2019
DOI: 10.1016/j.msec.2019.109831
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Co-responsive smart cyclodextrin-gated mesoporous silica nanoparticles with ligand-receptor engagement for anti-cancer treatment

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Cited by 47 publications
(33 citation statements)
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“…The obtained formulation demonstrated improved internalization ability and increased accumulation capacity in these cancer cells both in vitro and in vivo. The authors of [225] immobilized β-CD in combination with azobenzene/galactose-grafted polymer (GAP) on the surface of mesoporous silica nanoparticles. The latter is a well-known ligand for targeting asialoglycoprotein receptors of HepG2 cells and controllable release of encapsulated cargo.…”
Section: Mesoporous Silica Nanoparticles Modified By Synthetic Polymersmentioning
confidence: 99%
“…The obtained formulation demonstrated improved internalization ability and increased accumulation capacity in these cancer cells both in vitro and in vivo. The authors of [225] immobilized β-CD in combination with azobenzene/galactose-grafted polymer (GAP) on the surface of mesoporous silica nanoparticles. The latter is a well-known ligand for targeting asialoglycoprotein receptors of HepG2 cells and controllable release of encapsulated cargo.…”
Section: Mesoporous Silica Nanoparticles Modified By Synthetic Polymersmentioning
confidence: 99%
“…As a main contributor of redox status in cells, GSH plays a critical role in cellular activities. Disulfide bonds [54][55][56], ferrocene [57], boronic ester [58], and tetrathiafulvalene [50] are considered as promising tools for designing redox-responsive nanocarriers. These structures are highly stable in the extracellular environment with a low level of GSH, while they tend to breakdown in reductive environments.…”
Section: Redox Potentialmentioning
confidence: 99%
“…To improve the efficiency and precision of drug delivery, dual responsive nanoplatforms have been built [58,121,122]. For instance, β-cyclodextrin and azobenzene/galactosegrafted polymer were introduced for the fabrication and functionalization of mesoporous silica nanoparticles to impart both light and redox sensitivity for preventing leakage of the payload and for increasing the chemotherapeutic performance of DOX [54]. Upon UV radiation, azobenzene moieties were dissociated from the surface, which caused the release of DOX.…”
Section: Multi-responsive Systemmentioning
confidence: 99%
“…These biomolecules have also been explored as targeting agents owing to their ability to interact in a very specific manner with overexpressed lectin proteins present on the cell membrane. For instance, the asialoglycoprotein receptor can be targeted using MSNs functionalized with galactose [149] or lactobionic acid [150][151][152][153]. In addition, the conjugation of glucose derivatives with MSNs are useful for targeting overexpressed GLUT receptors [154,155].…”
Section: Carbohydratesmentioning
confidence: 99%
“…In this manner, enhanced drug release can be observed when MSNs reach the cytoplasm and GSH completely removes the β-CD caps [325,326]. A nice feature of β-CDs is that not only they serve as gatekeeper, but also provide possibilities for further functionalization, including PEGylation [327] and grafting of targeting agents [149,201,328,329].…”
Section: Small Nanoparticles and Nanovalvesmentioning
confidence: 99%