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聚乙二醇化聚-L-鸟氨酸复合物作为新型吸收促进剂的制备与评价

Preparation and Evaluation of PEGylated Poly-L-ornithine Complex as a Novel Absorption Enhancer.

作者信息

Kamiya Yusuke, Yamaki Tsutomu, Uchida Masaki, Hatanaka Tomomi, Kimura Mitsutoshi, Ogihara Masahiko, Morimoto Yasunori, Natsume Hideshi

机构信息

Faculty of Pharmaceutical Sciences, Josai University.

出版信息

Biol Pharm Bull. 2017;40(2):205-211. doi: 10.1248/bpb.b16-00781.

Abstract

Polycationic compounds, such as poly-L-arginine and poly-L-ornithine (PLO), enhance the nasal absorption of hydrophilic macromolecular drugs. However, the bio availability corresponding to the dose of these enhancers has not been obtained in an open system study, where an administered solution is transferred to the pharynx because they do not exhibit mucoadhesion/retention in the nasal cavity. In this study, we prepared PEGylated-poly-L-ornithine (PEG-PLO) and investigated the effects of PEGylation on in vitro adhesion/retention properties, permeation enhancement efficiency, and cytotoxicity. PEG-PLO bearing 3-4 polyethylene glycol (PEG) chains per PLO molecule was more retentive than unmodified PLO on an inclined plate. The permeability of a model drug, FD-4, across Caco-2 cell sheets was enhanced by PEG-PLO as well as by PLO. PLO showed cytotoxicity at high concentrations, whereas PEG-PLO did not decrease cell viability, even above the concentration giving a sufficient enhancement effect. These findings suggest that PEGylation of polycationic absorption enhancers improves their adhesion/retention and decreases their cytotoxicity, which may lead to enhancers with greater utility.

摘要

聚阳离子化合物,如聚-L-精氨酸和聚-L-鸟氨酸(PLO),可增强亲水性大分子药物的鼻腔吸收。然而,在开放系统研究中,尚未获得与这些增强剂剂量相对应的生物利用度,在该研究中,给药溶液会转移至咽部,因为它们在鼻腔中不表现出粘膜粘附/滞留。在本研究中,我们制备了聚乙二醇化聚-L-鸟氨酸(PEG-PLO),并研究了聚乙二醇化对体外粘附/滞留特性、渗透增强效率和细胞毒性的影响。每个PLO分子带有3-4条聚乙二醇(PEG)链的PEG-PLO在倾斜板上比未修饰的PLO更具滞留性。模型药物FD-4跨Caco-2细胞单层的渗透率通过PEG-PLO以及PLO得到增强。PLO在高浓度时表现出细胞毒性,而PEG-PLO即使在高于产生足够增强效果的浓度下也不会降低细胞活力。这些发现表明,聚阳离子吸收增强剂的聚乙二醇化改善了它们的粘附/滞留并降低了它们的细胞毒性,这可能会产生更具实用性的增强剂。

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