Specific Bioimaging Research Articles

Probe for simultaneous membrane and nucleus labeling in living cells and in vivo bioimaging using a two-photon absorption water-soluble Zn(ii) terpyridine complex with a reduced π-conjugation system.

Small, biocompatible and water-soluble molecules with high two-photon absorption (2PA) cross-section values (δ) are in high demand for specific bioimaging applications. Here, two novel terpyridine derivative ligands with donor-acceptor (D-A) (L1) and donor-π-acceptor (D-π-A) (L2) models, and their corresponding Zn(ii) complexes are designed and characterized. It was found that the two-photon absorption cross section values (δ) in the near-infrared region (NIR, about 800 nm) are significantly enhanced for complexes 1 and 2 compared to their free D-A type ligand L1, while those of complexes 3 and 4 were greatly decreased relative to their free ligand L2, thus confirming that the smaller ligand (D-A type) displays a suitable Turn-ON fluorescence pair for two-photon fluorescence microscopy (2PFM). Firstly, the potential of simultaneously labeling a live cell plasma membrane and nucleus using complex 1 is demonstrated. In addition, live larval and adult zebrafish incubated with an optimal concentration of 1 demonstrated clear brain uptake. Lastly and importantly, using such a probe to visualize the blood-brain-barrier (BBB) capillary endothelial cells and penetrate the BBB into the central nervous system (CNS) intravenously in a mouse model is also explored.

Hyaluronic acid functionalized nitrogen-doped carbon quantum dots for targeted specific bioimaging

Schematic illustration of the preparation of HA-CQDs (A) and the following bioimaging application (B).

Water‐Dispersed Near‐Infrared‐Emitting Quantum Dots of Ultrasmall Sizes for In Vitro and In Vivo Imaging

Near-infrared (NIR)-fluorescence imaging is widely recognized as an effective method for high-resolution and highsensitivity bioimaging because of its minimized biological autofluorescence background and the increased penetration of excitation and emission light through tissues in the NIR wavelength window (700–900 nm). There have been tremendous efforts to develop high-efficiency fluorescent biological probes for NIR-fluorescence imaging. Semiconductor quantum dots (QDs) have attracted much recent attention as a new generation of fluorescent probes because of their unique optical properties such as strong luminescence, high photostability, and size-tunable emission wavelength. While QDs emitting in the range of 450–650 nm have been well developed, NIR-emitting QDs have been much less explored because of their relatively complicated synthesis and post-treatment manipulations. Furthermore, NIR-emitting QDs are usually prepared in organic phase, and additional surface modification is employed to render them waterdispersible for biological applications. The relatively complicated surface modification often results in an increase in size of the QDs. Only recently, water-dispersed NIRemitting CdTe/CdS QDs with tetrahedral structure were directly prepared in aqueous phase through the epitaxialshell-growth method. Despite these advances, much work is still needed to obtain NIR-emitting QDs that can be facilely synthesized in aqueous phase for high-sensitivity and specific bioimaging. Herein, we report the first example of ultrasmall-sized NIR-emitting CdTe QDs with excellent aqueous dispersibility, robust storage, chemical, and photostability, and strong photoluminescence (photoluminescent quantum yield (PLQY): 15–20%). Significantly, the NIR QDs are directly synthesized in aqueous phase through a facile one-step microwave-assisted method (see the Supporting Information for experimental details and mechanisms) by utilizing several attractive properties of microwave irradiation such as prompt startup, easy heat control (on and off), prompt and homogeneous heating, and so forth. More importantly, highly spectrally and spatially resolved bioimaging was possible, and efficient tumor passive targeting in live mice was shown by using the prepared QDs. QDs with different emission wavelengths in the NIR range (lmax= 700–800 nm) can be readily prepared through fine adjustment of the experimental conditions (e.g., reaction time and temperature). Figure 1a,b displays the normalized ultraviolet photoluminescence (UV-PL) spectra for a series of as-prepared QDs with controllable maximum emission wavelength ranging from 700 to 800 nm in aqueous solution. Such QD solutions are transparent under ambient light conditions, suggesting the as-prepared QDs are well-dispersed in aqueous phase without further treatment (Figure 1c). The excellent aqueous dispersibility of the QDs arises from the surfacecovering mercaptopropionic acid (MPA) that acts as a stabilizer because of the presence of negatively charged carboxylic groups. Under UV irradiation the fluorescence of the as-prepared QDs became darker and the emission wavelength gradually shifted out of the visible region (Figure 1d). The transmission electron microscopy (TEM) and highresolution TEM (HRTEM) images reveal that the NIRemitting QDs are spherical particles with good monodispersibility (Figure 2a,b). The existence of a well-resolved crystal lattice in the HRTEM image further confirms the highly crystalline structures of the QDs (Figure 2b inset). Furthermore, the size distribution histogram (Figure 2c), which was determined by measuring more than 250 particles, shows that the average size and standard deviation of the as-prepared NIR-emitting QDs is (3.74 0.67) nm. Comparatively, the [*] Prof. Y. He, Y. L. Zhong, Dr. Y. Y. Su, Y. M. Lu, Z. Y. Jiang, F. Peng, T. T. Xu, Dr. S. Su Institute of Functional Nano & Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University Suzhou, Jiangsu 215123 (China) Fax: (+86)512-6588-2846 E-mail: yaohe@suda.edu.cn

NAC-Capped Quantum Dot as Nuclear Staining Agent for Living Cells via an In Vivo Steering Strategy

We describe a new nuclear staining strategy by in vivo anchoring Hoechst 33342, a commonly used nuclear staining organic dye, onto water-soluble N-acetylcysteine (NAC)-capped CdTe quantum dots (QDs). The strong H-bonding and electrostatic interaction between the organic dye and the QDs entice the positively charged nuclear staining agent in carrying effectively the bright QDs into the nucleus of living cells. Dynamic confocal imaging studies indicated that all visible light emitting NAC-capped QDs with emitting wavelength ranging from 530 to 602 nm can be successfully targeted to the nucleus of the living cells within 30 min. The minimum quantity of Hoechst 33342 as the anchoring agent required in carrying QDs to the nucleus is found to be 5 μg/mL. In essence, a simple, fast, and specific bioimaging of the nucleus in living cells by QDs is accomplished.

A Proposed Method for Thermal Specific Bioimaging and Therapy Technique for Diagnosis and Treatment of Malignant Tumors by Using Magnetic Nanoparticles

The objective of this research program is to develop a novel, noninvasive, low-cost infrared (8–12 μm spectral range) imaging technique that would improve upon current methods using nanostructured core/shell magnetic/noble metal-based imaging and therapies. The biocompatible magnetic nanoparticles are able to produce heat under AC magnetic field. This thermal radiation propagates along the tissue by thermal conduction reaching the medium's (tissue's) surface. The surface temperature distribution is acquired by a thermal camera and can be analyzed to retrieve and reconstruct nanoparticles' temperature and location within the tissue. The technique may function as a diagnostic tool thanks to the ability of specific bioconjugation of these nanoparticles to tumor's outer surface markers. Hence, by applying a magnetic field, we could cause a selective elevation of temperature of the targeted nanoparticles up to 5∘C, which detects the tumor. Furthermore, elevating the temperature over 65∘C and up to 100∘C stimulates a thermo ablating interaction which causes a localized irreversible damage to the cancerous site with no harm to the surrounding tissue. While functioning as a diagnostic tool, this procedure may serve as a targeted therapeutic tool under thermal feedback control as well.