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1.
Int J Pharm ; 585: 119480, 2020 Jul 30.
Artigo em Inglês | MEDLINE | ID: mdl-32479897

RESUMO

The aim of this research was the development and characterization of three gel dosage forms of Halobetasol propionate loaded lipid nanoparticles (HB-NLC) for the treatment of inflammatory skin diseases. A Pluronic gel (Pl-HB-NLC), a Carbopol gel (Cb-HB-NLC) and a Cremigel (Cg-HB-NLC), were characterized for stability, swelling, degradation, porosity and rheology. The biopharmaceutical behavior of in vitro release and ex vivo permeation, along with microbiological stability were also evaluated. Tolerance and therapeutic efficacy were determined in vivo. The gels proved to have eudermic pH and to be effective to improve HB-NLC stability for more than 6 months. In vitro drug release profiles were adjusted to a first order (Pl-HB-NLC, Cg-HB-NLC) and hyperbola (Cb-HB-NLC) kinetic models, revealing sustained drug release. Ex vivo biopharmaceutical behavior showed slow drug penetration through skin, delaying the drug entrance into systemic circulation. The formulations were effective in reducing inflammation with a lower drug dose in comparison with existing treatments, obtaining the fastest effect when using Pl-HB-NLC. After application of the formulations in volunteers, no irritation, redness or edema reactions were detected, plus, an enhancement of the biomechanical properties of the skin was evidenciated. Therefore, the results indicate that these formulations are a suitable alternative to current treatments.


Assuntos
Produtos Biológicos/síntese química , Clobetasol/análogos & derivados , Portadores de Fármacos/síntese química , Desenvolvimento de Medicamentos/métodos , Inflamação/tratamento farmacológico , Nanoestruturas/química , Administração Tópica , Adulto , Animais , Produtos Biológicos/administração & dosagem , Produtos Biológicos/metabolismo , Clobetasol/administração & dosagem , Clobetasol/síntese química , Clobetasol/metabolismo , Formas de Dosagem , Portadores de Fármacos/administração & dosagem , Portadores de Fármacos/metabolismo , Feminino , Géis , Humanos , Inflamação/metabolismo , Lipídeos , Masculino , Pessoa de Meia-Idade , Nanoestruturas/administração & dosagem , Técnicas de Cultura de Órgãos , Coelhos , Absorção Cutânea/efeitos dos fármacos , Absorção Cutânea/fisiologia , Resultado do Tratamento , Vasoconstritores/administração & dosagem , Vasoconstritores/síntese química , Vasoconstritores/metabolismo
2.
Curr Pharm Des ; 26(12): 1235-1250, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32067607

RESUMO

Glaucoma constitutes the second cause of blindness worldwide and it is considered a neurodegenerative disorder. In this sense, Alzheimer's disease, which is the most common type of dementia, also causes neurodegeneration. The association between both diseases remains unknown although it has been hypothesised that a possible connection might exist and it will be analysed throughout the review. In this sense, nanoparticulate systems and specially, lipid nanoparticles could be the key for effective neuroprotection. Lipid nanoparticles are the most recent type of drug nanoparticulate systems. These nanoparticles have shown great potential to encapsulate hydrophobic drugs increasing their bioavailability and being able to deliver them to the target tissue. In addition, they have shown great potential for ocular drug delivery. This review explores the most recent strategies employing lipid nanoparticles for AD and glaucoma.


Assuntos
Doença de Alzheimer , Glaucoma , Nanopartículas , Doença de Alzheimer/tratamento farmacológico , Portadores de Fármacos , Glaucoma/tratamento farmacológico , Humanos , Lipídeos
3.
Nanomedicine (Lond) ; 14(23): 3089-3104, 2019 12.
Artigo em Inglês | MEDLINE | ID: mdl-31769335

RESUMO

Aim: Development of fluorometholone-loaded PEG-PLGA nanoparticles (NPs) functionalized with cell-penetrating peptides (CPPs) for the treatment of ocular inflammatory disorders. Materials & methods: Synthesized polymers and peptides were used for elaboration of functionalized NPs, which were characterized physicochemically. Cytotoxicity and ability to modulate the expression of proinflammatory cytokines were evaluated in vitro using human corneal epithelial cells (HCE-2). NPs uptake was assayed in both in vitro and in vivo models. Results: NPs showed physicochemical characteristics suitable for ocular administration without evidence of cytotoxicity. TAT-NPs and G2-NPs were internalized and displayed anti-inflammatory activity in both HCE-2 cells and mouse eye. Conclusion: TAT-NPs and G2-NPs could be considered a novel strategy for the treatment of ocular inflammatory diseases of the anterior and posterior segment.


Assuntos
Peptídeos Penetradores de Células/química , Células Epiteliais/metabolismo , Epitélio Corneano/citologia , Fluormetolona/química , Nanopartículas/química , Poliésteres/química , Polietilenoglicóis/química , Animais , Linhagem Celular , Humanos , Camundongos
4.
Eur J Pharm Sci ; 129: 173-180, 2019 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-30639402

RESUMO

Pioglitazone (PGZ) is a member of the thiazolidinedione (TZDs) family of drugs and it is primarily used to treat type 2 diabetes. Previous studies have reported anti-inflammatory and neuroprotective effects in the central nervous system. Building on this, the aim of this study was to develop an oral solution of PGZ (PGZ-SOL) as an alternative treatment for geriatric patients with Alzheimer's disease (AD). Solubility of PGZ was evaluated to establish the solution composition. Parameters determined were pH, rheology, extensibility and retention time. In vitro diffusion kinetic profile and ex vivo permeation studies were carried out in Franz diffusion cells using buccal, sublingual, nasal and intestinal mucosae. The toxicity of PGZ-SOL was evaluated by in vivo model using BALB/c mice. PGZ-SOL exhibited a Newtonian behavior as well as physical and chemical stability during a period of three months. The diffusion profile of PGZ from formulation followed a first-order kinetic model. The biopharmaceutical parameters revealed high permeability of PGZ via intestinal mucosa. Finally, oral administration of PGZ-SOL did not cause damage of buccal, sublingual and intestinal mucosae which suggests that this formulation is a viable alternative for AD treatment in geriatric populations with difficulty swallowing conventional solid dosage forms.


Assuntos
Doença de Alzheimer/tratamento farmacológico , Tiazolidinedionas/administração & dosagem , Administração Sublingual , Animais , Diabetes Mellitus Tipo 2/tratamento farmacológico , Difusão , Humanos , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Permeabilidade , Pioglitazona/administração & dosagem , Suínos
5.
Colloids Surf B Biointerfaces ; 175: 365-374, 2019 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-30554015

RESUMO

Thermosensitive gels have been developed and optimized in such a way that they become gels at corneal temperature and with a viscosity that allows the adequate release of the Fluorometholone (FMT)-loaded PLGA nanoparticles (NPs) in order to improve ocular anti-inflammatory efficacy against a commercial formulation. It has been shown that gels avoid burst release of the drug in the first hours with a slow and increasing profile after administration. NPs have maintained their average size and spherical shape within the gels as confirmed by transmission electron microscopy (TEM). In turn, the in-situ gelling of the formulations allows the administration in eye drops dosage form due to its state of sol at temperatures below 25 °C. Ocular tolerance studies have shown that no formulation causes eye irritation. The administration of the developed formulations has improved the precorneal residence time reflected in the ocular bioavailability, where deep tissues as aqueous humour and crystalline were reached. In conclusion, the use of thermosensitive gels for the topical application of NPs has demonstrated their effectiveness in the acute and preventive treatment of ocular inflammatory conditions.


Assuntos
Anti-Inflamatórios/administração & dosagem , Sistemas de Liberação de Medicamentos , Oftalmopatias/tratamento farmacológico , Fluormetolona/química , Géis/química , Nanopartículas/administração & dosagem , Polímeros/química , Administração Oftálmica , Animais , Anti-Inflamatórios/química , Disponibilidade Biológica , Masculino , Nanopartículas/química , Coelhos
6.
Int J Pharm ; 547(1-2): 338-346, 2018 Aug 25.
Artigo em Inglês | MEDLINE | ID: mdl-29800741

RESUMO

The main objective of this study was the development and optimization of fluorometholone-loaded PLGA nanoparticles for the treatment of inflammatory conditions of the eye. Design of experiments was used to obtain nanoparticles with the best physicochemical characteristics. The optimized nanoparticles containing 1.5 mg·mL-1 of fluorometholone showed a negative surface charge (-30 mV) and an average size below 200 nm being suitable for ocular administration. Drug-polymer interaction studies confirmed no new bonds were formed during the synthesis. Nanoparticles performance was assessed with biopharmaceutical behavior studies, ocular tolerance, anti-inflammatory efficacy and bioavailability. The biopharmaceutical behavior of the drug from nanoparticles was adjusted to hyperbola order showing a significantly greater permeation in the cornea than in the sclera. The optimized formulation had significantly greater anti-inflammatory effects than the commercial formulation. In addition, nanoparticles increased drug penetration toward the vitreous. Polymeric nanoparticles of fluorometholone could provide a suitable alternative for the treatment of inflammatory disorders of the anterior and posterior segments of the eye against of conventional topical formulations.


Assuntos
Anti-Inflamatórios/administração & dosagem , Fluormetolona/administração & dosagem , Inflamação/tratamento farmacológico , Nanopartículas , Administração Oftálmica , Animais , Anti-Inflamatórios/farmacocinética , Anti-Inflamatórios/farmacologia , Disponibilidade Biológica , Galinhas , Membrana Corioalantoide/efeitos dos fármacos , Córnea/metabolismo , Modelos Animais de Doenças , Portadores de Fármacos/química , Sistemas de Liberação de Medicamentos , Oftalmopatias/tratamento farmacológico , Fluormetolona/farmacocinética , Fluormetolona/farmacologia , Ácido Láctico/química , Tamanho da Partícula , Ácido Poliglicólico/química , Copolímero de Ácido Poliláctico e Ácido Poliglicólico , Esclera/metabolismo , Suínos
7.
Environ Pollut ; 187: 202-5, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24485904

RESUMO

Air pollution in Santiago is a serious problem every winter, causing thousands of cases of breathing problems within the population. With more than 6 million people and almost two million vehicles, this large city receives rainfall only during winters. Depending on the frequency of storms, statistics show that every time it rains, air quality improves for a couple of days, followed by extreme levels of air pollution. Current regulations focus mostly on PM10 and PM2.5, due to its strong influence on respiratory diseases. Though more than 50% of the ambient PM10s in Santiago is represented by soil particles, most of the efforts have been focused on the remaining 50%, i.e. particulate material originating from fossil and wood fuel combustion, among others. This document emphasizes the need for the creation of erosion/sediment control regulations in Chile, to decrease respiratory diseases on Chilean polluted cities.


Assuntos
Poluentes Atmosféricos/análise , Poluição do Ar/estatística & dados numéricos , Material Particulado/análise , Doenças Respiratórias/epidemiologia , Chile/epidemiologia , Cidades/estatística & dados numéricos , Humanos , Estações do Ano
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