2020
DOI: 10.1016/j.jconrel.2020.05.033
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Megalin-targeting liposomes for placental drug delivery

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Cited by 33 publications
(20 citation statements)
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“…In animal models, targeted liposomes have been used for delivery of indomethacin to the uterus, for the treatment of pre-term labor [38,39]. Similarly, targeted liposomes have been used to deliver insulin-like growth factor-I and -II [7], SE175 [29] and gentamicin [40] to the placenta, to increase trophoblast proliferation, improve uteroplacental blood flow and enhance placental liposome uptake, respectively. There are few reported studies of liposomal uptake and drug delivery in human placental explants, other than our own.…”
Section: Discussionmentioning
confidence: 99%
“…In animal models, targeted liposomes have been used for delivery of indomethacin to the uterus, for the treatment of pre-term labor [38,39]. Similarly, targeted liposomes have been used to deliver insulin-like growth factor-I and -II [7], SE175 [29] and gentamicin [40] to the placenta, to increase trophoblast proliferation, improve uteroplacental blood flow and enhance placental liposome uptake, respectively. There are few reported studies of liposomal uptake and drug delivery in human placental explants, other than our own.…”
Section: Discussionmentioning
confidence: 99%
“…To go further, it could be interesting to design new nanosystems such as targeting nanoparticles, such as liposomes, for placental MRI. As liposomes already showed their value as contrast agent delivery systems but also as placental targeting nanocarriers, it seems natural to consider them to ensure a specific delivery of the contrast agent to the placenta to ensure the safety of usage for both the mother and the fetus [110][111][112]. Ultimately, any use of nanomaterials in pregnancy should still require a cautious and extensive risk-benefit evaluation.…”
Section: Discussionmentioning
confidence: 99%
“…Liposomes were synthesized using a thin‐film hydration method 39–41 . Specifically, in a round‐bottom flask, 2 mg of Fer‐1 (or 3 mg Dex), 8 mg of cholesterol, 10 mg of DSPE‐mPEG, and 30 mg of soybean lecithin (molar ratio, 2:5:1:10) were added to 10 ml of methylene chloride and dissolved completely.…”
Section: Methodsmentioning
confidence: 99%
“…Liposomes were synthesized using a thin-film hydration method. [39][40][41] Specifically, in a round-bottom flask, 2 mg of Fer-1 (or 3 mg Dex), 8 mg of cholesterol, 10 mg of DSPE-mPEG, and 30 mg of soybean lecithin (molar ratio, 2:5:1:10) were added to 10 ml of methylene chloride and dissolved completely. The mixture was evaporated using a rotary evaporator under reduced pressure until a homogeneous phospholipid film formed.…”
Section: Liposomes Preparation and Characterizationmentioning
confidence: 99%