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dc.contributor.authorHallaj-Nezhadi, S
dc.contributor.authorDass, CR
dc.contributor.authorLotfipour, F
dc.date.accessioned2018-08-26T08:04:04Z
dc.date.available2018-08-26T08:04:04Z
dc.date.issued2013
dc.identifier10.2217/FON.12.171
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/49462
dc.description.abstractNanoparticle-based gene delivery systems may be more efficient for administration of therapeutic genes to solid tumors and cancer metastases, owing to the numerous advantages in terms of enhanced tissue penetrability, improved cellular uptake and targeted gene delivery to the cells of interest compared with other gene delivery systems. Intraperitoneal (IP) delivery of therapeutic agents offers special merits because of the anatomical situation of peritoneum for local cancer therapy. Via the IP administration route, it is possible to target the therapeutic agents exactly to the target cells and protect healthy tissues outside the peritoneal cavity from side effects. IP delivery could be applicable for the treatment of disorders of organs in the peritoneal cavity covered with peritoneum and subperitoneal connective tissue, including cancers such as ovarian and gastric. The goal of this article is to review the current state of IP delivery of nanoparticles for cancer gene therapy.
dc.language.isoEnglish
dc.relation.ispartofFUTURE ONCOLOGY
dc.subjectcancer
dc.subjectgene delivery
dc.subjectgene therapy
dc.subjectintraperitoneal
dc.subjectnanoparticle
dc.subjectplasmid
dc.titleIntraperitoneal delivery of nanoparticles for cancer gene therapy
dc.typeReview
dc.citation.volume9
dc.citation.issue1
dc.citation.spage59
dc.citation.epage68
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.2217/FON.12.171


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