1. Academic Validation
  2. A c(RGDfE) conjugated multi-functional nanomedicine delivery system for targeted pancreatic cancer therapy

A c(RGDfE) conjugated multi-functional nanomedicine delivery system for targeted pancreatic cancer therapy

  • J Mater Chem B. 2015 Feb 14;3(6):1049-1058. doi: 10.1039/c4tb01402b.
Jing Sun 1 Dong-Hyun Kim Yang Guo Zhaogang Teng Yanjun Li Linfeng Zheng Zhuoli Zhang Andrew C Larson Guangming Lu
Affiliations

Affiliation

  • 1 Department of Medical Imaging, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, Jiangsu Province, P.R. China. [email protected].
Abstract

Pancreatic Cancer is one of the five most lethal malignancies and has a poor prognosis due to its abundant stromal barriers and lack of effective available therapies. Although gemcitabine has been used as a standard therapy for several decades, there has been little progress in the improvement of the 5 year survive rate due to the low targeting efficiency for pancreatic Cancer cells. To achieve a targeted delivery of gemcitabine to pancreatic Cancer cells, we have developed a c(RGDfE) [cyclic (Arg-Gly-Asp-d-Phe-Glu)] conjugated multi-functional nanomedicine delivery system composed of a magnetic core and mesoporous silica shell. These magnetic mesoporous nanoparticles demonstrated sufficient relaxivity properties for detection with magnetic resonance imaging (MRI). These c(RGDfE) peptide conjugated magnetic mesoporous silica nanoparticles [c(RGDfE)-pMMSNs] can target pancreatic Cancer cells and increase cellular uptake in human pancreatic Cancer cell lines that overexpress Integrin ανβ3. Gemcitabine loaded c(RGDfE)-pMMSNs were most efficiently targeted to pancreatic Cancer cells (BxPC-3). Growth inhibition of the BxPC-3 cell line was achieved in a time dependent manner consistent with observed drug release behavior. Intracellular targeted gemcitabine delivery using c(RGDfE)-pMMSNs offers a promising approach for the treatment of pancreatic Cancer.

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