{"title":"Targeted Gene Delivery to MCF-7 Cells via Polyspermine-PEG-Glucose/DNA Nanoparticles: Preparation and Characterization.","authors":"Sahar Mohajeri, Aytak Fathi Erdi, Hashem Yaghoubi","doi":"10.1007/s12033-025-01454-0","DOIUrl":null,"url":null,"abstract":"<p><p>Cationic polymers are positively charged polymers that have a high ability to electrostatically interact with negatively charged species, including nucleic acids. This property has led to the use of these polymers in various fields, including targeted drug delivery. In this study, biocompatible polyspermine-polyethylene glycol (PEG)-glucose (PSPG) nanoparticles were synthesized for DNA delivery to MCF-7 cells. Structural characterization was performed via Fourier transform infrared spectroscopy (FTIR), hydrogen nuclear magnetic resonance spectroscopy (<sup>1</sup>HNMR), thermogravimetric analysis (TGA), and differential thermal gravimetric (DTG) methods. The DNA-loaded nanoparticles exhibited a spherical morphology with smooth surfaces, as confirmed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Dynamic light scattering (DLS) revealed a particle size of 267 ± 10 nm and a surface charge of + 13.4 ± 1.3 mV. DNA release from PSPG was pH dependent, increasing at acidic pH (5.0, cancer cells) compared with physiological pH (7.4). The biocompatibility assessed via MTT demonstrated high gene transfer efficiency with minimal cytotoxicity. Agarose gel electrophoresis confirmed the protection of the DNA against enzymatic degradation. Gene delivery to MCF-7 cells was validated via fluorescence microscopy and flow cytometry, confirming successful transfection. These findings highlight the potential of polyspermine-PEG-glucose nanoparticles as efficient DNA carriers for targeted cancer therapy.</p>","PeriodicalId":18865,"journal":{"name":"Molecular Biotechnology","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Biotechnology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s12033-025-01454-0","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Cationic polymers are positively charged polymers that have a high ability to electrostatically interact with negatively charged species, including nucleic acids. This property has led to the use of these polymers in various fields, including targeted drug delivery. In this study, biocompatible polyspermine-polyethylene glycol (PEG)-glucose (PSPG) nanoparticles were synthesized for DNA delivery to MCF-7 cells. Structural characterization was performed via Fourier transform infrared spectroscopy (FTIR), hydrogen nuclear magnetic resonance spectroscopy (1HNMR), thermogravimetric analysis (TGA), and differential thermal gravimetric (DTG) methods. The DNA-loaded nanoparticles exhibited a spherical morphology with smooth surfaces, as confirmed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Dynamic light scattering (DLS) revealed a particle size of 267 ± 10 nm and a surface charge of + 13.4 ± 1.3 mV. DNA release from PSPG was pH dependent, increasing at acidic pH (5.0, cancer cells) compared with physiological pH (7.4). The biocompatibility assessed via MTT demonstrated high gene transfer efficiency with minimal cytotoxicity. Agarose gel electrophoresis confirmed the protection of the DNA against enzymatic degradation. Gene delivery to MCF-7 cells was validated via fluorescence microscopy and flow cytometry, confirming successful transfection. These findings highlight the potential of polyspermine-PEG-glucose nanoparticles as efficient DNA carriers for targeted cancer therapy.
期刊介绍:
Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.