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 | |
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| gdc.bip.impulseclass | C3 | |
| gdc.bip.influenceclass | C5 | |
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| 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 | |
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| 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 | |
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| gdc.openalex.toppercent | TOP 10% | |
| gdc.opencitations.count | 28 | |
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| 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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