» Articles » PMID: 33854311

Regression of Melanoma Following Intravenous Injection of Plumbagin Entrapped in Transferrin-Conjugated, Lipid-Polymer Hybrid Nanoparticles

Overview
Publisher Dove Medical Press
Specialty Biotechnology
Date 2021 Apr 15
PMID 33854311
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Plumbagin, a naphthoquinone extracted from the officinal leadwort presenting promising anti-cancer properties, has its therapeutic potential limited by its inability to reach tumors in a specific way at a therapeutic concentration following systemic injection. The purpose of this study is to assess whether a novel tumor-targeted, lipid-polymer hybrid nanoparticle formulation of plumbagin would suppress the growth of B16-F10 melanoma in vitro and in vivo.

Methods: Novel lipid-polymer hybrid nanoparticles entrapping plumbagin and conjugated with transferrin, whose receptors are present in abundance on many cancer cells, have been developed. Their cellular uptake, anti-proliferative and apoptosis efficacy were assessed on various cancer cell lines in vitro. Their therapeutic efficacy was evaluated in vivo after tail vein injection to mice bearing B16-F10 melanoma tumors.

Results: The transferrin-bearing lipid-polymer hybrid nanoparticles loaded with plumbagin resulted in the disappearance of 40% of B16-F10 tumors and regression of 10% of the tumors following intravenous administration. They were well tolerated by the mice.

Conclusion: These therapeutic effects, therefore, make transferrin-bearing lipid-polymer hybrid nanoparticles entrapping plumbagin a highly promising anti-cancer nanomedicine.

Citing Articles

Novel Strategies for Tumor Treatment: Harnessing ROS-Inducing Active Ingredients from Traditional Chinese Medicine Through Multifunctional Nanoformulations.

Zhang Z, Li M, Zhang X, Zhou F Int J Nanomedicine. 2024; 19:9659-9688.

PMID: 39309188 PMC: 11416109. DOI: 10.2147/IJN.S479212.


Pharmacological Features and Therapeutic Implications of Plumbagin in Cancer and Metabolic Disorders: A Narrative Review.

Sharma B, Dhiman C, Hasan G, Shamsi A, Hassan M Nutrients. 2024; 16(17).

PMID: 39275349 PMC: 11397539. DOI: 10.3390/nu16173033.


Transferrin-Modified Triptolide Liposome Targeting Enhances Anti-Hepatocellular Carcinoma Effects.

Zhao X, Yang Y, Su X, Xie Y, Liang Y, Zhou T Biomedicines. 2023; 11(10).

PMID: 37893242 PMC: 10604558. DOI: 10.3390/biomedicines11102869.


Lipid polymer hybrid nanoparticles: a custom-tailored next-generation approach for cancer therapeutics.

Gajbhiye K, Salve R, Narwade M, Sheikh A, Kesharwani P, Gajbhiye V Mol Cancer. 2023; 22(1):160.

PMID: 37784179 PMC: 10546754. DOI: 10.1186/s12943-023-01849-0.


Nanoparticle-Based Treatment Approaches for Skin Cancer: A Systematic Review.

Diaz M, Natarelli N, Aflatooni S, Aleman S, Neelam S, Tran J Curr Oncol. 2023; 30(8):7112-7131.

PMID: 37622997 PMC: 10453819. DOI: 10.3390/curroncol30080516.


References
1.
Daniels T, Bernabeu E, Rodriguez J, Patel S, Kozman M, Chiappetta D . The transferrin receptor and the targeted delivery of therapeutic agents against cancer. Biochim Biophys Acta. 2011; 1820(3):291-317. PMC: 3500658. DOI: 10.1016/j.bbagen.2011.07.016. View

2.
Guo L, Zhang H, Wang F, Liu P, Wang Y, Xia G . Targeted multidrug-resistance reversal in tumor based on PEG-PLL-PLGA polymer nano drug delivery system. Int J Nanomedicine. 2015; 10:4535-47. PMC: 4509529. DOI: 10.2147/IJN.S85587. View

3.
Mandala Rayabandla S, Aithal K, Anandam A, Shavi G, Nayanabhirama U, Arumugam K . Preparation, in vitro characterization, pharmacokinetic, and pharmacodynamic evaluation of chitosan-based plumbagin microspheres in mice bearing B16F1 melanoma. Drug Deliv. 2010; 17(3):103-13. DOI: 10.3109/10717540903548447. View

4.
Gao H, Yang Z, Zhang S, Cao S, Shen S, Pang Z . Ligand modified nanoparticles increases cell uptake, alters endocytosis and elevates glioma distribution and internalization. Sci Rep. 2013; 3:2534. PMC: 3755284. DOI: 10.1038/srep02534. View

5.
Toy R, Peiris P, Ghaghada K, Karathanasis E . Shaping cancer nanomedicine: the effect of particle shape on the in vivo journey of nanoparticles. Nanomedicine (Lond). 2013; 9(1):121-34. PMC: 4057606. DOI: 10.2217/nnm.13.191. View