TY - JOUR
T1 - Advanced dextran based nanogels for fighting Staphylococcus aureus infections by sustained zinc release
AU - Malzahn, Kerstin
AU - Jamieson, William D.
AU - Dröge, Melanie
AU - Mailänder, Volker
AU - Jenkins, A. Toby A.
AU - Weiss, Clemens K.
AU - Landfester, Katharina
PY - 2014/4/21
Y1 - 2014/4/21
N2 - The growth in numbers and severity of hospital acquired infections has increased the need to target bacteria locally and specifically. Consequently, smart drug-delivery systems are being developed for local bactericidal action. The approach takes the concept of nanogels in drug delivery of small molecules to the next level by enclosing them in a shell. Versatile polysaccharide nanogels were loaded with zinc ions as antibacterial agents in a miniemulsion process, in order to target methicillin resistant strains of Staphylococcus aureus (MRSA). The encapsulation of drugs in nanogels is limited by the crosslinking density of the gel and the size of the drug. The characterization of the nanogels with inductively coupled plasma optical emission spectroscopy (ICP-OES) revealed that zinc ions cannot be retained within without an additional 'shell' layer. The nanogels were surrounded by a dextran-polyurethane shell, which can retain substances by reduction of water penetration. A delayed zinc release compared to the nanogels was confirmed by ICP-OES. Bacterial tests revealed an antibacterial effect of the shell enhanced nanogels against S. aureus. The studied nanogel system shows potential in locally addressing bacterial infections. The platform is extremely versatile and can be tailored to application as dextran and Zn(NO) can be replaced by other polysaccharides (e.g. hyaluronic acid) and antibacterial agents, respectively.
AB - The growth in numbers and severity of hospital acquired infections has increased the need to target bacteria locally and specifically. Consequently, smart drug-delivery systems are being developed for local bactericidal action. The approach takes the concept of nanogels in drug delivery of small molecules to the next level by enclosing them in a shell. Versatile polysaccharide nanogels were loaded with zinc ions as antibacterial agents in a miniemulsion process, in order to target methicillin resistant strains of Staphylococcus aureus (MRSA). The encapsulation of drugs in nanogels is limited by the crosslinking density of the gel and the size of the drug. The characterization of the nanogels with inductively coupled plasma optical emission spectroscopy (ICP-OES) revealed that zinc ions cannot be retained within without an additional 'shell' layer. The nanogels were surrounded by a dextran-polyurethane shell, which can retain substances by reduction of water penetration. A delayed zinc release compared to the nanogels was confirmed by ICP-OES. Bacterial tests revealed an antibacterial effect of the shell enhanced nanogels against S. aureus. The studied nanogel system shows potential in locally addressing bacterial infections. The platform is extremely versatile and can be tailored to application as dextran and Zn(NO) can be replaced by other polysaccharides (e.g. hyaluronic acid) and antibacterial agents, respectively.
UR - http://www.scopus.com/inward/record.url?scp=84897888354&partnerID=8YFLogxK
UR - http://dx.doi.org/10.1039/c3tb21335h
U2 - 10.1039/c3tb21335h
DO - 10.1039/c3tb21335h
M3 - Article
AN - SCOPUS:84897888354
SN - 2050-7526
VL - 2
SP - 2175
EP - 2183
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
IS - 15
ER -