2011
DOI: 10.1021/jp2047147
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Measurement of Uptake and Release Capacities of Mesoporous Silica Nanoparticles Enabled by Nanovalve Gates

Abstract: The uptake and release capacities of mesoporous silica particles are measured on nanovalve-gated stimulated release systems, using a water soluble biological stain, Hoechst 33342, as the cargo model. Five different types of mesoporous silica nanoparticles: 2D-hexagonal MCM-41, swollen pore MCM-41, rod-like MCM-41, hollow mesoporous nanoparticles and radial mesoporous nanoparticles are studied and compared. Solid silica nanoparticles are used as the control. Because of the presence of the nanovalves, the loaded… Show more

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Cited by 54 publications
(50 citation statements)
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“…The uptake and release capacity of the MSNPs 2 loaded with the different fluorescent cargo molecules are summarized in Table 1. The trapped and releasable amounts of the cargo, in agreement with previous release experiments on nanovalve-gated MSNPs, 33 would provide a better control over the delivery process for both in vitro and in vivo applications.…”
Section: Resultssupporting
confidence: 86%
“…The uptake and release capacity of the MSNPs 2 loaded with the different fluorescent cargo molecules are summarized in Table 1. The trapped and releasable amounts of the cargo, in agreement with previous release experiments on nanovalve-gated MSNPs, 33 would provide a better control over the delivery process for both in vitro and in vivo applications.…”
Section: Resultssupporting
confidence: 86%
“…The observed 2% weight of Hoechst is a typical delivery capacity of MSN loaded with Hoechst. 41 Additionally, a 0.2% weight release of cobalt was observed. In terms of molar concentration, this amount is on the order of Hoechst released; 5 mg of gated particles can release ∼0.2 μmols of Hoechst and cobalt, demonstrating that the system is capable of delivering comparable molar quantities of both cargo types (Figure 3b1).…”
Section: Resultsmentioning
confidence: 93%
“…4 To be an effective drug delivery system, MSNs must be able to retain cargo molecules while in storage and in circulation, but capable of delivering their payload upon arriving at its target. A variety of methods have been employed to prepare MSN to meet these criteria; researchers have exploited hydrophobicity as a method of passive cargo retention, 5 and/or engineered nanomachines based on supramolecular nanovalves, 6a–c snap-tops, 6d metal nanocrystals,6 e–f nanoimpellers,6 g supported lipid bilayers,6 h biomolecules,6 i and reversible chelation6 j towards the goal of retaining cargo inside the pores of MSN. These systems have been designed to deliver their payload in response to a variety of stimuli; some of which may already be present inside the cell, or is externally applied in the form of magnetic fields 7 and light.…”
Section: Introductionmentioning
confidence: 99%