Investigation of microemulsion microstructure and its impact on skin delivery of flufenamic acid
[Display omitted] Microemulsions are well known penetration enhancing delivery systems. Several properties are described that influence the transdermal delivery of active components. Therefore, this study aimed to characterize fluorosurfactant-based microemulsions and to assess the impact of formula...
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| Vydáno v: | International journal of pharmaceutics Ročník 490; číslo 1-2; s. 292 - 297 |
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| Hlavní autoři: | , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
Netherlands
Elsevier B.V
25.07.2015
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| Témata: | |
| ISSN: | 0378-5173, 1873-3476 |
| On-line přístup: | Získat plný text |
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| Abstract | [Display omitted]
Microemulsions are well known penetration enhancing delivery systems. Several properties are described that influence the transdermal delivery of active components. Therefore, this study aimed to characterize fluorosurfactant-based microemulsions and to assess the impact of formulation variables on the transdermal delivery of incorporated flufenamic acid. The microemulsion systems prepared in this study consisted of bistilled water, oleic acid, isopropanol as co-solvent, flufenamic acid as active ingredient and either HexaforTM670 (Hex) or Chemguard S-550-100 (Sin) as fluorosurfactant. Characterization was performed by a combination of techniques including electrical conductivity measurements, small-angle X-ray scattering (SAXS) and nuclear magnetic resonance (NMR) self-diffusion experiments. In vitro skin permeation experiments were performed with each prepared microemulsion using Franz type diffusion cells to correlate their present microstructure with their drug delivery to skin. Electrical conductivity increased with added water content. Consequently, the absence of a conductivity maximum as well as the NMR and SAXS data rather suggest O/W type microemulsions with spherical or rod-like microstructures. Skin permeation data revealed enhanced diffusion for Hex- and Sin-microemulsions if the shape of the structures was rather elongated than spherical implying that the shape of droplets had an essential impact on the skin permeation of flufenamic acid. |
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| AbstractList | [Display omitted]
Microemulsions are well known penetration enhancing delivery systems. Several properties are described that influence the transdermal delivery of active components. Therefore, this study aimed to characterize fluorosurfactant-based microemulsions and to assess the impact of formulation variables on the transdermal delivery of incorporated flufenamic acid. The microemulsion systems prepared in this study consisted of bistilled water, oleic acid, isopropanol as co-solvent, flufenamic acid as active ingredient and either HexaforTM670 (Hex) or Chemguard S-550-100 (Sin) as fluorosurfactant. Characterization was performed by a combination of techniques including electrical conductivity measurements, small-angle X-ray scattering (SAXS) and nuclear magnetic resonance (NMR) self-diffusion experiments. In vitro skin permeation experiments were performed with each prepared microemulsion using Franz type diffusion cells to correlate their present microstructure with their drug delivery to skin. Electrical conductivity increased with added water content. Consequently, the absence of a conductivity maximum as well as the NMR and SAXS data rather suggest O/W type microemulsions with spherical or rod-like microstructures. Skin permeation data revealed enhanced diffusion for Hex- and Sin-microemulsions if the shape of the structures was rather elongated than spherical implying that the shape of droplets had an essential impact on the skin permeation of flufenamic acid. Microemulsions are well known penetration enhancing delivery systems. Several properties are described that influence the transdermal delivery of active components. Therefore, this study aimed to characterize fluorosurfactant-based microemulsions and to assess the impact of formulation variables on the transdermal delivery of incorporated flufenamic acid. The microemulsion systems prepared in this study consisted of bistilled water, oleic acid, isopropanol as co-solvent, flufenamic acid as active ingredient and either Hexafor(TM)670 (Hex) or Chemguard S-550-100 (Sin) as fluorosurfactant. Characterization was performed by a combination of techniques including electrical conductivity measurements, small-angle X-ray scattering (SAXS) and nuclear magnetic resonance (NMR) self-diffusion experiments. In vitro skin permeation experiments were performed with each prepared microemulsion using Franz type diffusion cells to correlate their present microstructure with their drug delivery to skin. Electrical conductivity increased with added water content. Consequently, the absence of a conductivity maximum as well as the NMR and SAXS data rather suggest O/W type microemulsions with spherical or rod-like microstructures. Skin permeation data revealed enhanced diffusion for Hex- and Sin-microemulsions if the shape of the structures was rather elongated than spherical implying that the shape of droplets had an essential impact on the skin permeation of flufenamic acid. |
| Author | Peterlik, Herwig Kählig, Hanspeter Binder, Lisa Kwizda, Kristina Partyka-Jankowska, Ewa Valenta, Claudia Mahrhauser, Denise-Silvia |
| Author_xml | – sequence: 1 givenname: Denise-Silvia surname: Mahrhauser fullname: Mahrhauser, Denise-Silvia organization: Department of Pharmaceutical Technology and Biopharmaceutics, Faculty of Life Sciences, Althanstraße 14, 1090 Vienna, Austria – sequence: 2 givenname: Hanspeter surname: Kählig fullname: Kählig, Hanspeter organization: Institute of Organic Chemistry, University of Vienna, Währingerstraße 38, 1090 Vienna, Austria – sequence: 3 givenname: Ewa surname: Partyka-Jankowska fullname: Partyka-Jankowska, Ewa organization: Faculty of Physics, University of Vienna, Boltzmanngasse 5, 1090 Vienna, Austria – sequence: 4 givenname: Herwig surname: Peterlik fullname: Peterlik, Herwig organization: Faculty of Physics, University of Vienna, Boltzmanngasse 5, 1090 Vienna, Austria – sequence: 5 givenname: Lisa surname: Binder fullname: Binder, Lisa organization: Department of Pharmaceutical Technology and Biopharmaceutics, Faculty of Life Sciences, Althanstraße 14, 1090 Vienna, Austria – sequence: 6 givenname: Kristina surname: Kwizda fullname: Kwizda, Kristina organization: Department of Pharmaceutical Technology and Biopharmaceutics, Faculty of Life Sciences, Althanstraße 14, 1090 Vienna, Austria – sequence: 7 givenname: Claudia surname: Valenta fullname: Valenta, Claudia email: claudia.valenta@univie.ac.at organization: Department of Pharmaceutical Technology and Biopharmaceutics, Faculty of Life Sciences, Althanstraße 14, 1090 Vienna, Austria |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26022888$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_3109_10837450_2016_1148722 crossref_primary_10_3390_ph13110329 crossref_primary_10_1016_j_jddst_2019_101245 crossref_primary_10_1016_j_molliq_2021_116361 crossref_primary_10_1016_j_molliq_2022_120405 crossref_primary_10_1016_j_colsurfb_2017_10_015 crossref_primary_10_1016_j_ejpb_2018_02_037 crossref_primary_10_1016_j_ijpharm_2017_06_050 crossref_primary_10_1007_s12032_025_02611_w crossref_primary_10_1016_j_colsurfb_2022_112474 crossref_primary_10_1016_j_molliq_2020_112742 crossref_primary_10_1080_10717544_2023_2234099 crossref_primary_10_1016_j_jddst_2017_08_002 crossref_primary_10_3390_molecules22091552 crossref_primary_10_1007_s11094_018_1858_6 crossref_primary_10_1016_j_colsurfb_2015_11_064 crossref_primary_10_1016_j_foodres_2023_112545 crossref_primary_10_1016_j_ijpharm_2017_11_041 crossref_primary_10_1080_02652048_2021_1957037 crossref_primary_10_1016_j_ejps_2023_106521 crossref_primary_10_1016_j_ijpharm_2016_07_043 crossref_primary_10_3390_pharmaceutics9040037 |
| Cites_doi | 10.1103/PhysRev.110.1 10.1159/000336787 10.1021/cm980756l 10.1006/jmra.1995.1176 10.1016/j.cocis.2012.07.002 10.1023/A:1022234305600 10.1016/j.ijpharm.2011.09.014 10.1016/j.ijpharm.2004.02.018 10.1016/S0927-7757(00)00744-5 10.1002/bip.1969.360080514 10.1081/DDC-100000125 10.1016/S0168-3659(00)00325-4 10.1007/s11095-011-0404-y 10.1016/j.ejpb.2014.04.019 10.1016/0022-3093(95)00021-6 10.1211/jpp.60.5.0003 10.1039/C2SM06903B 10.1016/j.addr.2012.09.032 10.1021/j100246a041 10.1016/j.fluid.2013.07.042 10.1016/j.ijpharm.2014.02.012 10.1016/S0169-409X(02)00116-3 10.1016/j.ijpharm.2009.10.052 |
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| Copyright | 2015 Elsevier B.V. Copyright © 2015 Elsevier B.V. All rights reserved. |
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| Keywords | Skin permeation studies NMR Electrical conductivity Microemulsion characterization ME Sin Hex SAXS |
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Microemulsions are well known penetration enhancing delivery systems. Several properties are described that influence the transdermal... Microemulsions are well known penetration enhancing delivery systems. Several properties are described that influence the transdermal delivery of active... |
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| SubjectTerms | Administration, Cutaneous Chemistry, Pharmaceutical - methods Drug Delivery Systems - methods Electrical conductivity Emulsions - administration & dosage Emulsions - chemistry Flufenamic Acid - administration & dosage Flufenamic Acid - chemistry Microemulsion characterization NMR Permeability SAXS Scattering, Small Angle Skin - metabolism Skin Absorption Skin permeation studies Solvents - chemistry Surface-Active Agents - chemistry Water - chemistry X-Ray Diffraction - methods |
| Title | Investigation of microemulsion microstructure and its impact on skin delivery of flufenamic acid |
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