Publication

Protein corona variation in nanoparticles revisited: A dynamic grouping strategy

Rezaei, G., Daghighi, S. M., Haririan, I., Yousefi, I., Raoufi, M., Rezaee, F. & Dinarvand, R., 1-Jul-2019, In : COLLOIDS AND SURFACES B-BIOINTERFACES. 179, p. 505-516 12 p.

Research output: Contribution to journalArticleAcademicpeer-review

APA

Rezaei, G., Daghighi, S. M., Haririan, I., Yousefi, I., Raoufi, M., Rezaee, F., & Dinarvand, R. (2019). Protein corona variation in nanoparticles revisited: A dynamic grouping strategy. COLLOIDS AND SURFACES B-BIOINTERFACES, 179, 505-516. https://doi.org/10.1016/j.colsurfb.2019.04.003

Author

Rezaei, Ghassem ; Daghighi, Seyed Mojtaba ; Haririan, Ismael ; Yousefi, Iman ; Raoufi, Mohammad ; Rezaee, Farhad ; Dinarvand, Rassoul. / Protein corona variation in nanoparticles revisited : A dynamic grouping strategy. In: COLLOIDS AND SURFACES B-BIOINTERFACES. 2019 ; Vol. 179. pp. 505-516.

Harvard

Rezaei, G, Daghighi, SM, Haririan, I, Yousefi, I, Raoufi, M, Rezaee, F & Dinarvand, R 2019, 'Protein corona variation in nanoparticles revisited: A dynamic grouping strategy', COLLOIDS AND SURFACES B-BIOINTERFACES, vol. 179, pp. 505-516. https://doi.org/10.1016/j.colsurfb.2019.04.003

Standard

Protein corona variation in nanoparticles revisited : A dynamic grouping strategy. / Rezaei, Ghassem; Daghighi, Seyed Mojtaba; Haririan, Ismael; Yousefi, Iman; Raoufi, Mohammad; Rezaee, Farhad; Dinarvand, Rassoul.

In: COLLOIDS AND SURFACES B-BIOINTERFACES, Vol. 179, 01.07.2019, p. 505-516.

Research output: Contribution to journalArticleAcademicpeer-review

Vancouver

Rezaei G, Daghighi SM, Haririan I, Yousefi I, Raoufi M, Rezaee F et al. Protein corona variation in nanoparticles revisited: A dynamic grouping strategy. COLLOIDS AND SURFACES B-BIOINTERFACES. 2019 Jul 1;179:505-516. https://doi.org/10.1016/j.colsurfb.2019.04.003


BibTeX

@article{1886c3050e044c059baf51dcb93886c5,
title = "Protein corona variation in nanoparticles revisited: A dynamic grouping strategy",
abstract = "Bio-nano interface investigation models are mainly based on the type of proteins present on corona, bio-nano interaction responses and the evaluation of final outcomes. Due to the extensive diversity in correlative models for investigation of nanoparticles biological responses, a comprehensive model considering different aspects of bio-nano interface from nanoparticles properties to protein corona fingerprints appeared to be essential and cannot be ignored. In order to minimize divergence in studies in the era of bio-nano interface and protein corona with following therapeutic implications, a useful investigation model on the basis of RADAR concept is suggested. The contents of RADAR concept consist of five modules: 1- Reshape of our strategy for synthesis of nanoparticles (NPs), 2- Application of NPs selected based on human fluid, 3- Delivery strategy of NPs selected based on target tissue, 4- Analysis of proteins present on corona using correct procedures and 5- Risk assessment and risk reduction upon the collection and analysis of results to increase drug delivery efficiency and drug efficacy. RADAR grouping strategy for revisiting protein corona phenomenon as a key of success will be discussed with respect to the current state of knowledge.",
keywords = "Corona, Biological fluid, Bio-nano interface, Grouping strategy, Protein, RADAR, HUMAN SERUM-ALBUMIN, ENABLED BLOOD-TEST, IN-VITRO, PLASMA-PROTEINS, CELLULAR UPTAKE, BIOMOLECULAR CORONA, PLGA NANOPARTICLES, DRUG-RELEASE, INTERACTIONS OPPORTUNITIES, POLYMERIC NANOPARTICLES",
author = "Ghassem Rezaei and Daghighi, {Seyed Mojtaba} and Ismael Haririan and Iman Yousefi and Mohammad Raoufi and Farhad Rezaee and Rassoul Dinarvand",
year = "2019",
month = "7",
day = "1",
doi = "10.1016/j.colsurfb.2019.04.003",
language = "English",
volume = "179",
pages = "505--516",
journal = "Colloids and Surfaces B: Biointerfaces",
issn = "0927-7765",
publisher = "ELSEVIER SCIENCE BV",

}

RIS

TY - JOUR

T1 - Protein corona variation in nanoparticles revisited

T2 - A dynamic grouping strategy

AU - Rezaei, Ghassem

AU - Daghighi, Seyed Mojtaba

AU - Haririan, Ismael

AU - Yousefi, Iman

AU - Raoufi, Mohammad

AU - Rezaee, Farhad

AU - Dinarvand, Rassoul

PY - 2019/7/1

Y1 - 2019/7/1

N2 - Bio-nano interface investigation models are mainly based on the type of proteins present on corona, bio-nano interaction responses and the evaluation of final outcomes. Due to the extensive diversity in correlative models for investigation of nanoparticles biological responses, a comprehensive model considering different aspects of bio-nano interface from nanoparticles properties to protein corona fingerprints appeared to be essential and cannot be ignored. In order to minimize divergence in studies in the era of bio-nano interface and protein corona with following therapeutic implications, a useful investigation model on the basis of RADAR concept is suggested. The contents of RADAR concept consist of five modules: 1- Reshape of our strategy for synthesis of nanoparticles (NPs), 2- Application of NPs selected based on human fluid, 3- Delivery strategy of NPs selected based on target tissue, 4- Analysis of proteins present on corona using correct procedures and 5- Risk assessment and risk reduction upon the collection and analysis of results to increase drug delivery efficiency and drug efficacy. RADAR grouping strategy for revisiting protein corona phenomenon as a key of success will be discussed with respect to the current state of knowledge.

AB - Bio-nano interface investigation models are mainly based on the type of proteins present on corona, bio-nano interaction responses and the evaluation of final outcomes. Due to the extensive diversity in correlative models for investigation of nanoparticles biological responses, a comprehensive model considering different aspects of bio-nano interface from nanoparticles properties to protein corona fingerprints appeared to be essential and cannot be ignored. In order to minimize divergence in studies in the era of bio-nano interface and protein corona with following therapeutic implications, a useful investigation model on the basis of RADAR concept is suggested. The contents of RADAR concept consist of five modules: 1- Reshape of our strategy for synthesis of nanoparticles (NPs), 2- Application of NPs selected based on human fluid, 3- Delivery strategy of NPs selected based on target tissue, 4- Analysis of proteins present on corona using correct procedures and 5- Risk assessment and risk reduction upon the collection and analysis of results to increase drug delivery efficiency and drug efficacy. RADAR grouping strategy for revisiting protein corona phenomenon as a key of success will be discussed with respect to the current state of knowledge.

KW - Corona

KW - Biological fluid

KW - Bio-nano interface

KW - Grouping strategy

KW - Protein

KW - RADAR

KW - HUMAN SERUM-ALBUMIN

KW - ENABLED BLOOD-TEST

KW - IN-VITRO

KW - PLASMA-PROTEINS

KW - CELLULAR UPTAKE

KW - BIOMOLECULAR CORONA

KW - PLGA NANOPARTICLES

KW - DRUG-RELEASE

KW - INTERACTIONS OPPORTUNITIES

KW - POLYMERIC NANOPARTICLES

U2 - 10.1016/j.colsurfb.2019.04.003

DO - 10.1016/j.colsurfb.2019.04.003

M3 - Article

VL - 179

SP - 505

EP - 516

JO - Colloids and Surfaces B: Biointerfaces

JF - Colloids and Surfaces B: Biointerfaces

SN - 0927-7765

ER -

ID: 95438487