Non-invasive, continuous oral delivery of solid levodopa-carbidopa for management of Parkinson’s disease

When short plasma half-life drugs act only briefly, they require frequent or continuous administration. We report the engineering of a non-invasive oral drug delivery system for long-term, continuous administration of these drugs. Their non-invasive, long-term, continuous administration at daily doses exceeding 100 mg has, for many years, been considered an insurmountable challenge. We show that over 1200 mg/day of 4:1 levodopa-carbidopa (LD-CD) can be non-invasively and continuously extruded when formulated as a semisolid paste, loaded with 63%w/w of the solid drugs. The drug delivery system comprises a reusable orthodontic retainer with a co-molded pocket into which the patient inserts after each meal a new 1 mL propellant-driven, prefilled, disposable, drug delivery extruder. The paste is delivered to the lingual side of the teeth where it is mixed with saliva and swallowed. As reported elsewhere, a 15-day, 16 patient open label clinical trial of the drug delivery system continuously extruding LD-CD paste significantly reduces the variability of the plasma LD concentration and alleviates symptoms of advanced Parkinson's disease (PD) as compared to LD-CD tablets.

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Publication Details

Journal
Scientific Reports
Published
2024-11-05
DOI
https://doi.org/10.1038/s41598-024-78145-4
Citations
4
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
1.48
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article

Non-invasive, continuous oral delivery of solid levodopa-carbidopa for management of Parkinson’s disease

Adam Heller, Ephraim Heller, William L. Murch, John Spiridigliozzi
4 citations
Scientific Reports
Parkinson's Disease Mechanisms and Treatments
1.48
article

Non-invasive, continuous oral delivery of solid levodopa-carbidopa for management of Parkinson’s disease

Adam Heller, Ephraim Heller, William L. Murch, John Spiridigliozzi
article en
4 citations

Abstract

When short plasma half-life drugs act only briefly, they require frequent or continuous administration. We report the engineering of a non-invasive oral drug delivery system for long-term, continuous administration of these drugs. Their non-invasive, long-term, continuous administration at daily doses exceeding 100 mg has, for many years, been considered an insurmountable challenge. We show that over 1200 mg/day of 4:1 levodopa-carbidopa (LD-CD) can be non-invasively and continuously extruded when formulated as a semisolid paste, loaded with 63%w/w of the solid drugs. The drug delivery system comprises a reusable orthodontic retainer with a co-molded pocket into which the patient inserts after each meal a new 1 mL propellant-driven, prefilled, disposable, drug delivery extruder. The paste is delivered to the lingual side of the teeth where it is mixed with saliva and swallowed. As reported elsewhere, a 15-day, 16 patient open label clinical trial of the drug delivery system continuously extruding LD-CD paste significantly reduces the variability of the plasma LD concentration and alleviates symptoms of advanced Parkinson's disease (PD) as compared to LD-CD tablets.

Scientific ReportsVol. 14(1)
SynAgile (United States) (US)
Openalex Percentile: Top 16%
Parkinson's Disease Mechanisms and Treatments
1.48
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