Light responsive Gold NPs-polymer hybrid LBL capsules for the Lysosomal Storage Disorder
Abstract
Abstract: GM1 gangliosidosis is a rare lysosomal storage disorder caused due to the malfunctioning of lysosomal ?-galactosidase that maintains the distribution of GM1 ganglioside within the body. Delivery of ? -galactosidase inside the cells is the only potential approach to cure such disease. However, trafficking of this therapeutic protein into a cell is highly challenging. In this regard, stimuli-responsive nanocarriers have gained a lot of attention as they precisely control the delivery of payload under the influence of a particular stimulus. To this end, we report the formulation of light-responsive gold NPs-polymer hybrid LBL capsule for the intracellular delivery of ?-gal enzyme and showed light-responsive breaking of gold NPs-polymer hybrid LBL capsule by using NIR laser exposure technique (980nm, a continuous laser beam of 1W power). The light-responsive breaking of gold NPs-polymer hybrid LBL capsules was verified by fluorescent microscopy and scanning electron microscope (SEM). We observed 1.5, 1.8- and 2.27-fold reduction in the capsules number after10 min, 15min and 20min laser exposure respectively. Further, ?-gal enzyme release from gold NPs-polymer hybrid LBL capsule was verified after capsule lysis using assay buffer (ONPG). We observed 1835mU±113 ?-gal entrapment within gold NPs-polymer hybrid LBL capsules (?500 nm). Gold NPs-polymer hybrid LBL capsules showed no cytotoxicity up to 150 capsules per cell concentration and were well internalized by the HeLa as well as L929 cells.
Keywords: Gangliosidosis, beta-galactosidase, gold nanoparticles, LBL capsules, light responsive, stimuli responsive nanocarriers