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Self-assembled oligomeric procyanidin-insulin hybrid nanoparticles: a novel strategy for controllable insulin delivery

机译:自组装的低聚原花青素-胰岛素杂化纳米颗粒:一种可控的胰岛素输送新策略

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摘要

Natural oligomeric procyanidin (OPC) with high biological and pharmacological activities was successfully used to synthesize OPC-insulin (OPC-INS) nanoparticles with different aggregation sizes for sustained and controlled delivery of hydrophilic insulin. The aggregation size of OPC-INS nanoparticles was regulated by OPC concentration, pH value, and incubation time. The fabrication mechanism would be that OPC and insulin self-assembled into a mixture of insulin aggregates via intermolecular interactions. In the self-assembly of insulin, OPC could serve both in the encompassing of insulin aggregates as a stabilizer and cross-linking different amounts of insulin aggregates into OPC-INS nanoparticles as interphase. OPC-INS nanoparticles not only demonstrated effective insulin drug loading but also exhibited aggregation-size-dependent and controlled insulin release performance in vitro. In the best case for OPC-INS nanoparticles, only ~21% of insulin was released in 37 days. This study showed that the OPC-INS nanosystem is promising to serve as a long-acting insulin release formulation, and OPC has great potential as a drug carrier for nanomedicine.
机译:具有高生物和药理活性的天然低聚原花青素(OPC)已成功用于合成具有不同聚集尺寸的OPC-胰岛素(OPC-INS)纳米粒子,以持续和控制地输送亲水性胰岛素。 OPC-INS纳米颗粒的聚集大小由OPC浓度,pH值和孵育时间调节。制造机制是OPC和胰岛素通过分子间相互作用自组装成胰岛素聚集体的混合物。在胰岛素的自组装中,OPC既可以作为稳定剂包含在胰岛素聚集体中,又可以作为中间相将不同量的胰岛素聚集体交联到OPC-INS纳米颗粒中。 OPC-INS纳米颗粒不仅表现出有效的胰岛素载药量,而且在体外还表现出聚集大小依赖性和受控的胰岛素释放性能。在OPC-INS纳米颗粒的最佳情况下,在37天内仅释放约21%的胰岛素。这项研究表明,OPC-INS纳米系统有望用作长效胰岛素释放制剂,OPC作为纳米药物的药物载体具有巨大潜力。

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