Local delivery to malignant brain tumors: potential biomaterial-based therapeutic/adjuvant strategies

dc.bibliographicCitation.firstPage6037eng
dc.bibliographicCitation.issue18eng
dc.bibliographicCitation.journalTitleBiomaterials Scienceeng
dc.bibliographicCitation.lastPage6051eng
dc.bibliographicCitation.volume9eng
dc.contributor.authorAlghamdi, Majed
dc.contributor.authorGumbleton, Mark
dc.contributor.authorNewland, Ben
dc.date.accessioned2022-03-18T10:25:19Z
dc.date.available2022-03-18T10:25:19Z
dc.date.issued2021
dc.description.abstractGlioblastoma (GBM) is the most aggressive malignant brain tumor and is associated with a very poor prognosis. The standard treatment for newly diagnosed patients involves total tumor surgical resection (if possible), plus irradiation and adjuvant chemotherapy. Despite treatment, the prognosis is still poor, and the tumor often recurs within two centimeters of the original tumor. A promising approach to improving the efficacy of GBM therapeutics is to utilize biomaterials to deliver them locally at the tumor site. Local delivery to GBM offers several advantages over systemic administration, such as bypassing the blood-brain barrier and increasing the bioavailability of the therapeutic at the tumor site without causing systemic toxicity. Local delivery may also combat tumor recurrence by maintaining sufficient drug concentrations at and surrounding the original tumor area. Herein, we critically appraised the literature on local delivery systems based within the following categories: polymer-based implantable devices, polymeric injectable systems, and hydrogel drug delivery systems. We also discussed the negative effect of hypoxia on treatment strategies and how one might utilize local implantation of oxygen-generating biomaterials as an adjuvant to enhance current therapeutic strategies. © 2021 The Royal Society of Chemistry.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/8273
dc.identifier.urihttps://doi.org/10.34657/7311
dc.language.isoengeng
dc.publisherCambridge : RSCeng
dc.relation.doihttps://doi.org/10.1039/d1bm00896j
dc.relation.essn2047-4849
dc.relation.issn2047-4830
dc.rights.licenseCC BY 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/eng
dc.subject.ddc540eng
dc.subject.otherBiochemistryeng
dc.subject.otherBraineng
dc.subject.otherChemotherapyeng
dc.subject.otherControlled drug deliveryeng
dc.subject.otherImplants (surgical)eng
dc.subject.otherPolymerseng
dc.subject.otherTargeted drug deliveryeng
dc.subject.otherTumorseng
dc.subject.otherAdjuvant chemotherapyeng
dc.subject.otherBlood-brain barriereng
dc.subject.otherDrug delivery systemeng
dc.subject.otherImplantable deviceseng
dc.subject.otherSurgical resectioneng
dc.subject.otherSystemic administrationeng
dc.subject.otherSystemic toxicitieseng
dc.subject.otherTherapeutic strategyeng
dc.subject.otherDiagnosiseng
dc.titleLocal delivery to malignant brain tumors: potential biomaterial-based therapeutic/adjuvant strategieseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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