Use of Polyvinyl Alcohol as a Solubility Enhancing Polymer for Poorly Water-Soluble Drug Delivery (Part 2)

被引:27
|
作者
Brough, Chris [1 ,2 ]
Miller, Dave A. [2 ]
Ellenberger, Daniel [1 ,2 ]
Lubda, Dieter [3 ]
Williams, Robert O., III [1 ]
机构
[1] Univ Texas Austin, Coll Pharm, Div Pharmaceut, 1 Univ Stn,Campus Mail Code A1902, Austin, TX 78712 USA
[2] DisperSol Technol LLC, 111 W Cooperat Way,Bldg 3, Georgetown, TX 78626 USA
[3] Merck KGaA, Frankfurter Str 250, D-64293 Darmstadt, Germany
来源
AAPS PHARMSCITECH | 2016年 / 17卷 / 01期
关键词
amorphous solid dispersion; itraconazole; polyvinyl alcohol; PVAL; solubility enhancement; AMORPHOUS SOLID DISPERSIONS; HOT-STAGE EXTRUSION; MELT-EXTRUSION; ORAL BIOAVAILABILITY; ITRACONAZOLE; FORMULATION; STABILITY; RELEASE; DISSOLUTION; ABSORPTION;
D O I
10.1208/s12249-016-0490-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The KinetiSol (R) 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 ITZ: PVAL 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 ITZ: PVAL 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.
引用
收藏
页码:180 / 190
页数:11
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