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16 protocols using ibuprofen

1

Measuring Thermodynamic Ibuprofen Solubility

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The thermodynamic solubility of ibuprofen was determined by the shake-flask method (25 RPM), incubating gastrointestinal fluids for 24 h with an excess amount of ibuprofen (Acros Organics, Morris Plains, NJ, USA) at 37 °C. The fluids that were used for measuring the thermodynamic solubility of ibuprofen were aspirated gastric, duodenal and jejunal fluids of three different time points of subject B005-F2. Following the 24 h incubation, samples were centrifuged for 15 min at 17,000 g (AccuSpin Micro 17, Fisher Scientific, Pittsburgh, PA, USA). The supernatant was diluted 10-fold with methanol (Fisher Scientific, Pittsburgh, PA, USA) and again centrifuged for 5 min in order to discard any proteins that could interfere with the HPLC analysis (see below). Solubility measurements were performed in triplicate.
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2

Ibuprofen-Loaded Alginate Microbeads for Controlled Drug Release

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Sodium alginate (≈39% in guluronic acid blocks, Mw ≈ 100 kDa), Span 80 (sorbitan monooleate), Tween 80 (polysorbate), isopropyl myristate (≥98%), calcium chloride (CaCl2), sodium chloride (NaCl), Nile red, vitamin E (α‐tocopherol, ≥ 99.5%), corn oil, poly(ethylene glycol) diacrylate (PEGDA, Mn = 700 g mol−1), silicone oil, and photoinitiator 2‐hydroxy‐2‐methyl‐1‐phenyl‐propan‐1‐one (Darocur 1173) were purchased from Sigma–Aldrich. Ibuprofen (99%, ACROS Organics) was purchased from Fisher Scientific to be used as an API. Sucrose (ultrapure) was purchased from VWR Life Science.
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3

Synthesis and Characterization of Iron-Based Metal-Organic Frameworks

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All
chemicals were reagent
grade or better and used as received, included: iron(III) chloride
(hexahydrate, 99 + %, Acros), terephthalic acid (TA, 99 + %, Acros), N,N-dimethylformamide (Fisher Chemical,
ACS Certified), sodium hydroxide (2.0 N Standardized Solution, Alfa
Aesar), hexanes (Fisher Chemical, ACS Certified), ibuprofen (99%,
Acros), phosphate-buffered saline (PBS, pH = 7.2, 1×, Gibco),
trifluoroacetic acid (HPLC Grade, Acros), Milli-Q water (18 MΩ·
cm, Millipore), and acetonitrile (HPLC Grade, Fisher Chemical).
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4

Cyclodextrin-Ibuprofen Formulation Development

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Ibuprofen (racemic mixture, sodium salt), sodium hydroxide and potassium dihydrogen phosphate were purchased from Acros Organics. β-CD, HPβ-CD (with a mean of 5.6 substitutions per cyclodextrin) were purchased from Wacker Chemie (Lyon, France). The water content (10% for β-CD, 6% for HPβ-CD) has been taken into account when preparing solutions. All products were of analytical grade and used as received. Distilled deionized water was used throughout this work.
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5

Analytical-Grade Chemicals for Research

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Bisphenol A, 4-chlorocatechol
(97%), 4-chlororesorcinol (98%), chloro-p-benzoquinone
(95%), and 4-isobutylacetophenone were purchased from Sigma-Aldrich.
Ibuprofen (99%), 2,4-dichlorophenol (99%), 4-ethylbenzadehyde (98%),
resorcinol (98%), chlorohydroquinone (90%), catechol (99%), and benzoqinone
(99%) were supplied by Acros. Triclosan (99.7%) was from Calbiochem,
and hydroquinone was from Fischer Scientific. Deionized (DI) water
(18.0 mΩ cm) obtained from a Millipore Milli-Q system was used
in all the experiments. All chemicals used in this study were above
analytical grade.
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6

Synthesis of Dextran-Ibuprofen Conjugates

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First, 0.5 g (2.42 mmol) ibuprofen[2-(4-isobutylphenyl) propanoic acid), Acros Organics Company, the United States] were added to a 5 mL Dimethyl sulfoxide (DMSO, Gibco company, the United States), then, 0.43 g (2.66 mmol) of N, N’-carbonyldiimidazole (Shanghai Sigma-Aldrich Company, China) were added to the solution and the reaction mixture was stirred at room temperature for 1 hour. 0.5 g (3.1 mmol, the fructose unit) of Dextran (Shanghai Alladin Reagent Company, China) was subsequently added to the mixture and the reaction was allowed to react for 24 hours at 80 °C under stirring. The resultant solution was precipitated into 100 mL cold water. The precipitates were filtered out, washed several times with water and dried under vacuum to obtain Dextran-ibprofen conjugates.
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7

Synthesis and Characterization of Organic Compounds

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Aspirin (ASP), ibuprofen (IBU), nicotinamide (NC), isonicotinamide (INC), isoniazid (INZ), and methyl nicotinate (MN) were bought from Acros (Geel, Belgium). 3,4-diaminopyridine (AMI) was acquired from Sigma-Aldrich (St. Louis, MO, USA), 4-aminobenzoic acid (PABA) from Alfa Aesar (Haverhill, MA, USA), and zinc oxide from Merck (Kenilworth, NJ, USA). All the solvents and reagents were used as received without further treatment.
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8

FeOCl Nanocatalyst for Fenton-like Treatment

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FeCl3•6H2O (Honeywell Fluka) was used to synthesize the FeOCl nanocatalyst, and H2O2 was purchased from Fisher Scientific. γ-Al2O3 (Alfa Aesar) was used as a support to immobilize FeOCl. BPA (Sigma-Aldrich), ibuprofen (Alfa Aesar), atrazine (Sigma-Aldrich), carbamazepine (Sigma-Aldrich), 4-chlorophenol (Acros Organics), 4-nitrophenol (Acros Organics), rhodamine B (Harleco), reactive blue 19 (Sigma-Aldrich), and orange II (Acros Organics) were used as substrates for the Fenton-like process treatment. Other chemicals (i.e., sodium sulfate [Na2SO4] as the supporting electrolyte, sodium carbonate [Na2CO3] for synthetic alkaline water, ethanol as a HO radical scavenger, and methanol and acetonitrile as the mobile phase for high-performance liquid chromatography [HPLC]) were purchased from Fisher Scientific. Pure water was used throughout the work, except in the field water studies.
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9

Pluronic-Based Ibuprofen Formulations

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Pluronics L92 and F108 were purchased from Sigma-Aldrich, and Pluronics F98, F88, F68, F87, and P84 were purchased from BASF Corporation. All these Pluronics were used as received without further purification. Their physicochemical and molecular characteristics are described in Table 1 and the molecular structure of Pluronic is schematically illustrated in Figure 1a. The drug α-methyl-4-(isobutyl) phenylacetic acid, known as ibuprofen, was bought from Alfa-Aesar and used as received. The molecular structure of ibuprofen is illustrated in Figure 1b. NaOH was bought from SHOWA, and its purity is 96%. Water was purified by double distillation followed by a PURELAB Maxima Series (ELGA Lab Water) purification system with a resistivity better than 18.2 MΩ cm.
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10

Titanium Foil Synthesis and Characterization

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Titanium foil (0.2 mm thick,
99.9% purity) was obtained from Ankuro Int. GmbH (Germany). Nitric
acid (HNO3, 65%) was bought from Carlo Erba Reagents GmbH
(Germany). Hydrofluoric acid (HF, 48–51%) and furfuryl alcohol
(FFA, 99%) were purchased from Fisher Scientific. Ethylene glycol
(99%), ammonium fluoride (NH4F, 99.8%), sodium borohydride
(NaBH4, 97%), sodium chloride (NaCl, 99%), sodium sulfate
(Na2SO4, >99%), Ibuprofen (IBF, ≥98%),
coumarin, and sodium hypochlorite (NaOCl) were purchased from Alfa
Aesar (U.K.). Ammonium chloride (NH4Cl, 98%) and 7-hydroxycoumarin
were obtained from Acros Organics. Ethylenediaminetetraacetic acid
(EDTA), sodium thiosulfate (Na2S2O3), and tert-butyl alcohol (TBA) were purchased from
Sigma-Aldrich. A graphite block (99.9%) was purchased from Beijing
Great Wall Co., Ltd. (China). Deionized water was used in all of the
experiments.
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