Tissue distribution pharmacokinetics of intrathecal U1 adaptor oligonucleotide in mice

U1 Adaptor is a novel gene-silencing technology, offering an innovative approach to target genes in the CNS for the treatment of diseases. Intrathecal delivery is a medically viable route of administration of CNS-bound nucleic acid drugs; therefore, it is important to investigate U1 Adaptor distribution after intrathecal drug delivery. We investigated the distribution patterns of U1 Adaptor upon intrathecal bolus administration in mice. It readily distributes to CNS tissues, including the lumbar and the cervical spinal cord, and the cerebellum. Over time, the U1 Adaptor also accumulates in the periphery, both in the liver and the kidneys, while plasma levels are undetectable. Our findings provide useful information for future in-depth pharmacokinetic modeling of U1 Adaptor distribution upon intrathecal administration.

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Publication Details

Journal
Current Research in Pharmacology and Drug Discovery
Published
2025-01-01
DOI
https://doi.org/10.1016/j.crphar.2025.100220
Citations
1
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
0.81
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Tissue distribution pharmacokinetics of intrathecal U1 adaptor oligonucleotide in mice

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1 citations
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article

Tissue distribution pharmacokinetics of intrathecal U1 adaptor oligonucleotide in mice

M Z Satti, Samuel Gunderson, Yash Patel, Lei Yu, Lawrence Walker, Kavita Prasad, Demi Poulathas, Esha Paghdal
article en
1 citations

Abstract

U1 Adaptor is a novel gene-silencing technology, offering an innovative approach to target genes in the CNS for the treatment of diseases. Intrathecal delivery is a medically viable route of administration of CNS-bound nucleic acid drugs; therefore, it is important to investigate U1 Adaptor distribution after intrathecal drug delivery. We investigated the distribution patterns of U1 Adaptor upon intrathecal bolus administration in mice. It readily distributes to CNS tissues, including the lumbar and the cervical spinal cord, and the cerebellum. Over time, the U1 Adaptor also accumulates in the periphery, both in the liver and the kidneys, while plasma levels are undetectable. Our findings provide useful information for future in-depth pharmacokinetic modeling of U1 Adaptor distribution upon intrathecal administration.

Current Research in Pharmacology and Drug DiscoveryVol. 8
Rutgers, The State University of New Jersey (US)
Openalex Percentile: Top 29%
RNA Interference and Gene Delivery
0.81
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