50:50 multimode fiber optic coupler Search Results


98
Ocean Optics core multimode fibre mmf patch cable
Optical setup to allow fibre based sensing. A 520 nm laser source (10 µW power and 100 ms exposure) was used as a pump source to excite both the pH and oxygen sensors. The pump illumination was launched from a single mode fibre (SMF) collimated by an aspheric lens (L1), passing through a band pass filter (BP) removing unwanted long wavelength light, and reflected by the dichroic mirror (DM), then focused with an identical aspheric lens (L2) and selectively coupled into the fibre core (with XY control of the sensing fibre mount). The returned light from the fibre core was collimated by L2, passed through the dichroic mirror and a long pass filter (LP, removing any reflected pump light). <t>The</t> <t>fluorescence</t> was then focused by lens L3 into a 50 µm core multimode fibre <t>(MMF)</t> patch cable, and directed to a spectrometer (Ocean Optics QEPro). The triggering unit (TTL pulse generator) controlled both laser and spectrometer allowing on demand short integration time (100 ms) synchronised measurements.
Core Multimode Fibre Mmf Patch Cable, supplied by Ocean Optics, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/core multimode fibre mmf patch cable/product/Ocean Optics
Average 98 stars, based on 1 article reviews
core multimode fibre mmf patch cable - by Bioz Stars, 2026-06
98/100 stars
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96
Revvity envision 2104 multilabel reader
Optical setup to allow fibre based sensing. A 520 nm laser source (10 µW power and 100 ms exposure) was used as a pump source to excite both the pH and oxygen sensors. The pump illumination was launched from a single mode fibre (SMF) collimated by an aspheric lens (L1), passing through a band pass filter (BP) removing unwanted long wavelength light, and reflected by the dichroic mirror (DM), then focused with an identical aspheric lens (L2) and selectively coupled into the fibre core (with XY control of the sensing fibre mount). The returned light from the fibre core was collimated by L2, passed through the dichroic mirror and a long pass filter (LP, removing any reflected pump light). <t>The</t> <t>fluorescence</t> was then focused by lens L3 into a 50 µm core multimode fibre <t>(MMF)</t> patch cable, and directed to a spectrometer (Ocean Optics QEPro). The triggering unit (TTL pulse generator) controlled both laser and spectrometer allowing on demand short integration time (100 ms) synchronised measurements.
Envision 2104 Multilabel Reader, supplied by Revvity, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/envision 2104 multilabel reader/product/Revvity
Average 96 stars, based on 1 article reviews
envision 2104 multilabel reader - by Bioz Stars, 2026-06
96/100 stars
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86
Thorlabs multimode fiber
Optical setup to allow fibre based sensing. A 520 nm laser source (10 µW power and 100 ms exposure) was used as a pump source to excite both the pH and oxygen sensors. The pump illumination was launched from a single mode fibre (SMF) collimated by an aspheric lens (L1), passing through a band pass filter (BP) removing unwanted long wavelength light, and reflected by the dichroic mirror (DM), then focused with an identical aspheric lens (L2) and selectively coupled into the fibre core (with XY control of the sensing fibre mount). The returned light from the fibre core was collimated by L2, passed through the dichroic mirror and a long pass filter (LP, removing any reflected pump light). <t>The</t> <t>fluorescence</t> was then focused by lens L3 into a 50 µm core multimode fibre <t>(MMF)</t> patch cable, and directed to a spectrometer (Ocean Optics QEPro). The triggering unit (TTL pulse generator) controlled both laser and spectrometer allowing on demand short integration time (100 ms) synchronised measurements.
Multimode Fiber, supplied by Thorlabs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/multimode fiber/product/Thorlabs
Average 86 stars, based on 1 article reviews
multimode fiber - by Bioz Stars, 2026-06
86/100 stars
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96
Revvity multimode optical in vivo imaging system mois
Optical setup to allow fibre based sensing. A 520 nm laser source (10 µW power and 100 ms exposure) was used as a pump source to excite both the pH and oxygen sensors. The pump illumination was launched from a single mode fibre (SMF) collimated by an aspheric lens (L1), passing through a band pass filter (BP) removing unwanted long wavelength light, and reflected by the dichroic mirror (DM), then focused with an identical aspheric lens (L2) and selectively coupled into the fibre core (with XY control of the sensing fibre mount). The returned light from the fibre core was collimated by L2, passed through the dichroic mirror and a long pass filter (LP, removing any reflected pump light). <t>The</t> <t>fluorescence</t> was then focused by lens L3 into a 50 µm core multimode fibre <t>(MMF)</t> patch cable, and directed to a spectrometer (Ocean Optics QEPro). The triggering unit (TTL pulse generator) controlled both laser and spectrometer allowing on demand short integration time (100 ms) synchronised measurements.
Multimode Optical In Vivo Imaging System Mois, supplied by Revvity, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/multimode optical in vivo imaging system mois/product/Revvity
Average 96 stars, based on 1 article reviews
multimode optical in vivo imaging system mois - by Bioz Stars, 2026-06
96/100 stars
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90
Corning Life Sciences multimode corning mmf 50/125
Optical setup to allow fibre based sensing. A 520 nm laser source (10 µW power and 100 ms exposure) was used as a pump source to excite both the pH and oxygen sensors. The pump illumination was launched from a single mode fibre (SMF) collimated by an aspheric lens (L1), passing through a band pass filter (BP) removing unwanted long wavelength light, and reflected by the dichroic mirror (DM), then focused with an identical aspheric lens (L2) and selectively coupled into the fibre core (with XY control of the sensing fibre mount). The returned light from the fibre core was collimated by L2, passed through the dichroic mirror and a long pass filter (LP, removing any reflected pump light). <t>The</t> <t>fluorescence</t> was then focused by lens L3 into a 50 µm core multimode fibre <t>(MMF)</t> patch cable, and directed to a spectrometer (Ocean Optics QEPro). The triggering unit (TTL pulse generator) controlled both laser and spectrometer allowing on demand short integration time (100 ms) synchronised measurements.
Multimode Corning Mmf 50/125, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/multimode corning mmf 50/125/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
multimode corning mmf 50/125 - by Bioz Stars, 2026-06
90/100 stars
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86
Amersham Life Sciences Inc leadseeker multimodality imaging system ic50 values
Optical setup to allow fibre based sensing. A 520 nm laser source (10 µW power and 100 ms exposure) was used as a pump source to excite both the pH and oxygen sensors. The pump illumination was launched from a single mode fibre (SMF) collimated by an aspheric lens (L1), passing through a band pass filter (BP) removing unwanted long wavelength light, and reflected by the dichroic mirror (DM), then focused with an identical aspheric lens (L2) and selectively coupled into the fibre core (with XY control of the sensing fibre mount). The returned light from the fibre core was collimated by L2, passed through the dichroic mirror and a long pass filter (LP, removing any reflected pump light). <t>The</t> <t>fluorescence</t> was then focused by lens L3 into a 50 µm core multimode fibre <t>(MMF)</t> patch cable, and directed to a spectrometer (Ocean Optics QEPro). The triggering unit (TTL pulse generator) controlled both laser and spectrometer allowing on demand short integration time (100 ms) synchronised measurements.
Leadseeker Multimodality Imaging System Ic50 Values, supplied by Amersham Life Sciences Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/leadseeker multimodality imaging system ic50 values/product/Amersham Life Sciences Inc
Average 86 stars, based on 1 article reviews
leadseeker multimodality imaging system ic50 values - by Bioz Stars, 2026-06
86/100 stars
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96
Revvity phome substrate
Optical setup to allow fibre based sensing. A 520 nm laser source (10 µW power and 100 ms exposure) was used as a pump source to excite both the pH and oxygen sensors. The pump illumination was launched from a single mode fibre (SMF) collimated by an aspheric lens (L1), passing through a band pass filter (BP) removing unwanted long wavelength light, and reflected by the dichroic mirror (DM), then focused with an identical aspheric lens (L2) and selectively coupled into the fibre core (with XY control of the sensing fibre mount). The returned light from the fibre core was collimated by L2, passed through the dichroic mirror and a long pass filter (LP, removing any reflected pump light). <t>The</t> <t>fluorescence</t> was then focused by lens L3 into a 50 µm core multimode fibre <t>(MMF)</t> patch cable, and directed to a spectrometer (Ocean Optics QEPro). The triggering unit (TTL pulse generator) controlled both laser and spectrometer allowing on demand short integration time (100 ms) synchronised measurements.
Phome Substrate, supplied by Revvity, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/phome substrate/product/Revvity
Average 96 stars, based on 1 article reviews
phome substrate - by Bioz Stars, 2026-06
96/100 stars
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99
Bruker Corporation bra loaded f127 micelles
Schematic experimental steps for ( A ) extraction and isolation of BRA from Arrabidaea brachypoda roots and ( B ) preparation of BRA-loaded <t>F127</t> micelles by the solid dispersion method.
Bra Loaded F127 Micelles, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/bra loaded f127 micelles/product/Bruker Corporation
Average 99 stars, based on 1 article reviews
bra loaded f127 micelles - by Bioz Stars, 2026-06
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90
Corning Life Sciences multimode fiber corning clearcurve om2
Schematic experimental steps for ( A ) extraction and isolation of BRA from Arrabidaea brachypoda roots and ( B ) preparation of BRA-loaded <t>F127</t> micelles by the solid dispersion method.
Multimode Fiber Corning Clearcurve Om2, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/multimode fiber corning clearcurve om2/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
multimode fiber corning clearcurve om2 - by Bioz Stars, 2026-06
90/100 stars
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90
Corning Life Sciences clearcurve® optical fiber
Schematic experimental steps for ( A ) extraction and isolation of BRA from Arrabidaea brachypoda roots and ( B ) preparation of BRA-loaded <t>F127</t> micelles by the solid dispersion method.
Clearcurve® Optical Fiber, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/clearcurve® optical fiber/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
clearcurve® optical fiber - by Bioz Stars, 2026-06
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86
Avantes Inc avantes fc uvir50
Schematic experimental steps for ( A ) extraction and isolation of BRA from Arrabidaea brachypoda roots and ( B ) preparation of BRA-loaded <t>F127</t> micelles by the solid dispersion method.
Avantes Fc Uvir50, supplied by Avantes Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/avantes fc uvir50/product/Avantes Inc
Average 86 stars, based on 1 article reviews
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86
Thorlabs multimode fibre
Schematic experimental steps for ( A ) extraction and isolation of BRA from Arrabidaea brachypoda roots and ( B ) preparation of BRA-loaded <t>F127</t> micelles by the solid dispersion method.
Multimode Fibre, supplied by Thorlabs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/multimode fibre/product/Thorlabs
Average 86 stars, based on 1 article reviews
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Image Search Results


Optical setup to allow fibre based sensing. A 520 nm laser source (10 µW power and 100 ms exposure) was used as a pump source to excite both the pH and oxygen sensors. The pump illumination was launched from a single mode fibre (SMF) collimated by an aspheric lens (L1), passing through a band pass filter (BP) removing unwanted long wavelength light, and reflected by the dichroic mirror (DM), then focused with an identical aspheric lens (L2) and selectively coupled into the fibre core (with XY control of the sensing fibre mount). The returned light from the fibre core was collimated by L2, passed through the dichroic mirror and a long pass filter (LP, removing any reflected pump light). The fluorescence was then focused by lens L3 into a 50 µm core multimode fibre (MMF) patch cable, and directed to a spectrometer (Ocean Optics QEPro). The triggering unit (TTL pulse generator) controlled both laser and spectrometer allowing on demand short integration time (100 ms) synchronised measurements.

Journal: Scientific Reports

Article Title: High fidelity fibre-based physiological sensing deep in tissue

doi: 10.1038/s41598-019-44077-7

Figure Lengend Snippet: Optical setup to allow fibre based sensing. A 520 nm laser source (10 µW power and 100 ms exposure) was used as a pump source to excite both the pH and oxygen sensors. The pump illumination was launched from a single mode fibre (SMF) collimated by an aspheric lens (L1), passing through a band pass filter (BP) removing unwanted long wavelength light, and reflected by the dichroic mirror (DM), then focused with an identical aspheric lens (L2) and selectively coupled into the fibre core (with XY control of the sensing fibre mount). The returned light from the fibre core was collimated by L2, passed through the dichroic mirror and a long pass filter (LP, removing any reflected pump light). The fluorescence was then focused by lens L3 into a 50 µm core multimode fibre (MMF) patch cable, and directed to a spectrometer (Ocean Optics QEPro). The triggering unit (TTL pulse generator) controlled both laser and spectrometer allowing on demand short integration time (100 ms) synchronised measurements.

Article Snippet: The fluorescence was then focused by lens L3 into a 50 µm core multimode fibre (MMF) patch cable, and directed to a spectrometer (Ocean Optics QEPro).

Techniques: Fluorescence

Schematic experimental steps for ( A ) extraction and isolation of BRA from Arrabidaea brachypoda roots and ( B ) preparation of BRA-loaded F127 micelles by the solid dispersion method.

Journal: Pharmaceutics

Article Title: Design of Liquid Formulation Based on F127-Loaded Natural Dimeric Flavonoids as a New Perspective Treatment for Leishmaniasis

doi: 10.3390/pharmaceutics16020252

Figure Lengend Snippet: Schematic experimental steps for ( A ) extraction and isolation of BRA from Arrabidaea brachypoda roots and ( B ) preparation of BRA-loaded F127 micelles by the solid dispersion method.

Article Snippet: The AFM analysis of the F127 and BRA-loaded F127 micelles was performed using a Multimode 8 microscope (Bruker, Santa Barbara, CA, USA). qpBioT (Nanosensor) probes were used with a nominal spring constant of 0.08 N/m.

Techniques: Extraction, Isolation, Dispersion

( A ) Schematic diagram of a typical force versus separation curve obtained with AFM. ( B ) Topographic maps of the nanostructured micelles. ( C ) Root mean square of the roughness plot. The values found for the empty F127 micelles (F127). Significant value differences were determined by ANOVA statistics with post-test Tukey p < 0.05. ( D ) Graph of adhesion forces with mean values of 3.5 ± 0.9 nN and 1.6 ± 0.3 nN, respectively, for F127 and LF-B500. The inner image represents the behavior of the AFM probe during the film interaction in the analysis of adhesion forces. ( E ) Young’s modulus plot with mean values of 12.4 ± 1.4 MPa for the F127 and 12.8 ± 1.0 MPa for the LF-B500. The inner image represents the behavior of the AFM probe during the film interaction in the analysis of elastic forces. (*) Values with a significant difference in the ANOVA statistics with post-test Tukey p < 0.05.

Journal: Pharmaceutics

Article Title: Design of Liquid Formulation Based on F127-Loaded Natural Dimeric Flavonoids as a New Perspective Treatment for Leishmaniasis

doi: 10.3390/pharmaceutics16020252

Figure Lengend Snippet: ( A ) Schematic diagram of a typical force versus separation curve obtained with AFM. ( B ) Topographic maps of the nanostructured micelles. ( C ) Root mean square of the roughness plot. The values found for the empty F127 micelles (F127). Significant value differences were determined by ANOVA statistics with post-test Tukey p < 0.05. ( D ) Graph of adhesion forces with mean values of 3.5 ± 0.9 nN and 1.6 ± 0.3 nN, respectively, for F127 and LF-B500. The inner image represents the behavior of the AFM probe during the film interaction in the analysis of adhesion forces. ( E ) Young’s modulus plot with mean values of 12.4 ± 1.4 MPa for the F127 and 12.8 ± 1.0 MPa for the LF-B500. The inner image represents the behavior of the AFM probe during the film interaction in the analysis of elastic forces. (*) Values with a significant difference in the ANOVA statistics with post-test Tukey p < 0.05.

Article Snippet: The AFM analysis of the F127 and BRA-loaded F127 micelles was performed using a Multimode 8 microscope (Bruker, Santa Barbara, CA, USA). qpBioT (Nanosensor) probes were used with a nominal spring constant of 0.08 N/m.

Techniques:

( A ) Picture of the liquid formulation LF-B500 showing physical stability after 72 h of preparation. ( B ) Chemical structure of brachy-dins A, B, and C. ( C ) Representation of the F127 copolymer composition. ( D ) Schematic representation of worm-like F127 micelles observed by morphology analysis.

Journal: Pharmaceutics

Article Title: Design of Liquid Formulation Based on F127-Loaded Natural Dimeric Flavonoids as a New Perspective Treatment for Leishmaniasis

doi: 10.3390/pharmaceutics16020252

Figure Lengend Snippet: ( A ) Picture of the liquid formulation LF-B500 showing physical stability after 72 h of preparation. ( B ) Chemical structure of brachy-dins A, B, and C. ( C ) Representation of the F127 copolymer composition. ( D ) Schematic representation of worm-like F127 micelles observed by morphology analysis.

Article Snippet: The AFM analysis of the F127 and BRA-loaded F127 micelles was performed using a Multimode 8 microscope (Bruker, Santa Barbara, CA, USA). qpBioT (Nanosensor) probes were used with a nominal spring constant of 0.08 N/m.

Techniques: Formulation

FTIR frequencies for neat BRA and  BRA-loaded F127 micelles  (LF-B500).

Journal: Pharmaceutics

Article Title: Design of Liquid Formulation Based on F127-Loaded Natural Dimeric Flavonoids as a New Perspective Treatment for Leishmaniasis

doi: 10.3390/pharmaceutics16020252

Figure Lengend Snippet: FTIR frequencies for neat BRA and BRA-loaded F127 micelles (LF-B500).

Article Snippet: The AFM analysis of the F127 and BRA-loaded F127 micelles was performed using a Multimode 8 microscope (Bruker, Santa Barbara, CA, USA). qpBioT (Nanosensor) probes were used with a nominal spring constant of 0.08 N/m.

Techniques:

AFM representative images for ( A ) empty F127 micelles and ( B ) BRA-loaded F127 micelles: height ( aI – aIII ), adhesion force maps ( bI – bIII ), and Young’s modulus ( cI – cIII ).

Journal: Pharmaceutics

Article Title: Design of Liquid Formulation Based on F127-Loaded Natural Dimeric Flavonoids as a New Perspective Treatment for Leishmaniasis

doi: 10.3390/pharmaceutics16020252

Figure Lengend Snippet: AFM representative images for ( A ) empty F127 micelles and ( B ) BRA-loaded F127 micelles: height ( aI – aIII ), adhesion force maps ( bI – bIII ), and Young’s modulus ( cI – cIII ).

Article Snippet: The AFM analysis of the F127 and BRA-loaded F127 micelles was performed using a Multimode 8 microscope (Bruker, Santa Barbara, CA, USA). qpBioT (Nanosensor) probes were used with a nominal spring constant of 0.08 N/m.

Techniques:

Peak (P) ± SD, area (A), hydrodynamic diameter (Dh), polydispersity Index (PDI), and ζ potential of empty and  BRA-loaded F127 micelles  acquired by the DLS technique in triplicate at 25° C.

Journal: Pharmaceutics

Article Title: Design of Liquid Formulation Based on F127-Loaded Natural Dimeric Flavonoids as a New Perspective Treatment for Leishmaniasis

doi: 10.3390/pharmaceutics16020252

Figure Lengend Snippet: Peak (P) ± SD, area (A), hydrodynamic diameter (Dh), polydispersity Index (PDI), and ζ potential of empty and BRA-loaded F127 micelles acquired by the DLS technique in triplicate at 25° C.

Article Snippet: The AFM analysis of the F127 and BRA-loaded F127 micelles was performed using a Multimode 8 microscope (Bruker, Santa Barbara, CA, USA). qpBioT (Nanosensor) probes were used with a nominal spring constant of 0.08 N/m.

Techniques:

Differential pulse voltammograms on the GCE were recorded in different conditions: supporting electrolyte only (blank), in the presence of BRA, F127, and BRA-loaded F127 micelles in 0.1 mol L −1 phosphate buffer, pH 5.5, pulse amplitude = 50 mV and v = 25 mV s −1 .

Journal: Pharmaceutics

Article Title: Design of Liquid Formulation Based on F127-Loaded Natural Dimeric Flavonoids as a New Perspective Treatment for Leishmaniasis

doi: 10.3390/pharmaceutics16020252

Figure Lengend Snippet: Differential pulse voltammograms on the GCE were recorded in different conditions: supporting electrolyte only (blank), in the presence of BRA, F127, and BRA-loaded F127 micelles in 0.1 mol L −1 phosphate buffer, pH 5.5, pulse amplitude = 50 mV and v = 25 mV s −1 .

Article Snippet: The AFM analysis of the F127 and BRA-loaded F127 micelles was performed using a Multimode 8 microscope (Bruker, Santa Barbara, CA, USA). qpBioT (Nanosensor) probes were used with a nominal spring constant of 0.08 N/m.

Techniques:

In vitro cytotoxicity assay of BRA-loaded F127 micelles against ( A ) RAW 264.7 cell line murine and ( B ) Leishmania amazonensis promastigotes. The assay was performed for different F127 copolymer concentrations ( w / v ): 0.5% (red bars), 0.25% (green bars), and 0.125% (blue bars), scanning a BRA concentration range of 500 to 1.9 µg/mL. The dose–response curves were accessed by linear regression for 0.125% w / v of the F127 copolymer. ( C ) 50% of RAW cell proliferation was achieved for a BRA concentration of 171 µg/mL, and ( D ) 50% of Leishmania amazonensis promastigotes proliferation was achieved for a BRA concentration of 16.06 µg/mL. The results correspond to (means ± SD) of individual samples tested in triplicate. (*) p < 0.05, compared to the positive controls (DMSO and pentamidine).

Journal: Pharmaceutics

Article Title: Design of Liquid Formulation Based on F127-Loaded Natural Dimeric Flavonoids as a New Perspective Treatment for Leishmaniasis

doi: 10.3390/pharmaceutics16020252

Figure Lengend Snippet: In vitro cytotoxicity assay of BRA-loaded F127 micelles against ( A ) RAW 264.7 cell line murine and ( B ) Leishmania amazonensis promastigotes. The assay was performed for different F127 copolymer concentrations ( w / v ): 0.5% (red bars), 0.25% (green bars), and 0.125% (blue bars), scanning a BRA concentration range of 500 to 1.9 µg/mL. The dose–response curves were accessed by linear regression for 0.125% w / v of the F127 copolymer. ( C ) 50% of RAW cell proliferation was achieved for a BRA concentration of 171 µg/mL, and ( D ) 50% of Leishmania amazonensis promastigotes proliferation was achieved for a BRA concentration of 16.06 µg/mL. The results correspond to (means ± SD) of individual samples tested in triplicate. (*) p < 0.05, compared to the positive controls (DMSO and pentamidine).

Article Snippet: The AFM analysis of the F127 and BRA-loaded F127 micelles was performed using a Multimode 8 microscope (Bruker, Santa Barbara, CA, USA). qpBioT (Nanosensor) probes were used with a nominal spring constant of 0.08 N/m.

Techniques: In Vitro, Cytotoxicity Assay, Concentration Assay