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首页> 外文期刊>Food biophysics >Preparation and Characterization of Zein/Sodium Caseinate/Xanthan Gum Complex for Encapsulation of Piperine and its In Vitro Release Study
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Preparation and Characterization of Zein/Sodium Caseinate/Xanthan Gum Complex for Encapsulation of Piperine and its In Vitro Release Study

机译:玉米醇素/黄原/黄原胶复合物的制备及表征哌啶封装及其体外释放研究

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摘要

To encapsulate piperine (Pip), as a poor water-soluble bioactive compound, zein-sodium caseinate-xanthan gum (Z-SG-XG) nanocomplex was prepared as a colloidal delivery system. The effect of different parameters involved in complexation process, including concentration of proteins, polysaccharide, and Pip on the encapsulation efficiency of Pip, particle size and stability of the nanocomplexes was investigated. Powders obtained by freeze-drying of the colloidal solution had relatively uniform particles compared to those obtained from conventional drying system and showed well redispersibility in water. At the optimal condition, a stable and homogeneous nanocomplex with a mean particle size of 145.9 +/- 2.7 nm, PDI of 0.27 +/- 0.01, and zeta-potential of -39.7 +/- 1.3 mV was obtained. The antioxidant activity of Pip was significantly improved by encapsulation into the Z-SC-XG nanocomplex. Also, the in vitro release of Pip from the synthesized nanocomplexes in phosphate-buffer saline (PBS) solution and simulated gastrointestinal fluids (SGIF) was investigated and the release kinetic was studied as well. The Pip/Z-SG-XG nanocomplex showed a slower release in SGIF compared to the free Pip and nanoparticles without XG and SC, while its antioxidant activity was remarkable. Results suggested a possible utilization of Z-SC-XG nanocomplex for improving the water solubility, bioavailability and storage stability of Pip.
机译:为了将哌啶(PIP)封装,作为较差的水溶性生物活性化合物,制备ZEIN-钠酪氨酸铝酸盐胶(Z-SG-XG)纳米麦单晶药作为胶体输送系统。研究了络合过程中涉及的不同参数的影响,包括蛋白质,多糖和PIP的浓度,粒径效率,粒径和纳米复合物的稳定性。与由常规干燥系统中获得的那些相比,通过胶体溶液的冷冻干燥获得的粉末具有相对均匀的颗粒,并在水中显示出良好的再分散性。在最佳条件下,获得稳定且均匀的纳米复合物,平均粒径为145.9 +/- 2.7nm,PDI为0.27 +/- 0.01,以及-39.7 +/- 1.3mV的Zeta-poly。通过封装到Z-SC-XG纳米核糖中,PIP的抗氧化活性显着改善。此外,研究了来自合成的纳米复合物中的磷酸盐缓冲盐(PBS)溶液和模拟胃肠流体(SGIF)的体外释放,并研究了释放动力学。与没有XG和SC的游离点和纳米颗粒相比,PIP / Z-SG-XG纳米键术在SGIF中显示出较慢的SGIF释放,而其抗氧化活性显着。结果表明,Z-SC-XG纳米键可采用Z-SC-XG纳米键,以改善PIP的水溶性,生物利用度和储存稳定性。

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