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1.
Data Brief ; 38: 107391, 2021 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-34604482

RESUMEN

Cochliomyia hominivorax is the dipteran that causes the worst and most serious types of myiasis in animals and humans in the Americas. The data described here show the effects of a commercial product formulated on the basis of citronella essential oil nanoemulsified (Nano Citronela Plus®) directly on eggs, first, second and third stage larvae of the C. hominivorax blowfly, in addition to the indirect effect on the oviposition of adult flies. These data make up the gross base that was used in the preparation of the article "Repellent, ovicidal, larvicidal and adulticidal action of a nanoemulsion of Citronella essential oil (Cymbopogon winterianus) on Cochliomyia hominivorax (Diptera: Calliphoridae)" Bricarello et al., 2021. Counting data of larvae, eggs and adult flies live and dead after contact with the product, data on weighing and counting of eggs from the repellency test are available, as well as photos of cuticular changes that occurred in the larvae and malformations observed after contact with Nano Citronela Plus®.

2.
An Acad Bras Cienc ; 92(4): e20200134, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33237141

RESUMEN

Pectin (PC) extracted from a solid residue from cassava roots (Manihot esculenta Crantz) was used to coat nanoparticles (NP) containing ß-carotene (BC) aiming at the gastrointestinal administration of this lipophilic nutraceutical. The NP were prepared by spontaneous emulsification method using food grade components. Pectin-coated NP have been successfully prepared as confirmed by the increased particle size and negative surface charges due to the pectin's anionic nature. NP showed spherical shape and monodisperse distribution, with a mean size of 21.3 nm (polydispersity index (PDI) 0.29) for BC PC T80-NP (nanoparticle with ß-carotene, pectin and Tween 80) and 261.4 nm (PDI 0.1) for BC PC T20-NP (nanoparticle with ß-carotene, pectin and Tween 20). BC was encapsulated at amounts of 530 and 324 µg/ml for BC PC T80-NP and BC PC T20-NP, respectively, with high encapsulation efficiency (> 95%), increasing its antioxidant capacity in vitro, besides no cytotoxic effect. However, only BC PC T20-NP was stable over a 90 days storage period (4°C) and revealed a strong interaction between pectin and mucin. These results suggest that pectin-coated BC PC T20-NP is a promising strategy to improve the bioavailability and permeation of BC for administration through mucosal surfaces.


Asunto(s)
Manihot , Nanopartículas , Celulosa , Pectinas , beta Caroteno
3.
Drug Dev Ind Pharm ; 44(4): 643-651, 2018 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-29139323

RESUMEN

OBJECTIVE: The aim of this work is to develop and characterize nanoemulsions containing jaboticaba extract (Plinia peruviana) aiming pharmaceutical and cosmetic applications. METHODS: Nanoemulsions were prepared by high-pressure homogenization method using different concentrations of components (oil, surfactant, and extract) and homogenization pressures, in order to optimize the preparation conditions. Both unloaded and extract-loaded nanoemulsions were characterized according to their size, polydispersity, zeta potential, pH, morphology, and physical stability. Total phenolic and flavonoid contents in free jaboticaba extract and jaboticaba-loaded nanoemulsions were determined spectrophotometrically, while ellagic acid content was determined by high-performance liquid chromatography (HPLC) analysis. In vitro antioxidant activity was investigated by 2, 2-diphenyl-1-picrylhydrazyl (DPPH) and ferric reducing antioxidant power (FRAP) methods. RESULTS: Colloidal dispersions exhibited a mean particle size around 200 nm, with monodisperse size distribution (PdI <0.3), and spherical shape. Stability studies showed that nanoemulsions were stable over 120 d of storage at room temperature. Jaboticaba nanoemulsions showed significant concentrations of phenolics, flavonoids, and ellagic acid, with encapsulation efficiency values higher than 90%. Antioxidant properties of jaboticaba nanoemulsions were demonstrated by its remarkable ability to scavenge DPPH free radicals and to reduce ferric-tripyridyltriazine complex, which can be attributed to their phenolic and flavonoid contents. CONCLUSIONS: The results suggest that nanoemulsions containing jaboticaba extract can be considered a promising candidate as a new antioxidant agent.


Asunto(s)
Antioxidantes/química , Antioxidantes/farmacología , Myrtaceae/química , Extractos Vegetales/química , Extractos Vegetales/farmacología , Antioxidantes/administración & dosificación , Compuestos de Bifenilo , Composición de Medicamentos , Estabilidad de Medicamentos , Ácido Elágico/química , Emulsiones , Flavonoides/análisis , Concentración de Iones de Hidrógeno , Nanopartículas , Tamaño de la Partícula , Fenoles/análisis , Picratos , Extractos Vegetales/administración & dosificación
4.
Methods Mol Biol ; 1391: 65-80, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27108310

RESUMEN

Plinia cauliflora (jaboticaba) is a native fruit tree from Brazilian rainforest widely used in popular medicine to prevent diarrhea, asthma, and infections. Studies have shown that the major therapeutic potential of jaboticaba fruits is on its peel, a rich source of anthocyanins. These secondary metabolites have well-known antioxidant and anti-inflammatory activities and have been claimed to be effective to treat diabetes, cancer, cardiovascular diseases, and stroke. This chapter describes a series of methodologies to evaluate important in vitro biological activities like cytotoxicity, proliferation, and migration of a hydroalcoholic extract of jaboticaba peel on mouse fibroblast L929 line. Assays to assess total phenolic, flavonoid, and anthocyanin contents and antioxidant activities are described as well.


Asunto(s)
Antocianinas/química , Antocianinas/farmacología , Evaluación Preclínica de Medicamentos/métodos , Myrtaceae/química , Animales , Antocianinas/aislamiento & purificación , Antioxidantes/química , Antioxidantes/aislamiento & purificación , Antioxidantes/farmacología , Línea Celular , Movimiento Celular/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Fibroblastos/citología , Fibroblastos/efectos de los fármacos , Flavonoides/química , Flavonoides/aislamiento & purificación , Flavonoides/farmacología , Ratones , Fenoles/química , Fenoles/aislamiento & purificación , Fenoles/farmacología , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/farmacología , Cicatrización de Heridas/efectos de los fármacos
5.
J Nanosci Nanotechnol ; 15(1): 781-91, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-26328442

RESUMEN

Mucoadhesive nanoparticles loaded with curcumin were developed as a new approach to deliver curcumin for the local treatment of oral cancer. PCL nanoparticles coated with chitosan displaying different molar masses were prepared by using the nanoprecipitation technique. The mucoadhesive properties of nanoparticle suspensions were demonstrated by their strong ability to interact with the glycoprotein mucin through electrostatic interactions. Similar permeation profiles of curcumin loaded in uncoated and chitosan-coated nanoparticles across porcine esophageal mucosa were verified. Curcumin concentrations retained in the mucosa suggest the possibility of a local effect of the drug. In vitro studies demonstrated that free curcumin.and curcumin loaded into nanoparticles coated with chitosan caused significant reduction of SCC-9 human oral cancer cell viability in a concentration and time-dependent manner. However, no significant cell death was observed after 24 h of treatment with unloaded nanoparticles coated with chitosan. In addition, curcumin-loaded nanoparticles showed reduced cytotoxicity, when compared with the free drug. Therefore, chitosan-coated PCL nanoparticles may be considered a promising strategy to deliver curcumin directly into the oral cavity for the treatment of oral cancer.


Asunto(s)
Antineoplásicos/farmacocinética , Quitosano/farmacocinética , Curcumina/farmacocinética , Neoplasias de la Boca/metabolismo , Nanopartículas/química , Animales , Antineoplásicos/química , Antineoplásicos/farmacología , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Quitosano/química , Quitosano/farmacología , Curcumina/química , Curcumina/farmacología , Esófago/química , Esófago/metabolismo , Humanos , Mucinas/metabolismo , Nanopartículas/toxicidad , Porcinos
6.
J Pharm Sci ; 104(10): 3524-34, 2015 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-26085173

RESUMEN

The study was aimed to evaluate the effect of orally administered chitosan-coated nanoparticles containing curcumin on metastatic melanoma. Chitosan-coated nanoparticles containing curcumin were prepared, and their antimetastatic activity was investigated both in vitro and in vivo. Curcumin decreased cell viability and induced apoptosis of B16F10 melanoma cells. We observed that curcumin significantly decreased the expression of metalloproteinases, which are known to be associated with migration and proliferation of cancer cells. Importantly, treatment with chitosan-coated nanoparticles containing curcumin decreased pulmonary tumor formation in a murine model of experimental metastasis. Histological analyses confirmed the macroscopic results in which lungs of mice treated with curcumin-loaded chitosan-coated polycaprolactone nanoparticles had only a few small nodules and most of them were free of melanoma. Our findings indicate that nanoparticles coated with the mucoadhesive polymer chitosan containing curcumin may be a promising approach and/or intervention for the treatment of malignant melanoma.


Asunto(s)
Antineoplásicos Fitogénicos/administración & dosificación , Antineoplásicos Fitogénicos/uso terapéutico , Curcumina/administración & dosificación , Curcumina/uso terapéutico , Melanoma Experimental/tratamiento farmacológico , Melanoma/tratamiento farmacológico , Animales , Apoptosis/efectos de los fármacos , Línea Celular Tumoral , Movimiento Celular/efectos de los fármacos , Quitosano , Femenino , Absorción Intestinal , Metaloproteinasa 2 de la Matriz/biosíntesis , Melanoma/patología , Melanoma Experimental/patología , Ratones , Ratones Endogámicos C57BL , Nanopartículas , Metástasis de la Neoplasia , Poliésteres , Neoplasias Cutáneas , Melanoma Cutáneo Maligno
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