Sustained Release of Vascular Endothelial Growth Factor from Poly(ε-caprolactone-PEG-ε-caprolactone)-b-Poly(l-lactide) Multiblock Copolymer Microspheres
نویسندگان
چکیده
منابع مشابه
Incomplete protein release from hydrophilic poly(D,L-lactide-PEG)-b-poly(ε-caprolactone) implants
In this study, novel hydrophilic multiblock copolymers composed of semi-crystalline poly(ε-caprolactone) [PCL] blocks and amorphous blocks consisting of poly(D,Llactide) (PDLA) and poly(ethylene glycol) (PEG) [PDLA-PEG] were synthesized. The block ratio of these [PDLA-PEG]-b-[PCL] multiblock copolymers was varied and the degradation of implants prepared of these polymers by hot melt extrusion (...
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Poly(L-lactide-co-ε-caprolactone) nanofibers with heparin incorporated were successfully fabricated by coaxial electrospinning. The morphologies of electrospun nanofibers were studied by scanning electron microscopy (SEM), and a significant decrease in fiber diameter was observed with increasing heparin concentration. The transmission electron microscopy (TEM) images indicated that coaxial elec...
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Bioresorbable, aliphatic polyesters are known in medicine where serve as orthopedic devices (e.g., rods, pins and screws) or sutures and staples in wound closure. Moreover, such materials are extensively stud- ied as scaffolds--three-dimensional structures for tissue engineering but also drug delivery systems (DDS). The aim of this study was to determine the release profile of paclitaxel, one o...
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Fully biodegradable and surface-functionalized poly(D,L-lactide) (PLA) nanoparticles have been prepared by a co-precipitation technique. Novel amphiphilic random copolyesters P(CL-co-γXCL) were synthesized by controlled copolymerization of ε-caprolactone and ε-caprolactone substituted in the γ-position by a hydrophilic X group, where X is either a cationic pyridinium (γPyCL) or a non-ionic hydr...
متن کاملFormulation, and Evaluation of Pentoxifylline-Loaded Poly(ε-caprolactone) Microspheres
Pentoxifylline-loaded poly(epsilon-caprolactone) microspheres were prepared by solvent evaporation technique with different drug to carrier ratio F1 (1:3), F2 (1:4), F3 (1:5) and F4 (1:6). The microspheres were characterized for particle size, scanning electron microscopy, FT-IR study, percentage yield, drug entrapment, stability studies and for in vitro release kinetics. The shape of microsphe...
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ژورنال
عنوان ژورنال: ACS Omega
سال: 2019
ISSN: 2470-1343,2470-1343
DOI: 10.1021/acsomega.9b01272