Quantification and qualitative effects of different PEGylations on Poly(butyl cyanoacrylate) nanoparticles

Protein adsorption on nanoparticles (NPs) used in nanomedicine leads to opsonization and activation of the complement system in blood, which substantially reduces the blood circulation time of NPs. The most commonly used method to avoid protein adsorption, is to coat the NPs with polyethylene glycol...

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Main Authors: Aslund, Andreas K.O, Sulheim, Einar, Snipstad, Sofie, von Haartman, Eva, Baghirov, Habib, Starr, Nichola J., Løvmo, Mia Kvåle, Lelú, Sylvie, Scurr, David J., Catharina, de Lange Davies, Ruth, Schmid, Ýrr, Mørch
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Published: American Chemical Society 2017
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Online Access:https://eprints.nottingham.ac.uk/41856/
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author Aslund, Andreas K.O
Sulheim, Einar
Snipstad, Sofie
von Haartman, Eva
Baghirov, Habib
Starr, Nichola J.
Løvmo, Mia Kvåle
Lelú, Sylvie
Scurr, David J.
Catharina, de Lange Davies
Ruth, Schmid
Ýrr, Mørch
author_facet Aslund, Andreas K.O
Sulheim, Einar
Snipstad, Sofie
von Haartman, Eva
Baghirov, Habib
Starr, Nichola J.
Løvmo, Mia Kvåle
Lelú, Sylvie
Scurr, David J.
Catharina, de Lange Davies
Ruth, Schmid
Ýrr, Mørch
author_sort Aslund, Andreas K.O
building Nottingham Research Data Repository
collection Online Access
description Protein adsorption on nanoparticles (NPs) used in nanomedicine leads to opsonization and activation of the complement system in blood, which substantially reduces the blood circulation time of NPs. The most commonly used method to avoid protein adsorption, is to coat the NPs with polyethylene glycol, so called PEGylation. Although PEGylation is of utmost importance for designing the in vivo behavior of the NP, there is still a considerable lack of methods for characterization and fundamental understanding related to the PEGylation of NPs. In this work we have studied four different poly(butyl cyanoacrylate) (PBCA) NPs , PEGylated with different types of PEG-based non-ionic surfactants–Jeffamine M-2070, Brij L23, Kolliphor HS 15, Pluronic F68–or combinations thereof. We evaluated the PEGylation, both quantitatively by nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA) and time-of-flight secondary ion mass spectrometry (ToF-SIMS), and qualitatively by studying zeta-potential, protein adsorption, diffusion, cellular interactions and blood circulation half-life. We found that NMR and ToF-SIMS are complementary methods, while TGA is less suitable to quantitate PEG on polymeric NPs. It was found that longer PEG increases both blood circulation time and diffusion of NPs in collagen gels.
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spelling nottingham-418562020-05-04T18:35:45Z https://eprints.nottingham.ac.uk/41856/ Quantification and qualitative effects of different PEGylations on Poly(butyl cyanoacrylate) nanoparticles Aslund, Andreas K.O Sulheim, Einar Snipstad, Sofie von Haartman, Eva Baghirov, Habib Starr, Nichola J. Løvmo, Mia Kvåle Lelú, Sylvie Scurr, David J. Catharina, de Lange Davies Ruth, Schmid Ýrr, Mørch Protein adsorption on nanoparticles (NPs) used in nanomedicine leads to opsonization and activation of the complement system in blood, which substantially reduces the blood circulation time of NPs. The most commonly used method to avoid protein adsorption, is to coat the NPs with polyethylene glycol, so called PEGylation. Although PEGylation is of utmost importance for designing the in vivo behavior of the NP, there is still a considerable lack of methods for characterization and fundamental understanding related to the PEGylation of NPs. In this work we have studied four different poly(butyl cyanoacrylate) (PBCA) NPs , PEGylated with different types of PEG-based non-ionic surfactants–Jeffamine M-2070, Brij L23, Kolliphor HS 15, Pluronic F68–or combinations thereof. We evaluated the PEGylation, both quantitatively by nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA) and time-of-flight secondary ion mass spectrometry (ToF-SIMS), and qualitatively by studying zeta-potential, protein adsorption, diffusion, cellular interactions and blood circulation half-life. We found that NMR and ToF-SIMS are complementary methods, while TGA is less suitable to quantitate PEG on polymeric NPs. It was found that longer PEG increases both blood circulation time and diffusion of NPs in collagen gels. American Chemical Society 2017-02-07 Article PeerReviewed Aslund, Andreas K.O, Sulheim, Einar, Snipstad, Sofie, von Haartman, Eva, Baghirov, Habib, Starr, Nichola J., Løvmo, Mia Kvåle, Lelú, Sylvie, Scurr, David J., Catharina, de Lange Davies, Ruth, Schmid and Ýrr, Mørch (2017) Quantification and qualitative effects of different PEGylations on Poly(butyl cyanoacrylate) nanoparticles. Molecular Pharmaceutics, 14 (8). pp. 2560-2569. ISSN 1543-8384 PACA PEG NMR ToF-SIMS TGA circulation time protein adsorption http://pubs.acs.org/doi/abs/10.1021/acs.molpharmaceut.6b01085 doi:10.1021/acs.molpharmaceut.6b01085 doi:10.1021/acs.molpharmaceut.6b01085
spellingShingle PACA
PEG
NMR
ToF-SIMS
TGA
circulation time
protein adsorption
Aslund, Andreas K.O
Sulheim, Einar
Snipstad, Sofie
von Haartman, Eva
Baghirov, Habib
Starr, Nichola J.
Løvmo, Mia Kvåle
Lelú, Sylvie
Scurr, David J.
Catharina, de Lange Davies
Ruth, Schmid
Ýrr, Mørch
Quantification and qualitative effects of different PEGylations on Poly(butyl cyanoacrylate) nanoparticles
title Quantification and qualitative effects of different PEGylations on Poly(butyl cyanoacrylate) nanoparticles
title_full Quantification and qualitative effects of different PEGylations on Poly(butyl cyanoacrylate) nanoparticles
title_fullStr Quantification and qualitative effects of different PEGylations on Poly(butyl cyanoacrylate) nanoparticles
title_full_unstemmed Quantification and qualitative effects of different PEGylations on Poly(butyl cyanoacrylate) nanoparticles
title_short Quantification and qualitative effects of different PEGylations on Poly(butyl cyanoacrylate) nanoparticles
title_sort quantification and qualitative effects of different pegylations on poly(butyl cyanoacrylate) nanoparticles
topic PACA
PEG
NMR
ToF-SIMS
TGA
circulation time
protein adsorption
url https://eprints.nottingham.ac.uk/41856/
https://eprints.nottingham.ac.uk/41856/
https://eprints.nottingham.ac.uk/41856/