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Assessing the Layer-by-Layer Assembly of Cellulose Nanofibrils and Polyelectrolytes in Pancreatic Tumor Spheroid Formation

Three-dimensional (3D) tumor spheroids are regarded as promising models for utilization as preclinical assessments of chemo-sensitivity. However, the creation of these tumor spheroids presents challenges, given that not all tumor cell lines are able to form consistent and regular spheroids. In this...

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Autores principales: Abbasi Aval, Negar, Lahchaichi, Ekeram, Tudoran, Oana, Fayazbakhsh, Farzaneh, Heuchel, Rainer, Löhr, Matthias, Pettersson, Torbjörn, Russom, Aman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669291/
https://www.ncbi.nlm.nih.gov/pubmed/38002061
http://dx.doi.org/10.3390/biomedicines11113061
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author Abbasi Aval, Negar
Lahchaichi, Ekeram
Tudoran, Oana
Fayazbakhsh, Farzaneh
Heuchel, Rainer
Löhr, Matthias
Pettersson, Torbjörn
Russom, Aman
author_facet Abbasi Aval, Negar
Lahchaichi, Ekeram
Tudoran, Oana
Fayazbakhsh, Farzaneh
Heuchel, Rainer
Löhr, Matthias
Pettersson, Torbjörn
Russom, Aman
author_sort Abbasi Aval, Negar
collection PubMed
description Three-dimensional (3D) tumor spheroids are regarded as promising models for utilization as preclinical assessments of chemo-sensitivity. However, the creation of these tumor spheroids presents challenges, given that not all tumor cell lines are able to form consistent and regular spheroids. In this context, we have developed a novel layer-by-layer coating of cellulose nanofibril–polyelectrolyte bilayers for the generation of spheroids. This technique builds bilayers of cellulose nanofibrils and polyelectrolytes and is used here to coat two distinct 96-well plate types: nontreated/non-sterilized and Nunclon Delta. In this work, we optimized the protocol aimed at generating and characterizing spheroids on difficult-to-grow pancreatic tumor cell lines. Here, diverse parameters were explored, encompassing the bilayer count (five and ten) and multiple cell-seeding concentrations (10, 100, 200, 500, and 1000 cells per well), using four pancreatic tumor cell lines—KPCT, PANC-1, MiaPaCa-2, and CFPAC-I. The evaluation includes the quantification (number of spheroids, size, and morphology) and proliferation of the produced spheroids, as well as an assessment of their viability. Notably, our findings reveal a significant influence from both the number of bilayers and the plate type used on the successful formation of spheroids. The novel and simple layer-by-layer-based coating method has the potential to offer the large-scale production of spheroids across a spectrum of tumor cell lines.
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spelling pubmed-106692912023-11-15 Assessing the Layer-by-Layer Assembly of Cellulose Nanofibrils and Polyelectrolytes in Pancreatic Tumor Spheroid Formation Abbasi Aval, Negar Lahchaichi, Ekeram Tudoran, Oana Fayazbakhsh, Farzaneh Heuchel, Rainer Löhr, Matthias Pettersson, Torbjörn Russom, Aman Biomedicines Article Three-dimensional (3D) tumor spheroids are regarded as promising models for utilization as preclinical assessments of chemo-sensitivity. However, the creation of these tumor spheroids presents challenges, given that not all tumor cell lines are able to form consistent and regular spheroids. In this context, we have developed a novel layer-by-layer coating of cellulose nanofibril–polyelectrolyte bilayers for the generation of spheroids. This technique builds bilayers of cellulose nanofibrils and polyelectrolytes and is used here to coat two distinct 96-well plate types: nontreated/non-sterilized and Nunclon Delta. In this work, we optimized the protocol aimed at generating and characterizing spheroids on difficult-to-grow pancreatic tumor cell lines. Here, diverse parameters were explored, encompassing the bilayer count (five and ten) and multiple cell-seeding concentrations (10, 100, 200, 500, and 1000 cells per well), using four pancreatic tumor cell lines—KPCT, PANC-1, MiaPaCa-2, and CFPAC-I. The evaluation includes the quantification (number of spheroids, size, and morphology) and proliferation of the produced spheroids, as well as an assessment of their viability. Notably, our findings reveal a significant influence from both the number of bilayers and the plate type used on the successful formation of spheroids. The novel and simple layer-by-layer-based coating method has the potential to offer the large-scale production of spheroids across a spectrum of tumor cell lines. MDPI 2023-11-15 /pmc/articles/PMC10669291/ /pubmed/38002061 http://dx.doi.org/10.3390/biomedicines11113061 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Abbasi Aval, Negar
Lahchaichi, Ekeram
Tudoran, Oana
Fayazbakhsh, Farzaneh
Heuchel, Rainer
Löhr, Matthias
Pettersson, Torbjörn
Russom, Aman
Assessing the Layer-by-Layer Assembly of Cellulose Nanofibrils and Polyelectrolytes in Pancreatic Tumor Spheroid Formation
title Assessing the Layer-by-Layer Assembly of Cellulose Nanofibrils and Polyelectrolytes in Pancreatic Tumor Spheroid Formation
title_full Assessing the Layer-by-Layer Assembly of Cellulose Nanofibrils and Polyelectrolytes in Pancreatic Tumor Spheroid Formation
title_fullStr Assessing the Layer-by-Layer Assembly of Cellulose Nanofibrils and Polyelectrolytes in Pancreatic Tumor Spheroid Formation
title_full_unstemmed Assessing the Layer-by-Layer Assembly of Cellulose Nanofibrils and Polyelectrolytes in Pancreatic Tumor Spheroid Formation
title_short Assessing the Layer-by-Layer Assembly of Cellulose Nanofibrils and Polyelectrolytes in Pancreatic Tumor Spheroid Formation
title_sort assessing the layer-by-layer assembly of cellulose nanofibrils and polyelectrolytes in pancreatic tumor spheroid formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669291/
https://www.ncbi.nlm.nih.gov/pubmed/38002061
http://dx.doi.org/10.3390/biomedicines11113061
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