2022
DOI: 10.1016/j.colsurfb.2022.112763
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Functionalized bosutinib liposomes for target specific delivery in management of estrogen-positive cancer

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Cited by 9 publications
(4 citation statements)
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“…The candidate compounds screened from CMap were further selected based on their efficacy in inhibiting BRCA cell growth measured with IC 50 and EC 50 . Among the six identified drugs, bosutinib is a small molecule functioning as a dual inhibitor of BCR-ABL and Src tyrosine kinase for treating chronic myeloid leukemia (CML) and advanced solid tumors [ 72 ], including estrogen-positive breast cancer [ 73 ]. Dasatinib is an oral inhibitor of multiple tyrosine kinases, including BCR-ABL, Src, c-KIT, PDGFR-α, PDGFR-β, and ephrin receptor kinases [ 74 ].…”
Section: Discussionmentioning
confidence: 99%
“…The candidate compounds screened from CMap were further selected based on their efficacy in inhibiting BRCA cell growth measured with IC 50 and EC 50 . Among the six identified drugs, bosutinib is a small molecule functioning as a dual inhibitor of BCR-ABL and Src tyrosine kinase for treating chronic myeloid leukemia (CML) and advanced solid tumors [ 72 ], including estrogen-positive breast cancer [ 73 ]. Dasatinib is an oral inhibitor of multiple tyrosine kinases, including BCR-ABL, Src, c-KIT, PDGFR-α, PDGFR-β, and ephrin receptor kinases [ 74 ].…”
Section: Discussionmentioning
confidence: 99%
“…For instance, folate ligands target folate receptor [ 82 - 84 ] , transferrin ligands target transferrin receptor [ 85 , 86 ] , epidermal growth factor (EGF) protein [ 87 ] , epidermal growth factor receptor (EGFR) antibody [ 88 ] , and cetuximab [ 89 , 90 ] target EGFR, and prostate-specific peptide [ 91 ] and prostate-specific antigen gene [ 92 ] target prostate-specific membrane antigen (PSMA). Additionally, single-stranded DNA aptamer [ 93 ] targets forkhead box M1 (FOXM1), biotin [ 94 - 97 ] and fructose [ 96 ] target biotin receptor, and humanized anti-human epidermal growth factor receptor 2 (HER2) antibody [ 98 ] , engineered peptide [ 99 ] , and bispecific antibody [ 100 ] target HER2 receptor. Liposomes can also be designed for controlled release drug delivery to combat cancer drug resistance when exposed to physicochemical or biochemical stimuli, e.g., changes in pH [ 82 , 101 , 102 ] , specific enzymes [ 103 , 104 ] , ultrasound [ 105 , 106 ] , and so on.…”
Section: Lipid-based Nanomaterials For Cancer Resistancementioning
confidence: 99%
“…Singh et al. [51] designed and developed surface-functionalized bosutinib liposomes that exhibit estrogen-positive cancer activity via estrogen response elements, that contributes to the malignancy of cancer cells. DSPC-based liposomes were synthesized by activating the biotin carboxylic end using NHS and DCC.…”
Section: Functionalization Strategies For Immunoliposomesmentioning
confidence: 99%
“…DSPC-based liposomes were synthesized by activating the biotin carboxylic end using NHS and DCC. The activated biotin-NHS was then allowed to react with the amino-PEG-modified lipid surface (DSPC-PEG-NH 2 ) to form liposome derivatives that have been reported to be effective for targeted delivery [51] . Lian et al.…”
Section: Functionalization Strategies For Immunoliposomesmentioning
confidence: 99%