TY - JOUR
T1 - Biodegradable polyphosphoester micelles act as both background-free 31P magnetic resonance imaging agents and drug nanocarriers
AU - Koshkina, Olga
AU - Rheinberger, Timo
AU - Flocke, Vera
AU - Windfelder, Anton
AU - Bouvain, Pascal
AU - Hamelmann, Naomi M.
AU - Paulusse, Jos M.J.
AU - Gojzewski, Hubert
AU - Flögel, Ulrich
AU - Wurm, Frederik R.
N1 - Funding Information:
We thank Dr. Diego Resendiz Lara (UT), Dr. Ricardo E.P. Martinho (UT), Dr. Mark Hempenius (UT), Dr. Sandra S.M.C. Michel-Souzy (UT), Bianca Ruel (UT), Clemens Padberg (UT), Ramon Ten Elshof (UT), Richard Egberink (UT), and Prof. Dr. Andreas Vilcinskas (IME). We acknowledge Alexander von Humboldt Foundation (OK), Dutch Research Council NWO grant OCENW.XS21.2.066 (OK), Deutsche Forschungsgemeinschaft DFG grant INST 208/764-1 FUGG (UF).
Funding Information:
We thank Dr. Diego Resendiz Lara (UT), Dr. Ricardo E.P. Martinho (UT), Dr. Mark Hempenius (UT), Dr. Sandra S.M.C. Michel-Souzy (UT), Bianca Ruel (UT), Clemens Padberg (UT), Ramon Ten Elshof (UT), Richard Egberink (UT), and Prof. Dr. Andreas Vilcinskas (IME). We acknowledge Alexander von Humboldt Foundation (OK), Dutch Research Council NWO grant OCENW.XS21.2.066 (OK), Deutsche Forschungsgemeinschaft DFG grant INST 208/764-1 FUGG (UF).
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/7/19
Y1 - 2023/7/19
N2 - In vivo monitoring of polymers is crucial for drug delivery and tissue regeneration. Magnetic resonance imaging (MRI) is a whole-body imaging technique, and heteronuclear MRI allows quantitative imaging. However, MRI agents can result in environmental pollution and organ accumulation. To address this, we introduce biocompatible and biodegradable polyphosphoesters, as MRI-traceable polymers using the 31P centers in the polymer backbone. We overcome challenges in 31P MRI, including background interference and low sensitivity, by modifying the molecular environment of 31P, assembling polymers into colloids, and tailoring the polymers’ microstructure to adjust MRI-relaxation times. Specifically, gradient-type polyphosphonate-copolymers demonstrate improved MRI-relaxation times compared to homo- and block copolymers, making them suitable for imaging. We validate background-free imaging and biodegradation in vivo using Manduca sexta. Furthermore, encapsulating the potent drug PROTAC allows using these amphiphilic copolymers to simultaneously deliver drugs, enabling theranostics. This first report paves the way for polyphosphoesters as background-free MRI-traceable polymers for theranostic applications.
AB - In vivo monitoring of polymers is crucial for drug delivery and tissue regeneration. Magnetic resonance imaging (MRI) is a whole-body imaging technique, and heteronuclear MRI allows quantitative imaging. However, MRI agents can result in environmental pollution and organ accumulation. To address this, we introduce biocompatible and biodegradable polyphosphoesters, as MRI-traceable polymers using the 31P centers in the polymer backbone. We overcome challenges in 31P MRI, including background interference and low sensitivity, by modifying the molecular environment of 31P, assembling polymers into colloids, and tailoring the polymers’ microstructure to adjust MRI-relaxation times. Specifically, gradient-type polyphosphonate-copolymers demonstrate improved MRI-relaxation times compared to homo- and block copolymers, making them suitable for imaging. We validate background-free imaging and biodegradation in vivo using Manduca sexta. Furthermore, encapsulating the potent drug PROTAC allows using these amphiphilic copolymers to simultaneously deliver drugs, enabling theranostics. This first report paves the way for polyphosphoesters as background-free MRI-traceable polymers for theranostic applications.
UR - http://www.scopus.com/inward/record.url?scp=85165328011&partnerID=8YFLogxK
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:001037980500004
U2 - 10.1038/s41467-023-40089-0
DO - 10.1038/s41467-023-40089-0
M3 - Article
C2 - 37468502
AN - SCOPUS:85165328011
SN - 2041-1723
VL - 14
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 4351
ER -