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diffusion  (Logan Instruments CORP)


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    Structured Review

    Logan Instruments CORP diffusion
    Diffusion, supplied by Logan Instruments CORP, used in various techniques. Bioz Stars score: 96/100, based on 434 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/diffusion/Diffusion/custom%40system-913%4042495156
    Average 96 stars, based on 434 article reviews
    diffusion - by Bioz Stars, 2026-10
    96/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Diffusion-based Assay:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Microscopy:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    In Vitro:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Concentration Assay:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    In Vivo:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Permeability:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Membrane:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Formulation:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Sampling:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Blocking Assay:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Injection:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Isolation:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Chromatography:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Liquid Chromatography:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    High Performance Liquid Chromatography:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Mass Spectrometry:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr

    Spectroscopy:

    Article Title: Microemulsion-embedded hyaluronic acid microneedles improve local triptolide delivery and anti-arthritic efficacy in rheumatoid arthritis
    Article Snippet: ned (5 μm), and stained with H&E. Microchannel morphology and insertion depth were examined by optical microscopy (CX43, Olympus, Japan). In vitro TP release was evaluated using Franz diffusion cells (LOGAN Instruments, USA) with excised rat skin mounted between donor and receptor chambers (stratum corneum facing donor). The receptor compartment contained PBS (pH 7.4) maintained at 37 °C with stirr



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    Image Search Results


     Formulation  Compositions for the Preparation of NM, NM-HA, and NM-HON by ABN

    Journal: International Journal of Nanomedicine

    Article Title: Improved Physicochemical Stability and Retinoblastoma Anticancer Activity of Salt-Caged Acid–Base Neutralized Melphalan Loaded in L-Glutathione and pH Responsive Fattigated Nanoparticles

    doi: 10.2147/IJN.S618075

    Figure Lengend Snippet: Formulation Compositions for the Preparation of NM, NM-HA, and NM-HON by ABN

    Article Snippet: Each formulation (NM, NM-HA, and NM-HON) and free MEL were analyzed using a DHC-6TD permeability testing system with a PB-M (Logan Instruments, Somerset, NJ, USA).

    Techniques: Formulation

    Comparative stability of MEL, neutralized MEL (NM) and NM-loaded formulations (NM-HA, and NM-HON) in pH 7.4 PBS (n = 3). **p < 0.01, ***p < 0.001. ****p<0.0001 One-way ANOVA compared with MEL.

    Journal: International Journal of Nanomedicine

    Article Title: Improved Physicochemical Stability and Retinoblastoma Anticancer Activity of Salt-Caged Acid–Base Neutralized Melphalan Loaded in L-Glutathione and pH Responsive Fattigated Nanoparticles

    doi: 10.2147/IJN.S618075

    Figure Lengend Snippet: Comparative stability of MEL, neutralized MEL (NM) and NM-loaded formulations (NM-HA, and NM-HON) in pH 7.4 PBS (n = 3). **p < 0.01, ***p < 0.001. ****p<0.0001 One-way ANOVA compared with MEL.

    Article Snippet: Each formulation (NM, NM-HA, and NM-HON) and free MEL were analyzed using a DHC-6TD permeability testing system with a PB-M (Logan Instruments, Somerset, NJ, USA).

    Techniques: Stability

    Solid-state stability of freeze-dried NM, NM-HA, and NM-HON at 25 °C and 70 % RH (n = 3). *p<0.05, **p < 0.01, ****p<0.0001 One-way ANOVA compared with MEL.

    Journal: International Journal of Nanomedicine

    Article Title: Improved Physicochemical Stability and Retinoblastoma Anticancer Activity of Salt-Caged Acid–Base Neutralized Melphalan Loaded in L-Glutathione and pH Responsive Fattigated Nanoparticles

    doi: 10.2147/IJN.S618075

    Figure Lengend Snippet: Solid-state stability of freeze-dried NM, NM-HA, and NM-HON at 25 °C and 70 % RH (n = 3). *p<0.05, **p < 0.01, ****p<0.0001 One-way ANOVA compared with MEL.

    Article Snippet: Each formulation (NM, NM-HA, and NM-HON) and free MEL were analyzed using a DHC-6TD permeability testing system with a PB-M (Logan Instruments, Somerset, NJ, USA).

    Techniques: Stability

    FE-SEM images of MEL ( a ), HA ( b ), HOC ( c ), NM ( d ), NM-HA ( e ), and NM-HON ( f ).

    Journal: International Journal of Nanomedicine

    Article Title: Improved Physicochemical Stability and Retinoblastoma Anticancer Activity of Salt-Caged Acid–Base Neutralized Melphalan Loaded in L-Glutathione and pH Responsive Fattigated Nanoparticles

    doi: 10.2147/IJN.S618075

    Figure Lengend Snippet: FE-SEM images of MEL ( a ), HA ( b ), HOC ( c ), NM ( d ), NM-HA ( e ), and NM-HON ( f ).

    Article Snippet: Each formulation (NM, NM-HA, and NM-HON) and free MEL were analyzed using a DHC-6TD permeability testing system with a PB-M (Logan Instruments, Somerset, NJ, USA).

    Techniques:

    Fourier transform-infrared (FT-IR) spectra ( a ), differential scanning calorimetry (DSC) thermograms ( b ), and high power X- ray diffraction (HP-XRD) patterns ( c) of MEL, NM, NM-HA, NM-HON, and raw materials.

    Journal: International Journal of Nanomedicine

    Article Title: Improved Physicochemical Stability and Retinoblastoma Anticancer Activity of Salt-Caged Acid–Base Neutralized Melphalan Loaded in L-Glutathione and pH Responsive Fattigated Nanoparticles

    doi: 10.2147/IJN.S618075

    Figure Lengend Snippet: Fourier transform-infrared (FT-IR) spectra ( a ), differential scanning calorimetry (DSC) thermograms ( b ), and high power X- ray diffraction (HP-XRD) patterns ( c) of MEL, NM, NM-HA, NM-HON, and raw materials.

    Article Snippet: Each formulation (NM, NM-HA, and NM-HON) and free MEL were analyzed using a DHC-6TD permeability testing system with a PB-M (Logan Instruments, Somerset, NJ, USA).

    Techniques: Fourier Transform Infrared Spectroscopy, Differential Scanning Calorimetry

    In vitro permeability profiles of MEL, NM, NM-HA, and NM-HON using permeation barrier membrane (PB-M) in pH 7.4 PBS (n = 3). **p < 0.01, ***p < 0.001. ****p<0.0001 One-Way ANOVA compared with MEL.

    Journal: International Journal of Nanomedicine

    Article Title: Improved Physicochemical Stability and Retinoblastoma Anticancer Activity of Salt-Caged Acid–Base Neutralized Melphalan Loaded in L-Glutathione and pH Responsive Fattigated Nanoparticles

    doi: 10.2147/IJN.S618075

    Figure Lengend Snippet: In vitro permeability profiles of MEL, NM, NM-HA, and NM-HON using permeation barrier membrane (PB-M) in pH 7.4 PBS (n = 3). **p < 0.01, ***p < 0.001. ****p<0.0001 One-Way ANOVA compared with MEL.

    Article Snippet: Each formulation (NM, NM-HA, and NM-HON) and free MEL were analyzed using a DHC-6TD permeability testing system with a PB-M (Logan Instruments, Somerset, NJ, USA).

    Techniques: In Vitro, Permeability, Membrane

    In vitro release profiles of MEL, NM, NM-HA, and NM-HON in pH 7.4 PBS ( a ), pH 5.2 ABS ( b ), and pH 7.4 PBS with 10 mM GSH ( c ) (n = 3). *p < 0.05, **p<0.01, ***p < 0.001. ****p<0.0001 One-way ANOVA compared with MEL.

    Journal: International Journal of Nanomedicine

    Article Title: Improved Physicochemical Stability and Retinoblastoma Anticancer Activity of Salt-Caged Acid–Base Neutralized Melphalan Loaded in L-Glutathione and pH Responsive Fattigated Nanoparticles

    doi: 10.2147/IJN.S618075

    Figure Lengend Snippet: In vitro release profiles of MEL, NM, NM-HA, and NM-HON in pH 7.4 PBS ( a ), pH 5.2 ABS ( b ), and pH 7.4 PBS with 10 mM GSH ( c ) (n = 3). *p < 0.05, **p<0.01, ***p < 0.001. ****p<0.0001 One-way ANOVA compared with MEL.

    Article Snippet: Each formulation (NM, NM-HA, and NM-HON) and free MEL were analyzed using a DHC-6TD permeability testing system with a PB-M (Logan Instruments, Somerset, NJ, USA).

    Techniques: In Vitro

    In vitro cytotoxicity of MEL, NM, NM-HA, and NM-HON in ARPE-19 normal cells ( a ) and WERI-Rb-1 cancer cells ( b ) after incubation for 24 h (n = 3). *p < 0.05, **p<0.01, ***p < 0.001. ****p<0.0001 One-way ANOVA compared with MEL.

    Journal: International Journal of Nanomedicine

    Article Title: Improved Physicochemical Stability and Retinoblastoma Anticancer Activity of Salt-Caged Acid–Base Neutralized Melphalan Loaded in L-Glutathione and pH Responsive Fattigated Nanoparticles

    doi: 10.2147/IJN.S618075

    Figure Lengend Snippet: In vitro cytotoxicity of MEL, NM, NM-HA, and NM-HON in ARPE-19 normal cells ( a ) and WERI-Rb-1 cancer cells ( b ) after incubation for 24 h (n = 3). *p < 0.05, **p<0.01, ***p < 0.001. ****p<0.0001 One-way ANOVA compared with MEL.

    Article Snippet: Each formulation (NM, NM-HA, and NM-HON) and free MEL were analyzed using a DHC-6TD permeability testing system with a PB-M (Logan Instruments, Somerset, NJ, USA).

    Techniques: In Vitro, Incubation