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13 protocols using potassium chloride (kcl)

1

Synthesis of Hybrid Nanocomposites

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Multi-walled carbon nanotubes (3–12 µm, 99.99%) were purchased from NANOGENSTORE (Chiang Mai, Thailand), and silicon carbide (50 nm, 99.9%) from Sigma-Aldrich (St. Louis, MO, USA). Silver nitrate (AgNO3, 99.9%) and Cetyltrimethylammonium bromide (CTAB, 99%) were purchased from Virotevittayapun Company Limited (Nakhon Ratchasima, Thailand). Corn starch was purchased at any market. Potassium hexacyanoferrate (II): K4(Fe(CN)6)·3H2O: Fe(II) was purchased from Sigma Aldrich. Potassium chloride (max. 0.0001%A) was purchased from Riedel de Haen. Chitosan (Mw = 125–500 kDa and 500–900 kDa, %DD = 90–95%) was purchased from BIO21 (Thailand). Acetic acid (99.7%) was purchased from APEX CHEMICALS (Singapore).
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2

Synthesis and Characterization of Nanomaterials

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Titanium tetra-isopropoxide (C12H28O4Ti) (98%), P-nitrophenyl phosphate (C6H6NO6P) (>99%), 2-methoxy Ethanol (C3H8O2) (>99.5%), sulphuric acid (H2SO4) (98%), and barium acetate (C4H6BaO4) (>98.5%) were obtained from Sigma-Aldrich. Ethanol (99.7–100%), de-ionized water (DI), distilled water (DW) and, potassium chloride (KCl) (≥99.0%) were acquired from Riedel-deHaen. Phenol (C6H6O) (99.6%), Di-Ethanol amine (DEA) (98%), potassium ferrocyanide (C6N6FeK4) (98.5%), and potassium ferricyanide (C6N6FeK3) (98%) were purchased from Daejung. Tenofovir hydrate drug (TFV) (98.0%), gemcitabine (GEM) (>99%), etoposide (ETO) (95–105%), ibuprofen (>98%), and diclofenac sodium (>98%) were bought from TCI. Alkaline phosphatase enzyme (ALP) was procured from Calbiochem, Human blood serum was obtained from a regional laboratory in Lahore. All chemicals and reagents used in this work were of analytical grade.
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3

Synthesis and Characterization of κ-Carrageenan Biomaterial

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κ-Carrageenan from Danisco S/A (Danisco SA, Copenhagen, Denmark now DuPont) was
received in food grade. All other chemicals were purchased in analytical grade
as follows: sodium chloride and calcium chloride (Carl Roth GmbH & Co. KG,
Karlsruhe, Germany), potassium chloride (Riedel-de Haën, Seelze, Germany now
Honeywell) and ethanol (EtOH) (Deuring GmbH & Co. KG, Hörbranz, Austria).
Compounds were used as received.
SBF fluid was adapted close to ionic concentrations of calcium (Ca2+),
potassium (K+) and sodium (Na+) levels present in the vasa
deferentia of human males, 1.5 mM, 100 mM (instead of 111 mM) and 30 mM
respectively.28 (link),29 (link)
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4

Antioxidant and Redox Activity Assays

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Thiobarbituric acid (TBA); lipoxygenase from soybean; nitroblue tetrazolium (NBT); reduced form of nicotinamide adenine dinucleotide (NADH) and N-phenylmethazonium methosulfate (PMS) were purchased from Fluka, Biochemika, Sigma-Aldrich, Steinheim, Germany. Linoleic acid sodium salt; 2,2’-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) diammonium salt (ABTS); 2,2-diphenyl-1-picrylhydrazyl (DPPH); nordihydroguaiaretic acid (NDGA) and 2-deoxyribose were purchased from Sigma-Aldrich, Steinheim, Germany. Trichloroacetic acid was purchased from VWR, Leuven, Belgium. Ferrozine iron reagent hydrate; ethylenediaminetetraacetic acid (EDTA); FeCl2.4H2O, FeCl3; and potassium persulfate were purchased from Acros organics, New Jersey, USA. L(+)-Ascorbic acid and boric acid were purchased from Merck, Darmstadt, Germany. KH2PO4-K2HPO4; FeSO4.7H2O were purchased from Panreac, Barcelona, Spain. H2O2 was purchased from Fisher Scientific, New Jersey, USA. L-α-lecithin of soybean was purchased from CALBIOCHEM, Darmstadt, Germany. Chloroform was purchased from lab-scan, Dublin; Folin Ciocalteu's phenol reagent, was purchased from Panreac Química SA (Barcelona, Spain). Gallic acid; Na2CO3; acetic acid; acetic acid; sodium dodecyl sulfate (SDS); KCl; butanol; butylated hydroxytoluene (BHT); mannitol KCl were purchased from Riedel de Haen (Seelze, Germany).
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5

Electrochemical Characterization of Catalysts

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All chemicals were used as received without further purification and all aqueous solutions were prepared using ultrapure water (Siemens Water Technologies, Barsbüttel, Germany). The electrochemical characterization of the SECM tips, microelectrodes, and recessed microelectrodes as sample surfaces were performed by means of cyclic voltammetry in an electrolyte containing 5 mM [Ru(NH3)6]Cl3 (ABCR, Karlsruhe, Germany) and 100 mM KCl (Riedel-de Haën, Seelze, Germany) as background electrolyte. As a model catalyst a commercial nanoporous ORR catalyst from ETEK (Natick, USA) with 20 wt % Pt on Vulcan XC72 was used. An air saturated 0.1 M sodium phosphate buffer (pH 7, VWR International, Darmstadt, Germany) was used for all investigations of the catalytic activity towards ORR.
Platinum wires with diameters of 25 µm, 100 µm and 250 µm and a gold wire with a diameter of 100 µm were from Goodfellow (Bad Nauheim, Germany). Borosilicate glass capillaries (length 100 mm, outside Ø 1.5 mm, inside Ø 0.75 mm) were purchased from Hilgenberg (Malsfeld, Germany) while quartz glass capillaries (length 95 mm, outside Ø 0.9 mm, inside Ø 0.3 mm) were from Quarzschmelze Illmenau (Illmenau, Germany).
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6

Linseed-based Moxifloxacin Delivery System

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Linseeds were procured from Pansari inn, Pakistan. Linseeds were de-dusted and cleaned from physical impurities, and stored in an airtight container at ambient temperature. Microcrystalline cellulose (Avicel® PH 102) and HPMC K100M were procured from Merck, Germany. Moxifloxacin used in this research was according to the specification of United States Pharmacopoeia (USP). The KCl, NaOH, n-hexane, potassium dihydrogen phosphate and HCl were purchased from Riedel-de Haën, Germany. Magnesium stearate, polyvinylpyrrolidone K30 (PVP K30), talcum, sodium bicarbonate and β-cyclodextrin were procured from Sigma-Aldrich, USA. Linseeds hydrogel (LSH) was separated from linseeds using a nylon mesh. Deionized water was used for the entire study.
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7

Hydrogel Carrier Synthesis for Drug Delivery

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Seeds of S. spinosa were brought from the local market of Sargodha, Pakistan (in May–June) and their taxonomy was verified by a botanist, Dr Hassan Sher from the Department of Botany, University of Swat, Mingora, Pakistan. The methacrylic acid (MAA, monomer; 99.0%), potassium persulfate (KPS, initiator; 99.0%), and N,N-methylenebisacrylamide (MBA, cross-linker; 99.5%) were purchased from Sigma-Aldrich, Germany. Potassium dihydrogen phosphate (KH2PO4; 99.0%), NaOH (98.0%), KCl (99.0%), ethanol (95.0%), and n-hexane (95.0%) were acquired from Riedel-de Haen, Germany. Venlafaxine HCl (United States Pharmacopeia (USP) standard) was used as a model drug for in vitro drug release studies from the synthesized hydrogel carrier. For swelling and drug release studies, the buffers of pH 7.4, 6.8, 4.5, and 1.2 were prepared according to the procedure given in USP. All other reagents and chemical ingredients were of lab-grade. Deionized water (DW) was used during the whole research work.
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8

Reverse Phase HPLC Method Development

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The investigated drugs included neutral, acidic, basic and zwitterionic species and they were donated by local pharmaceutical companies. They are listed in Table 1. All reagents were of analytical grade unless otherwise mentioned. For the preparation of mobile phases KCl (≥99.5%, Riedel-de Haen), KH 2 PO 4 (≥99.5%, Merck), Na 2 HPO 4 (≥99.0%, Sigma-Aldrich), NaCl (≥99.5%, Sigma-Aldrich), CH 3 CN (≥99.9%, LC gradient grade, Merck) and High Purity Water (HPW) were used. The HPW was obtained by means of an EASYpure II (Barnstead International, USA) water purification system. As void volume markers, sodium citrate•2x H 2 O (≥99.0%, Sigma-Aldrich), (COONH 4 ) 2 •H 2 O (≥99.5%, Riedel-de-Haen) and L-Cystine (≥99%, Fluka Biochemika) were used.
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9

Fabrication of ITO-Coated Glass Coverslips

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Potassium
chloride (KCl, Honeywell, 99.5%)
and 1,1′-ferrocenedimethanol (FcDM, Sigma-Aldrich, 97%) were
used as supplied. All solutions were prepared with deionized water
(ELGA PURELAB systems; 18.2 MΩ cm at 25 °C). Indium tin
oxide (ITO)-coated glass coverslips, 0.17 mm thick, 20 mm × 20
mm, 8–12 Ω/sq resistivity (SPI Supplies, West Chester,
PA), were cleaned following typical protocols of sonicating in isopropanol
followed by deionized water and then dried in an argon stream.20 (link),24 (link)
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10

Cultivation of Streptomyces chartreusis

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S. chartreusis NRRL 3882 was cultivated in chemically defined medium [21 mM NaCl (Carl Roth, Karlsruhe, Germany), 15 mM (NH4)2SO4 (Sigma-Aldrich, St. Louis, MO, USA), 8 mM MgSO4 (VWR International, Darmstadt, Germany), 27 mM KCl (Honeywell International, Morristown, NJ, USA), 50 mM Tris (Sigma-Aldrich, St. Louis, MO, USA), 0.6 mM KH2PO4 (VWR International, Darmstadt, Germany), 2 mM CaCl2 (Avantor, Radnor, PA, USA), 0.01 mM MnSO4 (Honeywell International, Morristown, NJ, USA), 11 mM D-glucose (Thermo Fisher Scientific, Waltham, MA, USA), pH 7.5]. The pH was adjusted to 7.5 with HCl. Amino acids were supplemented at a concentration of 0.78 mM. Glutamic acid was added as mono sodium salt. Cultures were incubated for two weeks at 30 °C and 180 rpm in an Innova orbital shaker. If not indicated otherwise, all experiments were conducted three times independently.
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