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
. 2024 Jan 14;10(1):61.
doi: 10.3390/gels10010061.

Single-, Dual-, and Multi-Stimuli-Responsive Nanogels for Biomedical Applications

Affiliations
Review

Single-, Dual-, and Multi-Stimuli-Responsive Nanogels for Biomedical Applications

Naveen Kumar et al. Gels. .

Abstract

In recent years, stimuli-responsive nanogels that can undergo suitable transitions under endogenous (e.g., pH, enzymes and reduction) or exogenous stimuli (e.g., temperature, light, and magnetic fields) for on-demand drug delivery, have received significant interest in biomedical fields, including drug delivery, tissue engineering, wound healing, and gene therapy due to their unique environment-sensitive properties. Furthermore, these nanogels have become very popular due to some of their special properties such as good hydrophilicity, high drug loading efficiency, flexibility, and excellent biocompatibility and biodegradability. In this article, the authors discuss current developments in the synthesis, properties, and biomedical applications of stimulus-responsive nanogels. In addition, the opportunities and challenges of nanogels for biomedical applications are also briefly predicted.

Keywords: drug delivery; nanogels; nanomedicine; stimuli-responsiveness; tissue engineering.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Schematic representation of (A) chemical and (B) physical cross-linking reactions during nanogel preparation.
Figure 2
Figure 2
Linkers and their cleavage susceptibility conditions.
Figure 3
Figure 3
Classification of materials used in nanogel synthesis.
Figure 4
Figure 4
Schematic representation of different nanogel preparation methods.
Figure 5
Figure 5
Schematic representation of cross-linked copolymer network structure of poly (Am-co-DADMAC) with NN-MBA.
Figure 6
Figure 6
Schematic representation of stimuli-responsive nanogels.
Figure 7
Figure 7
Chemical structure of some important pH-sensitive cationic and anionic polymers and their pKa values.
Figure 8
Figure 8
Structures of some temperature-sensitive polymers.
Figure 9
Figure 9
Different functional groups and photoreaction types used to design photoresponsive nanogels.
Figure 10
Figure 10
Dual- and multi-stimuli-responsive polymeric NPs as novel controlled drug delivery systems.

References

    1. Sana S.S., Arla S.K., Badineni V., Boya V.K.N. Development of poly (acrylamide-co-diallyldimethylammoniumchloride) nanogels and study of their ability as drug delivery devices. SN Appl. Sci. 2019;1:1716. doi: 10.1007/s42452-019-1742-3. - DOI
    1. Suner S.S., Sahiner M., Sengel S.B., Rees D., Reed W.F., Nurettin S. In: Responsive Biopolymer-Based Microgels/Nanogels for Drug Delivery Applications. In Stimuli Responsive Polymeric Nanocarriers for Drug Delivery Applications—Types and Triggers. Hamdy A.S., Abu-Thabit N.Y., editors. Woodhead Publishing; Sawston, UK: 2018. pp. 453–500.
    1. Shah S., Rangaraj N., Laxmikeshav K., Sampathi S. Nanogels as drug carriers—Introduction, chemical aspects, release mechanisms and potential applications. Int. J. Pharm. 2020;581:119268. doi: 10.1016/j.ijpharm.2020.119268. - DOI - PubMed
    1. Sahiner N., Sagbas S., Aktas N. Preparation of Macro-, Micro-, and Nano-Sized Poly(Tannic Acid) Particles with Controllable Degradability and Multiple Biomedical Uses. Polym. Degrad. Stab. 2016;129:96–105. doi: 10.1016/j.polymdegradstab.2016.04.010. - DOI
    1. Zha L., Banik B., Alexis F. Stimulus responsive nanogels for drug delivery. Soft Matter. 2011;7:5908–5916. doi: 10.1039/c0sm01307b. - DOI

LinkOut - more resources