2015
DOI: 10.1039/c5ra16004a
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pH- and glutathione-responsive release of curcumin from mesoporous silica nanoparticles coated using tannic acid–Fe(iii) complex

Abstract: A novel pH- and glutathione-responsive drug delivery system has been developed by deposition of tannic acid (TA)–Fe(iii) complex on the surface of mesoporous silica nanoparticles (MSN).

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Cited by 77 publications
(38 citation statements)
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“…The average particle size of MCM‐41 is 263.4 nm. Based on data, these results demonstrate that textural properties for MCM‐41 are agreement with previous published results …”
Section: Resultssupporting
confidence: 92%
“…The average particle size of MCM‐41 is 263.4 nm. Based on data, these results demonstrate that textural properties for MCM‐41 are agreement with previous published results …”
Section: Resultssupporting
confidence: 92%
“…Furthermore the zeta potential of the Curc-MSNP decreased from -23.9 ± 0.4 mV to -16.9 ± 0.9 mV (P ≤ 0.01) ( Figure 6B). This increase in particle size and PDI has been previously reported after loading curcumin in their mesoporous nanoparticles 51,79 . Furthermore the decrease in zeta potential following loading has previously been reported, however the polarity of the resultant charge is a function of the pH of the media that the zeta potential is measured in, with reports that a lower pH media often leads to more positive zeta potential with loading [82][83][84][85] .…”
Section: Phytochemical Loading Into Msnpsupporting
confidence: 82%
“…Furthermore, mesoporous silica nanoparticles have recently been used to demonstrate loading and release of curcumin 51 .…”
Section: Introductionmentioning
confidence: 99%
“…Owing to their unique advantages including well-defined morphology, uniform size, controllable structure, super high specific pore volume, tunable pore size, easily modified surface, high drug-loading capacity, and excellent biocompatibility, mesoporous silica nanoparticles (MSNs) have attracted increasing interest in biomedical applications in the recent decades, especially in controlled drug delivery system (Berger et al, 2016;Chen et al, 2013a;Chen et al, 2014;Chen et al, 2013b;Chin et al, 2014;Ge et al, 2015;Jia et al, 2015;Kim et al, 2015;Knežević et al, 2013;Li et al, 2011;Mamaeva et al, 2013;Niu et al, 2014;Tang and Cheng, 2013;Tao, 2014;von Haartman et al, 2013;. However, the simplex structure of MSNs is barely able to meet the demands of drug release in complicated in vivo environment.…”
Section: Introductionmentioning
confidence: 99%