2014
DOI: 10.1016/s1773-2247(14)50077-9
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Enhancement of dissolution rate and oral bioavailability in beagle dogs of oleanolic acid by adsorbing onto porous silica using supercritical carbon dioxide

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Cited by 17 publications
(7 citation statements)
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“…Despite limited absorption, the recovery of intact OA and UA has been reported in animal [ 53 , 54 , 58 , 59 , 60 , 61 , 62 , 63 , 64 , 65 , 66 ] and human [ 67 , 68 , 69 ] plasma after oral and parenteral administration. Nonetheless, several pharmacokinetic studies revealed that maximal plasma concentration following oral administration of doses up to 300 mg/kg was low (at nanogram quantities) and elimination half-life was relatively short (<1 h) [ 54 , 60 , 63 , 69 ].…”
Section: Bioavailability and Pharmacokinetic Properties Of Ursolic And Oleanolic Acidsmentioning
confidence: 99%
“…Despite limited absorption, the recovery of intact OA and UA has been reported in animal [ 53 , 54 , 58 , 59 , 60 , 61 , 62 , 63 , 64 , 65 , 66 ] and human [ 67 , 68 , 69 ] plasma after oral and parenteral administration. Nonetheless, several pharmacokinetic studies revealed that maximal plasma concentration following oral administration of doses up to 300 mg/kg was low (at nanogram quantities) and elimination half-life was relatively short (<1 h) [ 54 , 60 , 63 , 69 ].…”
Section: Bioavailability and Pharmacokinetic Properties Of Ursolic And Oleanolic Acidsmentioning
confidence: 99%
“…Despite limited absorption, the recovery of intact OA and UA has been reported in animal [53,54,[58][59][60][61][62][63][64][65][66] and human [67][68][69] plasma after oral and parenteral administration. Nonetheless, several pharmacokinetic studies revealed that maximal plasma concentration following oral administration of doses up to 300 mg/kg was low (at nanogram quantities) and elimination half-life was relatively short (<1 h) [54,60,63,69].…”
Section: Bioavailability and Pharmacokinetic Properties Of Ursolic And Oleanolic Acidsmentioning
confidence: 99%
“…Pharmacokinetic studies of oleanolic acid were carried out in beagle dog by Shi et al [ 87 ] and Li et al [ 88 ]. Shi et al [ 87 ] determined pharmacokinetic parameters of oleanolic acid after oral and intravenous administration of calenduloside E, a triterpene saponin of oleanolic acid conjugated with glucuronic acid, while Li et al [ 88 ] determined pharmacokinetic parameters of a solid dispersion of oleanolic acid prepared with fumed silica by a supercritical fluid technology ( Table 4 ). According to Shi et al [ 87 ], oleanolic acid was found in the plasma after administration of oral doses of calenduloside E, indicating its formation from its glucuronic acid conjugate.…”
Section: Bioavailability Of Pentacyclic Triterpenesmentioning
confidence: 99%
“…This conjugate undergoes biliary excretion and is transported through the bile to the gut where it is again hydrolyzed to oleanolic acid, and the cycle is repeated. On the basis of the AUC values ( Table 4 ), Li et al [ 88 ] concluded that the solid dispersion of oleanolic acid prepared with fumed silica bioavailability was 1.9-fold higher, as compared with commercial tablets.…”
Section: Bioavailability Of Pentacyclic Triterpenesmentioning
confidence: 99%