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Fluorescence microscopy images are presented in Figure 3.
All microscopy images are taken at a magnification of 1,000.
Confocal microscopy images are analyzed to find the location of tens of thousands of particles at each composition studied.
Atomic force microscopy images are usually affected by different kinds of artifacts due to either the microscope design and operation mode or external environmental factors.
In order to get more uniform distribution of PS spheres, the ICP etching is used to adjust the morphology (the scanning electron microscopy images are Appendix 1).
Water uptake data, colorimetric experiments and scanning electron microscopy images are given for the characterization of this new solid dosage form; the importance of the borax presence is also discussed.
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Confocal microscopy images were obtained using a fluorescence imaging system with laser excitation at 405 nm.
Microscopy images were recorded using an Olympus Cell^R imaging station with DIC setup.
Confocal microscopy images were acquired using an LSM 510 Meta microscope and imaging software (Zeiss).
Fluorescence images, together with transmission microscopy images were captured.
Light microscopy images were captured using ×2 and ×10 objectives.
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