» Articles » PMID: 30966270

Chitosan Based Self-Assembled Nanoparticles in Drug Delivery

Overview
Publisher MDPI
Date 2019 Apr 11
PMID 30966270
Citations 77
Authors
Affiliations
Soon will be listed here.
Abstract

Chitosan is a cationic polysaccharide that is usually obtained by alkaline deacetylation of chitin poly(-acetylglucosamine). It is biocompatible, biodegradable, mucoadhesive, and non-toxic. These excellent biological properties make chitosan a good candidate for a platform in developing drug delivery systems having improved biodistribution, increased specificity and sensitivity, and reduced pharmacological toxicity. In particular, chitosan nanoparticles are found to be appropriate for non-invasive routes of drug administration: oral, nasal, pulmonary and ocular routes. These applications are facilitated by the absorption-enhancing effect of chitosan. Many procedures for obtaining chitosan nanoparticles have been proposed. Particularly, the introduction of hydrophobic moieties into chitosan molecules by grafting to generate a hydrophobic-hydrophilic balance promoting self-assembly is a current and appealing approach. The grafting agent can be a hydrophobic moiety forming micelles that can entrap lipophilic drugs or it can be the drug itself. Another suitable way to generate self-assembled chitosan nanoparticles is through the formation of polyelectrolyte complexes with polyanions. This paper reviews the main approaches for preparing chitosan nanoparticles by self-assembly through both procedures, and illustrates the state of the art of their application in drug delivery.

Citing Articles

-Carrageenan/Chitosan Nanoparticles via Coacervation: Achieving Stability for Tiny Particles.

Klein R, de Almeida D, de Oliveira A, Bonafe E, Monteiro J, Sabino R Nanomaterials (Basel). 2025; 15(3).

PMID: 39940137 PMC: 11819667. DOI: 10.3390/nano15030161.


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

Zucca G, Vigani B, Valentino C, Ruggeri M, Marchesi N, Pascale A Int J Nanomedicine. 2025; 20:907-932.

PMID: 39867306 PMC: 11766310. DOI: 10.2147/IJN.S488507.


Chitosan and Its Nanoparticles: A Multifaceted Approach to Antibacterial Applications.

Akdasci E, Duman H, Eker F, Bechelany M, Karav S Nanomaterials (Basel). 2025; 15(2).

PMID: 39852740 PMC: 11768082. DOI: 10.3390/nano15020126.


Chitosan-Clay Mineral Nanocomposites with Antibacterial Activity for Biomedical Application: Advantages and Future Perspectives.

Krajisnik D, Uskokovic-Markovic S, Dakovic A Int J Mol Sci. 2024; 25(19).

PMID: 39408707 PMC: 11476839. DOI: 10.3390/ijms251910377.


-Venom-Loaded Cross-Linked Chitosan Nanoparticles Improve Antimicrobial Activity.

Glaucia-Silva F, Torres J, Torres-Rego M, Daniele-Silva A, Furtado A, Ferreira S Int J Mol Sci. 2024; 25(18).

PMID: 39337380 PMC: 11432167. DOI: 10.3390/ijms25189893.


References
1.
Tokumitsu H, Ichikawa H, Fukumori Y . Chitosan-gadopentetic acid complex nanoparticles for gadolinium neutron-capture therapy of cancer: preparation by novel emulsion-droplet coalescence technique and characterization. Pharm Res. 2000; 16(12):1830-5. DOI: 10.1023/a:1018995124527. View

2.
Bali J, Cousse H, Neuzil E . Biochemical basis of the pharmacologic action of chondroitin sulfates on the osteoarticular system. Semin Arthritis Rheum. 2001; 31(1):58-68. DOI: 10.1053/sarh.2000.24874. View

3.
Janes K, Fresneau M, Marazuela A, Fabra A, Alonso M . Chitosan nanoparticles as delivery systems for doxorubicin. J Control Release. 2001; 73(2-3):255-67. DOI: 10.1016/s0168-3659(01)00294-2. View

4.
Illum L, Jabbal-Gill I, Hinchcliffe M, Fisher A, Davis S . Chitosan as a novel nasal delivery system for vaccines. Adv Drug Deliv Rev. 2001; 51(1-3):81-96. DOI: 10.1016/s0169-409x(01)00171-5. View

5.
Kim Y, Gihm S, Park C, Lee K, Kim T, Kwon I . Structural characteristics of size-controlled self-aggregates of deoxycholic acid-modified chitosan and their application as a DNA delivery carrier. Bioconjug Chem. 2001; 12(6):932-8. DOI: 10.1021/bc015510c. View