Bacterial infection is a serious issue in wound healing. Extensive use of biocides in wound dressings have raised concerns like biocide resistance and unwanted harm to normal skin cells. In this thesis, I report a new approach to realize bacteria-triggered release of biocide to the sites of bacterial infections from core-shell polyhydroxyalkanoate (PHA)-based nanofibers prepared by coaxial electrospinning. The hydrophobic PHA-based shell can effectively prevent the biocide from undesirable payload release in physiological environments without pathogens. However, in the presence of pathogens, the PHA-based shell is degraded by pathogens, and the encapsulated biocide is released. The released biocide subsequently can impose targeted antimicrobial effects on the bacteria. Using Pseudomonas aeruginosa as a model bacterium and dodecyltrimethylammonium chloride as a model biocide, we demonstrated that the core-shell PHA-based nanofibers released encapsulated dodecyltrimethylammonium chloride in the presence of Pseudomonas aeruginosa, resulting in targeted inhibition of Pseudomonas aeruginosa growth. iii Acknowledgement Undertaking this master degree has been a challenging experience for me and I could not make it without the support and help received from many people. I would like to express my gratitude to my supervisor, Dr. Song Liu, for his support, guidance, and help during my M.Sc. program. I appreciate his vast knowledge, ideas, and encouragement to make my research experience motivational, productive, and enjoyable. It has been a great honour to work and learn from him. Thanks to his efforts, I have grown tremendously in both my academic and personal life. A special thanks goes to my co-advisor, Dr. Nazim Cicek, without whose financial support and encouragement I may not fully focus on my research program during my two-year M.Sc. program. I must also thank Dr. David B. Levin for all the guidance and assistance throughout my graduate studies. It has been such a valuable experience for me to cooperate with different students in Dr. Levin's group. I am also greatly thankful to Dr. Sarvesh Logsetty for his valuable comments in my committee meetings. I also want to thank all my friends who helped me get through my M.Sc. program. Some friends, like Seungil Kim and Dr. Hardev Singh, were kind and tolerant enough to teach me chemistry laboratory technique and professionalism. Sadegh Ghanbar, Zahra Abdali, Mohammad Reza Kazemian, Jie Li, and Lucy Wang, were good enough not to throw me overboard while at sea. And I would like to send my thanks out to Dr. Levin's PhD students Christopher Dartiailh and Warren Blunt, for their help in all aspects of our collaboration. I thank with love to my wife, Xing Xie, for her continuous support, understanding, and encouragement. She has made countless sacrifices to help me get to this point. This thesis has been written during my stay at the Department of Biosystems Engineering of the University of Manitoba. I would like to thank the University of Manitoba Faculty of Graduate Studies f...