Enhancement of iodinin solubility by encapsulation into cyclodextrin nanoparticles.

Enhancement of iodinin solubility by encapsulation into cyclodextrin nanoparticles.
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DOI:
10.1080/14756366.2017.1421638
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发表时间:
2018-12
影响因子:
5.6
通讯作者:
Perret F
Perret F
中科院分区:
医学2区
文献类型:
--
作者:
Prandina A;Herfindal L;Radix S;Rongved P;Døskeland SO;Le Borgne M;Perret F

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已知吩嗪可重组平面含氮杂环化合物。它被用于提高生物学上重要的化合物碘的生物利用度,碘在水溶液中几乎不溶。它的水溶性导致了使用不同两亲性α-环糊精(CD)的新制剂的开发。以全-[6-脱氧-6-(3-全氟己基丙硫基)-2,3-二-O-甲基]-α-CD为载体,成功制备了粒径为97.9 nm、包封率为62%、有效控释的碘化原氨酸纳米制剂。这项研究提出了一个有趣的替代优化碘的水溶性碘的化学修饰。
Phenazine is known to regroup planar nitrogen-containing heterocyclic compounds. It was used here to enhance the bioavailability of the biologically important compound iodinin, which is near insoluble in aqueous solutions. Its water solubility has led to the development of new formulations using diverse amphiphilic α-cyclodextrins (CDs). With the per-[6-desoxy-6-(3-perfluorohexylpropanethio)-2,3-di-O-methyl]-α-CD, we succeeded to get iodinin-loaded nanoformulations with good parameters such as a size of 97.9 nm, 62% encapsulation efficiency and efficient control release. The study presents an interesting alternative to optimizing the water solubility of iodinin by chemical modifications of iodinin.
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