Structured Review

Phenomenex phenomenex luna c18
Substrate scope study. Reaction condition: precursor (5 mg), [ 18 F]HF in target water (370–740 MBq), K 2 CO 3 (60 µg, 0.43 µmol), DMSO (0.3 mL), 150 °C MW, 20 min. RCC was determined by analytical HPLC and the identity of the product was confirmed by co-injection with the standard compounds. HPLC condition: <t>Phenomenex</t> Luna <t>C18</t> (2) column, 100 × 4.6 mm, 5 µm. Mobile phase: 5–95% acetonitrile in water (0.1% NH 4 OH) in 8 min; 1.0 mL/min.
Phenomenex Luna C18, supplied by Phenomenex, used in various techniques. Bioz Stars score: 86/100, based on 40 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/phenomenex luna c18/product/Phenomenex
Average 86 stars, based on 40 article reviews
Price from $9.99 to $1999.99
phenomenex luna c18 - by Bioz Stars, 2022-08
86/100 stars

Images

1) Product Images from "Radiosynthesis of 5-[18F]Fluoro-1,2,3-triazoles through Aqueous Iodine–[18F]Fluorine Exchange Reaction"

Article Title: Radiosynthesis of 5-[18F]Fluoro-1,2,3-triazoles through Aqueous Iodine–[18F]Fluorine Exchange Reaction

Journal: Molecules

doi: 10.3390/molecules26185522

Substrate scope study. Reaction condition: precursor (5 mg), [ 18 F]HF in target water (370–740 MBq), K 2 CO 3 (60 µg, 0.43 µmol), DMSO (0.3 mL), 150 °C MW, 20 min. RCC was determined by analytical HPLC and the identity of the product was confirmed by co-injection with the standard compounds. HPLC condition: Phenomenex Luna C18 (2) column, 100 × 4.6 mm, 5 µm. Mobile phase: 5–95% acetonitrile in water (0.1% NH 4 OH) in 8 min; 1.0 mL/min.
Figure Legend Snippet: Substrate scope study. Reaction condition: precursor (5 mg), [ 18 F]HF in target water (370–740 MBq), K 2 CO 3 (60 µg, 0.43 µmol), DMSO (0.3 mL), 150 °C MW, 20 min. RCC was determined by analytical HPLC and the identity of the product was confirmed by co-injection with the standard compounds. HPLC condition: Phenomenex Luna C18 (2) column, 100 × 4.6 mm, 5 µm. Mobile phase: 5–95% acetonitrile in water (0.1% NH 4 OH) in 8 min; 1.0 mL/min.

Techniques Used: High Performance Liquid Chromatography, Injection

2) Product Images from "Rugosic acid A, derived from Rosa rugosa Thunb., is novel inhibitory agent for NF‐κB and IL‐6/ STAT3 axis in acute lung injury model, et al. Rugosic acid A, derived from Rosa rugosa Thunb., is novel inhibitory agent for NF‐κB and IL‐6/ STAT3 axis in acute lung injury model"

Article Title: Rugosic acid A, derived from Rosa rugosa Thunb., is novel inhibitory agent for NF‐κB and IL‐6/ STAT3 axis in acute lung injury model, et al. Rugosic acid A, derived from Rosa rugosa Thunb., is novel inhibitory agent for NF‐κB and IL‐6/ STAT3 axis in acute lung injury model

Journal: Phytotherapy Research

doi: 10.1002/ptr.6767

Quantitative analysis of rugosic acid A in R. rugosa extract. (a) Structure of rugosic acid A. (b) Calibration curve of rugosic aicd A standard. (c) HPLC chromatogram pattern of rugosic acid A in extract from hexan fraction of R.rugosa .; HPLC model: Agilent 1100series (Agilent), column: Phenomenex Luna C18 (5 μm, 4.6 × 250 mm), column temperature: 25°C, mobile phase: (a) H 2 O, (b) ACN, gradient: 0–0, 5–0, 45–100, 65(min)‐100(B%) [Colour figure can be viewed at wileyonlinelibrary.com ]
Figure Legend Snippet: Quantitative analysis of rugosic acid A in R. rugosa extract. (a) Structure of rugosic acid A. (b) Calibration curve of rugosic aicd A standard. (c) HPLC chromatogram pattern of rugosic acid A in extract from hexan fraction of R.rugosa .; HPLC model: Agilent 1100series (Agilent), column: Phenomenex Luna C18 (5 μm, 4.6 × 250 mm), column temperature: 25°C, mobile phase: (a) H 2 O, (b) ACN, gradient: 0–0, 5–0, 45–100, 65(min)‐100(B%) [Colour figure can be viewed at wileyonlinelibrary.com ]

Techniques Used: High Performance Liquid Chromatography

3) Product Images from "Rugosic acid A, derived from Rosa rugosa Thunb., is novel inhibitory agent for NF‐κB and IL‐6/ STAT3 axis in acute lung injury model, et al. Rugosic acid A, derived from Rosa rugosa Thunb., is novel inhibitory agent for NF‐κB and IL‐6/ STAT3 axis in acute lung injury model"

Article Title: Rugosic acid A, derived from Rosa rugosa Thunb., is novel inhibitory agent for NF‐κB and IL‐6/ STAT3 axis in acute lung injury model, et al. Rugosic acid A, derived from Rosa rugosa Thunb., is novel inhibitory agent for NF‐κB and IL‐6/ STAT3 axis in acute lung injury model

Journal: Phytotherapy Research

doi: 10.1002/ptr.6767

Quantitative analysis of rugosic acid A in R. rugosa extract. (a) Structure of rugosic acid A. (b) Calibration curve of rugosic aicd A standard. (c) HPLC chromatogram pattern of rugosic acid A in extract from hexan fraction of R.rugosa .; HPLC model: Agilent 1100series (Agilent), column: Phenomenex Luna C18 (5 μm, 4.6 × 250 mm), column temperature: 25°C, mobile phase: (a) H 2 O, (b) ACN, gradient: 0–0, 5–0, 45–100, 65(min)‐100(B%) [Colour figure can be viewed at wileyonlinelibrary.com ]
Figure Legend Snippet: Quantitative analysis of rugosic acid A in R. rugosa extract. (a) Structure of rugosic acid A. (b) Calibration curve of rugosic aicd A standard. (c) HPLC chromatogram pattern of rugosic acid A in extract from hexan fraction of R.rugosa .; HPLC model: Agilent 1100series (Agilent), column: Phenomenex Luna C18 (5 μm, 4.6 × 250 mm), column temperature: 25°C, mobile phase: (a) H 2 O, (b) ACN, gradient: 0–0, 5–0, 45–100, 65(min)‐100(B%) [Colour figure can be viewed at wileyonlinelibrary.com ]

Techniques Used: High Performance Liquid Chromatography

4) Product Images from "Anti-Human Rhinoviral Activity of Polybromocatechol Compounds Isolated from the Rhodophyta, Neorhodomela aculeata"

Article Title: Anti-Human Rhinoviral Activity of Polybromocatechol Compounds Isolated from the Rhodophyta, Neorhodomela aculeata

Journal: Marine Drugs

doi: 10.3390/md10102222

RP-HPLC profile of sub-fractions of EtOAc-soluble fraction (ESF) of N. aculeata . Performed on an Agilent 1300 HPLC system fitted with a Phenomenex Luna C18 (2) column (150 × 4.6 mm, 5 μm). The elution solvent system was binary gradient of solvent A (0.02% trifluoroacetic acid (TFA) in water); solvent B (0.02% TFA in acetonitrile). The gradient flow program was, as follows: 0 min, 10% B; 30 min. The flow rate was 0.7 mL/min and detection wavelength was set at 280 nm and column temperature was 25 °C. The chromatogram of F1 was not shown.
Figure Legend Snippet: RP-HPLC profile of sub-fractions of EtOAc-soluble fraction (ESF) of N. aculeata . Performed on an Agilent 1300 HPLC system fitted with a Phenomenex Luna C18 (2) column (150 × 4.6 mm, 5 μm). The elution solvent system was binary gradient of solvent A (0.02% trifluoroacetic acid (TFA) in water); solvent B (0.02% TFA in acetonitrile). The gradient flow program was, as follows: 0 min, 10% B; 30 min. The flow rate was 0.7 mL/min and detection wavelength was set at 280 nm and column temperature was 25 °C. The chromatogram of F1 was not shown.

Techniques Used: High Performance Liquid Chromatography, Flow Cytometry

5) Product Images from "Radiosynthesis of 5-[18F]Fluoro-1,2,3-triazoles through Aqueous Iodine–[18F]Fluorine Exchange Reaction"

Article Title: Radiosynthesis of 5-[18F]Fluoro-1,2,3-triazoles through Aqueous Iodine–[18F]Fluorine Exchange Reaction

Journal: Molecules

doi: 10.3390/molecules26185522

Substrate scope study. Reaction condition: precursor (5 mg), [ 18 F]HF in target water (370–740 MBq), K 2 CO 3 (60 µg, 0.43 µmol), DMSO (0.3 mL), 150 °C MW, 20 min. RCC was determined by analytical HPLC and the identity of the product was confirmed by co-injection with the standard compounds. HPLC condition: Phenomenex Luna C18 (2) column, 100 × 4.6 mm, 5 µm. Mobile phase: 5–95% acetonitrile in water (0.1% NH 4 OH) in 8 min; 1.0 mL/min.
Figure Legend Snippet: Substrate scope study. Reaction condition: precursor (5 mg), [ 18 F]HF in target water (370–740 MBq), K 2 CO 3 (60 µg, 0.43 µmol), DMSO (0.3 mL), 150 °C MW, 20 min. RCC was determined by analytical HPLC and the identity of the product was confirmed by co-injection with the standard compounds. HPLC condition: Phenomenex Luna C18 (2) column, 100 × 4.6 mm, 5 µm. Mobile phase: 5–95% acetonitrile in water (0.1% NH 4 OH) in 8 min; 1.0 mL/min.

Techniques Used: High Performance Liquid Chromatography, Injection

6) Product Images from "Antiulcerogenic Activity and Toxicity of Bauhinia holophylla Hydroalcoholic Extract"

Article Title: Antiulcerogenic Activity and Toxicity of Bauhinia holophylla Hydroalcoholic Extract

Journal: Evidence-based Complementary and Alternative Medicine : eCAM

doi: 10.1155/2015/439506

HPLC-PAD analytical chromatogram of 70% EtOH leaf extract of Bauhinia holophylla . Experimental conditions: eluents A (H 2 O + 0.1% formic acid) and B (MeOH + 0.1% formic acid). Gradient system: 25–100% B over 70 min. Column: Phenomenex Luna C18 (250 × 4.6 mm i.d., 5 μ m). Flow rate: 0.8 mL·min −1 and λ = 360 nm. Injected volume: 10 μ L. Identified compounds: 1, myricetin-O-deoxyhexoside, 2, quercetin-O-hexoside, 3, quercetin-O-pentoside, 4, quercetin-O-deoxyhexoside, and 5, isorhamnetin.
Figure Legend Snippet: HPLC-PAD analytical chromatogram of 70% EtOH leaf extract of Bauhinia holophylla . Experimental conditions: eluents A (H 2 O + 0.1% formic acid) and B (MeOH + 0.1% formic acid). Gradient system: 25–100% B over 70 min. Column: Phenomenex Luna C18 (250 × 4.6 mm i.d., 5 μ m). Flow rate: 0.8 mL·min −1 and λ = 360 nm. Injected volume: 10 μ L. Identified compounds: 1, myricetin-O-deoxyhexoside, 2, quercetin-O-hexoside, 3, quercetin-O-pentoside, 4, quercetin-O-deoxyhexoside, and 5, isorhamnetin.

Techniques Used: High Performance Liquid Chromatography, Flow Cytometry, Injection

7) Product Images from "Radiosynthesis of 5-[18F]Fluoro-1,2,3-triazoles through Aqueous Iodine–[18F]Fluorine Exchange Reaction"

Article Title: Radiosynthesis of 5-[18F]Fluoro-1,2,3-triazoles through Aqueous Iodine–[18F]Fluorine Exchange Reaction

Journal: Molecules

doi: 10.3390/molecules26185522

Substrate scope study. Reaction condition: precursor (5 mg), [ 18 F]HF in target water (370–740 MBq), K 2 CO 3 (60 µg, 0.43 µmol), DMSO (0.3 mL), 150 °C MW, 20 min. RCC was determined by analytical HPLC and the identity of the product was confirmed by co-injection with the standard compounds. HPLC condition: Phenomenex Luna C18 (2) column, 100 × 4.6 mm, 5 µm. Mobile phase: 5–95% acetonitrile in water (0.1% NH 4 OH) in 8 min; 1.0 mL/min.
Figure Legend Snippet: Substrate scope study. Reaction condition: precursor (5 mg), [ 18 F]HF in target water (370–740 MBq), K 2 CO 3 (60 µg, 0.43 µmol), DMSO (0.3 mL), 150 °C MW, 20 min. RCC was determined by analytical HPLC and the identity of the product was confirmed by co-injection with the standard compounds. HPLC condition: Phenomenex Luna C18 (2) column, 100 × 4.6 mm, 5 µm. Mobile phase: 5–95% acetonitrile in water (0.1% NH 4 OH) in 8 min; 1.0 mL/min.

Techniques Used: High Performance Liquid Chromatography, Injection

8) Product Images from "Immobilization of NTPDase-1 from Trypanosoma cruzi and Development of an Online Label-Free Assay"

Article Title: Immobilization of NTPDase-1 from Trypanosoma cruzi and Development of an Online Label-Free Assay

Journal: Journal of Analytical Methods in Chemistry

doi: 10.1155/2016/9846731

Representative chromatogram for the separation of ATP (3), ADP (2), and AMP (1) by a Phenomenex Luna C18 (100 Å 250 × 4.6 mm, 5 μ m) analytical column at a flow rate of 1.0 mL·min −1 , eluent Buffer C : MeOH (84 : 16 v/v), and UV detection at λ = 254 nm. The chromatographic conditions of the two-dimensional method are described in Table 1 .
Figure Legend Snippet: Representative chromatogram for the separation of ATP (3), ADP (2), and AMP (1) by a Phenomenex Luna C18 (100 Å 250 × 4.6 mm, 5 μ m) analytical column at a flow rate of 1.0 mL·min −1 , eluent Buffer C : MeOH (84 : 16 v/v), and UV detection at λ = 254 nm. The chromatographic conditions of the two-dimensional method are described in Table 1 .

Techniques Used: Flow Cytometry

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  • 86
    Phenomenex c18 column luna
    Effect of iPLA 2 γ inhibitor, (R)-BEL, on SWCNT-induced pulmonary inflammation. ( A ) Production of pro- and anti-inflammatory cytokines in BAL of mice. Measurements were performed using Bio-Plex Pro Mouse Cytokine 23-Plex Immunoassay kit, composed of a combination of pro- and anti-inflammatory cytokines. ( B ) Representative images of lung sections from mice on day 1 post exposure to SWCNT or R-BEL alone, SWCNT/R-BEL together and control group (neutrophils indicated by arrows). ( C ) Average neutrophil counts per whole lung sections from 3 mice per group. ( D ) Tissue damage and fibrogenic response in BAL of mice. Pulmonary tissue damage was measured as protein in BAL of mice on day 1 after exposure to SWCNT (40 μ g/mouse; a). Fibrogenic response was assessed on day 7 post exposure to SWCNT (40 μ g/mouse) by the levels of collagen measured in the lung of mice (b). ( E ) Production of pro-inflammatory lipid mediators, LTB 4 (a), and HXB 3 (b) in lung of C57B6J mice. Structural formulas of LTB 4 and HXB 3 (inserts). ( F ) (R)-BEL treatment reversed the increases in PNLP8 expression (green) and cell death (TUNEL(magenta) positive nuclei, arrows) induced by SWCNT exposure in mouse lungs (a), % PNLP8 positive cells relative to total cell number (b), % TUNEL positive cells relative to total cell number (c). ( G ) MS spectrum of CL obtained from control mouse lung (a). Base peak chromatograms of CL molecular species with m / z 1475.992 from lung of control mouse and mouse exposed to SWCNT in the absence and in the presence of (R)-BEL on day 1 after treatment (b). MS 2 spectrum of CL molecular species with m / z 1475.992 containing arachidonic acid (C20:4), <t>CL-C18:1/C18:2/C18:1/C20:4,</t> obtained from control mouse lung (c). All data are mean ± SD ( n = 4–5 mice per group). * P
    C18 Column Luna, supplied by Phenomenex, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/c18 column luna/product/Phenomenex
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    c18 column luna - by Bioz Stars, 2022-08
    86/100 stars
      Buy from Supplier

    86
    Phenomenex luna c18
    HPLC overlay chromatogram of Bruguiera gymnorrhiza (BRG), n-butanol fraction of BRG and compound G. The HPLC fingerprint indicated the presence of compound G at retention time of 15.12 min. The analysis was carried out using Shimadzu high-performance liquid chromatography system attached with an ultraviolet detector and prepacked <t>C18</t> column (4.6 mm × 250 mm, 5 μm; Agilent Technologies). The separation was carried out using a gradient conc. of Solvent A (Water with 0.1% TFA) and Solvent B (Acetonitrile with 0.1% TFA). The total run time for the separation was 30 min (flow rate of 1 ml/min) at λ = 220 nm
    Luna C18, supplied by Phenomenex, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/luna c18/product/Phenomenex
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    luna c18 - by Bioz Stars, 2022-08
    86/100 stars
      Buy from Supplier

    86
    Phenomenex c18
    Chromatogram of concentrated methanol extract of ( a ) purified beeswax, ( b ) raw beeswax, and ( c ) green propolis. Chromatographic conditions: <t>C18</t> column with a mobile phase composed of (A) water containing 0.4% formic acid, 5% methanol, and 2% isopropanol, and (B) acetonitrile and 2% isopropanol. The flow was 1 mL/min in the concentration gradient, using 20% B for 3 min, 20–25% B for 3–4 min, 25% B for 4–15 min, 25–45% B for 15–20 min, 45% B for 20–40 min, 45–60% B for 40–45 min, 60–80% B for 45–68.83 min, 80–20% B for 68.86–70 min, and 20% B for 70–80 min. An injection volume of 15 µL, oven temperature of 30 °C, and wavelength of 300 nm were used.
    C18, supplied by Phenomenex, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/c18/product/Phenomenex
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    c18 - by Bioz Stars, 2022-08
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    86
    Phenomenex luna c18 column
    Effects of Guiera senegalensis hydroethanolic extract (GS: 1 µg/L, 4 µg/L and 8 µg/L) on Sco-induced increasing in the activity of the acetylcholinesterase (AChE). Each <t>column</t> represents mean ± S.E.M. of 10 zebrafish. For Tukey’s post hoc analyses: *** p
    Luna C18 Column, supplied by Phenomenex, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/luna c18 column/product/Phenomenex
    Average 86 stars, based on 1 article reviews
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    Image Search Results


    Effect of iPLA 2 γ inhibitor, (R)-BEL, on SWCNT-induced pulmonary inflammation. ( A ) Production of pro- and anti-inflammatory cytokines in BAL of mice. Measurements were performed using Bio-Plex Pro Mouse Cytokine 23-Plex Immunoassay kit, composed of a combination of pro- and anti-inflammatory cytokines. ( B ) Representative images of lung sections from mice on day 1 post exposure to SWCNT or R-BEL alone, SWCNT/R-BEL together and control group (neutrophils indicated by arrows). ( C ) Average neutrophil counts per whole lung sections from 3 mice per group. ( D ) Tissue damage and fibrogenic response in BAL of mice. Pulmonary tissue damage was measured as protein in BAL of mice on day 1 after exposure to SWCNT (40 μ g/mouse; a). Fibrogenic response was assessed on day 7 post exposure to SWCNT (40 μ g/mouse) by the levels of collagen measured in the lung of mice (b). ( E ) Production of pro-inflammatory lipid mediators, LTB 4 (a), and HXB 3 (b) in lung of C57B6J mice. Structural formulas of LTB 4 and HXB 3 (inserts). ( F ) (R)-BEL treatment reversed the increases in PNLP8 expression (green) and cell death (TUNEL(magenta) positive nuclei, arrows) induced by SWCNT exposure in mouse lungs (a), % PNLP8 positive cells relative to total cell number (b), % TUNEL positive cells relative to total cell number (c). ( G ) MS spectrum of CL obtained from control mouse lung (a). Base peak chromatograms of CL molecular species with m / z 1475.992 from lung of control mouse and mouse exposed to SWCNT in the absence and in the presence of (R)-BEL on day 1 after treatment (b). MS 2 spectrum of CL molecular species with m / z 1475.992 containing arachidonic acid (C20:4), CL-C18:1/C18:2/C18:1/C20:4, obtained from control mouse lung (c). All data are mean ± SD ( n = 4–5 mice per group). * P

    Journal: Journal of leukocyte biology

    Article Title: Redox (phospho)lipidomics of signaling in inflammation and programmed cell death

    doi: 10.1002/JLB.3MIR0119-004RR

    Figure Lengend Snippet: Effect of iPLA 2 γ inhibitor, (R)-BEL, on SWCNT-induced pulmonary inflammation. ( A ) Production of pro- and anti-inflammatory cytokines in BAL of mice. Measurements were performed using Bio-Plex Pro Mouse Cytokine 23-Plex Immunoassay kit, composed of a combination of pro- and anti-inflammatory cytokines. ( B ) Representative images of lung sections from mice on day 1 post exposure to SWCNT or R-BEL alone, SWCNT/R-BEL together and control group (neutrophils indicated by arrows). ( C ) Average neutrophil counts per whole lung sections from 3 mice per group. ( D ) Tissue damage and fibrogenic response in BAL of mice. Pulmonary tissue damage was measured as protein in BAL of mice on day 1 after exposure to SWCNT (40 μ g/mouse; a). Fibrogenic response was assessed on day 7 post exposure to SWCNT (40 μ g/mouse) by the levels of collagen measured in the lung of mice (b). ( E ) Production of pro-inflammatory lipid mediators, LTB 4 (a), and HXB 3 (b) in lung of C57B6J mice. Structural formulas of LTB 4 and HXB 3 (inserts). ( F ) (R)-BEL treatment reversed the increases in PNLP8 expression (green) and cell death (TUNEL(magenta) positive nuclei, arrows) induced by SWCNT exposure in mouse lungs (a), % PNLP8 positive cells relative to total cell number (b), % TUNEL positive cells relative to total cell number (c). ( G ) MS spectrum of CL obtained from control mouse lung (a). Base peak chromatograms of CL molecular species with m / z 1475.992 from lung of control mouse and mouse exposed to SWCNT in the absence and in the presence of (R)-BEL on day 1 after treatment (b). MS 2 spectrum of CL molecular species with m / z 1475.992 containing arachidonic acid (C20:4), CL-C18:1/C18:2/C18:1/C20:4, obtained from control mouse lung (c). All data are mean ± SD ( n = 4–5 mice per group). * P

    Article Snippet: Cardiolipins were separated on a C18 column Luna (2) 3 μ m, 100 Å, 150 × 1 mm (Phenomenex) at a flow rate of 0.050 mL/min on a Dionex Ultimate 3000 HPLC system.

    Techniques: Mouse Assay, Expressing, TUNEL Assay, Mass Spectrometry

    HPLC overlay chromatogram of Bruguiera gymnorrhiza (BRG), n-butanol fraction of BRG and compound G. The HPLC fingerprint indicated the presence of compound G at retention time of 15.12 min. The analysis was carried out using Shimadzu high-performance liquid chromatography system attached with an ultraviolet detector and prepacked C18 column (4.6 mm × 250 mm, 5 μm; Agilent Technologies). The separation was carried out using a gradient conc. of Solvent A (Water with 0.1% TFA) and Solvent B (Acetonitrile with 0.1% TFA). The total run time for the separation was 30 min (flow rate of 1 ml/min) at λ = 220 nm

    Journal: Indian Journal of Pharmacology

    Article Title: 5,7-dihydroxy-2-(3-hydroxy-4, 5-dimethoxy-phenyl)-chromen-4-one-a flavone from Bruguiera gymnorrhiza displaying anti-inflammatory properties

    doi: 10.4103/0253-7613.182890

    Figure Lengend Snippet: HPLC overlay chromatogram of Bruguiera gymnorrhiza (BRG), n-butanol fraction of BRG and compound G. The HPLC fingerprint indicated the presence of compound G at retention time of 15.12 min. The analysis was carried out using Shimadzu high-performance liquid chromatography system attached with an ultraviolet detector and prepacked C18 column (4.6 mm × 250 mm, 5 μm; Agilent Technologies). The separation was carried out using a gradient conc. of Solvent A (Water with 0.1% TFA) and Solvent B (Acetonitrile with 0.1% TFA). The total run time for the separation was 30 min (flow rate of 1 ml/min) at λ = 220 nm

    Article Snippet: A Luna C18 (30 mm × 2.0 mm and 5 µm particle size, Phenomenex, USA) column was used in liquid chromatography–mass spectrometry (LC/MS and LC/MS/MSs) analysis.

    Techniques: High Performance Liquid Chromatography, Flow Cytometry

    Chromatogram of concentrated methanol extract of ( a ) purified beeswax, ( b ) raw beeswax, and ( c ) green propolis. Chromatographic conditions: C18 column with a mobile phase composed of (A) water containing 0.4% formic acid, 5% methanol, and 2% isopropanol, and (B) acetonitrile and 2% isopropanol. The flow was 1 mL/min in the concentration gradient, using 20% B for 3 min, 20–25% B for 3–4 min, 25% B for 4–15 min, 25–45% B for 15–20 min, 45% B for 20–40 min, 45–60% B for 40–45 min, 60–80% B for 45–68.83 min, 80–20% B for 68.86–70 min, and 20% B for 70–80 min. An injection volume of 15 µL, oven temperature of 30 °C, and wavelength of 300 nm were used.

    Journal: Pharmaceutics

    Article Title: A New Approach to Atopic Dermatitis Control with Low-Concentration Propolis-Loaded Cold Cream

    doi: 10.3390/pharmaceutics13091346

    Figure Lengend Snippet: Chromatogram of concentrated methanol extract of ( a ) purified beeswax, ( b ) raw beeswax, and ( c ) green propolis. Chromatographic conditions: C18 column with a mobile phase composed of (A) water containing 0.4% formic acid, 5% methanol, and 2% isopropanol, and (B) acetonitrile and 2% isopropanol. The flow was 1 mL/min in the concentration gradient, using 20% B for 3 min, 20–25% B for 3–4 min, 25% B for 4–15 min, 25–45% B for 15–20 min, 45% B for 20–40 min, 45–60% B for 40–45 min, 60–80% B for 45–68.83 min, 80–20% B for 68.86–70 min, and 20% B for 70–80 min. An injection volume of 15 µL, oven temperature of 30 °C, and wavelength of 300 nm were used.

    Article Snippet: The column used was a C18 (Phenomenex LUNA, Torrance, CA, USA) of 250 mm × 4.6 × 5 μm with a precolumn C18 of 4 mm × 3.0 mm.

    Techniques: Purification, Concentration Assay, Injection

    Effects of Guiera senegalensis hydroethanolic extract (GS: 1 µg/L, 4 µg/L and 8 µg/L) on Sco-induced increasing in the activity of the acetylcholinesterase (AChE). Each column represents mean ± S.E.M. of 10 zebrafish. For Tukey’s post hoc analyses: *** p

    Journal: Plants

    Article Title: Neuroprotective Potential of Guiera senegalensis (Combretaceae) Leaf Hydroethanolic Extract against Cholinergic System Dysfunctions and Oxidative Stress in Scopolamine-Induced Cognitive Impairment in Zebrafish (Danio rerio)

    doi: 10.3390/plants11091149

    Figure Lengend Snippet: Effects of Guiera senegalensis hydroethanolic extract (GS: 1 µg/L, 4 µg/L and 8 µg/L) on Sco-induced increasing in the activity of the acetylcholinesterase (AChE). Each column represents mean ± S.E.M. of 10 zebrafish. For Tukey’s post hoc analyses: *** p

    Article Snippet: Volumes of 5 µL were injected in the LC-PDA Thermo UltiMate 3000 (Pro Analysis Systems, Bucharest, Romania) system equipped with a Luna C18 column (Phenomenex, CA, USA) (150 × 4.6 mm, 100 Å).

    Techniques: Activity Assay