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dc.contributor.authorHallaj-Nezhadi, S
dc.contributor.authorLotfipour, F
dc.contributor.authorDass, CR
dc.date.accessioned2018-08-26T06:15:42Z
dc.date.available2018-08-26T06:15:42Z
dc.date.issued2010
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/43132
dc.description.abstractWhile the systemic route of administration enables therapeutic genes to spread through the bloodstream and access target cells, it is a challenge to achieve this. Several studies demonstrate that systemic administration of therapeutic genes or other nucleic acid-based constructs such as siRNA to solid tumors as well as cancer metastases are better with nanoparticulate systems compared to administration of free (uncomplexed) nucleic acids. Nanoparticle-based nucleic acid delivery systems might be more pertinent, due to the several privileges in terms of enhanced tissue penetrability, improved cellular uptake and to a lesser extent, targeted gene delivery to the cells of interest provided targeting ligands are used. Systemic delivery of nanoplexes has already been reported with different nanoparticles containing DNA via various routes of administration. The goal of the present article is to review the current state of intravenous delivery of nanoparticles for gene therapy of cancer.
dc.language.isoEnglish
dc.relation.ispartofDie Pharmazie
dc.subjectDNA
dc.subjectDrug Delivery Systems
dc.subjectGene Transfer Techniques
dc.subjectGenetic Therapy
dc.subjectHumans
dc.subjectInjections, Intravenous
dc.subjectNanoparticles
dc.subjectNeoplasms
dc.subjectRNA, Small Interfering
dc.titleDelivery of nanoparticulate drug delivery systems via the intravenous route for cancer gene therapy.
dc.typearticle
dc.citation.volume65
dc.citation.issue12
dc.citation.spage855
dc.citation.epage9
dc.citation.indexPubmed


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