An in vitro and in vivo study on the properties of hollow polycaprolactone cell-delivery particles.

The field of dermal fillers is evolving rapidly and numerous products are currently on the market. Biodegradable polymers such as polycaprolactone (PCL) have been found to be compatible with several body tissues, and this makes them an ideal material for dermal filling purposes. Hollow PCL spheres w...

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Main Authors: Barend Andre Stander, Fiona A van Vollenstee, Karlien Kallmeyer, Marnie Potgieter, Annie Joubert, Andri Swanepoel, Lara Kotze, Sean Moolman, Michael S Pepper
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0198248&type=printable
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author Barend Andre Stander
Fiona A van Vollenstee
Karlien Kallmeyer
Marnie Potgieter
Annie Joubert
Andri Swanepoel
Lara Kotze
Sean Moolman
Michael S Pepper
author_facet Barend Andre Stander
Fiona A van Vollenstee
Karlien Kallmeyer
Marnie Potgieter
Annie Joubert
Andri Swanepoel
Lara Kotze
Sean Moolman
Michael S Pepper
author_sort Barend Andre Stander
collection DOAJ
description The field of dermal fillers is evolving rapidly and numerous products are currently on the market. Biodegradable polymers such as polycaprolactone (PCL) have been found to be compatible with several body tissues, and this makes them an ideal material for dermal filling purposes. Hollow PCL spheres were developed by the Council for Scientific and Industrial Research (CSIR) to serve both as an anchor point and a "tissue harbour" for cells. Particles were tested for cytotoxicity and cell adherence using mouse embryo fibroblasts (MEF). MEFs adhered to the particles and no significant toxic effects were observed based on morphology, cell growth, cell viability and cell cycle analysis, suggesting that the particles are suitable candidates for cell delivery systems in an in vivo setting. The objective of providing a "tissue harbour" was however not realized, as cells did not preferentially migrate into the ported particles. In vivo studies were conducted in BALB/c mice into whom particles were introduced at the level of the hypodermis. Mice injected with PCL particles (ported and non-ported; with or without MEFs) showed evidence of local inflammation and increased adipogenesis at the site of injection, as well as a systemic inflammatory response. These effects were also observed in mice that received apparently inert (polystyrene) particles. Ported PCL particles can therefore act as a cell delivery system and through their ability to induce adipogenesis, may also serve as a dermal bulking agent.
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spelling doaj-art-28825f3f641c4906b6cd8e8a7359a5762025-08-20T03:04:37ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01137e019824810.1371/journal.pone.0198248An in vitro and in vivo study on the properties of hollow polycaprolactone cell-delivery particles.Barend Andre StanderFiona A van VollensteeKarlien KallmeyerMarnie PotgieterAnnie JoubertAndri SwanepoelLara KotzeSean MoolmanMichael S PepperThe field of dermal fillers is evolving rapidly and numerous products are currently on the market. Biodegradable polymers such as polycaprolactone (PCL) have been found to be compatible with several body tissues, and this makes them an ideal material for dermal filling purposes. Hollow PCL spheres were developed by the Council for Scientific and Industrial Research (CSIR) to serve both as an anchor point and a "tissue harbour" for cells. Particles were tested for cytotoxicity and cell adherence using mouse embryo fibroblasts (MEF). MEFs adhered to the particles and no significant toxic effects were observed based on morphology, cell growth, cell viability and cell cycle analysis, suggesting that the particles are suitable candidates for cell delivery systems in an in vivo setting. The objective of providing a "tissue harbour" was however not realized, as cells did not preferentially migrate into the ported particles. In vivo studies were conducted in BALB/c mice into whom particles were introduced at the level of the hypodermis. Mice injected with PCL particles (ported and non-ported; with or without MEFs) showed evidence of local inflammation and increased adipogenesis at the site of injection, as well as a systemic inflammatory response. These effects were also observed in mice that received apparently inert (polystyrene) particles. Ported PCL particles can therefore act as a cell delivery system and through their ability to induce adipogenesis, may also serve as a dermal bulking agent.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0198248&type=printable
spellingShingle Barend Andre Stander
Fiona A van Vollenstee
Karlien Kallmeyer
Marnie Potgieter
Annie Joubert
Andri Swanepoel
Lara Kotze
Sean Moolman
Michael S Pepper
An in vitro and in vivo study on the properties of hollow polycaprolactone cell-delivery particles.
PLoS ONE
title An in vitro and in vivo study on the properties of hollow polycaprolactone cell-delivery particles.
title_full An in vitro and in vivo study on the properties of hollow polycaprolactone cell-delivery particles.
title_fullStr An in vitro and in vivo study on the properties of hollow polycaprolactone cell-delivery particles.
title_full_unstemmed An in vitro and in vivo study on the properties of hollow polycaprolactone cell-delivery particles.
title_short An in vitro and in vivo study on the properties of hollow polycaprolactone cell-delivery particles.
title_sort in vitro and in vivo study on the properties of hollow polycaprolactone cell delivery particles
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0198248&type=printable
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