Nanoparticle-mediated drug delivery for treating melanoma

Vaibhav Mundra, Wei Li, Ram I. Mahato

Research output: Contribution to journalReview article

21 Citations (Scopus)

Abstract

Melanoma originated from melanocytes is the most aggressive type of skin cancer with limited treatment options. New targeted therapeutic options with the discovery of BRAF and MEK inhibitors have shown significant survival benefits. Despite the recent progress, development of chemoresistance and systemic toxicity remains a challenge for treating metastatic melanoma. While the response from the first line of treatment against melanoma using dacarbazine remains only 5-10%, the prolonged use of targeted therapy against mutated oncogene BRAF develops chemoresistance. In this review, we will discuss the nanoparticle-based strategies for encapsulation and conjugation of drugs to the polymer for maximizing their tumor distribution through enhanced permeability and retention effect. We will also highlight photodynamic therapy and design of melanoma-targeted nanoparticles.

Original languageEnglish (US)
Pages (from-to)2613-2633
Number of pages21
JournalNanomedicine
Volume10
Issue number16
DOIs
StatePublished - Aug 1 2015

Fingerprint

Drug delivery
Nanoparticles
Melanoma
drug
Dacarbazine
Photodynamic therapy
encapsulation
permeability
Mitogen-Activated Protein Kinase Kinases
Encapsulation
tumor
Pharmaceutical Preparations
Toxicity
Tumors
inhibitor
cancer
skin
Skin
Polymers
polymer

All Science Journal Classification (ASJC) codes

  • Medicine (miscellaneous)
  • Bioengineering
  • Biomedical Engineering
  • Development
  • Materials Science(all)

Cite this

Nanoparticle-mediated drug delivery for treating melanoma. / Mundra, Vaibhav; Li, Wei; Mahato, Ram I.

In: Nanomedicine, Vol. 10, No. 16, 01.08.2015, p. 2613-2633.

Research output: Contribution to journalReview article

Mundra, Vaibhav ; Li, Wei ; Mahato, Ram I. / Nanoparticle-mediated drug delivery for treating melanoma. In: Nanomedicine. 2015 ; Vol. 10, No. 16. pp. 2613-2633.
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