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
相关论文
共 50 条
  • [21] Enhancing the solubility and bioavailability of poorly water-soluble drugs using supercritical antisolvent (SAS) process
    Abuzar, Sharif Md
    Hyun, Sang-Min
    Kim, Jun-Hee
    Park, Hee Jun
    Kim, Min-Soo
    Park, Jeong-Sook
    Hwang, Sung-Joo
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2018, 538 (1-2) : 1 - 13
  • [22] A DELIVERY DEVICE CONTAINING A POORLY WATER-SOLUBLE DRUG IN A HYDROPHOBIC MEDIUM - RUMINAL DELIVERY APPLICATION
    THOMBRE, AG
    CARDINAL, JR
    FOURNIER, LA
    JOURNAL OF CONTROLLED RELEASE, 1992, 18 (03) : 221 - 234
  • [23] Influence of Solid Drug Delivery System Formulation on Poorly Water-Soluble Drug Dissolution and Permeability
    Krstic, Marko
    Popovic, Miljana
    Dobricic, Vladimir
    Ibric, Svetlana
    MOLECULES, 2015, 20 (08) : 14684 - 14698
  • [24] Mesoporous drug carrier systems for enhanced delivery rate of poorly water-soluble drug: nimodipine
    Kiwilsza, Anna
    Milanowski, Bartlomiej
    Druzbicki, Kacper
    Coy, L. Emerson
    Grzeszkowiak, Mikolaj
    Jarek, Marcin
    Mielcarek, Jadwiga
    Lulek, Janina
    Pajzderska, Aleksandra
    Wasicki, Jan
    JOURNAL OF POROUS MATERIALS, 2015, 22 (03) : 817 - 829
  • [25] Recent trends of self-emulsifying drug delivery system for enhancing the oral bioavailability of poorly water-soluble drugs
    Phuong Tran
    Jeong-Sook Park
    Journal of Pharmaceutical Investigation, 2021, 51 : 439 - 463
  • [26] Recent trends of self-emulsifying drug delivery system for enhancing the oral bioavailability of poorly water-soluble drugs
    Tran, Phuong
    Park, Jeong-Sook
    JOURNAL OF PHARMACEUTICAL INVESTIGATION, 2021, 51 (04) : 439 - 463
  • [27] Mesoporous drug carrier systems for enhanced delivery rate of poorly water-soluble drug: nimodipine
    Anna Kiwilsza
    Bartłomiej Milanowski
    Kacper Drużbicki
    L. Emerson Coy
    Mikołaj Grzeszkowiak
    Marcin Jarek
    Jadwiga Mielcarek
    Janina Lulek
    Aleksandra Pajzderska
    Jan Wąsicki
    Journal of Porous Materials, 2015, 22 : 817 - 829
  • [28] Development of Clinical Dosage Forms for a Poorly Water-Soluble Drug II: Formulation and Characterization of a Novel Solid Microemulsion Preconcentrate System for Oral Delivery of a Poorly Water-Soluble Drug
    Li, Ping
    Hynes, Sara R.
    Haefele, Thomas F.
    Pudipeddi, Madhu
    Royce, Alan E.
    Serajuddin, Abu T. M.
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (05) : 1750 - 1764
  • [29] A review on solubility enhancement methods for poorly water-soluble drugs
    Ainurofiq, Ahmad
    Putro, David Sarono
    Ramadhani, Dhea Aqila
    Putra, Gemala Mahendra
    Santo, Laura Da Costa Do Espirito
    JOURNAL OF REPORTS IN PHARMACEUTICAL SCIENCES, 2021, 10 (01): : 137 - 147
  • [30] Polymeric micelles for delivery of poorly water-soluble compounds
    Kwon, GS
    CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS, 2003, 20 (05): : 357 - 403