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Improving normothermic machine perfusion and blood transfusion through biocompatible blood silicification.
Lei, Chuanyi; Li, Zeyu; Ma, Shuhao; Zhang, Qi; Guo, Jimin; Ouyang, Qing; Lei, Qi; Zhou, Liang; Yang, Junxian; Lin, Jiangguo; Ettlinger, Romy; Wuttke, Stefan; Li, Xuejin; Brinker, C Jeffrey; Zhu, Wei.
  • Lei C; MOE International Joint Research Laboratory on Synthetic Biology and Medicines, School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, People's Republic of China.
  • Li Z; MOE International Joint Research Laboratory on Synthetic Biology and Medicines, School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, People's Republic of China.
  • Ma S; State Key Laboratory of Fluid Power and Mechatronic Systems, Department of Engineering Mechanics, and Center for X-Mechanics, Zhejiang University, Hangzhou 310027, People's Republic of China.
  • Zhang Q; The Second Affiliated Hospital of Anhui Medical University, Hefei 23060, People's Republic of China.
  • Guo J; Center for Micro-Engineered Materials and the Department of Chemical and Biological Engineering, The University of New Mexico, Albuquerque, NM 87131.
  • Ouyang Q; Department of Hepatobiliary Surgery and Liver Transplant Center, The General Hospital of Southern Theater, Guangzhou 510010, People's Republic of China.
  • Lei Q; MOE International Joint Research Laboratory on Synthetic Biology and Medicines, School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, People's Republic of China.
  • Zhou L; MOE International Joint Research Laboratory on Synthetic Biology and Medicines, School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, People's Republic of China.
  • Yang J; Research Department of Medical Sciences, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China.
  • Lin J; Research Department of Medical Sciences, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China.
  • Ettlinger R; EastChem School of Chemistry, University of St Andrews, North Haugh, St. Andrews KY16 9ST, United Kingdom.
  • Wuttke S; BCMaterials, Basque Center for Materials, UPV/EHU Science Park, Leioa 48950, Spain.
  • Li X; Ikerbasque, Basque Foundation for Science, Bilbao 48009, Spain.
  • Brinker CJ; State Key Laboratory of Fluid Power and Mechatronic Systems, Department of Engineering Mechanics, and Center for X-Mechanics, Zhejiang University, Hangzhou 310027, People's Republic of China.
  • Zhu W; Center for Micro-Engineered Materials and the Department of Chemical and Biological Engineering, The University of New Mexico, Albuquerque, NM 87131.
Proc Natl Acad Sci U S A ; 121(35): e2322418121, 2024 Aug 27.
Article en En | MEDLINE | ID: mdl-39159377
ABSTRACT
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Materiales Biocompatibles / Dióxido de Silicio / Eritrocitos Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Materiales Biocompatibles / Dióxido de Silicio / Eritrocitos Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article