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Concentrated hydrochloric acid

Manufactured by Thermo Fisher Scientific
Sourced in United States

Concentrated hydrochloric acid is a clear, colorless, and highly corrosive liquid chemical compound. It is used as a common laboratory reagent and industrial chemical.

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18 protocols using concentrated hydrochloric acid

1

Lipid-based Nanoparticle Synthesis Protocol

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Tetraethylorthosilicate (TEOS) was purchased from Acros Organics. Dodecyltrichlorosilane was purchased from Gelest, Inc. Cetyltrimethylammonium chloride (CTAC, 25 wt.% in water) was purchased from Sigma. Water was deionized with a Milli-Q Advantage A10 system (MilliporeSigma, Inc.) and was used without degassing. Chloroform and hexanes were purchased from Merck. Concentrated hydrochloric acid was obtained from Fischer Scientific. Bovine plasma was ordered from Lampire Biological Laboratories. 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1,2-dibehenoyl-sn-glycero-3-phosphocholine (DBPC), 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), and 1,2-dilauroyl-sn-glycero-3-phosphocholine (DLPC), were all purchased from Avanti Polar Lipids, Inc. 1,2-distearoyl-sn-glycero-3-phospho-ethanolamine-N-[methoxy(polyethylene glycol)- 2000] (DSPE-PEG2k) was also ordered from Avanti Polar Lipids, Inc.
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2

Superhydrophobic Al Foil Fabrication

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Untreated Al foil
(AL000612, Goodfellow) with a thickness of 200 μm (similar to
the thickness of common soda can walls) was cut into rectangular samples,
which was performed with chemical and fs-laser treatments, as shown
in Figure 1b. The foils
were first chemically etched for 30 min under ultrasound in a mixed
solution of concentrated hydrochloric acid (37.2%, Thermo Fisher Scientific
Inc., USA) and 5% cuprous chloride (98% min, Alfa Aesar Inc., USA)
with a mixing ratio of 0.25 v/v % to obtain a surface with microroughness.
The ratio of the HCl/CuCl2 mixture solution volume to the
surface area of the sample was 1.25 mL cm–2. After
etching, the samples were cleaned with ethanol under ultrasound. To
yield a superhydrophobic surface, the etched samples were treated
in 0.01 mol L–1 stearic acid (98%, Alfa Aesar Inc.,
USA) ethanol solution for 24 h, followed by rinsing with ethanol and
drying at ambient temperature. Finally, the as-designed superhydrophilic
patterns were fs-laser-ablated on the superhydrophobic surface by
programmed scanning with a SCANcube III 10 galvanometer scanner (SCANLAB
GmbH, Germany) with a scanning speed of 5 mm s–1. The laser was generated by an Astrella-USP-1K ultrafast Ti/sapphire
amplifier system (Coherent Inc., USA) with the wavelength centered
at 800 nm, pulse width of 35 fs, repetition rate of 1 kHz, beam quality M2 < 1.25, and an average power of 1.25 W.
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3

Glass Surface Activation Protocol

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Glass substrates with dimensions of 1.2 cm × 1.2 cm (Thermo Fisher Scientific) were washed by immersing them in a mixture of methanol (Thermo Fisher Scientific) and concentrated hydrochloric acid (Thermo Fisher Scientific) (1:1 v/v) for at least 30 min followed by washing them with DI water thoroughly. The substrates were oxidized with concentrated H2SO4 (l) (Thermo Fisher Scientific) for at least 30 min to activate the hydroxyl groups and then washed with DI water thoroughly. Next, the Glass substrates were washed with methanol and immersed in a mixture of 3-mercapto-1-propanesulfonic acid (MPS) and methanol (1:1000) for 30 min. Finally, the Glass substrates were sequentially washed with methanol and DI water and then dried under nitrogen. The substrates could be stored in a desiccator for a short period.
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4

Detailed Isotopic Analysis Protocol

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The internal standard, sodium sulphite-34S (Na234SO3, 95%), in addition to formaldehyde (37%), toluene, ammonium acetate (Sigma Ultra, minimum 98%) and sodium sulphite (Na2SO3, ≥ 98%) were acquired from Sigma-Aldrich (St. Louis, MO, USA). LC-MS-grade acetonitrile, water and methanol, in addition to glacial acetic acid, ethanol, methylene chloride, hydrogen peroxide (30%), sodium hydroxide (certified 0.1 and 0.01 N), potassium hydroxide pellets (85%), potassium dihydrogen phosphate, barium chloride, concentrated phosphoric acid and concentrated hydrochloric acid, were purchased from Thermo Fisher Scientific (Pittsburgh, PA, USA). Methyl red from Mallinckrodt Baker (Phillipsburg, NJ, USA) was used in the MW titration. Samples were diluted and extracted using 18 MΩ water obtained from an Aqua Solutions water purification system (Jasper, GA, USA). Fresh vegetables and all ingredients used for making garlic products were purchased from grocery stores located in Greenbelt, MD, USA. All food samples were stored according to the manufacturers’ suggested storage conditions.
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5

Characterizing Dodecyl Drug Analogues

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Materials Brij 78, tetrahydrofuran, anhydrous materials (pyridine, dichloromethane) and deuterated solvents (CDCl 3 ) were all purchased from Sigma Aldrich. Each were used as received apart from CDCl 3 where 0.1% tetramethylsilane was added. All other solvents were reagent grade and purchased from Fischer Scientific and used as received. Alkyl chloroformates were purchased from Tokyo chemical industry and used as received. Magnesium sulphate (MgSO 4 ) and concentrated hydrochloric acid (HCl) Fig. 10 Graph showing the relationship between percentage of dodecyl drug analogue within the core and the crystallinity of dodecyl drug analogue relative to that of the bulk.
were also purchased from Fischer Scientific. HCl was diluted down to a 1M solution, meanwhile MgSO 4 was used as received. Imwitor s 900K (glyceryl monostearate) was kindly gifted from IOI Oleochemical, Hamburg. Lamivudine was purchased from Top Well Medipharma Group.
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6

Oat Flour Characterization and Enzyme Assays

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Medium bran oat flour (i.d. 112-001) with a particle size percentage distribution of 2.00 mm (0.8%), 0.841 mm (61.5%), 0.595 mm (32.1%), 0.420 mm (5.0%), and Pan (0.6%) was donated by Richardson Milling (Portage La Prairie, MB, Canada). The enzymes (α-amylase, Flavourzyme®, Alcalase®, and Papain, sodium tartrate, sodium dodecyl sulfate, cupric sulfate pentahydrate, Trolox, 1,10-phenanthroline, iron(II) sulfate heptahydrate, hydrogen peroxide (H2O2), Tris-HCl, Tris-Base, potassium bromide, pyrogallol, reduced glutathione, L-serine, 3,5-dinitrosalicylic acid, sodium potassium phosphate tartrate, starch, and bovine serum albumin (BSA) were purchased from Sigma-Aldrich Ltd. (Oakville, Ontario, Canada). The solvents, including concentrated hydrochloric acid, methanol and Folin-Ciocalteau Phenol reagent, fluorescein, and 2,2’-azobis(2-amidinopropane) dihydrochloride (AAPH), were purchased from Fisher Scientific Co. (Nepean, Ontario, Canada).
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7

Synthesis and Purification of Aromatic Diamines

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The diamines phenylene
diamine (PDA, ortho and para), 4,4′-diaminodiphenyl ether,
piperazine, 4,4′-diaminodiphenylmethane, 1,5-diaminonapthalene,
1,3-propylene diamine, and thionyl chloride were purchased from Aldrich
Chemical Company (Milwaukee, WI) or TCI America (Portland, OR) and
used as received without further purification. Anhydrous pyridine
and N-methyl-2-pyrrolidone (NMP) were purchased from
Aldrich and used as received. Other common reagents utilized in the
synthesis or work up such as sodium hydroxide, concentrated hydrochloric
acid, dichloromethane, methanol, acetone, dimethylformamide (DMF),
and hexamethylphosphoramide (HMPA) were purchased from Fisher Scientific
(Hampton, NH). Powdered, virgin PET for model reactions was purchased
from Goodfellow Corporation (Coraopolis, PA). TPA was obtained from
mixed-waste PET, composed of colored, clear, and opaque yellow bottles
whose labels and caps were not removed, via basic hydrolysis, and
the study is reported in detail elsewhere.9 (link)
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8

In vitro Gastrointestinal Digestion Assay

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All reagents used were of analytical grade. All solutions were prepared using ultra-high pure (UHP) 18 Ω water. All laboratory ware was soaked for 24 h in an acid bath containing 10% (v/v) nitric acid and then rinsed with UHP water. Concentrated hydrochloric acid (12 mol L−1), HNO3 69%, NaCl, NH4Cl, anhydrous Na2SO4, CaCl2.2H2O, NaHCO3, anhydrous D ( + )-glucose, sodium arsenate dibasic heptahydrate, cadmium acetate and lead acetate trihydrate were obtained from Fisher Scientific. d-glucuronic acid, Pancreatin (pig), pepsin (pig), Bovine serum albumin (BSA), KSCN, NaH2PO4, mucin (pig), D-glucosamine hydrochloride, lipase (pig), α-amylase (Bacillus species), urea and bile salts (bovine), modified eagle medium (DMEM) containing 4.5 g/L glucose, penicillin-streptomycin solution (10, 000 units penicillin and 10 mg streptomycin per mL), and Hank’s Balanced Salt Solution (HBSS) and glycine were obtained from Sigma–Aldrich (St. Louis, MO, USA). KH2PO4, MgCl2·6H2O, KCl, and uric acid were obtained from VWR. Caco-2 cells (HTB-37™) were purchased at passage 18 from the American Type Culture Collection (ATCC, Manassas, VA, USA). Fetal bovine serum and trypsin-EDTA were purchased from Invitrogen (Burlington, ON, Canada).
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9

Hydrochloric Acid-Based Extraction Protocol

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Concentrated
hydrochloric acid (HCl), 1 N
HCl, 1 N sodium hydroxide (NaOH), poly(vinylidine fluoride), and poly(tetrafluoroethylene)
syringe filters, and Wheaton glass scintillation vials were purchased
from Fisher Scientific (Fair Lawn, NJ). All other reagents, solvents,
and fine chemicals were obtained from Aldrich (Milwaukee, WI) and
used as received.
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10

Biodegradable Coating for Titanium Rods

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Titanium rods were coated with a biodegradable, 7ND-releasing coating following a previously established layer-by-layer (LBL) method.21 (link) Briefly, end-modified poly(β-amino ester) (C32–130) was synthesized as previously described, suspended in phosphate buffered saline (PBS) at 10 mg mL−1 and used as the positively charged polyelectrolyte. A 3 mg mL−1 polystyrene sulfonate was used as the negatively charged polyelectrolyte. The 7ND was dissolved in 0.1% (w/v) bovine serum albumin at 30 μg mL−1. Prior to coating hollow A-40 titanium rods (6 mm, 21 G, New England Small Tube, Litchfield, NH) were surface etched with concentrated hydrochloric acid (37.3% w/v, Fisher Scientific, Pittsburgh, PA) for 2 h to facilitate the attachment of the coating. Rods were then thoroughly washed with H2O, rinsed three times in 70% ethanol, air dried, and subjected the LBL deposition, with polyelectrolyte layers on bottom and the 7ND containing layer on top. Polyelectrolyte layers were deposited for 5 min, and the 7ND layer for 10 min. In between layer depositions rods were washed twice in H2O. The sustained release of 7ND from the surface coating was confirmed in vitro using CCL2 ELISA (Peprotech, Rocky Hill, NJ) as previously described.21 (link)
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