The development of artificial skin substitutes based on cultured cells and biomaterials such as collagen requires an understanding of cellular interactions with the substrate. In this study, human keratinocytes were cultured on the surface of collagen sponges, and confocal laser-scanning microscopy
Confocal laser scanning microscopy (CLSM) for the study of collagen sponge microstructure
β Scribed by Hanthamrongwit, M. ;Grant, M. H. ;Wilkinson, R.
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 414 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0021-9304
No coin nor oath required. For personal study only.
β¦ Synopsis
This study uses confocal laser scanning microscopy (CLSM) to assess the microstructure of collagen sponges providing an accurate quantification of porosity under conditions similar to those experienced by cells growing on the sponges during culture. CLSM offers several advantages over scanning electron microscopy (SEM) and conventional optical microscopy for this kind of study, the most important of which is probably the absence of artifacts associated with the extensive preparation of samples required for the latter two methods. When the "pan-side" surface of collagen sponges was studied, it was found that the pore sizes increased with increasing depth into the sponge. Collagen sponges frozen in a -70Β°C freezer had a more open structure than ones frozen on the stage of a tissue dryer. These different pore sizes are thought to reflect different freezing rates in the samples.
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