Dendrimer, Liposomes, Carbon Nanotubes and PLGA Nanoparticles: One Platform Assessment of Drug Delivery Potential

被引:83
|
作者
Mody, Nishi [1 ]
Tekade, Rakesh Kumar [1 ,2 ]
Mehra, Neelesh Kumar [1 ]
Chopdey, Prashant [1 ]
Jain, Narendra Kumar [1 ]
机构
[1] Dr Hari Singh Gour Vishwavidyalaya, Dept Pharmaceut Sci, Pharmaceut Res Lab, Sagar 470003, MP, India
[2] Univ Hawaii, Coll Pharm, Pharm Res Stn, Hilo, HI 96720 USA
来源
AAPS PHARMSCITECH | 2014年 / 15卷 / 02期
关键词
carbon nanotubes; dendrimer; drug delivery; liposomes; nanoparticles; nanotechnology; POLY(PROPYLENE IMINE) DENDRIMERS; CANCER-THERAPY; SOLUBILIZATION; FORMULATION; SIZE;
D O I
10.1208/s12249-014-0073-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Liposomes (LIP), nanoparticles (NP), dendrimers (DEN), and carbon nanotubes (CNTs), represent eminent classes of drug delivery devices. A study was carried out herewith by employing docetaxel (DTX) as model drug to assess their comparative drug delivery potentials. Under optimized conditions, highest entrapment of DTX was observed in CNT-based formulation (DTX-CNTs, 74.70 +/- 4.9%) followed by nanoparticles (DTX-NP, 62.34 +/- 1.5%), liposome (49.2 +/- 1.51%), and dendrimers (28.26 +/- 1.74%). All the formulations were found to be of nanometric size. In vitro release studies were carried out in PBS (pH 7.0 and 4.0), wherein all the formulations showed biphasic release pattern. Cytotoxicity assay in human cervical cancer SiHa cells inferred lowest IC50 value of 1,235.09 +/- 41.93 nM with DTX-CNTs, followed by DTX-DEN, DTX-LIP, DTX-NP with IC50 values of 1,571.22 +/- 151.27, 1,653.98 +/- 72.89, 1,922.75 +/- 75.15 nM, respectively. Plain DTX showed higher hemolytic toxicity of 22.48 +/- 0.94%, however loading of DTX inside nanocarriers drastically reduced its hemolytic toxicity (DTX-DEN, 17.22 +/- 0.48%; DTX-LIP, 4.13 +/- 0.19%; DTX-NP, 6.43 +/- 0.44%; DTX-CNTs, 14.87 +/- 1.69%).
引用
收藏
页码:388 / 399
页数:12
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