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Enhanced oral bioavailability of dexibuprofen via a novel solid sedds formulation
- In: Industrial Pharmacy- Posters
- At: Istanbul (Turkey) (2009)
- Type: Poster
- Poster code: IPS-P-019
- By: YONG, Chul Soon (College of Pharmacy, Yeungnam University, Gyeongsangbuk-do, South-Korea)
- Co-author(s): Balakrishnan, Prabagar (College of Pharmacy, Yeungnam University, GYEONGSANGBUK-DO, South-Korea)
Woo, Jong Soo (College of Pharmacy, Yeungnam University, GYEONGSANGBUK-DO, South-Korea)
Choi, Han-Gon (College of Pharmacy, Yeungnam University, GYEONGSANGBUK-DO, South-Korea)
Hong, Myung-Ja (College of Pharmacy, Yeungnam University, GYEONGSANGBUK-DO, South-Korea)
Sung, Jun Ho (College of Pharmacy, Yeungnam University, GYEONGSANGBUK-DO, South-Korea) - Abstract:
The main objective of this study was to prepare a solid form of lipid-based self emulsifying drug delivery system (SEDDS) by spray drying liquid SEDDS with an inert solid carrier Aerosil 200 to improve the oral bioavailability of poorly water soluble drug dexibuprofen. The liquid SEDDS was a system consisting of dexibuprofen, Labrasol, Capryol 90..
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Last update 28 September 2023