Microencapsulation of amorphous solid dispersions of fenretinide enhances drug solubility and release from PLGA in vitro and in vivo

Author:

Nieto Kari,Mallery Susan R.,Schwendeman Steven P.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference40 articles.

1. In-process crystallization of acidic drugs in acrylic microparticle systems: influence of physical factors and drug-polymer interactions;Alhnan;J. Pharm. Sci.,2011

2. Almarsson Ö, Hickey MB, Peterson ML, Zaworotko MJ, Moulton B, Rodriguez-Hornedo N. Pharmaceutical co-crystal compositions. Google Patents; 2011. https://patents.google.com/patent/EP1608339A1/en [Accessed 02/2017].

3. BASF. PVP and More. In: BASF, editor. 2009. https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=2&ved=2ahUKEwjHkIXY-9boAhVXJ80KHe8wBy4QFjABegQIARAB&url=https%3A%2F%2Fpharmaceutical.basf.com%2Fglobal%2Fimages%2Fb_03_110921e_solubility_enhance_compendium.pdf&usg=AOvVaw0w9X9XsNIv-xCALjtZi8S_ [Accessed 06/2016].

4. In vitro interaction of fenretinide with plasma retinol-binding protein and its functional consequences;Berni;FEBS Lett.,1992

5. Mechanism of amorphous itraconazole stabilization in polymer solid dispersions: role of molecular mobility;Bhardwaj;Mol. Pharm.,2014

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