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
. 2021 Nov 15;9(11):1694.
doi: 10.3390/biomedicines9111694.

Hydrogels: 3D Drug Delivery Systems for Nanoparticles and Extracellular Vesicles

Affiliations
Review

Hydrogels: 3D Drug Delivery Systems for Nanoparticles and Extracellular Vesicles

Yashna Chabria et al. Biomedicines. .

Abstract

Synthetic and naturally occurring nano-sized particles present versatile vehicles for the delivery of therapy in a range of clinical settings. Their small size and modifiable physicochemical properties support refinement of targeting capabilities, immune response, and therapeutic cargo, but rapid clearance from the body and limited efficacy remain a major challenge. This highlights the need for a local sustained delivery system for nanoparticles (NPs) and extracellular vesicles (EVs) at the target site that will ensure prolonged exposure, maximum efficacy and dose, and minimal toxicity. Biocompatible hydrogels loaded with therapeutic NPs/EVs hold immense promise as cell-free sustained and targeted delivery systems in a range of disease settings. These bioscaffolds ensure retention of the nano-sized particles at the target site and can also act as controlled release systems for therapeutics over a prolonged period of time. The encapsulation of stimuli sensitive components into hydrogels supports the release of the content on-demand. In this review, we highlight the prospect of the sustained and prolonged delivery of these nano-sized therapeutic entities from hydrogels for broad applications spanning tissue regeneration and cancer treatment. Further understanding of the parameters controlling the release rate of these particles and efficient transfer of cargo to target cells will be fundamental to success.

Keywords: biocompatible; bioscaffolds; cancer; extracellular vesicles; hydrogels; nanoparticles; tissue regeneration.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Sustained Delivery system of MSC derived Extracellular vesicles (EVs) for Tissue Regeneration. (Image created using www.Biorender.com-paid subscription, accessed on 29 June 2021, Biorender 2021).

References

    1. Davis M.E., Chen Z., Shin D.M. Nanoparticle therapeutics: An emerging treatment modality for cancer. Nat. Rev. Drug Discov. 2008;7:771–782. doi: 10.1038/nrd2614. - DOI - PubMed
    1. Hamidi M., Azadi A., Rafiei P. Hydrogel nanoparticles in drug delivery. Adv. Drug Deliv. Rev. 2008;60:1638–1649. doi: 10.1016/j.addr.2008.08.002. - DOI - PubMed
    1. Lim Y.H., Tiemann K.M., Hunstad D.A., Elsabahy M., Wooley K.L. Polymeric nanoparticles in development for treatment of pulmonary infectious diseases: Nanoparticles in treatment of pulmonary infectious diseases. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 2016;8:842–871. doi: 10.1002/wnan.1401. - DOI - PMC - PubMed
    1. Jin G.-Z., Chakraborty A., Lee J.-H., Knowles J.C., Kim H.-W. Targeting with nanoparticles for the therapeutic treatment of brain diseases. J. Tissue Eng. 2020;11:204173141989746. doi: 10.1177/2041731419897460. - DOI - PMC - PubMed
    1. Zolnik B.S., González-Fernández Á., Sadrieh N., Dobrovolskaia M.A. Minireview: Nanoparticles and the immune system. Endocrinology. 2010;151:458–465. doi: 10.1210/en.2009-1082. - DOI - PMC - PubMed

LinkOut - more resources