1,2-distearoylphosphatidylethanolamine

Known as: distearoyl-L-phosphatidylethanolamine, 1,2-dioctadecanoyl-sn-glycero-3-phosphoethanolamine, DSPE 
 
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
Successful further development of superhigh-constrast upconversion (UC) bioimaging requires addressing the existing paradox: 980… (More)
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Highly Cited
2009
Highly Cited
2009
We have previously shown that the PEGylated LPD (liposome-polycation-DNA) nanoparticles were highly efficient in delivering siRNA… (More)
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Highly Cited
2009
Highly Cited
2009
Site-specific delivery of drugs and therapeutics can significantly reduce drug toxicity and increase the therapeutic effect… (More)
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Highly Cited
2008
Highly Cited
2008
We have developed a nanoparticle formulation [liposomes-protamine-hyaluronic acid nanoparticle (LPH-NP)] for systemically… (More)
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Highly Cited
2006
Highly Cited
2006
Selective gene inhibition by antisense oligodeoxynucleotide (AS-ODN) or by small interference RNA (siRNA) therapeutics promises… (More)
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Highly Cited
2004
Highly Cited
2004
Sterically stabilized micelles (SSM) composed of poly(ethylene glycol-2000)-grafted distearoylphosphatidylethanolamine (DSPE-PEG… (More)
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Highly Cited
2000
Highly Cited
2000
Folic acid, attached to polyethyleneglycol-derivatized, distearoyl-phosphatidylethanolamine, was used to target in vitro… (More)
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Highly Cited
1993
Highly Cited
1993
The pharmacokinetics of doxorubicin (DOX) encapsulated in liposomes containing polyethylene glycol-derivatized… (More)
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Highly Cited
1991
Highly Cited
1991
Novel synthetic lipid derivatives of poly(ethylene glycol) (PEG) have been synthesized and tested for their ability to decrease… (More)
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Highly Cited
1990
Highly Cited
1990
New lipidic carriers suitable for the sustained drug release in vivo are presented. They consist of middle sized, compact… (More)
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