Nanoparticle encapsulation improves oral bioavailability of curcumin by at least 9-fold when compared to curcumin administered with piperine as absorption enhancer

被引:736
作者
Shaikh, J. [2 ]
Ankola, D. D. [1 ]
Beniwal, V. [2 ]
Singh, D. [2 ]
Kumar, M. N. V. Ravi [1 ]
机构
[1] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, Glasgow G4 0NR, Lanark, Scotland
[2] NIPER, Dept Pharmaceut, Sas Nagar 160062, Punjab, India
关键词
Curcumin; Bioavailability; Nanoparticles; Oral; Piperine; BEHAVIOR IN-VITRO; PLGA NANOPARTICLES; FORMULATION; ESTRADIOL; DELIVERY; PHARMACOKINETICS; STABILITY; THERAPY; DESIGN; VIVO;
D O I
10.1016/j.ejps.2009.02.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Curcumin, a derived product from common spice turmeric that is safe and beneficial in several aliments was formulated into biodegradable nanoparticles with a view to improve its oral bioavailability. The curcumin encapsulated nanoparticles prepared by emulsion technique were spherical in shape with particle size of 264 rim (polydispersity index 0.31) and 76.9% entrapment at 15% loading. The curcumin encapsulated nanoparticles were able to withstand the International Conference on Harmonisation (ICH) accelerated stability test conditions for refrigerated products for the studied duration of 3 months. X-ray diffraction analysis revealed the amorphous nature of the encapsulated curcumin. The in vitro release was predominantly by diffusion phenomenon and followed Higuchi's release pattern. The in vivo pharmacokinetics revealed that curcumin entrapped nanoparticles demonstrate at least 9-fold increase in oral bioavailability when compared to curcumin administered with piperine as absorption enhancer. Together the results clearly indicate the promise of nanoparticles for oral delivery of poorly bioavailable molecules like curcumin. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:223 / 230
页数:8
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