Nanocrystal technology for drug formulation and delivery

被引:55
作者
Chang, Tzu-Lan [1 ]
Zhan, Honglei [1 ]
Liang, Danni [2 ]
Liang, Jun F. [1 ]
机构
[1] Charles V Schaefer Sch Engn & Sci, Stevens Inst Technol, Dept Chem Chem Biol & Biomed Engn, Hoboken, NJ 07030 USA
[2] SUNY Stony Brook, Sch Med, Stony Brook, NY 11794 USA
关键词
drug nanocrystal; nanotechnology; formulation; bioavailability; stabilizers; drug delivery; NANOSUSPENSIONS; PARTICLES;
D O I
10.1007/s11705-015-1509-3
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
With the development of modern technology like high throughput screening, combinatorial chemistry and computer aid drug design, the drug discovery process has been dramatically accelerated. However, new drug candidates often exhibit poor aqueous or even organic medium solubility. Additionally, many of them may have low dissolution velocity and low oral bioavailability. Nanocrystal formulation sheds new light on advanced drug development. Due to small (nano- or micro- meters) sizes, the increased surface-volume ratio leads to dramatically enhanced drug dissolution velocity and saturation solubility. The simplicity in preparation and the potential for various administration routes allow drug nanocrystals to be a novel drug delivery system for specific diseases (i.e. cancer). In addition to the comprehensive review of different technologies and methods in drug nanocrystal preparation, suspension, and stabilization, we will also compare nano- and micro- sized drug crystals in pharmaceutical applications and discuss current nanocrystal drugs on the market and their limitations.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 85 条
[1]   Nanoparticle interaction with plasma proteins as it relates to particle biodistribution, biocompatibility and therapeutic efficacy [J].
Aggarwal, Parag ;
Hall, Jennifer B. ;
McLeland, Christopher B. ;
Dobrovolskaia, Marina A. ;
McNeil, Scott E. .
ADVANCED DRUG DELIVERY REVIEWS, 2009, 61 (06) :428-437
[2]   Specific interactions between diphenhydramine and α-helical poly(glutamic acid) -: A new ion-pairing complex for taste masking and pH-controlled diphenhydramine release [J].
Agresti, Ciara ;
Tu, Zhigang ;
Ng, Charlene ;
Yang, Yongsheng ;
Liang, Jun F. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 70 (01) :226-233
[3]   The function of gelatin in controlled precipitation processes of nanosize particles [J].
Auweter, H ;
Andre, V ;
Horn, D ;
Luddecke, E .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 1998, 19 (2-3) :163-184
[4]  
Auweter H, 2002, US Patent, Patent No. 6494924
[5]  
Bansal S., 2012, INT J RES PHARM BIOM, V3, P406
[6]   Production methods for nanodrug particles using the bottom-up approach [J].
Chan, Hak-Kim ;
Kwok, Philip Chi Lip .
ADVANCED DRUG DELIVERY REVIEWS, 2011, 63 (06) :406-416
[7]  
Chase A R, 1985, REMINGTONS PHARM SCI, P286
[8]   Synthesis of nanoparticles with novel technology: High-gravity reactive precipitation [J].
Chen, JF ;
Wang, YH ;
Guo, F ;
Wang, XM ;
Zheng, C .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2000, 39 (04) :948-954
[9]   Preparation and characterization of amorphous cefuroxime axetil drug nanoparticles with novel technology: high-gravity antisolvent precipitation [J].
Chen, Jian-Feng ;
Zhang, Ji-Yao ;
Shen, Zhi-Gang ;
Zhong, Jie ;
Yun, Jimmy .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2006, 45 (25) :8723-8727
[10]   A Brief Literature and Patent Review of Nanosuspensions to a Final Drug Product [J].
Chin, William Wei Lim ;
Parmentier, Johannes ;
Widzinski, Michael ;
Tan, En Hui ;
Gokhale, Rajeev .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2014, 103 (10) :2980-2999