Developing a hollow fiber infection model system to determine the PK/PD of conjugated oligoelectrolytes against clinically relevant pathogens
The ability of microbes to develop antimicrobial resistance gives rise to the emergence of drug resistant strains whose infections are difficult to treat. Therefore, there is a pressing need for the development of novel drugs. One of the key stages in the drug discovery pipeline is understanding...
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Format: | Thesis-Master by Research |
Language: | English |
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Nanyang Technological University
2023
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Online Access: | https://hdl.handle.net/10356/165631 |
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Institution: | Nanyang Technological University |
Language: | English |
Summary: | The ability of microbes to develop antimicrobial resistance gives rise to the emergence of
drug resistant strains whose infections are difficult to treat. Therefore, there is a pressing need
for the development of novel drugs. One of the key stages in the drug discovery pipeline is
understanding the pharmacokinetic/pharmacodynamic (PK/PD) of the new drug. The
conventional in vitro methods for evaluating drug efficacy are often static and hence may not
truly reflect the in vivo conditions. Recently, hollow fiber bioreactors have emerged as a
model system to mimic in vivo drug pharmacokinetics (PK) and pharmacodynamics (PD),
without the need to access animal model experiments which requires specialized handling
and are expensive to maintain. This is a useful technique that may accelerate the development
of novel antimicrobial compounds such as the conjugated oligoelectrolytes (COEs). COEs are
a class of synthetic water-soluble molecules containing a conjugated core and pendant ionic
groups. COEs that are sufficiently shorter in molecular length as compared to the lipid bilayer
inhibit microbial growth due to their membrane disrupting abilities. While COEs are
emerging as potential low-cost antimicrobial agents, an understanding of the PK/PD of COEs
is still required. Hence, this research would aim at developing the hollow fiber infection
model (HFIM) system to determine the PK/PD of COEs against clinically relevant pathogens
that are often difficult to infect in conventional mouse models due to the intrinsic host
defense mechanisms. |
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