Казанский (Приволжский) федеральный университет, КФУ
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PROPOXYLATION OF CATIONIC POLYMERS PROVIDES A NOVEL APPROACH TO CONTROLLABLE MODULATION OF THEIR CELLULAR TOXICITY AND INTERACTION WITH NUCLEIC ACIDS
Форма представленияСтатьи в зарубежных журналах и сборниках
Год публикации2016
Языканглийский
  • Абдуллин Тимур Илдарович, автор
  • Бадеев Юрий Владимирович, автор
  • Салахиева Диана Витальевна, автор
  • Шевченко Веста Денисовна, автор
  • Штырлин Юрий Григорьевич, автор
  • Библиографическое описание на языке оригинала Propoxylation of cationic polymers provides a novel approach to controllable modulation of their cellular toxicity and interaction with nucleic acids. Vesta D. Shevchenko, Diana V. Salakhieva, Abdulla A. Yergeshov, Yuriy V. Badeev, Yurii G. Shtyrlin, Timur I. Abdullin //Materials Science and Engineering C 69 (2016) 60–67.
    Аннотация An effective chemical approach to modulation of biological interactions of cationic polymers was proposed and tested using polyethyleneimine (PEI) as a drug carrier. Branched 25 kDa PEI was modified in the reaction with propylene oxide (PO) to produce a series of propoxylated PEIs with NH groups grafted by single or oligomer PO units. Clear relationships between the propoxylation degree and biological effects, such as interaction with plasmid DNA, hemolytic, cytotoxic, and pro-apoptotic activities were revealed for PEIs modified upon PO / NH molar ratio of 0.5, 0.75, 1.0 and 3.0. The partial modification of available cationic centers up to 100 % is predominantly accompanied by a significant gradual reduction in polycation adverse effects, while ability of complex formation with plasmid DNA is being preserved. Grafted PEI with 0.75 PO / NH ratio provides better protection from nuclease degradation and transfection activity compared with other modified PEIs.
    Ключевые слова Cationic polymers; Polyethyleneimine; Propoxylation; Biocompatibility; Cellular toxicity; Gene delivery
    Название журнала Materials Science & Engineering C
    URL http://dx.doi.org/10.1016/j.msec.2016.05.024
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