Das Beste aus drei Welten: Ein System bestehend aus Goldnanostäbchen mit Poly(styrol‐alt‐maleinsäure)‐Hülle (siehe Bild; pink), dem Photosensibilisator Indocyaningrün (schwarz) und Antikörpern (grüne „Y“) lässt sich nicht nur für die photodynamische Therapie und als hyperthermisches Reagens zur Zerstörung maligner Zellen einsetzen, sondern wirkt simultan auch als Kontrastfarbstoff zur Bildgebung von Zellen im Nah‐Infrarot.
Developing a nanomaterial, for use in highly efficient dual-modality two-photon photodynamic therapy (PDT) involving reactive oxygen species (ROS) generation and for use as a two-photon imaging contrast probe, is currently desirable. Here, graphene quantum dots (GQDs) doped with nitrogen and functionalized with an amino group (amino-N-GQDs) serving as a photosensitizer in PDT had the superior ability to generate ROS as compared to unmodified GQDs. Multidrug-resistant (MDR) species were completely eliminated at an ultralow energy (239.36 nJ pixel) through only 12 s two-photon excitation (TPE) in the near-infrared region (800 nm). Furthermore, the amino-N-GQDs had an absorption wavelength of approximately 800 nm, quantum yield of 0.33, strong luminescence, an absolute cross section of approximately 54 356 Göeppert-Mayer units, a lifetime of 1.09 ns, a ratio of the radiative to nonradiative decay rates of approximately 0.49, and high two-photon stability under TPE. These favorable properties enabled the amino-N-GQDs to act as a two-photon contrast probe for tracking and localizing analytes through in-depth two-photon imaging in a three-dimensional biological environment and concurrently easily eliminating MDR species through PDT.
Cordyceps militaris (C. militaris) is a fungus with a long history of widespread use in folk medicine, and its biological and medicinal functions are well studied. A crucial pharmacological effect of C. militaris is immunomodulation. In this review, we catalog the immunomodulatory effects of different extracts of C. militaris, namely total extracts, polysaccharides and cordycepin. Total extracts obtained using water or 50% ethyl alcohol and polysaccharides from C. militaris were discovered to tend to promote type 1 immunity, whereas total extracts obtained using 70–80% ethyl alcohol and cordycepin from C. militaris were more likely to promote type 2 immunity. This article is the first to classify the immunomodulatory effects of different extracts of C. militaris. In addition, we discovered a relationship between different segments or extracts and differing types of immunity. This review can provide the readers a comprehensive understanding on the immunomodulatory effects of the precious folk medicine and guidance on its use for both health people and those with an immunodeficiency.
Phototheranostics
has attracted considerable attention in the fields
of cancer diagnosis and treatment. However, the complete eradication
of solid tumors using traditional phototheranostics is difficult because
of the limited depth and range of laser irradiation. New phototheranostics
enabling precise phototherapy and post-treatment imaging-guided programmed
therapy for residual tumors is urgently required. Accordingly, this
study developed a novel transformable phototheranostics by assembling
hyaluronic acid (HA) with copper-nitrogen-coordinated carbon dots
(CDs). In this transformable nanoplatform, named copper-nitrogen-CDs@HA,
the HA component enables the specific targeting of cluster determinant
(CD) 44-overexpressing tumor cells. In the tumor cells, redox glutathione
converts Cu(II) (cupric ions) into Cu(I) (cuprous ions), which confers
the novel transformable functionality to phototheranostics. Both in vitro and in vivo results reveal that
the near-infrared-light-photoactivated CuII-N-CDs@HA could
target CD44-overexpressing tumor cells for precise synergistic photothermal
therapy and photodynamic therapy. This study is the first to observe
that CuII-N-CDs@HA could escape from lysosomes and be transformed in situ into CuI-N-CDs@HA in tumor cells, with
the d9 electronic configuration of Cu(II) changing to the
d10 electronic configuration of Cu(I), which turns on their
fluorescence and turns off their photothermal properties. This transformable
phototheranostics could be used for post-treatment imaging-guided
photodynamic therapy on residual tumor cells. Thus, the rationally
designed copper-nitrogen-coordinated CDs offer a simple in
situ transformation strategy for using multiple-stimulus-responsive
precise phototheranostics in post-treatment monitoring of residual
tumor cells and imaging-guided programmed therapy.
Airway and gut microbiota are important in asthma pathogenesis. Although several studies have revealed distinct microbiota in asthmatic airways at baseline compared to healthy controls, limited studies compared microbiota during acute exacerbation (AE) and in the recovery phase (RP) in the same asthmatic children. We aim to investigate association between microbiota and asthma status in children and explore their relationship with clinical features of asthma. We recruited 56 asthmatic children and investigated their nasal, throat, and stool microbiota during AE and in the RP. Totally, 320 samples were subjected to 16S rRNA sequencing. Although the microbial communities were clearly separated by body site, within each site the overall communities during AE and in the RP could not be distinguished. Most nasal microbiota were dominated by only one or two of six bacterial genera. The domination was associated with mite allergy and patient age only during AE but not in the RP. When moving into RP, the relative abundance of Staphylococcus increased while that of Moraxella decreased. Throat and stool microbiota were not associated with most of the clinical features. Interestingly, stool microbiota during AE was associated with ABO blood type and stool microbiota in the RP was associated with frequency of the subsequent exacerbations. In summary, the association between nasal microbiota and mite allergy only during AE suggests an altered local immunity and its interplay with nasal microbes. Our work provides a basis for studying microbes, and prevention or therapeutic strategy in childhood asthma, especially during AE.
We report that human mesenchymal stem cells (hMSCs) were successfully labeled with poly(lactideco-glycolide) nanoparticles (PLGA NPs) surface-conjugated quantum dots (QDs) (PLGA-QD NPs) via endocytosis pathway. These NPs were not toxicity even treated with PLGA-QD NPs at high concentrations for at least four weeks. Besides, PLGA-QD NPs-labeled hMSCs did not change their proliferation and differentiation capability toward the cell fates of adipocytes, osteocytes, and chrondrocytes. It's known that PLGA has been widely employed to act as delivery carrier which encapsulates drugs and releases them under a controlled way. Currently, we have also demonstrated that FITC-loaded PLGA-QD NPs degraded in hMSCs to achieve intracellular release of FITC. The aim of this research is to investigate viability, proliferation and differentiation capability and the potential for gene delivery of MSCs labeled with PLGA-QD NPs. In addition to PLGA-QD NPs, QDs alone were used to serve as a control set for comparison.
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