Current potential and challenges in the advances of liquid crystalline nanoparticles as drug delivery systems

被引:87
|
作者
Madheswaran, Thiagarajan [1 ]
Kandasamy, Murugesh [2 ]
Bose, Rajendran J. C. [3 ,4 ]
Karuppagounder, Vengadeshprabhu [5 ]
机构
[1] Int Med Univ, Sch Pharm, Dept Pharmaceut Technol, 126 Jalan Jalil Perkasa 19, Kuala Lumpur 57000, Malaysia
[2] Int Med Univ, Sch Pharm, Dept Pharmaceut Chem, 126 Jalan Jalil Perkasa 19, Kuala Lumpur 57000, Malaysia
[3] Stanford Univ, Sch Med, Dept Radiol, MIPS, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Radiol, Canary Ctr Stanford Canc Early Detect, Stanford, CA 94305 USA
[5] Penn State Coll Med, Dept Orthoped & Rehabil, 500 Univ Dr, Hershey, PA 17033 USA
关键词
IN-VITRO; CUBIC PHASE; LIPID NANOPARTICLES; GLYCERYL MONOOLEATE; STERIC STABILIZERS; CUBOSOMES; NANOCARRIERS; PHYTANTRIOL; DESIGN; ACID;
D O I
10.1016/j.drudis.2019.05.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lyotropic nonlamellar liquid crystalline nanoparticles (NPs) (LCN), such as cubosomes and hexosomes, are useful tools for applications in drug delivery because of their unique structural properties. LCNs are highly versatile carriers that can be applied for use with topical, oral, and intravenous treatments. In recent years, significant research has focused on improving their preparation and characterization, including controlling drug release and enhancing the efficacy of loaded bioactive molecules. Nevertheless, the clinical translation of LCN-based carriers has been slow. In this review, we highlight recent advances and challenges in the development and application of LCN, providing examples of their topical, oral, and intravenous drug delivery applications, and discussing translational obstacles to LCN as a NP technology.
引用
收藏
页码:1405 / 1412
页数:8
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