Please use this identifier to cite or link to this item: https://doi.org/10.3390/antibiotics6030014
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dc.titleMacromolecular conjugate and biological carrier approaches for the targeted delivery of antibiotics
dc.contributor.authorTram, N.D.T
dc.contributor.authorEe, P.L.R
dc.date.accessioned2020-09-09T05:01:41Z
dc.date.available2020-09-09T05:01:41Z
dc.date.issued2017
dc.identifier.citationTram, N.D.T, Ee, P.L.R (2017). Macromolecular conjugate and biological carrier approaches for the targeted delivery of antibiotics. Antibiotics 6 (3) : 14. ScholarBank@NUS Repository. https://doi.org/10.3390/antibiotics6030014
dc.identifier.issn20796382
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/175202
dc.description.abstractFor the past few decades, the rapid rise of antibiotic multidrug-resistance has presented a palpable threat to human health worldwide. Meanwhile, the number of novel antibiotics released to the market has been steadily declining. Therefore, it is imperative that we utilize innovative approaches for the development of antimicrobial therapies. This article will explore alternative strategies, namely drug conjugates and biological carriers for the targeted delivery of antibiotics, which are often eclipsed by their nanomedicine-based counterparts. A variety of macromolecules have been investigated as conjugate carriers, but only those most widely studied in the field of infectious diseases (e.g., proteins, peptides, antibodies) will be discussed in detail. For the latter group, blood cells, especially erythrocytes, have been successfully tested as homing carriers of antimicrobial agents. Bacteriophages have also been studied as a candidate for similar functions. Once these alternative strategies receive the amount of research interest and resources that would more accurately reflect their latent applicability, they will inevitably prove valuable in the perennial fight against antibiotic resistance. © 2017 by the authors. Licensee MDPI, Basel, Switzerland.
dc.sourceUnpaywall 20200831
dc.subjectaminoglycoside
dc.subjectampicillin
dc.subjectantibiotic agent
dc.subjectantigen
dc.subjectchloramphenicol
dc.subjecterythromycin
dc.subjectlincosamide
dc.subjectmacrolide
dc.subjectnanocarrier
dc.subjectpenicillin derivative
dc.subjectprotein
dc.subjecttetracycline
dc.subjectvancomycin
dc.subjectantibacterial activity
dc.subjectantibiotic resistance
dc.subjectantimicrobial activity
dc.subjectAspergillus fumigatus
dc.subjectatypical Mycobacterium
dc.subjectblood cell
dc.subjectelectroporation
dc.subjecterythrocyte
dc.subjectimmunogenicity
dc.subjectinflammation
dc.subjectminimum inhibitory concentration
dc.subjectnonhuman
dc.subjectPlasmodium falciparum
dc.subjectpriority journal
dc.subjectPseudomonas aeruginosa
dc.subjectReview
dc.subjectStaphylococcus aureus
dc.typeReview
dc.contributor.departmentPHARMACY
dc.description.doi10.3390/antibiotics6030014
dc.description.sourcetitleAntibiotics
dc.description.volume6
dc.description.issue3
dc.description.page14
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