Literature DB >> 17393074

Poly(ethylene glycol)-modified nanocarriers for tumor-targeted and intracellular delivery.

Lilian E van Vlerken1, Tushar K Vyas, Mansoor M Amiji.   

Abstract

The success of anti-cancer therapies largely depends on the ability of the therapeutics to reach their designated cellular and intracellular target sites, while minimizing accumulation and action at non-specific sites. Surface modification of nanoparticulate carriers with poly(ethylene glycol) (PEG)/poly(ethylene oxide) (PEO) has emerged as a strategy to enhance solubility of hydrophobic drugs, prolong circulation time, minimize non-specific uptake, and allow for specific tumor-targeting through the enhanced permeability and retention effect. Furthermore, PEG/PEO modification has emerged as a platform for incorporation of active targeting ligands, thereby providing the drug and gene carriers with specific tumor-targeting properties through a flexible tether. This review focuses on the recent developments surrounding such PEG/PEO-surface modification of polymeric nanocarriers to promote tumor-targeting capabilities, thereby enhancing efficacy of anti-cancer therapeutic strategies.

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Year:  2007        PMID: 17393074     DOI: 10.1007/s11095-007-9284-6

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  77 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-10       Impact factor: 11.205

5.  Intracellular delivery of saquinavir in biodegradable polymeric nanoparticles for HIV/AIDS.

Authors:  Lipa K Shah; Mansoor M Amiji
Journal:  Pharm Res       Date:  2006-09-13       Impact factor: 4.200

6.  Tumor-targeted gene delivery using poly(ethylene glycol)-modified gelatin nanoparticles: in vitro and in vivo studies.

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  105 in total

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Review 5.  Multi-modal strategies for overcoming tumor drug resistance: hypoxia, the Warburg effect, stem cells, and multifunctional nanotechnology.

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Review 6.  Strategies to target tumors using nanodelivery systems based on biodegradable polymers, aspects of intellectual property, and market.

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Review 7.  In vivo delivery of miRNAs for cancer therapy: challenges and strategies.

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8.  Folic acid-decorated polyamidoamine dendrimer exhibits high tumor uptake and sustained highly localized retention in solid tumors: Its utility for local siRNA delivery.

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9.  Cellular delivery and biological activity of antisense oligonucleotides conjugated to a targeted protein carrier.

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10.  Enhanced siRNA delivery using a combination of an arginine-grafted bioreducible polymer, ultrasound, and microbubbles in cancer cells.

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