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Oxaliplatin oxa

Manufactured by Merck Group
Sourced in United States

Oxaliplatin (OXA) is a platinum-based chemotherapeutic agent used in the laboratory setting for research purposes. It functions as a DNA-binding and -damaging agent, primarily interfering with DNA replication and transcription. The core function of OXA is to serve as a research tool for studying the effects of platinum-based compounds on cellular processes.

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5 protocols using oxaliplatin oxa

1

CRC Cell Line Sensitivity to 5-Fu and Oxa

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Human CRC cell lines HCT116 and SW480 were cultured in Dulbecco’s Modified Eagle Medium with 4.5 g/L glucose (DMEM; Gibco BRL, Grand Island, NY, USA) containing 10% fetal bovine serum (FBS; Gibco BRL) and 1% antibiotic/antimycotic solution. Cells were maintained at 37 °C in an atmosphere of 5% CO2 and 95% room air.
LncRNA CRNDE siRNA, control siRNA, miR-181a-5p and miR-181a-5p inhibitor were all obtained from GenePharma (Shanghai, China). 5-fluorouracil (5-Fu) and oxaliplatin (Oxa) were all purchased from Sigma Aldrich (St Louis, MO, USA). Lipofectamine™ 3000 (Life Technologies, San Diego, CA, USA) was used for cell transfection according to manufacturer’s instructions. After 48 h of transfection, cells were treated different concentration of 5-Fu (0, 3, 6, 12, 24 and 48 μg/ml) or Oxa (0, 4, 8, 16, 32 and 64 μg/ml).
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2

Oxaliplatin Cytotoxicity Evaluation

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KR158-luc or GL261-luc cells were seeded in triplicate in 96-well cell culture dishes in normal growth conditions. Cells were then left untreated or treated with 50, 100, 200, 300, 400 or 500 μM oxaliplatin (OXA; Sigma-Aldrich) dissolved in DMEM for 24 h and then WST-1 proliferation agent (Sigma-Aldrich) was added to the media. Cell growth was then determined by absorbance readings according to the manufacturer’s recommendations.
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3

Synthesis and Characterization of Polymer-based Drug Delivery System

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Iron (III) chloride hexahydrate (≥99%), iron (II) chloride tetrahydrate (98%), oleic acid (≥90%) (OA), potassium dihydrogen phosphate (≥98%), N-hydroxysuccinimide (NHS) (98%), N-(3-dimethyl aminoproyl)-N’-ethylcarbodiimide hydrochloride (EDC), N,N′-dicyclohexylcarbodiimide (DCC) (≥99.0%), poly(ethylene glycol diamine) (NH2-PEG-NH2, Mn = 3000), (≥98.0%), polyvinyl alcohol (PVA, Mowiol 4–88), deuterated chloroform (≥99%) and oxaliplatin (OXA) (≥99%) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Dialysis bags (Spectra/Por, MWCO: 3.5 and 12–14 kDa) and a monoclonal anti-CD133-TMP4 Ab conjugated to Alexa Fluor 488 were purchased from Thermo Fisher Scientific (Waltham, MA, USA). Commercial PLGA Mn of 10 kDa (Purasorb PDLG 7502A, 70/30 LA/GA) was kindly donated by Corbion (The Netherlands). Sodium hydroxide, chloroform, ethyl ether, tetrahydrofuran (THF), dichloromethane (DCM), ethanol, and ammonia p.a. were purchased from Penta (The Czech Republic). Media used for cell culture Eagle’s Minimum Essential Medium (EMEM) and Dulbecco’s Modified Eagles’ medium (DMEM) were bought from Thermo Fisher Scientific (Waltham, MA, USA). Microscopy dishes with glass bottom (ø35 mm, 1.5#) were supplied by MatTek Life Sciences (Boston, MA, USA). Filters with a 0.45-µm pore size were purchased from JetBiofil (China). For all experiments, Millipore water was used.
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4

Immunohistochemical Profiling of Colorectal Cancer

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Monoclonal mouse anti-human CD133 and mouse anti-human EpCAM antibodies were purchased from Miltenyi Biotec (Headquarters, Germany). Anti-α-SMA antibody was obtained from Dako (Denmark). Anti-FAP was purchased from Abcam (Cambridge, UK) and anti-vimentin was purchased from Cell Signaling Technology (Danvers, MA). Anti-Wnt3a and anti-beta Actin were purchased from Santa Cruz Biotechnology (CA, USA). Alexa Fluor 488-conjugated goat anti-mouse lgG was obtained from Jackson ImmunoResearch (Pennsylvania, USA). GW4869, 5-fluorouracil (5-Fu) and oxaliplatin (OXA) were purchased from Sigma (St. Louis, USA). Matrigel was obtained from B.D. (Franklin Lakes, NJ).
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5

Cytotoxicity of Chemotherapeutic Agents

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Breast cancer cells were seeded into 96-well plates (10,000 cells/well) and cultured in complete medium for 24 h and then treated with different concentrations (0–500 μM) of chemotherapy agents, including Doxorubicin (Dox) (MCE, NJ, USA), Gefitinib (Gef) (Sigma-Aldrich, MO, USA), Oxaliplatin (Oxa) (Sigma-Aldrich, MO, USA) and Fluorouracil (5-FU) (Sigma-Aldrich, MO, USA). After another 20 h incubation, 10 μl MTT was added to each well for 4 h at 37 °C. The formazan produced by viable cells was dissolved with DMSO (Sigma-Aldrich, MO, USA) and then measured the absorbance at 570 nm.
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