Title of article :
Grafting-from” synthesis and characterization of poly (2-ethyl-2- oxazoline)-b-poly (benzyl L-glutamate) micellar nanoparticles for potential biomedical applications
Author/Authors :
Mohammadi-Samani Soliman Department of Pharmaceutics - Shiraz School of Pharmacy - Shiraz University of Medical Sciences - Shiraz, Iran , Salmanpour Mohsen Department of Pharmaceutics - Shiraz School of Pharmacy - Shiraz University of Medical Sciences - Shiraz, Iran , Yousefi Gholamhossein Department of Pharmaceutics - Shiraz School of Pharmacy - Shiraz University of Medical Sciences - Shiraz, Iran , Tamaddon ali Center for Nanotechnology in Drug Delivery - Shiraz University of Medical Sciences - Shiraz, Iran
Abstract :
Recent advances in the field
of poly (2-oxazolines) as bio-inspired
synthetic pseudopeptides have proven
their potential biomedical applications
such as drug delivery and tissue
engineering.
Methods: In order to fabricate a
biodegradable micellar nanoparticle
of poly (2-ethyl 2-oxazoline)-b-poly
(benzyl L-glutamate) or pEOx-b-pBLG,
“grafting-from” synthesis approach
was used involving consecutive steps of cationic ring-opening polymerization of 2-ethyl-2-
oxazoline, amine functionalization of pEOx using 1-Boc-piperazine and N-carboxyanhydride
polymerization of γ-benzyl- L-glutamate. Following hydrolysis of the copolymer, the protecting
γ-benzyl groups were removed yielding a double-hydrophilic block ionomer of pEOx-bpoly
(L-glutamic acid). The polymers were characterized by FTIR, 1H-NMR, size exclusion
chromatography and differential scanning calorimetry (DSC). Aqueous assembly of the
polymers was investigated by pyrene assay, dynamic light scattering, and transmission electron
microscopy. MTT cytotoxicity assay was also performed to determine the cytocompatibility in
various tumor cell lines.
Results: The polymeric micelles presented a uni-modal size distribution with mean hydrodynamic
diameter of 149.8 ± 10.6 nm and critical aggregation concentration of 60 μg/mL. The average
molecular weight of pEOx increased from ~ 14 to 20 kDa for pEOx-b-poly (L-glutamic acid)
as determined by light scattering (Debye plot), indicating a successful copolymerization. MTT
assay showed little to no practical cytotoxicity at concentrations below 1 mg/mL.
Conclusion: Multi-step synthesis of pEOx-b-pBLG and subsequent alkaline hydrolysis were
performed to obtain the block ionomer pEOx-b-poly (L-glutamic acid). Both pEOx-based
copolymers can be considered for various potential applications such as loading and delivery of
drugs, genes, and contrast agents either by chemical conjugation or physical loading.
Keywords :
Grafting-from synthesis , Nano-assembly , Double hydrophilic block ionomer , Poly (2-oxazolines) functionalization , Ring-opening polymerization , Poly (L-glutamic acid)
Journal title :
Bioimpacts