Modified Polyethylenimine: Self Assemble Nanoparticle Forming Polymer for pDNA Delivery

سال انتشار: 1387
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 179

فایل این مقاله در 8 صفحه با فرمت PDF قابل دریافت می باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

JR_IJBMS-11-1_005

تاریخ نمایه سازی: 27 مهر 1400

چکیده مقاله:

Objective Polyethylenimine (PEI), a readily available synthetic polycation which has high transfection efficiency owing to its buffering capacity was introduced for transfection a few years ago. But it has been reported that PEI is cytotoxic in many cell lines. In this study, in order to enhance the transfection efficiency of ۱۰ kDa PEI and reduce its toxicity, hydrophobic residues were grafted on PEI. Materials and Methods PEI polymers were modified by adding hydrophobic chains to the primary amines of PEI in different degrees of grafting using bromoacetic acid derivatives with different lengths. These polymers were complexed with plasmid DNA at different C/P ratios and the resulting nanoparticles were characterized by dynamic light scattering and EtBr-DNA binding assay to determine particle sizes and complex formation, respectively. Cytotoxicity and transfection efficiency of the polymers were also tested in cultured Neuro۲a cell line. Results DNA condensation measurement revealed that the resulted polymers could form polyplexes with plasmid DNA and they have the ability to condense DNA in relatively low amounts of polymers. Particle size measurement of polyplexes showed that they form particles in the size range of below ۱۹۰ nm. Transfection experiments showed that polymers which have been modified with hexanoic derivative could transfect pDNA as good as ۲۵ kDa PEI with the advantage of being much less toxic. Conclusion Results indicate that the structure modifications of PEI accomplished in this study play a significant role in increasing the transfection efficiency and without inducing the cytotoxicity compared to PEI itself.  

نویسندگان

Reza K. Oskuee

Department of Biotechnology, Pharmaceutical and Biotechnology Research Centers, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

Ali Dehshahri

Department of Biotechnology, Pharmaceutical and Biotechnology Research Centers, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

Wayne. T. Shier

Department of Medicinal Chemistry, University of Minnesota-Twin Cities, Minneapolis, MN ۵۵۴۵۵, USA

Mohammad Ramezani

Department of Biotechnology, Pharmaceutical and Biotechnology Research Centers, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

مراجع و منابع این مقاله:

لیست زیر مراجع و منابع استفاده شده در این مقاله را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود مقاله لینک شده اند :
  • Cavazzano-Calvo M, Thrasher A, Mavilio F. The future of gene ...
  • Forrest LM, Meister EG, Koerber J, Pack D. Partial acetylation ...
  • Lungwitz U, Breunig MT, Blunk Gopferich A. Polyethylenimine-based non-viral gene ...
  • El-Aneed A. An overview of current delivery systems in cancer ...
  • Lehrman S. Virus treatment questioned after gene therapy death. Nature ...
  • Liu Q, Muruve DA. Molecular basis of the inflammatory response ...
  • Sun JY, Anand-Jawa V, Chatterjee S, Wong K K. Immune ...
  • Merdan T, Kopecek J, Kissel T. Prospects for cationic polymers ...
  • Zhang S, Xu Y, Wang B, Qiao W, Liu D, ...
  • Boussif O, Lezoualc’h F, Zanta MA. A versatile vector for ...
  • Cho YW, Kim J, Park K. Polycation gene delivery systems: ...
  • Kursa M, Walker GF, Roessler V, Ogris M, Roedl W, ...
  • Kircheis R, Schuller S, Brunner S, Ogris M, Heide KH, ...
  • Ogris M, Walker G, Blessing T, Kircheis R, Wolschek M, ...
  • Kircheis R, Wightman L, Schreiber A, Robitza B, Rossler V, ...
  • Tseng WC, Jong CM. Improved stability of polycationic vector by ...
  • Kim S, Choi JS, Jang HS, Suh H, Park J. ...
  • Thomas M, Klibanov AM. Non-viral gene therapy: polycation mediated DNA ...
  • Thomas M, Klibanov AM. Enhancing polyethylenimine’s delivery of plasmid DNA ...
  • Brownlie A, Uchegbu A, Schatzlein AG. PEI-based vesicle-polymer hybrid gene ...
  • Snyder SL, Sobocinski PZ. An improved ۲, ۴, ۶-trinitrobenzenesulfonic acid ...
  • Kichler A, Leborgne Ch, Coeytaux E, Danos O. Polyethylenimine-mediated gene ...
  • Liu D, Ren T, Gao X. Cationic transfection lipids. Curr ...
  • Neu M, Fischer D, Kissel T. Recent advances in rational ...
  • Doody AM, Korley JN, Dang KP, Zawaneh PN, Putnam D. ...
  • Chen DJ, Majors BS, Zelikin A, Putnam D. Structure–function relationships ...
  • Gabrielson NP, Pack DW. Acetylation of polyethylenimine enhances gene delivery ...
  • Fischer D, Bieber T, Li Y, Elsasser HP, Kissel T. ...
  • Godbey WT, Wu KK, Mikos AG. Size matters: molecular weight ...
  • Moghimi SM, Symonds P, Murray JC, Hunter AC, Debska G, ...
  • Hunter AC. Molecular hurdles in polyfectin design and mechanistic background ...
  • Thomas M, Lu JJ, Ge O, Zhang C, Chen J, ...
  • نمایش کامل مراجع