{"title":"Development and characterization of chitosan-pluronic nanoparticles for tamoxifen delivery and cytotoxicity to MCF-7 cells","authors":"Rajath Othayoth, V. Karthik, K. Santhosh Kumar","doi":"10.1109/ICANMEET.2013.6609328","DOIUrl":null,"url":null,"abstract":"In this study, tamoxifen-loaded chitosan-pluronic nanoparticles have been prepared by an ionic gelation (IG) method. Particle size analysis, Scanning electron microscopy (SEM), Zeta potential measurements, Fourier transform infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC) were used for nanoparticle characterization. The cytotoxicity of the nanoparticles was assayed in the MCF-7 cell line. The optimized tamoxifen loaded nanoparticles had a spherical shape with positive charge and mean diameter 150 to 300 nm. The FT-IR and DSC studies found that the drug was dispersed in amorphous form due to its potent interaction with nanoparticles matrix. The maximum encapsulation efficiency was obtained at 8mg/ml tamoxifen. The tamoxifen loaded chitosan-pluronic nanoparticles had good blood compatibility and the particles were nontoxic to the MCF-7 cell line. All study results suggest that the nanoparticles could be used as an effective drug delivery carrier for the breast cancer treatment.","PeriodicalId":13708,"journal":{"name":"International Conference on Advanced Nanomaterials & Emerging Engineering Technologies","volume":"94 1","pages":"394-401"},"PeriodicalIF":0.0000,"publicationDate":"2013-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Conference on Advanced Nanomaterials & Emerging Engineering Technologies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ICANMEET.2013.6609328","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
In this study, tamoxifen-loaded chitosan-pluronic nanoparticles have been prepared by an ionic gelation (IG) method. Particle size analysis, Scanning electron microscopy (SEM), Zeta potential measurements, Fourier transform infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC) were used for nanoparticle characterization. The cytotoxicity of the nanoparticles was assayed in the MCF-7 cell line. The optimized tamoxifen loaded nanoparticles had a spherical shape with positive charge and mean diameter 150 to 300 nm. The FT-IR and DSC studies found that the drug was dispersed in amorphous form due to its potent interaction with nanoparticles matrix. The maximum encapsulation efficiency was obtained at 8mg/ml tamoxifen. The tamoxifen loaded chitosan-pluronic nanoparticles had good blood compatibility and the particles were nontoxic to the MCF-7 cell line. All study results suggest that the nanoparticles could be used as an effective drug delivery carrier for the breast cancer treatment.