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1,2-distearoylphosphatidylethanolamine and camptothecin

1,2-distearoylphosphatidylethanolamine has been researched along with camptothecin in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Koo, OM; Onyuksel, H; Rubinstein, I1
Anderson, BD; Joguparthi, V; Xiang, TX1
Anderson, BD; Joguparthi, V1
Atyabi, F; Dinarvand, R; Esmaeili, F; Farkhondehfai, A1

Other Studies

4 other study(ies) available for 1,2-distearoylphosphatidylethanolamine and camptothecin

ArticleYear
Camptothecin in sterically stabilized phospholipid micelles: a novel nanomedicine.
    Nanomedicine : nanotechnology, biology, and medicine, 2005, Volume: 1, Issue:1

    Topics: Antineoplastic Agents, Phytogenic; Breast Neoplasms; Camptothecin; Capsules; Cell Line, Tumor; Cell Survival; Drug Compounding; Drug Stability; Humans; Liposomes; Micelles; Nanomedicine; Nanoparticles; Particle Size; Phosphatidylethanolamines; Solubility; Stereoisomerism

2005
Liposome transport of hydrophobic drugs: gel phase lipid bilayer permeability and partitioning of the lactone form of a hydrophobic camptothecin, DB-67.
    Journal of pharmaceutical sciences, 2008, Volume: 97, Issue:1

    Topics: Animals; Antineoplastic Agents, Phytogenic; Blood Proteins; Buffers; Camptothecin; Chemical Phenomena; Chemistry, Physical; Drug Carriers; Excipients; Gels; Hydrolysis; Kinetics; Lactones; Lipid Bilayers; Lipids; Liposomes; Models, Statistical; Organosilicon Compounds; Permeability; Phosphatidylethanolamines; Polyethylene Glycols; Rats; Reproducibility of Results; Solubility

2008
Liposomal delivery of hydrophobic weak acids: enhancement of drug retention using a high intraliposomal pH.
    Journal of pharmaceutical sciences, 2008, Volume: 97, Issue:1

    Topics: Acids; Antineoplastic Agents, Phytogenic; Buffers; Camptothecin; Chemical Phenomena; Chemistry, Pharmaceutical; Chemistry, Physical; Chromatography, High Pressure Liquid; Dialysis; Drug Carriers; Drug Delivery Systems; Hydrogen-Ion Concentration; Lipid Bilayers; Liposomes; Membranes, Artificial; Particle Size; Permeability; Pharmaceutical Preparations; Pharmaceutical Vehicles; Phosphatidylethanolamines; Polyethylene Glycols; Thiourea

2008
Preparation of pegylated nano-liposomal formulation containing SN-38: In vitro characterization and in vivo biodistribution in mice.
    Acta pharmaceutica (Zagreb, Croatia), 2009, Volume: 59, Issue:2

    Topics: Animals; Antineoplastic Agents, Phytogenic; Camptothecin; Chemistry, Pharmaceutical; Drug Stability; Female; Injections, Intravenous; Irinotecan; Liposomes; Mice; Mice, Inbred BALB C; Nanoparticles; Particle Size; Phosphatidylcholines; Phosphatidylethanolamines; Polyethylene Glycols; Solubility; Technology, Pharmaceutical; Tissue Distribution

2009