TY - JOUR
T1 - Nasal Tramadol delivery system
T2 - A new approach for improved pain therapy
AU - Duchi, Shaher
AU - Touitou, Elka
AU - Pradella, Lorenzo
AU - Marchini, Francesco
AU - Ainbinder, Denize
PY - 2011/11
Y1 - 2011/11
N2 - The present work investigates Tramadol nasal delivery for effective analgesia with a rapid onset of action.The pharmacokinetic and pharmacodynamic behavior of Tramadol, a non-opiate analgesic drug, following its administration to rodents from a nasal delivery system was compared to oral aqueous solution.Following Tramadol nasal administration in animals at a dose of 10mg/kg, a C max value of 2421±651ng/ml was obtained as compared to a four time lower value after oral delivery (644±349ng/ml). The high plasma concentration was achieved at 10min (t max), indicating a rapid systemic absorption of the drug.Tramadol nasal delivery system treatment in animal Writhing model at a relative low dose of only 5. mg/kg significantly increased the analgesic effect, as compared to the oral administration, both 30. min before and immediately with pain induction.The local safety of Tramadol nasal system was good with no histological or nasal cavity changes.The outcomes of this work are that nasal administration of Tramadol could improve pain therapy and shorten its onset of action.The treatment by the nasal pathway could overcome the side effects associated with parenteral and oral delivery. Furthermore, due to the rapid and efficient delivery of the drug to the blood, nasal administration of Tramadol could be considered for the treatment of breakthrough pain.
AB - The present work investigates Tramadol nasal delivery for effective analgesia with a rapid onset of action.The pharmacokinetic and pharmacodynamic behavior of Tramadol, a non-opiate analgesic drug, following its administration to rodents from a nasal delivery system was compared to oral aqueous solution.Following Tramadol nasal administration in animals at a dose of 10mg/kg, a C max value of 2421±651ng/ml was obtained as compared to a four time lower value after oral delivery (644±349ng/ml). The high plasma concentration was achieved at 10min (t max), indicating a rapid systemic absorption of the drug.Tramadol nasal delivery system treatment in animal Writhing model at a relative low dose of only 5. mg/kg significantly increased the analgesic effect, as compared to the oral administration, both 30. min before and immediately with pain induction.The local safety of Tramadol nasal system was good with no histological or nasal cavity changes.The outcomes of this work are that nasal administration of Tramadol could improve pain therapy and shorten its onset of action.The treatment by the nasal pathway could overcome the side effects associated with parenteral and oral delivery. Furthermore, due to the rapid and efficient delivery of the drug to the blood, nasal administration of Tramadol could be considered for the treatment of breakthrough pain.
KW - Analgesia
KW - Nasal delivery system
KW - Pain
KW - Tramadol
UR - http://www.scopus.com/inward/record.url?scp=83355177368&partnerID=8YFLogxK
U2 - 10.1016/j.eujps.2011.08.009
DO - 10.1016/j.eujps.2011.08.009
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AN - SCOPUS:83355177368
SN - 1754-3207
VL - 5
SP - 449
EP - 452
JO - European Journal of Pain Supplements
JF - European Journal of Pain Supplements
IS - 2
ER -