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Insulin-loaded calcium pectinate nanoparticles: effects of pectin molecular weight and formulation pH.

机译:胰岛素负载的果胶钙纳米颗粒:果胶分子量和配方pH的影响。

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摘要

Insulin-loaded calcium pectinate nanoparticles were prepared as a potential colonic delivery system by ionotropic gelation with calcium ions. The effects of pectin molecular weight (Mv) and formulation pH on the characteristics of the nanoparticles were evaluated. Commercial pectins, LM101 and LM104, with respective degrees of esterification of 36% and 28%, were depolymerized by mechanical milling to give Mv ranging from 89 to 5.6 kDa. Milled pectins did not yield nanoparticles with significantly different mean diameter and insulin association efficiency (AE) compared to nanoparticles of unmilled pectins. LM104 nanoparticles had smaller variation in mean size than the LM101 nanoparticles. Formulation pH significantly influenced the AE and stability of the nanoparticles. Increasing the pH from 2 to 3 enhanced the AE by three-fold, from 32.76% to 93.31%, at an insulin loading concentration of 80 U/mL. This increase in AE was correlated to the charge density on the pectin molecules as a function of pH. Subsequent release of associated insulin from the nanoparticles was dependent on the extent of dilution of the nanoparticle dispersion and the pH of the dissolution medium. Cross-flow filtration could be used to separate the nanoparticles from unassociated ions and molecules, without compromising the characteristics of the nanoparticles.
机译:通过与钙离子的离子凝胶化,将胰岛素负载的果胶钙纳米颗粒制备为潜在的结肠递送系统。评估了果胶分子量(Mv)和配方pH对纳米颗粒特性的影响。通过机械研磨使酯化度分别为36%和28%的市售果胶LM101和LM104解聚,得到的Mv为89至5.6 kDa。与未碾碎的果胶的纳米颗粒相比,碾碎的果胶的纳米颗粒的平均直径和胰岛素缔合效率(AE)没有明显不同。 LM104纳米颗粒的平均尺寸变化小于LM101纳米颗粒。制剂pH值显着影响纳米颗粒的AE和稳定性。在80 U / mL的胰岛素负载浓度下,将pH从2增加到3可将AE增加3倍,从32.76%增加到93.31%。 AE的这种增加与果胶分子上的电荷密度随pH值相关。随后从纳米颗粒释放缔合的胰岛素取决于纳米颗粒分散体的稀释程度和溶解介质的pH。可以使用错流过滤将纳米粒子与未缔合的离子和分子分离,而不会损害纳米粒子的特性。

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