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Article

PEG–Ursolic Acid Conjugate: Synthesis and In Vitro Release Studies

by
Marina ZACCHIGNA
1,*,
Francesca CATENI
1,
Sara DRIOLI
1,
Giuseppe PROCIDA
1 and
Tiziano ALTIERI
2
1
Department of Chemical and Pharmaceutical Sciences, University of Trieste, Piazzale Europa 1, 34127 Trieste, Italy
2
School of Advanced Studies ”G. D’Annunzio”, University of Chieti-Pescara, Via dei Vestini 31, 66100 Chieti Scalo, Chieti, Italy
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2014, 82(2), 411-422; https://doi.org/10.3797/scipharm.1309-17
Submission received: 25 September 2013 / Accepted: 6 April 2014 / Published: 6 April 2014

Abstract

A highly water-soluble macromolecular compound of ursolic acid with mono-methoxypoly(ethylene glycol) (mPEG) was prepared. The physicochemical properties and stabilities under different conditions were investigated. By PEG conjugation, greatly increased water solubility was obtained, and the results showed that this conjugate was a potential prodrug for the oral delivery of ursolic acid.
Keywords: Ursolic acid; Monomethoxypoly(ethylene glycol); Conjugation; Solubility Ursolic acid; Monomethoxypoly(ethylene glycol); Conjugation; Solubility

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MDPI and ACS Style

ZACCHIGNA, M.; CATENI, F.; DRIOLI, S.; PROCIDA, G.; ALTIERI, T. PEG–Ursolic Acid Conjugate: Synthesis and In Vitro Release Studies. Sci. Pharm. 2014, 82, 411-422. https://doi.org/10.3797/scipharm.1309-17

AMA Style

ZACCHIGNA M, CATENI F, DRIOLI S, PROCIDA G, ALTIERI T. PEG–Ursolic Acid Conjugate: Synthesis and In Vitro Release Studies. Scientia Pharmaceutica. 2014; 82(2):411-422. https://doi.org/10.3797/scipharm.1309-17

Chicago/Turabian Style

ZACCHIGNA, Marina, Francesca CATENI, Sara DRIOLI, Giuseppe PROCIDA, and Tiziano ALTIERI. 2014. "PEG–Ursolic Acid Conjugate: Synthesis and In Vitro Release Studies" Scientia Pharmaceutica 82, no. 2: 411-422. https://doi.org/10.3797/scipharm.1309-17

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