Modulating Pharmacokinetics, Tumor Uptake and Biodistribution by Engineered Nanoparticles 英文参考文献.docVIP
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Modulating Pharmacokinetics, Tumor Uptake and Biodistribution by Engineered Nanoparticles 英文参考文献
ModulatingPharmacokinetics,TumorUptakeand
BiodistributionbyEngineeredNanoparticles
RochelleR.Arvizo1,OscarR.Miranda2,DanielF.Moyano2,ChadA.Walden3,KarunaGiri1 ,Resham
Bhattacharya1,J.DavidRobertson5,VincentM.Rotello2,JoelM.Reid3,PriyabrataMukherjee1,4,6*
1DepartmentofBiochemistryandMolecularBiology,MayoClinicRochester,Rochester,Minnesota,UnitedStatesofAmerica,2DepartmentofChemistry,Universityof
Massachusetts,Amherst,Massachusetts,UnitedStatesofAmerica,3DepartmentofOncology,MayoClinicRochester,Rochester,Minnesota,UnitedStatesofAmerica,
4Department of Physiology and Biomedical Engineering, Mayo Clinic Rochester, Rochester, Minnesota, United States of America, 5Department of Chemistry and
UniversityofMissouriResearchReactor,UniversityofMissouri,Columbia,Missouri,UnitedStatesofAmerica,6MayoClinicCancerCenter,MayoClinicCollegeofMedicine,
Rochester,Minnesota,UnitedStatesofAmerica
Abstract
Background: Inorganic nanoparticles provide promising tools for biomedical applications including detection, diagnosis
andtherapy.Whilesurfacepropertiessuchaschargeareexpectedtoplayanimportantroleintheirinvivobehavior,very
little is known how the surface chemistry of nanoparticles influences their pharmacokinetics, tumor uptake, and
biodistribution.
Method/Principal Findings: Using a family of structurally homologous nanoparticles we have investigated how
pharmacological properties including tumor uptake and biodistribution are influenced by surface charge using neutral
(TEGOH),zwitterionic(Tzwit),negative(TCOOH)andpositive(TTMA)nanoparticles.Nanoparticleswereinjectedintomice
(normalandathymic)eitherinthetailveinorintotheperitoneum.
Conclusion:NeutralandzwitterionicnanoparticlesdemonstratedlongercirculationtimeviabothIPandIVadministration,
whereas negatively and positively charged nanoparticles possessed relatively short half-lives. These pharmacological
characteristics were reflected on the tumor uptake and biodistribution of the respective nanoparticles, with enhanced
tumoruptakebyn
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