博士申请用研究计划英文模板Word文件下载.docx
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博士申请用研究计划英文模板Word文件下载.docx
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A.Proposedareaofresearch
TheaimofthisproposedPhDprojectistodevelopandevaluatepHresponsive,endosomolyticpolymersforefficientintracellulardeliveryofbiologicaldrugpayloads.
Thereisaneedtobetterunderstandthemechanismsofentryintothecellcytoplasmandnucleusinordertodesignoptimaldeliverysystemsforbiologicalmolecules.Ontheonehand,thiswouldopenupsignificantopportunitiestodeliverpotentdrugpayloadsagainstintracellulartargetstopositivelyimpacthumanhealth.Inadditiontheprojectaimstodevelopamoregeneralunderstandingoftherulesgoverningtheuptakeofbiologicalmoleculesintocells.
Thisprojectproposestoinvestigatetheuseofsynthetic,biodegradablepolymersforintracellulardeliveryofdrugpayloads(includingsiRNA,therapeuticpeptideandantibody)againstawell-validatedintracellulardrugtarget,suchasBcl-2.ThenovelpH-responsivepolymershavebeendesignedbyDrRongjunChen’sLabtomimictheactivityofviruses,bothintheircellentryandendosomalescapemechanisms.Usingcancercelllines(JurkatorHL-60cells)asamodelsystem,thepolymerswouldbetestedwithavarietyofdifferentbiologicalpayloadsinaquantitativecomparisonoftheirabilitytoenterthecellandtriggerapoptosisandsubsequentlycelldeath.Withanefficientmodelsystemestablished,therewouldthenbescopetooptimizethesystemintermsofthekineticsandmechanismsofcellentry,cytoplasmicandnuclearlocalization,andthebiodegradationofthepolymers.Therewouldalsobescopetoexploretheefficiencyinothercellsystemsandwithfurtherintracellulartargets.ThismultidisciplinaryprojectisattheinterfaceofChemistry,BiologyandMedicine,andwillprovidethestudentwitharealopportunitytobeinvolvedinthedevelopmentandevaluationofnewnanomedicines.
B.Background
Advancesingenomicsandproteomicshaveenabledthedevelopmentofmacrodrugs,suchasnucleicacidsandproteins,withpotentialforthetreatmentofawidevarietyofdiseases.Amongstotherproblems,theirclinicalapplicationsmaybegreatlyimpairedbylowcellularuptakeandlysosomaldegradationbeforetheycanreachtheirtargetorganellesorcellnuclei.Inordertoachieveefficientintracellulardeliveryofsuchbiologicalmolecules,deliverysystemsarerequiredtoenablehighcellentryviaendocytosisandefficientreleaseintothecytoplasmbyendosomalmembranedisruptionundermildlyacidicconditions.
Recombinantvirusesandfusogenicviralpeptideshavebeenusedtomediategenetransfection,buttheirclinicaluseispotentiallylimitedbysafetyissuesanddifficultiesinlarge-scaleproduction.Avarietyofsyntheticpolymershavethereforebeendevelopedasnon-viralvectors.Cationicpolyethyleneimine,poly(2-(dimethylamino)ethylmethacrylate)andpolyamidoaminedendrimersmediategenedeliverythroughthe‘protonsponge’effect,butsufferfromcytotoxicityandrelativelylowtransductionefficiencies.Theintensivelystudiedvinyl-basedanionicpolymers,poly(a-alkylacrylicacid)s,displaypH-responsivemembranedisruptivebehavior,buttheyarenotbiodegradable,thuslowmolecularweightshavetobestrictlyrequiredtoallowrenalexcretionandtheirclinicalapplicationsareseriouslylimited.
DrRongjunChen’sLabhasrecentlydevelopedaclassofnovel,biodegradable,pH-responsivepolymerstomimicfactorsthatenableefficientviraltransfection,buttheyaresafe,easytomanufactureandhavemorecontrollablestructures.Theparentpolymerisapolyamide,poly(L-lysineisophthalamide),whichwasbasedonpolycondensationofdiacylchloridesandnaturalmetabolitetri-functionalaminoacidscontainingbothα-andω-aminegroups.Hydrophobicaminoacidsand/orpoly(ethyleneglycol)weregraftedontoitspendantcarboxylicacidgroupstomanipulateitsamphiphilicityandstructure.Themetabolite-derivedbiomimeticpolymerscanundergopH-mediatedcoil-globulechangesinconformation.Thispropertyenablesthesepolymerstobesignificantlymembrane-disruptivewithinpHrangetypicalofendosomalcompartments,butnecessarilynon-toxicatphysiologicalpH.Basedonprevioussuccessfulintracellulardeliveryofthemodel-drugssuchascalcein,dextran(withmolecularweightrangingfrom3kDato70kDa),andtherapeuticproteinapoptinandsiRNA,itisthoughtthatthesepolymersmaybeabletodeliverawidevarietyofdifferentbiologicalmolecules(nucleicacidsandproteins)intocellsforthetreatmentofvariousdiseasesincludingcancers.
C.Applicant’sworkpreparationinChina
TheapplicantisanexpectedbachelormajoringinPolymerScienceandEngineeringfromBeijingUniversityofChemicalTechnology(BUCT).Afterfouryearsofundergraduatestudies(2007-2011),Ihaveobtainedastrongresearchbackgroundinorganicchemistry,polymerphysicsandchemistry,physicalchemistry,etc.WorkingintheStateKeyLaboratoryofPolymerPhysicsandChemistryintheInstituteofChemistryofChineseAcademyofScienceformorethanhalfofayearhassetupmymindinresearchingpolymerdrugcarriers.Ourgroupcastoureyestowardssynthesizinggraftcopolymerswithaminoacidsasthemainmonomers,tocreateanovelcarrierwhichisbothpHandtemperaturesensitive.
WehadsynthesizedapolymerbrushfromZ-lysineand2-Bromoisobutyrylbromidethroughring-openingpolymerization.Thenwegraftedspecifictemperaturesensitiveresiduesontothepolymerbrushviaatomictransferradicalpolymerization,followedbycharacterizationandtheoreticalanalysisofthepolymers.
Inaddition,IwasaResearchAssistantinthestatekeylaboratoryofBeijingUniversityofChemicalTechnology,workingonthecharacterizationofcopolymersbyNMR.IwasalsoaResearchAssistantintheEnvironmentalMaterialsLaboratoryofChinaBuildingMaterialsAcademy,workingonsynthesisofFEVEcoating.Theseresearchexperienceshaveenrichedmyknowledgeandexperimentalskillsforpolymersynthesisandenabledmetooperatemanyfacilitiesdeftly,suchasNMR,GPC,FTIR,vacuumgloveboxandrotaryevaporator.
Inthesummerof2010,Iwasselectedtoattendtheprogram“BUCT-CambridgeSummerSchool”intheUniversityofCambridge.DuringthethreeweeksintheUK,IvisitedtheDepartmentofChemicalEngineeringandBiotechnologyanddidexperimentsrelevanttomyresearchitslabs.InCambridge,Ialsodidacasestudyaboutthebiopharmaceuticalmarket.Thisdeepenedmyunderstandingofcommercialprospectsofdrugdeliverytechnologies,suchasthedemandsofdifferentpatientsfordrugdeliverysystemsandcompetitivenessofdifferenthealthtestingequipments.BesidestheUniversityofCambridge,IalsovisitedtheUniversityofOxford,ImperialCollegeLondon,UniversityofBirmingham,andUniversityofLoughborough.IalsoestablishedthecontactwithDrRongjunChenwhoistheGroupLeaderofBiomaterialsandDrugDeliveryGroupattheUniversityofLeedswhenIwasintheUK,andhavebeencommunicatingwithhimviaemailssincethen,discussingaboutpolymersynthesisandcharacterizationanddrugdeliveryresearch.
IbelievetheabovementionedacademicbackgroundsandvariousrelevantexperienceshavepreparedmyselfwellforthePhDstudyonpolymerdrugdeliveryresearchforthetreatmentofvariousdiseasesincludingcancersinDrRongjunChen’sLabattheUniversityofLeeds.
D.Aimofoverseasstudy
TheaimofmyPhDstudyistoapplypolymernanotechnologytodrugdeliveryinordertoimprovethesafetyandpharmaceuticalefficacyofdrugsthatneedpreciseintracellulardelivery.Iwilldesignandsynthesizebiodegradableaminoacid-basedpolymervectors,whichareefficient,safe,cost-effectiveandamenabletolarge-scalemanufacturing.Iwillthenevaluatethepolymer-basedtargetedintracellulardeliveryofbiologicaldrugpayloads(includingsiRNA,therapeuticpeptideandantibody)againstawell-validatedintracellulardrugtarget,suchasBcl-2,forcancertreatment.Theintentionistocombinethehighlynovelchemistryexpertisesurroundingthedeliverypolymerwiththebiologicalexpertisearoundthediscoveryanddevelopmentofavarietyofdrugpayloads.Thenovelpolymerdeliverytechnologytobedevelopedwillopenthedoortoawidevarietyofcytoplasmicandnucleartargets,previouslythoughttobeinaccessibletobiologicaltherapyforvariousdiseaseincludingcancers.
Inaddition,Iwillinvestigatethefundamentalmechanismsoftheinteractionbetweenpolymers/polymer-drugentitiesanddifferentmembranemodels(artificiallipidmembranes,erythrocytesandmorecomplexnucleatedmammaliancells)andobtainabetterunderstandingoftherulescontrollingtheuptakeofmacromoleculesintocells.
E.Researchmethods
Theprojectwouldbreakdownintodiscretestagesasdescribedbelow:
(1)Polymersynthesis
Aminoacidderivatives(e.g.lysinederivative)willbeusedtocarryouttheN-Carboxyanhydrideringopeningpolymerizationinordertoobtainapolymerbrush,whichcouldbethebackboneoftargetpolymer.Thenenvironmentally(e.g.pHandtemperature)responsivegroupswillbegraftedtothemainchainbyATRPorMichaelAddition,etc.Fluorescentpolymerswouldbepreparedbycouplingorganicfluorophores(e.g.fluoresceinisothiocyanateandCy5)ontothepolymers.Cleavablelinkerchemistry(e.g.disulfidebond)wouldbeintroducedontothepolymerbackbonefordrugconjugation.Polyethyleneglycolwouldbeaddedtothepolymerstoincreasetheirbiocompatibilityandbioavailability.
(2)Characterizationofpolymers
Thestructures,molecularweightsandcompositionsofthesynthesizedpeptidepolymerswillbecharacterizedbyNMR,massspectrometry,GPCandHPLCetc.Th
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