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Synthesis and characterization of poly (N-isopropylacrylamide)-g-carboxymethyl chitosan copolymer-based doxorubicin-loaded polymeric nanoparticles for thermoresponsive drug release
被引:35
|作者:
Antoniraj, M. Gover
[1
]
Kumar, C. Senthil
[1
]
Kandasamy, Ruckmani
[1
,2
]
机构:
[1] Anna Univ, Dept Pharmaceut Technol, Ctr Excellence Nanobio Translat Res CENTRE, BIT Campus, Tiruchirappalli 620024, Tamil Nadu, India
[2] Anna Univ, Natl Facil Drug Dev Cademia Pharmaceut & Allied I, BIT Campus, Tiruchirappalli 620024, Tamil Nadu, India
关键词:
Poly (N-isopropylacrylamide);
O-carboxymethyl chitosan;
Polymer synthesis;
Smart polymers;
Thermal properties;
MICELLES;
CHITOSAN-GRAFT-POLY(N-ISOPROPYLACRYLAMIDE);
DELIVERY;
BEHAVIOR;
ACID);
D O I:
10.1007/s00396-015-3804-4
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Thermoresponsive graft copolymer (PNIPAm-g-OCMC) with PNIPAm and chitosan was prepared by conjugation of amine-terminated PNIPAm with O-carboxymethylchitosan through graft-onto method. The results of FTIR and proton NMR confirmed the synthesis of a copolymer. Furthermore, XRD analysis revealed conjugation reaction of polymeric materials. Doxorubicin-loaded polymeric nanoparticles (D-PNPs) were fabricated using copolymer by gelation method. Morphology illustration through TEM showed the spherical shape of D-PNPs. Particles size measurement study indicates thermoresponsive properties of D-PNPs at various temperatures. Lower critical solution temperature (LCST) of D-PNPs was obtained at 38 A degrees C predicted by turbidimetry analysis. Release studies at three different temperatures notified that thermoresponsive doxorubicin release of D-PNPs. The release of doxorubicin was slower at 25 A degrees C, moderately released at 37 A degrees C, and faster released at 42 A degrees C due to adjustment of the framework of the D-PNPs. Based on the results such as transmittance measurement, particle size observation, and release studies, we declare that the D-PNPs exhibit temperature-responsive behavior, which could make them appropriate for a thermoresponsive drug delivery.
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页码:527 / 535
页数:9
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