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Arch. latinoam. nutr ; 72(1): 11-22, mar. 2022. tab, graf
Article in Spanish | LILACS, LIVECS | ID: biblio-1368344


El arándano (Vaccinium corymbosum L.) posee un alto contenido de compuestos fenólicos los cuales han sido estudiados principalmente por su actividad antioxidante, antiobesogénica, antiinflamatoria, entre otras. Objetivo. Evaluar el efecto de la digestión gastrointestinal in vitro sobre la bioaccesibilidad de compuestos fenólicos y actividad antioxidante de una formulación nutracéutica de arándano (cápsula), comparado con arándano fresco y polvo. Materiales y métodos. Se obtuvieron extractos metanólicos de muestras de arándano fresco y liofilizado y se determinó su contenido de fenoles, flavonoides y antocianinas totales, así como también actividad antioxidante. Se llevó a cabo un ensayo de simulación de digestión gastrointestinal para evaluar la bioaccesibilidad de los compuestos fenólicos presentes en las muestras. Resultados. Los resultados mostraron que la digestión gástrica de arándano en polvo y en cápsula promovió una mayor bioaccesibilidad de fenoles (42% y 40%), flavonoides (52% y 33%) y antocianinas (45% y 40%) comparado con digestos de arándano fresco. Posterior a la digestión intestinal, la bioaccesibilidad de fenoles (63%) y flavonoides (67%) fue mayor en la cápsula de arándano comparada con su contraparte arándano en polvo. Las condiciones de digestión intestinal afectaron negativamente la bioaccesibilidad de las antocianinas independientemente del tipo de muestra evaluada. Conclusión. Las condiciones de digestión gástrica promueven una mayor estabilidad de los compuestos fenólicos en arándano en polvo y en cápsula lo que pudiera ser relevante para el mantenimiento de un ambiente antioxidante a este nivel. Las condiciones de digestión intestinal afectaron de manera particular a los compuestos fenólicos de arándano fresco y polvo, pero no a la cápsula, lo que puede sugerir que el encapsulamiento protegió de las condiciones alcalinas a los fenoles presentes. Se sugieren estudios posteriores sobre absorción in vitro de los componentes remanentes en intestino y sus posibles efectos sobre biomarcadores de estrés oxidativo en modelos in vivo(AU)

Blueberry (Vaccinium corymbosum L.) has a high content of phenolic compounds which have been studied mainly for their antioxidant, antiobesogenic, anti-inflammatory activity, among others. Objetive. The objective of the present study was to evaluate the effect of in vitro gastrointestinal digestion on the bioaccessibility of phenolic compounds and antioxidant activity of a nutraceutical formulation of blueberry (capsule), compared to fresh and powder blueberry. Materials and methods. Methanolic extracts of fresh and lyophilized blueberry were obtained and determined its total phenols, flavonoids, anthocyanins content, as well as antioxidant activity. A gastrointestinal digestion simulation test also was carried out to assess the bioaccessibility of the phenolic compounds found in samples. Results. The results showed that gastric digestion of powder and capsule blueberry promoted greater bioaccessibility of phenols (42% and 40%), flavonoids (52% and 33%) and anthocyanins (45% and 40%), compared to fresh blueberry digests. After intestinal digestion, the bioaccessibility of phenols (63%) and flavonoids (67%) was higher in the blueberry capsule compared to its powdered blueberry counterpart. The intestinal digestion conditions negatively affected the bioaccessibility of anthocyanins regardless of the type of sample evaluated. Conclusion. Gastric digestion conditions promote greater stability of phenolic compounds in powdered and capsule blueberries, which could be relevant for the maintenance of an antioxidant environment at this level. The intestinal digestion conditions particularly affected the phenolic compounds of fresh and lyophilized blueberry, but not the capsule, which may suggest that encapsulation protected the phenols present from alkaline conditions. Further studies on in vitro absorption of the remaining components in the intestine and their possible effects on oxidative stress biomarkers in in vivo models are suggested(AU)

Tannins , Flavonoids , Blueberry Plants , Phenolic Compounds , Gastrointestinal Absorption , In Vitro Techniques , Chronic Disease , Digestion , Freeze Drying
Braz. J. Pharm. Sci. (Online) ; 58: e18946, 2022. tab, graf
Article in English | LILACS | ID: biblio-1364411


Abstract To investigate structure-property relationship of polymer-based curcumin solid dispersion (SD), three acrylic polymers were used to formulate curcumin SD by solvent evaporation method. Curcumin Eudragit EPO SD (cur@EPO), curcumin Eudragit RS PO SD (cur@RSPO) and curcumin Eudragit RL PO SD (cur@RLPO) showed deep red, golden orange and reddish orange color, respectively. Cur@RSPO entrapped 15.42 wt% of curcumin followed by cur@RL PO and cur@EPO. FTIR spectra indicated that in cur@EPO, curcumin may transfer hydrogen to the dimethylaminoethyl methacrylate group and thus change its color to red. In contrast, curcumin may form hydrogen bonding with Eudragit RS PO and Eudragit RL. Curcumin exists in amorphous state in three SDs as proved by differential scanning calorimetry and X-Ray diffraction measurement. In vitro digestion presented that lower pH value in simulated gastric fluid (SGF) stimulates the curcumin release from cur@EPO while permeability influences the release profile in other two SDs. When in simulated intestinal fluid (SIF), first order release model governs the release behaviors of all three SDs which showed sustained release pattern. Our results are helpful to elucidate how structure of polymer may impact on the major properties of curcumin contained SD and will be promising to broaden its therapeutic applications.

Polymers , Curcumin/analysis , Methods , Solvents/administration & dosage , X-Ray Diffraction/instrumentation , In Vitro Techniques/methods , Calorimetry, Differential Scanning/methods , Evaporation/classification , Spectroscopy, Fourier Transform Infrared , Color , Citrus sinensis/classification , Hydrogen-Ion Concentration
Braz. J. Pharm. Sci. (Online) ; 58: e18594, 2022. graf
Article in English | LILACS | ID: biblio-1364422


Abstract Traditionally dates is consumed as a rich source of iron supplement and the current research discuss the synthesis of silver nanoparticles (AgNPs) using methanolic seed extract of Rothan date and its application over in vitro anti-arthritic, anti-inflammatory and antiproliferative activity against lung cancer cell line (A549). FTIR result of synthesised AgNPs reveals the presence of functional group OH as capping agent. XRD pattern confirms the crystalline nature of the AgNPs with peaks at 38º, 44º, 64º and 81º, indexed by (111), (200), (220) and (222) in the 2θ range of 10-90, indicating the face centered cubic (fcc) structure of metallic Ag. HR- TEM results confirm the morphology of AgNPs as almost spherical with high surface areas and average size of 42 ± 9nm. EDX spectra confirmed that Ag is only the major element present and the Dynamic light scattering (DLS) assisted that the Z-average size was 203nm and 1.0 of PdI value. Zeta potential showed − 26.5mv with a single peak. The results of the biological activities of AgNPs exhibited dose dependent activity with 68.44% for arthritic, antiinflammatory with 63.32% inhibition and anti-proliferative activity illustrated IC50 value of 59.66 µg/mL expressing the potential of AgNPs to combat cancer

Silver , In Vitro Techniques/methods , Chronology as Topic , Nanoparticles , Phoeniceae/adverse effects , Lung Neoplasms/classification , Seeds , zeta Potential , Spectroscopy, Fourier Transform Infrared , Inhibitory Concentration 50 , Dosage/methods
Braz. J. Pharm. Sci. (Online) ; 58: e18809, 2022. tab, graf
Article in English | LILACS | ID: biblio-1364420


Abstract Risperidone is an atypical antipsychotic drug widely prescribed all over the world due to its clinical advantages. The currently available long acting marketed depot formulation of risperidone is a microsphere based preparation using poly-[lactide-co-glycolide] (PLGA) as drug release barrier. It is however, a cold chain product due to thermal instability of PLGA at room temperature. After beginning the depot injection therapy it is administered every two weeks but associated with another drawback of about 3 weeks lag time due to which its tablets are also administered for three weeks so as to attain and maintain therapeutic drug concentration in the body. The present work attempts to develop a long acting depot delivery system of risperidone for once a month administration based on the combination of sucrose acetate isobutyrate and polycaprolactone dissolved in benzyl benzoate to provide an effective drug release barrier for one month without any lag time and which can be stored at room temperature precluding the requirement of cold supply chain. The developed depot formulation showed a sustained in vitro drug release profile with 88.95% cumulative drug release in 30 days with little burst release. The in vivo pharmacokinetic studies of the developed formulation conducted on rats showed attainment of mean peak plasma drug concentration of 459.7 ng/mL in 3 days with a mean residence time of 31.2 days, terminal half-life of 20.6 days, terminal elimination rate constant of 0.0336 per day, and a good in vitro- in vivo correlation.

Pharmaceutical Preparations/administration & dosage , Risperidone/agonists , Sucrose , In Vitro Techniques/methods , Drug Liberation/drug effects
Braz. J. Pharm. Sci. (Online) ; 58: e18630, 2022. tab, graf
Article in English | LILACS | ID: biblio-1364418


Abstract The objective of the present investigation was to design, optimize and characterize the gastro retentive floating levofloxacin tablets and perform in-vivo evaluation using radiographic imaging. The floating tablets were prepared by using polymers i.e hydroxy propyl methyl cellulose (HPMC-K4M) and carbopol-940 individually and in combination by nonaquous granulation method. All the Formulations were evaluated for swelling index (S.I), floating behavior and in-vitro drug release kinetics. The compatibility study of levofloxacin with other polymers was investigated by FTIR, DSC, TGA and XRD. Results from FTIR and DSC revealed no chemical interaction amongst the formulation components. The optimized formulation (F11) showed floating lag time (FLT), total floating time (TFT) swelling index (S.I) of 60 sec, >16h and approximately 75 %, respectively. Moreover, F11 showed zero order levofloxacin release in simulated gastric fluid over the period of 6 h. X-ray studies showed that total buoyancy time was able to delay the gastric emptying of levofloxacin floating tablets in rabbits for more than 4 hours. In conclusion the optimized formulation (F11) can be used for the sustained delivery of levofloxacin for the treatment of peptic ulcer.

Drug Liberation , Peptic Ulcer/classification , Tablets/pharmacology , X-Rays/adverse effects , In Vitro Techniques/instrumentation , Spectroscopy, Fourier Transform Infrared , Drug Compounding/instrumentation , Process Optimization/analysis , Levofloxacin/analysis , Gastric Emptying/drug effects
Braz. J. Pharm. Sci. (Online) ; 58: e18655, 2022. tab, graf
Article in English | LILACS | ID: biblio-1364423


Abstract Periodontitis is an oral disease associated with inflammation and pain with swollen and bleeding gums. In the present study, dental pastes containing NSAIDs, namely, diclofenac sodium and nimesulide (1 % w/w) were prepared to treat periodontitis. Dental pastes of diclofenac sodium and nimesulide (1 % w/w) were prepared with/without mucoadhesive hydrocolloid polymers such as sodium carboxy methyl cellulose (NaCMC), hydroxyl ethyl cellulose (HEC) and methyl cellulose (MC) by conventional trituration method. The pH, drug content, viscosity, tube spreadability and tube extrudability of these prepared dental pastes were measured. These dental pastes of diclofenac sodium and nimesulide (1 % w/w) were characterized by FTIR analyses for drug-excipient compatibility. The in vitro drug releases from these dental pastes in 6.4 pH phosphate buffer solution displayed sustained release over longer period and the drug release rate was found to be decreased when the concentration of mucoadhesive polymer was increased. These dental pastes displayed good adhesion to the oral mucosa revealing more retention time in mouth when tested for ex vivo mucoadhesion using bovine cheek pouch. The stability study results reveal that the DC3 and NC3 dental paste formulations were found stable enough over a longer period in different storage conditions. The present study revealed that the prepared mucoadhesive dental pastes of diclofenac sodium and nimesulide (1 % w/w) had good adhesion with the oral mucosa to maintain consistent release of drugs over prolonged time.

Toothpastes/analysis , Pharmaceutical Preparations , Anti-Inflammatory Agents, Non-Steroidal/analysis , Mouth , Mouth Mucosa/abnormalities , Periodontitis , In Vitro Techniques/methods , Diclofenac/adverse effects , Disease/classification , Spectroscopy, Fourier Transform Infrared , Drug Liberation , Gingiva/abnormalities , Inflammation/complications
J. venom. anim. toxins incl. trop. dis ; 28: e20210067, 2022. graf
Article in English | LILACS, VETINDEX | ID: biblio-1365078


Background: Melittin has shown antiproliferative effects on tumor cells. Therefore, it comprises a valuable compound for studies on cancer treatment. To the best of our knowledge, no studies have reported melittin effects on bone metastasis. Herein, we propose an approach based on intrametastatic melittin injection to treat bone metastases in colorectal cancer. Methods: Following the characterization of melittin and antiproliferative tests in vitro, a single dose was injected through intrametastatic route into the mouse bone metastasis model. Following treatment, metastasis growth was evaluated. Results: A single dose of melittin was able to inhibit metastasis growth. Histological analysis showed necrosis and inflammatory processes in melittin-treated metastasis. Except by mild weight loss, no other systemic effects were observed. Conclusion: Our data suggest that melittin might be a promising agent for the future development of treatment strategies aiming to reduce the bone metastasis skeletal-related impact in colorectal cancer patients with bone metastasis.(AU)

Animals , Bone and Bones , In Vitro Techniques , Colorectal Neoplasms , Neoplasm Metastasis
Arch. latinoam. nutr ; 71(4): 241-251, dic. 2021. tab
Article in Spanish | LILACS, LIVECS | ID: biblio-1355032


El basul es el fruto de la planta Erythrina edulis que posee un alto contenido de proteínas, fibra dietética y antioxidantes, pero también con contenido de antinutrientes. Objetivo. El objetivo del estudio fue evaluar el efecto del germinado sobre las características nutricionales, propiedades bioactivas y funcionales de las semillas de basul. Materiales y métodos. Mediante un diseño aleatorizado con arreglo factorial de 2x2x2 (tiempo de remojo, tiempo de germinado, presencia o ausencia de luz), las semillas de basul fueron germinadas y convertidas en harina (HBG) para determinar la composición proximal y la digestibilidad in vitro de la proteína. Además, se ha determinado los fenoles totales (CFT), la capacidad antioxidante (métodos ABTS y DPPH) y las propiedades de hidratación y adsorción de aceite. Resultados. Las diferentes condiciones de germinado no han modificado la composición proximal de la HBG; sin embargo, la digestibilidad in vitro de la proteína incrementó hasta en 6,25% en uno de los tratamientos respecto a la muestra no germinada. El CFT, también ha incrementado de 241,49 mg AGE/100g (sin germinar) a 267,15 mg AGE/100g (germinado); al igual que la capacidad antioxidante (ABTS) de 173,04 µmolTE/g (sin germinar) a 195,67 µmolTE/g (germinado). También se tuvo incrementos en la solubilidad, la capacidad de absorción de agua y la capacidad de hinchamiento. Conclusión. La calidad de la proteína, el contenido de fenoles totales, la capacidad antioxidante y propiedades funcionales de interacción con el agua de la semilla de basul mejora con el germinado(AU)

Basul is the fruit of the Erythrina edulis plant. It has a high content of proteins, dietary fiber, and antioxidants, but it also contains antinutrients. Objective. The study objective was to evaluate the effect of sprouting on the nutritional characteristics, bioactive and functional properties of basul seeds. Materials and methods. Basul seeds were germinated to produce flour (HBG) and determine its proximal composition and in vitro digestibility of the protein through a randomized design with a 2x2x2 factorial arrangement (soaking time, germination time, and presence or absence of light). Total phenols (CFT), antioxidant capacity (ABTS and DPPH methods), and hydration and oil adsorption properties were also determined. Results. The different germination conditions did not modify the proximal composition of HBG. However, the in vitro digestibility of the protein increased up to 6.25% in one of the treatments compared to the non-germinated sample. The CFT also increased from 241.49 mg AGE/100g (without germination) to 267.15 mg AGE/100g (germinated) and the antioxidant capacity (ABTS) from 173.04 µmolTE/g (without germination) to 195.67 µmolTE/g (germinated). Solubility, water absorption capacity, and swelling capacity also increased. Conclusion. The quality of the protein, the content of total phenols, the antioxidant capacity, and the functional properties of interaction with the water of the basul seed improved with germination(AU)

In Vitro Techniques , Dietary Fiber , Dietary Proteins , Germination , Erythrina , Phenolic Compounds , Flour/analysis , Proteins , Absorption , Fabaceae , Antioxidants , Nutritive Value
Con-ciencia (La Paz) ; 9(2): [1-15], nov. 2021.
Article in Spanish | LILACS | ID: biblio-1348987


El hígado es el órgano principal del cuerpo encargado de mantener la homeostasis interna, además cumple un rol fundamental en el metabolismo de medicamentos (xenobióticos) por lo tanto es vulnerable a lesiones fisiológicas o anatómicas. La lesión hepática inducida por fármacos (DILI) es la causa más común del fracaso del desarrollo pre-clínico y clínico de nuevos medicamentos, y de las advertencias de recuadro negro y el retiro de un medicamento del mercado. Por lo tanto, representa un problema grave para las industrias farmacéuticas, así también para el paciente, profesionales de la salud y las entidades reguladoras. Cabe mencionar que existen dos tipos de lesión hepática inducida por fármacos: farmacológicas o intrínsecas y la idiosincrásica. Durante la etapa pre-clínica del proceso de desarrollo de un medicamento se realiza un panel de cribado a los medicamentos candidatos empleando modelos celulares in vitro que incluyen sistemas de cultivos en 2D, 3D y líneas celulares de hepatoma humano, aunque también existen otros enfoques en el cual utilizan al pez cebra (reemplazo a los modelos animales) o modelos celulares basados en cribado de alto contenido. Posteriormente se emplean animales que, aunque presenten diferencias específicas respecto al humano a nivel hepatocelular igualmente se utiliza, para realizar predicciones cuantitativas y cualitativas de las principales propiedades farmacodinámicas, farmacocinéticas y toxicológicas del medicamento candidato. Actualmente existe un mayor esfuerzo para ir mejorando algunos modelos in vitro ya existentes, acoplando alguna herramienta o modificándolo genéticamente hacia el producto de interés proporcionando nuevos enfoques útiles para la predicción potencial tóxico a nivel hepático de los medicamentos candidatos.(AU)

The liver is the main organ of the body whose function is to maintain internal homeostasis, it also plays a fundamental role in the metabolism of drugs (xenobiotics), therefore it is vulnerable to physiological or anatomical injuries. Drug-induced liver injury (DILI) is the most common cause of preclinical and clinical development failure of new drugs, black box warnings, and drug recall. Therefore, it represents a serious problem for the pharmaceutical industries, as well as for the patient, health professionals and regulatory entities. It should be mentioned that there are two types of drug-induced liver injury: pharmacological or intrinsic and idiosyncratic. During the pre-clinical stage of the drug development process, candidate drugs are screened using in vitro cell models that include 2D, 3D culture systems and human hepatoma cell lines, although other approaches use zebrafish (replacement for animal models), or cell models based on high content screening. Subsequently, animals are used, which despite having specific differences with respect to humans at the hepatocellular level are also used to make quantitative and qualitative predictions of the main pharmacodynamic, pharmacokinetic and toxicological properties of the candidate drug. Currently, there is a major effort to improve some existing in vitro models, coupling a tool or genetically modifying it towards the product of interest, providing new useful approaches for the potential prediction of liver toxicity, of the candidate drugs.(AU)

In Vitro Techniques , Liver , Zebrafish , Drug Industry
Arq. Ciênc. Vet. Zool. UNIPAR (Online) ; 24(2, cont.): e2407, jul-dez. 2021. tab, graf
Article in English | LILACS, VETINDEX | ID: biblio-1352314


The factors that arouse interest in the study of essential oils as biocidal agents are numerous, such as the fact that they have antibacterial, antifungal, insecticidal, antioxidant, anti-inflammatory and larvicidal properties. The objective of this work was to evaluate the antimicrobial activity, in vitro, of the laurel (Laurus nobilis L) essential oil on the growth of pathogenic bacteria Salmonella enterica serovar Typhimurium ATCC 14028 and Staphylococcus aureus ATCC 25923, at different exposure times, as well as to perform the chemical characterization. Twenty compounds were identified and quantified, representing 96.57% of the total composition. The class of oxygenated monoterpenes represented the majority class of the essential oil, with 1,8-cineol (33.8%) as the substance found in greater quantity, followed by linalool (17.79%). The third constituent in greater quantity was sabinene (12.23%), belonging to the group of monoterpene hydrocarbons. Terpinyl acetate (9.41%) was also considered to be quantitatively representative. Laurel essential oil showed bacteriostatic activity against S. Typhimurium ATCC 14028 and S. aureus ATCC 25923.(AU)

Os fatores que despertam interesse no estudo dos óleos essenciais como agentes biocidas são inúmeros, como o fato de possuírem propriedades antibacteriana, antifúngica, inseticida, antioxidante, antiinflamatória e larvicida. O objetivo deste trabalho foi avaliar a atividade antimicrobiana, in vitro, do óleo essencial de louro (Laurus nobilis L) sobre o crescimento das bactérias patogênicas Salmonella enterica sorovar Typhimurium ATCC 14028 e Staphylococcus aureus ATCC 25923, em diferentes tempos de exposição, assim como realizar a caracterização química do óleo. Vinte compostos foram identificados e quantificados, representando 96,57% da composição total. A classe dos monoterpenos oxigenados representou a classe majoritária do óleo essencial, sendo o 1,8-cineol (33,8%) a substância encontrada em maior quantidade, seguido do linalol (17,79%). O terceiro constituinte em maior quantidade foi o sabineno (12,23%), pertencente ao grupo dos hidrocarbonetos monoterpênicos. O acetato de terpinila (9,41%) também foi considerado quantitativamente representativo. O óleo essencial de louro apresentou atividade bacteriostática contra S. Typhimurium ATCC 14028 e S. aureus ATCC 25923.(AU)

Los factores que despiertan interés en el estudio de los aceites esenciales como agentes biocidas son innumerables, como el hecho de que tienen propiedades antibacterianas, anti fúngicas, insecticidas, antioxidantes, antiinflamatorias y larvicidas. El objetivo de este trabajo ha sido evaluar la actividad antimicrobiana, in vitro, del aceite esencial de laurel (Laurus nobilis L) sobre el crecimiento de bacterias patógenas Salmonella enterica serovar Typhimurium ATCC 14028 y Staphylococcus aureus ATCC 25923, en diferentes momentos de exposición, así como realizar la caracterización química del aceite. Se identificaron y cuantificaron veinte compuestos, que representan el 96,57% de la composición total. La clase de mono terpenos oxigenados representó la clase principal de aceite esencial, siendo el 1,8-cineol (33,8%) la sustancia que se encuentra en mayor cantidad, seguida del linalol (17,79%). El tercer constituyente en mayor cantidad fue el sabineno (12,23%), perteneciente al grupo de los hidrocarburos monoterpénicos. El acetato de terpinilo (9,41%) también se consideró cuantitativamente representativo. El aceite esencial de laurel mostró actividad bacteriostática contra S. Typhimurium ATCC 14028 y S. aureus ATCC 25923.(AU)

Staphylococcus aureus , Salmonella enterica , Laurus/chemistry , Antioxidants , In Vitro Techniques , Anti-Bacterial Agents
Rev. cuba. med. mil ; 50(3): e1336, 2021. tab
Article in Spanish | LILACS, CUMED | ID: biblio-1357306


Introducción: En la medicina militar, la aplicación de las sustancias antibacterianas en las infecciones tópicas, es importante en el tratamiento de las tropas. Objetivos: Evaluar el efecto antibacteriano sinérgico de rifamicina en propóleo sobre bacterias grampositivas. Métodos: Estudio experimental in vitro y comparativo. Se efectuó el análisis fitoquímico preliminar del propóleo de Apis mellífera. Se utilizaron 96 placas de agar Muller Hinton (Britania®) (48 placas para cada especie bacteriana) repartidas en 6 grupos (n = 8). grupo I (agua destilada), grupo II (alcohol etílico al 96 por ciento), grupo III (rifamicina al 0,5 por ciento), grupo IV (rifamicina al 1 por ciento), grupo V (propóleo al 20 por ciento) y grupo VI (rifamicina al 1 por ciento en propóleo al 40 por ciento); se empleó la metodología de Kirby - Bauer; las cepas usadas fueron Staphylococcus aureus ATCC 25923, Streptococcus pyogenes ATCC 19615 y las mediciones de las zonas de inhibición se efectuaron a las 24 horas. Resultados: Se detectaron compuestos fenólicos, taninos, flavonoides, alcaloides y triterpenoides en propóleo. Se comprobó el efecto antibacteriano del grupo V con 18,627 ± 0,1008 mm (92,59 por ciento) y 19,247 ± 0,0762 mm (96,74 por ciento), y el efecto antibacteriano sinérgico del grupo VI con 19,316 ± 0,1202 mm (96,02 por ciento) y 19,613 ± 0,0820 mm (98,58 por ciento), comparados con rifamicina al 1 por ciento (100 por ciento) sobre S. aureus ATCC 25923 y S. pyogenes ATCC 19615. Conclusiones: La combinación de rifamicina al 1 por ciento unida al propóleo al 40 por ciento presenta una mayor actividad antibacteriana in vitro sobre bacterias grampositivas debido a su efecto sinérgico(AU)

Introduction: In military medicine, the application of antibacterial substances in topical infections are important in the treatment of troops. Objectives: To evaluate the synergistic antibacterial effect of rifamycin in propolis on gram-positive bacteria. Methods: In vitro and comparative experimental study. Preliminary phytochemical analysis of Apis mellifera propolis was carried out. 96 Muller Hinton agar plates (Britania®) (48 plates for each bacterial species) divided into 6 groups (n = 8) were used group I (distilled water), group II (96 percent ethyl alcohol), group III (rifamycin 0,5 percent), group IV (rifamycin 1 percent), group V (propolis 20 percent) and group VI (rifamycin 1 percent in 40 percent propolis); Kirby-Bauer methodology was used; the strains used were Staphylococcus aureus ATCC 25923, Streptococcus pyogenes ATCC 19615 and the measurements of the zones of inhibition were carried out at 24 hours. Results: Phenolic compounds, tannins, flavonoids, alkaloids and triterpenoids were detected in propolis. The antibacterial effect of group V was verified with 18,627 ± 0,1008 mm (92,59 percent) and 19,247 ± 0,0762 mm (96,74 percent), and the synergistic antibacterial effect of group VI with 19,316 ± 0,1202 mm (96,02 percent) and 19,613 ± 0,0820 mm (98,58 percent), compared with rifamycin 1 percent (100 percent) on S. aureus ATCC 25923 y S. pyogenes ATCC 19615. Conclusions: The combination of rifamycin 1 percent together with propolis 40 percent has a greater antibacterial activity in vitro on gram-positive bacteria due to its synergistic effect(AU)

Humans , Rifamycins , Gram-Positive Bacteria , Military Medicine , In Vitro Techniques , Anti-Bacterial Agents/analysis
Rev. cuba. med. trop ; 73(2): e607, 2021. tab, graf
Article in Spanish | LILACS, CUMED | ID: biblio-1347484


Introducción: Streptococcus mutans participa en el origen y progreso de la caries dental, una de las enfermedades más prevalentes a nivel mundial. Su control requiere métodos seguros y accesibles para la población. Myrciaria dubia (Kunth) McVaugh (Myrtaceae) (camu camu) es un árbol nativo de la amazonía peruana. La capacidad antimicrobiana de los componentes de su fruto ya se ha comprobado. Objetivo: Evaluar la actividad antibacteriana in vitro del extracto hidroetanólico de M. dubia contra S. mutans ATCC 35658. Métodos: Investigación experimental con posprueba y grupos controles. El extracto de la pulpa del fruto de M. dubia se obtuvo mediante maceración hidroetanólica. Las concentraciones evaluadas fueron 25 mg/mL, 50 mg/mL y 75 mg/mL. La capacidad antibacteriana se determinó mediante el método de difusión en disco. Gluconato de clorhexidina 0,12 por ciento fue el control positivo y el dimetilsulfóxido al 1 por ciento el control negativo. Resultados: La actividad antibacteriana se incrementó de manera directamente proporcional a la concentración del extracto. La concentración de 75 mg/mL mostró una media de inhibición de 18,2 ± 0,774 mm, seguido de la concentración de 50 mg/mL con una media de inhibición de 14,6 ± 1,055 mm y la concentración de 25 mg/mL con un halo de inhibición promedio de 10,1± 0,833 mm. La zona de inhibición del control positivo fue de 16,5 ± 0,516 mm. Existe diferencia estadísticamente significativa entre la concentración de 75 mg/mL y el control positivo (p< 0,05). Conclusiones: El extracto hidroetanólico de M. dubia muestra actividad antibacteriana in vitro de tipo bactericida sobre S. mutans ATCC 35668(AU)

Introduction: Streptococcus mutans is involved in the genesis and progress of dental caries, one of the most prevalent diseases worldwide, whose control requires safe methods accessible to the population. Myrciaria dubia (Kunth) McVaugh (Myrtaceae) (camu camu) is a tree native to the Peruvian Amazon. The antimicrobial capacity of the components of its fruit has already been verified. Objective: Evaluate the in vitro antibacterial activity of M. dubia hydroethanolic extract against S. mutans ATCC 35658. Methods: An experimental study was conducted with post-test analysis and control groups. The extract from the pulp of the fruit of M. dubia was obtained by hydroethanolic maceration. The concentrations evaluated were 25 mg/mL, 50 mg/mL and 75 mg/mL. Antibacterial capacity was determined by the disc diffusion method. The positive control was 0.12 percent chlorhexidine gluconate, whereas the negative control was 1 percent dimethyl sulfoxide. Results: The antibacterial activity increased directly proportional to the concentration of the extract. The concentration of 75 mg/mL showed a mean inhibition of 18.2 ± 0.774 mm, followed by the concentration of 50 mg/mL with a mean inhibition of 14.6 ± 1.055 mm and the concentration of 25 mg/mL with an average inhibition halo of 10.1 ± 0.833 mm. The zone of inhibition of the positive control was 16.5 ± 0.516 mm. There is a statistically significant difference between the concentration of 75 mg / mL and the positive control (p< 0.05). Conclusions: The M. dubia hydroethanolic extract displays in vitro antibacterial bactericidal activity against S. mutans ATCC 35668(AU)

Humans , Male , Female , Streptococcus mutans , Myrtaceae , Dental Caries , Herpes Zoster , Anti-Bacterial Agents , In Vitro Techniques
Rev. habanera cienc. méd ; 20(4): e3901, 2021. tab, graf
Article in Spanish | LILACS, CUMED | ID: biblio-1289616


Introducción: Uno de los derivados de los clorofenoles más utilizado en Estomatología, lo constituye el p-clorofenol (4-clorofenol), empleado como agente antibacteriano en la desinfección del conducto radicular durante el tratamiento pulporradicular. Son escasos los reportes científicos sobre sus efectos en la musculatura lisa vascular arterial y la regulación del flujo sanguíneo local. Objetivo: Determinar el efecto del 4-clorofenol sobre el músculo liso vascular de aorta abdominal de ratas Wistar. Material y Métodos: Se realizó una investigación experimental preclínica, utilizando 30 anillos de aorta abdominal (porción superior) obtenidos de ratas Wistar adultas. Las preparaciones de unos 5 mm se colocaron en baño de órganos, registrándose la tensión desarrollada por el músculo liso vascular tras la adición de 4-clorofenol en diferentes concentraciones y durante diferentes intervalos de tiempo. Resultados: El 4-clorofenol, tras la preactivación del musculo liso vascular de anillos de aorta abdominal, indujo relajación del vaso, la que se incrementó durante todo el tiempo de estudio y al aumento de la concentración del medicamento. Existieron diferencias significativas entre los valores de tensión promedios registrados en los diferentes intervalos de tiempo con los de la tensión base inicial. Conclusiones: El p-clorofenol indujo in vitro, relajación del músculo liso vascular de aorta abdominal de ratas Wistar(AU)

Introduction: In Dentistry, p-chlorophenol (4-chlorophenol) is one of the most widely used derivatives of chlorophenols. It is used as an antibacterial agent in root canal disinfection during pulp-radicular treatment. There are few scientific reports on its effects on vascular smooth musculature and the regulation of local blood flow. Objective: To determine the effect of 4-chlorophenol on vascular smooth muscle of abdominal aorta from Wistar rats. Material and Methods: A preclinical experimental research was carried out using 30 abdominal aortic rings (upper portion) obtained from adult Wistar rats. The preparations of about 5 mm were placed in an organ bath, recording the tension developed by the vascular smooth muscle after the addition of 4-chlorophenol at different concentrations and during different time intervals. Results: The results demonstrate that 4-Chlorophenol induced vasorelaxation after the preactivation of the vascular smooth muscle of the abdominal aortic rings, which increased during the entire study time and with increased drug concentration. There were significant differences among average tension values registered at different intervals of time in relation to the initial base tension. Conclusions: It is concluded that in vitro, p-chlorophenol induced relaxation of abdominal aorta vascular smooth muscle in Wistar rats(AU)

Rats , Oral Medicine , Dentistry , Anti-Bacterial Agents , Muscle, Smooth, Vascular , In Vitro Techniques , Chlorophenols/therapeutic use , Chromatography, Gas/methods , Rats, Wistar
Arq. bras. med. vet. zootec. (Online) ; 73(4): 799-811, Jul.-Aug. 2021. tab, ilus
Article in English | LILACS, VETINDEX | ID: biblio-1285263


This study aimed to evaluate the ultrastructural morphometry of bovine embryos produced in vitro grown at different concentrations of antioxidants. After in vitro maturation and fertilization, the presumptive zygotes were assigned into five treatments. T1) without the addition of any antioxidants (negative control); T2) addition of 50µM/mL cysteamine; and T3, T4 and T5) adding 2.5µg/mL, 5.0µg/mL or 10.0µg/mL of the antioxidants derived from the oily extract from Lippia origanoides, respectively. On D7 of culture, the embryos in the blastocyst stage were fixed and prepared for electron transmission microscopy. These were evaluated for the proportion of cytoplasm-to-nucleus, cytoplasm-to-mitochondria, cytoplasm-to-vacuoles, cytoplasm-to-autophagic vacuoles and cytoplasm-to-lipid droplets. Blastocysts cultured in media containing oily extract of Lippia origanoides presented morphological characteristics such as high cell:mitochondria ratio and low cell:vacuoles and cell:autophagic vacuole ratio, possibly been morphological indicators of embryonic quality. Inner cell mass (ICM) from blastocysts cultured in media without any antioxidants had the highest cell:vacuole ratio. Similar results were found in the trophectoderm (TE) cells of blastocysts from treatment 2. Embryo culture media supplemented with antioxidants derived from Lippia origanoides oil produced embryos with a higher cytoplasmic proportion of organelles, such as mitochondria. Also, treatments without any antioxidants or with the addition of cysteamine presented cytoplasmic vacuolization, a characteristic related to production of poor-quality embryos.(AU)

Este estudo teve como objetivo avaliar a morfometria ultraestrutural de embriões bovinos produzidos in vitro e cultivados em diferentes concentrações de antioxidantes. Após a maturação e a fertilização in vitro, os possíveis zigotos foram divididos em cinco tratamentos: T1) sem adição de antioxidantes (controle negativo); T2) adição de 50µM/mL de cisteamina; e T3, T4 e T5) adição de 2,5µg/mL, 5,0µg/mL ou 10,0µg/mL dos antioxidantes derivados do extrato oleoso de Lippia origanoides, respectivamente. No D7 de cultivo, os embriões em estágio de blastocisto foram fixados e preparados para microscopia eletrônica de transmissão. Estes foram avaliados para a proporção entre citoplasma e núcleo, citoplasma e mitocôndria, citoplasma e vacúolos, citoplasma e vacúolos autofágicos e citoplasma e gotículas lipídicas. Blastocistos cultivados em meio contendo extrato oleoso de Lippia origanoides apresentaram características morfológicas como alta relação célula:mitocôndria e baixa relação célula:vacúolos e célula:vacúolo autofágico, possíveis indicadores morfológicos de qualidade embrionária. A massa celular interna (MCI) de blastocistos cultivados em meio sem quaisquer antioxidantes teve a maior razão célula:vacúolo. Resultados semelhantes foram encontrados nas células do trofectoderma (TE) de blastocistos do tratamento 2. Portanto, o meio de cultivo embrionário suplementado com antioxidantes derivados do óleo de Lippia origanoides produziu embriões com maior proporção citoplasmática de organelas, como mitocôndrias. Além disso, tratamentos sem antioxidantes ou com adição de cisteamina apresentaram vacuolização citoplasmática, característica relacionada à produção de embriões de baixa qualidade.(AU)

Blastocyst , Cysteamine , Lippia , Embryo, Mammalian/ultrastructure , In Vitro Techniques/veterinary , Antioxidants
Rev. cuba. invest. bioméd ; 40(2): e1104, 2021. tab, graf
Article in Spanish | LILACS, CUMED | ID: biblio-1347458


Introducción: Las plantas medicinales han demostrado poseer propiedades antibacterianas para el control de la periodontitis. Objetivo: Determinar la actividad antibacteriana frente a Porphyromonas gingivalis ATCC 33277 de un gel experimental compuesto por aceite esencial de Eucalyptus globulus Labill. Métodos: Se realizó un estudio experimental in vitro. Se empleó el programa EPi InfoTM para el cálculo de las repeticiones. El aceite esencial se obtuvo por el método de arrastre de vapor; se identificó su composición química por cromatografía de gases acoplada a espectrometría de masas. Se evaluó la concentración mínima inhibitoria (CMI) y concentración mínima bactericida (CMB). Se realizó un ensayo de difusión en Agar para medir los halos de inhibición del gel experimental al 4,46 por ciento frente a P. gingivalis, la comparación con clorhexidina al 0,12 por ciento se evaluó con la prueba U de Mann-Whitney. Se adoptó un nivel de significancia del 5 por ciento . Resultados: Se identificaron 11 constituyentes en el aceite esencial, los principales componentes químicos fueron 3-heptadecene, (Z)- (36,13 por ciento ), 1-tridecene (14,7 por ciento ) y 1,8-cineole (9,72 por ciento ). La CMI del aceite esencial fue 36,195 mg/mL y la CMB fue 39,114 mg/mL. Los halos de inhibición del gel experimental de P. gingivalis fueron 25,533 mm ± 0,960. mm. Se observaron diferencias estadísticamente significativas frente a clorhexidina al 0,12 por ciento (23,282 ± 0,345) (p < 0,05). Conclusiones: El gel experimental al 4,46 por ciento compuesto por aceite esencial de Eucalyptus globulus Labill presentó una actividad antibacteriana importante frente a Porphyromonas gingivalis ATCC 33277(AU)

Introduction: Medicinal plants have proved to have antibacterial properties for the control of periodontitis. Objective: Determine the antibacterial activity against Porphyromonas gingivalis ATCC 33277 of an experimental gel composed of essential Eucalyptus globulus Labill oil. Methods: An in vitro experimental study was conducted. The software EPi InfoTM was used to estimate the repetitions. The essential oil was obtained by steam entrainment, and its chemical composition was determined by gas chromatography / mass spectrometry. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were also evaluated. An agar diffusion test was performed to measure the inhibition haloes of the 4.46 percent experimental gel against P. gingivalis. Comparison with 0.12 percent chlorhexidine was evaluated with the Mann-Whitney U test. A 5 percent significance level was adopted. Results: A total 11 constituents were identified in the essential oil. The main chemical components were 3-Heptadecene, (Z)- (36.13 percent), 1-Tridecene (14.7 percentand 1,8-cineole (9.72 percent). MIC of the essential oil was 36.195 mg/ml, whereas MBC was 39.114 mg/ml. The inhibition haloes of the experimental P. gingivalis gel were 25.533 mm ± 0.960 mm. Statistically significant differences were observed versus 0.12 percent chlorhexidine (23.282 ± 0.345) (p < 0.05). Conclusions: The 4.46 percent experimental gel composed of Eucalyptus globulus Labill essential oil displayed considerable antibacterial activity against Porphyromonas gingivalis ATCC 33277(AU)

Humans , Male , Female , Periodontitis , Oils, Volatile , Chlorhexidine , Mass Spectrometry/methods , In Vitro Techniques , Microbial Sensitivity Tests , Chromatography, Gas/methods , Anti-Bacterial Agents/therapeutic use
Rev. cient. odontol ; 9(2): e054, abr.-jun. 2021. ilus, tab, graf
Article in Spanish | LIPECS, LILACS, LIPECS | ID: biblio-1254593


Objetivo: Comparar la microdureza superficial de discos de acrílico de autocurado y termocurado en distintos periodos de tiempo. Metodología: Este estudio experimental, un ensayo en laboratorio in vitro, incluyó 80 discos de acrílico (Vitalloy), 40 de autocurado (A) y 40 de termocurado (T) divididos en 8 subgrupos: grupo control de autocurado GA0 (n = 10), grupo control de termocurado GT0 (n = 10), grupo de autocurado almancenado 1 día GA1 (n = 10), grupo de termocurado almacenado 1 día GT1 (n = 10), grupo de autocurado almacenado 7 días GA7 (n = 10), grupo de termocurado almacenado 7 días GT7 (n = 10), grupo de autocurado almacenado 21 días GA21 (n = 10), grupo de termocurado almacenado 21 días GT21 (n = 10); luego se evaluó la microdureza superficial Vickers de los discos de resina acrílica previamente almacenados en suero fisiológico en los distintos periodos de tiempo. Posteriormente, los datos fueron analizados estadísticamente mediante test de Anova y Tukey. El nivel de significancia estadística se tomó como p < 0,05. Resultados: Los valores encontrados fueron en el GT0 (20,45 ± 0,93 VHN); GA0(16,25 ± 0,79 VHN); GT1 (20,08 ± 0,66 VHN); GA1 (15,97 ± 0,78 VHN); GT7 (19,57 ± 1,54 VHN); GA7 (14,33 ± 0,48 VHN); GT21 (19,17 ± 1,26 VHN); GA21 (14,64 ± 0,52 VHN), presentando diferencias estadísticamente significativas ambos grupos autocurado y termocurado (p < 0,001). Conclusión: Los grupos de resinas acrílicas de termocurado presentaron mejores valores de microdureza que los grupos de resinas acrílicas de autocurado en los distintos periodos de tiempo evaluados. (AU)

Objective: To compare surface microhardness of self-curing and heat-curing acrylic discs in different periods of time. Methodology: This in vitro laboratory study, consisted of 80 acrylic discs (Vitalloy), 40 self-cured (A) and 40 heat-cured (T) divided into 8 subgroups: self-cure control group GA0 (n=10), heat-cure control group GT0 (n=10), self-cure group stored 1 day GA1 (n=10), heat-cure group stored 1 day GT1 (n=10), self-cure group stored 7 days GA7 (n=10), heat-cure group stored 7 days GT7 (n=10), self-cure group stored 21 days GA21 (n=10), and heat-cure group stored 21 days GT21 (n=10). Vickers surface microhardness of the acrylic resin discs previously stored in physiological serum was then evaluated at the different time periods. Subsequently, the data was statistically analyzed using ANOVA and TUKEY tests. The level of statistical significance was set at P <0.05. Results: The values found were in GT0 (20.45±0.93 Vickers hardness number [VHN]); GA0 (16.25±0.79 VHN); GT1 (20.08±0.66 VHN); GA1 (15.97±0.78 VHN); GT7(19.57±1.54 VHN); GA7 (14.33±0.48 VHN); GT21 (19.17±1.26 VHN); GA21 (14.64±0.52 VHN), with statistically significant differences between the self-cure and heat-cure groups (P<0.001). Conclusion: The groups of heat-curing acrylic resins presented better microhardness values than the groups of self-curing acrylic resins in the different time periods evaluated. (AU)

Acrylic Resins , Hardness , In Vitro Techniques , Epidemiology, Experimental
Rev. cient. odontol ; 9(2): e058, abr.-jun. 2021. ilus, tab
Article in Spanish | LIPECS, LILACS, LIPECS | ID: biblio-1254597


Objetivo: Comparar el pH de cuatro marcas de geles aclaradores a base de peróxido de hidrógeno de altas concentraciones (30%-35%) Whiteness HP Maxx (HPM), Lase Peroxide (LP), Whiteness HP Automixx (HPA)y Dash (DA), a través del tiempo de aplicación clínica (inicio, 15', 30' y 45'). Materiales y métodos: El estudio fue experimental in vitro. Se evaluaron 40 muestras (dientes bovinos) divididos en 4 grupos, uno para cada marca comercial de gel. Se preparó cada gel de acuerdo con las instrucciones del fabricante y se colocó una cantidad necesaria en la superficie vestibular; posteriormente, se registró el pH del gel con un pHmetro digital al inicio, 15, 30 y 45 minutos. Los datos se analizaron con las pruebas Anova, Friedman y Wilcoxon. Resultados: Hubo una tendencia a la disminución del pH desde el tiempo inicial de aplicación hasta el tiempo final, con excepción del grupo de la marca DA, el cual mostró que los valores del pH fueron aumentando a través del tiempo. En la marca HPM, existe una diferencia significativa entre el tiempo inicial de aplicación del gel y el resto de tiempos. En la marca LP, a partir de los 15' de aplicación, sí hay diferencia significativa entre los tiempos. En cuanto a la marca HPA, existieron diferencias significativas entre el tiempo inicial de aplicación y los demás tiempos. Finalmente, con la marca DA se encontró únicamente una diferencia significativa entre el tiempo inicial de aplicación y el tiempo final. Conclusiones: El pH de los geles aclaradores disminuyó a través del tiempo de aplicación clínica en todas las marcas estudiadas, con excepción de la marca Dash 30%, la cual mostró un aumento. (AU)

Objective: The aim of this in vitro study was to evaluate the pH of four bleaching agents based on high concentration hydrogen peroxide (30-35%) Whiteness HP Maxx (HPM), Lase Peroxide (LP), Whiteness HP Automixx (HPA) and Dash (DA) in different clinical periods (baseline, 15', 30' and 45'). Materials and methods: 40 specimens (bovine teeth) were divided into 4 groups; one group for each bleaching agent. Each bleaching agent was prepared according to the manufacturer's instructions and was applied on the vestibular surface. The pH of the bleaching agent was measured with a digital pH meter at baseline, 15, 30 and 45 minutes. ANOVA, Friedman and Wilcoxon tests were applied. Results: The pH values showed a trend to decreasing from the initial time of application to the final time, except for the DA group, which showed increasing pH values over time. The HPM group showed significant differences between baseline and the remaining periods. The LP group LP showed significant difference between 15' and the other periods. The HPA group showed significant differences between baseline and the remaining periods. Finally, the DA group, showed a significant difference between baseline and 45'. Conclusions: The pH values of 3 of the bleaching agents decreased over time, with the exception of Dash which increased in the different time periods. (AU)

Tooth Bleaching , Hydrogen-Ion Concentration , Hydrogen Peroxide , In Vitro Techniques , Epidemiology, Experimental
Bol. latinoam. Caribe plantas med. aromát ; 20(3): 226-243, may. 2021. ilus, tab
Article in English | LILACS | ID: biblio-1342815


Several species of the Myrcia genus have been used in folk medicine to treat diabetes. Therefore, the aim of this work was to investigate the inhibitory activity of α-glucosidase and pancreatic lipase in the crude extract (EBF) and in the ethyl acetate fraction (FFA) of Myrcia hatschbachii, as well as to identify isolated phenolic compounds and to evaluate the antioxidant property and preliminary in vitro toxicity against Artemia salina. EBF (IC50: 3.21 µg/mL) and FFA (IC50: 1.14 µg/mL) showed inhibitory activity superior to acarbose (IC50: 193.65 µg/mL). In addition, they showed inhibitory effects of pancreatic lipase (IC50: 556.58 µg/mL for EBF and 532.68 µg/mL for FFA), antioxidant potential, absence of preliminary toxicity and presence of gallic andellagic acids in FFA. The relevant results in the inhibition of α-glucosidase and pancreatic lipase motivate new studies for the development of herbal medicines that assist in the treatment of diabetic patients.

Varias especies del género Myrcia se han utilizado en la medicina popular para tratar la diabetes. Por lo tanto, el objetivo de este trabajo fue investigar la actividad inhibitoria de la α-glucosidasa y la lipasa pancreática en el extracto crudo (EBF) y en la fracción de acetato de etilo (FFA) de Myrcia hatschbachii, así como identificar compuestos fenólicos aislados y evaluar la propiedad antioxidante y toxicidad in vitro preliminar contra Artemia salina. EBF (IC50: 3.21 µg/mL) y FFA (IC50: 1.14 µg/mL) mostraron una actividad inhibitoria superior a la acarbosa (IC50: 193.65 µg/mL). Además, mostraron efectos inhibitorios de la lipasa pancreática (IC50: 556.58 µg/mL para EBF y 532.68 µg/mL para FFA), potencial antioxidante, ausencia de toxicidad preliminar y presencia de ácidos gálico y elágico en FFA. Los resultados relevantes en la inhibición de la α-glucosidasa y la lipasa pancreática motivan nuevos estudios para el desarrollo de medicamentos a base de hierbas que ayudan en el tratamiento de pacientes diabéticos.

Plant Extracts/pharmacology , Myrtaceae/chemistry , Glycoside Hydrolase Inhibitors/pharmacology , Lipase/drug effects , Antioxidants/pharmacology , Pancreas/enzymology , Phenols/analysis , X-Ray Diffraction , In Vitro Techniques , Plant Extracts/toxicity , Plant Extracts/chemistry , Free Radical Scavengers , Complex Mixtures , Ellagic Acid , Gallic Acid , Antioxidants/chemistry
Rev. Ciênc. Plur ; 7(2): 61-73, maio 2021. tab
Article in Portuguese | LILACS, BBO | ID: biblio-1282737


Introdução:Os sistemas adesivos possibilitama execução de restaurações estéticas e minimamente invasivas, sendo, portanto,objeto de pesquisas para contornar os problemas que se apresentam no procedimento restaurador.Objetivo:Avaliar in vitroa resistência de união de um sistema adesivo autocondicionante, e deste modificado com soluções extrativas de semente de uva.Metodologia:Duas soluções extrativas foram preparadas comextrato de semente de uva em pó dissolvido em acetona e etanol. A partir delas e de umadesivo,seis sistemas adesivos autocondicionantes experimentais foram preparados, diferindo quanto aosolvente utilizado eàsproporções entre adesivo puro e solução extrativa(7,5%, 15% e 30%). Setenta incisivos bovinos hígidos tiveram as raízes removidas com disco de carborundum e as faces vestibulares desgastadas comlixas d'água de granulação 120, 240, 600 e 1200 sob refrigeração até expor a dentina superficial. Os dentes foram distribuídos aleatoriamenteem sete grupos distintos: Controle; A7,5; A15; A30; E7,5; E15; e E30, contendo 10 elementos cada. A aplicação dos adesivos foi executada de acordo com as recomendações do fabricante do adesivo controle. A restauração foi realizada com uma matriz de silicone com dimensões 2mm de altura e 4mm de diâmetro e inserido o material restaurador em incremento único e fotopolimerizado por 40s. Após três meses armazenados em água destilada, os espécimes foram submetidos ao teste de resistência de união. Foi empregado ométodo estatísticoTeste Paramétrico Anova 1 Fator e pós-teste de Tamhane (p<0,05). Resultados:Os grupos A7,5, E7,5 e E30 não apresentaram diferença em relação ao grupo Controle; A15 e A30 mostraram desempenho estatisticamente semelhante entre si; e E15 não apresentou diferença estatística em relação aos outros adesivos.Conclusões:A adição de proantocianidina teve efeitos diferentes,dependendodos solventes e das concentrações utilizadas, mas sem alterar significativamente o desempenho do adesivo (AU).

Introduction:Adhesive systems make it possible to perform aestheticand minimally invasive restorations, being the subject of research to circumvent the problems that arise in the restorative procedure.Objective:Evaluate in vitrothe bond strength of a self-etching adhesive system,and modified with extractive grape seed solutions. Methodology:Two extractive solutions were prepared with powdered grape seed extract dissolved in acetone and ethanol. From them and an adhesive, six experimental self-etching adhesive systems were prepared, differing in terms of the solvent used and the proportions between pure adhesive and extractive solution(7.5%, 15% and 30%). Seventy healthy bovine incisors had their roots removed with carborundum disc and the vestibular faces were worn with sandpaper with granulation water 120, 240, 600 and 1200 under refrigeration until the superficial dentin was exposed. The teeth were randomly assigned to seven different groups: Control; A7.5; A15; A30; E7.5; E15; and E30, containing 10 elements each. The application of the adhesives was carried out according to the recommendations of the manufacturer of the control adhesive. The restoration was performed with a silicone matrix with dimensions 2mm high and 4mm indiameter and the restorative material was inserted in a single increment and light cured for 40s. After three months stored in distilled water, the specimens were submitted to the bond strength test. The statistical method Parametric Test Anova 1 Factor and Tamhane post-test (p<0.05) were used. Results:Groups A7.5, E7.5 and E30 showed no difference in relation to the Control group; A15 and A30 showed a statistically similar performance; and E15 showed no statistical difference in relation to the other adhesives. Conclusions:The addition of proanthocyanidin had different effects, depending on the solvents and concentrations used, but without significantly altering the performance ofthe adhesive (AU).

Introducción: Sistemas adhesivos permiten realizar restauraciones estéticas y mínimamente invasivas, siendo objeto de investigación para sortear problemas que surgen en elprocedimiento restaurador. Objetivo: Evaluar in vitrola fuerza de unión de un sistema adhesivoautograbante y modificado con soluciones extractivas de semilla de uva. Metodología: Se prepararon dos soluciones extractivas con extracto de semilla de uva en polvo disuelto en acetona y etanol. A partir de ellos y de un adhesivo, se prepararon seis sistemas experimentales de adhesivos autograbantes, que se diferencian en cuanto al solvente utilizado y las proporciones entre adhesivo puro y solución extractiva (7,5%, 15% y 30%). Setenta incisivos bovinos sanos fueron removidos con un disco de carborundo y las caras vestibulares fueron usadas com lija de agua de granulación 120, 240, 600 y 1200 bajo refrigeración hasta que la dentina superficial quedo expuesta. Los dientes se asignaron aleatoriamente a siete grupos diferentes: Control; A7,5; A15; A30; E7,5; E15; y E30, que contiene 10 elementos cada uno. La aplicación de los adhesivos se realizó siguiendo las recomendaciones del fabricante del adhesivo de control. La restauración se realizó con matriz de silicona con 2mm de altura y 4mm de diámetro y el material restaurador se insertó en un solo incremento y se fotopolimerizó durante 40s. Tres meses después, almacenados em agua destilada, las muestras se sometieron a la prueba de resistencia de la unión. Se utilizó el método estadístico Prueba Paramétrica Factor Anova 1 y post-prueba de Tamhane (p<0,05). Resultados: Los grupos A7,5, E7,5 y E30 no mostraron diferencias em relación con el grupo Control; A15 y A30 mostraron un desempeño estadísticamente similar; y E15 no mostró diferencia estadística en relación con los otros adhesivos. Conclusiones: La adición de proantocianidina tuvo diferentes efectos, dependiendo de los disolventes y concentraciones utilizadas, pero sin alterar significativamente el rendimiento del adhesivo (AU).

Animals , Cattle , Dental Polishing/instrumentation , Proanthocyanidins , Material Resistance , Flexural Strength , Solvents , In Vitro Techniques/methods , Brazil , Epidemiology, Experimental , Analysis of Variance , Dental Cements/chemistry , Grape Seed Extract
Rev. Ciênc. Plur ; 7(2): 47-60, maio 2021. ilus, tab
Article in Portuguese | LILACS, BBO | ID: biblio-1282724


Introdução:As atuaisresinas Bulk-Fill apresentamcomovantagens e propriedades: menor tempo clínico, baixa contração de polimerização, maior translucidez, entre outros. Objetivo:Avaliar a topografia superficial de restaurações com diferentes tipos de resina composta antes e após submetê-las a diferentes sistemas de acabamento e polimento. Metodologia:Confecção de100 corpos de prova, sendo 50 de cada composto resinoso, apresentando cinco grupos (n=10) sorteados de forma aleatória, de acordo com o sistema de acabamento e polimento empregado. Foram utilizadas as resinas Filtek Z350 XT e a Bulk Fill Filtek One Bulk Fill e os sistemas de acabamento e polimento: Discos de Lixa Sof-Lex Pop On Kit;Discos Diamantado Espiral Sof-Lex; Ponta Enhance e Broca Carbide Multilaminada nº 0283F, que foram comparados com superfície deixada pela Tira de Poliester (Controle Negativo). Após 7 dias de armazenamento em água destilada, os corpos de provaforam submetidos aoMicroscópio Eletrônico de Varredura.Resultados:Os corpos de provada resina Bulk Fill tiveram como melhor resultado o sistema de acabamento e polimentocom broca carbidee resultado não satisfatório com discodiamantado espiral Sof-lex, enquanto a ponta Enhance e lixa Sof-lex Pop Ontiveram resultados semelhantes. Os corpos de prova da resina Filtek Z350 XT tiveram melhor aspecto visual de lisura no grupo controle negativoe pior resultado no grupo com disco diamantado espiral Sof-lex. Conclusões:Dessa forma, o sistema que apresentou melhor resultado foi a broca Carbidena resina Bulk Fill, enquanto a Filtek Z350 XT apresentou-se melhor no grupo controle. Porém, ainda são necessáriosestudos para se chegar em um protocolo de acabamento e polimento mais eficiente (AU).

Introduction:The current Bulk-Fill resins have the following advantages and properties: less clinical time, low polymerization shrinkage, greater translucency, among others.Objective:Toevaluate the topography of restorations with different types of composite resin before and after submitting them to different finishing and polishing systems.Methodology:Manufacture of 100 specimens, 50 of each resin compound, presenting five groups (n = 10) drawn at random, according to the finishing and polishing system employed. Filtek Z350 XT resins and Bulk Fill Filtek One Bulk Fill andfinishing and polishing systems were used: Sof-Lex Pop On Kit Sanding Discs; Diamond Spiral Sof-Lex Discs; Tip Enhance and Multilaminated Carbide Drill nº 0283F, which were compared with the surface left by the Polyester Strip (Negative Control). After 7 days of storage in distilled water, the specimens were submitted to a Scanning Electron Microscope.Results:The Bulk Fill resin specimens had the best result of the finishing and polishing system with carbide drill and unsatisfactory result with Sof-lex spiral diamond disc, while the Enhance tip and Sof-lex Pop On sandpaper had similar results. The Filtek Z350 XT resin specimens had a better visual aspect of smoothness in the negative control group and a worse result in the group with Sof-lex spiral diamond wheel.Conclusions:Thus, the system that showed the best result was the Carbide drill in Bulk Fill resin, while Filtek Z350 XT was better in the control group. However, studies are still needed to arrive at a more efficient finishing and polishing protocol (AU).

Introducción:Las actuales resinas Bulk-Fill tienen las siguientes ventajas y propiedades: menor tiempo clínico, baja contracción de polimerización, mayor translucidez, entre otras.Objetivo: Evaluar la topografía de restauraciones con diferentes tipos de resina compuesta antes y después de someterlas a diferentes sistemas de acabado y pulido.Metodología: Fabricación de 100 probetas, 50 de cada resina compuesta, presentando cinco grupos (n = 10) extraídos al azar, según el sistema de acabado y pulido empleado. Se utilizaron resinas Filtek Z350 XT y Bulk Fill Filtek One Bulk Fill y sistemas de acabado y pulido: Discos de lijado Sof-Lex Pop On Kit; Discos Sof-Lex en espiral de diamante; Broca Realce de Punta y Carburo Multilaminado nº 0283F, que fueron comparadas con la superficie dejada por la Tira de Poliéster (Control Negativo). Después de 7 días de almacenamiento en agua destilada, lasmuestras se sometieron a un Las muestras de resina Bulk Fill tuvieron el mejor resultado del sistema de acabado y pulido con broca de carburo y un resultado insatisfactorio con el disco de diamante en espiral Sof-lex, mientras que la punta Enhance y el papel de lija Sof-lex Pop On tuvieron resultados similares. Las muestras de resina Filtek Z350 XT tuvieron un mejor aspecto visual de suavidad en el grupo de control negativo y un peor resultado en el grupo con disco de diamante en espiral Sof-lex.Conclusiones: Así, el sistema que mejor resultado mostró fue la broca Carbide en resina Bulk Fill, mientras que Filtek Z350 XT fue mejor en el grupo control. Sin embargo, aún se necesitan estudios para llegar a un protocolo de acabado y pulido más eficiente (AU).

Surface Properties , Microscopy, Electron, Scanning/instrumentation , Composite Resins , Dental Polishing/instrumentation , In Vitro Techniques/methods , Brazil , Protocols , Polymerization