药物输送
药品
亲脂性
反离子
化学
体内
组合化学
药理学
纳米技术
材料科学
有机化学
离子
医学
生物技术
生物
作者
Jinghan Xin,Mengdi Qin,Genyang Ye,Haonan Gong,Mo Li,Xiaofan Sui,Bingyang Liu,Qiang Fu,Zhonggui He
标识
DOI:10.1080/17425247.2023.2150758
摘要
Hydrophobic ion pairing (HIP) is a technology that combines lipophilic structures on polar counterions to increase the lipophilicity through electrostatic interaction. Recent studies showed that HIP-based SEDDS offer an effective way to increase the mucosal permeability and improve the chemical stability for antibiotics, proteases, DNA-based drugs, and other water-soluble macromolecular drugs. It is believed that HIP-based SEDDS offer a potential and attractive method capable of delivering hydrophilic macromolecules with ionizable groups for oral administration.
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