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1.
Braz. J. Pharm. Sci. (Online) ; 56: e18363, 2020. tab, graf
Article in English | LILACS | ID: biblio-1132057

ABSTRACT

This paper reports on the development of nanoparticles aiming at the in vitro controlled release of simvastatin (SVT). The nanoparticles were prepared by the nanoprecipitation method with polymers Eudragit® FS30D (EDGFS) or Eudragit® NE30D (EDGNE). EDGFS+SVT nanoparticles showed mean size of 148.8 nm and entrapment efficiency of 76.4%, whereas EDGNE+SVT nanoparticles showed mean size of 105.0 nm and entrapment efficiency of 103.2%. Infrared absorption spectra demonstrated that SVT incorporated into the polymer matrix, especially EDGNE. Similarly, the differential scanning calorimeter (DSC) curve presented no endothermic peak of fusion, indicating that the system is amorphous and the drug is not in the crystalline state. The maintenance of SVT in the amorphous state may favors its solubilization in the target release sites. In the in vitro dissolution assay, the SVT incorporated into the EDGFS+SVT nanoparticles showed a rapid initial release, which may be related to the pH of the dissolution medium used. Regarding the EDGNE+SVT nanoparticles, the in vitro release occurred in a bimodal behavior, i.e., an initial "burst" followed by a sustained delivery, with the kinetics of drug release following Baker-Lonsdale's mathematical model. All these features suggest the nanoparticulate system's potential to modulate SVT delivery and enhance its bioavailability.


Subject(s)
Simvastatin/pharmacology , Nanoparticles/analysis , Drug Liberation , In Vitro Techniques/classification , Pharmaceutical Preparations/administration & dosage , Dissolution/adverse effects
2.
Electron. j. biotechnol ; 16(1): 2-2, Jan. 2013. ilus, tab
Article in English | LILACS | ID: lil-663681

ABSTRACT

Background: Aloe vera L., member of the Liliaceae family, has been shown to stimulate cell proliferation and contribute to healing and angiogenesis, has anti-bacterial, anti-fungal and anti-inflammatory activity. In addition, Aloe vera can be used as a support for drug transport. Our objective is to evaluate antimicrobial activity and cytotoxicity of sponges of Aloe vera L. for use as a carrying support of drugs. Results: In this work, sponge of free Aloe vera (AV) loaded with amoxicillin (AMX) or nystatin (NYS) at 1% w/w, were prepared and physico-chemically characterized via X-ray diffraction, Fourier Transform Infrared Spectroscopy and thermal analysis. Antimicrobial potency of AV sponge alone, loaded with AMX or NYS, against strains of Streptococcus mutans, Staphylococcus aureus, Aggregatibacter actinomycetemcomitans, Enterococcus faecalis and Candida albicans was determined. Osteoblasts and human gingival fibroblasts were cultivated on AV, Aloe vera loaded with amoxicillin (AV/AMX) and Aloe vera loaded with nystatin (AV/NYS) and cellular viability was assessed. The physico-chemical characterization performed suggested that the loaded drugs were dispersed in the sponge and those interactions between the AV sponge and the loaded drugs were weak. Furthermore, AV loaded with AMX or NYS demonstrated antimicrobial potency and osteoblasts and fibroblasts were viable after 24 hrs on free AV, and AV loaded with AMX or NYS. Conclusions: Our results indicate that sponges of free AV, loaded with AMX or NYS, are biocompatible and exhibit antimicrobial activity.


Subject(s)
Humans , Aloe/chemistry , Anti-Infective Agents/pharmacology , Osteoblasts/drug effects , Porifera , Staphylococcus aureus/drug effects , Streptococcus mutans/drug effects , X-Ray Diffraction , Biocompatible Materials , Candida albicans/drug effects , Drug Carriers , Cell Survival/drug effects , Nystatin/pharmacology , Spectroscopy, Fourier Transform Infrared , Agar , Fibroblasts/drug effects , Gingiva/cytology , Amoxicillin/pharmacology
3.
Braz. oral res ; 24(1): 08-14, Jan.-Mar. 2010. ilus, graf, tab
Article in English | LILACS | ID: lil-541506

ABSTRACT

The aim of this study was to observe the histopathological pulp response following direct pulp capping of mechanically exposed teeth in rats with a composite of beta-tricalcium phosphate-hydroxyapatite bioceramic (BC) and poly (glycolic)-poly (lactic acid) (PLGA) material or a calcium hydroxide [Ca(OH)2] material, compared to BC alone and a negative control of water. Pulp of the maxillary molars was exposed, followed by capping with the experimental material. The pulpal tissue response was assessed post-operatively at 1, 7, 14 and 30 d, followed by histological analysis. The Ca(OH)2 group exhibited severe acute inflammatory cell infiltration at day 14. However after 30 d, a new hard tissue with macro porous obliteration of the pulp chamber and a characteristic necrotic area had appeared. BC and Ca(OH)2 capping were associated with moderate inflammation and dentinal bridge similar. Meanwhile, in the BC/PLGA composite group, there was moderate inflammatory infiltrate and formation of a dense and complete dentinal bridge. In conclusion, the BC/PLGA composite material showed a large zone of tertiary dentin, and effectively reorganized the dentin-pulp complex.


Subject(s)
Animals , Rats , Biocompatible Materials/therapeutic use , Calcium Hydroxide/therapeutic use , Dental Pulp Capping/methods , Dental Pulp/drug effects , Bone Cements/therapeutic use , Calcium Phosphates/therapeutic use , Disease Models, Animal , Dental Pulp/pathology , Dentin/pathology , Durapatite/therapeutic use , Lactic Acid/therapeutic use , Polyglycolic Acid/therapeutic use , Time Factors
4.
Pesqui. odontol. bras ; 17(1): 78-81, jan.-mar. 2003. tab, graf
Article in English | LILACS, BBO | ID: lil-343779

ABSTRACT

A efetividade da associaçäo fluoreto-clorexidina na prevençäo da gengivite e da cárie vem sendo defendida desde alguns anos 5,7,14. O propósito dessa associaçäo é ter um desempenho sinergistico da mesma. O objetivo do presente estudo foi avaliar a substantividade da clorexidina em associaçäo ou näo ao fluoreto de sódio em diferentes intervalos de tempo, in vitro. Foram tratadas superfícies de esmalte bovino com soluções de digluconato de clorexidina 0,12 por cento, Periogardâ - Colgateâ ou fluoreto de sódio 0,5 por cento-clorexidina 0,12 por cento Duplakâ -Dentsplyâ durante um minuto. A substantividade foi medida pela dessorçäo da clorexidina a partir dos fragmentos previamente imersos nas soluções teste e colocados em água destilada. Alíquotas foram removidas em intervalos de 5`, 30` e 6 horas e analisadas através da espectroscopia na regiäo do ultravioleta visível. Os valores obtidos foram analisados estatisticamente pelo teste de T-student. Os resultados mostraram que a concentraçäo da clorexidina foi significativamente reduzida quando em associaçäo com fluoreto de sódio (p <0.05). Os resultados in vitro sugerem que a associaçäo da clorexidina com fluoreto de sódio nas concentrações estudadas parece näo ter efeito benéfico devido à reduçäo da substantividade da clorexidina


Subject(s)
Chlorhexidine , Sodium Fluoride
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