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Originpro 8.5.0 sr1

Manufactured by OriginLab
Sourced in United States

OriginPro 8.5.0 SR1 is a data analysis and graphing software. It provides tools for data manipulation, statistical analysis, and visualization.

Automatically generated - may contain errors

13 protocols using originpro 8.5.0 sr1

1

Software-Assisted Data Processing Protocol

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Data were acquired using WSxM 4.0 software, treated using a custom-generated MATLAB code (The MATHWORKS, Inc.; code available in the Supplementary Information), and analyzed with OriginPro 8.5.0 SR1 (OriginLab Corp.). Errors are indicated as standard deviation of the mean.
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2

MTX Cytotoxicity Determination in A549 Cells

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For the determination of the half maximal inhibitory concentrations (IC50) of mitoxantrone dihydrochloride (MTX; CAS no.: 70476-82-3; HPLC grade from Sigma-Aldrich), MTT assay was performed as previously reported [26] (link). Briefly, 40 h after cell seeding and cultivation in normoxia and hypoxia, MTX was added to cells for another 24 or 48 h. IC50 values were evaluated based on the changes in the metabolic activity of A549 cells and extrapolated from a dose–response fit to the metabolic activity data using OriginPro 8.5.0 SR1 (OriginLab Corp., Northampton, MA, USA).
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3

AFM Measurements of Force-Separation Curves

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Force-separation curves were measured with either an MFP3D AFM (Asylum Research, Oxford Instruments) or a NanoWizard 3 BioScience AFM (JPK Instruments, Bruker Nano GmbH) at room temperature and under liquid environment (sodium phosphate buffer 50 mM, pH 6.5). After having measured the sensitivity (V·m−1), the cantilever spring constants were individually calibrated by using the equipartition theorem (thermal noise routine)69 (link). Force-separation curves were recorded by approaching and retracting the AFM tip at constant velocity (0.5 to 4 μm·s−1) and in the force map mode over an area of 3 × 3 μm2. The maximum applied (contact) force in each cycle was set to 300 pN. At least two independent experiments were conducted in each case. AFM data were acquired and treated using the AFM software and analyzed with OriginPro 8.5.0 SR1 (OriginLab Corp.). Errors are indicated as the standard deviation of the mean.
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4

Evaluating Acridine Compound Cytotoxicity

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MTT assays were performed in order to evaluate changes in the metabolic activity of cells that had occurred as a consequence of treatment with the acridine compounds. A549 cells (15 × 103 cells/cm2) and CCD-18Co (15.625 × 103 cells/cm2) were seeded in 96-well microplates. The A549 cells were treated for 24 and 48 h, and the CCD-18Co cells were treated for 48 h with different concentrations (5, 25, 50 and 75 µM) of the derivatives. After the treatment, the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltertrazolium bromide) solution in PBS (5 mg mL−1) was added to each well. The reaction was stopped after 4 h incubation, and the formazan was dissolved by the addition of SDS at a final concentration of 3.3%. The absorbance of formazan (λ = 584 nm) was measured using a BMG FLUOstar Optima spectrometer (BMG Labtech GmbH, Offenburg, Germany). The results were evaluated as percentages of the absorbance of the untreated control. Results are presented as the average percentage of cells from three independent experiments. IC50 values for the derivatives were extrapolated from a sigmoidal fit (dose-response curve) to the metabolic activity data using OriginPro 8.5.0 SR1 (OriginLab Corp., Northampton, MA, USA).
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5

Comparative Statistical Analysis Protocol

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All mathematical and statistical computations were made using Excel 2007 (Microsoft Office) and OriginPro 8.5.0 SR1 (OriginLab Corporation, USA). Data were reported as mean ± SD. Student t test was used for comparison of the developed method with standard method.
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6

Triplicate Experiment Data Analysis

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In this work, all experiments and measurements were carried out in triplicate, and data were expressed as a mean ± standard deviation (SD). The resulting data were analyzed by the use of OriginPro 8.5.0 SR1 (OriginLab Corporation, Northampton, MA, USA).
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7

Statistical Analysis of Experimental Data

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All analyses were completed using MedCalc version 20.010 (MedCalc Software Ltd., Ostend, Belgium) and OriginPro 8.5.0 SR1 (OriginLab Corporation, Northampton, MA, USA). Descriptive statistics were used to characterize the variables. A one-way repeated measures analysis of variances (ANOVA) followed by a Tukey post hoc test was used to determine whether three group means within each study group were different. Student’s t-test (unpaired two-sample test) was performed to test differences between groups at each follow-up. For comparison of nominal variables, the X2 test for a 2 × 2 or higher contingency table was used. p values less than 0.05 were considered statistically significant.
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8

Evaluating Biscoumarin Derivatives' Effects on Cell Metabolism

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MTT assays were performed in order to evaluate changes in the metabolic activity of cells that had occurred as a consequence of treatment with the biscoumarin derivatives. A549 cells (15 × 103 cells/cm2) and CCD-18Co (15 625 × 103 cells/cm2) were seeded in 96-well microplates. The cells were treated for 24 and 48 h with different concentrations (10, 25, 35, 50, 65, 75, and 100 µM) of the derivatives. After the treatment, the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltertrazolium bromide) solution in PBS (5 mg mL−1) was added to each well. The reaction was stopped after 4 h incubation, and the formazan was dissolved by the addition of sodium dodecyl sulfate (SDS) at a final concentration of 3.3%. The absorbance of formazan (λ = 584 nm) was measured using a BMG FLUOstar Optima spectrometer (BMG Labtech GmbH, Offenburg, Germany). The results were evaluated as percentages of the absorbance of the untreated control. Results are presented as the average percentage of cells from three independent experiments. IC50 values for the derivatives were extrapolated from a sigmoidal fit (dose–response curve) to the metabolic activity data using OriginPro 8.5.0 SR1 (OriginLab Corp., Northampton, MA, USA).
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9

Statistical Analysis of Experimental Data

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Experimental data were analyzed for statistical significance by analysis of variance (ANOVA) and Tukey’s test with a p < 0.05 significance level with the help of statistical software OriginPro 8.5.0 SR1 (OriginLab Corporation, Northampton, MA, USA).
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10

Tensile Strength and Elongation Analysis

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The tensile strength and percentage of elongation at break were determined using the methodology proposed by Fonseca-García, Jiménez-Regalado [11 (link)]. The experimental data regarding the mechanical properties were analyzed using OriginPro 8.5.0 SR1 software (OriginLab Corporation, Northampton, MA, USA) through an analysis of variance and the Tukey test with a significance level of p < 0.05.
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