INQUIMAE, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina.
Gerencia Química - Centro Atómico Constituyentes, Comisión Nacional de Energía Atómica, Av. Gral. Paz 1499, B1650KNA San Martín, Buenos Aires, Argentina.
Photochem Photobiol Sci. 2019 Jan 1;18(1):155-165. doi: 10.1039/c8pp00133b. Epub 2018 Oct 30.
We prepared water soluble, biocompatible fluorescent turn-on pH nanosensors and characterized their behavior as a function of changes in pH. The response relies on a halochromic reaction of a spirorhodamineamide derived from the bright and highly chemically and photo-stable rhodamine 6G, encapsulated in core/nanoporous shell silica nanoparticles. The fluorescent sensors displayed a fast response in the pH range of intracellular compartments. The encapsulation conferred solubility in aqueous environments and biocompatibility. We assessed the two main properties of the sensor, namely the useful pH range and the kinetics of the response, and compared them to those of the free probe. We found that such properties are strongly dependent on the functionalization and position in the silica matrix relative to the core/shell structure. Finally, we demonstrated the cellular uptake of the nanosensors, and their localization in lysosomes of living cells, by fluorescence confocal microscopy.
我们制备了水溶性、生物相容性的荧光开启型 pH 纳米传感器,并研究了它们在 pH 变化下的行为。这种响应依赖于从明亮且高度稳定的罗丹明 6G 衍生的螺旋罗丹明酰胺的变色反应,该反应被包裹在核/纳米多孔壳二氧化硅纳米粒子中。荧光传感器在细胞内隔室的 pH 范围内表现出快速响应。封装赋予了在水相环境中的溶解性和生物相容性。我们评估了传感器的两个主要特性,即有用的 pH 范围和响应动力学,并将其与游离探针的特性进行了比较。我们发现,这些特性强烈依赖于功能化和在相对于核/壳结构的二氧化硅基质中的位置。最后,我们通过荧光共焦显微镜证明了纳米传感器的细胞摄取及其在活细胞溶酶体中的定位。