Chemical Engineering Department, Columbia University, New York, New York 10027, USA.
Langmuir. 2010 Aug 17;26(16):13183-94. doi: 10.1021/la101796p.
Using microbubbles as model systems, we examined molecular diffusion and binding to colloidal surfaces in bimodal poly(ethylene glycol) (PEG) brush layers. A microbubble is a gaseous colloidal particle with a diameter of less than 10 mum, of which the surface comprises amphiphilic phospholipids self-assembled to form a lipid monolayer shell. Due to the compressible gas core, microbubbles provide a sensitive acoustic response and are currently used as ultrasound contrast agents. Similar to the design of long circulating liposomes, PEG chains are typically incorporated into the shell of microbubbles to form a steric barrier against coalescence and adsorption of macromolecules to the microbubble surface. We introduced a buried-ligand architecture (BLA) design where the microbubble surface was coated with a bimodal PEG brush. After microbubbles were generated, fluorescent ligands with different molecular weights were conjugated to the tethered functional groups on the shorter PEG chains, while the longer PEG chains served as a shield to protect these ligands from exposure to the surrounding environment. BLA microbubbles reduced the binding of macromolecules (>10 kDa) to the tethers due to the steric hindrance of the PEG overbrush while allowing the uninhibited attachment of small molecules (<1 kDa). Roughly 40% less fluorescein-conjugated streptavidin (SA-FITC) bound to BLA microbubbles compared to exposed-ligand architecture (ELA) microbubbles. The binding of SA-FITC to BLA microbubbles suggested a possible phase separation between the lipid species on the surface leading to populations of revealed and concealed ligands. Ligand conjugation kinetics was independent of microbubble size, regardless of ligand size or microbubble architecture. We observed, for the first time, streptavidin-induced surface structure formation for ELA microbubbles and proposed that this phenomenon may be correlated to flow cytometry scattering measurements. We therefore demonstrated the feasibility of postlabeling for small-molecule ligands to BLA microbubbles to generate stealth targeted ultrasound contrast agents.
我们使用微泡作为模型系统,研究了在两亲性聚乙二醇(PEG)刷层中分子扩散和与胶体表面的结合。微泡是一种直径小于 10 微米的气态胶体颗粒,其表面由两亲性磷脂自组装形成脂质单层壳。由于可压缩的气核,微泡提供了灵敏的声响应,目前被用作超声造影剂。类似于长循环脂质体的设计,PEG 链通常被引入到微泡的壳中,以形成阻止大分子聚合并吸附到微泡表面的空间位阻。我们引入了一种埋藏配体结构(BLA)设计,其中微泡表面涂有两亲性 PEG 刷。在生成微泡后,将不同分子量的荧光配体与较短 PEG 链上的连接基团缀合,而较长的 PEG 链则作为保护这些配体免受周围环境暴露的屏蔽。BLA 微泡由于 PEG 过度刷的空间位阻,减少了大分子(>10 kDa)与连接物的结合,同时允许小分子(<1 kDa)不受抑制地附着。与暴露配体结构(ELA)微泡相比,BLA 微泡上结合的荧光素结合链霉亲和素(SA-FITC)减少了约 40%。BLA 微泡上 SA-FITC 的结合表明表面上的脂质种类之间可能发生了相分离,导致了暴露和隐藏配体的群体。配体缀合动力学与微泡大小无关,与配体大小或微泡结构无关。我们首次观察到 ELA 微泡上链霉亲和素诱导的表面结构形成,并提出这种现象可能与流式细胞术散射测量有关。因此,我们证明了对 BLA 微泡进行小分子配体后标记以产生隐形靶向超声造影剂的可行性。