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  • Source: New Journal of Chemistry. Unidade: IQ

    Subjects: SOLUÇÕES AQUOSAS, NEOPLASIAS MAMÁRIAS

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      PANSURIYA, Raviraj et al. A dual responsive ionic liquid-based polymeric hydrogel: a promising drug delivery vehicle for the treatment of breast cancer. New Journal of Chemistry, v. 47, n. 30, p. 14261-14272, 2023Tradução . . Disponível em: https://doi.org/10.1039/D3NJ01914D. Acesso em: 06 jun. 2024.
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      Pansuriya, R., Patel, T., Mehra, S., Kumar, A., El Seoud, O. A., Kumar, S., et al. (2023). A dual responsive ionic liquid-based polymeric hydrogel: a promising drug delivery vehicle for the treatment of breast cancer. New Journal of Chemistry, 47( 30), 14261-14272. doi:10.1039/D3NJ01914D
    • NLM

      Pansuriya R, Patel T, Mehra S, Kumar A, El Seoud OA, Kumar S, Aswal VK, Kailasa SK, Malek NI. A dual responsive ionic liquid-based polymeric hydrogel: a promising drug delivery vehicle for the treatment of breast cancer [Internet]. New Journal of Chemistry. 2023 ; 47( 30): 14261-14272.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1039/D3NJ01914D
    • Vancouver

      Pansuriya R, Patel T, Mehra S, Kumar A, El Seoud OA, Kumar S, Aswal VK, Kailasa SK, Malek NI. A dual responsive ionic liquid-based polymeric hydrogel: a promising drug delivery vehicle for the treatment of breast cancer [Internet]. New Journal of Chemistry. 2023 ; 47( 30): 14261-14272.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1039/D3NJ01914D
  • Source: Journal of Molecular Liquids. Unidade: IQ

    Subjects: TENSOATIVOS, LÍQUIDOS IÔNICOS, CALORÍMETROS, SURFACTANTES

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      KEPPELER, Nicolas et al. Effects of head-group volume on the thermodynamic parameters and species distribution of ionic liquid-based surfactants in water: 1-(n-hexadecyl)-3-alkylimidazolium bromides and chlorides. Journal of Molecular Liquids, v. 362, p. 1-10 art. 119681, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.molliq.2022.119681. Acesso em: 06 jun. 2024.
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      Keppeler, N., Galgano, P. D., Schönhoff, M., Naved I. Malek,, & El Seoud, O. A. (2022). Effects of head-group volume on the thermodynamic parameters and species distribution of ionic liquid-based surfactants in water: 1-(n-hexadecyl)-3-alkylimidazolium bromides and chlorides. Journal of Molecular Liquids, 362, 1-10 art. 119681. doi:10.1016/j.molliq.2022.119681
    • NLM

      Keppeler N, Galgano PD, Schönhoff M, Naved I. Malek, El Seoud OA. Effects of head-group volume on the thermodynamic parameters and species distribution of ionic liquid-based surfactants in water: 1-(n-hexadecyl)-3-alkylimidazolium bromides and chlorides [Internet]. Journal of Molecular Liquids. 2022 ; 362 1-10 art. 119681.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.molliq.2022.119681
    • Vancouver

      Keppeler N, Galgano PD, Schönhoff M, Naved I. Malek, El Seoud OA. Effects of head-group volume on the thermodynamic parameters and species distribution of ionic liquid-based surfactants in water: 1-(n-hexadecyl)-3-alkylimidazolium bromides and chlorides [Internet]. Journal of Molecular Liquids. 2022 ; 362 1-10 art. 119681.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.molliq.2022.119681
  • Source: ACS Omega. Unidade: IQ

    Subjects: LÍQUIDOS IÔNICOS, AMIDAS

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      KUDDUSHI, Muzammil et al. Concentration- and temperature-responsive reversible transition in amide-functionalized surface-active ionic liquids: micelles to vesicles to organogel. ACS Omega, v. 5, p. 24272−24284, 2020Tradução . . Disponível em: https://doi.org/10.1021/acsomega.0c02397. Acesso em: 06 jun. 2024.
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      Kuddushi, M., Kumar, A., Ray, D., Aswal, V. K., & El Seoud, O. A. (2020). Concentration- and temperature-responsive reversible transition in amide-functionalized surface-active ionic liquids: micelles to vesicles to organogel. ACS Omega, 5, 24272−24284. doi:10.1021/acsomega.0c02397
    • NLM

      Kuddushi M, Kumar A, Ray D, Aswal VK, El Seoud OA. Concentration- and temperature-responsive reversible transition in amide-functionalized surface-active ionic liquids: micelles to vesicles to organogel [Internet]. ACS Omega. 2020 ; 5 24272−24284.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1021/acsomega.0c02397
    • Vancouver

      Kuddushi M, Kumar A, Ray D, Aswal VK, El Seoud OA. Concentration- and temperature-responsive reversible transition in amide-functionalized surface-active ionic liquids: micelles to vesicles to organogel [Internet]. ACS Omega. 2020 ; 5 24272−24284.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1021/acsomega.0c02397
  • Source: ACS Omega. Unidade: IQ

    Subjects: LÍQUIDOS IÔNICOS, SURFACTANTES

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      SHAH, Ankit et al. Ionic liquid-based catanionic coacervates: novel microreactors for membrane-free sequestration of dyes and curcumin. ACS Omega, v. 3, n. 12, p. 17751-17761, 2019Tradução . . Disponível em: https://doi.org/10.1021/acsomega.8b02455. Acesso em: 06 jun. 2024.
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      Shah, A., Kuddushi, M., Rajput, S., El Seoud, O. A., & Malek, N. I. (2019). Ionic liquid-based catanionic coacervates: novel microreactors for membrane-free sequestration of dyes and curcumin. ACS Omega, 3( 12), 17751-17761. doi:10.1021/acsomega.8b02455
    • NLM

      Shah A, Kuddushi M, Rajput S, El Seoud OA, Malek NI. Ionic liquid-based catanionic coacervates: novel microreactors for membrane-free sequestration of dyes and curcumin [Internet]. ACS Omega. 2019 ; 3( 12): 17751-17761.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1021/acsomega.8b02455
    • Vancouver

      Shah A, Kuddushi M, Rajput S, El Seoud OA, Malek NI. Ionic liquid-based catanionic coacervates: novel microreactors for membrane-free sequestration of dyes and curcumin [Internet]. ACS Omega. 2019 ; 3( 12): 17751-17761.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1021/acsomega.8b02455
  • Source: Acta Crystallographica. Unidade: IQ

    Assunto: QUÍMICA DE SUPERFÍCIE

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      CARACELLI, Ignez et al. 2-[(4-Bromophenyl)sulfanyl]-2-methoxy-1-phenylethan-1-one: crystal structure, Hirshfeld surface analysis and computational chemistry. Acta Crystallographica, v. 75, p. 816-822 :+ Supplementary materials (S1-S4), 2019Tradução . . Disponível em: https://doi.org/10.1107/S2056989019006765. Acesso em: 06 jun. 2024.
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      Caracelli, I., Zukerman-Schpector, J., Traesel, H. J., Olivato, P. R., Jotani, M. M., & Tiekink, E. R. T. (2019). 2-[(4-Bromophenyl)sulfanyl]-2-methoxy-1-phenylethan-1-one: crystal structure, Hirshfeld surface analysis and computational chemistry. Acta Crystallographica, 75, 816-822 :+ Supplementary materials (S1-S4). doi:10.1107/S2056989019006765
    • NLM

      Caracelli I, Zukerman-Schpector J, Traesel HJ, Olivato PR, Jotani MM, Tiekink ERT. 2-[(4-Bromophenyl)sulfanyl]-2-methoxy-1-phenylethan-1-one: crystal structure, Hirshfeld surface analysis and computational chemistry [Internet]. Acta Crystallographica. 2019 ; 75 816-822 :+ Supplementary materials (S1-S4).[citado 2024 jun. 06 ] Available from: https://doi.org/10.1107/S2056989019006765
    • Vancouver

      Caracelli I, Zukerman-Schpector J, Traesel HJ, Olivato PR, Jotani MM, Tiekink ERT. 2-[(4-Bromophenyl)sulfanyl]-2-methoxy-1-phenylethan-1-one: crystal structure, Hirshfeld surface analysis and computational chemistry [Internet]. Acta Crystallographica. 2019 ; 75 816-822 :+ Supplementary materials (S1-S4).[citado 2024 jun. 06 ] Available from: https://doi.org/10.1107/S2056989019006765
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: COLESTEROL, LÍQUIDOS IÔNICOS, SURFACTANTES

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      VAID, Zuber S et al. Synergistic interaction between cholesterol and functionalized ionic liquid based surfactant leading to the morphological transition. ChemistrySelect, v. 3, n. 4, p. 1300-1308, 2018Tradução . . Disponível em: https://doi.org/10.1002/slct.201702561. Acesso em: 06 jun. 2024.
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      Vaid, Z. S., Rajput, S. M., Kuddushi, M., Kumar, A., El Seoud, O. A., & Malek, N. I. (2018). Synergistic interaction between cholesterol and functionalized ionic liquid based surfactant leading to the morphological transition. ChemistrySelect, 3( 4), 1300-1308. doi:10.1002/slct.201702561
    • NLM

      Vaid ZS, Rajput SM, Kuddushi M, Kumar A, El Seoud OA, Malek NI. Synergistic interaction between cholesterol and functionalized ionic liquid based surfactant leading to the morphological transition [Internet]. ChemistrySelect. 2018 ; 3( 4): 1300-1308.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/slct.201702561
    • Vancouver

      Vaid ZS, Rajput SM, Kuddushi M, Kumar A, El Seoud OA, Malek NI. Synergistic interaction between cholesterol and functionalized ionic liquid based surfactant leading to the morphological transition [Internet]. ChemistrySelect. 2018 ; 3( 4): 1300-1308.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/slct.201702561
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: SURFACTANTES, LÍQUIDOS IÔNICOS

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      VAID, Zuber S et al. Salt induced microstructural transitions in aqueous dispersions of ionic liquids based surfactants. ChemistrySelect, v. 3, n. 17, p. 4851-4858, 2018Tradução . . Disponível em: https://doi.org/10.1002/slct.201800041. Acesso em: 06 jun. 2024.
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      Vaid, Z. S., Rajput, S. M., Shah, A., Kadam, Y., Kumar, A., El Seoud, O. A., et al. (2018). Salt induced microstructural transitions in aqueous dispersions of ionic liquids based surfactants. ChemistrySelect, 3( 17), 4851-4858. doi:10.1002/slct.201800041
    • NLM

      Vaid ZS, Rajput SM, Shah A, Kadam Y, Kumar A, El Seoud OA, Mata JP, Malek NI. Salt induced microstructural transitions in aqueous dispersions of ionic liquids based surfactants [Internet]. ChemistrySelect. 2018 ; 3( 17): 4851-4858.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/slct.201800041
    • Vancouver

      Vaid ZS, Rajput SM, Shah A, Kadam Y, Kumar A, El Seoud OA, Mata JP, Malek NI. Salt induced microstructural transitions in aqueous dispersions of ionic liquids based surfactants [Internet]. ChemistrySelect. 2018 ; 3( 17): 4851-4858.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/slct.201800041
  • Source: ChemPhysChem. Unidade: IQ

    Subjects: SURFACTANTES, SOLUÇÕES AQUOSAS

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      RAJPUT, Sargam M et al. Drug induced micelle to vesicle transition of a cationic gemini surfactant: Potential applications in drug delivery. ChemPhysChem, v. 19, p. 865–872, 2018Tradução . . Disponível em: https://doi.org/10.1002/cphc.201701134. Acesso em: 06 jun. 2024.
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      Rajput, S. M., Kumar, S., Aswal, V. K., El Seoud, O. A., Malek, N. I., & Kailasa, S. K. (2018). Drug induced micelle to vesicle transition of a cationic gemini surfactant: Potential applications in drug delivery. ChemPhysChem, 19, 865–872. doi:10.1002/cphc.201701134
    • NLM

      Rajput SM, Kumar S, Aswal VK, El Seoud OA, Malek NI, Kailasa SK. Drug induced micelle to vesicle transition of a cationic gemini surfactant: Potential applications in drug delivery [Internet]. ChemPhysChem. 2018 ; 19 865–872.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/cphc.201701134
    • Vancouver

      Rajput SM, Kumar S, Aswal VK, El Seoud OA, Malek NI, Kailasa SK. Drug induced micelle to vesicle transition of a cationic gemini surfactant: Potential applications in drug delivery [Internet]. ChemPhysChem. 2018 ; 19 865–872.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/cphc.201701134
  • Source: Acta Crystallographica Section E. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, QUÍMICA DE SUPERFÍCIE

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      CARACELLI, Ignez et al. 2-[(4-Chlorophenyl)sulfanyl]-2-methoxy-1-phenyl-ethan-1-one: crystal structure and Hirshfeld surface analysis. Acta Crystallographica Section E, v. 74 , n. 5, p. 703-708 :+ Supplementary materials (S1-S4), 2018Tradução . . Disponível em: https://doi.org/10.1107/S2056989018006072. Acesso em: 06 jun. 2024.
    • APA

      Caracelli, I., Schpector, J. Z., Traesel, H. J., Olivato, P. R., Jotani , M. M., & Tiekink, E. R. T. (2018). 2-[(4-Chlorophenyl)sulfanyl]-2-methoxy-1-phenyl-ethan-1-one: crystal structure and Hirshfeld surface analysis. Acta Crystallographica Section E, 74 ( 5), 703-708 :+ Supplementary materials (S1-S4). doi:10.1107/S2056989018006072
    • NLM

      Caracelli I, Schpector JZ, Traesel HJ, Olivato PR, Jotani MM, Tiekink ERT. 2-[(4-Chlorophenyl)sulfanyl]-2-methoxy-1-phenyl-ethan-1-one: crystal structure and Hirshfeld surface analysis [Internet]. Acta Crystallographica Section E. 2018 ; 74 ( 5): 703-708 :+ Supplementary materials (S1-S4).[citado 2024 jun. 06 ] Available from: https://doi.org/10.1107/S2056989018006072
    • Vancouver

      Caracelli I, Schpector JZ, Traesel HJ, Olivato PR, Jotani MM, Tiekink ERT. 2-[(4-Chlorophenyl)sulfanyl]-2-methoxy-1-phenyl-ethan-1-one: crystal structure and Hirshfeld surface analysis [Internet]. Acta Crystallographica Section E. 2018 ; 74 ( 5): 703-708 :+ Supplementary materials (S1-S4).[citado 2024 jun. 06 ] Available from: https://doi.org/10.1107/S2056989018006072
  • Source: Lenzinger Berichte. Unidade: IQ

    Subjects: LÍQUIDOS IÔNICOS, CELULOSE

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      BIONI, Thais de Almeida e MALEK, Naved I e EL SEOUD, Omar A. Kinetics of cellulose acylation with carboxylic anhydrides and N-acylimidazoles in ionic liquid/molecular solvent mixtures: relevance to the synthesis of mixed cellulose esters. Lenzinger Berichte, v. 94, p. 57-66, 2018Tradução . . Disponível em: https://www.lenzing.com/index.php?type=88245&tx_filedownloads_file%5bfileName%5d=fileadmin/content/PDF/03_Forschung_u_Entwicklung/Lenzinger_Berichte_94_2018.pdf. Acesso em: 06 jun. 2024.
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      Bioni, T. de A., Malek, N. I., & El Seoud, O. A. (2018). Kinetics of cellulose acylation with carboxylic anhydrides and N-acylimidazoles in ionic liquid/molecular solvent mixtures: relevance to the synthesis of mixed cellulose esters. Lenzinger Berichte, 94, 57-66. Recuperado de https://www.lenzing.com/index.php?type=88245&tx_filedownloads_file%5bfileName%5d=fileadmin/content/PDF/03_Forschung_u_Entwicklung/Lenzinger_Berichte_94_2018.pdf
    • NLM

      Bioni T de A, Malek NI, El Seoud OA. Kinetics of cellulose acylation with carboxylic anhydrides and N-acylimidazoles in ionic liquid/molecular solvent mixtures: relevance to the synthesis of mixed cellulose esters [Internet]. Lenzinger Berichte. 2018 ; 94 57-66.[citado 2024 jun. 06 ] Available from: https://www.lenzing.com/index.php?type=88245&tx_filedownloads_file%5bfileName%5d=fileadmin/content/PDF/03_Forschung_u_Entwicklung/Lenzinger_Berichte_94_2018.pdf
    • Vancouver

      Bioni T de A, Malek NI, El Seoud OA. Kinetics of cellulose acylation with carboxylic anhydrides and N-acylimidazoles in ionic liquid/molecular solvent mixtures: relevance to the synthesis of mixed cellulose esters [Internet]. Lenzinger Berichte. 2018 ; 94 57-66.[citado 2024 jun. 06 ] Available from: https://www.lenzing.com/index.php?type=88245&tx_filedownloads_file%5bfileName%5d=fileadmin/content/PDF/03_Forschung_u_Entwicklung/Lenzinger_Berichte_94_2018.pdf
  • Source: RSC Advances. Unidade: IQ

    Subjects: SURFACTANTES, SOLUÇÕES AQUOSAS

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      VAID, Zuber S et al. Drug induced micelle-to-vesicle transition in aqueous solutions of cationic surfactants. RSC Advances, v. 7, n. 7, p. 3861-3869, 2017Tradução . . Disponível em: https://doi.org/10.1039/c6ra25577a. Acesso em: 06 jun. 2024.
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      Vaid, Z. S., Kumar, A., El Seoud, O. A., & Malek, N. I. (2017). Drug induced micelle-to-vesicle transition in aqueous solutions of cationic surfactants. RSC Advances, 7( 7), 3861-3869. doi:10.1039/c6ra25577a
    • NLM

      Vaid ZS, Kumar A, El Seoud OA, Malek NI. Drug induced micelle-to-vesicle transition in aqueous solutions of cationic surfactants [Internet]. RSC Advances. 2017 ; 7( 7): 3861-3869.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1039/c6ra25577a
    • Vancouver

      Vaid ZS, Kumar A, El Seoud OA, Malek NI. Drug induced micelle-to-vesicle transition in aqueous solutions of cationic surfactants [Internet]. RSC Advances. 2017 ; 7( 7): 3861-3869.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1039/c6ra25577a
  • Source: Abstracts. Conference titles: American Chemical Society National Meeting & Exposition. Unidade: IQ

    Subjects: SURFACTANTES, LÍQUIDOS IÔNICOS

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      VAID, Zuber S e MALEK, Naved Anjum e EL SEOUD, Omar A. Diclofenac sodium-induced micelle-to-vesicle transition in ionic liquid based surfactant systems: relevance to drug delivery. 2016, Anais.. Washington: American Chemical Society (ACS), 2016. . Acesso em: 06 jun. 2024.
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      Vaid, Z. S., Malek, N. A., & El Seoud, O. A. (2016). Diclofenac sodium-induced micelle-to-vesicle transition in ionic liquid based surfactant systems: relevance to drug delivery. In Abstracts. Washington: American Chemical Society (ACS).
    • NLM

      Vaid ZS, Malek NA, El Seoud OA. Diclofenac sodium-induced micelle-to-vesicle transition in ionic liquid based surfactant systems: relevance to drug delivery. Abstracts. 2016 ;[citado 2024 jun. 06 ]
    • Vancouver

      Vaid ZS, Malek NA, El Seoud OA. Diclofenac sodium-induced micelle-to-vesicle transition in ionic liquid based surfactant systems: relevance to drug delivery. Abstracts. 2016 ;[citado 2024 jun. 06 ]

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