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- W2891820530 endingPage "A0070" @default.
- W2891820530 startingPage "A0070" @default.
- W2891820530 abstract "Oligonucleotide-based therapeutics such as antisense oligonucleotides, small interfering RNAs (siRNAs), decoy and aptamer have been extensively developed. To investigate the pharmacokinetics of oligonucleotide therapeutics, it is common to label a radioisotope in a nucleic acid and visualize it. However, if the labeled terminal nucleotide is decomposed by a nuclease in vivo, only the labeled nucleotide is detected, and it is impossible to observe the nucleic acid exhibiting the drug effect. The distribution of biomolecules, such as phospholipids, proteins, and glycolipids, can be obtained and visualized without labeling using matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI-IMS). MALDI-IMS is also used in pharmacokinetic analysis to visualize a parent drug and its metabolites simultaneously. In this study, we reported a methodology for oligonucleotides analysis by MALDI-IMS. When phosphorothioate antisense oligonucleotide was administered into the eyeball of rats, it reached the retina after 30 min without undergoing decomposition by nucleases." @default.
- W2891820530 created "2018-09-27" @default.
- W2891820530 creator A5000457572 @default.
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- W2891820530 date "2018-09-11" @default.
- W2891820530 modified "2023-10-12" @default.
- W2891820530 title "Distribution of Antisense Oligonucleotides in Rat Eyeballs Using MALDI Imaging Mass Spectrometry" @default.
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- W2891820530 doi "https://doi.org/10.5702/massspectrometry.a0070" @default.
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