Multiple cell plasma membranes have been utilized for surface functionalization of synthetic nanomaterials and construction of biomimetic drug delivery systems for cancer treatment. The natural characters and facile isolation of original cells facilitate the biomedical applications of plasma membranes in functionalizing nanocarriers. Human umbilical cord-derived mesenchymal stem cells (MSCs) have been identified to show tropism toward malignant lesions and have great advantages in ease of acquisition, low immunogenicity, and high proliferative ability. Here, we developed a poly(lactic- co-glycolic acid) (PLGA) nanoparticle with a layer of plasma membrane from umbilical cord MSC coating on the surface for tumor-targeted delivery of chemotherapy. Functionalization of MSC plasma membrane significantly enhanced the cellular uptake efficiency of PLGA nanoparticles, the tumor cell killing efficacy of PLGA-encapsulated doxorubicin, and most importantly the tumor-targeting and accumulation of the nanoparticles. As a result, this MSC-mimicking nanoformulation led to remarkable tumor growth inhibition and induced obvious apoptosis within tumor lesions. This study for the first time demonstrated the great potential of umbilical cord MSC plasma membranes in functionalizing nanocarriers with inherent tumor-homing features and the high feasibility of such biomimetic nanoformulations in cancer therapy.
Thermally induced domain wall motion in a magnetic insulator was observed using spatiotemporally resolved polar magneto-optical Kerr effect microscopy. The following results were found: (i) the domain wall moves towards hot regime; (ii) a threshold temperature gradient (5 K/mm), i.e., a minimal temperature gradient required to induce domain wall motion; (iii) a finite domain wall velocity outside of the region with a temperature gradient, slowly decreasing as a function of distance, which is interpreted to result from the penetration of a magnonic current into the constant temperature region; and (iv) a linear dependence of the average domain wall velocity on temperature gradient, beyond a threshold thermal bias. Our observations can be qualitatively explained using a magnonic spin transfer torque mechanism, which suggests the utility of magnonic spin transfer torque for controlling magnetization dynamics.
In this work, large-scale three-dimensional "flake-ball" microarchitectures of Eu(3+) doped white light hydroxyl sodium yttrium tungstate were prepared by the well-known hydrothermal approach at 180 degrees C for 48 h in the presence of triblock-copolymer poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) (P123). NaY(WO(4))(2):Eu(3+) phosphor was formed by annealing the hydrothermal product at approximately 630 degrees C for 2 h. A time-dependent microstructure evolution study was performed under hydrothermal reaction. The evolution process is the self-assembly process of P123, and the effects of other reaction parameters, such as influence of the concentration of P123 on morphology, and the influence of temperature on PL. The mechanism by which the "flake-ball" particles are formed is discussed in detail. The PL spectra of Eu(3+)-doped hydroxyl sodium yttrium tungstate phosphor contain two parts: the broad blue-green band and the (5)D(0)-->(7)F(J) (J = 1, and 2) characteristic transition of Eu(3+). This approach provides a facile route for the production of high-quality hydroxyl sodium yttrium tungstate microstructures with an interesting optical property.
Introduction. The equiatomic rare-earth aluminium silicides and germanides have been studied by Yanson (1975), who reported the" a-ThSi2 type for the large rare-earth elements and a new type, the so-called DyA1Ge type, for small rare-earth elements. However, the R--A1 distances for compounds with the 'DyA1Ge type' show unreasonably short values. This gave us an incentive for a reinvestigation of the structures of the RA1Ge compounds.
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