Abstract
Hyperbranched polyglycerol (hPG) has been used as a multivalent scaffold to develop a series of nanocarriers capable of high-affinity encapsulation of copper (Cu). A rationally selected set of Cu-complexing motifs has been conjugated to hPG hydroxyl groups to render the constructs potentially usable as exogenous sources of Cu for addressing different pathological conditions associated with Cu-deficiency. We have utilized a newly discovered route to attach Cu-binding domains exclusively within a hPG core by selective differentiation between the primary and secondary hydroxyl groups of the polyol. These hPG-derivatives were found to form a stable complex with Cu ions depending on the type of immobilized ligands and corresponding degree of functionalization. In addition, these Cu-bearing nano-complexes demonstrated moderately cationic surface charge resulting in adjustable protein-binding characteristics and low cellular toxicity profile. We envision that these Cu-loaded hPG nanocarriers can be used as a stable platform to transport the metal ion across the systemic circulation to supply bioavailable quantity of Cu in disease-afflicted tissues.
Highlights
Recapitulation of homeostatic level of electrolytes or trace element concentration is one of the mainstays of clinical management for a number of pathological conditions, including but not limited to blood disorders, renal failure, acute poisoning, cancer and skeletal system-related diseases
Molecules 2018, 23, 1281 complex instability, bioavailability, circulation lifetime and dosing frequency, we have reported a library of macromolecular, multivalent, Cu-encapsulating nanocarrier platforms based on hyperbranched polyglycerol [12,13,14]
Compared to linear polymers of analogous molecular weight, spatially globular architecture of solubility, both of which can be readily modulated by post-synthetic functionalization of peripheral hyperbranched polyglycerol (hPG) gives rise to a number of interesting properties such as reduced viscosities and enhanced water hydroxyl functional group through alcohol-group chemistry
Summary
Recapitulation of homeostatic level of electrolytes or trace element concentration is one of the mainstays of clinical management for a number of pathological conditions, including but not limited to blood disorders, renal failure, acute poisoning, cancer and skeletal system-related diseases. Exogenous supply of Cu is mediated by soluble oral administration of soluble metal salts or metal complexes in disease conditions where Cu supplementation is required. Potential beneficial effects of oral intake of Cu (II)-orotate-dihydrate (8 mg Cu daily) were investigated in AD patients. Results demonstrated that oral Cu intake has neither a detrimental nor a promoting effect on the progression of AD, Cu treatment stabilized plasma and CSF levels in AD patients and antagonized the unbalanced Cu levels likely by activating the homeostatic system [6,7]. Studies with the antibiotic clioquinol (CQ), an 8-OH quinoline with a moderate affinity for Cu2+ and Zn2+ , the lipophilic chelator (DP109), isatin-Schiff base Cu (II)-complexes and metal bis(thiosemicarbazonato) complexes confirmed that promoting Cu uptake is a reasonable treatment strategy [8,9,10,11] in
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