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1.
Bol. latinoam. Caribe plantas med. aromát ; 18(4): 411-424, jul. 2019. tab, ilus
Article in English | LILACS | ID: biblio-1008180

ABSTRACT

Thymol (2-isopropyl-5-methylphenol) is an aromatic monoterpene found in essential oils extracted from plants belonging to the Lamiaceae family, such as Thymus, Ocimum, Origanum, Satureja, Thymbra and Monarda genera. Growth and biofilm formation by Listeria monocytogenes CLIP 74902 were evaluate using three carbon sources in the presence of thymol. Specific growth rate (h-1) values at 37o with glucose, trehalose and cellobiose with the addition of thymol (µg/mL) 0 (control) and 750, were respectively: 0.22, 0.07; 0.14, 0.04; 0.11, 0.04. Lag periods obtained under the same conditions were (h): 8.19, 13.2; 22.5, 27.5; 23.1, 28.1. A marked antibiofilm activity was observed against the exposure with 750 µg/mL of thymol, showing a high percentage of inhibition: glucose (99 %), trehalose (97 %) and cellobiose (98%), compared to the control. The results suggest that thymol could be used to inhibit the growth and production of biofilms by L. monocytogenes in the food industry.


Timol (2-isopropil-5-metilfenol) es un monoterpeno aromático presente en los aceites esenciales extraídos de plantas pertenecientes a la familia Lamiaceae, como los géneros Thymus, Ocimum, Origanum, Satureja, Thymbra y Monarda. El crecimiento y formación de biopelícula por Listeria monocytogenes CLIP 74902 fueron evaluados utilizando tres fuentes de carbono en presencia de timol. La velocidad específica de crecimiento (h-1) a 37o con glucosa, trehalosa y celobiosa con la adición de timol (µg/mL) 0 (control) y 750, fueron respectivamente: 0.22, 0.07; 0.14, 0.04, 0.11, 0,04. Los períodos lag obtenidos en las mismas condiciones fueron (h): 8.19, 13.2; 22.5, 27.5; 23.1, 28.1. Una marcada actividad antibiofilm fue obtenida con 750 µg/mL de timol, mostrando un alto porcentaje de inhibición con glucosa (99%), trehalosa (97%) y celobiosa (98%), respecto al control. Los resultados sugieren que timol podría ser usado para inhibir el crecimiento y producción de biopelículas por L. monocytogenes en la industria alimentaria.


Subject(s)
Thymol/pharmacology , Biofilms/drug effects , Listeria monocytogenes/drug effects , Terpenes/pharmacology , Kinetics , Biofilms/growth & development , Environment , Fermentation , Food Microbiology , Listeria monocytogenes/growth & development
2.
Braz. j. biol ; 78(4): 691-696, Nov. 2018. tab
Article in English | LILACS | ID: biblio-951593

ABSTRACT

Abstract This study aimed to evaluate the in vitro antibacterial activity of the phytochemicals thymol, linalool, and citronellol against Streptococcus mutans, Streptococcus salivarius and Streptococcus oralis. Disk diffusion screening on solid medium and measurement of the diameter of the bacterial growth inhibition halos was the technique utilized. The Minimum Inhibitory Concentration (MIC) of the substances was determined using serial substance dilutions and microdilution technique in Brain Heart Infusion culture medium. After incubation for 24 hours in an oven at 37 °C, plate reading was completed and confirmed by visual method using 2,3,5 triphenyl tetrazolium chloride dye. The Minimum Bactericidal Concentration (MBC) was determined from MIC subcultures. Assays were performed in triplicate, and chlorhexidine was used as a positive control. The diameters in mm of the growth inhibition halos ranged between 7.3 and 10.7 for S. mutans, 7.3 and 10.0 for S. oralis, and 8.2 and 9.8 for S. salivarius. The MIC and MBC values obtained converged, ranging from maximum values in the presence of Linalool (1,250.0 mg/mL, 2,500.0 mg/mL and 2,500.0 mg/mL, respectively, for S. mutans, S. oralis, and S. salivarius); and minimum values with Thymol (312.5 μg/ml, 156.2 μg/mL and 156.2 μg/ml, respectively for S. mutans, S. oralis, and S. salivarius). All the tested phytochemicals displayed antibacterial activity, thus representing substances with potential applications in preventing tooth decay.


Resumo Este estudo objetivou avaliar a atividade antibacteriana in vitro dos fitoquímicos timol, linalol e citronelol sobre Streptococcus mutans, Streptococcus salivaris e Streptococcus oralis. Utilizou-se a técnica de discos de difusão em meio sólido e medição do diâmetro dos halos de inibição. A concentração inibitória mínima (CIM) das substâncias foi determinada utilizando diluições em série das substâncias e técnica de microdiluição em meio de cultura de Brain Heart Infusion. Após incubação durante 24 horas em estufa a 37 °C, a leitura da placa foi confirmada pelo método visual usando o corante 2,3,5 trifenil cloreto de tetrazólio. A concentração bactericida mínima (CBM) foi determinada a partir de subculturas de MIC. Os ensaios foram realizados em triplicata, e clorexidina foi usada como um controle positivo. Os diâmetros dos halos de inibição do crescimento variaram entre 7,3 e 10,7 por S. mutans, 7,3 e 10,0 por S. oralis, e 8,2 e 9,8 para S. salivaris. Os valores de CIM e CBM obtidos variaram de valores máximos na presença de linalol (1.250,0 mg/mL, 2.500.0 mg/mL e 2.500.0 mg/mL, respectivamente, para o S. mutans, S oralis e S. salivaris); a valores mínimos com timol (312,5 μg/ml, 156,2 μg/mL e 156,2 μg/ml, respectivamente para S. mutans, S. oralis e S. salivaris). Todos os fitoquímicos testados apresentaram atividade antibacteriana, representando, assim, substâncias com potencial de aplicações na prevenção da cárie dentária.


Subject(s)
Streptococcus/drug effects , Thymol/pharmacology , Monoterpenes/pharmacology , Anti-Bacterial Agents/pharmacology , Microbial Sensitivity Tests/methods , Dental Caries/microbiology , Phytochemicals/pharmacology , Acyclic Monoterpenes
3.
Acta cir. bras ; 33(5): 431-438, May 2018. tab, graf
Article in English | LILACS | ID: biblio-949342

ABSTRACT

Abstract Purpose: To evaluate the effects of this thymol-rich oil in the proliferation of human adipose tissue-derived stem cells. Methods: Stem cells were isolated from human adipose tissue by liposuction. After the first passage, cells were cultivated in triplicate for three days in control medium and medium supplemented with three oil samples (1.0 μg/mL, 5.0 μg/mL, and 25.0 μg/mL). Cells were analyzed by the MTT assay at passage 1 (P1), and cell proliferation of control and 1 μg/mL groups was determined with a hemocytometer at P2 and P3. Results: Viability of the essential oil-treated cells was significantly higher than the control group at P1 (p = 0.0008). The treatment with the oil, at a concentration of 1 µg/mL, led to increases of 24.8% at P1 and 43.0% at P3 in the rate of cell proliferation compared with control cells. Conclusion: Supplementing culture medium with essential oil of Lippia origanoides increased cell proliferation, especially at later passages.


Subject(s)
Humans , Adult , Thymol/pharmacology , Plant Oils/pharmacology , Oils, Volatile/pharmacology , Lippia/chemistry , Cell Proliferation/drug effects , Antioxidants/pharmacology , Stem Cells/drug effects , Plant Oils/chemistry , Oils, Volatile/chemistry , Lipectomy , Adipose Tissue/cytology , Culture Media
4.
Rev. bras. parasitol. vet ; 26(3): 323-330, July-Sept. 2017. tab, graf
Article in English | LILACS | ID: biblio-899288

ABSTRACT

Abstract Thymol is a monoterpene and acetylation form of this compound can reduce the toxicity and enhance its biological effects. The objective of this study was to evaluate the effect of thymol and thymol acetate (TA) on egg, larva and adult Haemonchus contortus and the cuticular changes, acute toxicity in mice and the efficacy on sheep gastrointestinal nematodes. In vitro tests results were analyzed by analysis of variance (ANOVA) and followed by comparison with Tukey test or Bonferroni. The efficacy of in vivo test was calculated by the BootStreet program. In the egg hatch test (EHT), thymol (0.5 mg/mL) and TA (4 mg/mL) inhibited larval hatching by 98% and 67.1%, respectively. Thymol and TA (8 mg/mL) inhibited 100% of larval development. Thymol and TA (800 µg/mL) reduced the motility of adult worms, by 100% and 83.4%, respectively. Thymol caused cuticular changes in adult worm teguments. In the acute toxicity test, the LD50 of thymol and TA were 1,350.9 mg/kg and 4,144.4 mg/kg, respectively. Thymol and TA reduced sheep egg count per gram of faeces (epg) by 59.8% and 76.2%, respectively. In in vitro tests thymol presented better anthelmintic activity than TA. However TA was less toxic and in in vivo test efficacy was similar.


Resumo Timol é um monoterpeno e a acetilação deste composto pode reduzir a toxicidade e potencializar os seus efeitos biológicos. O objetivo deste trabalho foi avaliar o efeito do timol e acetato de timolila (AT) sobre ovos, larvas e adultos de Haemonchus contortus e suas alterações cuticulares, toxicidade aguda em camundongos e a eficácia sobre nematoides gastrintestinais de ovinos. Os resultados dos testes in vitro foram analisados por análise de variância (ANOVA) e comparados pelo testes de Tukey ou Bonferroni. A eficácia do teste de redução da contagem de ovos nas fezes (RCOF) foi calculada pelo programa BootStreet. No teste de inibição da eclosão de ovos (TEO), timol (0,5 mg/mL) e AT (4 mg/mL) inibiram a eclosão das larvas em 98% e 67,1%, respectivamente. Timol e AT (8 mg/mL) inibiram 100% do desenvolvimento larval. Timol e AT (800 μg/mL) reduziram a motilidade dos nematoides adultos, em 100% e 83,4%, respectivamente. O timol provocou alterações cuticulares nos nematoides adultos. No teste de toxicidade aguda, a DL50 do timol e AT foi de 1.350,9 mg/kg e 4.144,4 mg/kg, respectivamente. Timol e AT reduziram a contagem de ovos por gramas de fezes (OPG) dos ovinos em 59,8% e 76,2%, respectivamente. Nos testes in vitro timol apresentou atividade melhor anti-helmíntica do que AT. Entretanto, AT foi menos tóxico do que o timol e no teste in vivo apresentaram eficácia semelhante.


Subject(s)
Animals , Female , Mice , Sheep Diseases/parasitology , Sheep Diseases/drug therapy , Thymol/toxicity , Thymol/therapeutic use , Nematoda/drug effects , Nematode Infections/veterinary , Acetylation , Thymol/pharmacology , Sheep , Haemonchus/drug effects , Anthelmintics/therapeutic use , Anthelmintics/pharmacology , Acetates/therapeutic use , Acetates/pharmacology , Nematode Infections/drug therapy
5.
Rev. Soc. Bras. Med. Trop ; 50(1): 75-79, Jan.-Feb. 2017. tab
Article in English | LILACS | ID: biblio-842827

ABSTRACT

ABSTRACT INTRODUCTION: This study evaluated the susceptibilities of oral candidiasis-derived Candida albicans, fluconazole-resistant (FR) Candida dubliniensis, and fluconazole-susceptible (FS) C. dubliniensis to synthetic antiseptics [chlorhexidine gluconate (CHX), cetylpyridinium chloride (CPC), and triclosan (TRC)] and natural compounds (carvacrol, eugenol and thymol). METHODS: Susceptibility tests were performed based on the M27-A3 reference method. The fluconazole-resistant C. dubliniensis strains were obtained after prolonged in vitro exposure to increasing fluconazole concentrations. The geometric mean values for minimum inhibitory concentrations and minimum fungicidal concentrations were compared among the groups. RESULTS: Fluconazole-susceptible C. dubliniensis was more sensitive to CPC and TRC than FR C. dubliniensis and C. albicans were. However, eugenol and thymol were more active against FR C. dubliniensis. The fungicidal activities of CHX and TRC were similar for the three groups, and FR C. dubliniensis and C. albicans had similar sensitivities to CPC. CONCLUSIONS: The resistance of C. dubliniensis to fluconazole affects its sensitivity the synthetic antiseptics and natural compounds that were tested.


Subject(s)
Humans , Candida/drug effects , Fluconazole/pharmacology , Anti-Infective Agents, Local/pharmacology , Antifungal Agents/pharmacology , Thymol/pharmacology , Triclosan/pharmacology , Candida/isolation & purification , Candida/classification , Candida albicans/drug effects , Eugenol/pharmacology , Microbial Sensitivity Tests , Cetylpyridinium/pharmacology , Chlorhexidine/pharmacology
6.
Braz. j. med. biol. res ; 50(12): e6351, 2017. graf
Article in English | LILACS | ID: biblio-888959

ABSTRACT

Lippia sidoides Cham is a typical herb species of Northeast Brazil with widespread use in folk medicine. The major constituents of the essential oil of L. sidoides (EOLs) are thymol, p-cymene, myrcene, and caryophyllene. Several studies have shown that the EOLs and its constituents have pharmacological effects, including antibacterial, anti-inflammatory, antioxidant and neuroprotective activity. Therefore, this work aimed to investigate the effects of the EOLs and their main constituents on rat sciatic nerve excitability. The sciatic nerves of adult Wistar rats were dissected and mounted in a moist chamber. Nerves were stimulated by square wave pulses, with an amplitude of 40 V, duration of 100 μs to 0.2 Hz. Both EOLs and thymol inhibited compound action potential (CAP) in a concentration-dependent manner. Half maximal inhibitory concentration for CAP peak-to-peak amplitude blockade were 67.85 and 40 µg/mL for EOLs and thymol, respectively. CAP peak-to-peak amplitude was significantly reduced by concentrations ≥60 µg/mL for EOLs and ≥30 µg/mL for thymol. EOLs and thymol in the concentration of 60 µg/mL significantly increased chronaxie and rheobase. The conduction velocities of 1st and 2nd CAP components were also concentration-dependently reduced by EOLs and thymol in the range of 30-100 µg/mL. Differently from EOLs and thymol, p-cymene, myrcene and caryophyllene did not reduce CAP in the higher concentrations of 10 mM. These data demonstrated that EOLs and thymol inhibited neuronal excitability and were promising agents for the development of new drugs for therapeutic use.


Subject(s)
Animals , Male , Female , Alkenes/pharmacology , Lippia/chemistry , Monoterpenes/pharmacology , Oils, Volatile/pharmacology , Sciatic Nerve/drug effects , Sesquiterpenes/pharmacology , Thymol/pharmacology , Action Potentials/drug effects , Action Potentials/physiology , Nerve Block/methods , Neural Conduction/drug effects , Oils, Volatile/chemistry , Rats, Wistar , Reproducibility of Results , Sciatic Nerve/physiology , Time Factors
7.
Braz. j. med. biol. res ; 50(12): e6346, 2017. tab, graf
Article in English | LILACS | ID: biblio-888962

ABSTRACT

This study evaluated the anesthetic potential of thymol and carvacrol, and their influence on acetylcholinesterase (AChE) activity in the muscle and brain of silver catfish (Rhamdia quelen). The AChE activity of S-(+)-linalool was also evaluated. We subsequently assessed the effects of thymol and S-(+)-linalool on the GABAergic system. Fish were exposed to thymol and carvacrol (25, 50, 75, and 100 mg/L) to evaluate time for anesthesia and recovery. Both compounds induced sedation at 25 mg/L and anesthesia with 50-100 mg/L. However, fish exposed to carvacrol presented strong muscle contractions and mortality. AChE activity was increased in the brain of fish at 50 mg/L carvacrol and 100 mg/L thymol, and decreased in the muscle at 100 mg/L carvacrol. S-(+)-linalool did not alter AChE activity. Anesthesia with thymol was reversed by exposure to picrotoxin (GABAA antagonist), similar to the positive control propofol, but was not reversed by flumazenil (antagonist of benzodiazepine binding site), as observed for the positive control diazepam. Picrotoxin did not reverse the effect of S-(+)-linalool. Thymol exposure at 50 mg/L is more suitable than carvacrol for anesthesia in silver catfish, because this concentration did not cause any mortality or interference with AChE activity. Thymol interacted with GABAA receptors, but not with the GABAA/benzodiazepine site. In contrast, S-(+)-linalool did not act in GABAA receptors in silver catfish.


Subject(s)
Animals , Acetylcholinesterase/metabolism , Anesthetics/pharmacology , Catfishes , Monoterpenes/pharmacology , Receptors, GABA-A/metabolism , Thymol/pharmacology , Acetylcholinesterase/physiology , Adjuvants, Anesthesia/pharmacology , Analysis of Variance , Anesthesia/veterinary , Brain/drug effects , Brain/enzymology , Catfishes/metabolism , Diazepam/pharmacology , GABA Antagonists/pharmacology , Muscles/drug effects , Muscles/enzymology , Oils, Volatile/chemistry , Picrotoxin/pharmacology , Receptors, GABA-A/physiology , Reproducibility of Results , Statistics, Nonparametric , Time Factors
8.
Braz. dent. j ; 25(4): 277-281, 2014. tab
Article in English | LILACS | ID: lil-722610

ABSTRACT

Candida albicans is a commensal fungus, but circumstantially it may cause superficial infections of the mucous membranes, such as denture stomatitis, when a biofilm is formed on the surface of dental prostheses. This study evaluated the cell viability of C. albicans biofilms against the antifungal activity of thymol when compared with miconazole, by the fluorescence imaging using SYTO 9 and propidium iodide dyes, and counting of colony forming units. C. albicans standard strains (ATCC 11006) were used. The minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of drugs were determined by broth microdilution tests and the inoculum was standardized to match 0.5 on the McFarland scale (106 cfu/mL). Biofilms were grown on the surface of acrylic resin disks in parallel flow chambers from Sabouraud broth supplemented with 10% dextrose. For counting of colony forming units, the fungal solution was sequentially diluted and plated in Sabouraud dextrose agar. Data were analyzed using two-way ANOVA and Tukey's test (a=5%). Biofilms treated with thymol and miconazole presented low numbers of viable cells at the evaluated exposure times. There was statistically significant difference (p<0.05) when compared with control, and the mean value of the exposure times between miconazole and thymol did not differ significantly (p>0.05). In conclusion, both drugs have similar efficiency as antifungal agents against biofilms of C. albicans formed on acrylic surfaces.


Candida albicans é um fungo comensal que circunstancialmente pode causar infecções superficiais das mucosas, como a estomatite protética, na qual o biofilme se forma sobre a superfície das próteses dentárias. Este estudo avaliou a viabilidade celular de biofilmes de C. albicans frente à ação antifúngica do timol em comparação com o miconazol por meio da técnica de fluorescência, empregando os corantes SYTO 9 e iodeto de propídio, e contagem das unidades formadoras de colônia. Utilizaram-se cepas de C. albicans (ATCC 11006). As concentrações inibitórias mínimas (CIM) e fungicidas mínimas (CFM) das drogas foram determinadas com testes de microdiluição em caldo, sendo o inóculo padronizado para corresponder a 0,5 da escala de McFarland (106 UFC/mL). Os biofilmes foram cultivados sobre a superfície de discos de resina acrílica, em células paralelas de fluxo, a partir de caldo Sabouraud suplementado com dextrose 10%. Para a contagem das unidades formadoras de colônia, as soluções fúngicas foram sequencialmente diluídas e semeadas em agar Sabouraud dextrose Os dados foram analisados por meio de estatística ANOVA A dois fatores e teste de Tukey (α = 5%). Biofilmes tratados com o timol e miconazol apresentaram baixos números percentuais de células viáveis nos tempos de exposição avaliados. Houve diferença estatística significante (p<0.05) em comparação com o controle, e o valor médio dos tempos de exposição entre miconazol e timol não diferiu estatisticamente (p>0.05). Concluindo, ambas as drogas possuem similar eficiência como agentes antifúngicos contra a viabilidade de biofilmes de C. albicans formados em superfícies de resinas acrílicas.


Subject(s)
Antifungal Agents/pharmacology , Candida albicans/drug effects , Thymol/pharmacology , Candida albicans/cytology
9.
Pakistan Journal of Pharmaceutical Sciences. 2013; 26 (5): 893-896
in English | IMEMR | ID: emr-138406

ABSTRACT

In our present research we studied physiochemical properties and antimicrobial activity of T. ammi [Trachyuspermum ammi] seeds. The seeds yielded 2.86% essential oil. Refractive index, specific gravity, acid value, and easter values were 1.496, 0.9212, 1.12 and 2.80 respectively. GLC was used to determine the composition of oil. The major component of oil was Thymol [55.308%]. Antimicrobial activity of the oil was carried out against four species of bacteria and fungs. The oil was used to formulate a cream and the pH, physiochemical stability, phase separation and dermal irritation of cream were investigated. The cream was examined for healing wound in rabbits in comparison with Iodine tincture


Subject(s)
Animals , Chemistry, Pharmaceutical , Drug Stability , Models, Animal , Oils, Volatile/pharmacology , Plant Oils/pharmacology , Thymol/pharmacology , Wound Healing/drug effects , Rabbits , Seeds , Skin Cream , Phytotherapy , Anti-Infective Agents
10.
Biol. Res ; 45(4): 399-402, 2012. ilus
Article in English | LILACS | ID: lil-668692

ABSTRACT

Leishamaniasis is a disease that affects more than 2 million people worldwide, whose causative agent is Leishmania spp. The current therapy for leishmaniasis is far from satisfactory. All available drugs, including pentavalent antimony, require parenteral administration and are potentially toxic. Moreover, an increase in clinical resistance to these drugs has been reported. In this scenario, plant essential oils used traditionally in folk medicine are emerging as alternative sources for chemotherapeutic compounds. In this study, in vitro leishmanicidal effects of a thymol- and a carvacrol-rich essential oil from leaves of Lippia sidoides Cham. were investigated. The essential oils were extracted and their constituents were characterized by gas chromatography coupled to mass spectrometry (GC/MS). Both essential oils showed significant activity against promastigote forms of Leishmania chagasi. However, we found that carvacrol-rich essential oil was more effective, with IC50/72 h of 54.8 μg/mL compared to 74.1 μg/mL for thymol-rich oil. Carvacrol also showed lower IC50 than thymol. Our data suggest that L. sidoides essential oils are indeed promising sources of leishmanicidal compounds.


Subject(s)
Antiprotozoal Agents/pharmacology , Leishmania/drug effects , Lippia/chemistry , Monoterpenes/pharmacology , Oils, Volatile/pharmacology , Plant Oils/pharmacology , Thymol/pharmacology , Gas Chromatography-Mass Spectrometry , Monoterpenes/isolation & purification , Plant Leaves/chemistry , Thymol/isolation & purification
11.
J. appl. oral sci ; 19(5): 511-516, Sept.-Oct. 2011. tab
Article in English | LILACS | ID: lil-600852

ABSTRACT

OBJECTIVE: This study evaluated the response of periapical tissues to the endodontic sealer Endométhasone in root canal fillings short of or beyond the apical foramen. MATERIAL AND METHODS: Twenty root canals of premolars and incisors of 2 mongrel dogs were used. After coronal access and pulp extirpation, the canals were instrumented up to a size 55 K-file and the apical cemental barrier was penetrated with a size 15 K-file to obtain a main apical foramen, which was widened to a size 25 K-file. The canals were irrigated with saline at each change of file. The root canals were obturated either short of or beyond the apical foramen by the lateral condensation of gutta-percha and Endométhasone, originating 2 experimental groups: G1: Endométhasone/short of the apical foramen; G2: Endométhasone/beyond the apical foramen. The animals were killed by anesthetic overdose 90 days after endodontic treatment. The individual roots were obtained and serial histological sections were prepared for histomorphological analysis (H&E and Brown & Brenn techniques) under light microscopy. The following parameters were examined: closure of the apical foramen of the main root canal and apical opening of accessory canals, apical cementum resorption, intensity of the inflammatory infiltrate, presence of giant cells and thickness and organization of the apical periodontal ligament. Each parameter was scored 1 to 4, 1 being the best result and 4 the worst. Data were analyzed statistically by the Wilcoxon nonparametric tests (p=0.05). RESULTS: Comparing the 2 groups, the best result (p<0.05) was obtained with root canal filling with Endométhasone short of the apical foramen but a chronic inflammatory infiltrate was present in all specimens. CONCLUSIONS: Limiting the filling material to the root canal space apically is important to determine the best treatment outcome when Endométhasone is used as sealer.


Subject(s)
Animals , Dogs , Dental Pulp Cavity/drug effects , Dexamethasone/pharmacology , Formaldehyde/pharmacology , Hydrocortisone/pharmacology , Periapical Tissue/drug effects , Root Canal Filling Materials/pharmacology , Thymol/analogs & derivatives , Tooth Apex/drug effects , Biocompatible Materials/pharmacology , Drug Combinations , Dental Pulp Cavity/pathology , Dexamethasone/adverse effects , Formaldehyde/adverse effects , Hydrocortisone/adverse effects , Materials Testing , Periapical Tissue/pathology , Root Canal Filling Materials/adverse effects , Root Canal Obturation/methods , Thymol/adverse effects , Thymol/pharmacology , Tooth Apex/pathology
12.
Arq. bras. med. vet. zootec ; 59(3): 700-704, jun. 2007.
Article in Portuguese | LILACS | ID: lil-461148

ABSTRACT

Verificou-se a atividade repelente do timol, mentol, ácido salicílico e salicilato de metila sobre larvas de Boophilus microplus. Essas substâncias foram usadas em emulsões em dimetilsulfuxido aquoso a 1 por cento ou solução aquosa. Para cada substância foram testadas três concentrações, 1,0 por cento; 0,5 por cento e 0,25 por cento, com cinco repetições cada. Cerca de 100 larvas, com 21 dias de idade, foram inseridas na base de hastes de madeira para avaliação da repelência, a cada duas horas, totalizando 12 horas. As concentrações mais elevadas apontaram que as quatro substâncias causaram alteração no comportamento das larvas. Timol, com mortalidade de 65 por cento e 35 por cento de repelência e mentol e salicilato de metila, ambos com 80 por cento de repelência foram os mais eficientes.


The repellent activity of thymol, menthol, salicylic acid and methyl salicylate on Boophilus microplus larvae was studied. These substances were tested according to their solubility: emulsions in 1 percent aqueous dimethylsulphoxide or in pure water. Three concentrations were tested for each substance, 1.0 percent, 0.5 percent and 0.25 percent, with five repetitions for each. Approximately 100 larvae at 21 days of age were placed on the base of wooden sticks and then observed for repellent action every two hours, during twelve hours. The results obtained from the higher concentrations showed that the four substances caused alterations on the larvae behavior. However, thymol (65 percent of mortality and 35 percent of repellency), menthol (80 percent of repellency) and methyl salicylate (80 percent of repellency) were the most efficient.


Subject(s)
Animals , Cattle , Insecticides/pharmacology , Ixodidae/drug effects , Menthol/pharmacology , Salicylates/pharmacology , Salicylic Acid/pharmacology , Thymol/pharmacology , Ixodidae/growth & development , Larva/drug effects
13.
J Indian Soc Pedod Prev Dent ; 1997 Dec; 15(4): 134-40
Article in English | IMSEAR | ID: sea-115095

ABSTRACT

Four materials viz. zinc oxide-eugenol, iodoform paste, Kri paste, Maisto's paste and Vitapex (Calcium hydroxide + iodoform) were tested for their antibacterial effect against the aerobic and anerobic bacteria, viz. Staphylococcus aureus, Streptococcus viridans, Streptococcus faecalis, Bacteroides melaninogenicus and mixed bacterial culture; obtained from infected non-vital deciduous anterior teeth. The antimicrobial sensitivity was checked on BHI-agar plates using well method. The results showed that all the 4 materials were distinctly different from each other in their antimicrobial activity. Maisto's paste was invariably the superior most in its antibacterial efficacy (in comparison to all the 5 micro-organism strains). Iodoformized zincoxide eugenol appeared to be the second best followed by Kri paste. Vitapex showed the least antibacterial activity.


Subject(s)
Anti-Infective Agents, Local/pharmacology , Calcium Hydroxide/pharmacology , Camphor/pharmacology , Child , Child, Preschool , Chlorophenols/pharmacology , Data Interpretation, Statistical , Drug Combinations , Evaluation Studies as Topic , Humans , Hydrocarbons, Iodinated/pharmacology , Microbial Sensitivity Tests , Root Canal Filling Materials/pharmacology , Silicones/pharmacology , Thymol/pharmacology , Zinc Oxide/pharmacology , Zinc Oxide-Eugenol Cement/pharmacology
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