Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Jan 28:10:483-507.
doi: 10.2147/DDDT.S99651. eCollection 2016.

Preparation, characterization, and potential application of chitosan, chitosan derivatives, and chitosan metal nanoparticles in pharmaceutical drug delivery

Affiliations
Review

Preparation, characterization, and potential application of chitosan, chitosan derivatives, and chitosan metal nanoparticles in pharmaceutical drug delivery

Tarek A Ahmed et al. Drug Des Devel Ther. .

Abstract

Naturally occurring polymers, particularly of the polysaccharide type, have been used pharmaceutically for the delivery of a wide variety of therapeutic agents. Chitosan, the second abundant naturally occurring polysaccharide next to cellulose, is a biocompatible and biodegradable mucoadhesive polymer that has been extensively used in the preparation of micro-as well as nanoparticles. The prepared particles have been exploited as a potential carrier for different therapeutic agents such as peptides, proteins, vaccines, DNA, and drugs for parenteral and nonparenteral administration. Therapeutic agent-loaded chitosan micro- or nanoparticles were found to be more stable, permeable, and bioactive. In this review, we are highlighting the different methods of preparation and characterization of chitosan micro- and nanoparticles, while reviewing the pharmaceutical applications of these particles in drug delivery. Moreover, the roles of chitosan derivatives and chitosan metal nanoparticles in drug delivery have been illustrated.

Keywords: characterization; microparticles; nanoparticles; pharmaceutical application; preparation.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Chemical structure of chitosan showing the repeating subunits.
Figure 2
Figure 2
Schematic representation of production of chitosan micro/nanoparticles by chemical cross-linking.
Figure 3
Figure 3
Scanning electron micrograph of chitosan nanoparticles produced using nanoemulsion internal cross-linking technique.
Figure 4
Figure 4
Schematic representation of the spray-drying technique used for the manufacturing of chitosan particulate systems.
Figure 5
Figure 5
Schematic representation of reverse micellar technique.
Figure 6
Figure 6
Structure of the skin and subcutaneous layers and common routes of parenteral drug administration.

Similar articles

Cited by

References

    1. Chirra HD, Desai TA. Emerging microtechnologies for the development of oral drug delivery devices. Adv Drug Deliv Rev. 2012;64(14):1569–1578. - PMC - PubMed
    1. Des Rieux A, Fievez V, Garinot M, Schneider YJ, Preat V. Nanoparticles as potential oral delivery systems of proteins and vaccines: a mechanistic approach. J Control Release. 2006;116(1):1–27. - PubMed
    1. Sahoo SK, Parveen S, Panda JJ. The present and future of nanotechnology in human health care. Nanomedicine. 2007;3(1):20–31. - PubMed
    1. Park JH, Lee S, Kim JH, Park K, Kim K, Kwon IC. Polymeric nanomedicine for cancer therapy. Prog Polym Sci. 2008;33(1):113–137.
    1. Sumer B, Gao J. Theranostic nanomedicine for cancer. Nanomedicine. 2008;3(2):137–140. - PubMed