Page last updated: 2024-10-15

lucinactant

Description

lucinactant: a pulmonary surfactant composed of sinapultide, colfosceril palmitate, palmitoyloleaoylphosphatidylglycerol, and palmitic acid [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID155886531
MeSH IDM0487844

Synonyms (4)

Synonym
825600-90-6
lucinactant
l-lysyl-l-leucyl-l-leucyl-l-leucyl-l-leucyl-l-lysyl-l-leucyl-l-leucyl-l-leucyl-l-leucyl-l-lysyl-l-leucyl-l-leucyl-l-leucyl-l-leucyl-l-lysyl-l-leucyl-l-leucyl-l-leucyl-l-leucyl-l-lysine, acetate; sinapultide acetate
B0084-462251

Research Excerpts

Overview

Lucinactant (Surfaxin®) is a new synthetic surfactant. It contains sinapultide, a bioengineered peptide mimic of surfactants-associated protein B. LucinActant is a more effective surfactent preparation than colfosceril palmitate.

ExcerptReference
"Lucinactant is a synthetic surfactant containing sinapultide, a bioengineered peptide mimic of surfactant-associated protein B."( Lucinactant for the prevention of respiratory distress syndrome in premature infants.
Donn, SM; Jordan, BK, 2013
)
"Lucinactant (Surfaxin®) is a new synthetic surfactant with a pulmonary surfactant-associated protein B mimic that recently received FDA approval."( Lucinactant for the treatment of respiratory distress syndrome in neonates.
Fernandez-Bustamante, A; Piehl, E, 2012
)
"Lucinactant is a new synthetic peptide-containing surfactant that contains sinapultide, a novel, 21-amino acid peptide (leucine and lysine repeating units, KL4 peptide) designed to mimic human SP-B."( A multicenter, randomized, controlled trial of lucinactant versus poractant alfa among very premature infants at high risk for respiratory distress syndrome.
Bernstein, G; d'Agostino, R; Gadzinowski, J; Hajdu, J; Lacaze-Masmonteil, T; Massaro, J; Sanchez-Luna, M; Schaber, CJ; Segal, R; Sinha, SK; Valls i Soler, A; Wiswell, TE, 2005
)
"Lucinactant is a more effective surfactant preparation than colfosceril palmitate for the prevention of RDS. "( A multicenter, randomized, masked, comparison trial of lucinactant, colfosceril palmitate, and beractant for the prevention of respiratory distress syndrome among very preterm infants.
Bancalari, A; Bancalari, E; d'Agostino, R; Gadzinowski, J; Kopelman, B; Kornacka, MK; Massaro, J; Merritt, TA; Moya, FR; Salinas, V; Schaber, CJ; Segal, R; Tsai, H, 2005
)

Dosage Studied

ExcerptReference
" There were no differences in major dosing complications."( A multicenter, randomized, controlled trial of lucinactant versus poractant alfa among very premature infants at high risk for respiratory distress syndrome.
Bernstein, G; d'Agostino, R; Gadzinowski, J; Hajdu, J; Lacaze-Masmonteil, T; Massaro, J; Sanchez-Luna, M; Schaber, CJ; Segal, R; Sinha, SK; Valls i Soler, A; Wiswell, TE, 2005
)
" We conducted a masked, multicenter, multinational, randomized, controlled, pilot study to estimate the effects of treating infants at high risk for developing bronchopulmonary dysplasia with lucinactant, a synthetic, peptide-containing surfactant, on safety during dosing and the incidence of death or bronchopulmonary dysplasia."( A pilot randomized, controlled trial of later treatment with a peptide-containing, synthetic surfactant for the prevention of bronchopulmonary dysplasia.
Aschner, J; Bose, C; Cummings, JJ; Donn, SM; Guardia, C; Laughon, M; Liu, G; Morabito, C; Moya, F; Segal, R, 2009
)
" Aerosurf was well tolerated, with transient desaturations observed during dosing without bradycardia or hypotension."( An open label, pilot study of Aerosurf® combined with nCPAP to prevent RDS in preterm neonates.
Bernstein, G; Finer, NN; Job, L; Mazela, J; Merritt, TA; Segal, R, 2010
)
" One retreatment was allowed 12-24 hrs after initial dosing if hypoxemia persisted."( A pilot, randomized, controlled clinical trial of lucinactant, a peptide-containing synthetic surfactant, in infants with acute hypoxemic respiratory failure.
Barton, P; Cheifetz, IM; Cruces, P; Guardia, CG; Markovitz, B; Moya, FR; Randolph, AG; Segal, R; Simmons, P; Thomas, NJ, 2012
)
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (34)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's15 (44.12)29.6817
2010's18 (52.94)24.3611
2020's1 (2.94)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 (%)
Trials6 (17.65%)5.53%
Reviews11 (32.35%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other17 (50.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]