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Oleic Acid

Oleic Acid is a monounsaturated fatty acid found in various plant and animal oils.
It plays a crucial role in biological processes, including cell membrane structure and function.
Oleic Acid has been associated with potential health benefits, such as improved cardiovascular health and reduced inflammation.
Researchers can leverage PubCompare.ai's AI-driven protocol comparison tool to optimize their Oleic Acid studies, identify the best products and procedures, and ensure reproducibility and accuracy in their findings.
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Most cited protocols related to «Oleic Acid»


M. smegmatis mc2155 [72] (link), M. tuberculosis H37Rv and Escherichia coli NEB-10β (New England Biolabs UK Ltd) were used in this work. M. smegmatis and M. tuberculosis were grown on Middlebrook 7H11 agar medium (BD Diagnostics) supplemented with 0.5% glycerol and 10% oleic acid albumin-dextrose-catalase (OADC) (BD Diagnostics). When required, filter-sterilised luciferin was added at a final concentration of 0.157 mM. Liquid cultures of M. smegmatis and M. tuberculosis were grown either in Middlebrook 7H9 broth (BD Diagnostics) containing 0.05% Tween 80 (Sigma) and 10% albumin-dextrose-catalase (ADC) enrichment (BD Diagnostics), or (for M. smegmatis Gluc assays) in Luria-Bertani (LB) medium with 0.05% Tween. LB medium was preferred for the Gluc assays because the background of coelenterazine was 100 times lower in that medium than in 7H9 broth. LB medium was used for culturing E. coli. All the strains were grown at 37°C. The following antibiotics were added when appropriate: ampicillin [100 µg ml−1 (Sigma)], hygromycin B [150 µg ml−1 (Invitrogen)] and kanamycin [25 µg ml−1, for mycobacteria, 50 µg ml−1 for E. coli (Sigma)].
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Publication 2010
Agar Albumins Ampicillin Antibiotics, Antitubercular Biological Assay Catalase coelenterazine Diagnosis Escherichia coli Glucose Glycerin Hygromycin B Kanamycin Luciferins Mycobacterium Mycobacterium tuberculosis Mycobacterium tuberculosis H37Rv Oleic Acid Strains Tween 80 Tweens
Except where indicated, we grew all strains (M. smegmatis, M. smegmatis-pBP10, Mtb H37Rv and Mtb H37Rv-pBP10 at 37 °C in Middlebrook 7H9 medium (Becton Dickinson) with 0.05% Tween-80 and albumin, dextrose, catalase (Middlebrook ADC Enrichment, BBL Microbiology) with or without 30 μg ml−1 kanamycin or on Middlebrook 7H10 (Becton Dickinson) medium with oleic acid plus albumin, dextrose, catalase (Middlebrook ADC Enrichment, BBL Microbiology) with or without 30 μg ml−1 kanamycin. We grew strains to an optical densityof ~1 at A600 (OD600) and stored them in 15% glycerol at −80 °C. For in vitro log-phase experiments, we maintained replicate rolling cultures in log phase by subculturing every 1–3 d for ~40 generations in the absence of antibiotics. We recorded each dilution to calculate total bacterial numbers. We determined the percentage of mycobacteria carrying plasmid as the number of CFUs on 7H10 agar with kanamycin over the number of CFUs on 7H10 agar without kanamycin. We compared different media conditions to achieve a variety of growth rates, including 7H9 medium diluted with sterile water, with 0.05% Tween to minimize clumping. For the starvation experiments, we grew Mtb in minimal medium consisting of 3.33 mM L-asparagine, 5.74 mM KH2PO4, 10.6 mM Na2HPO4, 40.6 μM MgSO4·7H20, 4.50 μM CaCl2, 0.619 μM ZnSO4 and 50 mg/L ferric ammonium citrate. We measured log-phase growth rates at the initiation of growth (high plasmid frequency) and again at the end (low plasmid frequency) to assess the fitness cost of plasmid carriage. We grew hypoxic cultures in 7H9 medium in spinner flasks with 2% oxygen flow-through as previously described32 (link). Before plating, we brought cultures to their original volumes to account for evaporation from the constant air flow. For in vitro stationary phase and starvation experiments with Mtb, we grew rolling cultures for ~20 d without subculturing. For the hypoxic experiments, we maintained Mtb in 7H9 medium in 96-well plates placed inside airtight bags with a Gaspak EZ Anaerobe Container System Sachet (Becton Dickinson) and a Gaspak Dry Anaerobic Indicator Strip (Becton Dickinson).
Publication 2009
Agar Albumins Antibiotics, Antitubercular Asparagine Bacteria Bacteria, Anaerobic Catalase DNA Replication ferric ammonium citrate Glucose Glycerin Hypoxia Kanamycin Mycobacterium Oleic Acid Oxygen Plasmids Sterility, Reproductive Sulfate, Magnesium Technique, Dilution Tween 80 Tweens Vision

E. coli DH5α was cultured in LB medium. M. smegmatis mc2-155 was grown in Lemco medium (10 g L−1 peptone, 5 g L−1 Lemco powder, 5 g L−1 NaCl) containing 0.05% w/v Tween 80 for liquid cultures or 15 g L−1 agar for agar plates, minimal medium as described previously [50] (link) or Dubos-Tween Albumin (DTA) medium (Dubos medium, 0.05% w/v Tween 80, 10% v/v Dubos Albumin supplement (Becton Dickinson)). M. tuberculosis H37Rv (ATCC 25618) and M. marinum (ATCC BAA-535 /strain M) strains were grown in Middlebrook 7H9 medium plus 10% v/v OADC (oleic acid, albumin, dextrose, catalase) supplement (Becton Dickinson) and 0.05% w/v Tween 80 or on Middlebrook 7H10 agar (Becton Dickinson) plus 10% v/v OADC. Chloramphenicol was used at 8 µg/ml, hygromycin at 100 µg/ml and kanamycin at 20 µg/ml where required.
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Publication 2010
Agar Albumins Catalase Chloramphenicol Dietary Supplements Escherichia coli Glucose hygromycin A Kanamycin Mycobacterium tuberculosis H37Rv Oleic Acid Peptones Powder Sodium Chloride Strains Tween 80 Tweens
A chemical library of 658-natural compounds was kindly provided by Dr. Sang Jeon Chung of Sungkyunkwan University (Suwon, Korea). Kaempferide (69545), dimethylsulfoxide (D2650), bafilomycin A1 (B1793), rapamycin (553210), tiliroside (79257), chloroquine (C6628), orlistat (O4139), palmitic acid (P5585), oleic acid (O1383), acridine orange (A6014), oil-red-O (O0625), dexamethasone (D8893), insulin (I0516), and 3-isobutyl-1-methylxanthine (I5879) were purchased from Sigma-Aldrich. BODIPY 493/503 (D3922), Hoechst33342 (H3570), lipofectamine LTX (94756), lipofectamine 2000 (52887), Plus reagent (10964), protease and phosphatase inhibitor solution (78441), M-PER kit (89842Y), DMEM, fetal bovine serum (FBS), bovine serum, and antibiotics were purchased from Invitrogen ThermoFisher Scientific. For in vivo experiments, Kaempferide (K0057) was purchased from TCI Chemicals. siRNA targeting TUFM was purchased from Dharmacon. mRFP-GFP-LC3B plasmids were kindly provided by Dr. Jaewhan Song of Yonsei University (Seoul, Korea).
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Publication 2021
1-Methyl-3-isobutylxanthine 4,4-difluoro-1,3,5,7,8-pentamethyl-4-bora-3a,4a-diaza-s-indacene Acridine Orange Antibiotics, Antitubercular bafilomycin A1 Bos taurus Chloroquine Dexamethasone Fetal Bovine Serum Hoechst33342 Insulin kaempferide Lipofectamine lipofectamine 2000 Oleic Acid Orlistat Palmitic Acid Peptide Hydrolases Phosphoric Monoester Hydrolases Plasmids RNA, Small Interfering Serum Sirolimus solvent red 27 Sulfoxide, Dimethyl tiliroside

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Publication 2012
2-Mercaptoethanol Adult Germline Stem Cells Cells DyeCycle Violet Fibroblast Growth Factor 2 Formaldehyde Glial Cell Line-Derived Neurotrophic Factor Glutamine Haploid Cell HEPES Homo sapiens Human Embryonic Stem Cells Human Induced Pluripotent Stem Cells Insulin Linoleic Acid Linolenic Acid Lysine Mus NRG1 protein, human Oleic Acid Palmitic Acid palmitoleic acid Parent Penicillins Poly A Putrescine Selenite, Sodium Serum Albumin, Bovine Stains stearic acid Streptomycin Transferrin

Most recents protocols related to «Oleic Acid»

Example 5

Additional formulations which vary the amounts of transcutol and ethyl alcohol were examined by the same procedure.

Formulations tested (Table 4):

Formula
D1C
PENNSAID
2%FormulaFormulaFormulaFormula
DiclofenacD37D38D39D40
IngredientWt %Wt %Wt %Wt %Wt %
Oleic Acid08.08.08.08.0
DMSO45.516.021.016.021.0
Transcutol026.021.021.016.0
Sodium Diclofenac2.02.02.02.02.0
Propylene Glycol11.011.011.011.011.0
Poloxamer P18800000
Ethyl Alcohol31.3534.034.039.039.0
Hydroxypropyl3.03.03.03.03.0
Cellulose
Water7.150000
TOTAL100100100100100

FIGS. 9, 10, and 11 depict a head-to-head comparison of Pennsaid and Formulation D34 as a delivered transdermal dose, dose retained in the skin, and calculated as percent delivery of diclofenac.

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Patent 2024
Acids Cyclooxygenase Inhibitors Diclofenac Diclofenac Sodium Ethanol Figs Head hydroxypropylcellulose Obstetric Delivery Oleic Acid Poloxamer Propylene Glycol Skin Sodium Sulfoxide, Dimethyl Transcutol

Example 2

A composition comprising Tretinoin as an active ingredient:

IngredientsConcentration (w/w %)
Oleic acid4.00
Isopropanol6.00
BHT (Butylated Hydroxytoluene)0.02
Sorbic acid0.10
Tretinoin0.10
Silica microspheres0.70
Natrosol (HEC)1.50
Xanthan gum0.80
Trolamine1.20
Benzyl alcohol0.80
Glycerin15.00
Waterq.s. 100%

The process for the preparation of the composition was as follows:

    • 1. Trolamine, Natrosol (HEC) and xanthan gum were added gradually to the water while stirring at high speed using mixer propeller;
    • 2. The mixture of oleic acid, isopropanol, BHT, sorbic acid and tretinoin was heated to 50° C. while stirring then cooled to the room temperature;
    • 3. Silica microspheres were added to the stage 2 and the resultant mixture was stirred for at least one hour;
    • 4. Benzyl alcohol and Glycerin were added to stage 1
    • 5. Stage 4 was added to the mixer reactor and stirred vigorously.

An opaque yellowish gel was obtained.

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Patent 2024
Benzyl Alcohol Glycerin Isopropyl Alcohol Microspheres Oleic Acid Pharmaceutical Preparations Silicon Dioxide Sorbic Acid Tretinoin triethanolamine xanthan gum

Example 4

Additional formulations which vary the amounts of oleic acid, propylene glycol, and ethyl alcohol were examined by the same procedure.

Formulations tested (Table 3):

Formula
D1C
PENNSAID
2%FormulaFormulaFormulaFormulaFormula
DiclofenacD51D52D53D54D55
IngredientWt %Wt %Wt %Wt %Wt %Wt %
Oleic Acid08.08.08.04.04.0
DMSO45.520.020.020.020.020.0
Transcutol024.524.524.524.524.5
Sodium Diclofenac2.02.02.02.02.02.0
Propylene Glycol11.011.06.03.011.03.0
Poloxamer P188000000
Ethyl Alcohol31.3531.536.539.535.543.5
Hydroxypropyl3.03.03.03.03.03.0
Cellulose
Water7.1500000
TOTAL100100100100100100

FIG. 7 depicts skin permeation delivered dose data for 2% diclofenac formulations from Table 1, while FIG. 8 depicts skin permeation flux data for 2% diclofenac formulations from Table 1. As shown, these formulae can deliver equivalent amounts of diclofenac to that of Formula D1C with substantially less DMSO and at a much lower amount of the formula applied.

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Patent 2024
Acids Cyclooxygenase Inhibitors Diclofenac Diclofenac Sodium Ethanol hydroxypropylcellulose Oleic Acid Poloxamer Propylene Glycol Skin Sodium Sulfoxide, Dimethyl Transcutol
Not available on PMC !

Example 4

A composition comprising Tretinoin as active ingredient:

IngredientConcentration (w/w %)
Oleic acid5.00
Isopropanol10.00
BHT (Butylated Hydroxytoluene)0.02
Sorbic acid0.10
Tretinoin0.10
Silica microspheres0.70
CMC Na (carboxymethyl cellulose sodium)2.40
Natrosol (HBC)0.50
Glycerin5.00
Benzyl alcohol0.80
Poloxamer 4070.20
P. Waterq.s. 100%

The process for the preparation of the composition was as follows:

    • 1. CMC Na (carboxymethyl cellulose sodium) and Natrosol (HEC) were dispersed in water until a clear gel was formed
    • 2. Glycerin and benzyl alcohol were added to stage 1 and mixed;
    • 3. Oleic acid, isopropanol, BHT, sorbic acid, Poloxamer 407 and tretinoin were heated to 50° C. while stirring until clear solution was obtained. Then the solution was cooled to the room temperature;
    • 4. Silica Microspheres were added to the cooled oily phase and resultant mixture was stirred for at least one hour;
    • 5. Stage 4 was added to the stage 2 and stirred for one hour under vacuum.

An opaque yellowish gel was obtained.

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Patent 2024
Benzyl Alcohol Ethanol Glycerin Isopropyl Alcohol Microspheres Oils Oleic Acid Pharmaceutical Preparations Poloxamer 407 Silicon Dioxide Sodium Carboxymethylcellulose Sorbic Acid Tretinoin Vacuum
Not available on PMC !

Example 6

Strain 5 was subjected to another round of mutagenesis with increasing concentrations and exposure time to 4-NQO (37 μM for 30 minutes at 28° C.). This population of cells was subsequently subdivided and grown in standard lipid production medium supplemented with a range of cerulenin concentrations (7-50 μM). Cells from all concentrations were pooled and fractionated over a 60% Percoll/0.15 M NaCl density gradient. Oil laden cells recovered from a density zone of 1.02 g/mL were plated and assessed for glucose consumption and fatty acid profile. One of these clones was subsequently stabilized and given the strain designation “Strain 6”.

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Patent 2024
Cells Cerulenin Clone Cells Fatty Acids Glucose Lipids Microalgae Mutagenesis Oleic Acid Percoll Sodium Chloride Strains Triglycerides

Top products related to «Oleic Acid»

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Oleic acid is a long-chain monounsaturated fatty acid commonly used in various laboratory applications. It is a colorless to light-yellow liquid with a characteristic odor. Oleic acid is widely utilized as a component in various laboratory reagents and formulations, often serving as a surfactant or emulsifier.
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1-octadecene is a linear alkene with the molecular formula C18H36. It is a colorless, oily liquid that is commonly used as a chemical intermediate in various industrial and laboratory applications.
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Oleylamine is a chemical compound used as a surfactant, emulsifier, and lubricant in various industrial applications. It is a long-chain aliphatic amine with a hydrocarbon backbone and an amino group at one end. Oleylamine is commonly used in the formulation of lubricants, coatings, and personal care products.
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Tween 80 is a non-ionic surfactant and emulsifier. It is a viscous, yellow liquid that is commonly used in laboratory settings to solubilize and stabilize various compounds and formulations.
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Palmitic acid is a saturated fatty acid with the chemical formula CH3(CH2)14COOH. It is a colorless, odorless solid at room temperature. Palmitic acid is a common constituent of animal and vegetable fats and oils.
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Fetal Bovine Serum (FBS) is a cell culture supplement derived from the blood of bovine fetuses. FBS provides a source of proteins, growth factors, and other components that support the growth and maintenance of various cell types in in vitro cell culture applications.
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Oleic acid is a long-chain monounsaturated fatty acid. It is a clear, colorless to pale yellow liquid with a slightly unpleasant odor. Oleic acid is commonly used in various laboratory applications and industrial processes.
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Sodium hydroxide is a chemical compound with the formula NaOH. It is a white, odorless, crystalline solid that is highly soluble in water and is a strong base. It is commonly used in various laboratory applications as a reagent.
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Methanol is a clear, colorless, and flammable liquid that is widely used in various industrial and laboratory applications. It serves as a solvent, fuel, and chemical intermediate. Methanol has a simple chemical formula of CH3OH and a boiling point of 64.7°C. It is a versatile compound that is widely used in the production of other chemicals, as well as in the fuel industry.
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Toluene is a colorless, flammable liquid with a distinctive aromatic odor. It is a common organic solvent used in various industrial and laboratory applications. Toluene has a chemical formula of C6H5CH3 and is derived from the distillation of petroleum.

More about "Oleic Acid"

Oleic acid, a monounsaturated fatty acid, is a crucial component found in various plant and animal oils.
It plays a vital role in biological processes, including cell membrane structure and function.
Researchers have associated oleic acid with potential health benefits, such as improved cardiovascular health and reduced inflammation.
Experts can leverage the AI-driven protocol comparison tool from PubCompare.ai to optimize their oleic acid studies.
This powerful platform helps identify the best products and procedures, ensuring reproducibility and accuracy in their findings.
Whether you're working with related compounds like 1-octadecene, oleylamine, or Tween 80, or exploring the interactions with palmitic acid, FBS, sodium hydroxide, methanol, or toluene, PubCompare.ai can streamline your research and enhance reproducibility.
By utilizing the insights gained from the MeSH term description and Metadescription, researchers can delve deeper into the world of oleic acid and its applications.
With the help of PubCompare.ai's innovative tools, they can navigae the complexities of this important lipid molecule and make breakthroughs in their studies.