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Use of Polyvinyl Alcohol as a Solubility Enhancing Polymer for Poorly Water-Soluble Drug Delivery (Part 2).
Brough, Chris; Miller, Dave A; Ellenberger, Daniel; Lubda, Dieter; Williams, Robert O.
Affiliation
  • Brough C; Division of Pharmaceutics, College of Pharmacy, The University of Texas at Austin, 1 University Station, Campus Mail Code A1902, Austin, Texas, 78712, USA. chris.brough@dispersoltech.com.
  • Miller DA; DisperSol Technologies, LLC, 111 W. Cooperative Way, Building 3, Georgetown, Texas, 78626, USA. chris.brough@dispersoltech.com.
  • Ellenberger D; DisperSol Technologies, LLC, 111 W. Cooperative Way, Building 3, Georgetown, Texas, 78626, USA.
  • Lubda D; Division of Pharmaceutics, College of Pharmacy, The University of Texas at Austin, 1 University Station, Campus Mail Code A1902, Austin, Texas, 78712, USA.
  • Williams RO; DisperSol Technologies, LLC, 111 W. Cooperative Way, Building 3, Georgetown, Texas, 78626, USA.
AAPS PharmSciTech ; 17(1): 180-90, 2016 Feb.
Article in En | MEDLINE | ID: mdl-26863889
ABSTRACT
The KinetiSol® Dispersing (KSD) technology has enabled the investigation into the use of polyvinyl alcohol (PVAL) as a concentration enhancing polymer for amorphous solid dispersions. Our previous study revealed that the 88% hydrolyzed grade of PVAL was optimal for itraconazole (ITZ) amorphous compositions with regard to solid-state properties, non-sink dissolution performance, and bioavailability enhancement. The current study investigates the influence of molecular weight for the 88% hydrolyzed grades of PVAL on the properties of KSD processed ITZPVAL amorphous dispersions. Specifically, molecular weights in the processable range of 4 to 18 mPa · s were evaluated and the 4-88 grade provided the highest AUC dissolution profile. Amorphous dispersions at 10, 20, 30, 40, and 50% ITZ drug loads in PVAL 4-88 were also compared by dissolution performance. Analytical tools of diffusion-ordered spectroscopy and Fourier transform infrared spectroscopy were employed to understand the interaction between drug and polymer. Finally, results from a 30-month stability test of a 30% drug loaded ITZPVAL 4-88 composition shows that stable amorphous dispersions can be achieved. Thus, this newly enabled polymer carrier can be considered a viable option for pharmaceutical formulation development for solubility enhancement.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymers / Polyvinyl Alcohol / Solubility / Water / Itraconazole Language: En Journal: AAPS PharmSciTech Journal subject: FARMACOLOGIA Year: 2016 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymers / Polyvinyl Alcohol / Solubility / Water / Itraconazole Language: En Journal: AAPS PharmSciTech Journal subject: FARMACOLOGIA Year: 2016 Document type: Article Affiliation country: United States