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35 protocols using curcumin cur

1

Glycol Chitosan-Based Curcumin Delivery System

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Glycol chitosan (GC, ≥60% (by titration), crystalline, Mw ≅ 585,000 g/mol), glycidyl methacrylate (GM), and curcumin (CUR) were purchased from Sigma-Aldrich (St. Louis, MO, USA). 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) was obtained from Wako Pure Chemical Industries, Ltd. (Osaka, Japan). Dialysis tubing (Spectrum Laboratories Inc., Rancho Dominguez, CA, USA) was used for purification. The mouse L-929 fibroblast cell line was supplied by Korean Cell Line Bank (Seoul, Korea). All the chemicals were used as received without further purification.
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2

Curcumin-Encapsulated Biomaterial Evaluation

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Fetal bovine serum (FBS), Dulbecco’s phosphate buffered saline (PBS), Dulbecco’s modified Eagle’s medium (DMEM), penicillin/streptomycin, and trypsin were obtained from Gibco (Carlsbad, CA, USA), Fetal bovine serum (FBS) and curcumin (CUR) were obtained from Sigma-Aldrich, Australia. Thiazolyl Blue Tetrazolium Bromide (MTT), dimethylsulfoxide (DMSO), PEG, alginate (ALG), and collagen (COL) were purchased from Sigma (Sigma–Aldrich, St. Louis, MO, USA). All other materials utilized in this study were from domestic providers at analytical grade.
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3

Cell Proliferation Evaluation by MTT Assay

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Cell proliferation was evaluated in TUBO and SALTO cells by 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay (Sigma-Aldrich, MO, USA). Briefly, 5 × 103 cells/well were plated in 96-well plates in 100 µL of complete medium. The day after, cells were treated singly or in combination with curcumin (CUR) (15 µM) (Sigma-Aldrich, MO, USA) and resveratrol (RES) (15 µM) (Sigma-Aldrich, MO, USA) for 48 h. Untreated cells were used as control (CT). The MTT assay was performed following manufacturer’s instruction. The plates were analyzed with Absorbance 96 (Byonoy, Germany). The experiments were performed in triplicate and repeated three times.
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4

Bioactive Curcumin-Loaded Polymer Scaffolds

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Poly(ε-caprolactone) (PCL molecular weight of 80,000 Da) was purchased from Sigma Aldrich while poly (l-lactide-co-d,l-lactide) (PLA 4032 D-Mw = 160,000 g/mol) was purchased from NatureWorks (Minnetonka, MN, USA). Tetrahydrofuran (THF pure-CAS: 109-99-9), Ethanol (EtOH purity > 96%-CAS 64-17-5) and Phosphate Buffer Solution (PBS-pH = 7 ± 0.02-CAS: 7558-79-4) were purchased from Carlo Erba Reagents (Cornaredo-Milano). N,N-Dimethylformamide (DMF-CAS 68-12-2) and Curcumin (Cur) were purchased from Sigma Aldrich (Milan, Italy). Cell Counting Kit-8 (CCK-8) assay and Lactate dehydrogenase assay were from Roche Applied Science (Milan, Italy). Human dermal fibroblasts were purchased from the American Type Culture Collection ATCC (LGC Standards S.R.L., Sesto San Giovanni, Milan, Italy) and cultured in accordance with the manufacturer’s instructions. Fetal bovine serum (FBS), Dulbecco’s Modified Eagle’s Medium (DMEM), sodium pyruvate, L-glutamine, penicillin, and streptomycin were purchased from Hyclone (Milan, Italy).
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5

Nanomedicine Formulation Development

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1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000] (PEG2000–PE) was purchased from Corden Pharma International (Plankstadt, Germany). Curcumin (CUR) was purchased from Sigma (St. Louis, MO, USA catalog #C7727). Paclitaxel was purchased from LC laboratories (Woburn, MA catalog #P-9600). Vitamin E (>96% catalogue #T3251) was purchased from Sigma (St. Louis, MO, USA). Matrigel™ basement membrane matrix was purchased from BD Biosciences (Bedford, MA). CellTiter-blue® was purchased from Promega (Madison, WI). All buffer solution components were analytical grade preparations and deionized reverse osmosis treated water was used in all the experiments. All the organic solvents were HPLC grade.
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6

Curcumin Pretreatment of OM-MSCs

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Curcumin (CUR) was purchased from Sigma-Aldrich (St. Louis, MO, USA), prepared in DMSO, and stored at −20 °C. The OM-MSCs were pretreated with CUR at a final concentration of 10 μM in 10% FBS-containing culture medium for 24 h.
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7

Pretreatment Conditions for Cell Assays

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Zebularine (Zeb) (Sigma, USA) and trichostatin A (TSA) (Sigma, USA) were dissolved and further diluted in dimethyl sulfoxide (DMSO) (Sigma, USA). Recombinant human TRAIL/TNFSF10 protein (TRAIL) (375-TL-010, R&D System) was dissolved in the 1X phosphate buffered saline (PBS) and 0.1% bovine serum albumin (BSA). Curcumin (Cur) (Sigma, USA) was dissolved in the absolute ethanol and further diluted with Dulbecco's Modified Eagle Medium (DMEM) (Cellgro, USA). Doxorubicin (Dox) (D1515, Sigma) was dissolved in sterile water.
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8

ANIT and Curcumin Pharmacological Evaluation

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Alpha-naphthylisothiocyanate (ANIT) and curcumin (CUR) were obtained from Sigma-Aldrich (Sigma-Aldrich, USA). All the bile acid standards were purchased from Sigma-Aldrich as well. Danning tablet used in this study were produced by Shanghai Huchison Pharmaceuticals Co. Ltd (batch No. Z10910040). Ammonium acetate, formic acid, acetonitrile and methanol (HPLC grade) were purchased from Fisher Scientific (Nepean, Ont, Canada). Ultrapure water was prepared by a Milli-Q50 SP Reagent Water System (Millipore Corporation, MA, USA) for the preparation of samples and buffer solutions.
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9

Lipid-based Nanocarrier Formulation Development

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L-α-Phosphatidylcholine (egg yolk, ~60%, confirmed by thin layer-chromatography (TLC)) and sodium cholate hydrate (≥97%; dried material) were purchased from Sigma-Aldrich. Cholesterol was provided by CRODA Inc. (East Yorkshire, England). Poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) Pluronic® P-123 (average Mn ~5800) employed as a polymer for nanocarriers stabilization, was acquired from Sigma-Aldrich (Poznań, Poland). Methylene Blue (MB) Injection (1%; Akorn, Inc., Lake Forest, IL, USA) and curcumin (CUR) (Sigma-Aldrich, Poznań, Poland) were used as active model compounds. Chloroform and tetrahydrofuran (THF) was supplied by Avantor Performance Materials Poland S.A. (formerly POCH S.A., Gliwice, Poland). Distilled water was used for all experiments. All the above-mentioned chemicals were of commercial grade and were applied as received.
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10

Preparation and Storage of Photosensitizers and Chemotherapeutics

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All drugs and photosensitizers were prepared and stored protected from light.
Photogem (PG; Photogem LLC. Co., Moscow, Russia) and Methylene blue (MB; Sigma Co., St. Louis, USA) were dissolved in PBS and stored at −20 °C. Cisplatin (CisPT) was obtained as a 0.5 mg/mL solution (Tecnoplatin, Zodiac Produtos Farmaceuticos S/A, Brazil), stored at room temperature. Curcumin (CUR; Sigma Co., St. Louis, USA) was solubilized in dimethyl sulfoxide (DMSO) and stored at −20 °C. All drugs above were diluted to working concentrations prior to use. Doxorubicin (DOX) was obtained as doxorubicin hydrochloride powder (Cloridrato de doxorrubicina, Eurofarma, Brazil) and solutions were prepared in sterile distilled water immediately prior to use.
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