Are demineralized bone allografts (cortical or cancellous) fully bio-resorbable?

Have there been any conclusive studies to show whether or not allografts, particularly demineralized allografts, are fully bio-resorbable? Also, is there any difference in clinical performance between demineralized particulate bone and demineralized bone matrix?

17 Comments on Are demineralized bone allografts (cortical or cancellous) fully bio-resorbable?

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greg steiner
9/28/2016
The mineralized portion of an allograft is never resorbed once the mineralization process has begun because osteoclasts will not resorb this material. Demineralized allografts usually contiain approximatly 3% to 5% residual mineralized material not removed in processing and that material is also not resorbed. Both products heal by the same mechanism producing sclertoic bone. I don't understand what you are talking about in regard to demineralized particulate bone and demineralized bone matrix. When you remove the minerals you are left with the matrix. Greg Steiner Steiner Biotechnology
vtt
9/28/2016
Demineralized allografts are commercially available in two different forms: particulate or putty. The latter is often referred to as demineralized bone matrix (DBM), hence my question regarding whether or not there is any differences in clinical performance between the two. If demineralized allografts only contain 3-5% residual mineralized material (quite insignificant), how can they produce "sclerotic" bone? Is it correct to say that demineralized allografts produce significantly better bone quality than mineralized allografts? Interestingly, demineralized particulate costs less than mineralized particulate. Any idea why?
greg steiner
10/1/2016
The sclerosis is a result of the immune response to the foreign proteins and not the mineral portion. In regard to bone quality produced by demineralized vs mineralized both of these graft materials produce such poor bone quality that I refuse to place implants in sites grafted with these materials. These graft materials produce high mineralization with very poor vitality and no ability to adapt or remodel. Greg Steiner Steiner Biotechnology
JDA360
9/29/2016
J Periodontol. 2016 Sep;87(9):1022-9. doi: 10.1902/jop.2016.160139. Epub 2016 Apr 30. Effect of Healing Time on New Bone Formation After Tooth Extraction and Ridge Preservation With Demineralized Freeze-Dried Bone Allograft: A Randomized Controlled Clinical Trial. Whetman J1, Mealey BL1. Suggest reading this article. Demineralized bone should actually cost more as you lose more bone during the demineralization process.
Sam
9/29/2016
I can't comment on the studies, but in terms of pricing demineralized bone graft particles/particulate do not cost more. You can see prices here: https://www.ddsgadget.com/biologics/bone-grafting/allografts.html What does cost more are putty-type bone grafts (not particles), and especially the DBM's. That's because they contain carriers, and because of other characteristics of the putty, like syringe delivery, are obviously more expensive to manufacture. Our most popular putty is the C-Blast Putty.
Andre
10/1/2016
How can the foreign proteins hang around long enough to cause sclerosis? Wouldn't they be resorbed completely by the osteoclasts?
greg steiner
10/4/2016
Andre Osteoclasts have never been found resorbing allografts. With over 200 allograft histologic studies in the literature the allograft particles are encased in sclerotic bone and there has never been histology showing an osteoclast on an allograft particle in a resorption pit. Resorption and remodeling of allografts do not occur. Greg Steiner Steiner Biotechnology
Andre
10/5/2016
Hi Greg It would help if there is an explanation as to why the foreign proteins in the allografts can't be resorbed by the osteoclasts. If these foreign proteins always cause bone sclerosis which is quite undesirable, then why are allografts still being a very popular graft material?
Greg Steiner
10/10/2016
Andre That is a complex issue but the short version is osteoclasts do not destroy bone they process bone and the proteins in the mineralixed matrix of bone are moved through the cytoplasm of the osteoclast into the surrounding extracellular matrix to be reused. Osteoclasts are multinucleated cells made by the joining together of macrophages. Macrophages patrol the body and look for pathogens or foreign proteins to destroy and present them to our acquired immune system. A cells whose role in life was to destroy foreign proteins is not going to process those foreign proteins and release them into the extracellular fluid. An osteoclast has never been found on a allograft particle in a resorption lacunae and allografts are never resorbed once mineralization occurs. Failure of allografts will be shown to be the largest reason for implant failure and the reason they are still popular grafts is because the people using them and the people promoting them do not understand their biology. You will note that there are those that challenge me personally but they never provide an intellectual debate because they have no science to support their position. Greg Steiner Steiner Biotechnology
Andre
10/12/2016
Greg I'm here to learn with an open mind. Unfortunately, despite several posts you still have not provided any explanation as to WHY the foreign proteins in allografts can't be resorbed. For a meaningful discussion, simply making claims is not helpful. So again I would ask the same question and hope for a real, stimulating explanation: Once swallowed by the osteoclasts, WHY are the foreign proteins not digested completely by acid, collagenase and enzymes inside the osteoclasts?
greg steiner
10/19/2016
Andre When an allograft is placed the site is filled with inflammatory cells for a few months while mineralization occurs. Mineralization forms on the surface of the allograft particles and when the allograft particles care covered with mineralized material then the inflammation subsides. At this point you have sclerotic bone that will never be modified through remodeling and that is why it is called sclerotic. Osteoclasts never come in contact with the allograft particles in this process. So proving or disproving weather an osteoclast will process foreign proteins is a moot point. If you really want to understand the process come to the course we are putting on in Las Vegas next month. Greg Steiner Steiner Biotechnology
Robert
10/22/2016
Greg There seems to be a self contradiction between your last 2 posts in this thread. In your last post you said "osteoclasts never come in contact with the allograft particles". But in the post prior to that you said "the proteins in the mineralized matrix of bone are moved through the cytoplasm of the osteoclast into the surrounding extracellular matrix to be reused". This implies the foreign substance must have been engulfed by the osteoclast, which means a direct contact between osteoclasts and allograft particles. Would you care to explain this self contradiction?
dphil
10/5/2016
Greg Steiner sells synthetic grafts...just saying... I think the routine and very successful use of allografts in implant dentistry by many practitioners, over many years, has significant merit.
Peter Fairbairn
10/5/2016
Agree , I used and liked DMFD materials in the 90s ......... but when the bodies were stolen and the Bone bank compromised it effected us in the UK more as everyone knew about it here . Sadly we could not buy them for many years which led me to move to synthetics and their improved performance . Having a highly osteo-inductive potential we can now get over 50 % new host bone in as little as 8 weeks , so a big step forward ..... All the research in proper high Impact factor journals ... is showing this .. But I liked allografts , just can do a lot more with new synthetics ... Yes I sell synthetics as well , but only make them for my own patients needs ...... Regards Peter
dphil
10/6/2016
Peter, well said, as always! A balanced approach.
greg steiner
10/24/2016
Robert The two statements are both correct and not contradictory. Osteoclasts form on normal bone but not on allografts. When an osteoclast forms on normal bone it processes the bone and moves the proteins from the matrix of the bone through the cytoplasm of the osteoclast and the proteins are expelled into the extracelluar fluid to be reused (paracrines and endocrines). Osteoclasts do not form on allografts and that is why mineralized allografts are never resorbed. Greg Steiner Steiner Biotechnology
hamideh reza
11/30/2016
I,d like to know what will be the fate of allograft and xenogaft particle in the site of GBR

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