Evidence map›Paper›PMID 39159377›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Improving normothermic machine perfusion and blood transfusion through biocompatible blood silicification.

Chuanyi Lei, Zeyu Li, Shuhao Ma, Qi Zhang, Jimin Guo, Qing Ouyang, Qi Lei, Liang Zhou, Junxian Yang, Jiangguo Lin and 5 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Stomata biosilica andChemical science · 2025
    Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Chuanyi Lei *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.ORCID 0009-0003-4948-9257
Zeyu Li *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.
Shuhao Ma *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.ORCID 0000-0002-7464-1471
Qi Zhang *The Second Affiliated Hospital of Anhui Medical University, Hefei 23060, People's Republic of China.
Jimin GuoCenter for Micro-Engineered Materials and the Department of Chemical and Biological Engineering, The University of New Mexico, Albuquerque, NM 87131.
Qing OuyangDepartment of Hepatobiliary Surgery and Liver Transplant Center, The General Hospital of Southern Theater, Guangzhou 510010, People's Republic of China.
Qi LeiMOE 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.
Liang ZhouMOE 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.
Junxian YangResearch Department of Medical Sciences, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China.
Jiangguo LinResearch Department of Medical Sciences, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China.
Romy EttlingerEastChem School of Chemistry, University of St Andrews, North Haugh, St. Andrews KY16 9ST, United Kingdom.
Stefan WuttkeBCMaterials, Basque Center for Materials, UPV/EHU Science Park, Leioa 48950, Spain.
Xuejin LiState 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.ORCID 0000-0002-4446-2480
C Jeffrey BrinkerCenter for Micro-Engineered Materials and the Department of Chemical and Biological Engineering, The University of New Mexico, Albuquerque, NM 87131.
Wei ZhuMOE 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.

Funding

Guangdong Basic and Applied Basic Research Foundation 2020B1515120031| Guangdong Provincial Pearl River Talents Program () 2019QN01Y314National Natural Science Foundation of China 21972047 52003086 12072318Natural Science Foundation of Guangdong-Foshan Joint Funds 20201910250000091Natural Science Foundation of Guangdong Province, China 2021A1515010724Science and Technology Project of Guangzhou, China 202102020352 202102020259the Program for Guangdong Introducing Innovative and Entrepreneurial Teams 2019ZT08Y318
6 · The paper itself

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.

Indexed as

Biocompatible MaterialsErythrocytesSilicon DioxideAnimalsBlood PreservationBlood TransfusionHumansMicePerfusionBiocompatible MaterialsSilicon Dioxideantigen blockingnormothermic machine perfusionred blood cellsilicification

Identifiers

PMID39159377
PMCPMC11363281

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.