Inorganic Polyphosphate: Coacervate Formation and Functional Significance in Nanomedical Applications.

Heinz C Schröder, Meik Neufurth, Huan Zhou, Shunfeng Wang, Xiaohong Wang, Werner E G Müller

Journal: International journal of nanomedicine 2022;17():5825-5850

PMID: 36474526

Abstract

["Inorganic polyphosphates (polyP) are long-chain polymers of orthophosphate residues, which, depending on the external conditions, can be present both physiologically and synthetically in either soluble, nanoparticulate or coacervate form. In recent years, these polymers have received increasing attention due to their unprecedented ability to exhibit both morphogenetic and metabolic energy delivering properties. There are no other physiological molecules that contain as many metabolically utilizable, high-energy bonds as polyP, making these polymers of particular medical interest as components of advanced hydrogel scaffold materials for potential applications in ATP-dependent tissue regeneration and repair. However, these polymers show physiological activity only in soluble form and in the coacervate phase, but not as stable metal-polyP nanoparticles. Therefore, understanding the mechanisms of formation of polyP coacervates and nanoparticles as well as their transformations is important for the design of novel materials for tissue implants, wound healing, and drug delivery and is discussed here.",{"copyright":"\u00a9 2022 Schr\u00f6der et al."}]
Address: ERC Advanced Investigator Group, Institute for Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.; School of Health Sciences and Biomedical Engineering, Heibei University of Technology, Tianjin, People's Republic of China.
MeSH Terms: Polyphosphates
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.