...
首页> 外文期刊>Biomacromolecules >Investigating the Influence of Aromatic Moieties on the Formulation of Hydrophobic Natural Products and Drugs in Poly(2-oxazoline)-Based Amphiphiles
【24h】

Investigating the Influence of Aromatic Moieties on the Formulation of Hydrophobic Natural Products and Drugs in Poly(2-oxazoline)-Based Amphiphiles

机译:调查芳香部分对聚(2-恶唑啉)基于两亲疏水性天然产物和药物制剂的影响

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Many natural compounds with interesting biomedical properties share one physicochemical property, namely, low water solubility. Polymer micelles are, among others, a popular means to solubilize hydrophobic compounds. The specific molecular interactions between the polymers and the hydrophobic drugs are diverse, and recently it has been discussed that macromolecular engineering can be used to optimize drug-loaded micelles. Specifically, pi-pi stacking between small molecules and polymers has been discussed as an important interaction that can be employed to increase drug loading and formulation stability. Here, we test this hypothesis using four different polymer amphiphiles with varying aromatic content and various natural products that also contain different relative amounts of aromatic moieties. In the case of paclitaxel, having the lowest relative content of aromatic moieties, the drug loading decreases with increasing relative aromatic amount in the polymer, whereas the drug loading of curcumin, having a much higher relative aromatic content, is increased. Interestingly, the loading using schizandrin A, a dibenzo[a,c]cyclooctadiene lignan with intermediate relative aromatic content is not influenced significantly by the aromatic content of the polymers employed. The very high drug loading, long-term stability, ability to form stable highly loaded binary coformulations in different drug combinations, small-sized formulations, and amorphous structures in all cases corroborate earlier reports that poly(2-oxazoline)-based micelles exhibit an extraordinarily high drug loading and are promising candidates for further biomedical applications. The presented results underline that the interaction between the polymers and the incorporated small molecules may be more complex and are significantly influenced by both sides, the used carrier and drug, and must be investigated in each specific case.
机译:许多具有有趣生物医学性质的天然化合物共享一种物理化学性质,即低水溶性。聚合物胶束等是溶解疏水化合物的普遍方法。聚合物和疏水药物之间的特定分子相互作用是多种多样的,最近讨论了大分子工程可用于优化药物负载的胶束。具体地,已经讨论了小分子和聚合物之间的PI-PI堆叠作为可以采用的重要相互作用来增加药物载荷和制剂稳定性。在这里,我们使用具有不同芳族含量的四种不同的聚合物两亲性和各种天然产物来测试该假设,以及还含有不同相对量的芳族部分的各种天然产物。在具有紫杉醇的紫杉醇的情况下,具有最低的芳族部分的相对含量,药物负载随着聚合物中的相对芳族量的增加而降低,而姜黄素的药物载荷具有更高的相对芳族含量。有趣的是,使用Schizandrin A的装载是具有中间相对芳族含量的二苯脲[A,C]环辛酰胺Lignan不受所用聚合物的芳族含量的显着影响。在不同药物组合中的药物负荷非常高的药物负载,长期稳定性,形成稳定的高负荷二元共体,在不同的药物组合中,所有情况下的小尺寸配方和无定形结构都证实了聚(2-恶唑啉)的胶束表现出来的早期报告非常高的药物负荷,并且是进一步生物医学应用的承诺候选人。所呈现的结果强调,聚合物和掺入的小分子之间的相互作用可能更复杂,并且受到两侧,二手载体和药物的显着影响,并且必须在每个特定情况下研究。

著录项

  • 来源
    《Biomacromolecules》 |2018年第7期|共10页
  • 作者单位

    Julius Maximilians Univ Wurzburg Dept Chem &

    Pharm Chair Adv Mat Synth Funct Polymer Mat Rontgenring 11 D-97070 Wurzburg Germany;

    Julius Maximilians Univ Wurzburg Dept Chem &

    Pharm Chair Adv Mat Synth Funct Polymer Mat Rontgenring 11 D-97070 Wurzburg Germany;

    Julius Maximilians Univ Wurzburg Dept Chem &

    Pharm Chair Adv Mat Synth Funct Polymer Mat Rontgenring 11 D-97070 Wurzburg Germany;

    Julius Maximilians Univ Wurzburg Dept Chem &

    Pharm Chair Adv Mat Synth Funct Polymer Mat Rontgenring 11 D-97070 Wurzburg Germany;

    Univ Klinikum Wurzburg Lehrstuhl Tissue Engn &

    Regenerat Med Rontgenring 11 D-97070 Wurzburg Germany;

    Univ Bayreuth Organ Chem Lab Univ Str 30 D-95447 Bayreuth Germany;

    Julius Maximilians Univ Wurzburg Dept Chem &

    Pharm Chair Adv Mat Synth Funct Polymer Mat Rontgenring 11 D-97070 Wurzburg Germany;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号