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Meta-Analysis of Drug Delivery Approaches for Treating Intracellular Infectionsoa mark
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Publication Year
2022-06-01
Publisher
Springer
Citation
Pharmaceutical Research, Vol.39, pp.1085-1114
Keyword
AntimicrobialsDrug carriersIntracellular drug deliveryIntracellular pathogens
Mesh Keyword
Anti-Bacterial AgentsDrug Delivery Systems
All Science Classification Codes (ASJC)
BiotechnologyMolecular MedicinePharmacologyPharmaceutical ScienceOrganic ChemistryPharmacology (medical)
Abstract
This meta-analysis aims to evaluate the trend, methodological quality and completeness of studies on intracellular delivery of antimicrobial agents. PubMed, Embase, and reference lists of related reviews were searched to identify original articles that evaluated carrier-mediated intracellular delivery and pharmacodynamics (PD) of antimicrobial therapeutics against intracellular pathogens in vitro and/or in vivo. A total of 99 studies were included in the analysis. The most commonly targeted intracellular pathogens were bacteria (62.6%), followed by viruses (16.2%) and parasites (15.2%). Twenty-one out of 99 (21.2%) studies performed neither microscopic imaging nor flow cytometric analysis to verify that the carrier particles are present in the infected cells. Only 31.3% of studies provided comparative inhibitory concentrations against a free drug control. Approximately 8% of studies, albeit claimed for intracellular delivery of antimicrobial therapeutics, did not provide any experimental data such as microscopic imaging, flow cytometry, and in vitro PD. Future research on intracellular delivery of antimicrobial agents needs to improve the methodological quality and completeness of supporting data in order to facilitate clinical translation of intracellular delivery platforms for antimicrobial therapeutics.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32533
DOI
https://doi.org/10.1007/s11095-022-03188-z
Fulltext

Type
Review
Funding
This study was supported by the National Institutes of Health (R01 CA232419, R01 CA258737), Basic Science Research Program through the National Research Foundation of Korea (NRF) grant funded by the Ministry of Science and ICT (No. 2021R1C1C1003735) and by Ajou University re-search fund (S-2021-G0001-00310). The authors report no conflicts of interest in this research.
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Shin, Soo Young  Image
Shin, Soo Young 신수영
Division of Pharmacy Sciences
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