TY - JOUR
T1 - Improving normothermic machine perfusion and blood transfusion through biocompatible blood silicification
AU - Lei, Chuanyi
AU - Li, Zeyu
AU - Ma, Shuhao
AU - Zhang, Qi
AU - Guo, Jimin
AU - Ouyang, Qing
AU - Lei, Qi
AU - Zhou, Liang
AU - Yang, Junxian
AU - Lin, Jiangguo
AU - Ettlinger, Romy
AU - Wuttke, Stefan
AU - Li, Xuejin
AU - Brinker, C. Jeffrey
AU - Zhu, Wei
N1 - Publisher Copyright:
Copyright © 2024 the Author(s).
PY - 2024/8/27
Y1 - 2024/8/27
N2 - The growing world population and increasing life expectancy are driving the need to improve the quality of blood transfusion, organ transplantation, and preservation. Here, to improve the ability of red blood cells (RBCs) for normothermic machine perfusion, a biocompatible blood silicification approach termed “shielding-augmenting RBC-in-nanoscale amorphous silica (SARNAS)” has been developed. The key to RBC surface engineering and structure augmentation is the precise control of the hydrolysis form of silicic acid to realize stabilization of RBC within conformal nanoscale silica-based exoskeletons. The formed silicified RBCs (Si-RBCs) maintain membrane/structural integrity, normal cellular functions (e.g., metabolism, oxygen-carrying capability), and enhance resistance to external stressors as well as tunable mechanical properties, resulting in nearly 100% RBC cryoprotection. In vivo experiments confirm their excellent biocompatibility. By shielding RBC surface antigens, the Si-RBCs provide universal blood compatibility, the ability for allogeneic mechanical perfusion, and more importantly, the possibility for cross-species transfusion. Being simple, reliable, and easily scalable, the SARNAS strategy holds great promise to revolutionize the use of engineered blood for future clinical applications.
AB - The growing world population and increasing life expectancy are driving the need to improve the quality of blood transfusion, organ transplantation, and preservation. Here, to improve the ability of red blood cells (RBCs) for normothermic machine perfusion, a biocompatible blood silicification approach termed “shielding-augmenting RBC-in-nanoscale amorphous silica (SARNAS)” has been developed. The key to RBC surface engineering and structure augmentation is the precise control of the hydrolysis form of silicic acid to realize stabilization of RBC within conformal nanoscale silica-based exoskeletons. The formed silicified RBCs (Si-RBCs) maintain membrane/structural integrity, normal cellular functions (e.g., metabolism, oxygen-carrying capability), and enhance resistance to external stressors as well as tunable mechanical properties, resulting in nearly 100% RBC cryoprotection. In vivo experiments confirm their excellent biocompatibility. By shielding RBC surface antigens, the Si-RBCs provide universal blood compatibility, the ability for allogeneic mechanical perfusion, and more importantly, the possibility for cross-species transfusion. Being simple, reliable, and easily scalable, the SARNAS strategy holds great promise to revolutionize the use of engineered blood for future clinical applications.
KW - antigen blocking
KW - normothermic machine perfusion
KW - red blood cell
KW - silicification
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U2 - 10.1073/pnas.2322418121
DO - 10.1073/pnas.2322418121
M3 - Article
C2 - 39159377
AN - SCOPUS:85201742993
SN - 0027-8424
VL - 121
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 35
M1 - e2322418121
ER -