An Overview of Nanoparticle Protein Corona Literature

Author:

Hajipour Mohammad J.12,Safavi‐Sohi Reihaneh13,Sharifi Shahriar1,Mahmoud Nouf145,Ashkarran Ali Akbar1,Voke Elizabeth6,Serpooshan Vahid789,Ramezankhani Milad10,Milani Abbas S.10,Landry Markita P.6111213ORCID,Mahmoudi Morteza1ORCID

Affiliation:

1. Department of Radiology and Precision Health Program Michigan State University East Lansing MI 48824 USA

2. Department of Radiology Stanford University Stanford CA 94304 USA

3. Department of Chemistry and Biochemistry University of Notre Dame Notre Dame IN 46556 USA

4. Faculty of Pharmacy Al‐Zaytoonah University of Jordan Airport Rd. 11733 Amman Jordan

5. Department of Biomedical Sciences, College of Health Sciences, QU Health Qatar University Doha 2713 Qatar

6. Department of Chemical and Biomolecular Engineering University of California Berkeley CA 94720 USA

7. Wallace H. Coulter Department of Biomedical Engineering Emory University School of Medicine and Georgia Institute of Technology Atlanta GA 30322 USA

8. Department of Pediatrics Emory University Atlanta GA 30322 USA

9. Children's Healthcare of Atlanta Atlanta GA 30322 USA

10. School of Engineering University of British Columbia Kelowna BC V1V 1V7 Canada

11. Innovative Genomics Institute Berkeley CA 94720 USA

12. California Institute for Quantitative Biosciences University of California Berkeley Berkeley CA 94720 USA

13. Chan Zuckerberg Biohub San Francisco CA 94158 USA

Abstract

AbstractThe protein corona forms spontaneously on nanoparticle surfaces when nanomaterials are introduced into any biological system/fluid. Reliable characterization of the protein corona is, therefore, a vital step in the development of safe and efficient diagnostic and therapeutic nanomedicine products. 2134 published manuscripts on the protein corona are reviewed and a down‐selection of 470 papers spanning 2000–2021, comprising 1702 nanoparticle (NP) systems is analyzed. This analysis reveals: i) most corona studies have been conducted on metal and metal oxide nanoparticles; ii) despite their overwhelming presence in clinical practice, lipid‐based NPs are underrepresented in protein corona research, iii) studies use new methods to improve reliability and reproducibility in protein corona research; iv) studies use more specific protein sources toward personalized medicine; and v) careful characterization of nanoparticles after corona formation is imperative to minimize the role of aggregation and protein contamination on corona outcomes. As nanoparticles used in biomedicine become increasingly prevalent and biochemically complex, the field of protein corona research will need to focus on developing analytical approaches and characterization techniques appropriate for each unique nanoparticle formulation. Achieving such characterization of the nano‐bio interface of nanobiotechnologies will enable more seamless development and safe implementation of nanoparticles in medicine.

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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