TY - JOUR
T1 - PH-Induced Transformation of Biodegradable Multilamellar Nanovectors for Enhanced Tumor Penetration
AU - Cao, Shoupeng
AU - Abdelmohsen, Loai K.E.A.
AU - Shao, Jingxin
AU - Van Den Dikkenberg, Joep
AU - Mastrobattista, Enrico
AU - Williams, David S.
AU - Van Hest, Jan C.M.
PY - 2018/11/20
Y1 - 2018/11/20
N2 - Herein we describe biodegradable nanovectors comprised of block copolymers of poly(ethylene glycol) and poly(trimethylene carbonate) (PEG-PTMC) that change their morphology and surface charge when exposed to tumor environment conditions. Well-defined, drug-loaded nanovectors were prepared via direct hydration using liquid oligo(ethylene glycol) as a dispersant. Systematic introduction of basic imidazole-functional TMC derivatives, through modular polymerization, resulted in polymers that self-assembled in multilamellar nanoparticles (at neutral pH) and that were loaded with hydrophobic drugs. The resultant multilamellar nanovectors demonstrated a significant size reduction and charge reversal at pH ≈ 6.5, which yielded cationic nanovectors that were tailored for tumor penetration. In vitro studies using 3D heterospheroids demonstrate that this platform has excellent potential to promote enhanced tumor penetration under physiological conditions.
AB - Herein we describe biodegradable nanovectors comprised of block copolymers of poly(ethylene glycol) and poly(trimethylene carbonate) (PEG-PTMC) that change their morphology and surface charge when exposed to tumor environment conditions. Well-defined, drug-loaded nanovectors were prepared via direct hydration using liquid oligo(ethylene glycol) as a dispersant. Systematic introduction of basic imidazole-functional TMC derivatives, through modular polymerization, resulted in polymers that self-assembled in multilamellar nanoparticles (at neutral pH) and that were loaded with hydrophobic drugs. The resultant multilamellar nanovectors demonstrated a significant size reduction and charge reversal at pH ≈ 6.5, which yielded cationic nanovectors that were tailored for tumor penetration. In vitro studies using 3D heterospheroids demonstrate that this platform has excellent potential to promote enhanced tumor penetration under physiological conditions.
UR - http://www.scopus.com/inward/record.url?scp=85056739142&partnerID=8YFLogxK
U2 - 10.1021/acsmacrolett.8b00807
DO - 10.1021/acsmacrolett.8b00807
M3 - Article
AN - SCOPUS:85056739142
SN - 2161-1653
VL - 7
SP - 1394
EP - 1399
JO - ACS Macro Letters
JF - ACS Macro Letters
IS - 11
ER -