TY - JOUR
T1 - Enhancing the antibacterial effect of Chitosan to combat orthopaedic implant-associated infections
AU - Rahayu, Dien Puji
AU - De Mori, Arianna
AU - Yusuf, Rahmi
AU - Draheim, Roger
AU - Lalatsa, Aikaterini
AU - Roldo, Marta
PY - 2022/8/1
Y1 - 2022/8/1
N2 - The development of antibacterial resistance imposes the development of novel materials to relieve the burden of infection. Chitosan, a material of natural and sustainable origin, possesses ideal characteristics to translate into a novel biomaterial with antibacterial properties, as it already has these properties and it allows easy and scalable chemical modification to enhance its activity. The aim of the present work was that of producing low molecular weight chitosans that have higher solubility and can remain protonated at physiological pH, thus enhancing the antimicrobial action. This was achieved by reacting acid hydrolysed low molecular weight chitosan with 2-bromoethyleneamine hydrobromide or Fmoc-Lys(Fmoc)-OH to elicit N-(2-ethylamino)-chitosan and N-2(2,6-diaminohexanamide)-chitosan polymers. The latter derivative, CS3H Lys, that was synthesised for the first time, showed superior efficacy against Staphylococcus aureus, supporting further studies for its inclusion in implant coating materials to tackle the burden of orthopaedic implant-associated infections.
AB - The development of antibacterial resistance imposes the development of novel materials to relieve the burden of infection. Chitosan, a material of natural and sustainable origin, possesses ideal characteristics to translate into a novel biomaterial with antibacterial properties, as it already has these properties and it allows easy and scalable chemical modification to enhance its activity. The aim of the present work was that of producing low molecular weight chitosans that have higher solubility and can remain protonated at physiological pH, thus enhancing the antimicrobial action. This was achieved by reacting acid hydrolysed low molecular weight chitosan with 2-bromoethyleneamine hydrobromide or Fmoc-Lys(Fmoc)-OH to elicit N-(2-ethylamino)-chitosan and N-2(2,6-diaminohexanamide)-chitosan polymers. The latter derivative, CS3H Lys, that was synthesised for the first time, showed superior efficacy against Staphylococcus aureus, supporting further studies for its inclusion in implant coating materials to tackle the burden of orthopaedic implant-associated infections.
KW - Chitosan
KW - Chitosan derivatives
KW - antibacterial activity
KW - S. aureus
KW - implant-associated infection
UR - https://linkinghub.elsevier.com/retrieve/pii/S0144861722002892
U2 - 10.1016/j.carbpol.2022.119385
DO - 10.1016/j.carbpol.2022.119385
M3 - Article
SN - 0144-8617
VL - 289
JO - Carbohydrate Polymers
JF - Carbohydrate Polymers
M1 - 119385
ER -