药剂学英文名词解释整理.docx
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药剂学英文名词解释整理
1.Whatispharmaceutics?
Howmanybranchesofpharmaceutics?
2.Whatisadrug?
Givesomeexamples
Adrugisdefinedasanagentintendedforuseinthediagnosis,mitigation,treatment,cure,orpreventionofdiseaseinhumansorinotheranimals.
药物是有目的地用于诊断、缓解、治疗、治愈或预防人类或动物疾病的物质。
●Emetic(inducevomiting催吐剂)andantiemetic(preventvomiting止吐剂)drugs
●Diureticdrugs(increasetheflowofurine利尿剂)
●Expectorantdrugs(increaserespiratorytractfluid除痰剂)
●Catharticsorlaxatives(evacuatethebowel泻药)
●Otherdrugsdecreasetheflowofurine,diminishbodysecretions,orinduceconstipation(便秘)
Drugstandards
●Theunitedstatespharmacopeia(药典)andthenationalformulary(国家药品标准)
●Pharmakon,meaning“drug〞;poiein,meaning“make〞;
●Thebinationindicatesanyrecipeorformulaorotherstandardsrequiredtomakeorprepareadrug.
●Organizedsetsofmonographsorbooksofthesestandardsarecalledpharmacopeiasorformularies.
InternationalOrganizationforstandardization(ISO)
isaninternationalconsortiumofrepresentativebodiesconstitutedtodevelopandpromoteuniformorharmonizedinternationalstandards.
国际标准化组织是一个代表性的国际联合会,其设立是为了开展和增进国际标准的均一性和协调性。
ISO9000-ISO9004usedinthepharmaceuticalindustry
●ISOincludedstandardspertainingtodevelopment,production,qualityassurance,qualitycontrol,detectionofdefectiveproducts,qualitymanagement,andotherissuesasproductsafetyandliability.
●ISO包括标准适合开发、生产、质量保证、质量控制、缺陷产品的检测、质量管理和其他如产品平安性和责任的问题。
●Internationallyrecognizedquality-managementsystem.
Prodrugs
isatermusedtodescribeapoundthatrequiresmetabolicbiotransformationafteradministrationtoproducethedesiredpharmacologicallyactivepound.
(前体药物使之能够在给药后经体代性生物转化成具有期望的药理活性化合物的化合物。
〕
aleadpound
isaprototype〔原形化学物质〕chemicalpoundthathasafundamentaldesiredbiologicorpharmacologicactivity.
〔先导化合物是一种具有生物学和药理学活性根本要求的原型化学物质。
〕
agoaldrug
Intheory,a“goaldrug〞
●wouldproducethespecificallydesiredeffect,
●beadministeredbythemostdesiredroute(generallyorally)atminimaldosageanddosingfrequency,
●haveoptimalonsetanddurationofactivity,
理论上,目标药物应能通过最理想的途径〔通常为口服〕以最小的剂量和给药频率给药,能产生特异的期望疗效,具有最理想的起效和持续时间,
●exhibitnosideeffects,
●followingitsdesiredeffectwouldbeeliminatedfromthebodyefficiently,pletely,andwithoutresidualeffect.
●itwouldbeeasilyproducedatlowcost,
●bepharmaceuticallyelegant,
●physicallyandchemicallystableundervariousconditionsofuseandstorage.
●〔无副作用,并在发挥疗效后能完全有效地从体消除,且无残留效应。
它应该易于生产,费用低,制剂产品美观,在不同的使用和贮藏条件下物理和化学上稳定。
〕
5(知)
●Pharmacodynamicsisthestudyofthebiochemicalandphysiologicaleffectsofdrugsandtheirmechanismsofaction.
●Pharmacokineticsdealswiththeabsorption,distribution,metabolismorbiotransformation,andexcretionofdrugs.
●Clinicalpharmacologyappliespharmacologicprinciplestothestudyoftheeffectsandactionsofdrugsinhumans.
AtreatmentIND
oratreatmentprotocolpermitstheuseofaninvestigationaldruginthetrentmentofpatientsnotenrolledintheclinicalstudybutwhohaveaseriousorimmediatelylife-threateningdiseaseforwhichthereisnonsatisfactoryalternativetherapy.
1药剂学定义
Thegeneralareaofstudyconcernedwiththe
formulation
manufacture
stability
effectiveness
ofpharmaceuticaldosageformsistermedpharmaceutics.
Biopharmaceutics
istheareaofstudyembracingtherelationshipbetweenthephysical,chemical,andbiologicalsciencesastheyapplytodrugs,dosageforms,andtodrugaction.
〔生物药剂学是围绕物理学、化学和生物科学及它们关于药物、剂型和药物作用相互关系的研究领域。
〕
药物动力学
Theareaofstudywhichelucidatesthetimecourseofdrugconcentrationinthebloodandtissuesistermedpharmacokinetics.
Itisthestudyofthekineticsofabsorption,distribution,metabolismandexcretion(ADME)ofdrugsandtheircorrespondingpharmacologic,therapeutic,ortoxicresponseinanimalsandman.
Pharmacokineticsalsomaybeappliedinthestudyofinteractionsbetweendrugs.
Activetransport
denotesaprocessofthesoluteordrugbeingmovedacrossthemembraneagainstaconcentrationgradient,thatis,fromasolutionoflowerconcentrationtooneofahigherconcentrationor,ifthesoluteisanion,againstanelectrochemicalpotentialgradient
〔主动转运是指溶质或药物穿过生物膜的转运的过程是逆浓度梯度进展,即从低浓度向高浓度转运或当溶质是离子时逆电化学电势梯度转运。
〕
endocytosis(吞)
Manylargemoleculesandparticlescannotentercellsviapassiveoractivemechanisms.However,somemayenter,asyet,byaprocessknownasendocytosis(吞)
Inphagocytosis(吞噬)(celleating),
largeparticlessuspendedintheextracellularfluidareengulfedandeithertransportedintocellsoraredestroyedwithinthecell.Thisisaveryimportantprocessforlungphagocytesandcertainliverandspleencells.
Pinocytosis(胞饮)(celldrinking)
isasimilarprocessbutinvolvestheengulfingofliquidsorverysmallparticlesthatareinsuspensionwithintheextracellularfluid.
Thebioavailability
describestherateandextenttowhichanactivedrugingredientortherapeuticmoietyisabsorbedfromadrugproductandbeesavailableatthesiteofdrugaction.
Thebioequivalence
referstotheparisonofbioavailabilitiesofdifferentformulations,drugproducts,orbatchesofthesamedrugproduct.
Peakheight(Cmax)
concentrationisthemaximumdrugconcentrationobservedinthebloodplasmaorserumfollowingadoseofthedrug.
Forconventionaldosageforms,astabletsandcapsules,theCmaxwillusuallyoccuratonlyasingletimepoint,referredtoasTmax.
Timeofpeak(Tmax),
maximumlevelofdrugintheblood
Thisparameterreflectstherateofdrugabsorptionfromaformulation.Itistherateofdrugabsorptionthatdeterminesthetimeneededfortheminimumeffectiveconcentrationtobereachedandthusfortheinitiationofthedesiredpharmacologiceffect.
Areaundertheserumconcentrationtimecurve(AUC)
TheAUCofaconcentration-timeplotisconsideredrepresentativeofthetotalamountofdrugabsorbedintothecirculationfollowingtheadministrationofasingledoseofthatdrug.
ThesmallertheAUC,thelessdrugabsorbed.
Pharmaceuticalequivalents
aredrugproductsthatcontainidenticalamountsoftheidenticalactivedrugingredient,i.e.,thesamesaltoresterofthesametherapeuticmoiety,inidenticaldosageforms,butnotnecessarilycontainingthesameinactiveingredients,andthatmeettheidenticalpendialorotherapplicablestandardofidentity,strength,quality,andpurity,includingpotencyand,whereapplicable,contentuniformity,disintegrationtimes,and/ordissolutionrates.
〔制剂等效指包含等量同种活性药物成分的药品,即:
有一样治疗效应的一样盐或酯的形式,一样剂型。
但并不一定包含一样的非活性成分,具有一样的外观或其他相应的性质如规格、质量、纯度,包括效价、含量均匀性、崩解时间和溶出速率。
〕
Pharmaceuticalalternatives
aredrugproductsthatcontaintheidenticaltherapeuticmoiety,oritsprecursor,butnotnecessarilyinthesameamountordosageformorasthesamesaltorester.Eachsuchproductindividuallymeetseithertheidenticaloritsownrespectivependialorotherapplicablestandardofidentity,strength,quality,andpurity,includingpotencyand,whereapplicable,contentuniformity,disintegrationtimes,and/ordissolutionrates.
〔制剂替代品指含有一样治疗效果的组成局部或它的前体药物,不需要一样剂量、一样剂型、一样的盐或酯的形式。
每种药品符合同样的或各自的外观和其他相应的性质如规格、质量、纯度,包括效价,含量均匀性、崩解时间和溶出速率。
)
Bioequivalentdrug
productsarepharmaceuticalequivalentsorpharmaceuticalalternativeswhoserateandextentofabsorptiondonotshowasignificantdifferencewhenadministeredatthesamemolardoseofthetherapeuticmoietyundersimilarexperimentalconditions,eithersingledoseormultipledose.
(生物等效性药品指在一样的试验条件下,单次或屡次给予一样治疗剂量的药物,其吸收的速率和程度没有显示显著性差异的制剂等效品或制剂替代品。
〕
Therapeuticequivalents
hasbeenusedtoindicatepharmaceuticalequivalentswhich,whenadministeredtothesameindividualsinthesamedosageregimens,willprovideessentiallythesametherapeuticeffect.
Thehalf-life(T1/2)
ofadrugdescribesthetimerequiredforadrug’sbloodorplasmaconcentrationtodecreasebyonehalf.
4〔复〕WhatisNoyes-Whitneyequation?
ThedissolutionofasubstancemaybedescribedbythemodifiedNoyes-Whitneyequation:
dc/dt=kS(cs-ct)
inwhichdc/dtistherateofdissolution
kisthedissolutionrateconstant
Sisthesurfaceareaofthedissolvingsolid,
Csisthesaturationconcentrationofdruginthediffusionlayer
Ctistheconcentrationofthedruginthedissolutionmediumattimet
Biotransformation
isatermusedtoindicatethechemicalchangesthatoccurwithdrugswithinthebodyastheyaremetabolizedandalteredbyvariousbiochemicalmechanisms.
Theprocessofbiotransformationismonlyreferredtoasthe“detoxification〞or“inactivation〞process.
8〔复〕Explainshortlyaboutonepartmentmodelandtwopartmentmodel?
●Thesimplestpharmacokineticmodelisthesinglepartmentopen-modelsystem.
Thismodeldepictsthebodyasonepartmentcharacterizedbyacertainvolumeofdistribution(Vd)thatremainsconstant.
●Inthetwo-partmentsystem,adrugentersintoandisinstantaneouslydistributedthroughoutthecentralpartment.
Itssubsequentdistributionintothesecondorperipheralpartmentisslower.
8Powders
areintimatemixturesofdry,finelydivideddrugsand/orchemicalsthatmaybeintendedforinternalorexternaluse.e.g.tablets,capsules,liquiddosageforms,ointmentsandcreams.
粘附性(adhesion)
是指不同分子间产生的引力,如粉体粒子与器壁间的粘附。
凝聚性(cohesion,粘着性)
是指同分子间产生的引力,如粉体粒子之间发生粘附而形成聚集体(randomfloc)
6Capsules
aresoliddosageformsinwhichmedicinalagentsand/orinertsubstancesareenclosedinasmallshellofgelatin.Gelatincapsuleshellsmaybehardorsoft,dependingontheirposition.
1〔知〕sustained-releasepreparations缓释制剂
系指在规定释放介质中,按要求缓慢地非恒速释放药物,其与相应的普通制剂比拟,给药频率比普通制剂减少一半或给药频率比普通制剂有所减少,且能显著增加患者的顺应性的制剂。
controlled-releasepreparations控释制剂
系指在规定释放介质中,按要求缓慢地恒速或接近恒速释放