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- Pharmacokinetics and distribution of 2-hydroxypropyl-β-cyclodextrin following a single intrathecal dose to cats.
Pharmacokinetics and distribution of 2-hydroxypropyl-β-cyclodextrin following a single intrathecal dose to cats.
Citation | “Pharmacokinetics And Distribution Of 2-Hydroxypropyl-Β-Cyclodextrin Following A Single Intrathecal Dose To Cats.”. Journal Of Inherited Metabolic Disease, pp. 618-634. . |
Center | Washington University in St Louis |
Author | Mark L Kao, Susan Stellar, Eric Solon, Alfred Lordi, Nicole Kasica, Gary Swain, Jessica H Bagel, Brittney L Gurda, Charles H Vite |
Keywords | Niemann Pick type C, animal model, brain, cholesterol, drug therapy, inborn errors of metabolism, storage diseases |
Abstract |
2-Hydroxypropyl-β-cyclodextrin (HP-β-CD) is an experimental therapy for Niemann-Pick disease type C (NPC) that reduced neuronal cholesterol and ganglioside storage, reduced Purkinje cell death, and increased lifespan in npc1-/- mice and NPC1 cats. In this study, tissue distribution was investigated in normal cats that received a single 120-mg dose of [ C]-HP-β-CD (approximately 200 μCi/cat) via the cerebellomedullary cistern (CBMC) and lumbar cistern. One cat was euthanized at each of various time points up to 24 hours postdose for subsequent processing and quantitative whole-body autoradiographic analysis. HP-β-CD-derived radioactivity absorbed from the CBMC was widely distributed to cat tissues; most tissues were observed to have reached their highest concentration at 1 hour postdose. HP-β-CD-derived radioactivity penetrated into the deeper parts of the central nervous system with the highest concentration at 4 hours (403 μg Eq/g or 0.28 mM) and remained high (49.7 μg Eq/g or 0.03 mM) at 24 hours. The relatively long half-life (11-30 hours) in cerebral ventricles and the subarachnoid space surrounding the brain and spinal cord might contribute to the efficacy of HP-β-CD in NPC1 cats. Other tissues with high concentrations of radioactivity were nasal turbinates, pituitary gland, and urinary bladder, while relatively low concentrations were observed in blood and bile. |
Year of Publication |
2020
|
Journal |
Journal of inherited metabolic disease
|
Volume |
43
|
Issue |
3
|
Number of Pages |
618-634
|
Date Published |
05/2020
|
ISSN Number |
1573-2665
|
DOI |
10.1002/jimd.12189
|
Alternate Journal |
J. Inherit. Metab. Dis.
|
PMID |
31707730
|
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