TY - JOUR
T1 - Nanoparticle-mediated active and passive drug targeting in oral squamous cell carcinoma
T2 - current trends and advances
AU - Manikkath, Jyothsna
AU - Manikkath, Aparna
AU - Lad, Hitesh
AU - Vora, Lalitkumar K.
AU - Mudgal, Jayesh
AU - Shenoy, Rekha R.
AU - Ashili, Shashaanka
AU - Radhakrishnan, Raghu
N1 - Publisher Copyright:
© 2024 Expert Publishing Medicine Ltd trading as Taylor & Francis.
PY - 2023/11/1
Y1 - 2023/11/1
N2 - Oral squamous cell carcinoma (OSCC) is an invasive and highly malignant cancer with significant morbidity and mortality. Existing treatments including surgery, chemotherapy and radiation have poor overall survival rates and prognosis. The intended therapeutic effects of chemotherapy are limited by drug resistance, systemic toxicity and adverse effects. This review explores advances in OSCC treatment, with a focus on lipid-based platforms (solid lipid nanoparticles, nanostructured lipid carriers, lipid-polymer hybrids, cubosomes), polymeric nanoparticles, self-assembling nucleoside nanoparticles, dendrimers, magnetic nanovectors, graphene oxide nanostructures, stimuli-responsive nanoparticles, gene therapy, folic acid receptor targeting, gastrin-releasing peptide receptor targeting, fibroblast activation protein targeting, urokinase-type plasminogen activator receptor targeting, biotin receptor targeting and transferrin receptor targeting. This review also highlights oncolytic viruses as OSCC therapy candidates.
AB - Oral squamous cell carcinoma (OSCC) is an invasive and highly malignant cancer with significant morbidity and mortality. Existing treatments including surgery, chemotherapy and radiation have poor overall survival rates and prognosis. The intended therapeutic effects of chemotherapy are limited by drug resistance, systemic toxicity and adverse effects. This review explores advances in OSCC treatment, with a focus on lipid-based platforms (solid lipid nanoparticles, nanostructured lipid carriers, lipid-polymer hybrids, cubosomes), polymeric nanoparticles, self-assembling nucleoside nanoparticles, dendrimers, magnetic nanovectors, graphene oxide nanostructures, stimuli-responsive nanoparticles, gene therapy, folic acid receptor targeting, gastrin-releasing peptide receptor targeting, fibroblast activation protein targeting, urokinase-type plasminogen activator receptor targeting, biotin receptor targeting and transferrin receptor targeting. This review also highlights oncolytic viruses as OSCC therapy candidates.
UR - https://www.scopus.com/pages/publications/85182955753
UR - https://www.scopus.com/inward/citedby.url?scp=85182955753&partnerID=8YFLogxK
U2 - 10.2217/nnm-2023-0247
DO - 10.2217/nnm-2023-0247
M3 - Review article
C2 - 38197397
AN - SCOPUS:85182955753
SN - 1743-5889
VL - 18
SP - 2061
EP - 2080
JO - Nanomedicine (London, England)
JF - Nanomedicine (London, England)
IS - 27
ER -