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通过去除光不稳定保护基团实现光触发脂质体中亲水性药物的释放。

Light-triggered hydrophilic drug release from liposomes through removal of a photolabile protecting group.

作者信息

Goto Yuya, Ueda Masafumi, Sugikawa Kouta, Yasuhara Kazuma, Ikeda Atsushi

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Hiroshima University 1-4-1 Kagamiyama Higashi-Hiroshima 739-8527 Japan.

School of Science, Kitasato University 1-15-1 Kitasato, Minami-ku Sagamihara Kanagawa 252-0373 Japan.

出版信息

RSC Adv. 2018 Dec 21;9(1):166-171. doi: 10.1039/c8ra08584f. eCollection 2018 Dec 19.

Abstract

The antibiotic penicillin G cannot be completely incorporated into hydrophobic lipid-membranes owing to its hydrophilicity. Through modification with a hydrophobic and photolabile protecting group, penicillin G was effectively incorporated into liposomes and released by photoirradiation at 365 nm.

摘要

由于青霉素G具有亲水性,它无法完全融入疏水性脂质膜中。通过用疏水性且对光不稳定的保护基团进行修饰,青霉素G被有效地包入脂质体中,并在365纳米波长的光照射下释放出来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/185a/9059325/64c9f6b843b7/c8ra08584f-s1.jpg

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