全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
药学学报  2015 

固体药物的转晶现象

, PP. 521-527

Keywords: 药物稳定性,多晶型,转晶

Full-Text   Cite this paper   Add to My Lib

Abstract:

在药物开发过程中,有些药物的稳定晶型可能会存在某些缺陷,如溶解度太差等,从而不得不考虑将一些动力学上可以稳定存在的亚稳晶型作为药用晶型开发上市。使用亚稳晶型存在晶型转变的风险。对固体药物转晶现象的研究可以帮助这些使用亚稳晶型的药物选择合适的生产和储存条件,避免因转晶而获得不需要的晶型。

References

[1]  hilfikerr.polymorphisminthepharmaceuticalindustry[m].weinheim:wiley-vchverlaggmbh&co.kgaa,2006:218.
[2]  kumarss,nangiaa.asolubilitycomparisonofneutralandzwitterionicpolymorphs[j].crystgrowthdes,2014,14:1865-1881.
[3]  aldawsarih,altafa,banjarzm,etal.crystallizationofanewpolymorphofacetohexamidefrom2-hydroxybutyl-β-cyclodextrinsolution:formviwithahighaqueoussolubility[j].intjpharm,2013,453:315-321.
[4]  pudipeddim,serajuddinatm.trendsinsolubilityofpolymorphs[j].jpharmsci,2005,94:929-939.
[5]  bonfilior,lealjs,santosomm,etal.analysisofchlorthalidonepolymorphsinrawmaterialsandtabletsandtheeffectofformsiandiionthedissolutionpropertiesofdrugproducts[j].jpharmbiomedanal,2014,88:562-570.
[6]  liuc,danglp,tongy,etal.influenceofpolymorphsonthetransformationwateractivityoftheophylline[j].indengchemres,2013,52:14979-14983.
[7]  orolal,veidismv,sarcevicai,etal.theeffectofphonpolymorphformationofthepharmaceuticallyactivecompoundtianeptine[j].intjpharm,2012,432:50-56.
[8]  anjh,choigj,kimws.polymorphicandkineticinvestigationofadefovirdipivoxilduringphasetransformation[j].intjpharm,2012,422:185-193.
[9]  matsumotot,ichikawaji,kaneniwan,etal.effectofenvironmentaltemperatureonthepolymorphictransformationofphenylbutazoneduringgrinding[j].chempharmbull,1988,36:1074-1085.
[10]  traskav,shann,motherwellwds,etal.selectivepolymorphtransformationviasolvent-dropgrinding[j].chemcommun(camb),2005,(7):880-882.
[11]  takahashiy,nakashimak,ishiharat,etal.polymorphismoffostedil:chracterizationandpolymophicchangebymechanicaltreatments[j].drugdevindpharm,1985,11:1543-1563.
[12]  lefebvrec,guyothermannam,draguetbrughmansm,etal.polymorphictransitionsofcarbamazepineduringgrindingandcompression[j].drugdevindpharm,1986,12:1913-1927.
[13]  boldyrevaev.combinedx-raydiffractionandramanspectroscopystudiesofphasetransitionsincrystallineaminoacidsatlowtemperaturesandhighpressures:selectedexamples[j].phasetransitions,2009,82:303-321.
[14]  barriom,maccaronie,rietveldib,etal.pressure-temperaturestatediagramforthephaserelationshipsbetweenbenfluorexhydrochlorideformsiandii:acaseofenantiotropicbehavior[j].jpharmsci,2012,101:1073-1078.
[15]  xuj,pingqn,liugj.studiesonthecharacteristicsofpolymorphsofmetoclopramide[j].jchinpharmuniv(中国药科大学学报),1996,27:722-725.
[16]  yuanhj,chendw,reng,etal.conversionconditionsandinfluencefactorsofnitrendipinecrystalpolymorphism[j].actachimsin(化学学报),2008,66:2429-2433.
[17]  grooffd,liebenbergw,devilliersmm.preparationandtransformationoftruenifedipinepolymorphs:investigatedwithdifferentialscanningcalorimetryandx-raydiffractionpatternfittingmethods[j].jpharmsci,2011,100:1944-1957.
[18]  sonoday,hirayamaf,arimah,etal.selectivecrystallizationofthemetastableformivpolymorphoftolbutamideinthepresenceof2,6-di-o-methyl-β-cyclodextrininaqueoussolution[j].crystgrowthdes,2006,6:1181-1185.
[19]  ishigurot,hirayamaf,ioharad,etal.crystallizationandpolymorphictransitionsofchlorpropamideinaqueous2-hydroxybutyl-β-cyclodextrinsolution[j].eurjpharmsci,2010,39:248-255.
[20]  kogawaac,salgadohrn.developmentandvalidationofinfraredspectroscopymethodforthedeterminationofdarunavirintablets[j].physchem,2013,3:1-6.
[21]  araya-sibajaam,paulinoas,raubergs,etal.dissolutionproperties,solid-statetransformationandpolymorphiccrystal­lization:progesteronecasestudy[j].pharmdevtechnol,2014,19:779-788.
[22]  silvaapc,meneghinilz,bajerskil,etal.discriminatorydissolutiontestfortabletscontainingalpha-andbeta-thalidomidepolymorphs[j].dissoluttechnol,2013,20:19-25.
[23]  yuanhj,chendw,reny,etal.studyonpharmacokineticsandbioavailabilityofnirendipinecrystalpolymorphsinrabbits[j].chinhosppharmj(中国医院药学杂志),2009,29:29-32.
[24]  yuanhj,chendw,liuyl,etal.studyonpharmacokineticsofnimodipinepolymorphsinrabbits[j].chinpharmj(中国药学杂志),2005,40:609-612.
[25]  kobayashiy,itos,itais,etal.physicochemicalpropertiesandbioavailabilityofcarbamazepinepolymorphsanddihydrate[j].intjpharm,2000,193:137-146.
[26]  yangc,rentk,wangj,etal.thermodynamicstabilityanalysisofm-nisoldipinepolymorphs[j].jchemthermodyn,2013,58:300-306.
[27]  wangjr,wangxj,luly,etal.highlycrystallineformsofvalsartanwithsuperiorphysicochemicalstability[j].crystgrowthdes,2013,13:3261-3269.
[28]  upadhyayp,dantuluriak,kumarl,etal.estimatingrelativestabilityofpolymorphsbygenerationofconfigurationalfreeenergyphasediagram[j].jpharmsci,2012,101:1843-1851.
[29]  khomaneks,bansalak.differentialcompactionbehaviourofrollercompactedgranulesofclopidogrelbisulphatepolymorphs[j].intjpharm,2014,472:288-295.
[30]  khomaneks,morepk,raghavendrag,etal.molecularunderstandingofthecompactionbehaviorofindomethacinpolymorphs[j].molpharm,2013,10:631-639.
[31]  perumallasr,shilm,suncc.ionizedformofacetaminophenwithimprovedcompactionproperties[j].crystengcomm,2012,14:2389-2390.
[32]  chengm.polymorphismofchloramphenicolpalmitate[j].chinpharmbull(药学通报),1982,17:29-32.
[33]  zhangmf,guym,daizy.studiesonthebloodconcentrationsofdifferentpreparationsofchloramphenicolpalmitate[j].actaacadmedprimshanghai(上海第一医学院学报),1979,6:409-413.
[34]  zhangq,luly,daiwj,etal.newpolymorphsofhuperzinea:preparation,structures,andphysicochemicalpropertiesofanhydrouscrystalforms[j].crystgrowthdes,2013,13:2198-2207.
[35]  mahera,crokerdm,seatoncc,etal.solution-mediatedpolymorphictransformation:formiitoformiiipiracetaminorganicsolvents[j].crystgrowthdes,2014,14:3967-3974.
[36]  zhangg,gaolp,zhangzx,etal.heating-inducedphasetransitionofbupropionhydrobromidepolymorphs[j].jpharmsci,2012,101:3091-3095.
[37]  chanhk,doelkere.polymorphictransformationofsomedrugsundercompression[j].drugdevindpharm,1985,11:315-332.
[38]  otsukam,kaneniwan.effectofseedcrystalsonsolid-statetransformationofpolymorphsofchloramphenicolpalmitateduringgrinding[j].jpharmsci,1986,75:506-511.
[39]  berzinsa,actinsa,kreismanisjp.hydrationanddehydrationkineticsofxylazinehydrochloride[j].pharmdevtechnol,2009,14:388-399.
[40]  crispjl,dannse,edgarm,etal.theeffectofparticlesizeonthedehydration/rehydrationbehaviouroflactose[j].intjpharm,2010,391:38-47.
[41]  kangf,vogtfg,brumj,etal.effectofparticlesizeandmorphologyonthedehydrationmechanismofanon-stoichiometrichydrate[j].crystgrowthdes,2012,12:60-74.
[42]  daveyrj,guypd,ruddickaj.theiv-iiipolymorphicphasetransitioninaqueousslurriesofammoniumnitrate[j].jcolloidinterfacesci,1985,108:189-192.
[43]  grecok,bognerr.solution-mediatedphasetransformation:significanceduringdissolutionandimplicationsforbioavailability[j].jpharmsci,2012,101:2996-3018.
[44]  kraljd,brecevicl,kontrecj.vateritegrowthanddissolutioninaqueoussolutioniii:kineticsoftransformation[j].jcrystgrowth,1997,177:248-257.
[45]  kitamuram.controllingfactorofpolymorphismincrystallizationprocess[j].jcrystgrowth,2002,237:2205-2214.
[46]  kakumanuv,bansala.enthalpyrelaxationstudiesofcelecoxibamorphousmixtures[j].pharmres,2002,19:1873-1878.
[47]  linsy,hsuch,kewt.solid-statetransformationofdifferentgabapentinpolymorphsuponmillingandco-milling[j].intjpharm,2010,396:83-90.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133