2016
DOI: 10.1007/s11434-016-1056-4
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Nanoparticle-based oral delivery systems for colon targeting: principles and design strategies

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Cited by 57 publications
(28 citation statements)
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“…Various carriers based on synthesized NPs (e.g., lipid, chitosan, polymer and silica NPs) have been designed to release the loaded drug at a specific pH value to resist digestive enzymes, and/or to require bacterial cleavage for activation. Several of these carriers are currently being investigated for clinical use [8]. We recently demonstrated that artificially synthesized NPs can deliver low doses of drugs, proteins, or siRNA to specific cell types and tissues, decreasing the systemic side effects of medications in IBD therapy [9].…”
Section: Nanoparticle Drug Delivery Systems In Ibdmentioning
confidence: 99%
“…Various carriers based on synthesized NPs (e.g., lipid, chitosan, polymer and silica NPs) have been designed to release the loaded drug at a specific pH value to resist digestive enzymes, and/or to require bacterial cleavage for activation. Several of these carriers are currently being investigated for clinical use [8]. We recently demonstrated that artificially synthesized NPs can deliver low doses of drugs, proteins, or siRNA to specific cell types and tissues, decreasing the systemic side effects of medications in IBD therapy [9].…”
Section: Nanoparticle Drug Delivery Systems In Ibdmentioning
confidence: 99%
“…There are also polyester systems containing a reductively labile azo group. These polyesters containing the azo linkages can be used in colon-specific therapy [93,94,95]. Most precisely, the aromatic poly(ether-ester) has been synthetized by classical polycondensation of 4-[(4-hydroxyphenyl)azo]benzoic acid and its derivatives.…”
Section: Polyesters With Stimuli-sensitive Linkagesmentioning
confidence: 99%
“…Furthermore, surface modification of the NP can facilitate its specific cell-targeting functions, enabling nano-drugs to exhibit controlled release at the site of inflamed cells and minimizing systemic toxicity. 25 The published studies have largely focused on treating IBD with mechanism-driven DDSs (including size-, charge-, pH-, pressure-, enzymatic hydrolysis-, degradation-, ligandreceptor-, and microbiome-dependent) and synthetic NPmediated DDSs (including amphiphilic prodrugs, hydrogels, mesoporous silica, and solid lipid NPs), and such applications have been extensively reviewed. 14,21,24,25 This review will touch only lightly on these topics, instead focusing on deliverable targets in IBD treatment, including the intestinal epithelium and mucus, immune cells, the lamina propria, the extracellular matrix (ECM), and the microbiota (a newly emerged target).…”
Section: Introductionmentioning
confidence: 99%