[引用][C] Comparative study of acyclovir solid dispersion for bioavailability enhancement
A Kushwaha, SK Prajapati, B Sharma - American research of pharmtech research, 2011
[PDF][PDF] Comparative study of acyclovir solid dispersion for bioavailability enhancement
K Anjali, K Prajapati Sunil, S Bhawna - 2012 - researchgate.net
The objective of present study is to improve the dissolution rate of Acyclovir a poorly water
soluble drug by solid dispersion technique using a water soluble carrier, PEG-6000, urea,
mannitol. The solid dispersions are prepared by physical method, co-grinding method and
solvent evaporation method. The prepared solid dispersions showed an enhancement in
dissolution rate and solubility compared to plain drug. In vitro release profiles of all SDs
were comparatively evaluated and also studied against pure acyclovir. Faster dissolution …
soluble drug by solid dispersion technique using a water soluble carrier, PEG-6000, urea,
mannitol. The solid dispersions are prepared by physical method, co-grinding method and
solvent evaporation method. The prepared solid dispersions showed an enhancement in
dissolution rate and solubility compared to plain drug. In vitro release profiles of all SDs
were comparatively evaluated and also studied against pure acyclovir. Faster dissolution …
以上显示的是最相近的搜索结果。 查看全部搜索结果