Chorion Membrane Allograft dHAICM
AmchoPlast™ is a cutting-edge, sterile, minimally manipulated, dehydrated allograft designed to support homologous use in clinical applications. It is meticulously derived from human placental membranes, specifically the amnion, intermediate layer, and chorion, obtained from healthy, consenting donors. The allograft incorporates a basement membrane and a stromal matrix collagen layer, providing structural integrity and biological compatibility for therapeutic purposes.
Applications For Use of AmchoPlast
AmchoPlast can be used for non-infected, acute & chronic wounds that occur due to conditions such as:
Usage Guidelines
- The wound site should be assessed and prepared for wound debridement.
- The site bed should be cleared of all necrotic tissue and cleared of possible infections.
Clinical Applications and Benefits
The unique composition of AmchoPlast, which includes a basement membrane and stromal matrix collagen, supports a variety of clinical applications. It provides an optimal scaffold for tissue regeneration and repair, promoting wound healing and cellular integration. Its biocompatible properties make it ideal for use in managing acute and chronic wounds, surgical procedures, and other tissue repair scenarios.
AmchoPlast represents a significant advancement in regenerative medicine, offering a reliable and safe solution for clinicians seeking effective tools to enhance patient outcomes.
AmchoPlast: Amnion—Intermediate Layer—Chorion Membrane Allograft
Amnion, intermediate layer, chorion membranes are procured from healthy donors under aseptic conditions with necessary informed consent and health history of the donor. Donors are screened for various infectious diseases (Table 1), to minimize risk to patients. In addition, donors are physically examined by the physicians for signs and symptoms of any untested illness.
AmchoPlast is a sterile minimally manipulated, dehydrated, human amnion, chorion membrane allograft intended for homologous use. The allograft is derived from human placental membrane collected from consenting donors. It consists of a basement membrane and stromal matrix collagen layer.
Only tissues from donors meeting the prescribed criteria are processed for manufacturing of AmchoPlast.
Table 1: Infectious disease screened in blood specimens of donor
| HIV - I & II (Antibody) | HIV - I & HCV (NAT) | Anti HTLV - I & Anti HTLV - II |
| Anti - HBC | Anti - HCV | CMV - IgM & CMV - IgG |
| HBsAg | Syphilis | Malaria |
Procurement and Donor Screening
The placental tissues used in AmchoPlast are procured under stringent aseptic conditions to ensure the highest level of safety and quality. Informed consent is obtained from donors after a thorough review of their health history. Each donor undergoes extensive screening for a broad spectrum of infectious diseases (as detailed in Table 1), minimizing the risk of pathogen transmission to recipients.
Beyond standard laboratory testing, donors are also subjected to a comprehensive physical examination by qualified medical professionals to identify any signs or symptoms of undetected illnesses. This dual-layer screening process ensures that only tissues from donors meeting the most rigorous eligibility criteria are selected for processing.
Manufacturing Excellence
AmchoPlast is produced following strict guidelines to maintain the sterility and integrity of the tissues. The manufacturing process involves careful dehydration, a method that preserves the biological properties of the placental membranes while enhancing their shelf life and handling convenience. By minimizing manipulation, the process retains the inherent structural and biochemical properties of the tissue, ensuring its efficacy in homologous applications.