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. 2023 May 18;18:2659–2676. doi: 10.2147/IJN.S406415

Table 3.

Recent Studies Presenting Different Liposome-Based Bioformulations for Drug Delivery in LC Treatment

Liposome Drug Formulation Name In vitro or in vivo/Model Cancer Type Result References
Liposome Doxorubicin (Dox) SA-5-Dox-LP In vivo/mice with lung tumors
In vitro/BT-474, A549, Calu-3, and MCF-7 cells
NSCLC Targeted SA-5-Dox-LP showed better anti-proliferative activity [94]
Chitosan oligosaccharide-modified liposomes Paclitaxel (PTX) PTX-loaded CP50-LSs In vitro/A549
In vivo/mice
LC CSO modification provides promising applicability for nanomedicine [95]
RGD-modified liposomes DOX DOX-RGD-LPs In vitro/A549
In vivo/Balb/c nude mice
LC The DOX-loaded pH-sensitive liposome, which has been modified with 5% cRGD-lipid, could be used to enhance cancer therapy [96]
Liposome Lonidamine or Epirubicin - In vitro/A549 cells
In vivo/Female BALB/c mice
NSCLC The formulation used as an anticancer agent to treat drug-resistant LC [97]
Folate-modified submicron-sized liposome (ssLip) Rapamycin (RM) RM/FA-ssLip In vitro/KB and LL2 cells and A549 cells
In vivo/Male C57BL/6NCr mice
LC Administration of this formulation extended the survival of LL2 cell tumor-bearing mice [98]
pH-sensitive liposomes (PSL) Thymoquinone (TQ) TQPSL In vivo/Swiss Albino Mice LC It shows potential of TQPSL as a LC therapeutic agent [99]
PEGylated liposome Lycobetaine
Olic acid
RGD
LBT-OA-PEG-Lipo + nRGD In vivo/ mice xenograft Lung carcinoma Improved tumor penetration, and increased extravasation of formulations and antitumor efficacy [93]
PSL Afatinib (tyrosine kinase inhibitor) AFT loaded PSL In vitro/human LC cells (H-1975) NSCLC cells AFT loaded-PSL prompted apoptosis in H-1975 cells [100]
Liposome Betulinic parthenolide, honokiol and ginsenoside Rh2 Drug-loaded liposome In vivo/mice
In vitro/A549 cells
LC Cocktail liposome systems could offer a more efficient and safer treatment for LC [101]
PEGylated cationic liposomes PTX MLV-PEG-PTX In vivo/Female C57BL/6 mice
In vitro/A549 and the murine lung
carcinoma cell line LL/2
LC MLV-PEG-PTX exhibited biocompatibility and anticancer activity against CSCs [53]
DSPE-PEG2000-PFV Daunorubicin and Dioscin Daunorubicin and dioscin co-delivery liposomes In vitro/A549 cells
In vivo/Male BALB/c nude mice
NSCLC Increased the cellular uptake facilitated by PFV cell-penetrating peptide; augmented inhibitory effects on vasculogenic mimicry formation and tumor metastasis from the inclusion of dioscin [102]
Liposome Docetaxel and CD133 aptamers CD133-DTX LP In vitro/A549 tumor mice
In vivo/mice xenograft
LC CD133-DTX LP significantly decreased cell proliferation and improved the therapeutic efficiency [103]
Folate-modified liposomes Metallothionein 1D pseudogene (MT1DP)
Erastin
Erastin/MT1DP@FA-LPs (E/M@FA-LPs) In vitro/A549 and H1299 cells
In vivo/BALB/c nude mice
NSCLS The combination increased the bioavailability and effectiveness of the drug/gene [104]
Folate-modified liposome (F-PLP) Plasmid BIM F-PLP/pBIM In vitro/LL/2 and A549 LC
In vivo/Female C57BL/6 mice
NSCLS Developed formulation considerably blocked tumor growth by inducing apoptosis in tumor cells, and inhibited proliferation and angiogenesis [105]
Liposome Curcumin Liposomal curcumin dry powder inhaler (LCD) In vitro/A549 cells Primary LC Formulation having notable anticancer effects compared with the other two medications with reference to the pathology [90]
Liposome Inhalable Pirfenidone (PFD) PFD-loaded liposomes In vitro/H4006, A549 cell lines NSCLC PFD-loaded liposomes induced cell migration, apoptosis, and angiogenesis assays [92]
Cationic liposome PTX and Survivin siRNA L-PTX-PSur In vitro/NCI-H460 LC cells LC Developed formulation synergistically inhibits cancer cell growth [106]
Liposome PTX
Curcumin (CUR)
RGD
RGD- PTX-CUR LPs In vitro/A549 LC cell lines
In vivo/BALB/c nude mice
LC The present formulation shows the antitumor effect in vivo, compared with the non-modified LPs [52]
Liposome PTX LP (liposomal paclitaxel)-in-E. coli (LPE) In vitro/A549 LC cell lines LC LPE significantly down-regulated the VEGF and HIF-1α in rat primary LC, and exacerbated apoptosis in the same cells [107]