Cited by 23Advanced Drug Delivery SystemsNanoparticle-Based Drug DeliveryDrug Solubulity and Delivery Systems

Chitosan Oleate Coated Poly Lactic-Glycolic Acid (PLGA) nanoparticles versus chitosan oleate self-assembled polymeric micelles, loaded with resveratrol.

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Miele, Dalila, Catenacci, Laura, Sorrenti, Milena, Rossi, Silvia, Sandri, Giuseppina, Malavasi, Lorenzo, Dacarro, Giacomo, Ferrari, Franca +1 more·2019·Marine Drugs

Abstract

Chitosan oleate (CS-OA), a chitosan salt with amphiphilic properties, has demonstrated the ability to self-assemble in aqueous environment to give polymeric micelles useful to load poorly soluble drugs. More recently, CS-OA was proposed to stabilize nanoemulsions during the preparation by emulsification and solvent evaporation of poly lactic-glycolic acid (PLGA) nanoparticles (NPs) loaded with curcumin. Positive mucoadhesive behavior and internalization properties were demonstrated for these NPs attributable to the presence of positive charge at the NP surface. In the present paper, two CS-OA-based nanosystems, micelles and PLGA NPs, were compared with the aim of elucidating their physico-chemical characteristics, and especially their interaction with cell substrates. The two systems were loaded with resveratrol (RSV), a hydrophobic polyphenol endowed with anti-cancerogenic, anti-inflammatory, and heart/brain protective effects, but with low bioavailability mainly due to poor aqueous solubility. Calorimetric analysis and X-ray spectra demonstrated amorphization of RSV, confirming its affinity for hydrophobic domains of polymeric micelles and PLGA core of NPs. TGA decomposition patterns suggest higher stability of PLGA-NPs compared with polymeric micelles, that anyway resulted more stable than expected, considering the RSV release profiles, and the cell line interaction results.

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  • PLGA nanoparticles coated with Chitosan oleate (CS-OA) were found to be more stable compared with polymeric micelles based on release profiles, TGA analysis, and cell line interaction results.

    “micelles and PLGA NPs, loaded with lipophillic model drug i.e., resveratrol, based on release profiles, TGA analysis and the cell line interaction results PLGA-CS-OA found to be more stable compared with polymeric micelles (Miele et al., 2019).”

    From Nanotechnology: A Promising Approach for Delivery of Neuroprotective Drugs (2020) · cites this paper as Miele et al., 2019

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Authors
Miele, D., Catenacci, L., Sorrenti, M., Rossi, S., Sandri, G., Malavasi, L., Dacarro, G., Ferrari, F., & Bonferoni, M. C.
Affiliations
University of Pavia (IT)
Corresponding author
Bonferoni, Maria Cristina
Venue
Marine Drugs
Publisher
MDPI AG
Published
2019-09-01
Volume
17
Issue
9
Pages
515
ISSN
1660-3397 (ISSN-L)
OpenAlex
W2970791469
Cited by
23
References
28
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 4 · 2022: 4 · 2021: 5 · 2020: 6
FWCI
1.60
Type
journal article
Language
en
Open access
Locations
  • Marine Drugs (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Drug Solubulity and Delivery Systems
Keywords
PLGA nanoparticles, polymeric micelles, resveratrol, drug delivery systems, poorly water-soluble drugs, drug loading, amorphization, thermal stability, drug release, cellular uptake, mucoadhesion, anticancer polyphenols
MeSH terms
Polylactic Acid-Polyglycolic Acid Copolymer, Resveratrol, Biological Availability, Curcumin, Drug Carriers, Glycolates, Glycols, HeLa Cells, Humans, Micelles, Particle Size, Polymers, Solubility, Surface Properties, Drug Delivery Systems, Caco-2 Cells, Oleic Acid, Cell Line, Tumor, Chitosan, Nanoparticles, Hydrophobic and Hydrophilic Interactions

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