A small library of polyethylene glycol esters of palmitoylethanolamide (PEA) was synthesized with the aim of improving the pharmacokinetic profile of the parent drug after topical administration. Synthesized prodrugs were studied for their skin accumulation, pharmacological activities, in vitro chemical stability, and in silico enzymatic hydrolysis. Prodrugs proved to be able to delay and prolong the pharmacological activity of PEA by modification of its skin accumulation profile. Pharmacokinetic improvements were particularly evident when specific structural requirements, such as flexibility and reduced molecular weight, were respected. Some of the synthesized prodrugs prolonged the pharmacological effects 5 days following topical administration, while a formulation composed by PEA and two pegylated prodrugs showed both rapid onset and long-lasting activity, suggesting the potential use of polyethylene glycol prodrugs of PEA as a suitable candidate for the treatment of skin inflammatory diseases.

Improvement of Topical Palmitoylethanolamide Anti-Inflammatory Activity by Pegylated Prodrugs / D. Tronino, R. Russo, C. Ostacolo, A. Mazzolari, C. De Caro, C. Avagliano, S. Laneri, G. La Rana, A. Sacchi, F. Della Valle, G. Vistoli, A. Calignano. - In: MOLECULAR PHARMACEUTICS. - ISSN 1543-8384. - 12:9(2015), pp. 3369-3379. [10.1021/acs.molpharmaceut.5b00397]

Improvement of Topical Palmitoylethanolamide Anti-Inflammatory Activity by Pegylated Prodrugs

A. Mazzolari;G. Vistoli
Penultimo
;
2015

Abstract

A small library of polyethylene glycol esters of palmitoylethanolamide (PEA) was synthesized with the aim of improving the pharmacokinetic profile of the parent drug after topical administration. Synthesized prodrugs were studied for their skin accumulation, pharmacological activities, in vitro chemical stability, and in silico enzymatic hydrolysis. Prodrugs proved to be able to delay and prolong the pharmacological activity of PEA by modification of its skin accumulation profile. Pharmacokinetic improvements were particularly evident when specific structural requirements, such as flexibility and reduced molecular weight, were respected. Some of the synthesized prodrugs prolonged the pharmacological effects 5 days following topical administration, while a formulation composed by PEA and two pegylated prodrugs showed both rapid onset and long-lasting activity, suggesting the potential use of polyethylene glycol prodrugs of PEA as a suitable candidate for the treatment of skin inflammatory diseases.
No
English
anti-inflammatory effects; antihyperalgesic effects; N-palmitoylethanolamide; pegylated prodrugs; topical delivery; Administration, Cutaneous; Administration, Topical; Animals; Anti-Inflammatory Agents, Non-Steroidal; Dermatologic Agents; Drug Stability; Ethanolamines; Hydrolysis; Male; Mice; Models, Molecular; Palmitic Acids; Polyethylene Glycols; Prodrugs; Skin Absorption; 3003; Molecular Medicine; Drug Discovery3003 Pharmaceutical Science; Medicine (all)
Settore CHIM/08 - Chimica Farmaceutica
Articolo
Esperti anonimi
Ricerca di base
Pubblicazione scientifica
2015
American Chemical Society
12
9
3369
3379
11
Pubblicato
Periodico con rilevanza internazionale
scopus
pubmed
crossref
NON aderisco
info:eu-repo/semantics/article
Improvement of Topical Palmitoylethanolamide Anti-Inflammatory Activity by Pegylated Prodrugs / D. Tronino, R. Russo, C. Ostacolo, A. Mazzolari, C. De Caro, C. Avagliano, S. Laneri, G. La Rana, A. Sacchi, F. Della Valle, G. Vistoli, A. Calignano. - In: MOLECULAR PHARMACEUTICS. - ISSN 1543-8384. - 12:9(2015), pp. 3369-3379. [10.1021/acs.molpharmaceut.5b00397]
none
Prodotti della ricerca::01 - Articolo su periodico
12
262
Article (author)
no
D. Tronino, R. Russo, C. Ostacolo, A. Mazzolari, C. De Caro, C. Avagliano, S. Laneri, G. La Rana, A. Sacchi, F. Della Valle, G. Vistoli, A. Calignano...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/451670
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