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1.
J Pharm Biomed Anal ; 111: 209-14, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25898315

RESUMEN

As [(18)F]fluoride is a starting reagent in the radiosynthesis of most fluorine-18 labeled positron emission tomography (PET) tracers, its chromatographic behavior on reversed phase (RP) HPLC columns is important for the purification performance and accuracy of RP HPLC quality control methods. We have investigated the chromatographic behavior and recovery of [(18)F]fluoride as a function of the type and brand of RP HPLC column, the pH and the composition of the mobile phase. Elution and elution profile of [(18)F]fluoride from six RP-HPLC columns (Waters XBridge C18 3 mm × 100 mm 3.5 µm; Grace Platinum EPS C18 4.6 mm × 100 mm, 3 µm; Waters XTerra C18 4.6 mm × 250 mm, 5 µm; Phenomenex C18 4.6 mm × 150 mm, 5 µm; Hamilton PRP-1 column 4.1 mm × 150 mm, 5 µm; Merck KGaA Chromolith Performance C18 3 mm × 100 mm) eluted with mobile phase composed of phosphate or acetate buffers (pH 2, 3, 4, 5, 7.3 and 9) and acetonitrile or ethanol as organic modifier were characterized. The elution profile was determined by on-line radioactivity measurement in the column eluate and recovery was calculated by comparison of radioactivity eluted with the HPLC column present or absent in the chromatographic flow path. Interestingly, [(18)F]fluoride recovery increased with increasing pH. At pH 3 all packed silica-based columns showed significant retention of fluorine-18, whereas almost no retention was observed on a polymeric PRP-1 column. However at pH 5, [(18)F]fluoride recovery was above 90% for each tested column. In addition, small differences were observed when changing the composition of the mobile phase. We therefore recommend to use a mobile phase with pH > 5 for silica based C18 columns for both quality control and semi-preparative HPLC of fluorine-18 labeled PET radiopharmaceuticals. If required a lower pH can be used in combination with a polymer based HPLC column.


Asunto(s)
Fluoruros/química , Radioisótopos de Flúor/química , Cromatografía Líquida de Alta Presión/métodos , Cromatografía de Fase Inversa/métodos , Concentración de Iones de Hidrógeno , Polímeros/química , Tomografía de Emisión de Positrones/métodos , Radiofármacos/química , Dióxido de Silicio/química
2.
J Pharm Sci ; 103(11): 3696-3703, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25231545

RESUMEN

In this study, we investigated the potential of supersaturation for the formulation of the poorly water-soluble microbicide dapivirine (DPV) in an aqueous vaginal gel in order to enhance its vaginal tissue uptake. Different excipients such as hydroxypropylmethylcellulose, polyethylene glycol 1000, and cyclodextrins were evaluated for their ability to inhibit precipitation of supersaturated DPV in the formulation vehicle as such as well as in biorelevant media. In vitro permeation assessment across HEC-1A cell layers demonstrated an enhanced DPV flux from supersaturated gels compared with suspension gels. The best performing supersaturated gel containing 500 µM DPV (supersaturation degree of 4) in the presence of sulfobutyl ether-beta-cyclodextrin (2.5%) appeared to be stable for at least 3 months. In addition, the gel generated a significant increase in vaginal drug uptake in rabbits as compared with suspension gels. We conclude that supersaturation is a possible strategy to enhance the vaginal concentration of hydrophobic microbicides, thereby increasing permeation into the vaginal submucosa.


Asunto(s)
Fármacos Anti-VIH/administración & dosificación , Pirimidinas/administración & dosificación , Inhibidores de la Transcriptasa Inversa/administración & dosificación , Tecnología Farmacéutica/métodos , Animales , Fármacos Anti-VIH/química , Fármacos Anti-VIH/farmacocinética , Fármacos Anti-VIH/toxicidad , Línea Celular , Precipitación Química , Química Farmacéutica , Estabilidad de Medicamentos , Excipientes/química , Estudios de Factibilidad , Femenino , Geles , Interacciones Hidrofóbicas e Hidrofílicas , Membrana Mucosa/metabolismo , Permeabilidad , Pirimidinas/química , Pirimidinas/farmacocinética , Pirimidinas/toxicidad , Conejos , Inhibidores de la Transcriptasa Inversa/química , Inhibidores de la Transcriptasa Inversa/farmacocinética , Inhibidores de la Transcriptasa Inversa/toxicidad , Solubilidad , Vagina/metabolismo , beta-Ciclodextrinas/química
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