Abstract

Melanoma is an aggressive form of skin cancer with a very high mortality rate. Early diagnosis of the disease, the utilization of more potent pharmacological agents, and more effective drug delivery systems are essential to achieve an optimal treatment plan. The applications of nanotechnology to improve therapeutic efficacy and early diagnosis for melanoma treatment have received great interest among researchers and clinicians. In this review, we summarize the recent progress of utilizing various nanomaterials for theranostics of melanoma. The key importance of using nanomaterials for theranostics of melanoma is to improve efficacy and reduce side effects, ensuring safe implementation in clinical use. As opposed to conventional in vitro diagnostic methods, in vivo medical imaging technologies have the advantages of being a type of non-invasive, real-time monitoring. Several common nanoparticles, including ultrasmall superparamagnetic iron oxide nanoparticles, silica nanoparticles, and carbon-based nanoparticles, have been applied to deliver chemotherapeutic agents for the theranostics of melanoma. The application of nanomaterials for theranostics in molecular imaging (MRI, PET, US, OI, etc.) plays an important role in targeting drug delivery of melanoma, by monitoring the distribution site of the molecular imaging probe and the therapeutic drug in the body in real-time. Hence, it is worthwhile to anticipate the approval of these nanomaterials for theranostics in molecular imaging by the US Food and Drug Administration in clinical trials.

Highlights

  • Malignant melanoma (MM) is one of the deadliest skin cancers that may occur in any anatomical site of melanocytes

  • With the recent development of clinical trials for triple therapy and drug tolerance to target therapy analyzed at single cell level in melanoma, we expect that the combination of treatments can enhance treatment efficacy and prevent the emergence of drug resistance

  • human protein ferritin (HFt)-MSH-poly(ethylene glycol) (PEG) NPs exhibited very high selectivity, accumulating and targeting at the primary melanoma as compared to the control HFt-PEG NPs with no α-melanocyte-stimulating hormone (α-MSH) moiety. These results indicated that HFt-MSH-PEG NPs can be used as promising carriers to deliver diagnostic or therapeutic agents to cutaneous melanoma sites selectively in vivo

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Summary

Introduction

Malignant melanoma (MM) is one of the deadliest skin cancers that may occur in any anatomical site of melanocytes. With the recent development of clinical trials for triple therapy (combined BRAF/MEK inhibition with PD-1 blockade) and drug tolerance to target therapy analyzed at single cell level in melanoma, we expect that the combination of treatments can enhance treatment efficacy and prevent the emergence of drug resistance. Among these new diagnostic and therapeutic technologies, the integration of imaging and treatment technology has received great attention recently. This review is focused on the recent progress on the treatments of malignant melanoma by theranostic nanoparticles

Introduction of Melanoma
Melanoma Animal Model
Molecular Imaging for Diagnosis
Optical Imaging
Molecular Imaging for Theranostics
Findings
Outlook
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