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Métodos Terapéuticos y Terapias MTCI
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1.
PeerJ ; 6: e5476, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30402343

RESUMEN

Medicinal plants play a crucial role in the search for components that are capable of neutralizing the multiple mechanisms of fungal resistance. Psidium salutare (Kunth) O. Berg is a plant native to Brazil used as both food and traditional medicine to treat diseases and symptoms such as stomach ache and diarrhea, whose symptoms could be related to fungal infections from the genus Candida. The objective of this study was to investigate the influence of seasonal variability on the chemical composition of the Psidium salutare essential oil, its antifungal potential and its effect on the Candida albicans morphogenesis. The essential oils were collected in three different seasonal collection periods and isolated by the hydrodistillation process in a modified Clevenger apparatus with identification of the chemical composition determined by gas chromatography coupled to mass spectrometry (GC/MS). The antifungal assays were performed against Candida strains through the broth microdilution method to determine the minimum fungicidal concentration (MFC). Fungal growth was assessed by optical density reading and the Candida albicans dimorphic effect was evaluated by optical microscopy in microculture chambers. The chemical profile of the essential oils identified 40 substances in the different collection periods with γ-terpinene being the predominant constituent. The antifungal activity revealed an action against the C. albicans, C. krusei and C. tropicalis strains with an IC50 ranging from 345.5 to 2,754.2 µg/mL and a MFC higher than 1,024 µg/mL. When combined with essential oils at sub-inhibitory concentrations (MIC/16), fluconazole had its potentiated effect, i.e. a synergistic effect was observed in the combination of fluconazole with P.salutare oil against all Candida strains; however, for C. albicans, its effect was reinforced by the natural product in all the collection periods. The results show that the Psidium salutare oil affected the dimorphic transition capacity, significantly reducing the formation of hyphae and pseudohyphae in increasing concentrations. The results show that P. salutare oil exhibits a significant antifungal activity against three Candida species and that it can act in synergy with fluconazole. These results support the notion that this plant may have a potential use in pharmaceutical and preservative products.

2.
Biomed Pharmacother ; 89: 201-207, 2017 May.
Artículo en Inglés | MEDLINE | ID: mdl-28226293

RESUMEN

Cyclodextrins (CDs) have been used as important pharmaceutical excipients for improve the physicochemical properties of the drugs of low solubility as the essential oil of Hyptis martiusii. This oil is important therapeutically, but the low solubility and bioavailability compromises your use. Therein, the aim of this study was to obtain and to characterize physico-chemically the samples obtained by physical mixture (PM), paste complexation (PC) and slurry complexation (SC) of the essential oil Hyptis martiusii (EOHM) in ß-CD, and to compare the antibacterial and modulatory-antibiotic activity of products obtained and oil free. The physicochemical characterization was performed by differential scanning calorimetry (DSC), thermogravimetry/derivative thermogravimetry (TG/DTG), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Karl Fischer titration. Additionally, the antibacterial tests were performed by microdilution technique. Thus, it was observed that the PM method showed low complexing capacity, unlike PC and SC in which it was observed the formation of inclusion complexes. In addition, the second stage of the TG/DTG curves showed that SC was the best method inclusion with mass loss of 6.9% over the PC that was 6.0%. The XRD results corroborate with the results above suggesting the formation of new solid phase and the SEM photomicrographs showed the porous surface of the samples PC and SC. The essential oil alone demonstrated an antibacterial and modulatory effect against the S. aureus and the Gram negative strain, respectively. However, the ß-CD and the inclusion complex did not demonstrate any biological activity in the performed antibacterial assays.


Asunto(s)
Antibacterianos/química , Hyptis/química , Aceites Volátiles/química , beta-Ciclodextrinas/química , Antibacterianos/farmacología , Rastreo Diferencial de Calorimetría/métodos , Ciclodextrinas/química , Ciclodextrinas/farmacología , Composición de Medicamentos/métodos , Bacterias Gramnegativas/efectos de los fármacos , Aceites Volátiles/farmacología , Extractos Vegetales/química , Extractos Vegetales/farmacología , Solubilidad , Espectroscopía Infrarroja por Transformada de Fourier/métodos , Staphylococcus aureus/efectos de los fármacos , Difracción de Rayos X/métodos , beta-Ciclodextrinas/farmacología
3.
Nat Prod Res ; 27(11): 992-6, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-22568530

RESUMEN

Leishmaniasis is caused by parasites of the genus Leishmania. Recent reports about leishmaniasis show a few number of drugs available, indicating the necessity of new drugs. In this study, the ethanol extract and fractions of Pityrogramma calomelanos (L.) link. (Pteridaceae) were assayed to verify the cytotoxicity and in vitro leishmanicidal activity against promastigote forms of Leishmania brasiliensis. The cytotoxic assay was performed using fibroblasts NCTC929. The studies indicated a leishmanicidal effect of the ethanol extract and the ethyl-acetate fraction. However, a high cytotoxic effect was observed. The hexane and methanol fractions did not show leishmanicidal activity, nor cytotoxic effect. The phytochemical screening detected the presence of alkaloids, a class of secondary metabolites with a known leishmanicidal activity. This is the first study reporting an anti-Leishmania and cytotoxic effect of P. calomelanos, being an interesting approach in the search for drugs against this disease.


Asunto(s)
Helechos/química , Leishmania/efectos de los fármacos , Extractos Vegetales/farmacología , Hojas de la Planta/química , Animales , Evaluación Preclínica de Medicamentos , Etanol/química
4.
Fitoterapia ; 82(2): 208-11, 2011 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-20875845

RESUMEN

The study examined the antiinflammatory and antinociceptive effects of the sesquiterpene (-)-α-bisabolol (BISA). The antiinflammatory effect was evaluated on acute models of dermatitis induced by Croton oil, arachidonic acid, phenol and capsaicin, respectively, in mouse ear. BISA inhibited the dermatitis induced by all noxious agents, except capsaicin. BISA was assessed in two established mouse models of visceral nociception. Mice were pretreated orally with BISA, and the pain-related behavioral responses to intraperitoneal cyclophosphamide or to intracolonic mustard oil were analyzed. BISA showed a dose-unrelated significant antinociception. Collectively, the results suggest that BISA may be an topical antiinflammatory and visceral antinociceptive agent.


Asunto(s)
Dolor Abdominal/tratamiento farmacológico , Analgésicos/uso terapéutico , Antiinflamatorios/uso terapéutico , Conducta Animal/efectos de los fármacos , Dermatitis/tratamiento farmacológico , Extractos Vegetales/uso terapéutico , Sesquiterpenos/uso terapéutico , Dolor Abdominal/inducido químicamente , Enfermedad Aguda , Analgésicos/farmacología , Animales , Antiinflamatorios/farmacología , Colon/efectos de los fármacos , Ciclofosfamida , Modelos Animales de Enfermedad , Oído , Masculino , Ratones , Sesquiterpenos Monocíclicos , Planta de la Mostaza , Aceites Volátiles/química , Peritoneo/efectos de los fármacos , Extractos Vegetales/farmacología , Aceites de Plantas , Sesquiterpenos/farmacología , Piel/efectos de los fármacos
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