Highly Fluorescent and Stable Quantum Dot-Polymer-Layered Double Hydroxide Composites

We report a designed strategy for a synthesis of highly luminescent and photostable composites by incorporating quantum dots (QDs) into layered double hydroxide (LDH) matrices without deterioration of a photoluminescence (PL) efficiency of the fluorophores during the entire processes of composite formations. The QDs synthesized in an organic solvent are encapsulated by polymers, poly­(maleic acid-alt-octadecene) to transfer them into water without altering the initial surface ligands. The polymer-encapsulated QDs with negative zeta potentials (−29.5 ± 2.2 mV) were electrostatically assembled with positively charged (24.9 ± 0.6 mV) LDH nanosheets to form QD-polymer-LDH composites (PL quantum yield: 74.1%). QD-polymer-LDH composite films are fabricated by a drop-casting of the solution on substrates. The PL properties of the films preserve those of the organic QD solutions. We also demonstrate that the formation of the QD-polymer-LDH composites affords enhanced photostabilities through multiple protections of QD surface by polymers and LDH nanosheets from the environment

Quantum Dots in an Amphiphilic Polyethyleneimine Derivative Platform for Cellular Labeling, Targeting, Gene Delivery, and Ratiometric Oxygen Sensing

Amphiphilic polyethyleneimine derivatives (amPEIs) were synthesized and used to encapsulate dozens of quantum dots (QDs). The QD–amPEI composite was ∼100 nm in hydrodynamic diameter and had the slightly positive outer surface that suited well for cellular internalization. The QD–amPEI showed very efficient QD cellular labeling with the labeled cell fluorescence intensity more than 10 times higher than conventional techniques such as Lipofectamine-assisted QD delivery. QD–amPEI was optimal for maximal intracellular QD delivery by the large QD payload and the rapid endocytosis kinetics. QD–amPEI platform technology was demonstrated for gene delivery, cell-specific labeling, and ratiometric oxygen sensing. Our QD–amPEI platform has two partitions: positive outer surface and hydrophobic inside pocket. The outer positive surface was further exploited for gene delivery and targeting. Co-delivery of QDs and GFP silencing RNAs was successfully demonstrated by assembling siRNAs to the outer surfaces, which showed the transfection efficiency an order of magnitude higher than conventional gene transfections. Hyaluronic acids were tethered onto the QD–amPEI for cell-specific targeted labeling which showed the specific-to-nonspecific signal ratio over 100. The inside hydrophobic compartment was further applied for cohosting oxygen sensing phosphorescence Ru dyes along with QDs. The QD-Ru-amPEI oxygen probe showed accurate and reversible oxygen sensing capability by the ratiometric photoluminescence signals, which was successfully applied to cellular and spheroid models