维普期刊资源整合服务平台（V6.5）

维普中文期刊产品整合服务

7篇 您的检索式：作者名="Nadda"

选中清除导出查看参考文献查看引证文献引用追踪共1页首页上一页第1页下一页末页 /1 跳转

		题名	作者	年代	出处	被引量
	1	Microscopic identification of early myocardial infarcts by dehydrogenase alterations显示文摘	Naddas MM Sandriter TK	1963	Am J Pathol1963，42，：	1
	2	The ecology of the Bithynia first intermediate hosts of Opisthorchis viverrini显示文摘	Trevor Petney Paiboon Sithithaworn Ross Andrews Nadda Kiatsopit Smarn Tesana Carl Grundy-Warr Alan Ziegler	2011	Parasitology International2011，，1：	1
	3	Determination of chlor- pyrifos 20% EC (Dursban 20 EC) in scented rose and its prod- ucts 显示文摘	KUMAR A NADDA G SHANKER A	2004	Journal of Chromatography A2004，1050，2：	1
	4	Microscopic identification of early myocardial infarcts by dehydrogenase alterations显示文摘	Naddas MM Sandriter TK	1963	Am J Pathol1963，42，：	1
	5	Age,growth and reproduction of the Caspian roach(Rutilus rutilus caspicus)in the Anzali and Gomishan wetlands,North Iran显示文摘	Nadda R Abdoli A Kiabi B H	2005	J Appli Ichthyol2005，21，：	1
	6	Characterization and biocompatibility of bacterial cellulose/alginate composite sponges with human keratinocytes and gingival fibroblasts显示文摘	Nadda Chiaoprakobkij Neeracha Sanchavanakit Keskanya Subbalekha Prasit Pavasant Muenduen Phisalaphong	2011	Carbohydrate Polymers2011，，3：	1
	7	Atractylodin-loaded PLGA nanoparticles:formulation and characterization显示文摘OBJECTIVE To formulate atractylodin-loaded poly(lactic-co-glycolic acid)(PLGA)nanoparticles and characterize the prepared nanoparticle formulation.METHODS The nanoparticle formulation was developed using solvent displacement method.The encapsulation and loading efficiency were characterized and particle size,and zeta potential were determined by dynamic light scattering technique.Drug release was assessed in vitro.RESULTS The size(mean±SD of diameter) of the prepared atractylodin-loaded PLGA nanoparticles were(161.27 ± 1.87)nm with narrow size distribution(mean PDI:0.068±0.015) and zeta potential(28.83±0.35)mV.The encapsulation and loading efficiency were(48.31±0.83)% and(2.15±0.04)%,respectively.Drug release from atractylodin-loaded PLGA nanoparticles was observed up to(87.70±0.47)% in 72 h with biphasic manner.Moreover,the nanoparticles were found to be freely dispersible in water without aggregation.CONCLUSION Results suggest that PLGA nanoparticles may be used as an effective drug delivery system for atractylodin.The anti-cholangiocarcinoma activity of this nanoparticle formulation is required.	Nadda MUHAMAD Tullayakorn PLENGSURIYAKARN Chuda CHITTASUPHO Kesara NA-BANGCHANG	2018	中国药理学与毒理学杂志2018，32，4：	0

返回顶部每页显示：

共1页首页上一页第1页下一页末页 /1 跳转

goolge学术搜索-维普

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1　渝公网安备 50019002500403号　违法和不良信息举报中心

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费