2014
DOI: 10.1002/adma.201400136
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Facile Synthesis of Yolk–Shell Structured Inorganic–Organic Hybrid Spheres with Ordered Radial Mesochannels

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Cited by 185 publications
(160 citation statements)
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“…The Fourier transform infrared (FT‐IR) spectra of the PB, PB@PMO, and PB@PMO‐Ce6 display a vibration peak at 2070 cm −1 , which is assigned the CN groups of PB. The PB@PMO and PB@PMO‐Ce6 also show the Si—O—Si vibration peak at 1050 cm −1 , C—S band at 650 cm −1 , and C—H band at 2900 cm −1 ,21, 30 confirming that the PB nanoparticles are successfully coated with PMO shells. The C=O vibration peak at 1700 cm −1 in PB@PMO‐Ce6 further indicates successful Ce6 conjugation (Figure 1f) 31, 32, 33.…”
Section: Resultsmentioning
confidence: 67%
“…The Fourier transform infrared (FT‐IR) spectra of the PB, PB@PMO, and PB@PMO‐Ce6 display a vibration peak at 2070 cm −1 , which is assigned the CN groups of PB. The PB@PMO and PB@PMO‐Ce6 also show the Si—O—Si vibration peak at 1050 cm −1 , C—S band at 650 cm −1 , and C—H band at 2900 cm −1 ,21, 30 confirming that the PB nanoparticles are successfully coated with PMO shells. The C=O vibration peak at 1700 cm −1 in PB@PMO‐Ce6 further indicates successful Ce6 conjugation (Figure 1f) 31, 32, 33.…”
Section: Resultsmentioning
confidence: 67%
“…However, pure PB nanoparticles cannot deliver drug for cancer chemotherapy because of their small micropores and limited loading capacity. Periodic mesoporous organosilicas (PMOs) synthesized via surfactant‐directed sol–gel process has been used for drug delivery because of their uniform and large mesopore size, high surface area, organic groups incorporated frameworks, and excellent biodegradation and biocompatibility 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43. Based on the unique features, we presumed that an imaging‐guided combination therapy strategy can be developed by intergating the advantages of PMO and PB.…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, the incorporation of organic groups into the MON framework can substantially reduce the surface-exposed silanol groups, fortunately leading to extremely low hemolytic effects of MONs against red blood cells (RBCs). Ethenylene-bridged MONs, [ 132 ] ethane-bridged yolk-shell MONs, [ 131 ] and phenylene-bridged HMONs [ 66 ] have all exhibited an extremely low hemolytic percentage against RBCs even at a co-incubation concentration as high as 2000 µg mL −1 (Figure 12 a 3 ) attributed to the same reason regarding the reduction of silanol groups. [215][216][217] In contrast, the organic-inorganic hybrid composition of MONs can also lead to enhanced biodegradability of silica in the presence of a high content (ca.…”
Section: Reviewmentioning
confidence: 98%
“…Reproduced with permission. [ 131 ] Copyright 2014, Wiley-VCH. e) UCNP@MONs yolk-shell NPs ( R = ethane).…”
Section: Structure/morphology Control Of Monsmentioning
confidence: 99%
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