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 Jun;44(6):1946-58.
doi: 10.1007/s10439-016-1637-z. Epub 2016 May 9.

Methods for Generating Hydrogel Particles for Protein Delivery

Affiliations
Review

Methods for Generating Hydrogel Particles for Protein Delivery

Allen L Liu et al. Ann Biomed Eng. 2016 Jun.

Abstract

Proteins represent a major class of therapeutic molecules with vast potential for the treatment of acute and chronic diseases and regenerative medicine applications. Hydrogels have long been investigated for their potential in carrying and delivering proteins. As compared to bulk hydrogels, hydrogel microparticles (microgels) hold promise in improving aspects of delivery owing to their less traumatic route of entry into the body and improved versatility. This review discusses common methods of fabricating microgels, including emulsion polymerization, microfluidic techniques, and lithographic techniques. Microgels synthesized from both natural and synthetic polymers are discussed, as are a series of microgels fashioned from environment-responsive materials.

Keywords: Growth factor; Hydrogel; Microgel; Microparticle; PEG; PNIPAM; Protein delivery.

PubMed Disclaimer

Conflict of interest statement

Statement No conflicts of interest.

Figures

Figure 1
Figure 1
Advantages of microgels as a delivery vehicle as compared to bulk hydrogels. (A) Microgels have a less traumatic route of administration, as they can be injected via needle or catheter as compared to a more-involved surgery to implant a bulk hydrogel. (B) Microgels conform to the defect or cavity in which they are placed, which results in superior coverage of the defect as compared to preformed bulk hydrogels. (C) Microgels have the potential to be simultaneously delivered with other microgels carrying different therapeutics.
Figure 2
Figure 2
Strategies to control protein release from microgels. Control over mesh size, the ability to utilize protease-degradable crosslinkers, and incorporation of stimuli-responsive polymers all modulate protein release.
Figure 3
Figure 3
Summary of common microgel synthesis schemes.

References

    1. Albrecht K, Bernkop-Schnurch A. Thiomers: forms, functions and applications to nanomedicine. Nanomedicine (Lond) 2007;2:41–50. - PubMed
    1. Allazetta S, Hausherr TC, Lutolf MP. Microfluidic synthesis of cell-type-specific artificial extracellular matrix hydrogels. Biomacromolecules. 2013;14:1122–1131. - PubMed
    1. Allazetta S, Kolb L, Zerbib S, Bardy J, Lutolf MP. Cell-Instructive Microgels with Tailor-Made Physicochemical Properties. Small. 2015;11:5647–5656. - PubMed
    1. An Y, Zhang L, Xiong S, Wu S, Xu M, Xu Z. Fluorine-containing thermo-sensitive microgels as carrier systems for biomacromolecules. Colloids and Surfaces B: Biointerfaces. 2012;92:246–253. - PubMed
    1. Bae KH, Lee F, Xu K, Keng CT, Tan SY, Tan YJ, Chen Q, Kurisawa M. Microstructured dextran hydrogels for burst-free sustained release of PEGylated protein drugs. Biomaterials. 2015;63:146–157. - PubMed

Publication types