variação do pH e a concentração do hormônio liberado em função do tempo. Resultado: A concentração do hormônio liberado em função do tempo foi aumentando até o terceiro dia. No quarto dia, houve uma queda e, no sétimo, ocorreu um aumento do hormônio liberado, estendendo-se até o décimo dia; no 14° dia, houve queda novamente. O pH teve uma queda brusca de 7,4 para 3,2 no primeiro dia, mantendo uma pequena queda até o 14° dia. A perda de massa foi gradual em relação ao tempo, como já era esperado. Conclusão: O PLGA é um bom biomaterial para confecção de matrizes com hormônio do crescimento. Revelou-se possível incorporar o rhGH nessa matriz, de modo a, então, desenvolver-se um substituto ósseo.


Objective: Incorporate recombinant human growth hormone in a biodegradable polymer (PLGA). Material and method: The arrays were fabricated by solvent evaporation technique. A mixture of polymer (poly lactic glycolic acid) and recombinant human growth (Saizen® Merck Serono SA Aubonne, Switzerland) was performed hormone. This mixture was poured into circular molds silicone 01cm in diameter and about 02mm thick, and carried into a drying chamber for evaporation of solvent for 48 hours. After this period, the matrices were immersed in PBS and passed through a constant temperature bath (test for hydrolytic degradation) in vitro, at a temperature of 37°C. The samples were removed from the bath in the range of 01, 02, 03, 04, 07, 10, 14 days. Mass loss, pH and concentration of hormone released as a function of time was measured. Result: The concentration of hormone released versus time was increased until the third day. On the fourth day had a fall and on the seventh day there have been increased hormone released by the tenth day, the fourteenth day was falling again. The pH had a sharp drop from 7.4 to 3.2 on the first day and keeping a small drop until the fourteenth day. The mass loss was a gradual loss in relation to time as was to be expected. Conclusion: PLGA is a good biomaterial for making breeders of growth hormone. It has proved possible to incorporate the rhGH in the array so as to then develop a bone substitute.


Subject(s)
Polymers , Spectrophotometry , Biocompatible Materials , In Vitro Techniques , Growth Hormone , Microscopy, Electron, Scanning , Bone Transplantation , Osteogenesis , Wound Healing , Bone Regeneration , Hydrogen-Ion Concentration
5.
Rev. odonto ciênc ; 25(3): 288-291, 2010. tab
Article in English | LILACS | ID: lil-574138

ABSTRACT

Purpose: This in vitro study assessed the amount of debris extruded apically after preparation with different techniques. Methods: Sixty healthy, extracted, human mandibular incisors were randomly divided into 3 groups: Group A - hand crown-down technique; Group B - crown-down technique with engine-driven rotary reciprocating instruments; Group C - Protaper: engine-driven continuous rotary instrumentation. The roots were immersed in 2.3 mL of distilled water. After preparation, the water in each tube was filtered to collect solid material extruded, and the filters were weighed using a precision scale. Data were analyzed by Kolmogorov-Smirnov and Kruskal-Wallis tests at the 0.05 level of significance. Results: The statistical analysis showed that group C had significantly higher values of debris than groups A and B. Conclusion: The instrumentation using a continuous rotary technique, Protaper, produced greater apical extrusion than the hand and engine-driven crown-down techniques. The direction of instrumentation, whether cervical-apical or apical-cervical, seems to be a more important factor influencing apical extrusion than whether the instrumentation was performed by hand or was engine-driven.


Objetivo: Este estudo, in vitro, avaliou a quantidade de extrusão apical de "debris", após o preparo químico-mecânico do canal radicular, utilizando diferentes técnicas. Metodologia: Sessenta incisivos inferiores humanos hígidos foram aleatoriamente divididos em três grupos: Grupo A: técnica coroa-ápice manual; Grupo B: técnica coroa-ápice mecanizada com sistema de rotação oscilatória; Grupo C: Protaper, técnica mecanizada com sistema derotação contínua. As raízes foram imersas em 2,3 mL de água destilada. Após os preparos, a água destilada de cada amostra foi filtrada, e o filtro de papel, contendo o material sólido extruído, foi pesado em uma balança analítica de precisão. Os dados foram analisados estatisticamente pelos testes Kolmogorov-Smirnov e Kruskal-Wallis ao nível de significância de 0,05. Resultados: A análise estatística demonstrou que o grupo C apresentou valores superiores de "debris" do que os grupos A e B. Conclusão: A técnica rotatória contínua com Pro-taper produziu maior quantidade de extrusão apical do que as técnicas coroa-ápice manual e mecanizada com sistema de rotação oscilatória. A direção da instrumentação, se cérvico-apical ou ápico-cervical, parece ser o fator mais determinante na extrusão de "debris" independente desta ser realizada manual ou mecanizada.


Subject(s)
Humans , In Vitro Techniques , Root Canal Preparation/methods , Periapical Tissue
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