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.
引用
收藏
页码:527 / 535
页数:9
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