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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chitkara, Deepak | - |
dc.contributor.author | Mittal, Anupama | - |
dc.date.accessioned | 2024-01-05T07:13:18Z | - |
dc.date.available | 2024-01-05T07:13:18Z | - |
dc.date.issued | 2022-10 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0168365922005296 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13680 | - |
dc.description.abstract | Temozolomide (TMZ), an imidazotetrazine, is a second-generation DNA alkylating agent used as a first-line treatment of glioblastoma multiforme (GBM). It was approved by FDA in 2005 and declared a blockbuster drug in 2008. Although TMZ has shown 100% oral bioavailability and crosses the blood-brain barrier effectively, however it suffers from limitations such as a short half-life (∼1.8 h), rapid metabolism, and lesser accumulation in the brain (∼10–20%). Additionally, development of chemoresistance has been associated with its use. Since it is a potential chemotherapeutic agent with an unmet medical need, advanced delivery strategies have been explored to overcome the associated limitations of TMZ. Nanocarriers including liposomes, solid lipid nanoparticles (SLNs), nanostructure lipid carriers (NLCs), and polymeric nanoparticles have demonstrated their ability to improve its circulation time | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.subject | Pharmacy | en_US |
dc.subject | Glioblastoma multiforme | en_US |
dc.subject | Temozolomide | en_US |
dc.subject | Polymer drug conjugates | en_US |
dc.subject | Prodrugs | en_US |
dc.subject | Small molecules | en_US |
dc.title | Polymeric and small molecule-conjugates of temozolomide as improved therapeutic agents for glioblastoma multiforme | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Pharmacy |
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