药物不良反应杂志
藥物不良反應雜誌
약물불량반응잡지
ADVERSE DRUG REACTIONS JOURNAL
2015年
1期
44-48
,共5页
唐红波%周志敏%闫素英%梁欣韫%李轶凡%代荫梅%冯欣
唐紅波%週誌敏%閆素英%樑訢韞%李軼凡%代蔭梅%馮訢
당홍파%주지민%염소영%량흔운%리질범%대음매%풍흔
纳米技术%胚胎研究%毒性试验
納米技術%胚胎研究%毒性試驗
납미기술%배태연구%독성시험
Nanotechnology%Embryo research%Toxicity tests
纳米递药系统(NDDS)是指药物与药物载体形成的、粒径在1 000 nm以内的药物输送系统,一般是以聚合物胶束、脂质体、纳米囊、微乳以及有机或无机纳米粒子为载体,将药效物质以一定的方式与载体结合制成新型控/缓释制剂,或直接将原药加工制成纳米粒子.NDDS的胚胎毒性是评价其非临床安全性的重要内容.体外研究显示,NDDS的胚胎毒性与纳米粒子的理化性质如尺度和表面修饰物、纳米粒子暴露时间和剂量相关.已有的研究显示,氧化锌纳米粒子胚胎毒性明显,二氧化钛、二氧化硅、氧化镁纳米粒子和碲化镉量子点也有不同程度的胚胎毒性,而聚苯乙烯基纳米粒子无胚胎毒性.体内研究结果显示,氧化锌纳米粒子、含镉或硒量子点和高浓度纳米银对大鼠、小鼠、斑马鱼、海胆、爪蟾和紫贻贝等动物中的一种或几种胚胎有毒性作用;不同剂量、不同尺寸的二氧化钛、二氧化硅、壳聚糖纳米粒子和碳纳米管对不同种属动物胚胎发育的影响不同.NDDS的胚胎毒性反应主要表现为发育停滞、流产和畸形,其胚胎毒性机制主要与氧化应激和炎症有关.NDDS的胚胎毒性研究虽然在模型、方法和内容方面都有待进一步探索和深入,但已开展的研究为后续的纳米药物胚胎毒性研究提供了重要的参考依据.
納米遞藥繫統(NDDS)是指藥物與藥物載體形成的、粒徑在1 000 nm以內的藥物輸送繫統,一般是以聚閤物膠束、脂質體、納米囊、微乳以及有機或無機納米粒子為載體,將藥效物質以一定的方式與載體結閤製成新型控/緩釋製劑,或直接將原藥加工製成納米粒子.NDDS的胚胎毒性是評價其非臨床安全性的重要內容.體外研究顯示,NDDS的胚胎毒性與納米粒子的理化性質如呎度和錶麵脩飾物、納米粒子暴露時間和劑量相關.已有的研究顯示,氧化鋅納米粒子胚胎毒性明顯,二氧化鈦、二氧化硅、氧化鎂納米粒子和碲化鎘量子點也有不同程度的胚胎毒性,而聚苯乙烯基納米粒子無胚胎毒性.體內研究結果顯示,氧化鋅納米粒子、含鎘或硒量子點和高濃度納米銀對大鼠、小鼠、斑馬魚、海膽、爪蟾和紫貽貝等動物中的一種或幾種胚胎有毒性作用;不同劑量、不同呎吋的二氧化鈦、二氧化硅、殼聚糖納米粒子和碳納米管對不同種屬動物胚胎髮育的影響不同.NDDS的胚胎毒性反應主要錶現為髮育停滯、流產和畸形,其胚胎毒性機製主要與氧化應激和炎癥有關.NDDS的胚胎毒性研究雖然在模型、方法和內容方麵都有待進一步探索和深入,但已開展的研究為後續的納米藥物胚胎毒性研究提供瞭重要的參攷依據.
납미체약계통(NDDS)시지약물여약물재체형성적、립경재1 000 nm이내적약물수송계통,일반시이취합물효속、지질체、납미낭、미유이급유궤혹무궤납미입자위재체,장약효물질이일정적방식여재체결합제성신형공/완석제제,혹직접장원약가공제성납미입자.NDDS적배태독성시평개기비림상안전성적중요내용.체외연구현시,NDDS적배태독성여납미입자적이화성질여척도화표면수식물、납미입자폭로시간화제량상관.이유적연구현시,양화자납미입자배태독성명현,이양화태、이양화규、양화미납미입자화제화력양자점야유불동정도적배태독성,이취분을희기납미입자무배태독성.체내연구결과현시,양화자납미입자、함력혹서양자점화고농도납미은대대서、소서、반마어、해담、조섬화자이패등동물중적일충혹궤충배태유독성작용;불동제량、불동척촌적이양화태、이양화규、각취당납미입자화탄납미관대불동충속동물배태발육적영향불동.NDDS적배태독성반응주요표현위발육정체、유산화기형,기배태독성궤제주요여양화응격화염증유관.NDDS적배태독성연구수연재모형、방법화내용방면도유대진일보탐색화심입,단이개전적연구위후속적납미약물배태독성연구제공료중요적삼고의거.
Nano drug delivery system (NDDS) is a kind of drug delivery system which are made up of drugs and drug carriers and their particle sizes are less than 1 000 nm.In general,polymeric micelles,liposome,nano capsule,microemulsion,and organic or inorganic nanoparticles are used as carriers in NDDS,pharmacodynamic substance and carriers are combined into new type of controlled/slow release preparations or the drugs are directly processed into nanoparticles.Embryo toxicity is an important index for non-clinic safety evaluation of NDDS.The in vitro studies showed that embryo toxicity of NDDS is related to physical and chemical properties of nanoparticles,such as size and modification materials on surface,exposure time of nanoparticles,and dosage.It has been shown that zinc oxide nanoparticles have embryo toxicity,titanium dioxide,silica,magnesium oxide,and quantum dots have different degrees of embryo toxicity,and polystyrene based nanoparticles have no embryo toxicity.The in vivo studies showed that zinc oxide nanoparticles,quantum dots containing cadmium or selenium,and high concentrations of nano silver have embryo toxicity in one or several animal models,such as rat,mouse,zebrafish,Paracentrotus lividus,Xenopus laevis,and Mytilus Galloprovincialis.Silica,titanium dioxide,chitosan nanoparticles and singlewalled carbon nanotubes at different dose and size showed different effects on embryonic development of different animal models.Embryotoxic or teratogenic effects of NDDS include stagnation,miscarriage,and deformity,and the mechanism of toxicity is mainly related to oxidative stress and inflammation.Though embryo toxicity of NDDS in models,methods and content need further exploration and research,studies which have been carried out provide important references for further research.