Page last updated: 2024-11-11

solufenum

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

solufenum: water-soluble salt of ibuprofen; structure in fourth source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID9841440
CHEMBL ID1201141
SCHEMBL ID44617
MeSH IDM0065869

Synonyms (60)

Synonym
p-isobutylphenyl-2-propionate lysine
l-lysine mono(4-isobutyl-alpha-methylbenzeneacetate)
soluphene
l-lysine, mono(alpha-methyl-4-(2-methylpropyl)benzeneacetate)
solufen [spanish]
einecs 260-751-7
ibuprofen lysinate
saren
dolormin
neoprofen (tn)
D06606
ibuprofen l-lysine (jan)
57469-77-9
solufenum
ibuprofen lysine (usan)
neoprofen
lisiprofen
ibuprofen l-lysine
imbun
CHEMBL1201141
ibuprofen lysine
A831448
(2s)-2,6-diaminohexanoic acid; 2-(4-isobutylphenyl)propanoic acid;ibuprofen lysine
AKOS015994629
BCP9000769
unii-n01orx9d6s
n01orx9d6s ,
arflamin
ibuprofen lysine [usan]
S1518
SCHEMBL44617
HS-0089
AB01274868-01
(s)-2,6-diaminohexanoic acid compound with 2-(4-isobutylphenyl)propanoic acid (1:1)
DTXSID50432054 ,
AB01274868_02
l-lysine mono((2rs)-2-(4-(2-methylpropyl)phenyl)propanoate
l-lysine compound with 2-(4-isobutylphenyl)propanoic acid (1:1)
HY-100586
ibuprofen (l-lysine)
l-lysine, .alpha.-methyl-4-(2-methylpropyl)benzeneacetate (1:1)
ibuprofen lysinate [who-dd]
ibuprofen lysine [vandf]
ibuprofen l-lysine [jan]
l-lysine, mono(.alpha.-methyl-4-(2-methylpropyl)benzeneacetate)
ibuprofen lysine [mart.]
ibuprofen lysine [orange book]
ibuprofen lysine (neoprofen)
(s)-2,6-diaminohexanoic acid 2-(4-isobutylphenyl)propanoic acid salt
(2s)-2,6-diaminohexanoic acid;2-[4-(2-methylpropyl)phenyl]propanoic acid
CCG-268058
Q27284326
D81763
[(5s)-5-amino-5-carboxypentyl]azanium;2-[4-(2-methylpropyl)phenyl]propanoate
ibuprofen-lysinat
DTXSID201024433
CS-0019739
ibuprofen lysine (mart.)
l-lysine, alpha-methyl-4-(2-methylpropyl)benzeneacetate (1:1)
dtxcid10382884

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
"A population pharmacokinetic study was performed on 66 neonates to characterize the concentration-time courses of ibuprofen."( An optimized ibuprofen dosing scheme for preterm neonates with patent ductus arteriosus, based on a population pharmacokinetic and pharmacodynamic study.
Eisinger, MJ; Hirt, D; Langhendries, JP; Marguglio, A; Schepens, P; Treluyer, JM; Urien, S; Van Overmeire, B, 2008
)
0.35
" A population pharmacokinetic model was developed with NONMEM."( An optimized ibuprofen dosing scheme for preterm neonates with patent ductus arteriosus, based on a population pharmacokinetic and pharmacodynamic study.
Eisinger, MJ; Hirt, D; Langhendries, JP; Marguglio, A; Schepens, P; Treluyer, JM; Urien, S; Van Overmeire, B, 2008
)
0.35
"Two randomized, single-dose, open-label, five-way crossover pharmacokinetic studies."( Ibuprofen sodium is absorbed faster than standard Ibuprofen tablets: results of two open-label, randomized, crossover pharmacokinetic studies.
Kellstein, D; Laurent, AL; Legg, TJ; Leyva, R, 2014
)
0.4
"Log-transformed area under the plasma concentration versus time curve to last observable concentration (AUCL) and maximum plasma concentration (C max) were the primary pharmacokinetic parameters; time to maximum measured plasma concentration (T max) was analyzed post hoc."( Ibuprofen sodium is absorbed faster than standard Ibuprofen tablets: results of two open-label, randomized, crossover pharmacokinetic studies.
Kellstein, D; Laurent, AL; Legg, TJ; Leyva, R, 2014
)
0.4

Bioavailability

ExcerptReferenceRelevance
"* To assess the absolute bioavailability of ibuprofen after its oral application as a lysine salt, intravenous injections of ibuprofen solutions containing 200 mg and 400 mg of the drug served as reference application."( Pharmacokinetics and absolute bioavailability of ibuprofen after oral administration of ibuprofen lysine in man.
Augustin, J; Kerkmann, T; Koselowske, G; Mangold, B; Martin, W; Töberich, H, 1990
)
0.28
" The absorption rate constants (ka) were estimated on the presumption of complete absorption and dose-dependent elimination."( Bioavailability of racemic ibuprofen and its lysinate from suppositories in rabbits.
Garrett, ER; Gtówka, FK; Hermann, TW, 1993
)
0.29
" An analysis of variance (ANOVA) model was used, and the 90% confidence intervals (CI) were calculated; further analyses were made regarding rate of absorption and variability."( Ibuprofen lysinate, quicker and less variable: relative bioavailability compared to ibuprofen base in a pediatric suspension dosage form.
Antonijoan, RM; Ballester, MR; Coimbra, J; Ferrero-Cafiero, JM; Font, X; Gich, I; Martínez, J; Mathison, Y; Puntes, M; Tarré, M, 2015
)
0.42
"While S-ibuprofen shows a similar bioavailability for AUC0t, AUC0∞, and Cmax, R-ibuprofen shows suprabioavailability for the lysinate formulation."( Ibuprofen lysinate, quicker and less variable: relative bioavailability compared to ibuprofen base in a pediatric suspension dosage form.
Antonijoan, RM; Ballester, MR; Coimbra, J; Ferrero-Cafiero, JM; Font, X; Gich, I; Martínez, J; Mathison, Y; Puntes, M; Tarré, M, 2015
)
0.42

Dosage Studied

ExcerptRelevanceReference
" From the results of intravenous injections one can deduce linear ibuprofen pharmacokinetics within the considered dosage range, with corresponding AUC0-infinity values of 3786 micrograms * min ml-1 and 7260 micrograms * min ml-1 for the 200 mg and 400 mg doses, respectively."( Pharmacokinetics and absolute bioavailability of ibuprofen after oral administration of ibuprofen lysine in man.
Augustin, J; Kerkmann, T; Koselowske, G; Mangold, B; Martin, W; Töberich, H, 1990
)
0.28
" Dosing schemes were proposed as a function of postnatal age, to achieve this AUC and to improve the efficacy of treatment for patent ductus arteriosus in neonates."( An optimized ibuprofen dosing scheme for preterm neonates with patent ductus arteriosus, based on a population pharmacokinetic and pharmacodynamic study.
Eisinger, MJ; Hirt, D; Langhendries, JP; Marguglio, A; Schepens, P; Treluyer, JM; Urien, S; Van Overmeire, B, 2008
)
0.35
"Pharmaceutical industry has been encountering antimicrobial activity of non-antibiotics during suitability tests carried out prior to routine pharmacopoeial microbiological purity analysis of finished dosage forms."( Antimicrobial activity of ibuprofen: new perspectives on an "Old" non-antibiotic drug.
Kos, B; Obad, J; Šušković, J, 2015
)
0.42
" The aim of the study was to evaluate the taste masking effectiveness of Smartseal 30D and ReadyMix on a range of bitter drug substances such as diphenhydramine HCl (DPD), ibuprofen lysine (IBU-LS), and phenylephrine HCl (PPH) for the development of paediatric dosage forms."( Comparative taste-masking evaluation of microencapsulated bitter drugs using Smartseal 30D and ReadyMix for paediatric dosage forms.
Douroumis, D; Mithu, MSH; Muoka, LC; Nandi, U; Ross, SA, 2021
)
0.62
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (41)

TimeframeStudies, This Drug (%)All Drugs %
pre-19907 (17.07)18.7374
1990's6 (14.63)18.2507
2000's12 (29.27)29.6817
2010's15 (36.59)24.3611
2020's1 (2.44)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials14 (31.82%)5.53%
Reviews1 (2.27%)6.00%
Case Studies2 (4.55%)4.05%
Observational0 (0.00%)0.25%
Other27 (61.36%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]