TABLE 5.
The use of anti-HER2 ligand in various nano formulations to target HER2 receptors.
| Nanocarrier | Therapeutic agent(s) | Conjugates | Clinical outcome | References |
|---|---|---|---|---|
| HER2 immunoliposomes and liposomes in combination | Bevacizumab in a liposome and doxorubicin in an immunoliposome | Inhibition in HER2/MDR BC patiemts | Reduced the tumour size and lower toxicity | Tang et al. (2021) |
| Polymalic acid based nano drug | Antisense oligonucleotides | The polymer-attached 12-mer peptide mimicking trastuzumab recognises HER2+ cells | Decrease the tumour size | Ding et al. (2017) |
| Ethylenediamine functionalized single-walled nanotube | Oncogene suppressor p53 | Increased uptake by MCF-7 cells | Leading to enhanced caspase-3-induced apoptosis | Karmakar et al. (2011) |
| HER2 antibody-coated gold nanoparticles and gold sulphide | Gold–gold sulphide for high- intensity photoablation | Bind with SK-BR-3 cells overexpressing HER2 | Promotes thermal damage to tumour | Day et al. (2010) |
| Trastuzumab-modified gold nanoparticles with 111-In labelling | Radioactive-111-in | Local its injection to mice with sc MDA-MB-361 | Tumours arrested | Chinen et al. (2015) |