The aim of present investigation was to screen different solvents for optimizing nanoparticle preparation in terms of particle size, entrapment efficiency, and finally, release behavior using a model drug estradiol. Nanoparticles were prepared following emulsion-diffusion-evaporation method using di
β¦ LIBER β¦
Estradiol loaded PLGA nanoparticles for oral administration: Effect of polymer molecular weight and copolymer composition on release behavior in vitro and in vivo
β Scribed by G. Mittal; D.K. Sahana; V. Bhardwaj; M.N.V. Ravi Kumar
- Book ID
- 113691503
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 380 KB
- Volume
- 119
- Category
- Article
- ISSN
- 0168-3659
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