Critical Material Attributes of Strip Films Loaded With Poorly Water-Soluble Drug Nanoparticles: II. Impact of Polymer Molecular Weight

被引:27
作者
Krull, Scott M. [1 ]
Ammirata, Jennifer [1 ]
Bawa, Sonia [1 ]
Li, Meng [1 ]
Bilgili, Ecevit [1 ]
Dave, Rajesh N. [1 ]
机构
[1] New Jersey Inst Technol, Otto H York Dept Chem Biol & Pharmaceut Engn, Newark, NJ 07102 USA
基金
美国国家科学基金会;
关键词
biodegradable polymers; content uniformity; controlled release/delivery; dissolution rate; formulation; nanoparticles; particle sizing; polymeric drug delivery systems; thermogravimetric analysis; UV/vis spectroscopy; ORAL FILMS; MECHANICAL-PROPERTIES; RELEASE PROFILE; IN-VITRO; DISSOLUTION; CELLULOSE; PLASTICIZER; TEMPERATURE; STABILIZERS; SURFACTANT;
D O I
10.1016/j.xphs.2016.10.009
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Recent work established polymer strip films as a robust platform for delivery of poorly water-soluble drug particles. However, a simple means of manipulating rate of drug release from films with minimal impact on film mechanical properties has yet to be demonstrated. This study explores the impact of film-forming polymer molecular weight ( MW) and concentration on properties of polymer films loaded with poorly water-soluble drug nanoparticles. Nanoparticles of griseofulvin, a model Biopharmaceutics Classification System class II drug, were prepared in aqueous suspension via wet stirred media milling. Aqueous solutions of 3 viscosity grades of hydroxypropyl methylcellulose ( 14, 21, and 88 kDa) at 3 viscosity levels (similar to 9500, similar to 12,000, and similar to 22,000 cP) were mixed with drug suspension, cast, and dried to produce films containing griseofulvin nanoparticles. Few differences in film tensile strength or elongation at break were observed between films within each viscosity level regardless of polymer MW despite requiring up to double the time to achieve 100% drug release. This suggests film-forming polymer MW can be used to manipulate drug release with little impact on film mechanical properties by matching polymer solution viscosity. In addition, changing polymer MW and concentration had no negative impact on drug content uniformity or nanoparticle redispersibility. (C) 2017 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:619 / 628
页数:10
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