Coating of DNA/poly(L-lysine) complexes by covalent attachment of poly[N-(2-hydroxypropyl)methacrylamide]
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
16398506
DOI
10.1021/bm050524x
Knihovny.cz E-zdroje
- MeSH
- aminace MeSH
- chlorid sodný MeSH
- DNA chemie MeSH
- hydrolýza MeSH
- kinetika MeSH
- kyseliny polymethakrylové chemie MeSH
- molekulární struktura MeSH
- molekulová hmotnost MeSH
- nitrobenzeny chemie MeSH
- polylysin chemie MeSH
- spektrofotometrie ultrafialová MeSH
- thiazolidiny MeSH
- thiazoly chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 2-mercaptothiazoline MeSH Prohlížeč
- chlorid sodný MeSH
- DNA MeSH
- Duxon MeSH Prohlížeč
- kyseliny polymethakrylové MeSH
- nitrobenzeny MeSH
- polylysin MeSH
- thiazolidiny MeSH
- thiazoly MeSH
N-(2-Hydroxypropyl)methacrylamide (HPMA) copolymers (pHPMA) containing 4-nitrophenyl ester (ONp) or thiazolidine-2-thione (TT) reactive groups in side chains and telechelic/semitelechelic pHPMA with TT groups were designed as highly hydrophilic biocompatible polymers suitable for chemical coating of polyelectrolyte-based DNA-containing nanoparticles bearing amino groups on the surface. The course of the coating reaction carried out in aqueous solution was evaluated on model self-assembling polyelectrolyte DNA/poly(L-lysine) (DNA/PLL) complexes either by monitoring the amount of residual polymer reactive groups by UV spectroscopy or by monitoring changes in the weight-average molecular weight and hydrodynamic size of the complexes using light scattering methods. Physicochemical stability of the coated complexes in buffered saline solution was also investigated. Contrary to uncoated particles, the coated complexes showed remarkable stability to aggregate in 0.15 M NaCl. Coating with pHPMA had practically no effect on the size distribution of the most stable complexes prepared by complexation of DNA with high-molecular-weight PLL (M(w) = 134 000) as shown by dynamic light scattering. The coating reaction was faster and more efficient with multivalent HPMA copolymers containing TT reactive groups than that with HPMA copolymers containing ONp groups.
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