کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2505476 | 1557494 | 2008 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Voriconazole into PLGA nanoparticles: Improving agglomeration and antifungal efficacy Voriconazole into PLGA nanoparticles: Improving agglomeration and antifungal efficacy](/preview/png/2505476.png)
This study is concerned with preparing PLGA nanoparticles loaded with voriconazole (PNLV), investigating the burst release and agglomeration of PNLV, and also evaluating antifungal efficacy of PNLV compared with voriconazole (VRC). The emulsion–solvent evaporation technique for nanoparticles and tests against fungi were completed. The amount of VRC in PNLV with sodium hexametaphosphate was 2.01 ± 0.27%, and burst release of PNLV was reduced by about 33% using 20% ethanol solution (n = 3). The mean D50 of PNLV with or without this salt was 132.8 nm and 6.3 μm, respectively (n = 5). In vitro; the fungal numbers treated with PNLV (3.5 mg/ml, equal amount calculated by VRC) and VRC (70 μg/ml) in tubes at the day 7 were 5.74 log10 and 6.72 log10, respectively (P < 0.05). In vivo; the fungal burden treated with PNLV and VRC in tissue from mice kidneys at day 7 after administration was 0.64 log10 and 2.61 log10, respectively (5 mg/kg, P < 0.001). The hematoxylin–eosin stain in mice kidney showed that the pathological lesions treated with PNLV were relieved in contrast with those with VRC. These results suggest that the emulsion–solvent evaporation process is feasible in preparing PNLV. Moreover, ethanol solution decreased burst release and Na-HMP inhibited agglomeration. PNLV could improve the VRC antifungal efficacy.
Journal: International Journal of Pharmaceutics - Volume 352, Issues 1–2, 20 March 2008, Pages 29–35