NDLI: Topical Delivery of a Model Phenolic Drug: Alkyloxycarbonyl Prodrugs of Acetaminophen

Content Provider	Springer Nature Link
Author	Wasdo, Scott C. Sloan, Kenneth B.
Copyright Year	2004
Abstract	Purpose. To determine whether the delivery of a phenolic parent drug by its alkyloxycarbonyl (AOC) prodrugs through hairless mouse skin would show similar dependencies on water and lipid solubilities that similar prodrugs of more polar heterocyclic amide and imide parent drugs have shown. Methods. Flux through hairless mouse skin from suspensions in isopropyl myristate (J$_{MIPM}$), solubilities in IPM (S$_{IPM}$) and water (S$_{AQ}$), and partition coefficients between isopropyl myristate (IPM) and pH 4.0 buffer (K$_{IPM:4.0}$) were measured for two series of AOC derivatives of acetaminophen (APAP); their solubilities in pH 4.0 buffer (S$_{4.0}$) were estimated from S$_{IPM}$/K$_{IPM: 4.0}$. Log J$_{MIPM}$ values were calculated from the n = 43 coefficients for the parameters in the transformed Potts-Guy (Roberts-Sloan) equation, and the average error of prediction (Δ log J`$_{IPM}$) was calculated. The J$_{MIPM}$, S$_{IPM}$, S$_{4.0}$, and molecular weight (MW) data for this series and two other series were combined with the n = 43 database to give a n = 61 database, and new best fit coefficients were determined for the Roberts-Sloan equation: log J$_{MIPM}$ = x + y log S$_{IPM}$ + (1 - y) log S$_{4.0}$ - z MW. Results. All of the 4-AOC-APAP derivatives underperformed based on their predicted log J$_{MIPM}$ (Δ log J`$_{MIPM}$ = 0.275 ± 0.147 log units) and, although the two more water soluble members of this more lipid soluble series were more effective than APAP, they were only marginally so: <2 times. Addition of three new series to the n = 43 database for the Roberts-Sloan equation did not substantially change the coefficients to the parameters: x, y, z, and r$^{2}$ = -0.322, 0.530, 0.00337 and 0.92, respectively. Conclusions. The topical delivery of a model phenolic drug by its AOC prodrugs through hairless mouse skin from IPM shows the same dependence on S$_{IPM}$, S$_{4.0}$, and MW as the delivery of polar heterocycles by their similar prodrugs.
Starting Page	940
Ending Page	946
Page Count	7
File Format	PDF
ISSN	07248741
Journal	Pharmaceutical Research
Volume Number	21
Issue Number	6
e-ISSN	1573904X
Language	English
Publisher	Kluwer Academic Publishers-Plenum Publishers
Publisher Date	2004-01-01
Publisher Place	New York
Access Restriction	One Nation One Subscription (ONOS)
Subject Keyword	Pharmacology/Toxicology Pharmacy Biochemistry Medical Law Biomedical Engineering
Content Type	Text
Resource Type	Article
Subject	Organic Chemistry Pharmacology Molecular Medicine Pharmacology (medical) Biotechnology Pharmaceutical Science

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