Hi!
I have been reading this forum for a while and I wanted to share an idea that I had. I\'m not sure this is the right sub-forum to put this topic, but since the stem-cell database should probably be restricted to sharing links that didn\'t seem like a good fit either. Anyway, feel free to move it. =)
After looking into autologous fibroblasts (this technique has been shown to be viable for penile girth enhancement in several studies, both on humans
www.ncbi.nlm.nih.gov/pubmed/21164145
,
www.ncbi.nlm.nih.gov/pubmed/16310926
,
www.ncbi.nlm.nih.gov/pubmed/20796201
and on animals
www.term.or.kr/journal/view.php?number=236
) I got to some thinking. For those of you who haven\'t explored this as obsessively as I have, fibroblasts are the cells which synthesize connective tissue (part of which is collagen) in the body and autologous means that the cells are from the patient who will receive them which removes the problem of rejection and inflammatory reactions. The basis of this method is that after taking a small biopsy of scrotal skin and culturing fibroblasts on a tube-shaped scaffold made of PLGA, a biodegradable material, the PLGA scaffold is surgically implanted and the fibroblasts will then start generating new tissue. The disadvantages are the invasive surgical techniques required for implanting the tube-shaped PLGA scaffold and possibly the difficulty in predicting gains of the procedure. Cost could be imagined to be a prohibitive factor, but in fact there is a patented and FDA approved autologous biofiller called Laviv that calls for twice the amount of fibroblasts as used in the studies (~20 million) and which carries a total treatment price of about $3-4000 (and that is to the plastic surgeon).
My idea, admittedly not a huge leap, was to replace the PLGA scaffold tube with PLGA microspheres that are mixed with cultured autologous fibroblasts. One study in rabbits has shown that injected PLGA microspheres mixed with chondrocytes (cartilage producing cells, which are about the same size as fibroblasts) produced healthy cartilage after implantation: \"Four and 9 weeks after implantation, chondrocytes implanted with PLGA microspheres formed solid, white cartilaginous tissues, whereas no gross evidence of cartilage tissue formation was noted in the control groups. Histological analysis of the implants by hematoxylin and eosin staining showed mature and well-formed cartilage.\" This appears to suggest that the structure provided by grouped microspheres as opposed to a cohesive tube can also support the growth of viable tissue.
www.ncbi.nlm.nih.gov/pubmed/15869422
Another study has shown that PLGA microspheres when injected into mice were not associated with migration and remained at their site of injection: \"After injection of PLGA microspheres into the subcutaneous dorsum of mice, inflammation, new tissue volume change, and microsphere migration were examined. Host cells from the surrounding tissues migrated to the implanted microspheres and formed new hybrid tissue structures. The volume of the newly generated tissues was maintained approximately constant for 7 weeks. Histological analyses showed no evidence of migration of the implanted microspheres to the distant organs. In summary, PLGA microspheres were injectable and able to induce a new hybrid tissue formation without initial volume decrease or particle migration.\"
www.ncbi.nlm.nih.gov/pubmed/15449255
The significance of this could be that instead of surgically implanting a PLGA scaffold tube, microspheres mixed with fibroblasts could be injected (presumably even with a microcanula) in the same way as PMMA. In addition to being a much less invasive procedure this could perhaps allow for greater control of the amount of girth gained by varying the amount or concentration of the microspheres and/or fibroblasts and for a more gradual process by repeated injections as opposed to a single major surgical procedure.
I can\'t really be the judge of whether this is a good idea but it might be something worth exploring. What\'s your take on this?