The synthesis of well-defined and complex hollow structures via a simple method is still a major challenge. In this work, a facile and controllable "multi-interface transformation" approach for preparation of monodisperse multi-shelled periodic mesoporous organosilica (PMO) hollow spheres has been established by a one-step hydrothermal treatment of successively grown organosilica particles. The multi-shelled PMO hollow spheres have inorganic-organic hybrid frameworks, controllable number (1-4) of shells, high surface area (∼805 m(2)/g), accessible ordered mesochannels (∼3.2 nm), large pore volume (1.0 cm(3)/g), and uniform and tunable diameter (300-550 nm), chamber size (4-54 nm), and shell thickness (10-30 nm). In addition, various organic groups (alkyl, aromatic, and heteroelement fragments) are successfully incorporated into the multi-shelled PMO hollow spheres by successively adding different bridged organosilica precursors. Notably, the distribution of different kinds of organic groups in the multi-shelled PMO hollow spheres can be precisely controlled, showing great potential for future applications. We propose that the formation of the multi-shelled PMO hollow structures is ascribed to the creation of multiple highly cross-linked organosilica interfaces, providing a new and interesting fundamental principle for PMO materials. Due to their unique structure and frameworks, triple-shelled ethane-bridged PMO hollow spheres were successfully loaded with an anti-cancer drug doxorubicin and perfluoropentane gas, which present excellent effects in the killing of cancer cells and ultrasound imaging. It is expected that the multi-interface transformation strategy provides a simple, controllable, versatile, and template-free method for preparation of various multifunctional PMOs for different applications.

Mesoporous solids have been widely used in various biomedical areas such as drug delivery and tumor therapy. Although deformability has been recognized as a prime important characteristic influencing cellular uptake, the synthesis of deformable mesoporous solids is still a great challenge. Herein, deformable thioether-, benzene-, and ethane-bridged hollow periodic mesoporous organosilica (HPMO) nanocapsules have successfully been synthesized for the first time by a preferential etching approach. The prepared HPMO nanocapsules possess uniform diameters (240-310 nm), high surface areas (up to 878 m·g), well-defined mesopores (2.6-3.2 nm), and large pore volumes (0.33-0.75 m·g). Most importantly, the HPMO nanocapsules simultaneously have large hollow cavities (164-270 nm), thin shell thicknesses (20-38 nm), and abundant organic moiety in the shells, which endow a lower Young's modulus (E) of 3.95 MPa than that of solid PMO nanoparticles (251 MPa). The HPMOs with low E are intrinsically flexible and deformable in the solution, which has been well-characterized by liquid cell electron microscopy. More interestingly, it is found that the deformable HPMOs can easily enter into human breast cancer MCF-7 cells via a spherical-to-oval morphology change, resulting in a 26-fold enhancement in cellular uptake (43.1% cells internalized with nanocapsules versus 1.65% cells with solid counterparts). The deformable HPMO nanocapsules were further loaded with anticancer drug doxorubicin (DOX), which shows high killing effects for MCF-7 cells, demonstrating the promise for biomedical applications.

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We demonstrate a self-transformation approach for the synthesis of ordered mesoporous silica hollow spheres with radially oriented mesochannels. The method is simple and facile, in which mesostructured silica spheres synthesized in a Stober solution can spontaneously transform to hollow structure when they are incubated with water. The formation of the hollow structure does not require any sacrificial templates, emulsion droplets, or surface protective agents. The obtained mesoporous silica hollow spheres possess controllable diameter, tunable shell thickness, high specific surface area, and uniform mesopore. Transmission electron microscopy (TEM) observations show that the formation of the hollow spheres undergoes a selective etching process in the inner section. 29 Si NMR spectra and detailed reactions demonstrate that the solid-to-hollow transformation of the Stober silica spheres in water is attributed to the difference in the degree of condensation of silica between their outer layer and inner section. Cytotoxicity and histological assays confirm that the obtained mesoporous silica hollow spheres possess good biocompatibility. Besides, the capability of the hollow spheres as contrast agents for untrasound imaging is conducted in vitro. Moreover, yolk−shell microspheres with a Fe 3 O 4 @ nSiO 2 core and a mesoporous silica shell are successfully prepared based on the facile self-transformation strategy, which provides a general method to create various yolk−shell structured multifunctional composites for different applications.

The prevalence of pterygium in Dali is 39.0% among Chinese Bai aged 50 years and older. Independent associations with increasing age (>59 years), female sex, lack of education, and occupations linked to outdoor work suggest a multifactorial cause of this condition.

Organic functionalization and structural control of mesoporous materials are important for their applications. This study reports here that yolk–shell structured mesoporous nanoparticles with thioether-bridged organosilica frameworks can be successfully prepared by hydrothermal treatment of mesostructured organic–inorganic hybrid nanospheres. The thioether-bridged yolk–shell nanoparticles have ultrahigh condensation degree, i.e., (T3+Q4)/(Q n +T m ) = 94%, large surface area (400 m2 g–1), accessible ordered mesochannels (2.0 nm), large pore volume (0.67 cm3 g–1), and uniform diameter (290–90 nm), core size (180–40 nm), and shell thickness (19–8 nm). Thanks to the abundant thioether groups and the unique structure, the yolk–shell mesoporous nanoparticles can be used as nanoreactors to generate in situ polyhedral gold nanoparticles into their hollow spaces in a hot tetrachloride aurate aqueous solution. The gold loaded yolk–shell nanoparticles show two strong plasmon resonance bands at 577 and 633 nm with excellent photothermal efficiency. This shows a great potential for photothermal treatment. Furthermore, the thioether-bridged yolk–shell mesoporous nanoparticles exhibited excellent capability for convenient covalent connection of near-infrared dyes, which make them promising candidates for applications in cell and tumor imaging.

Mesenchymal stem cells (MSCs) have attracted increasing attention as vehicles for cancer treatment. Herein, MSC-based synergistic oncotherapy strategy is presented for the first time. To achieve this goal, yolk-shell structured gold nanorod embedded hollow periodic mesoporous organosilica nanospheres (GNR@HPMOs) with high paclitaxel (PTX) loading capability and excellent photothermal transfer ability upon near-infrared (NIR) light irradiation are first prepared. Cytotoxicity and migration assays show that the viability and tumor-homing capability of MSCs are well-retained after internalization of high content of PTX loaded GNR@HPMOs (denoted as GNR@HPMOs-PTX). In vitro experiments show the GNR@HPMOs-PTX loaded MSCs (GNR@HPMOs-PTX@MSCs) possess synergistic chemo-photothermal killing effects for breast cancer cells. Also, photoacoustic imaging shows that the MSCs can improve dispersion and distribution in tumor tissue for GNR@HPMOs-PTX after intratumoral injection. In vivo experiments in breast cancer model of nude mice further demonstrate that the GNR@HPMOs-PTX@MSCs significantly inhibit tumor growth, suggesting their great potential for synergistic therapy of cancer.

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