Chondroitin Sulphate-Chitosan Based Nanogels Loaded with Naringenin-β-Cyclodextrin Complex as Potential Tool for the Treatment of Diabetic Retinopathy: A Formulation Study

Gaia Zucca,1 Barbara Vigani,1 Caterina Valentino,1 Marco Ruggeri,1 Nicoletta Marchesi,1 Alessia Pascale,1 Giulia Giovilli,2 Lorenzo Malavasi,2 Giuseppina Sandri,1 Silvia Rossi1 1Department of Drug Sciences, University of Pavia, Pavia, 27100, Italy; 2Department of Chemistry and INSTM, University of P...

Full description

Saved in:
Bibliographic Details
Main Authors: Zucca G, Vigani B, Valentino C, Ruggeri M, Marchesi N, Pascale A, Giovilli G, Malavasi L, Sandri G, Rossi S
Format: Article
Language:English
Published: Dove Medical Press 2025-01-01
Series:International Journal of Nanomedicine
Subjects:
Online Access:https://www.dovepress.com/chondroitin-sulphate-chitosan-based-nanogels-loaded-with-naringenin--c-peer-reviewed-fulltext-article-IJN
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832592083553091584
author Zucca G
Vigani B
Valentino C
Ruggeri M
Marchesi N
Pascale A
Giovilli G
Malavasi L
Sandri G
Rossi S
author_facet Zucca G
Vigani B
Valentino C
Ruggeri M
Marchesi N
Pascale A
Giovilli G
Malavasi L
Sandri G
Rossi S
author_sort Zucca G
collection DOAJ
description Gaia Zucca,1 Barbara Vigani,1 Caterina Valentino,1 Marco Ruggeri,1 Nicoletta Marchesi,1 Alessia Pascale,1 Giulia Giovilli,2 Lorenzo Malavasi,2 Giuseppina Sandri,1 Silvia Rossi1 1Department of Drug Sciences, University of Pavia, Pavia, 27100, Italy; 2Department of Chemistry and INSTM, University of Pavia, Pavia, 27100, ItalyCorrespondence: Silvia Rossi; Barbara Vigani, Department of Drug Sciences, University of Pavia, Via Taramelli 12, Pavia, 27100, Italy, Email silvia.rossi@unipv.it; barbara.vigani@unipv.itPurpose: The main purpose of the study was the formulation development of nanogels (NHs) composed of chondroitin sulfate (CS) and low molecular weight chitosan (lCH), loaded with a naringenin-β-cyclodextrin complex (NAR/β-CD), as a potential treatment for early-stage diabetic retinopathy.Methods: Different formulations of NHs were prepared by varying polymer concentration, lCH ratio, and pH and, then, characterized for particle size, zeta potential, particle concentration (particles/mL) and morphology. Cytotoxicity and internalization were assessed in vitro using Human Umbilical Vein Endothelial Cells (HUVEC). The NAR/β-CD complex was prepared and evaluated for morphology, complexation efficiency, and solubility. Finally, the most promising NH prototype was loaded with NAR/β-CD (NH@NAR/β-CD) and further characterized for encapsulation efficiency, loading capacity, opacity and cytotoxicity on HUVEC; in vitro release test and DPPH assay were performed to investigate NH capability to sustain NAR release and NH@NAR/β-CD antioxidant properties, respectively.Results: NH properties were influenced by polymer concentration, lCH ratio, and pH. N3 (0.5 mg/mL; lCH=1.5:1; pH = 5) and N9 (0.5 mg/mL; lCH=1:1; pH = 5) showed optimal characteristics, including small size (< 350 nm) and positive zeta potential, facilitating cellular uptake. The NAR/β-CD complex showed 71% complexation efficiency and enhanced NAR solubility. Since characterized by superior properties and better in vitro biocompatibility, N3 was loaded with NAR/β-CD. N3@NAR/β-CD capability to sustain in vitro NAR release, radical scavenging activity and in vitro biocompatibility were finally demonstrated.Conclusion: The physico-chemical properties of N3@NAR/β-CD were responsible for their cell uptake, suggesting their potential to target retinal endothelial cells. The high NAR/β-CD complexation efficiency and the sustained NAR release over 72 hours could guarantee the maintenance of an effective drug concentration at the damage site while reducing the injection number. Further studies about the safety and the effectiveness of the intravitreal injection of NHs@NAR/β-CD will be performed on a diabetic animal model. Keywords: polyelectrolyte complexation, cellular uptake, inclusion complex, antioxidant properties, intravitreal administration
format Article
id doaj-art-b1211e2259d3414ba015b7204df6e925
institution Kabale University
issn 1178-2013
language English
publishDate 2025-01-01
publisher Dove Medical Press
record_format Article
series International Journal of Nanomedicine
spelling doaj-art-b1211e2259d3414ba015b7204df6e9252025-01-21T16:58:06ZengDove Medical PressInternational Journal of Nanomedicine1178-20132025-01-01Volume 2090793299456Chondroitin Sulphate-Chitosan Based Nanogels Loaded with Naringenin-&beta;-Cyclodextrin Complex as Potential Tool for the Treatment of Diabetic Retinopathy: A Formulation StudyZucca GVigani BValentino CRuggeri MMarchesi NPascale AGiovilli GMalavasi LSandri GRossi SGaia Zucca,1 Barbara Vigani,1 Caterina Valentino,1 Marco Ruggeri,1 Nicoletta Marchesi,1 Alessia Pascale,1 Giulia Giovilli,2 Lorenzo Malavasi,2 Giuseppina Sandri,1 Silvia Rossi1 1Department of Drug Sciences, University of Pavia, Pavia, 27100, Italy; 2Department of Chemistry and INSTM, University of Pavia, Pavia, 27100, ItalyCorrespondence: Silvia Rossi; Barbara Vigani, Department of Drug Sciences, University of Pavia, Via Taramelli 12, Pavia, 27100, Italy, Email silvia.rossi@unipv.it; barbara.vigani@unipv.itPurpose: The main purpose of the study was the formulation development of nanogels (NHs) composed of chondroitin sulfate (CS) and low molecular weight chitosan (lCH), loaded with a naringenin-β-cyclodextrin complex (NAR/β-CD), as a potential treatment for early-stage diabetic retinopathy.Methods: Different formulations of NHs were prepared by varying polymer concentration, lCH ratio, and pH and, then, characterized for particle size, zeta potential, particle concentration (particles/mL) and morphology. Cytotoxicity and internalization were assessed in vitro using Human Umbilical Vein Endothelial Cells (HUVEC). The NAR/β-CD complex was prepared and evaluated for morphology, complexation efficiency, and solubility. Finally, the most promising NH prototype was loaded with NAR/β-CD (NH@NAR/β-CD) and further characterized for encapsulation efficiency, loading capacity, opacity and cytotoxicity on HUVEC; in vitro release test and DPPH assay were performed to investigate NH capability to sustain NAR release and NH@NAR/β-CD antioxidant properties, respectively.Results: NH properties were influenced by polymer concentration, lCH ratio, and pH. N3 (0.5 mg/mL; lCH=1.5:1; pH = 5) and N9 (0.5 mg/mL; lCH=1:1; pH = 5) showed optimal characteristics, including small size (< 350 nm) and positive zeta potential, facilitating cellular uptake. The NAR/β-CD complex showed 71% complexation efficiency and enhanced NAR solubility. Since characterized by superior properties and better in vitro biocompatibility, N3 was loaded with NAR/β-CD. N3@NAR/β-CD capability to sustain in vitro NAR release, radical scavenging activity and in vitro biocompatibility were finally demonstrated.Conclusion: The physico-chemical properties of N3@NAR/β-CD were responsible for their cell uptake, suggesting their potential to target retinal endothelial cells. The high NAR/β-CD complexation efficiency and the sustained NAR release over 72 hours could guarantee the maintenance of an effective drug concentration at the damage site while reducing the injection number. Further studies about the safety and the effectiveness of the intravitreal injection of NHs@NAR/β-CD will be performed on a diabetic animal model. Keywords: polyelectrolyte complexation, cellular uptake, inclusion complex, antioxidant properties, intravitreal administrationhttps://www.dovepress.com/chondroitin-sulphate-chitosan-based-nanogels-loaded-with-naringenin--c-peer-reviewed-fulltext-article-IJNpolyelectrolyte complexationcellular uptakeinclusion complexantioxidant propertiesintravitreous administration
spellingShingle Zucca G
Vigani B
Valentino C
Ruggeri M
Marchesi N
Pascale A
Giovilli G
Malavasi L
Sandri G
Rossi S
Chondroitin Sulphate-Chitosan Based Nanogels Loaded with Naringenin-&beta;-Cyclodextrin Complex as Potential Tool for the Treatment of Diabetic Retinopathy: A Formulation Study
International Journal of Nanomedicine
polyelectrolyte complexation
cellular uptake
inclusion complex
antioxidant properties
intravitreous administration
title Chondroitin Sulphate-Chitosan Based Nanogels Loaded with Naringenin-&beta;-Cyclodextrin Complex as Potential Tool for the Treatment of Diabetic Retinopathy: A Formulation Study
title_full Chondroitin Sulphate-Chitosan Based Nanogels Loaded with Naringenin-&beta;-Cyclodextrin Complex as Potential Tool for the Treatment of Diabetic Retinopathy: A Formulation Study
title_fullStr Chondroitin Sulphate-Chitosan Based Nanogels Loaded with Naringenin-&beta;-Cyclodextrin Complex as Potential Tool for the Treatment of Diabetic Retinopathy: A Formulation Study
title_full_unstemmed Chondroitin Sulphate-Chitosan Based Nanogels Loaded with Naringenin-&beta;-Cyclodextrin Complex as Potential Tool for the Treatment of Diabetic Retinopathy: A Formulation Study
title_short Chondroitin Sulphate-Chitosan Based Nanogels Loaded with Naringenin-&beta;-Cyclodextrin Complex as Potential Tool for the Treatment of Diabetic Retinopathy: A Formulation Study
title_sort chondroitin sulphate chitosan based nanogels loaded with naringenin beta cyclodextrin complex as potential tool for the treatment of diabetic retinopathy a formulation study
topic polyelectrolyte complexation
cellular uptake
inclusion complex
antioxidant properties
intravitreous administration
url https://www.dovepress.com/chondroitin-sulphate-chitosan-based-nanogels-loaded-with-naringenin--c-peer-reviewed-fulltext-article-IJN
work_keys_str_mv AT zuccag chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy
AT viganib chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy
AT valentinoc chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy
AT ruggerim chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy
AT marchesin chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy
AT pascalea chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy
AT giovillig chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy
AT malavasil chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy
AT sandrig chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy
AT rossis chondroitinsulphatechitosanbasednanogelsloadedwithnaringeninbetacyclodextrincomplexaspotentialtoolforthetreatmentofdiabeticretinopathyaformulationstudy