4.7 Article

Development of P22 Viral Capsid Nanocomposites as Anti-Cancer Drug, Bortezomib (BTZ), Delivery Nanoplatforms

期刊

MACROMOLECULAR BIOSCIENCE
卷 14, 期 4, 页码 557-564

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/mabi.201300401

关键词

BTZ; catechol ligands; drug delivery; hepatocellular carcinoma cells; viral capsids

资金

  1. National Research Foundation of Korea (NRF)
  2. Korean government [NRF-2010-0028684, NRF-2013R1A1A1008228]
  3. Collaborative Research Program for Convergence Technology of the Korea (KRCF) [Seed-11-6]
  4. National Research Council of Science & Technology (NST), Republic of Korea [Seed-11-6] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Genetic and chemical engineering approaches are used to employ P22 viral capsids as nanoplatforms for developing an efficient delivery vehicle. Catechol ligands are chemically attached to the interior surface of P22 viral capsid for subsequent encapsulation of an anticancer drug, bortezomib (BTZ), through boronic acid-diol complexation. For targeted delivery, hepatocellular carcinoma (HCC)-targeting peptide (SP94, SFSIIHTPILPL) is synthesized and chemically conjugated to the exterior surface of the P22 viral capsid nanocomposites. Effective targeted delivery of synthesized P22 viral capsid nanocomposites is demonstrated by fluorescent cell imaging and the efficacy of delivered P22 viral capsid nanocomposites is evaluated using a cell viability assay.

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