Polyelectrolyte Complex Nanoparticles: Chitosan-Chondroitin Complex for Drug Delivery

Polyelectrolyte complex nanoparticles (PEC) have emerged as promising vehicles for drug delivery due to their unique physicochemical properties and biocompatibility. This study investigated the formulation characteristics of PEC nanoparticles based on interpolymer ionic interaction between cationic...

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Main Author: Daníel Óskarsson 1999-
Other Authors: Háskóli Íslands
Format: Master Thesis
Language:English
Published: 2024
Subjects:
Online Access:http://hdl.handle.net/1946/47452
id ftskemman:oai:skemman.is:1946/47452
record_format openpolar
spelling ftskemman:oai:skemman.is:1946/47452 2024-06-23T07:54:06+00:00 Polyelectrolyte Complex Nanoparticles: Chitosan-Chondroitin Complex for Drug Delivery Daníel Óskarsson 1999- Háskóli Íslands 2024-05 application/pdf http://hdl.handle.net/1946/47452 en eng http://hdl.handle.net/1946/47452 Lyfjafræði Lyfjagjöf Efnasambönd Fjölliður Thesis Master's 2024 ftskemman 2024-06-04T14:31:44Z Polyelectrolyte complex nanoparticles (PEC) have emerged as promising vehicles for drug delivery due to their unique physicochemical properties and biocompatibility. This study investigated the formulation characteristics of PEC nanoparticles based on interpolymer ionic interaction between cationic chitosan derivative and anionic chondroitin sulfate. The objective was to optimize formulation parameters and assess the potential of PEC for drug delivery applications. The cationic derivatives were chitosan betaine (CB) and chitosan oligomer betaine (COS). The anionic components used for preparing the PECs were chondroitin sulfate (CS) polymer and sulfobutyl-ether-β-cyclodextrin (CD). The CB and COS were synthesized at the University of Iceland, while CS and CD were commercial products. CD was also used in the study because is a well-known excipient used as a solubilizer and stabilizer. CB had to be tested for solubility and all samples freeze-dried to confirm their concentrations. Once sample solutions of all the polymers had been prepared, PEC formulation studies were carried out with dynamic light scattering (DLS). Through systematic experimentation, DLS revealed optimal ratios for CB+CS, COS+CS, and these complexes with CD and indicated the successful formation of PEC in terms of size (size < 200 nm, polydispersity index < 0.2) Fluorescence resonance energy transfer (FRET) was employed using fluorescently labeled polymers. FRET verified that PEC was formed between the polymers and showed exciting results regarding CD potential to enhance PEC properties, suggesting a potential avenue for further research. TEM imaging then ultimately confirmed the formation of PEC. Cell uptake studies were then performed on individual polymers and PECs, which indicated that using PECs increased the cell uptake of the polymers compared to polymers used on their own. Cytotoxicity test confirmed that only CB was cytotoxic and that the PEC reduced this toxicity. Overall, the findings suggest that these PECs hold significant ... Master Thesis Iceland Skemman (Iceland)
institution Open Polar
collection Skemman (Iceland)
op_collection_id ftskemman
language English
topic Lyfjafræði
Lyfjagjöf
Efnasambönd
Fjölliður
spellingShingle Lyfjafræði
Lyfjagjöf
Efnasambönd
Fjölliður
Daníel Óskarsson 1999-
Polyelectrolyte Complex Nanoparticles: Chitosan-Chondroitin Complex for Drug Delivery
topic_facet Lyfjafræði
Lyfjagjöf
Efnasambönd
Fjölliður
description Polyelectrolyte complex nanoparticles (PEC) have emerged as promising vehicles for drug delivery due to their unique physicochemical properties and biocompatibility. This study investigated the formulation characteristics of PEC nanoparticles based on interpolymer ionic interaction between cationic chitosan derivative and anionic chondroitin sulfate. The objective was to optimize formulation parameters and assess the potential of PEC for drug delivery applications. The cationic derivatives were chitosan betaine (CB) and chitosan oligomer betaine (COS). The anionic components used for preparing the PECs were chondroitin sulfate (CS) polymer and sulfobutyl-ether-β-cyclodextrin (CD). The CB and COS were synthesized at the University of Iceland, while CS and CD were commercial products. CD was also used in the study because is a well-known excipient used as a solubilizer and stabilizer. CB had to be tested for solubility and all samples freeze-dried to confirm their concentrations. Once sample solutions of all the polymers had been prepared, PEC formulation studies were carried out with dynamic light scattering (DLS). Through systematic experimentation, DLS revealed optimal ratios for CB+CS, COS+CS, and these complexes with CD and indicated the successful formation of PEC in terms of size (size < 200 nm, polydispersity index < 0.2) Fluorescence resonance energy transfer (FRET) was employed using fluorescently labeled polymers. FRET verified that PEC was formed between the polymers and showed exciting results regarding CD potential to enhance PEC properties, suggesting a potential avenue for further research. TEM imaging then ultimately confirmed the formation of PEC. Cell uptake studies were then performed on individual polymers and PECs, which indicated that using PECs increased the cell uptake of the polymers compared to polymers used on their own. Cytotoxicity test confirmed that only CB was cytotoxic and that the PEC reduced this toxicity. Overall, the findings suggest that these PECs hold significant ...
author2 Háskóli Íslands
format Master Thesis
author Daníel Óskarsson 1999-
author_facet Daníel Óskarsson 1999-
author_sort Daníel Óskarsson 1999-
title Polyelectrolyte Complex Nanoparticles: Chitosan-Chondroitin Complex for Drug Delivery
title_short Polyelectrolyte Complex Nanoparticles: Chitosan-Chondroitin Complex for Drug Delivery
title_full Polyelectrolyte Complex Nanoparticles: Chitosan-Chondroitin Complex for Drug Delivery
title_fullStr Polyelectrolyte Complex Nanoparticles: Chitosan-Chondroitin Complex for Drug Delivery
title_full_unstemmed Polyelectrolyte Complex Nanoparticles: Chitosan-Chondroitin Complex for Drug Delivery
title_sort polyelectrolyte complex nanoparticles: chitosan-chondroitin complex for drug delivery
publishDate 2024
url http://hdl.handle.net/1946/47452
genre Iceland
genre_facet Iceland
op_relation http://hdl.handle.net/1946/47452
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