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. 2022 May 20;10(5):1187. doi: 10.3390/biomedicines10051187

Table 3.

The examples of Res–loaded delivery systems for anticancer therapy.

DDS Material Size [nm] EE [%] Preparation Method Location Status Ref.
NPs Au 30.75 ± 3.41 n/d Reduction with chloroauric acid Breast In vitro—MCF-7 cells [133]
NPs PCL 132 ± 4 a 98.4 ± 0.3 a Interfacial deposition Skin In vitro—B16F10 cells
In vivo—mice
[134]
NPs PLC, PLGA, PEG 150 83.30 ± 13.47 Nanoprecipitation Prostate In vitro—DU-145, PC-3 and LNCaP cells [135]
NPs PLGA 202.8 ± 2.64 89.32 ± 3.51 Solvent displacement Prostate In vitro—LNCaP cells [136]
NPs CB n/d n/d N/d Lung In vitro—A549 cells [137]
NPs FA-HSA 102.1 ± 4.9 98.36 High pressure fluid nano-homogeneous emulsification Liver In vitro—HepG2 cells
In vivo—mice
[138]
NPs Pluronic F127 block copolymer, vitamin E-TPGS 179 ± 22 73 ± 0.9 Emulsification Breast In vitro—MCF-7,
MDA-MB-231, MCF-10A cells
[139]
SLNPs SA, saturated monoacid, triglyceride, Myrj52 168 ± 10.7 n/d Emulsification and low-temperature solidification Breast In vitro—MDA-MB-231 cells [140]
SLNPs Apolipoprotein E, DSPE, palmitic acid 217.1 ± 5.8 98.9 ± 0.6 High shear homogenization Brain hCMEC/D3 cells [141]

Au—gold; CB—carbon black; CS—chitosan; DDS—drug delivery system; DSPE—1,2-distearoyl-sn-glycero-3-phosphorylethanolamine; FA—folic acid; HSA—human serum albumin; Myrj52-polyoxyethylene (40) stearate; PCL—poly(ε-caprolactone); PLGA—poly(lactide-co-glycolide); SA—stearic acid. a nanoparticles containing 10 mg of Res.