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Adenoviral vectors modified by heparin-polyethyleneimine nanogels enhance targeting to the lung and show therapeutic potential for pulmonary metastasis in vivo.

Abstract
Polyethyleneimine (PEI) is a well-known cationic polymer that has previously been shown to have significant potential to deliver genes in vitro and in vivo. However, PEI is non-degradable and exhibits a high cytotoxicity as its molecular weight increases. The clinical application for systemic administration of adenoviral (Ad) vectors is limited, as these vectors do not efficiently penetrate solid tumor masses due to a common deficiency of Coxsackie Adenovirus Receptor (CAR) on the tumor surface. In this study, we conjugated low molecular weight PEI (Mn = 1,800) to heparin (Mn = 4,000-6,000) to create a new type of cationic degradable nanogel (HPEI) that was then used to modify Ad vectors. The resulting HPEI-Ad complexes were used to infect CT26 and HeLa cells in vitro. Additionally, the HPEI-Ad complexes were administrated in vivo via intravenous injection, and tissue distribution was assessed using luciferase assays; the therapeutic potential of HPEI-Ad complexes for pulmonary metastasis mediated by CT26 cells was also investigated. In vitro, HPEI-Ad complexes enhanced the transfection efficiency in CT26 cells, reaching 36.3% compared with 0.1% of the native adenovirus. In vivo, HPEI-Ad complexes exhibited greater affinity for lung tissue than the native adenovirus and effectively inhibited the growth of pulmonary metastases mediated by CT26 cells. Our results indicate that Ad vectors modified by HPEI nanogels to form HPEI-Ad complexes enhanced transfection efficiency in CT26 cells that lacked CAR, targeted to the lung and demostrated a potential therapy for pulmonary metastasis.
AuthorsWei Wei, Yandong Mu, XiaoPeng Li, MaLing Gou, HaiLong Zhang, ShunTao Luo, Ke Men, YongQiu Mao, ZhiYong Qian, Li Yang
JournalJournal of biomedical nanotechnology (J Biomed Nanotechnol) Vol. 7 Issue 6 Pg. 768-75 (Dec 2011) ISSN: 1550-7033 [Print] United States
PMID22416575 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Drug Carriers
  • Nanogels
  • polyethylene glycol polyethyleneimine nanogel
  • Polyethylene Glycols
  • Polyethyleneimine
  • Heparin
Topics
  • Adenoviridae (genetics)
  • Animals
  • Cell Proliferation (drug effects)
  • Drug Carriers (administration & dosage, chemistry, pharmacokinetics, pharmacology)
  • Female
  • Genetic Therapy (methods)
  • Genetic Vectors (administration & dosage, genetics, pharmacokinetics, pharmacology)
  • HeLa Cells
  • Heparin (administration & dosage, chemistry, pharmacokinetics)
  • Histocytochemistry
  • Humans
  • Lung (chemistry, metabolism)
  • Lung Neoplasms (metabolism, secondary, therapy)
  • Mice
  • Mice, Inbred BALB C
  • Nanogels
  • Neoplasm Metastasis
  • Polyethylene Glycols (administration & dosage, chemistry, pharmacokinetics, pharmacology)
  • Polyethyleneimine (administration & dosage, chemistry, pharmacokinetics, pharmacology)
  • Transfection (methods)
  • Xenograft Model Antitumor Assays

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