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23 protocols using da hydrochloride

1

Drug Preparation for Electrophysiology and Microdialysis

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(-)Nicotine hydrogen tartrate salt, DA hydrochloride and CNQX were obtained from Sigma-Aldrich (St. Louis, MO, USA), whereas picrotoxin and MK-801 were obtained from Tocris (UK). AZD1446 was obtained from AstraZeneca (Sweden). For electrophysiological experiments, drugs were prepared in stock solutions and bath-applied at known concentrations via a three-way tap system. A complete exchange of the solution in the recording chamber occurred in about 1 min. For microdialysis, nicotine was dissolved in aCSF and pH adjusted to 7.4. AZD1446 was prepared in stock solution in aCSF for striatal infusion and in water for systemic injections.
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2

Preparation of Bioactive Compounds

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DA hydrochloride and 3-HPBA were purchased from Sigma-Aldrich (U. S). Tyrosine, ascorbic acid, alanine, serine, glycine, tryptophan, lysine, cysteine, glucose, glutathione, norepinephrine, saccharide, and sodium hydroxide were obtained from Aladdin Co., Ltd. (Shanghai, China). All reagents were of analytical grade and used without further purification.
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3

Cocaine and Neurotransmitter Regulation

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Cocaine was provided by the Research Technology Branch, National Institute on Drug Abuse (Rockville, MD) and dissolved in sterile 0.9% saline. DA hydrochloride, DOPAC, ascorbic acid, Nafion (5%), chloralose, and urethane were purchased from Sigma-Aldrich (St. Louis, MO). chloralose, urethane, DA, DOPAC, and ascorbic acid were dissolved in 0.1M phosphate buffered saline. Drug and saline were administered i.p. in a volume of 1mL/kg.
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4

Dopaminergic modulation of behavior

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Rats were administered DA hydrochloride (0.3 and 3 mg/kg; Sigma-Aldrich) by i.p. injection twice per week for four weeks. All of the rats were subjected to the OF, YM, EPM and WFT tests. Following the final injection, NMDA (0.3 mM; Sigma-Aldrich) was also administered to the rats for 30 min by intraperitoneal injection. Liver, serum and cerebral cortex specimens were collected for fluorescent staining, immunoblotting and determination of DA.
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5

Antimicrobial Catheter Coating Development

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Allylamine, MeOH, EtOH, IPOH, DMF, DMSO,
DA hydrochloride, silver nitrate, and LMW-PEI (700 Da) were purchased
from Sigma. PDMA (uhPDMA, 900 kDa) was synthesized based on the procedure
which was previously developed in our lab.48 (link) The PU sheet was purchased from Professional Plastics. The polymeric
catheters including Foley catheters, 24G PU IV, 10 Fr silicone urinary,
and 16 Fr PVC urinary catheter were supplied by BD. The PDMS sheets
were cast in the lab using reagents purchased from Dow Corning. All
cell culture-related media and supplements [trypsin–EDTA, Dulbecco’s
phosphate-buffered saline (DPBS), heat-inactivated FBS, P/S, RPMI
1640 medium, modified eagle medium, and MeOH] were received from Thermo
Fisher Scientific unless otherwise specified. T24 bladder carcinoma
cells were purchased from American Type Culture Collection (ATCC CRL-2922
Manassas, VA) and were used between passage numbers 5 and 10.
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6

Cocaine Hydrochloride Dosing and Treatment

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Cocaine hydrochloride was dissolved in sterile 0.9% sodium chloride. Drugs were purchased from Sigma-Aldrich (St. Louis, MO) and intraperitoneally injected at a dose of 20 or 10 mg/kg for locomotor testing and locomotor sensitization, respectively. Cocaine solution was made fresh immediately before behavioral testing and protected from light. For in vitro experiments, drugs were diluted in Neurobasal medium (Invitrogen) immediately before treating cell culture plates. DA hydrochloride (Sigma-Aldrich, H8502-5G) was dissolved in Neurobasal medium, and cells were treated at a dose of 1 μM for RT-qPCR experiments or 50 μM for snRNA-seq experiments. R(+)–SCH-23390 hydrochloride (Sigma-Aldrich, D054-5MG) and R(+)–SKF-38393 hydrochloride (Sigma-Aldrich, S101-5MG) were dissolved in sterile Milli-Q water, and cells were treated at a dose of 1 μM. For MEK inhibitor experiments, U0124 (1 μM; Millipore, 662006-1MG) and U0126 (1 μM; Millipore, 662005-1MG) were dissolved in dimethyl sulfoxide (DMSO) (Invitrogen, D12345). The CREB inhibitor 666-15 (1 μM; Tocris, 5661), also called 3-(3-aminopropoxy)-N-[2-[[3-[[(4-chloro-2-hydroxyphenyl)amino]carbonyl]-2-naphthalenyl]oxy]ethyl]-2-naphthalenecarboxamine hydrochloride, was dissolved in DMSO. KCl (Fisher Scientific, P330-500) was dissolved in Neurobasal media, and cells were treated with a 25 mM dose.
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7

GO-based Membrane Filtration

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All chemicals
were commercially available and used without further purification
as follows. The GO suspension (4 mg mL–1 in H2O), tris (hydroxymethyl) amino methane (Tris, 1 mol L–1), DA hydrochloride (98.00 wt %), hydrochloric acid
(HCl, 0.1 mol L–1), and sodium hydroxide solution
(NaOH, 0.1 mol L–1) were purchased from Sigma-Aldrich
Co., Ltd. PES microfiltration membranes (diameter of 47 mm, average
pore size of 220 nm) were purchased from Merck Millipore Co., Ltd.
strontium nitrate (Sr(NO3)2, 98.00 wt %), and
strontium standard solution(1000 mg/L) were obtained from FUJIFILM
Wako Pure Chemical Industries Co. Ltd. Ultrapure water was obtained
from a Milli-Q system (Millipore, MA, USA).
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8

Dopamine Resistance Assay in C. elegans

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For DA resistance assay, 1-day-old adult hermaphrodites were incubated in a droplet of 20 μL of M9 buffer containing DA hydrochloride (Sigma-Aldrich) at a final concentration of 40 mM. Animal were scored for paralysis every 10 minutes. Nematodes were considered paralyzed when they did not exhibit any spontaneous body bend during a period of 5 s. Three distinct populations of 20 adults (for each strain) were scored over the assay period. We performed three independent measurements per strain. We used the Prism software package (GraphPad Software) for statistical analysis.
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9

Synthesis and Characterization of Copper(II) Complexes

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Materials in all
synthesis procedures were used without any further purifications.
DA hydrochloride (CAS: 62-31-7, s, >98%), trizma base (CAS: 77-86-1,
s, >99%), hydrochloric acid (CAS: 7647-01-0, l, 25%), copper(II)
sulfate
pentahydrate (CAS: 7758-99-8, s, ≥98.0%), acetic acid (CAS:
64-19-7, l, ≥99%), sodium acetate (CAS: 127-09-3, s, ≥99%),
BA (CAS: 10043-35-3, s, ≥99.5%), sodium hydroxide (CAS: 1310-73-2,
s, ≥98%), and silicon wafer (Si 100, CAS: 7440-21-3, s) from
Sigma-Aldrich and ultrapure deionized water from a Hydrolab Ultra
UV system were used.
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10

Zinc-based Metal-Organic Framework Synthesis

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Zinc
nitrate hexahydrate (Zn(NO3)2·6H2O, 98%), terephthalic acid (98%),
DA hydrochloride, and tris(hydroxymethyl)aminomethane (Tris, 99.8%)
were purchased from Sigma-Aldrich. N,N-dimethylformamide (DMF, 99.8%) was purchased from Caledon, CA. All
chemicals were used without further purification. Deionized water
was used throughout all the experiments.
Two different substrates
were used in the experiments: paper strips and cotton bulbs. The paper
was a coffee filter paper (GK Connaisseur 03-2644637 from Dollarama
in CA). Commercially available cotton balls made for medical uses
were used.
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