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Cacl2 solution

Manufactured by Thermo Fisher Scientific
Sourced in United States

CaCl2 solution is a laboratory reagent that provides a source of calcium ions (Ca2+) and chloride ions (Cl-) in aqueous solution. It is a common inorganic compound used in various scientific and industrial applications. The solution's core function is to serve as a chemical reagent for procedures that require the introduction of calcium and chloride ions into an experimental setup.

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4 protocols using cacl2 solution

1

Aged Bovine Blood Clots for Thrombolysis

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We used aged (4–5 d old) bovine blood clots in this study. Blood clot samples were prepared following the previously described method (Sutton et al. 2013 (link); Zhang et al. 2016 (link)), with the exception of sample storage materials. Briefly, bovine blood (Densco Marketing, Inc., Woodstock, IL, USA) was mixed with 2.5%–3.0% calcium chloride (CaCl2) solution (Fisher Scientific, Fair Lawn, NJ, USA) with a volume ratio of 10:1 (100 mL blood and 10 mL CaCl2; Kim et al. 2016 (link); Suo et al. 2017 ). The mixture was transferred to 1.8 mL transfer pipettes (outer diameter 6.6 mm; 33620 S, Thermo Fisher Scientific, Waltham, MA, USA). After 3 h in a 37°C water bath, the blood clot-filled pipettes were stored at 4°C for 4 d. A 302 ± 19 mg clot sample (approximate dimensions of 15 mm length and 5 mm diameter) was used for each thrombolysis test (Fig. 1d).
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2

In Vitro Bovine Blood Clot Preparation

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The blood clots were prepared following a similar procedure used in our previous work [29 (link)]. First, the fresh bovine blood obtained from Densco Marketing, Inc. (Woodstock, IL, USA) was mixed with 2.75% W/V CaCl2 solution (Fisher Scientific, Fair Lawn, NJ) in a volume ratio of 10:1 (50 mL blood /5 mL CaCl2 solution). Second, the mixed blood solution was drained to Tygon tubes (6.35 mm ID, 7.94 mm OD). Then the Tygon tubes were immersed in a 37 °C water bath for 3 h. Finally, the tubes with coagulated blood were stored at low temperature (4 °C) for 1 to 7 days to generate clots with different ages. Clot samples for thrombolysis tests were cut into a cylindrical shape (length: 12 ± 2 mm, diameter 3 ± 0.5 mm) and weighted as 130 mg ± 10% in mass and then positioned into a customized polydimethylsiloxane (PDMS) blood vessel mimicking phantom (microchannel, ID: 2-3 mm with 33.3 % stenosis) as shown in Fig. 2.
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3

Synthesis and Characterization of Organic Compounds

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Anhydrous
organic solvents (dichloromethane, hexanes, and ethyl acetate) were
obtained from Fisher Scientific (Pittsburgh, PA) and used as they
were received. 1-Ethyl-3-(3-(dimethylamino)propyl)carbodiimide (EDCI),
4-dimethylaminopyridine (DMAP), 1-hydroxy benzotriazole (HOBt), and
molecules 1118 were obtained from
Milipore-Sigma (Burlington, MA). For analytical TLC, UNIPLATETM silica
gel GHLF 250 μm precoated plates from ANALTECH, Newark, DE,
were employed. Column chromatography utilized Sigma-Aldrich’s
silica gel (200–400 mesh, 60 Å). All reactions were conducted
in oven-dried glassware. Flash chromatography was carried out using
Teledyne ISCO’s Combiflash RF system and disposable normal
silica cartridges with a particle size of 30–50 μm, mesh
size of 230–400, and pore size of 60 Å. The flow rate
of the mobile phase was in the range of 18–35 mL/min, and mobile
phase gradients of ethyl acetate/hexanes were used to elute inhibitors.
Human plasmas were purchased from George King Bio-Medical, Inc. (Overland
Park, KS). Reagents for clotting assays, including APTT reagent, thromboplastin
D, and CaCl2 solution, were all from Fisher Scientific.
UFHs were from Milipore-Sigma, whereas argatroban HCl, rivaroxaban,
and C6B7 were from Fisher Scientific.
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4

Preparation and Characterization of Bovine Blood Clots

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The unretracted and retracted bovine blood clots were utilized in this test. The fresh bovine blood clots were made with a similar process described in our earlier study [41 (link),42 (link)]. Initially, the 2.75 % W/V 10 mL CaCl2 solution (Fisher Scientific, Fair Lawn, NJ, USA) was blended with the 100 mL fresh bovine blood (Densco Marketing, Inc., Wood stock, IL, USA) in a volume ratio of 10:1. Next, half of the mixed-blood solution was transferred to a 2 mL micro-centrifuge plastic tube batch to form the unretracted clot. The other half of the mixed-blood solution was injected into the 2 mL borosilicate glass pipettes to form the retracted blood clot. Then the unretracted and retracted blood clots were incubated in the water bath (PolyPro Bath, Model RS-PB-100, USA) at 37 °C for three hours. Finally, the blood clots were put in storage in a freezer at ~4 °C for 72 h to two weeks to form clots of different ages. In each thrombolysis test, the clot samples were sliced into the cylinder shape with a length of about 10 ± 2 mm and a diameter of about 3 ± 0.5 mm. The weight of the clot samples was maintained at about 120 ± 12 mg in mass for each test. The prepared clot was finally placed into a venous flow model (Fig.3) for the in-vitro thrombolysis test.
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