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Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : orange juiceType of experiment : in vivoType of animal : ratType of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : Oral administrationDose/Conc.(herb) : 10 mL/kg for orange juiceDuration : Single administrationType of interaction : PharmacokineticsInteraction with drug : TacrolimusDose/Conc.(drug) : -Result : NegativeRemark : There was no significant difference in the AUC values between pre-treated with orange juice and pre-treated with water.
Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : -Type of experiment : humanType of animal : -Type of study : Open trialN(Total) : 16 (M/F = 8/8)N(Treatment) : 16 (M/F = 8/8)Sex : Both sexAge : 37.9 +/- 8.6 yearsRoute : Oral administrationDose/Conc.(herb) : 12 ounces of commercially available orange juiceDuration : -Type of interaction : PharmacokineticsInteraction with drug : LevofloxacinDose/Conc.(drug) : 500 mgResult : PositiveRemark : The coadministration of levofloxacin and calcium-fortified orange juice results in a lack of bioequivalence as compared to when it is administered with water in a fasting state. It also demonstrates the ability of nonfortified orange juice to significantly change key pharmacokinetic parameters of levofloxacin.Note : Subjects: healthy volunteers. Each subject received the following dosage regimens in random order: (1) a single 500-mg tablet of levofloxacin with 12 ounces of water, (2) a single 500-mg tablet of levofloxacin with 12 ounces of commercially available orange juice, and (3) a single 500-mg tablet of levofloxacin with 12 ounces of commercially available calcium-fortified orange juice.
Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : -Type of experiment : humanType of animal : -Type of study : Open trialN(Total) : 16 (M/F = 8/8)N(Treatment) : 16 (M/F = 8/8)Sex : Both sexAge : 37.9 +/- 8.6 yearsRoute : Oral administrationDose/Conc.(herb) : 12 ounces of commercially available calcium-fortified orange juiceDuration : -Type of interaction : PharmacokineticsInteraction with drug : LevofloxacinDose/Conc.(drug) : 500 mgResult : PositiveRemark : The coadministration of levofloxacin and calcium-fortified orange juice results in a lack of bioequivalence as compared to when it is administered with water in a fasting state. It also demonstrates the ability of nonfortified orange juice to significantly change key pharmacokinetic parameters of levofloxacin.Note : Subjects: healthy volunteers. Each subject received the following dosage regimens in random order: (1) a single 500-mg tablet of levofloxacin with 12 ounces of water, (2) a single 500-mg tablet of levofloxacin with 12 ounces of commercially available orange juice, and (3) a single 500-mg tablet of levofloxacin with 12 ounces of commercially available calcium-fortified orange juice.
Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : Water layer from ethyl acetate extraction of orange juiceType of experiment : in vitroType of animal : -Type of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : -Dose/Conc.(herb) : Uptake experiments were performed in 250 ml of incubation buffer containing 10 nM [3H]vinblastine in the presence of the water layer from ethyl acetate extraction of orange juice (diluted to be equivalent to 50% of the original orange juice strength).Duration : 60 min.Type of interaction : PharmacokineticsInteraction with drug : Vinblastine*/VLBDose/Conc.(drug) : 10 nM [3H]vinblastineResult : NegativeRemark : Result: No significant effect (uptake of [3H]vinblastine by Caco-2 cells) of the remaining aqueous layer after ethyl acetate extraction was seen (100 +/- 4.33% compared with the control), indicating that the active components were entirely extracted in ethyl acetate.
Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : orange juiceType of experiment : in vitroType of animal : -Type of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : -Dose/Conc.(herb) : Uptake experiments were performed in 250 ml of incubation buffer containing 10 nM [3H]vinblastine in the presence of orange juice (diluted to be equivalent to 50% of the original orange juice strength).Duration : 60 min.Type of interaction : PharmacokineticsInteraction with drug : Vinblastine*/VLBDose/Conc.(drug) : 10 nM [3H]vinblastineResult : PositiveRemark : Result: The steady-state uptake of [3H]vinblastine by Caco-2 cells was significantly increased to 178 +/- 5.5% in the presence of orange juice, compared with the control.
Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : ethyl acetate extracts of orange juiceType of experiment : in vitroType of animal : -Type of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : -Dose/Conc.(herb) : Uptake experiments were performed in 250 ml of incubation buffer containing 10 nM [3H]vinblastine in the presence of the ethyl acetate extracts of orange juice (diluted to be equivalent to 50% of the original orange juice strength).Duration : 60 min.Type of interaction : PharmacokineticsInteraction with drug : Vinblastine*/VLBDose/Conc.(drug) : 10 nM [3H]vinblastineResult : PositiveRemark : Result: The steady-state uptake of [3H]vinblastine by Caco-2 cells was significantly increased to 228 +/- 2.8% in the presence of ethyl acetate extracts of orange juice, compared with the control.
Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : diethyl ethyl acetate extracts of orange juiceType of experiment : in vitroType of animal : -Type of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : -Dose/Conc.(herb) : Uptake experiments were performed in 250 ml of incubation buffer containing 10 nM [3H]vinblastine in the presence of the diethyl ether extracts of orange juice (diluted to be equivalent to 50% of the original orange juice strength).Duration : 60 min.Type of interaction : PharmacokineticsInteraction with drug : Vinblastine*/VLBDose/Conc.(drug) : 10 nM [3H]vinblastineResult : PositiveRemark : Result: The steady-state uptake of [3H]vinblastine by Caco-2 cells was significantly increased to 203 +/- 14% in the presence of diethyl ether extracts of orange juice, compared with the control.
Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : methylene chloride extracts of orange juiceType of experiment : in vitroType of animal : -Type of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : -Dose/Conc.(herb) : Uptake experiments were performed in 250 ml of incubation buffer containing 10 nM [3H]vinblastine in the presence of the methylene chloride extracts of orange juice (diluted to be equivalent to 50% of the original orange juice strength).Duration : 60 min.Type of interaction : PharmacokineticsInteraction with drug : Vinblastine*/VLBDose/Conc.(drug) : 10 nM [3H]vinblastineResult : PositiveRemark : Result: The steady-state uptake of [3H]vinblastine by Caco-2 cells was significantly increased to 198 +/- 4.5% in the presence of methylene chloride extracts of orange juice, compared with the control.
Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : ethyl acetate extracts of orange juiceType of experiment : in vitroType of animal : -Type of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : -Dose/Conc.(herb) : Uptake experiments were performed in 250 ml of incubation buffer containing 10 nM [3H]vinblastine in the presence of the ethyl acetate extracts of orange juice (diluted to be equivalent to 50% of the original orange juice strength).Duration : 60 min.Type of interaction : PharmacokineticsInteraction with drug : Phenylalanine*/L-phenylalanineDose/Conc.(drug) : 500 nM [14C]phenylalanineResult : NegativeRemark : Result: No significant effect on the uptake of [14C]phenylalanine by Coaco-2 cells was found, compared with the control. This finding indicated that the effect is specific to the vinblastine efflux transporter.
Part Used : น้ำจากผลActivity : DRUG INTERACTIONSolvent/Active Compound : 3,3'4',5,6,7,8-heptamethoxyflavone (HMF)Type of experiment : in vitroType of animal : -Type of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : -Dose/Conc.(herb) : Uptake experiments were performed in 250 ml of incubation buffer containing 10 nM [3H]vinblastine in the presence of HMF 0.1, 1, 10, 100 microMDuration : 60 min.Type of interaction : PharmacokineticsInteraction with drug : Vinblastine*/VLBDose/Conc.(drug) : 10 nM [3H]vinblastineResult : PositiveRemark : Result: The steady-state uptake of [3H]vinblastine by Caco-2 cells was increased by HMF in a concentration-dependent manner, and the uptakes amounted to 578 +/- 15.9% of the control, in the presence of 50 microM methoxyflavones.