Plaunt Adam J, Harmatys Kara M, Hendrie Kyle A, Musso Anthony J, Smith Bradley D
Department of Chemistry and Biochemistry, 236 Nieuwland Science Hall, University of Notre Dame, Notre Dame, 46556 IN, USA.
RSC Adv. 2014 Oct 29;4(101):57983-57990. doi: 10.1039/C4RA10340H.
5-Aminolevulinic acid (5-ALA), a prodrug of Protoporphyrin IX (PpIX), is used for photodynamic therapy of several medical conditions, and as an adjunct for fluorescence guided surgery. The clinical problem of patient photosensitivity after systemic administration could likely be ameliorated if the 5-ALA was delivered more selectivity to the treatment site. Liposomal formulations are inherently attractive as targeted delivery vehicles but it is hard to regulate the spatiotemporal release of aqueous contents from a liposome. Here, we demonstrate chemically triggered leakage of 5-ALA from stealth liposomes in the presence of cell culture. The chemical trigger is a zinc(II)-dipicolylamine (ZnBDPA) coordination complex that selectively targets liposome membranes containing a small amount of anionic phosphatidylserine. Systematic screening of several ZnBDPA complexes uncovered a compound with excellent performance in biological media. Cell culture studies showed triggered release of 5-ALA from stealth liposomes followed by uptake into neighboring mammalian cells and intracellular biosynthesis to form fluorescent PpIX.
5-氨基乙酰丙酸(5-ALA)是原卟啉IX(PpIX)的前体药物,用于多种疾病的光动力治疗,并作为荧光引导手术的辅助手段。如果能将5-ALA更有选择性地递送至治疗部位,全身给药后患者光敏性这一临床问题可能会得到改善。脂质体制剂作为靶向递送载体本身具有吸引力,但很难调节脂质体中水相内容物的时空释放。在此,我们证明了在细胞培养存在的情况下,5-ALA可从隐形脂质体中通过化学触发而泄漏。化学触发剂是一种锌(II)-二吡啶甲胺(ZnBDPA)配位络合物,它能选择性地靶向含有少量阴离子磷脂酰丝氨酸的脂质体膜。对几种ZnBDPA络合物的系统筛选发现了一种在生物介质中具有优异性能的化合物。细胞培养研究表明,5-ALA从隐形脂质体中触发释放,随后被邻近的哺乳动物细胞摄取并在细胞内生物合成形成荧光性的PpIX。