Skip to main content

Table 1 Phospholipids characteristics

From: Nanomedicine review: clinical developments in liposomal applications

Phospholipid

Abbreviation

C:U

TC (º C)

Chargea

Advantages

Drawbacks

Hydrogenated soy phosphatidylcholine

HSPC

16–18:0

52

Neutral

Important role in membrane fusion, combined cationic lipids

Low cellular incorporation rate

Low cytotoxicity (Kolašinac et al. 2018; Zhao and Song Zhuang 2011)

Dilauroyl phosphatidylcholine

DLPC

12:0

− 2

Dimyristoyl phosphatidylcholine

DMPC

14:0

24

Dipalmitoyl phosphatidylcholine

DPPC

16:0

41

Distearoyl phosphatidylcholine

DSPC

18:0

55

Dioleoyl phosphatidylcholine

DOPC

18:1c9

− 17

Dilauroyl phosphatidylethanolamine

DLPE

12:0

29

Dimyristoyl phosphatidylethanolamine

DMPE

14:0

50

Dipalmitoyl phosphatidylethanolamine

DPPE

16:0

60

Distearoyl phosphatidylethanolamine

DSPE

18:0

74

Dioleoyl phosphatidylethanolamine

DOPE

18:1

− 16

Dilauroyl phosphatidylglycerol

DLPG

12:0

− 3

Negative

Prevent the aggregation of liposomes due to electrostatic repulsion

Laterally assemble into nanoclusters and this occurs in a charge-dependent manner

Accumulation in tumor

Adsorptive endocytosis and enhance stability

Rapidly removed from circulation by the reticuloendothelial system (RES)

Negatively charged liposomes do not significantly adsorb protein (Tsermentseli et al. 2018; Ma et al. 2017)

Dimyristoyl phosphatidylglycerol

DMPG

14:0

23

Dipalmitoyl phosphatidylglycerol

DPPG

16:0

41

Distearoyl phosphatidylglycerol

DSPG

18:0

55

Dioleoyl phosphatidylglycerol

DOPG

18:1

− 18

Dilauroyl phosphatidylserine

DLPS

12:0

 

Dimyristoyl phosphatidylserine

DMPS

14:0

35

Dipalmitoyl phosphatidylserine

DPPS

16:0

51

Distearoyl phosphatidylserine

DSPS

18:0

68

Dioleoyl phosphatidylserine

DOPS

18:1

− 11

Dilauroyl phosphatidic acid

DLPA

12:0

31

Dimyristoyl phosphatidic acid

DMPA

14:0

52

Dipalmitoyl phosphatidic acid

DPPA

16:0

65

Distearoyl phosphatidic acid

DSPA

18:0

75

Dioleoyl phosphatidic acid

DOPA

18:1

− 4

Diacyl dimethylammonium-propane

DAP

  

Positive

Strong gene transfer ability

The head group helps to attract the liposome to the negatively charged cell membrane, thus increasing the cell incorporation rate

Good protein adsorption, through adsorptive endocytosis

High cytotoxicity

Low efficiency

Positively charged lipids are not approved by FDA for clinical use (Li et al. 2019; Honary and Zahir 2013)

Dioleoyl trimethylammonium-propane

DOTAP

18:1

< 5

  1. C:U number of carbons:number of unsaturation, TC transition temperature
  2. aAt pH 7