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sln gel  (ATCC)


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    Structured Review

    ATCC sln gel
    Lipid-based systems for delivery of amphotericin B currently under development.
    Sln Gel, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sln+gel/Microbotryum+violaceum+(Persoon)+Deml+et+Oberwinkler%2C+teleomorph/pmc07023008-40-0-39
    Average 90 stars, based on 16 article reviews
    sln gel - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Lipid Systems for the Delivery of Amphotericin B in Antifungal Therapy"

    Article Title: Lipid Systems for the Delivery of Amphotericin B in Antifungal Therapy

    Journal: Pharmaceutics

    doi: 10.3390/pharmaceutics12010029

    Lipid-based systems for delivery of amphotericin B currently under development.
    Figure Legend Snippet: Lipid-based systems for delivery of amphotericin B currently under development.

    Techniques Used: Formulation, Conjugation Assay, Permeability, In Vitro, Activity Assay, Produced, MTT Assay, In Vivo, Concentration Assay, Spectroscopy, Shear, Liposomes, Modification, Dispersion, Injection, Incubation, Saline, Sonication, Infection, Solubility, Encapsulation, Homogenization, Titration, Ex Vivo, Viscosity, Inhibition, Diffusion-based Assay, Emulsion, Clinical Proteomics, Fluorescence, Imaging, Adjuvant, Expressing, RNA Expression, Solvent, Control, Histopathology, Polymer, Evaporation, Emulsification, Eye Drops

    Related Articles

    Solvent:

    Article Title: Lipid Systems for the Delivery of Amphotericin B in Antifungal Therapy
    Article Snippet: Nanodisk (ND) , Sinonasal (a) , 44–80 , , DMPC:DMPG (7:3 weight ratio), ApoA-I, AmB. Thin film method; sonication and dialysis after addition of AmB and ApoA-I. , HSNE exposed to toxic conc. of AmB-ND (18 h): apical membranes permeable to K + ions at 10 μg/mL AmB; reduction of apical cell K + permeability at 75 μg/mL AmB with 85% reduction of LDH and no increase in LDH release at 150 μg/mL AmB. In vitro expression of A. fumigatus (ATCC 13073) conidia after 4 h exposure to AmB-ND (10 μg/mL) smaller than exposure to AmB; AmB-ND (50 μg/mL) RNA expression without statistical significance between AmB and AmB-ND. AmB-ND protected human nasal epithelia membranes from AmB toxicity. , [ , ] . .. SLN gel , Skin , 111.1 ± 2.2 (0.13 ± 0.04) , 93.8 ± 1.8 , AmB:lipid (1:10 weight ratio), Pluronic F127 (0.25% w / v ). Solvent diffusion method in aqueous system. , Antifungal activity against Trichophyton rubrum (ATCC 28188, KWIK-STIK 0444P), ZOI (72 h) 2.81 ± 0.13 mm. Stability (ζ –23.98 ± 1.36 mV) at 2–8 °C and 25 ± 2 °C, for 3 months. AmB in aqueous phase: 90.2 ± 1.1% (compritol ATO 888), 96.5 ± 1.4% (Precirol ATO 5, selected for preparation of SLNs gel), and 72.1 ± 2.7% (stearic acid). Ex vivo permeation studies on abdomen skin of female albino Wistar rats: AmB efflux 22.34 μg/cm 2 . PII (SLN gel) 0.11 ± 0.19 Higher skin deposition, lower skin irritation, high antifungal activity, localized delivery with minimal side effects. , [ ] . .. Glyceride dilaurate-based SLN (AmbiOnp) , Oral , 392.8 ± 6.97 , , GDL, PC-enriched lecithin, PEG-660-12-hydroxystearate, AmB. Probe sonication-assisted nanoprecipitation technique. , Easy redispersion of AmbiOnp in water (3 months, 2–8 °C). Significant increase in particle size at 25 and 40 °C after 3 months. AmB content in AmbiOnp (ζ –27.9 ± 0.2 mV) ≈ 100% (after 1 month), showing significant reduction after 3 months when stored at 25 °C and 40 °C. In vitro antifungal activity against C. albicans in SGF, MIC 7.812 μg/mL.In vivo PK studies (adult female Sprague-Dawley rats): C máx 1109.31 ± 104.79 ng/mL, AmbiOnp (3.6 mg/kg of AmB) oral, 24 h, comparable to C máx 1417.49 ± 85.52 ng/mL Fungizone ® (0.8 mg/kg of AmB), i.v. Low renal tissue levels of AmB in AmbiOnp at 8 h: 84.50 ± 22.896 ng/mL; without detectable levels post 8 h. , [ , ] .

    Diffusion-based Assay:

    Article Title: Lipid Systems for the Delivery of Amphotericin B in Antifungal Therapy
    Article Snippet: Nanodisk (ND) , Sinonasal (a) , 44–80 , , DMPC:DMPG (7:3 weight ratio), ApoA-I, AmB. Thin film method; sonication and dialysis after addition of AmB and ApoA-I. , HSNE exposed to toxic conc. of AmB-ND (18 h): apical membranes permeable to K + ions at 10 μg/mL AmB; reduction of apical cell K + permeability at 75 μg/mL AmB with 85% reduction of LDH and no increase in LDH release at 150 μg/mL AmB. In vitro expression of A. fumigatus (ATCC 13073) conidia after 4 h exposure to AmB-ND (10 μg/mL) smaller than exposure to AmB; AmB-ND (50 μg/mL) RNA expression without statistical significance between AmB and AmB-ND. AmB-ND protected human nasal epithelia membranes from AmB toxicity. , [ , ] . .. SLN gel , Skin , 111.1 ± 2.2 (0.13 ± 0.04) , 93.8 ± 1.8 , AmB:lipid (1:10 weight ratio), Pluronic F127 (0.25% w / v ). Solvent diffusion method in aqueous system. , Antifungal activity against Trichophyton rubrum (ATCC 28188, KWIK-STIK 0444P), ZOI (72 h) 2.81 ± 0.13 mm. Stability (ζ –23.98 ± 1.36 mV) at 2–8 °C and 25 ± 2 °C, for 3 months. AmB in aqueous phase: 90.2 ± 1.1% (compritol ATO 888), 96.5 ± 1.4% (Precirol ATO 5, selected for preparation of SLNs gel), and 72.1 ± 2.7% (stearic acid). Ex vivo permeation studies on abdomen skin of female albino Wistar rats: AmB efflux 22.34 μg/cm 2 . PII (SLN gel) 0.11 ± 0.19 Higher skin deposition, lower skin irritation, high antifungal activity, localized delivery with minimal side effects. , [ ] . .. Glyceride dilaurate-based SLN (AmbiOnp) , Oral , 392.8 ± 6.97 , , GDL, PC-enriched lecithin, PEG-660-12-hydroxystearate, AmB. Probe sonication-assisted nanoprecipitation technique. , Easy redispersion of AmbiOnp in water (3 months, 2–8 °C). Significant increase in particle size at 25 and 40 °C after 3 months. AmB content in AmbiOnp (ζ –27.9 ± 0.2 mV) ≈ 100% (after 1 month), showing significant reduction after 3 months when stored at 25 °C and 40 °C. In vitro antifungal activity against C. albicans in SGF, MIC 7.812 μg/mL.In vivo PK studies (adult female Sprague-Dawley rats): C máx 1109.31 ± 104.79 ng/mL, AmbiOnp (3.6 mg/kg of AmB) oral, 24 h, comparable to C máx 1417.49 ± 85.52 ng/mL Fungizone ® (0.8 mg/kg of AmB), i.v. Low renal tissue levels of AmB in AmbiOnp at 8 h: 84.50 ± 22.896 ng/mL; without detectable levels post 8 h. , [ , ] .

    Activity Assay:

    Article Title: Lipid Systems for the Delivery of Amphotericin B in Antifungal Therapy
    Article Snippet: Nanodisk (ND) , Sinonasal (a) , 44–80 , , DMPC:DMPG (7:3 weight ratio), ApoA-I, AmB. Thin film method; sonication and dialysis after addition of AmB and ApoA-I. , HSNE exposed to toxic conc. of AmB-ND (18 h): apical membranes permeable to K + ions at 10 μg/mL AmB; reduction of apical cell K + permeability at 75 μg/mL AmB with 85% reduction of LDH and no increase in LDH release at 150 μg/mL AmB. In vitro expression of A. fumigatus (ATCC 13073) conidia after 4 h exposure to AmB-ND (10 μg/mL) smaller than exposure to AmB; AmB-ND (50 μg/mL) RNA expression without statistical significance between AmB and AmB-ND. AmB-ND protected human nasal epithelia membranes from AmB toxicity. , [ , ] . .. SLN gel , Skin , 111.1 ± 2.2 (0.13 ± 0.04) , 93.8 ± 1.8 , AmB:lipid (1:10 weight ratio), Pluronic F127 (0.25% w / v ). Solvent diffusion method in aqueous system. , Antifungal activity against Trichophyton rubrum (ATCC 28188, KWIK-STIK 0444P), ZOI (72 h) 2.81 ± 0.13 mm. Stability (ζ –23.98 ± 1.36 mV) at 2–8 °C and 25 ± 2 °C, for 3 months. AmB in aqueous phase: 90.2 ± 1.1% (compritol ATO 888), 96.5 ± 1.4% (Precirol ATO 5, selected for preparation of SLNs gel), and 72.1 ± 2.7% (stearic acid). Ex vivo permeation studies on abdomen skin of female albino Wistar rats: AmB efflux 22.34 μg/cm 2 . PII (SLN gel) 0.11 ± 0.19 Higher skin deposition, lower skin irritation, high antifungal activity, localized delivery with minimal side effects. , [ ] . .. Glyceride dilaurate-based SLN (AmbiOnp) , Oral , 392.8 ± 6.97 , , GDL, PC-enriched lecithin, PEG-660-12-hydroxystearate, AmB. Probe sonication-assisted nanoprecipitation technique. , Easy redispersion of AmbiOnp in water (3 months, 2–8 °C). Significant increase in particle size at 25 and 40 °C after 3 months. AmB content in AmbiOnp (ζ –27.9 ± 0.2 mV) ≈ 100% (after 1 month), showing significant reduction after 3 months when stored at 25 °C and 40 °C. In vitro antifungal activity against C. albicans in SGF, MIC 7.812 μg/mL.In vivo PK studies (adult female Sprague-Dawley rats): C máx 1109.31 ± 104.79 ng/mL, AmbiOnp (3.6 mg/kg of AmB) oral, 24 h, comparable to C máx 1417.49 ± 85.52 ng/mL Fungizone ® (0.8 mg/kg of AmB), i.v. Low renal tissue levels of AmB in AmbiOnp at 8 h: 84.50 ± 22.896 ng/mL; without detectable levels post 8 h. , [ , ] .

    Ex Vivo:

    Article Title: Lipid Systems for the Delivery of Amphotericin B in Antifungal Therapy
    Article Snippet: Nanodisk (ND) , Sinonasal (a) , 44–80 , , DMPC:DMPG (7:3 weight ratio), ApoA-I, AmB. Thin film method; sonication and dialysis after addition of AmB and ApoA-I. , HSNE exposed to toxic conc. of AmB-ND (18 h): apical membranes permeable to K + ions at 10 μg/mL AmB; reduction of apical cell K + permeability at 75 μg/mL AmB with 85% reduction of LDH and no increase in LDH release at 150 μg/mL AmB. In vitro expression of A. fumigatus (ATCC 13073) conidia after 4 h exposure to AmB-ND (10 μg/mL) smaller than exposure to AmB; AmB-ND (50 μg/mL) RNA expression without statistical significance between AmB and AmB-ND. AmB-ND protected human nasal epithelia membranes from AmB toxicity. , [ , ] . .. SLN gel , Skin , 111.1 ± 2.2 (0.13 ± 0.04) , 93.8 ± 1.8 , AmB:lipid (1:10 weight ratio), Pluronic F127 (0.25% w / v ). Solvent diffusion method in aqueous system. , Antifungal activity against Trichophyton rubrum (ATCC 28188, KWIK-STIK 0444P), ZOI (72 h) 2.81 ± 0.13 mm. Stability (ζ –23.98 ± 1.36 mV) at 2–8 °C and 25 ± 2 °C, for 3 months. AmB in aqueous phase: 90.2 ± 1.1% (compritol ATO 888), 96.5 ± 1.4% (Precirol ATO 5, selected for preparation of SLNs gel), and 72.1 ± 2.7% (stearic acid). Ex vivo permeation studies on abdomen skin of female albino Wistar rats: AmB efflux 22.34 μg/cm 2 . PII (SLN gel) 0.11 ± 0.19 Higher skin deposition, lower skin irritation, high antifungal activity, localized delivery with minimal side effects. , [ ] . .. Glyceride dilaurate-based SLN (AmbiOnp) , Oral , 392.8 ± 6.97 , , GDL, PC-enriched lecithin, PEG-660-12-hydroxystearate, AmB. Probe sonication-assisted nanoprecipitation technique. , Easy redispersion of AmbiOnp in water (3 months, 2–8 °C). Significant increase in particle size at 25 and 40 °C after 3 months. AmB content in AmbiOnp (ζ –27.9 ± 0.2 mV) ≈ 100% (after 1 month), showing significant reduction after 3 months when stored at 25 °C and 40 °C. In vitro antifungal activity against C. albicans in SGF, MIC 7.812 μg/mL.In vivo PK studies (adult female Sprague-Dawley rats): C máx 1109.31 ± 104.79 ng/mL, AmbiOnp (3.6 mg/kg of AmB) oral, 24 h, comparable to C máx 1417.49 ± 85.52 ng/mL Fungizone ® (0.8 mg/kg of AmB), i.v. Low renal tissue levels of AmB in AmbiOnp at 8 h: 84.50 ± 22.896 ng/mL; without detectable levels post 8 h. , [ , ] .



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    Lipid-based systems for delivery of amphotericin B currently under development.

    Journal: Pharmaceutics

    Article Title: Lipid Systems for the Delivery of Amphotericin B in Antifungal Therapy

    doi: 10.3390/pharmaceutics12010029

    Figure Lengend Snippet: Lipid-based systems for delivery of amphotericin B currently under development.

    Article Snippet: SLN gel , Skin , 111.1 ± 2.2 (0.13 ± 0.04) , 93.8 ± 1.8 , AmB:lipid (1:10 weight ratio), Pluronic F127 (0.25% w / v ). Solvent diffusion method in aqueous system. , Antifungal activity against Trichophyton rubrum (ATCC 28188, KWIK-STIK 0444P), ZOI (72 h) 2.81 ± 0.13 mm. Stability (ζ –23.98 ± 1.36 mV) at 2–8 °C and 25 ± 2 °C, for 3 months. AmB in aqueous phase: 90.2 ± 1.1% (compritol ATO 888), 96.5 ± 1.4% (Precirol ATO 5, selected for preparation of SLNs gel), and 72.1 ± 2.7% (stearic acid). Ex vivo permeation studies on abdomen skin of female albino Wistar rats: AmB efflux 22.34 μg/cm 2 . PII (SLN gel) 0.11 ± 0.19 Higher skin deposition, lower skin irritation, high antifungal activity, localized delivery with minimal side effects. , [ ] .

    Techniques: Formulation, Conjugation Assay, Permeability, In Vitro, Activity Assay, Produced, MTT Assay, In Vivo, Concentration Assay, Spectroscopy, Shear, Liposomes, Modification, Dispersion, Injection, Incubation, Saline, Sonication, Infection, Solubility, Encapsulation, Homogenization, Titration, Ex Vivo, Viscosity, Inhibition, Diffusion-based Assay, Emulsion, Clinical Proteomics, Fluorescence, Imaging, Adjuvant, Expressing, RNA Expression, Solvent, Control, Histopathology, Polymer, Evaporation, Emulsification, Eye Drops

    Schematic representation of formulation of FLB SLN using HME technique

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: Schematic representation of formulation of FLB SLN using HME technique

    Article Snippet: Anti‐inflammatory Effect of FLB SLN In Vivo Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Formulation

    A SEM image of FLB SLN showing spherical SLN particles with particle size below 250 nm. B DSC thermogram showing sharp endotherm of FLB at its melting point which was disappeared in FLB SLN formulation

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: A SEM image of FLB SLN showing spherical SLN particles with particle size below 250 nm. B DSC thermogram showing sharp endotherm of FLB at its melting point which was disappeared in FLB SLN formulation

    Article Snippet: Anti‐inflammatory Effect of FLB SLN In Vivo Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Formulation

    A Spreadability testing setup using texture analyzer equipment. B Spreadability curve showing significant decrease in peak adhesive force in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: A Spreadability testing setup using texture analyzer equipment. B Spreadability curve showing significant decrease in peak adhesive force in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation

    Article Snippet: Anti‐inflammatory Effect of FLB SLN In Vivo Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Adhesive, Formulation

    Table Showing Peak Adhesive Force, Work Area, and Stiffness of 0.5%  FLB SLN Gel  and 5% Marketed FLB Gel

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: Table Showing Peak Adhesive Force, Work Area, and Stiffness of 0.5% FLB SLN Gel and 5% Marketed FLB Gel

    Article Snippet: Anti‐inflammatory Effect of FLB SLN In Vivo Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Adhesive

    Rheological studies of 0.5% w/v FLB SLN gel and 5% w/w FLB marketed gel formulation showing decrease in viscosity upon increase in shear rate

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: Rheological studies of 0.5% w/v FLB SLN gel and 5% w/w FLB marketed gel formulation showing decrease in viscosity upon increase in shear rate

    Article Snippet: Anti‐inflammatory Effect of FLB SLN In Vivo Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Formulation, Viscosity, Shear

    A In vitro permeation test (IVPT) showing significant increase in percent drug permeation in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation at the end of 24 h. B Skin deposition study showing significant increase in drug deposition in dermal layer in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation at the end of 24 h

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: A In vitro permeation test (IVPT) showing significant increase in percent drug permeation in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation at the end of 24 h. B Skin deposition study showing significant increase in drug deposition in dermal layer in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation at the end of 24 h

    Article Snippet: Anti‐inflammatory Effect of FLB SLN In Vivo Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: In Vitro, Formulation

    In vivo anti-inflammatory study showing equivalent edema inhibition effect after application of 0.5% w/v FLB SLN gel and 5% w/w marketed FLB gel

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: In vivo anti-inflammatory study showing equivalent edema inhibition effect after application of 0.5% w/v FLB SLN gel and 5% w/w marketed FLB gel

    Article Snippet: Anti‐inflammatory Effect of FLB SLN In Vivo Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: In Vivo, Inhibition

    Schematic representation of formulation of FLB SLN using HME technique

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: Schematic representation of formulation of FLB SLN using HME technique

    Article Snippet: Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Formulation

    A SEM image of FLB SLN showing spherical SLN particles with particle size below 250 nm. B DSC thermogram showing sharp endotherm of FLB at its melting point which was disappeared in FLB SLN formulation

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: A SEM image of FLB SLN showing spherical SLN particles with particle size below 250 nm. B DSC thermogram showing sharp endotherm of FLB at its melting point which was disappeared in FLB SLN formulation

    Article Snippet: Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Formulation

    A Spreadability testing setup using texture analyzer equipment. B Spreadability curve showing significant decrease in peak adhesive force in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: A Spreadability testing setup using texture analyzer equipment. B Spreadability curve showing significant decrease in peak adhesive force in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation

    Article Snippet: Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Adhesive, Formulation

    Table Showing Peak Adhesive Force, Work Area, and Stiffness of 0.5%  FLB SLN Gel  and 5% Marketed FLB Gel

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: Table Showing Peak Adhesive Force, Work Area, and Stiffness of 0.5% FLB SLN Gel and 5% Marketed FLB Gel

    Article Snippet: Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Adhesive

    Rheological studies of 0.5% w/v FLB SLN gel and 5% w/w FLB marketed gel formulation showing decrease in viscosity upon increase in shear rate

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: Rheological studies of 0.5% w/v FLB SLN gel and 5% w/w FLB marketed gel formulation showing decrease in viscosity upon increase in shear rate

    Article Snippet: Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: Formulation, Viscosity, Shear

    A In vitro permeation test (IVPT) showing significant increase in percent drug permeation in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation at the end of 24 h. B Skin deposition study showing significant increase in drug deposition in dermal layer in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation at the end of 24 h

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: A In vitro permeation test (IVPT) showing significant increase in percent drug permeation in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation at the end of 24 h. B Skin deposition study showing significant increase in drug deposition in dermal layer in case of 0.5% w/v FLB SLN formulation as compared to 5% w/w FLB marketed gel formulation at the end of 24 h

    Article Snippet: Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: In Vitro, Formulation

    In vivo anti-inflammatory study showing equivalent edema inhibition effect after application of 0.5% w/v FLB SLN gel and 5% w/w marketed FLB gel

    Journal: AAPS PharmSciTech

    Article Title: Formulation of Topical Flurbiprofen Solid Lipid Nanoparticle Gel Formulation Using Hot Melt Extrusion Technique

    doi: 10.1208/s12249-022-02410-w

    Figure Lengend Snippet: In vivo anti-inflammatory study showing equivalent edema inhibition effect after application of 0.5% w/v FLB SLN gel and 5% w/w marketed FLB gel

    Article Snippet: Three groups: no treatment, 0.5% FLB SLN gel, and 5% FLB gel marketed product of SD rats (Envigo, IN, USA) were divide for this experiment.

    Techniques: In Vivo, Inhibition