Abstract

Two high molecular weight copolymers of poly(N-isopropylacrylamide) (PNIPAM) densely grafted with short poly(ethylene oxide) (PEO) chains (PNIPAM-g-PEO) were studied by NMR and laser light scattering. The long PNIPAM chains with densely grafted PEO branches had a random coil conformation at very dilute concentrations and low temperatures (i.e., T ≤ 30 °C), When the temperature was increased above 31 °C, the copolymers could undergo a broad coil-to-globule transition. The collapsed copolymer chains had a / value of about 1.0 with PNIPAM chains inside the core and the hydrophilic PEO chains on the surface. This kind of PNIPAM-g-PEO copolymers was studied as a DNA separation medium in capillary electrophoresis. Several advantages of the copolymers as a separation medium for DNA fragments were achieved, such as an automatic coating ability for the capillary inner wall, an easier injection into the capillary channel due to the slightly adjustable viscosity with temperature (up to 31 °C), a high resolution (i.e., one base pair resolution), and fast separation time. In contrast, the homo-PNIPAM or PEO showed worse DNA separation efficiency under similar conditions. The high DNA separation efficiency of the PNIPAM-g-PEO copolymers is related to the polymer chain conformation. The long copolymer chains in a random coil conformation with densely grafted PEO branches could form a physical network with a relatively stable and uniform pore size at high concentrations (i.e., ≥10 wt %). The separation medium has a high sieving ability for DNA separation in terms of DNA migration mechanisms. The collapsed copolymer chains in the globule state could destroy the chain network and thus lose the DNA separation ability.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.