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Combinatory interpretation of protein corona and shear stress for active cancer targeting of bioorthogonally clickable gelatin-oleic nanoparticles
  • Meghani, Nileshkumar M. ;
  • Amin, Hardik ;
  • Park, Chulhun ;
  • Cui, Jing Hao ;
  • Cao, Qing Ri ;
  • Choi, Kyung Hyun ;
  • Lee, Beom Jin
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dc.contributor.authorMeghani, Nileshkumar M.-
dc.contributor.authorAmin, Hardik-
dc.contributor.authorPark, Chulhun-
dc.contributor.authorCui, Jing Hao-
dc.contributor.authorCao, Qing Ri-
dc.contributor.authorChoi, Kyung Hyun-
dc.contributor.authorLee, Beom Jin-
dc.date.issued2020-06-01-
dc.identifier.urihttps://dspace.ajou.ac.kr/dev/handle/2018.oak/31192-
dc.description.abstractNanoparticle-protein interactions under conditions mimicking physiology determine how nanoparticles (NPs) will behave inside blood vessels and, therefore, the overall outcome of the drug-delivery system. Here, for the first time, we explore the effects of bio-mimicking shear stress and protein corona conditions on novel active targeting of clickable fattigation nanoparticles (NPs) for cancer therapy. Active targeting dibenzocyclooctyne-functionalized biocompatible gelatin-oleic NPs (GON-DBCOs) via a bioorthogonal click reaction were prepared by the desolvation method for delivery of docetaxel (DTX) to lung and breast cancer models. The effect of shear stress (5 dyne/cm2) and human serum albumin (HSA) protein corona on the cellular behavior of NPs was explored under a dynamic microfluidic system in lung (A549) and breast (MCF-7) cancer cell lines. The developed drug-loaded NPs had a particle size of 300 nm, a narrow size distribution, positive zeta potential, high encapsulation efficacy (72.4%), and spherical morphology. The particle size of the protein corona-coated NPs increased to 341 nm with a negative zeta potential. The inhibitory dose (IC50) increased approximately 3- and 42-fold in A549 and MCF-7 cells, respectively, under dynamic microfluidic conditions compared to static conditions. Cellular uptake was significantly decreased in the presence of shear stress and a protein corona, compared with static conditions, in both lung (A549, **p < 0.01) and breast (MCF-7, *p < 0.05) cancer cell lines. Clathrin-and energy-dependent pathways were found to be involved in the cellular uptake of NPs. This study could serve as a vital tool for the evaluation of NPs under aggressive bio-mimicking conditions comprising shear stress and a protein corona to predict the in vivo performance of NPs and support the preclinical and clinical translation of NP drug delivery systems.-
dc.description.sponsorshipThis work was primarily supported by a grant from the Ministry of Food and Drug Safety ( 16173MFDS542 ) in 2016, Republic of Korea.-
dc.language.isoeng-
dc.publisherElsevier Ltd-
dc.subject.meshCancer-targeting-
dc.subject.meshDynamic flows-
dc.subject.meshHuman serum albumins-
dc.subject.meshMicro fluidic system-
dc.subject.meshNarrow size distributions-
dc.subject.meshNegative zeta potentials-
dc.subject.meshProtein coronas-
dc.subject.meshSpherical morphologies-
dc.subject.meshBiocompatible Materials-
dc.subject.meshCell Line, Tumor-
dc.subject.meshCell Survival-
dc.subject.meshClick Chemistry-
dc.subject.meshDocetaxel-
dc.subject.meshDrug Carriers-
dc.subject.meshDrug Liberation-
dc.subject.meshGelatin-
dc.subject.meshHumans-
dc.subject.meshMicroscopy, Confocal-
dc.subject.meshNanoparticles-
dc.subject.meshParticle Size-
dc.subject.meshProtein Corona-
dc.subject.meshSerum Albumin, Human-
dc.subject.meshShear Strength-
dc.titleCombinatory interpretation of protein corona and shear stress for active cancer targeting of bioorthogonally clickable gelatin-oleic nanoparticles-
dc.typeArticle-
dc.citation.titleMaterials Science and Engineering C-
dc.citation.volume111-
dc.identifier.bibliographicCitationMaterials Science and Engineering C, Vol.111-
dc.identifier.doi10.1016/j.msec.2020.110760-
dc.identifier.pmid32279783-
dc.identifier.scopusid2-s2.0-85081176908-
dc.identifier.urlhttps://www.journals.elsevier.com/materials-science-and-engineering-c-
dc.subject.keywordActive cancer targeting-
dc.subject.keywordClickable fattigation nanoparticles-
dc.subject.keywordDynamic flow-
dc.subject.keywordHuman serum albumin-
dc.subject.keywordProtein corona-
dc.subject.keywordShear stress-
dc.description.isoafalse-
dc.subject.subareaMedicine (all)-
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