1986
DOI: 10.1007/978-1-4613-2179-8_63
|View full text |Cite
|
Sign up to set email alerts
|

A Novel Transdermal Therapeutic System as a Potential Treatment for Alzheimer’s Disease

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

1989
1989
2023
2023

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 8 publications
0
2
0
Order By: Relevance
“…designed a formulation pad (3.6 cm × 3.6 cm) in 1986 which consisted of physostigmine in enhancer vehicle propionic acid and an ethylene/vinylacetate copolymer membrane with an adhesive on one side and an aluminum foil cover on its back. [ 40 41 ] The human study with this structure showed that a stable plasma concentration was recorded at 0.56 ± 0.1 ng/ml during the test and correlated well with blood acetyl-cholinesterase inhibition. [ 18 ] Consequently, physostigmine transdermal system was fabricated by Lohmann Therapie-Systeme GmbH that contained 30 mg active molecular in surface area 30.2 cm 2 .…”
Section: Transdermal For Alzheimer's Diseasementioning
confidence: 99%
“…designed a formulation pad (3.6 cm × 3.6 cm) in 1986 which consisted of physostigmine in enhancer vehicle propionic acid and an ethylene/vinylacetate copolymer membrane with an adhesive on one side and an aluminum foil cover on its back. [ 40 41 ] The human study with this structure showed that a stable plasma concentration was recorded at 0.56 ± 0.1 ng/ml during the test and correlated well with blood acetyl-cholinesterase inhibition. [ 18 ] Consequently, physostigmine transdermal system was fabricated by Lohmann Therapie-Systeme GmbH that contained 30 mg active molecular in surface area 30.2 cm 2 .…”
Section: Transdermal For Alzheimer's Diseasementioning
confidence: 99%
“…One reason could be its low bioavailability in humans ( Whelpton and Hurst, 1985). Attempts have been made to improve this situation by developing a transdermal delivery system (Levy et aL, 1986) (Marta et aL, 1988b andYu et aL, 1988).…”
Section: Cholinesterase Inhibitors (Fig 5)mentioning
confidence: 99%