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Intrinsic cell factors are essential regulating tissue organization; however, understanding extrinsic cells constituents (extra cellular matrix, ECM) and its interface are critical issues regarding early restoring of functional tissues.
 
In general, our materials attempt to restore connective tissues where damage, weakness or loose exist. The different devices stimulate the migration, seed and proliferation of functional tissues. Over a period of time, at implant sites, the implants will be biodegraded without impaired function or immune rejection, taking the texture and appearance of normal host tissues.
 
Aongen™ Collagen Matrix is a 3-D scaffold resulted from applying tissue engineering technology. Aongen™ Collagen Matrix contains a connected porous structure made of cross- link ≥90% lyophilized porcine type I atelocollagen and ≤10% chondrotin 6-sulfate (glycosaminoglycan, GAG)
 
Our implant material functions as a scaffold for cellular invasion and capillary growth due to its chemotactics and adhesion properties. Its porous and connected structure is a stable soft skeleton which tolerates adequately protease activity, providing sufficient volume for cells to attach, grow randomly, and synthesize their own macromolecules. (Fig. 1)
 
Tissue ingrowths occurred first in the periphery and proceeded toward the center, accompanied by implant absorption. The biocompatibility observed is evident by the lack of adverse, inflammatory or immune rejection due in part our products do not contain antigenic telopeptides and show adequate protease resistance activity.
 
 
Fig. 1: Aongen™ promotes cells to seed and proliferate into a suitable tissue bed.
 
1.
Aongen™ Collagen Matrix may stimulate seed and proliferation of suitable tissues remaining indistinguishable from the surrounding. This will depend of age, stress tissue site, and predetermined intrinsic remodeling mechanisms.
2.
Aongen™ Collagen Matrix may minimize secondary effects seen after extensive removal of connective, adipose or epithelium tissue such as loose skin, flattened tissues or poor wound healing. The results are able to persist depending of age, stress tissue site, and predetermined intrinsic mechanisms.
3.
Eventually, Aongen™ Collagen Matrix will be biodegraded without impaired function, immune rejection or production of toxic elements due to its particular protease resistance structure and lack of antigenic telopeptides (atelocollagen structure)
4.
Aongen™ Collagen Matrix does not need prior preparation and is easy to place. Simple, put Aongen™ Collagen Matrix at the level of the subcutaneous tissue previous skin closure. Aongen™ Collagen Matrix can be trimmed and left in situ securing for surrounding tissues to best achieve its singular heal-expansive effects.
 
Coming pipelines include develops in ocular implants, long lasting biodegradable matrices and drug delivery compounds.


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