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A continuously oxygenated macroencapsulation system enables high-density packing and delivery of insulin-secreting cells

Author

Listed:
  • Tung T. Pham

    (Cornell University)

  • Phuong L. Tran

    (Cornell University)

  • Linda A. Tempelman

    (89 Rumford Ave)

  • Simon G. Stone

    (89 Rumford Ave)

  • Christopher Piccirillo

    (Cornell University)

  • Alan Li

    (Cornell University)

  • James A. Flanders

    (Cornell University)

  • Minglin Ma

    (Cornell University)

Abstract

The encapsulation of insulin-secreting cells offers a promising strategy for curative treatment of type 1 diabetes without immunosuppression. However, insufficient oxygen within encapsulation systems remains a major challenge, restricting cell survival, function, and scalability. Here, we report an encapsulation platform combining a miniaturized implantable electrochemical oxygen generator (iEOG) with a scalable, linear cell pouch designed for minimally invasive implantation and retrieval. This system enables continuous oxygen supply via electrolysis of tissue moisture, supporting high-density cell encapsulation (60,000 IEQ/mL). Oxygen generated by our system was stable, controllable, and sufficient to maintain cell viability and function under hypoxic (1% O₂) conditions in vitro. In an allogeneic rat model, the oxygenated system implanted subcutaneously reversed diabetes for up to three months without immunosuppression, while non-oxygenated controls remained hyperglycemic. These findings demonstrate the feasibility of sustained oxygenation to enable functional, high-density islet encapsulation in subcutaneous sites, advancing the development of clinically translatable cell-based therapies.

Suggested Citation

  • Tung T. Pham & Phuong L. Tran & Linda A. Tempelman & Simon G. Stone & Christopher Piccirillo & Alan Li & James A. Flanders & Minglin Ma, 2025. "A continuously oxygenated macroencapsulation system enables high-density packing and delivery of insulin-secreting cells," Nature Communications, Nature, vol. 16(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62271-2
    DOI: 10.1038/s41467-025-62271-2
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