noninvasive biomedical images are created through optical and tomographic imaging such as X-ray, positron emission tomography (PET), magnetic resonance imaging (MRI), and computed tomography (CT). [1] These modalities however, depend on the use of heavy doses of ionizing radiation and/or hazardous optical contrast agents such as radioactive 18 F in the form of flurodeoxyglucose for PET, paramagnetic 64 Gd for MRI, and iodine or barium for X-ray and CT scans. [1,2] Even with the use of such harmful radiocontrast agents or ionizing radiation, these present imaging tools are still predominantly limited by their low millimeter spatial and temporal resolution for reconstructing 3D images of biological systems. [1] On the other hand, fluorescence labeling and imaging are not subject to the adverse use of ionizing radiation or radioactive tracing agents that hinder conventional tomographic imaging tools. Furthermore, fluorescent probes afford real-time image acquisition with a vastly improved spatial resolution, all while employing medically-safe visible light, near-infrared (NIR), or infrared (IR) radiation. [3,4] Amongst the different classes of fluorescent probes such as organic molecular dyes, carbon dots, and metallic clusters, colloidal semiconductor quantum dots (QDs) have emerged as promising candidates for clinical applications beyond the laboratory setting. This is due, in part, to their superior optical qualities such as a broad-based absorption spectrum with a large absorption cross-section and high photoluminescence quantum yield (PLQY). [2,5,6] Flexible tuning of QD photoluminescence (PL) to emit from ultraviolet to IR radiation through size and compositional control also realizes the possibility of multiplex detection (through dual PL emissions) and multimodal imaging to combine more than one imaging tool such as MRI and fluorescence optical imaging. [7,8] In particular, tuning the QDs' PL emission to either of the two biological spectral windows (in the NIR from 650-900 nm, or IR from 1000-1350 nm) have facilitated bioimaging with minimal tissue scattering and autofluorescence, accompanied by a significant improvement in imaging depth and spatial resolution as compared to imaging using visible light. [9-11]