Exploration of the Effect of Chitosan and Crosslinking Agent Concentration on the Properties of Dual Responsive Chitosan-g-Poly (N-Isopropylacrylamide) Co-polymeric Particles

被引:13
作者
Patil, Archana S. [1 ]
Gadad, Anand P. [1 ]
Hiremath, Ravindra D. [2 ]
Dandagi, Panchakshari M. [1 ]
机构
[1] KLE Univ, Coll Pharm, Dept Pharmaceut, Belagavi 590010, Karnataka, India
[2] KLE Soc, Coll Pharm, Dept Pharmaceut Chem, Akkol Rd, Nippani, Karnataka, India
关键词
Chitosan; N-isopropylacrylamide; N; N-methylenebisacrylamide; Chitosan-g-poly (N-isopropylacrylamide); Co-polymer; TUMOR EXTRACELLULAR PH; SHELL COPOLYMER LATEX; SELF-ASSEMBLY METHOD; DRUG-DELIVERY; CONTROLLED-RELEASE; NANOPARTICLES; TEMPERATURE; MICROGELS; HYDROGELS; POLY(N-ISOPROPYLACRYLAMIDE);
D O I
10.1007/s10924-017-0971-z
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The objective of the present study was to synthesize and evaluate the effect of change in concentration of chitosan (CS) and N,N-methylenebisacrylamide (MBA)- a cross linking agent, on various properties such as lower critical solution temperature (LCST), zeta potential, particle size and poly dispersity index (PDI) of the synthesized co-polymer. Nine different formulations of chitosan-g-poly (N-isopropylacrylamide) (CS-g-PNIPAAm) co-polymer with varying CS and MBA concentrations were synthesized by a surfactant free dispersion copolymerization method. The synthesized co-polymer was further characterized and confirmed for its structure, morphology, particle size, zeta-potential, thermo and pH responsive properties, in-vitro cyto-compatability and stability studies using various analytical tools. The data confirms the successful synthesis of co-polymer. The increase in the concentrations of CS and MBA during the polymerization of co-polymer, resulted in proportional increase of LCST and zeta potential with decrease in particle size of co-polymeric nanoparticles. pH responsive studies showed that as the pH of the medium increases particle size and zeta potential decreases with increase in LCST of co-polymeric nanoparticles. From the results, it can be inferred that the synthesized co-polymeric nanoparticles exerted thermo and pH responsive properties with biocompatibility. By varying the CS and MBA concentrations in the co-polymer, desired LCST, particle size and zeta potential for co-polymeric nanoparticles can be obtained and thus the synthesized co-polymer may have great potential to be used as a drug carrier (nanoform) with both thermo and pH responsiveness.
引用
收藏
页码:596 / 606
页数:11
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