Development of a novel probe sonication assisted enhanced loading of 5-FU in SPION encapsulated pectin nanocarriers for magnetic targeted drug delivery system

被引:35
作者
Dutta, Raj Kumar [1 ]
Sahu, Saurabh [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Analyt Chem Lab, Roorkee 247667, Uttar Pradesh, India
关键词
Pectin; SPIONs; Polymer nanocarrier; 5-Fluorouacil; Controlled release; Cell viability; IRON-OXIDE NANOPARTICLES; RELEASE; 5-FLUOROURACIL; CYTOTOXICITY; PERMEABILITY; FORMULATION; MECHANISMS; CHITOSAN; ASSAY;
D O I
10.1016/j.ejpb.2012.05.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A novel probe sonication method is developed to enhance loading of 5-fluorouracil (5-FU) in SPION encalsulated pectin nanocarriers of 100-150 nm size (referred here as MP-5FU nanocarriers). Probe sonication at 20 kHz for 60 min resulted in 5-FU loading efficiency of 33.2 +/- 2.5% w/w and corresponding drug loading content of 18.2 +/- 1.1 wt%. These are two folds higher than literature report of 5-FU loading in pectin. The enhanced loading is attributed to increase in the rate of dissolution of 5-FU in pectin due to transmission of kHz order sonic waves which increases temperature and pressure in the medium due to formation and collapsing of cavitation bubbles. The fabricated MP-5FU nanocarriers with saturation magnetization (43.13 emu/g) exhibited pH responsive, swelling controlled in vitro release of 5-FU in simulated gastric fluid at pH 1.2, in simulated intestinal fluid at pH 6.8, in simulated colonic fluid at pH 5.5, and in phosphate buffer solution at pH 7.4. The cytotoxicity of MP-5FU was measured by sulforhodamine B (SRB) assay and its GI(50) was more than 5 mg/mL for cancer cells of HT-29 (colon) and Hep G2 (liver), while it was 3.7 mg/mL for cancer cells of MIA-PaCa-2 (Pancreas). (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:58 / 65
页数:8
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