Department of Biomedical Engineering, University at Buffalo, State University of New York, Buffalo, NY 14260, USA.
Gordon Center for Medical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
Theranostics. 2019 Jan 1;9(2):381-390. doi: 10.7150/thno.28376. eCollection 2019.
Near infrared (NIR) dyes are useful for optical imaging. Liposomes have been used extensively for delivery of diverse cargos, including hydrophilic cargos which are passively loaded in the aqueous core. However, most currently available NIR dyes are only slightly soluble in water, making passive entrapment in liposomes challenging for achieving high optical contrast. : We modified a commercially-available NIR dye (IR-820) via one-step Suzuki coupling with dicarboxyphenylboronic acid, generating a disulfonated heptamethine; dicarboxyphenyl cyanine (DCP-Cy). DCP-Cy was loaded in liposomes and used for optical imaging. Owing to increased charge in mildly basic aqueous solution, DCP-Cy had substantially higher water solubility than indocyanine green (by an order of magnitude), resulting in higher NIR absorption. Unexpectedly, DCP-Cy tended to form J-aggregates with pronounced spectral red-shifting to 934 nm (from 789 nm in monomeric form). J-aggregate formation was dependent on salt and DCP-Cy concentration. Dissolved at 20 mg/mL, DCP-Cy J-aggregates could be entrapped in liposomes. Full width at half maximum absorption of the liposome-entrapped dye was just 25 nm. The entrapped DCP-Cy was readily detectable by fluorescence and photoacoustic NIR imaging. Upon intravenous administration to mice, liposomal DCP-Cy circulated substantially longer than the free dye. Accumulation was largely in the spleen, which was visualized with fluorescence and photoacoustic imaging. DCP-Cy is simple to synthesize and exhibits high aqueous solubility and red-shifted absorption from J-aggregate formation. Liposomal dye entrapment is possible, which facilitates photoacoustic and fluorescence imaging around 930 nm.
近红外 (NIR) 染料可用于光学成像。脂质体已广泛用于递送各种载药,包括被动载入水核中的亲水性载药。然而,目前大多数可用的 NIR 染料在水中的溶解度仅略高,因此对于实现高光学对比度,被动包封在脂质体中具有挑战性。我们通过一步铃木偶联反应,用二羧基苯基硼酸对市售的 NIR 染料(IR-820)进行修饰,生成了二磺酸基七甲川菁(DCP-Cy)。DCP-Cy 被载入脂质体中并用于光学成像。由于在轻度碱性水溶液中带电量增加,DCP-Cy 的水溶性比吲哚菁绿(ICG)高了一个数量级,因此具有更高的近红外吸收。出人意料的是,DCP-Cy 倾向于形成 J-聚集物,光谱明显红移至 934nm(从单体形式的 789nm)。J-聚集物的形成取决于盐和 DCP-Cy 浓度。以 20mg/mL 的浓度溶解时,DCP-Cy J-聚集物可被包封在脂质体中。包封在脂质体中的染料的最大吸收峰全宽仅为 25nm。包封的 DCP-Cy 很容易通过荧光和光声 NIR 成像检测到。将脂质体 DCP-Cy 静脉注射到小鼠体内后,游离染料的循环时间显著延长。积累主要在脾脏中,荧光和光声成像可以观察到。DCP-Cy 合成简单,具有高水溶性和 J-聚集物形成引起的红移吸收。脂质体染料包封是可行的,这有利于 930nm 附近的光声和荧光成像。