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Glass capillaries

Manufactured by A-M Systems
Sourced in United States, United Kingdom

Glass capillaries are hollow, cylindrical tubes made of glass. They are used for the transfer, measurement, and manipulation of small volumes of liquids.

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10 protocols using glass capillaries

1

Carbon Fiber Electrodes for Neurotransmitter Measurement

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Carbon fiber microelectrodes were manufactured by aspirating 7 μm diameter carbon-fibers (Goodfellow Inc, Coraopolis, PA) into glass capillaries (0.6mm external diameter, 0.4mm internal diameter, A-M Systems Inc., Sequim, WA). Fibers were sealed into the capillaries with a vertical pipette puller (Narishige Group, Tokyo, Japan). The exposed fiber was trimmed to approximately 150 μm under a low-light power microscope for evaluation of serotonin and histamine and to 50 μm for evaluation of dopamine. Nafion was electrodeposited onto the exposed carbon fiber portion of serotonin and histamine electrodes as previously described and then dried at 70° C for 10 minutes (Hashemi et al. 2009 (link)).
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2

Fabrication of Carbon Fiber Microelectrodes

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CFMs were fabricated as previously described. Briefly, 7 μm diameter carbon fibers (Goodfellow Cambridge LTD, Huntingdon, UK) were aspirated into glass capillaries (1.2 mm D.D. and 0.68 mm I.D., 4 in long; A-M Systems, Inc., Carlsborg, WA) using a vacuum pump. The capillaries were then pulled using a PE-22 heated coil puller (Narishige Int. USA, East Meadow, NY) to form two electrodes. Exposed carbon fibers were trimmed to a length of 40–60 μm. CFMs were sealed by dipping in epoxy resin (EPON resin 815C and EPIKURE 3234 curing agent, Miller-Stephenson, Danbury, CT) for 45 seconds and cured at 100°C for 1 hr. Prior to experiments, electrodes were soaked in isopropanol for at least 10 min.
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3

Carbon Fiber Microelectrode Fabrication and Calibration

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CFMEs were fabricated as previously described. Briefly, a vacuum pump was used to aspirate 7 μm diameter carbon fibers (Goodfellow Cambridge LTD, Huntingdon, UK) into glass capillaries (1.2 mm D.D. and 0.68 mm I.D., 4 in long; A-M Systems, Inc., Carlsborg, WA) which were then pulled using a PE-22 heated coil puller (Narishige Int. USA, East Meadow, NY) to form two electrodes. Exposed carbon fibers were trimmed to a length of 50–100 μm. To seal the CFMEs, the tips were dipped in epoxy resin (EPON resin 815C and EPIKURE 3234 curing agent, Miller-Stephenson, Danbury, CT) for 45 seconds and cured at 100°C for 1 h. CFMEs were treatment via an isopropanol soak for at least 20 min prior to initial use.
All CFMEs were pre-calibrated against standard solutions of 5-HT, introduced to a flow cell through a six-port valve (Valco Instruments Company Incorporated, Houston, TX, USA). The flow solution, which consisted of mouse aCSF without D-glucose, was pumped at a rate of 2 mL min−1 using a syringe pump (Chemyx Inc, Stafford, TX, USA). Injections were conducted in triplicate to determine the 5-HT concentration per nanoamp of current for each CFME.
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4

Voltammetric Analysis of Serotonin

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Voltammetric analysis of serotonin was performed as described previously (Hashemi et al., 2009 (link); Wood and Hashemi, 2013 (link); Wood et al., 2014 (link)). Briefly, CFMs were constructed by aspirating 7 μm carbon fibers (Goodfellow Corporation, Coraopolis, PA, United States) into glass capillaries (0.4 mm internal diameter, 0.6 mm outer diameter, AM Systems, Carlsborg, WA, United States). A vertical pipette puller (Narishige Group, Tokyo, Japan) was employed to create a carbon-glass seal. Subsequently, the exposed carbon fiber was cut to 150 μm and silver paint was used to forge an electrical connection to a connection pin. Finally, electrodes were electrodeposited with NafionTM as described previously (Hashemi et al., 2009 (link)).
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5

Fabrication of Carbon-Fiber Microelectrodes

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CFMs were fabricated employing 7 μm diameter carbon-fibers (Goodfellow Corporation, Coraopolis, PA, USA) aspirated into glass capillaries (0.6 mm external diameter, 0.4 mm internal diameter; AM Systems, Inc., Sequim, WA, USA). A carbon-glass seal was formed using a vertical micropipette puller (Narishige Group, Tokyo, Japan). The exposed length of the carbon fiber was trimmed to 150 μm under an optical microscope. Microelectrodes were electro-plated with Nafion as described previously (Hashemi et al. 2009 (link)).
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6

Carbon Fiber Microelectrodes Fabrication

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CFMs were fabricated with 7 μm diameter carbon-fibers (Good-fellow Corporation, PA, USA) aspirated into glass capillaries (0.6 mm external diameter, 0.4 mm internal diameter, A-M systems, Inc., Sequim, WA). A carbon-glass seal was formed via a vertical micropipette puller (Narishige Group, Tokyo, Japan). The exposed length of the carbon fiber was trimmed to 150 μm under an optical microscope. Microelectrodes were electro-plated with Nafion as described previously.4 (link)
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7

Carbon Fiber Microelectrode Fabrication

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Carbon fiber microelectrodes were manufactured by aspirating 7 μm diameter carbon-fibers (Goodfellow Inc, Coraopolis, PA) into glass capillaries (0.6 mm external diameter, 0.4 mm internal diameter, A-M Systems Inc., Sequim, WA). Fibers were sealed into the capillaries with a vertical pipette puller (Narishige Group, Tokyo, Japan). The exposed fiber was trimmed to approximately 50 μm for evaluation of dopamine and precisely 150 μm under a low-light power microscope for evaluation of serotonin, as this length is critical for proper measurement of serotonin (Hashemi et al. 2009 (link); Denton et al., 2019 (link)). Nafion, a cation exchange polymer, was electrodeposited onto the carbon fiber portion of each serotonin electrode and dried for 10 minutes at 70º C (Hashemi et al. 2009 (link); Denton et al., 2019 (link)).
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8

Carbon-Fiber Microelectrode Fabrication and Calibration

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Carbon‐fiber cylinder microelectrodes were prepared as previously described (Huffman and Venton 2009). T‐650 carbon‐fibers (7 μm diameter, Cytec Engineering Materials, West Patterson, NJ) were pulled in glass capillaries (A‐M Systems Inc., Seqium, WA) and cylinders were cut between 75–125 μm in length. Cyclic voltammetry data were collected with TarHeel CV software and High‐Definition Cyclic‐Voltammetry (gift from Mark Wightman, UNC) using a Dagan ChemClamp (Dagan Corporation, Minneapolis, MN). Electrodes were scanned from −0.40 to 1.45 V and back at 400 V/sec at 10 Hz against a Ag/AgCl reference electrode. Electrodes were postcalibrated with 1.0 μmol/L adenosine after each experiment.
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9

Fabrication of Carbon Fiber Microelectrodes

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CFMs were fabricated in house using ~7 μm diameter carbon fibers (Goodfellow Corporation, PA, USA). The carbon fibers were aspirated into glass capillaries (ED 0.6 mm, ID 0.4 mm; A-M systems, Inc., Sequim, WA, USA) and pulled via a vertical micropipette puller (Narishige Group, Tokyo, Japan). Under an optical microscope, carbon fibers were cut to 150 μm. An electrical connection was forged between the carbon fiber and connection wire using silver paint. CFMs were then electroplated with nafion (Hashemi et al., 2009 (link)).
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10

Fabrication of Carbon-Fiber Microelectrodes

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Carbon-fiber cylindrical microelectrodes
were fabricated as previously described.28 (link),80 (link) Briefly, individual 7 μm carbon fibers, purchased from Goodfellow
Cambridge Ltd. (Huntingdon, England), were loaded into glass capillaries
(4 in, 1.2 mm OD; A-M Systems, Inc. Carlsborg, WA) and pulled using
a heated coil puller (Narishige International USA, East Meadow, NY).
Carbon-fiber tips were then cut with a scalpel 25 μm from the
end of the glass seal. Electrodes were sealed by dipping into a well-mixed
epoxy mixture of 0.24 g of EPI-CURE 3234 Curing Agent (lot FCXC4114/0886GG)
and 2.00 g of EPON Resin 815C (lot HADN0003/1307GG). Excess resin
was removed by dipping several times in toluene, and electrodes were
then baked for 1 h at 100 °C. The electrodes were backfilled
with 0.5 M potassium acetate to establish electrical connections between
the carbon-fibers and the inserted silver wires. For 5-HT detection,
electrodes were coated with Nafion (Nafion perfluorinated ion-exchange
resin, 5 wt % solution in a mixture of lower aliphatic alcohols and
water, Sigma-Aldrich, St. Louis, MO) via electrodeposition using an
adaptation of previously described methods.81 (link),82 (link) Electrodes were dipped in Nafion, and a potential of 1.0 V was applied
for 30 s. Nafion-coated electrodes were then cured at 70 °C for
10 min and stored for no longer than 1 week prior to use.
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