Myristica

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David Carriere - One of the best experts on this subject based on the ideXlab platform.

  • Molten fatty acid based microemulsions †
    Physical Chemistry Chemical Physics, 2016
    Co-Authors: Cecile Noirjean, Fabienne Testard, Christophe Déjugnat, Jacques Jestin, David Carriere
    Abstract:

    a We show that ternary mixtures of water (polar phase), myristic acid (MA, apolar phase) and cetyltrimethyl-ammonium bromide (CTAB, cationic surfactant) studied above the melting point of myristic acid allow the preparation of microemulsions without adding a salt or a co-surfactant. The combination of SANS, SAXS/ WAXS, DSC, and phase diagram determination allows a complete characterization of the structures and interactions between components in the molten fatty acid based microemulsions. For the different structures characterized (microemulsion, lamellar or hexagonal phases), a similar thermal behaviour is observed for all ternary MA/CTAB/water monophasic samples and for binary MA/CTAB mixtures without water: crystalline myristic acid melts at 52 1C, and a thermal transition at 70 1C is assigned to the breaking of hydrogen bounds inside the mixed myristic acid/CTAB complex (being the surfactant film in the ternary system). Water determines the film curvature, hence the structures observed at high temperature, but does not influence the thermal behaviour of the ternary system. Myristic acid is partitioned in two ''species'' that behave independently: pure myristic acid and myristic acid associated with CTAB to form an equimolar complex that plays the role of the surfactant film. We therefore show that myristic acid plays the role of a solvent (oil) and a co-surfactant allowing the fine tuning of the structure of oil and water mixtures. This solvosurfactant behaviour of long chain fatty acid opens the way for new formulations with a complex structure without the addition of any extra compound.

  • Molten fatty acid based microemulsions
    Physical Chemistry Chemical Physics, 2016
    Co-Authors: Cecile Noirjean, Fabienne Testard, Christophe Déjugnat, Jacques Jestin, David Carriere
    Abstract:

    a We show that ternary mixtures of water (polar phase), myristic acid (MA, apolar phase) and cetyltrimethyl-ammonium bromide (CTAB, cationic surfactant) studied above the melting point of myristic acid allow the preparation of microemulsions without adding a salt or a co-surfactant. The combination of SANS, SAXS/ WAXS, DSC, and phase diagram determination allows a complete characterization of the structures and interactions between components in the molten fatty acid based microemulsions. For the different structures characterized (microemulsion, lamellar or hexagonal phases), a similar thermal behaviour is observed for all ternary MA/CTAB/water monophasic samples and for binary MA/CTAB mixtures without water: crystalline myristic acid melts at 52 1C, and a thermal transition at 70 1C is assigned to the breaking of hydrogen bounds inside the mixed myristic acid/CTAB complex (being the surfactant film in the ternary system). Water determines the film curvature, hence the structures observed at high temperature, but does not influence the thermal behaviour of the ternary system. Myristic acid is partitioned in two ''species'' that behave independently: pure myristic acid and myristic acid associated with CTAB to form an equimolar complex that plays the role of the surfactant film. We therefore show that myristic acid plays the role of a solvent (oil) and a co-surfactant allowing the fine tuning of the structure of oil and water mixtures. This solvosurfactant behaviour of long chain fatty acid opens the way for new formulations with a complex structure without the addition of any extra compound.

Cecile Noirjean - One of the best experts on this subject based on the ideXlab platform.

  • Molten fatty acid based microemulsions †
    Physical Chemistry Chemical Physics, 2016
    Co-Authors: Cecile Noirjean, Fabienne Testard, Christophe Déjugnat, Jacques Jestin, David Carriere
    Abstract:

    a We show that ternary mixtures of water (polar phase), myristic acid (MA, apolar phase) and cetyltrimethyl-ammonium bromide (CTAB, cationic surfactant) studied above the melting point of myristic acid allow the preparation of microemulsions without adding a salt or a co-surfactant. The combination of SANS, SAXS/ WAXS, DSC, and phase diagram determination allows a complete characterization of the structures and interactions between components in the molten fatty acid based microemulsions. For the different structures characterized (microemulsion, lamellar or hexagonal phases), a similar thermal behaviour is observed for all ternary MA/CTAB/water monophasic samples and for binary MA/CTAB mixtures without water: crystalline myristic acid melts at 52 1C, and a thermal transition at 70 1C is assigned to the breaking of hydrogen bounds inside the mixed myristic acid/CTAB complex (being the surfactant film in the ternary system). Water determines the film curvature, hence the structures observed at high temperature, but does not influence the thermal behaviour of the ternary system. Myristic acid is partitioned in two ''species'' that behave independently: pure myristic acid and myristic acid associated with CTAB to form an equimolar complex that plays the role of the surfactant film. We therefore show that myristic acid plays the role of a solvent (oil) and a co-surfactant allowing the fine tuning of the structure of oil and water mixtures. This solvosurfactant behaviour of long chain fatty acid opens the way for new formulations with a complex structure without the addition of any extra compound.

  • Molten fatty acid based microemulsions
    Physical Chemistry Chemical Physics, 2016
    Co-Authors: Cecile Noirjean, Fabienne Testard, Christophe Déjugnat, Jacques Jestin, David Carriere
    Abstract:

    a We show that ternary mixtures of water (polar phase), myristic acid (MA, apolar phase) and cetyltrimethyl-ammonium bromide (CTAB, cationic surfactant) studied above the melting point of myristic acid allow the preparation of microemulsions without adding a salt or a co-surfactant. The combination of SANS, SAXS/ WAXS, DSC, and phase diagram determination allows a complete characterization of the structures and interactions between components in the molten fatty acid based microemulsions. For the different structures characterized (microemulsion, lamellar or hexagonal phases), a similar thermal behaviour is observed for all ternary MA/CTAB/water monophasic samples and for binary MA/CTAB mixtures without water: crystalline myristic acid melts at 52 1C, and a thermal transition at 70 1C is assigned to the breaking of hydrogen bounds inside the mixed myristic acid/CTAB complex (being the surfactant film in the ternary system). Water determines the film curvature, hence the structures observed at high temperature, but does not influence the thermal behaviour of the ternary system. Myristic acid is partitioned in two ''species'' that behave independently: pure myristic acid and myristic acid associated with CTAB to form an equimolar complex that plays the role of the surfactant film. We therefore show that myristic acid plays the role of a solvent (oil) and a co-surfactant allowing the fine tuning of the structure of oil and water mixtures. This solvosurfactant behaviour of long chain fatty acid opens the way for new formulations with a complex structure without the addition of any extra compound.

Youssouf Secka - One of the best experts on this subject based on the ideXlab platform.

  • Composition and cytotoxic activity of essential oils from Xylopia aethiopica (Dunal) A. Rich, Xylopia parviflora (A. Rich) Benth.) and Monodora Myristica (Gaertn) growing in Chad and Cameroon.
    BMC Complementary and Alternative Medicine, 2014
    Co-Authors: Issakou Bakarnga-via, Jean-baptiste Hzounda Fokou, Patrick Valere Tsouh Fokou, Lauve Rachel Yamthe Tchokouaha, Magali Gary-bobo, Audrey Gallud, Marcel Garcia, Lucain Walbadet, Youssouf Secka, Pierre Michel Jazet Dongmo
    Abstract:

    BackgroundCancer has become a global public health problem and the search for new control measures is urgent. Investigation of plant products such as essential oils from Monodora Myristica, Xylopia aethiopica and Xylopia parviflora might lead to new anticancer therapy. In this study, we have investigated the antineoplastic activity of essential oils from fruits of these plants growing in Chad and Cameroon.MethodsThe essential oils obtained by hydrodistillation of fruits of Monodora Myristica, Xylopia aethiopica and Xylopia parviflora collected in Chad and Cameroon were analyzed by GCFID and GC-MS and investigated for their antiproliferative activity against the breast cancer cell line (MCF7).ResultsOverall, monoterpenes were mostly found in the six essential oils. Oils from X. aethiopica and X. parviflora from Chad and Cameroon mainly contain β-pinene at 24.6%, 28.2%, 35.7% and 32.9% respectively. Monodora Myristica oils from both origins contain mainly α- phellandrene at 52.7% and 67.1% respectively. The plant origin did not significantly influence the chemical composition of oils. The six essential oils exerted cytotoxic activity against cancer (MCF-7) and normal cell lines (ARPE-19), with more pronounced effect on neoplastic cells in the majority of cases. The highest selectivity was obtained with the essential oils of X. parviflora from Chad and Cameroon (5.87 and 5.54) which were more cytotoxic against MCF-7 than against normal cell line (ARPE-19) with IC50 values of 0.155 μL/mL and 0.166 μL/mL respectively.ConclusionsEssential oils from fruits of Monodora Myristica, Xylopia aethiopica and Xylopia parviflora have shown acceptable antineoplastic potency, and might be investigated further in this regard.

  • composition and cytotoxic activity of essential oils from xylopia aethiopica dunal a rich xylopia parviflora a rich benth and monodora Myristica gaertn growing in chad and cameroon
    BMC Complementary and Alternative Medicine, 2014
    Co-Authors: Lauve Rachel Yamthe Tchokouaha, Audrey Gallud, Marcel Garcia, Lucain Walbadet, Issakou Bakarngavia, Jean Baptiste Hzounda, Patrick Valere Tsouh Fokou, Magali Garybobo, Youssouf Secka
    Abstract:

    Cancer has become a global public health problem and the search for new control measures is urgent. Investigation of plant products such as essential oils from Monodora Myristica, Xylopia aethiopica and Xylopia parviflora might lead to new anticancer therapy. In this study, we have investigated the antineoplastic activity of essential oils from fruits of these plants growing in Chad and Cameroon. The essential oils obtained by hydrodistillation of fruits of Monodora Myristica, Xylopia aethiopica and Xylopia parviflora collected in Chad and Cameroon were analyzed by GC-FID and GC-MS and investigated for their antiproliferative activity against the breast cancer cell line (MCF7). Overall, monoterpenes were mostly found in the six essential oils. Oils from X. aethiopica and X. parviflora from Chad and Cameroon mainly contain β-pinene at 24.6%, 28.2%, 35.7% and 32.9% respectively. Monodora Myristica oils from both origins contain mainly α-phellandrene at 52.7% and 67.1% respectively. The plant origin did not significantly influence the chemical composition of oils. The six essential oils exerted cytotoxic activity against cancer (MCF-7) and normal cell lines (ARPE-19), with more pronounced effect on neoplastic cells in the majority of cases. The highest selectivity was obtained with the essential oils of X. parviflora from Chad and Cameroon (5.87 and 5.54) which were more cytotoxic against MCF-7 than against normal cell line (ARPE-19) with IC50 values of 0.155 μL/mL and 0.166 μL/mL respectively. Essential oils from fruits of Monodora Myristica, Xylopia aethiopica and Xylopia parviflora have shown acceptable antineoplastic potency, and might be investigated further in this regard.

Issakou Bakarngavia - One of the best experts on this subject based on the ideXlab platform.

  • composition and cytotoxic activity of essential oils from xylopia aethiopica dunal a rich xylopia parviflora a rich benth and monodora Myristica gaertn growing in chad and cameroon
    BMC Complementary and Alternative Medicine, 2014
    Co-Authors: Lauve Rachel Yamthe Tchokouaha, Audrey Gallud, Marcel Garcia, Lucain Walbadet, Issakou Bakarngavia, Jean Baptiste Hzounda, Patrick Valere Tsouh Fokou, Magali Garybobo, Youssouf Secka
    Abstract:

    Cancer has become a global public health problem and the search for new control measures is urgent. Investigation of plant products such as essential oils from Monodora Myristica, Xylopia aethiopica and Xylopia parviflora might lead to new anticancer therapy. In this study, we have investigated the antineoplastic activity of essential oils from fruits of these plants growing in Chad and Cameroon. The essential oils obtained by hydrodistillation of fruits of Monodora Myristica, Xylopia aethiopica and Xylopia parviflora collected in Chad and Cameroon were analyzed by GC-FID and GC-MS and investigated for their antiproliferative activity against the breast cancer cell line (MCF7). Overall, monoterpenes were mostly found in the six essential oils. Oils from X. aethiopica and X. parviflora from Chad and Cameroon mainly contain β-pinene at 24.6%, 28.2%, 35.7% and 32.9% respectively. Monodora Myristica oils from both origins contain mainly α-phellandrene at 52.7% and 67.1% respectively. The plant origin did not significantly influence the chemical composition of oils. The six essential oils exerted cytotoxic activity against cancer (MCF-7) and normal cell lines (ARPE-19), with more pronounced effect on neoplastic cells in the majority of cases. The highest selectivity was obtained with the essential oils of X. parviflora from Chad and Cameroon (5.87 and 5.54) which were more cytotoxic against MCF-7 than against normal cell line (ARPE-19) with IC50 values of 0.155 μL/mL and 0.166 μL/mL respectively. Essential oils from fruits of Monodora Myristica, Xylopia aethiopica and Xylopia parviflora have shown acceptable antineoplastic potency, and might be investigated further in this regard.

Christophe Déjugnat - One of the best experts on this subject based on the ideXlab platform.

  • Molten fatty acid based microemulsions †
    Physical Chemistry Chemical Physics, 2016
    Co-Authors: Cecile Noirjean, Fabienne Testard, Christophe Déjugnat, Jacques Jestin, David Carriere
    Abstract:

    a We show that ternary mixtures of water (polar phase), myristic acid (MA, apolar phase) and cetyltrimethyl-ammonium bromide (CTAB, cationic surfactant) studied above the melting point of myristic acid allow the preparation of microemulsions without adding a salt or a co-surfactant. The combination of SANS, SAXS/ WAXS, DSC, and phase diagram determination allows a complete characterization of the structures and interactions between components in the molten fatty acid based microemulsions. For the different structures characterized (microemulsion, lamellar or hexagonal phases), a similar thermal behaviour is observed for all ternary MA/CTAB/water monophasic samples and for binary MA/CTAB mixtures without water: crystalline myristic acid melts at 52 1C, and a thermal transition at 70 1C is assigned to the breaking of hydrogen bounds inside the mixed myristic acid/CTAB complex (being the surfactant film in the ternary system). Water determines the film curvature, hence the structures observed at high temperature, but does not influence the thermal behaviour of the ternary system. Myristic acid is partitioned in two ''species'' that behave independently: pure myristic acid and myristic acid associated with CTAB to form an equimolar complex that plays the role of the surfactant film. We therefore show that myristic acid plays the role of a solvent (oil) and a co-surfactant allowing the fine tuning of the structure of oil and water mixtures. This solvosurfactant behaviour of long chain fatty acid opens the way for new formulations with a complex structure without the addition of any extra compound.

  • Molten fatty acid based microemulsions
    Physical Chemistry Chemical Physics, 2016
    Co-Authors: Cecile Noirjean, Fabienne Testard, Christophe Déjugnat, Jacques Jestin, David Carriere
    Abstract:

    a We show that ternary mixtures of water (polar phase), myristic acid (MA, apolar phase) and cetyltrimethyl-ammonium bromide (CTAB, cationic surfactant) studied above the melting point of myristic acid allow the preparation of microemulsions without adding a salt or a co-surfactant. The combination of SANS, SAXS/ WAXS, DSC, and phase diagram determination allows a complete characterization of the structures and interactions between components in the molten fatty acid based microemulsions. For the different structures characterized (microemulsion, lamellar or hexagonal phases), a similar thermal behaviour is observed for all ternary MA/CTAB/water monophasic samples and for binary MA/CTAB mixtures without water: crystalline myristic acid melts at 52 1C, and a thermal transition at 70 1C is assigned to the breaking of hydrogen bounds inside the mixed myristic acid/CTAB complex (being the surfactant film in the ternary system). Water determines the film curvature, hence the structures observed at high temperature, but does not influence the thermal behaviour of the ternary system. Myristic acid is partitioned in two ''species'' that behave independently: pure myristic acid and myristic acid associated with CTAB to form an equimolar complex that plays the role of the surfactant film. We therefore show that myristic acid plays the role of a solvent (oil) and a co-surfactant allowing the fine tuning of the structure of oil and water mixtures. This solvosurfactant behaviour of long chain fatty acid opens the way for new formulations with a complex structure without the addition of any extra compound.