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
. 2011 Jul;28(7):1500-19.
doi: 10.1007/s11095-010-0339-8. Epub 2010 Dec 23.

Designing dendrimers for drug delivery and imaging: pharmacokinetic considerations

Affiliations
Review

Designing dendrimers for drug delivery and imaging: pharmacokinetic considerations

Wassana Wijagkanalan et al. Pharm Res. 2011 Jul.

Abstract

Dendrimers have well-organized high branches with a layered architecture providing a series of versatile chemical modification for various purposes. Consequently, this dendrimer nanotechnology explores a new promising class of nanoscale carriers for therapeutic drugs and imaging reagents using passive and active targeting approaches. By controlling dendritic structures, the biological fate of dendrimer/dendrimer-based drugs can be significantly altered based on their intrinsic physicochemical properties, including the hydrophilicity of the unit molecules, particle size, surface charge, and modification. Accordingly, pharmacokinetic aspects play an important role in the design and development of dendrimer systems for successful in vivo application and clinical translation. This review focuses on the recent progress regarding dendritic architectures, structure-related toxicity, and critical factors affecting the pharmacokinetics and biodistribution of dendrimer/dendrimer-based drugs. A better understanding of the basic aspects of dendritic systems and their pharmacokinetics will help to develop a rationale for the design of dendrimers for the controlled delivery of drugs and imaging reagents for therapeutic or diagnostic purposes.

PubMed Disclaimer

References

    1. Int J Pharm. 2006 Jan 3;307(1):93-102 - PubMed
    1. Angew Chem Int Ed Engl. 2004 Jul 26;43(30):3928-32 - PubMed
    1. Radiology. 2003 Oct;229(1):217-23 - PubMed
    1. Bioconjug Chem. 2000 Nov-Dec;11(6):910-7 - PubMed
    1. Adv Drug Deliv Rev. 2005 Dec 14;57(15):2203-14 - PubMed

Publication types

MeSH terms

LinkOut - more resources