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1.
Curr Pharm Biotechnol ; 14(4): 464-9, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23590143

RESUMO

Potency and activity of SR13668 in cancer prevention have been proven in several in vitro and in vivo cancer models. However, the compound is highly hydrophobic and its limited oral bioavailability has hindered its clinical translation. In this study, we encapsulated SR13668 into polymeric nanoparticles to increase compound aqueous solubility and therefore bioavailability. Poly(lactic-co-glycolic acid) (PLGA) nanoparticles (100-200 nm) encapsulating SR13668 with narrow size distribution and high drug loading were generated by a continuous and scalable process of flash nanoprecipitation integrated with spray dry. A single gavage dose of SR13668-PLGA nanoparticles at 2.8 mg/kg was administered in eight beagle dogs. Drug levels in animal whole blood and plasma were measured over 24 hours. Enhanced bioavailability of SR13668 using nanoparticles compared with formulations of Labrasol® and neat drug in 0.5% methylcellulose is reported. This is the first attempt to study pharmacokinetics of SR13668 in large animals with orally administrated nanoparticle suspension.


Assuntos
Disponibilidade Biológica , Carbazóis/química , Carbazóis/farmacocinética , Administração Oral , Animais , Carbazóis/administração & dosagem , Química Farmacêutica/métodos , Cães , Feminino , Ácido Láctico/administração & dosagem , Ácido Láctico/química , Ácido Láctico/farmacocinética , Masculino , Nanopartículas/administração & dosagem , Nanopartículas/química , Tamanho da Partícula , Ácido Poliglicólico/administração & dosagem , Ácido Poliglicólico/química , Ácido Poliglicólico/farmacocinética , Copolímero de Ácido Poliláctico e Ácido Poliglicólico , Solubilidade , Suspensões/administração & dosagem , Suspensões/química , Suspensões/farmacocinética
2.
J Pharm Sci ; 101(10): 3877-85, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22821759

RESUMO

SR13668 [2,10-Dicarbethoxy-6-methoxy-5,7-dihydro-indolo-(2,3-b)carbazole] has been proven effective in cancer prevention, but the limited bioavailability has hindered its clinical translation. In this study, we have developed a continuous, scalable process to form stable poly(lactic-co-glycolic acid) nanoparticles encapsulating SR13668, based on understanding of the competitive kinetics of nanoprecipitation and spray drying. The optimized formulation achieved high drug loading (33.3 wt %) and small particles (150 nm) with narrow size distribution. The prepared nanoparticle suspensions through flash nanoprecipitation were spray dried to achieve long-term stability and to conveniently adjust the nanoparticle concentration before use. In vitro release of SR13668 from the nanosuspensions was measured in a solution with separated organic and aqueous phases to overcome the limit of SR13668 low water solubility. Higher oral bioavailability of SR13668 by employing polymeric nanoparticles compared with the Labrasol® formulation was demonstrated in a mouse model.


Assuntos
Carbazóis/administração & dosagem , Carbazóis/química , Nanopartículas/administração & dosagem , Nanopartículas/química , Polímeros/química , Administração Oral , Animais , Disponibilidade Biológica , Carbazóis/farmacologia , Química Farmacêutica/métodos , Estabilidade de Medicamentos , Cinética , Ácido Láctico/administração & dosagem , Ácido Láctico/química , Camundongos , Tamanho da Partícula , Ácido Poliglicólico/administração & dosagem , Ácido Poliglicólico/química , Copolímero de Ácido Poliláctico e Ácido Poliglicólico , Polímeros/administração & dosagem , Solubilidade , Suspensões/administração & dosagem , Suspensões/química , Suspensões/farmacologia
3.
Anal Chim Acta ; 661(2): 167-72, 2010 Feb 28.
Artigo em Inglês | MEDLINE | ID: mdl-20113731

RESUMO

Simvastatin (SS) is an effective cholesterol-lowering medicine, and is hydrolyzed to simvastatin acid (SSA) after oral administration. Due to SS and SSA inter-conversion and its pH and temperature dependence, SS and SSA quantitation is analytically challenging. Here we report a high-throughput salting-out assisted liquid/liquid extraction (SALLE) method with acetonitrile and mass spectrometry compatible salts for simultaneous LC-MS/MS analysis of SS and SSA. The sample preparation of a 96-well plate using SALLE was completed within 20 min, and the SALLE extract was diluted and injected into an LC-MS/MS system with a cycle time of 2.0 min/sample. The seamless interface of SALLE and LC-MS eliminated drying down step and thus potential sample exposure to room or higher temperature. The stability of SS and SSA in various concentration ratios in plasma was evaluated at room and low (4 degrees C) temperature and the low temperature (4 degrees C) was found necessary to maintain sample integrity. The short sample preparation time along with controlled temperature (2-4 degrees C) and acidity (pH 4.5) throughout sample preparation minimized the conversion of SS-->SSA to < or = 0.10% and the conversion of SSA-->SS to 0.00% The method was validated with a lower limit of quantitation (LLOQ) of 0.094 ng mL(-1) for both SS and SSA and a sample volume of 100 microL. The method was used for a bioequivalence study with 4048 samples. Incurred sample reproducibility (ISR) analysis of 362 samples from the study exceeded ISR requirement with 99% re-analysis results within 100+/-20% of the original analysis results.


Assuntos
Acetonitrilas/química , Análise Química do Sangue/métodos , Fracionamento Químico/métodos , Ensaios de Triagem em Larga Escala , Sais/química , Sinvastatina/análogos & derivados , Sinvastatina/sangue , Métodos Analíticos de Preparação de Amostras , Calibragem , Fenômenos Químicos , Cromatografia Líquida , Estabilidade de Medicamentos , Humanos , Reprodutibilidade dos Testes , Sinvastatina/química , Sinvastatina/isolamento & purificação , Sinvastatina/farmacocinética , Temperatura , Equivalência Terapêutica , Fatores de Tempo
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