Stimuli-responsive polymeric nanoparticles for nanomedicine
- PMID: 25319803
- DOI: 10.1002/cmdc.201402290
Stimuli-responsive polymeric nanoparticles for nanomedicine
Abstract
Nature continues to be the ultimate in nanotechnology, where polymeric nanometer-scale architectures play a central role in biological systems. Inspired by the way nature forms functional supramolecular assemblies, researchers are trying to make nanostructures and to incorporate these into macrostructures as nature does. Recent advances and progress in nanoscience have demonstrated the great potential that nanomaterials have for applications in healthcare. In the realm of drug delivery, nanomaterials have been used in vivo to protect the drug entity in the systemic circulation, ensuring reproducible absorption of bioactive molecules that do not naturally penetrate biological barriers, restricting drug access to specific target sites. Several building blocks have been used in the formulation of nanoparticles. Thus, stability, drug release, and targeting can be tailored by surface modification. Herein the state of the art of stimuli-responsive polymeric nanoparticles are reviewed. Such systems are able to control drug release by reacting to naturally occurring or external applied stimuli. Special attention is paid to the design and nanoparticle formulation of these so-called smart drug-delivery systems. Future strategies for further developments of a promising controlled drug delivery responsive system are also outlined.
Keywords: drug delivery; nanomedicine; nanoparticles; polymers; stimuli-responsive.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Similar articles
-
Classification of stimuli-responsive polymers as anticancer drug delivery systems.Drug Deliv. 2015 Feb;22(2):145-55. doi: 10.3109/10717544.2014.887157. Epub 2014 Feb 19. Drug Deliv. 2015. PMID: 24547737 Review.
-
Recent advances towards the fabrication and biomedical applications of responsive polymeric assemblies and nanoparticle hybrid superstructures.Dalton Trans. 2015 Mar 7;44(9):3904-22. doi: 10.1039/c4dt03609c. Dalton Trans. 2015. PMID: 25579704
-
Functional block copolymer assemblies responsive to tumor and intracellular microenvironments for site-specific drug delivery and enhanced imaging performance.Chem Soc Rev. 2013 Sep 7;42(17):7289-325. doi: 10.1039/c3cs60048c. Epub 2013 Apr 3. Chem Soc Rev. 2013. PMID: 23549663 Review.
-
Polymeric micelles with stimuli-triggering systems for advanced cancer drug targeting.J Drug Target. 2014 Aug;22(7):584-99. doi: 10.3109/1061186X.2014.936872. J Drug Target. 2014. PMID: 25012066 Review.
-
Recent Developments in the Application of Polymeric Nanoparticles as Drug Carriers.Adv Clin Exp Med. 2015 Sep-Oct;24(5):749-58. doi: 10.17219/acem/31802. Adv Clin Exp Med. 2015. PMID: 26768624
Cited by
-
Recent advances of bioresponsive polymeric nanomedicine for cancer therapy.Nano Res. 2023;16(2):2660-2671. doi: 10.1007/s12274-022-5002-2. Epub 2022 Nov 15. Nano Res. 2023. PMID: 36405982 Free PMC article. Review.
-
Self-Catalyzed Hydrolysis of Nitrile-Containing RAFT Chain-Transfer Agent and Its Impact upon Polymerization Control of Methacrylic Monomers.ACS Macro Lett. 2024 May 21;13(5):565-570. doi: 10.1021/acsmacrolett.4c00112. Epub 2024 Apr 18. ACS Macro Lett. 2024. PMID: 38636106 Free PMC article.
-
Strategies for the development of metalloimmunotherapies.Nat Biomed Eng. 2024 Sep;8(9):1073-1091. doi: 10.1038/s41551-024-01221-7. Epub 2024 Jun 24. Nat Biomed Eng. 2024. PMID: 38914800 Free PMC article. Review.
-
Ultrasound-Activated Nanomaterials for Therapeutics.Bull Chem Soc Jpn. 2020 Feb 15;93(2):220-229. doi: 10.1246/bcsj.20190346. Epub 2019 Dec 12. Bull Chem Soc Jpn. 2020. PMID: 39650549 Free PMC article.
-
Exploring the Potential of Nanogels: From Drug Carriers to Radiopharmaceutical Agents.Adv Healthc Mater. 2024 Jan;13(1):e2301404. doi: 10.1002/adhm.202301404. Epub 2023 Sep 28. Adv Healthc Mater. 2024. PMID: 37717209 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources