Nanocarrier for Poorly Water-Soluble Anticancer Drugs-Barriers of Translation and Solutions

被引:187
作者
Narvekar, Mayuri [1 ]
Xue, Hui Yi [1 ]
Eoh, June Young [1 ]
Wong, Ho Lun [1 ]
机构
[1] Temple Univ, Sch Pharm, Philadelphia, PA 19140 USA
来源
AAPS PHARMSCITECH | 2014年 / 15卷 / 04期
基金
美国国家卫生研究院;
关键词
anti-cancer drug; drug delivery; nanocarrier; poorly water-soluble drugs; translation; SOLID LIPID NANOPARTICLES; IN-VITRO; PARENTERAL DELIVERY; CARRIERS NLC; MULTIDRUG-RESISTANCE; HYBRID NANOPARTICLES; ANTITUMOR-ACTIVITY; CELLULAR UPTAKE; CO-DELIVERY; PACLITAXEL;
D O I
10.1208/s12249-014-0107-x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Many existing chemotherapeutic drugs, repurposed drugs and newly developed small-molecule anticancer compounds have high lipophilicity and low water-solubility. Currently, these poorly water-soluble anticancer drugs (PWSAD) are generally solubilized using high concentrations of surfactants and co-solvents, which frequently lead to adverse side effects. In recent years, researchers have been actively exploring the use of nanotechnology as an alternative to the solvent-based drug solubilization approach. Several classes of nanocarrier systems (lipid-based, polymer-based and albumin-based) are widely studied for encapsulation and delivery of the existing and new PWSAD. These nanocarriers were also shown to offer several additional advantages such as enhanced tumour accumulation, reduced systemic toxicity and improved therapeutic effectiveness. In this article, the recent nanotechnological advances in PWSAD delivery will be reviewed. The barriers commonly encountered in the development of PWSAD nanoformulations (e.g. formulation issues and nanotoxicity issues) and the strategies to overcome these barriers will also be discussed. It is our goal to provide the pharmaceutical scientists and clinicians with more in-depth information about the nanodelivery approach, thus, more efficacious and safe PWSAD nanoformulations can be developed with improved translational success.
引用
收藏
页码:822 / 833
页数:12
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