Engineered Liposomes in Interventional Theranostics of Solid Tumors

dc.contributor.author Kommineni, Nagavendra
dc.contributor.author Chaudhari, Ruchita
dc.contributor.author Conde, Joao
dc.contributor.author Cecen, Berivan
dc.contributor.author Chandra, Pranjal
dc.contributor.author Prasad, Rajendra
dc.contributor.author Tamburacı, Sedef
dc.date.accessioned 2023-10-03T07:15:29Z
dc.date.available 2023-10-03T07:15:29Z
dc.date.issued 2023
dc.description.abstract Engineered liposomal nanoparticles have unique characteristicsas cargo carriers in cancer care and therapeutics. Liposomal theranosticshave shown significant progress in preclinical and clinical cancermodels in the past few years. Liposomal hybrid systems have not onlybeen approved by the FDA but have also reached the market level. Nanosizedliposomes are clinically proven systems for delivering multiple therapeuticas well as imaging agents to the target sites in (i) cancer theranosticsof solid tumors, (ii) image-guided therapeutics, and (iii) combinationtherapeutic applications. The choice of diagnostics and therapeuticscan intervene in the theranostics property of the engineered system.However, integrating imaging and therapeutics probes within lipidself-assembly liposome may compromise their overalltheranostics performance. On the other hand, liposomal systems sufferfrom their fragile nature, site-selective tumor targeting, specificbiodistribution and premature leakage of loaded cargo molecules beforereaching the target site. Various engineering approaches, viz., grafting,conjugation, encapsulations, etc., have been investigated to overcomethe aforementioned issues. It has been studied that surface-engineeredliposomes demonstrate better tumor selectivity and improved therapeuticactivity and retention in cells/or solid tumors. It should be notedthat several other parameters like reproducibility, stability, smoothcirculation, toxicity of vital organs, patient compliance, etc. mustbe addressed before using liposomal theranostics agents in solid tumorsor clinical models. Herein, we have reviewed the importance and challengesof liposomal medicines in targeted cancer theranostics with theirpreclinical and clinical progress and a translational overview. en_US
dc.description.sponsorship R.P. thanks the director of IIT-BHU, Varanasi, U.P., for encouraging and providing the necessary facility and support and would also like to thank the school of biochemical engineering, IIT-BHU. N.K. would like to thank CBR, Population Council, for providing the Sheldon J. Segal Post-Doctoral Fellowship. P.C. acknowledges the support from the DST-funded I-DAPT Hub Foundation, IIT BHU [DST/NMICPS/TIH11/IIT(BHU)2020/02]. The authors thank Leander Corrie, Arun Butreddy, Sachin Kumar, and Qing He for reading this manuscript. J.C. acknowledges the European Research Council Starting Grant (ERC-StG-2019-848325). The author dedicates this article to Prof. Sanjiv Sam Gambhir, a molecular imaging scientist. All reproduced images and figures have been cited in this review. en_US
dc.identifier.doi 10.1021/acsbiomaterials.3c00510
dc.identifier.issn 2373-9878
dc.identifier.scopus 2-s2.0-85166769715
dc.identifier.uri https://doi.org/10.1021/acsbiomaterials.3c00510
dc.identifier.uri https://hdl.handle.net/11147/13769
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.relation.ispartof ACS Biomaterials Science and Engineering en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Liposomes en_US
dc.subject Interventional theranostic en_US
dc.subject Solid tumors en_US
dc.subject Nanoimaging en_US
dc.title Engineered Liposomes in Interventional Theranostics of Solid Tumors en_US
dc.type Review en_US
dspace.entity.type Publication
gdc.author.id 0000-0003-3234-226X
gdc.author.id 0000-0003-3234-226X en_US
gdc.author.institutional Tamburacı, Sedef
gdc.author.scopusid 57194060362
gdc.author.scopusid 58523336800
gdc.author.scopusid 56992468300
gdc.author.scopusid 57194413931
gdc.author.scopusid 24461480700
gdc.author.scopusid 42961281300
gdc.author.scopusid 57077644900
gdc.bip.impulseclass C3
gdc.bip.influenceclass C5
gdc.bip.popularityclass C4
gdc.coar.access open access
gdc.coar.type text::review
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Chemical Engineering en_US
gdc.description.endpage 4557 en_US
gdc.description.issue 8 en_US
gdc.description.publicationcategory Diğer en_US
gdc.description.scopusquality Q1
gdc.description.startpage 4527 en_US
gdc.description.volume 9 en_US
gdc.description.wosquality Q2
gdc.identifier.openalex W4384282391
gdc.identifier.pmid 37450683
gdc.identifier.wos WOS:001029698700001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.diamondjournal false
gdc.oaire.impulse 34.0
gdc.oaire.influence 3.1351604E-9
gdc.oaire.isgreen false
gdc.oaire.keywords Neoplasms
gdc.oaire.keywords Liposomes
gdc.oaire.keywords Humans
gdc.oaire.keywords Reproducibility of Results
gdc.oaire.keywords Tissue Distribution
gdc.oaire.keywords Precision Medicine
gdc.oaire.keywords Phospholipids
gdc.oaire.popularity 2.3788505E-8
gdc.oaire.publicfunded false
gdc.openalex.collaboration International
gdc.openalex.fwci 6.21070599
gdc.openalex.normalizedpercentile 0.96
gdc.openalex.toppercent TOP 10%
gdc.opencitations.count 28
gdc.plumx.mendeley 44
gdc.plumx.pubmedcites 13
gdc.plumx.scopuscites 38
gdc.scopus.citedcount 37
gdc.wos.citedcount 39
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4003-8abe-a4dfe192da5e

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