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Carvacrol

Manufactured by Merck Group
Sourced in United States, Germany, Italy, Spain, Sao Tome and Principe, United Kingdom, Canada, India, Poland, France, Portugal, Brazil

Carvacrol is a monoterpenic phenol compound that is a naturally occurring ingredient found in the essential oils of various plants, such as oregano, thyme, and savory. It is a colorless or pale yellow liquid with a characteristic aroma. Carvacrol exhibits antimicrobial and antioxidant properties, making it a potentially useful compound for various industrial and research applications.

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280 protocols using carvacrol

1

Carvacrol Counteracts LPS-Induced Neuroinflammation

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Rats were randomly classified into four groups (n = 8), including control group, LPS group, LPS + CAR25 group, and LPS + CAR50 group. Carvacrol-treated groups received Carvacrol intraperitoneally at doses of 25 and 50 mg/kg every day.[25 (link)] Carvacrol (Sigma-Aldrich Co., USA) was emulsified with 1% Tween 80 and dissolved in normal saline. The control and LPS groups received 1% Tween 80 dissolved in saline at the same volume as the treated groups. Injection of Carvacrol or 1% Tween was started 2 weeks before LPS injection and continued during LPS injections.[26 (link)]
LPS from Escherichia coli (Sigma-Aldrich Co., USA) was freshly prepared in saline and was injected intraperitoneally at a dose of 1 mg/kg, 2 h before behavioral testing[26 (link)] in the Morris water maze (MWM), which was performed on days 15–19. Treatments with Carvacrol or 1% Tween 80 were performed 30 min prior to behavioral task. After behavioral testing, rats were euthanized and their brains were immediately removed. The hippocampus and cerebral cortex were dissected, weighed, and homogenized with NaCl solution 10 times (w/v) for biochemical assessments. All chemicals for biochemical measurements (thiobarbituric acid reactive substances [TBARS] and total thiol concentration) were purchased from Merck Co. (Germany).
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2

Evaluation of Bioactive Compounds for In Vitro and In Vivo Applications

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Geraniol (NO: 48798), eugenol (NO: 35995), carvacrol (NO: 42632), 1,8-cineol (NO: 29210), Tween-80 (NO: P1754), paraffin oil (NO: 18512) and mineral oil (NO: M5904) were purchased from Sigma-Aldrich (Brussels, Belgium) for in vitro assays. carvacrol (NO: W224511) was purchased from Sigma-Aldrich for an in vivo assay. All compounds were commercially available as samples purified to 99% (analytical reagent > 99%).
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3

Carvacrol Solubilization in DMSO

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Carvacrol (98% purity) was purchased from Sigma-Aldrich (St. Louis, MO, USA). Dimethyl sulfoxide (DMSO; Sigma-Aldrich, France) with a final concentration of 2% (v/v) was used to prepare F-CARV solution, while E-CARV did not require DMSO since microcapsule already contain emulsifier that solubilize Carvacrol.
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4

Oral Treatment of C. jejuni Infection

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Treatment through oral administration via drinking water of carvacrol, deferoxamine, deoxycholic acid (all from Sigma-Aldrich, Munich, Germany), 2′-fucosyl-lactose (Chr. Hansen HMO GmbH, Rheinbreitbach, Germany), and the quadruple combination commenced 2 days following the onset of C. jejuni infection. Dosages were calculated considering an average body weight of approximately 25 g per mouse and an estimated drinking volume of 5 mL per day. All compounds were dissolved in autoclaved tap water. The daily doses and their previously determined minimal inhibitory concentrations (MICs) are illustrated in Table 1. To enhance the water solubility of carvacrol, 50 mg of the compound were dissolved in 250 μL Tween® 80 (Sigma-Aldrich, Munich, Germany). The placebo group received vehicle dissolved in autoclaved tap water.
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5

Carvacrol Dose-Dependent Antidiabetic Effects

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A preliminary experiment was carried out to explore the effective dose of Carvacrol on the plasma glucose level in diabetic mice. After 4 weeks of induction of DM, the plasma glucose level in diabetic mice increased persistently and stably. Carvacrol (Sigma-Aldrich) was administered at various doses (10, 20, 40 mg/kg bodyweight [BW]) to eight mice in each group, respectively. Carvacrol was dissolved in 1% dimethyl sulfoxide (DMSO) (Sigma-Aldrich) and given by intraperitoneal injection once a day for 2 weeks. Then, the plasma glucose level was measured using the glucometer.
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6

Carvacrol Treatment for Campylobacter Infection

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Four days prior C. jejuni infection treatment with carvacrol (Sigma-Aldrich, Munich, Germany; daily dose of 100 mg carvacrol per kg body weight) was initiated by dissolving the compound in Tween 80 (0.2% v/v) to a final concentration of 500 mg/l autoclaved tap water (ad libitum). Placebo control mice received Tween 80 only.
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7

Oral Administration of Satureja montana Dry Extract and Active Compounds

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The dry extract of Satureja montana was prepared by "Veselino EOOD", Kazanlak, Bulgaria from dried leaves of the medicinal plant, bought from an herbal pharmacy in Plovdiv, Bulgaria. The used method was methanol-aqueous extraction, followed by drying in a spray dryer at 40 °C. Carvacrol and Rosmarinic acid were bought from Sigma-Aldrich (St. Louis, Missouri, USA).
All substances were administered orally by stomach gavage after dissolving in distilled water for the dry extract and Rosmarinic acid and olive oil for Carvacrol. Doses and volumes of the administered solutions are presented in Table 1.
The doses of the dry extract of Satureja montana were calculated in accordance to the results of previous acute and chronic toxicity experiments conducted by our team. The dose of Rosmarinic acid was determined according to the content of this phenolic compound in the composition of the extract -44.730 ± 3.500 mg/g. The dose of Carvacrol was determined in accordance to the results of our previous chronic toxicity experiment and not with its content in the extract which was found to be 0.020 ± 0.001 mg/g. The quantity of both active ingredients was determined in our previous study.
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8

Determining Carvacrol's Subinhibitory Concentration Against Campylobacter jejuni

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Carvacrol was purchased from Sigma-Aldrich Co., St. Louis, MO (catalog no. W224502). The SIC of Carvacrol was determined using a previously published protocol (Amalaradjou et al., 2011 (link)) with slight modifications. Sterile 96-well polystyrene plates (Costar; Corning Incorporated, Corning, NY) containing serial dilutions of Carvacrol in CEB (100 μL/well) were inoculated with ∼6 log cfu of C. jejuni wild-type S-8 or NCTC 81-176 in equal volume (100 μL) of CEB, followed by incubation at 42°C for 24 h. Bacterial growth was determined by culturing on Campylobacter Line Agar (CLA) plates (Line, 2001 (link)). The highest concentration of Carvacrol that did not inhibit the growth of C. jejuni after 24 h of incubation was selected as the SIC for the study. Because 100% ethanol (catalog no. E7023; Sigma-Aldrich) was used as a diluent of Carvacrol, it was included as a control in all the experiments.
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9

Carvacrol-Chitosan Nanoparticle Formulation

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The carvacrol loaded chitosan nanoparticles were manufactured through ionic gelation method during first component of the project. For this purpose, commercially available carvacrol (Sigma Aldrich) was mixed with different concentrations of commercially available chitosan (Sigma Aldrich) to attain different carvacrol to chitosan ratios such as 1:0, 1:0.25, 1:0.50, 1:0.75, 1:1 and 1:1.25. Based upon maximum yield, carvacrol to chitosan ratio 1:1 found suitable (results not shown here) and recommended for further studies. The vials containing carvacrol loaded chitosan nanoparticles in lyophilized form were collected from Quality Operations Laboratory, UVAS and characterized as per standard protocol.
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10

Chitosan-based Antimicrobial Formulations

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High-molecular-weight chitosan (CAS 9012-76-4; 310 to 375 kDa) was sourced from Hangzhou Simit Chem. & Tech. Co. (Hangzhou, China). Neutrase® enzyme was provided by Novozymes A/S (Bagsværd, Denmark). Sodium carboxymethylcellulose (CAS 9004-32-4; USP reference standard), sodium alginate (CAS 9005-38-3; pharmaceutical secondary standard), acetic acid (CAS 64-19-7; purum, 80% in H2O), methacrylic anhydride (CAS 760-93-0; ≥94%), sodium tripolyphosphate (CAS 7758-29-4; ≥98%), carvacrol (CAS 499-75-2, 98%), chitosanase from Streptomyces griseus (Krainsky) Waksman and Henrici (EC 3.2.1.132, CAS 51570-20-8), methanol (UHPLC, suitable for mass spectrometry, CAS 67-56-1), tetrahydrofuran (THF, CAS 109-99-9; ≥99.9%), and Tween® 20 (CAS 9005-64-5) were procured from Merck (Darmstadt, Germany). Potato dextrose broth (PDB) and potato dextrose agar (PDA) were supplied by Becton, Dickinson, and Company (Franklin Lakes, NJ, USA).
Botrytis cinerea (CECT 20973) and P. expansum (CECT 20906) were obtained from the Spanish Type Culture Collection (Valencia, Spain), while C. coccodes (CRD 246/190) was sourced from the Regional Diagnostic Center of Aldearrubia (Junta de Castilla y León; Castilla y León, Spain).
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