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dc.date.accessioned2021-09-20T15:05:46Z
dc.date.available2021-09-20T15:05:46Z
dc.date.created2021-06-17T18:19:58Z
dc.date.issued2021
dc.identifier.citationZhu, Geyunjian Harry Azharuddin, Mohammad Islam, Rakibul Rahmoune, Hassan Deb, Suryyani Kanji, Upasona Das, Jyotirmoy Osterrieth, Johannes Aulakh, Parminder Ibrahim-Hashi, Hashi Manchanda, Raghav Nilsson, Per Mollnes, Tom Eirik Bhattacharyya, Maitreyee Islam, Mohammad Mirazul Hinkula, Jorma Slater, Nigel K. H. Patra, Hirak K. . Innate Immune Invisible Ultrasmall Gold Nanoparticles - Framework for Synthesis and Evaluation. ACS Applied Materials & Interfaces. 2021
dc.identifier.urihttp://hdl.handle.net/10852/88140
dc.description.abstractNanomedicine is seen as a potential central player in the delivery of personalized medicine. Biocompatibility issues of nanoparticles have largely been resolved over the past decade. Despite their tremendous progress, less than 1% of applied nanosystems can hit their intended target location, such as a solid tumor, and this remains an obstacle to their full ability and potential with a high translational value. Therefore, achieving immune-tolerable, blood-compatible, and biofriendly nanoparticles remains an unmet need. The translational success of nanoformulations from bench to bedside involves a thorough assessment of their design, compatibility beyond cytotoxicity such as immune toxicity, blood compatibility, and immune-mediated destruction/rejection/clearance profile. Here, we report a one-pot process-engineered synthesis of ultrasmall gold nanoparticles (uGNPs) suitable for better body and renal clearance delivery of their payloads. We have obtained uGNP sizes of as low as 3 nm and have engineered the synthesis to allow them to be accurately sized (almost nanometer by nanometer). The synthesized uGNPs are biocompatible and can easily be functionalized to carry drugs, peptides, antibodies, and other therapeutic molecules. We have performed in vitro cell viability assays, immunotoxicity assays, inflammatory cytokine analysis, a complement activation study, and blood coagulation studies with the uGNPs to confirm their safety. These can help to set up a long-term safety-benefit framework of experimentation to reveal whether any designed nanoparticles are immune-tolerable and can be used as payload carriers for next-generation vaccines, chemotherapeutic drugs, and theranostic agents with better body clearance ability and deep tissue penetration.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleInnate Immune Invisible Ultrasmall Gold Nanoparticles - Framework for Synthesis and Evaluation
dc.typeJournal article
dc.creator.authorZhu, Geyunjian Harry
dc.creator.authorAzharuddin, Mohammad
dc.creator.authorIslam, Rakibul
dc.creator.authorRahmoune, Hassan
dc.creator.authorDeb, Suryyani
dc.creator.authorKanji, Upasona
dc.creator.authorDas, Jyotirmoy
dc.creator.authorOsterrieth, Johannes
dc.creator.authorAulakh, Parminder
dc.creator.authorIbrahim-Hashi, Hashi
dc.creator.authorManchanda, Raghav
dc.creator.authorNilsson, Per
dc.creator.authorMollnes, Tom Eirik
dc.creator.authorBhattacharyya, Maitreyee
dc.creator.authorIslam, Mohammad Mirazul
dc.creator.authorHinkula, Jorma
dc.creator.authorSlater, Nigel K. H.
dc.creator.authorPatra, Hirak K.
cristin.unitcode185,50,0,0
cristin.unitnameDet medisinske fakultet
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1916578
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=ACS Applied Materials & Interfaces&rft.volume=&rft.spage=&rft.date=2021
dc.identifier.jtitleACS Applied Materials & Interfaces
dc.identifier.volume13
dc.identifier.issue20
dc.identifier.startpage23410
dc.identifier.endpage23422
dc.identifier.pagecount0
dc.identifier.doihttps://doi.org/10.1021/acsami.1c02834
dc.identifier.urnURN:NBN:no-90767
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1944-8244
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/88140/2/article95186.pdf
dc.type.versionPublishedVersion


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