1999
DOI: 10.1016/s0750-7658(99)80059-8
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Le propacétamol: des données fondamentales à l'utilisation clinique

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Cited by 20 publications
(2 citation statements)
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“…71 As a result, its onset of analgesia is more rapid than that from APAP ordered orally or rectally. [72][73][74] Thus, propacetamol cannot be administered orally due to its greater water solubility. Interestingly, 4-AAC-APAP derivatives were proposed by Kovach et al in 1981 as potentially useful prodrugs.…”
Section: Carrier-linked O/n-modied Apap Prodrugsmentioning
confidence: 99%
“…71 As a result, its onset of analgesia is more rapid than that from APAP ordered orally or rectally. [72][73][74] Thus, propacetamol cannot be administered orally due to its greater water solubility. Interestingly, 4-AAC-APAP derivatives were proposed by Kovach et al in 1981 as potentially useful prodrugs.…”
Section: Carrier-linked O/n-modied Apap Prodrugsmentioning
confidence: 99%
“…However, only a few prodrug salts have been reported, including Na + or K + salts of acetaminophen derivatized with phosphoric acid moieties 23d and Cl À salts derived from the attachment of an amine moiety, e.g., propacetamol HCl. 25 All of these salts are crystalline solids.…”
mentioning
confidence: 99%