Developing photothermal-responsive and anti-oxidative silk/dopamine nanoparticles decorated with drugs which were incorporated into silk films as a depot-based drug delivery
“…Silk cocoons were provided by a silk center, MDARES (Miaoli Agricultural Research and Extension Station, Council of Agriculture, Executive Yuan, Miaoli, Taiwan). A solution of SF (MW~185 kDa) was prepared as described in a previous study by the authors [7,25] and involved degumming in 9.3 M LiBr and removal of Li + using dialysis with deionized (DI) water. In brief, silk cocoons were boiled in 0.02 M Na 2 CO 3 for 90 min and then rinsed thoroughly in DI water to extract the glue-like sericin proteins from silk fibroin.…”
Section: Preparing Sf Solutionsmentioning
confidence: 99%
“…The extracted SFs were dissolved in 9.3 M LiBr solution at 75 • C for 1 h and then dialyzed in DI water using a dialysis membrane (MWCO 6000) (Spectra/Por1, Repligen Co., Waltham, MA, USA) at room temperature for 48 h to remove salts. The final concentration of the SF aqueous solution was 20% (w/v) [7,25].…”
Section: Preparing Sf Solutionsmentioning
confidence: 99%
“…The particle size and zeta potentials of the SF/NAC NPs were measured using a dynamic light scattering particle size/zeta potential analyzer (Particulate Systems NanoPlus, Norcross, GA, USA). The SF/NAC NPs were suspended at a concentration of 0.05 mg/mL in DI water for further measurements [7,26]. The morphological images of SF/NAC NPs were carried out by a transmission electron microscopy (TEM) with an accelerating voltage of 100 kV (JEOL JEM-2000EX II, Tokyo, Japan) after they were stained with 2% (w/v) phosphotungstic acid and placed on copper grids [7,26].…”
Section: Characteristics Of Sf and Sf/nac Npsmentioning
confidence: 99%
“…Sericin-free SF has a low immune-inflammatory response and excellent biological response [2], so it is a suitable biomaterial for engineering various tissues, such as cardiac patches, hydrogels and scaffolds, refs. [3][4][5] and drug delivery in varying forms (e.g., NPs or hydrogels) or with multifunctional properties such as photothermal responses [6][7][8]. The SF polymer also contains several hydrophilic and hydrophobic segments, and the crystallinity of the polymer is easily modulated, so it is a suitable biomaterial for drug delivery vehicles [9,10].…”
Using nasal routes to deliver drugs to the brain using multifunctional nanoparticles (NPs) to bypass the blood–brain barrier (BBB) might enhance the delivery efficacy. Anti-oxidative N-Acetyl-L-cysteine (NAC)-loaded silk fibroin (SF/NAC) NPs are produced, characterized and studied as a potential delivery vehicle for NAC delivered to the brain via nasal for both in vitro and in vivo studies. The NPs are not cytotoxic to RPMI 2650 cells, mucosal model cells, at a concentration of 6000 μg/mL. The anti-oxidative activities of SF/NAC NPs are demonstrated by high H2O2 scavenge capacities of the NPs and shown by mitochondrial superoxide (MitoSOX) immunostaining of human mesenchymal stem cells. Tight junctions in RPMI 2650 cells are opened after 30 min of incubation with SF/NAC NPs, which are demonstrated by measuring the decrease in trans-epithelial electrical resistance (TEER) values and discreteness in ZO-1 stains. The cellular uptake of SF/NAC NPs by RPMI 2650 cells is significantly greater than that for SF NPs and increased with increasing incubation time. In an in vivo imaging study (IVIS) using rats shows that the amount of NAC that is delivered to the brain by SF/NAC NPs increased by 1.40–2.60 times and NAC is retained longer in the nasal cavity than NAC solutions in a 2-h study.
“…Silk cocoons were provided by a silk center, MDARES (Miaoli Agricultural Research and Extension Station, Council of Agriculture, Executive Yuan, Miaoli, Taiwan). A solution of SF (MW~185 kDa) was prepared as described in a previous study by the authors [7,25] and involved degumming in 9.3 M LiBr and removal of Li + using dialysis with deionized (DI) water. In brief, silk cocoons were boiled in 0.02 M Na 2 CO 3 for 90 min and then rinsed thoroughly in DI water to extract the glue-like sericin proteins from silk fibroin.…”
Section: Preparing Sf Solutionsmentioning
confidence: 99%
“…The extracted SFs were dissolved in 9.3 M LiBr solution at 75 • C for 1 h and then dialyzed in DI water using a dialysis membrane (MWCO 6000) (Spectra/Por1, Repligen Co., Waltham, MA, USA) at room temperature for 48 h to remove salts. The final concentration of the SF aqueous solution was 20% (w/v) [7,25].…”
Section: Preparing Sf Solutionsmentioning
confidence: 99%
“…The particle size and zeta potentials of the SF/NAC NPs were measured using a dynamic light scattering particle size/zeta potential analyzer (Particulate Systems NanoPlus, Norcross, GA, USA). The SF/NAC NPs were suspended at a concentration of 0.05 mg/mL in DI water for further measurements [7,26]. The morphological images of SF/NAC NPs were carried out by a transmission electron microscopy (TEM) with an accelerating voltage of 100 kV (JEOL JEM-2000EX II, Tokyo, Japan) after they were stained with 2% (w/v) phosphotungstic acid and placed on copper grids [7,26].…”
Section: Characteristics Of Sf and Sf/nac Npsmentioning
confidence: 99%
“…Sericin-free SF has a low immune-inflammatory response and excellent biological response [2], so it is a suitable biomaterial for engineering various tissues, such as cardiac patches, hydrogels and scaffolds, refs. [3][4][5] and drug delivery in varying forms (e.g., NPs or hydrogels) or with multifunctional properties such as photothermal responses [6][7][8]. The SF polymer also contains several hydrophilic and hydrophobic segments, and the crystallinity of the polymer is easily modulated, so it is a suitable biomaterial for drug delivery vehicles [9,10].…”
Using nasal routes to deliver drugs to the brain using multifunctional nanoparticles (NPs) to bypass the blood–brain barrier (BBB) might enhance the delivery efficacy. Anti-oxidative N-Acetyl-L-cysteine (NAC)-loaded silk fibroin (SF/NAC) NPs are produced, characterized and studied as a potential delivery vehicle for NAC delivered to the brain via nasal for both in vitro and in vivo studies. The NPs are not cytotoxic to RPMI 2650 cells, mucosal model cells, at a concentration of 6000 μg/mL. The anti-oxidative activities of SF/NAC NPs are demonstrated by high H2O2 scavenge capacities of the NPs and shown by mitochondrial superoxide (MitoSOX) immunostaining of human mesenchymal stem cells. Tight junctions in RPMI 2650 cells are opened after 30 min of incubation with SF/NAC NPs, which are demonstrated by measuring the decrease in trans-epithelial electrical resistance (TEER) values and discreteness in ZO-1 stains. The cellular uptake of SF/NAC NPs by RPMI 2650 cells is significantly greater than that for SF NPs and increased with increasing incubation time. In an in vivo imaging study (IVIS) using rats shows that the amount of NAC that is delivered to the brain by SF/NAC NPs increased by 1.40–2.60 times and NAC is retained longer in the nasal cavity than NAC solutions in a 2-h study.
“…Curcumin is a nontoxic, very promising natural chemical with antiinflammatory [4], hepato-and nephroprotective [5,6], antioxidant, antibacterial, anticarcinogenic [7], and thrombosis-suppressing activities [8]. Curcumin comes from the root of the Curcuma longa Linn plant (family Zingiberaceae).…”
The metabolic syndrome, which includes obesity, insulin resistance, dyslipidemia, and hypertension, has gained importance due to its link to the development of cardiovascular disease and type 2 diabetes.
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