检索结果-内蒙古大学图书馆

您好，读者！请登录

内蒙古大学图书馆

首页
概况
党建
资源
服务
科研支持
- 论文收录引用证明
- 科技查新
知识产权
档案馆
帮助

咨询与建议

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

您的常用邮箱：*

您的手机号码：*

问题描述：

当前已输入0个字，您还可以输入200个字

全部搜索
期刊论文
图书
学位论文
标准
纸本馆藏
外文资源发现
数据库导航
超星发现

高级检索

时间限定

出版年份：

文献类型

图书期刊文献学位论文多媒体

馆藏选择

电子馆藏纸本馆藏

核心期刊

全部期刊 SCI 收录期刊 SSCI 收录期刊 EI 收录期刊 CSCD 收录期刊 CSSCI 收录期刊

语言

中文英文

文献类型

期刊文献图书学位论文标准纸本馆藏

帮助

文字说明：

T=题名（书名、题名），A=作者（责任者），K=主题词，P=出版物名称，PU=出版社名称，O=机构（作者单位、学位授予单位、专利申请人），L=中图分类号，C=学科分类号，U=全部字段，Y=年（出版发行年、学位年度、标准发布年）

检索规则说明：

AND代表“并且”；OR代表“或者”；NOT代表“不包含”；(注意必须大写,运算符两边需空一格)

检索范例：

范例一：(K=图书馆学 OR K=情报学) AND A=范并思 AND Y=1982-2016
范例二：P=计算机应用与软件 AND (U=C++ OR U=Basic) NOT K=Visual AND Y=2011-2016

分类表

所选分类

>> <<

限定检索结果

文献类型

590 篇 会议
2 篇 期刊文献

馆藏范围

592 篇 电子文献
0 种 纸本馆藏

日期分布

学科分类号

395 篇 医学
- 314 篇 中西医结合
- 299 篇 药学(可授医学、理...
- 49 篇 临床医学
- 26 篇 中药学(可授医学、...
- 8 篇 公共卫生与预防医...
- 6 篇 中医学
- 5 篇 基础医学(可授医学...
- 3 篇 医学技术（可授医学...
12 篇 工学
- 10 篇 材料科学与工程（可...
- 1 篇 化学工程与技术
- 1 篇 环境科学与工程（可...
8 篇 理学
- 8 篇 物理学
8 篇 管理学
- 7 篇 公共管理
- 1 篇 工商管理
2 篇 经济学
- 2 篇 应用经济学
2 篇 农学
- 1 篇 作物学
- 1 篇 兽医学

主题

16 篇 doxorubicin
16 篇 nanoparticles
14 篇 nanoparticle
12 篇 paclitaxel
12 篇 chitosan
11 篇 delivery
11 篇 sirna
11 篇 polymeric micell...
10 篇 bioavailability
10 篇 cytotoxicity
10 篇 presentation
10 篇 liposomes
9 篇 hyaluronic acid
9 篇 pharmacokinetics
9 篇 drug
8 篇 drug delivery
8 篇 multidrug resist...
8 篇 sustained releas...
8 篇 p-glycoprotein
8 篇 ph-sensitive

机构

8 篇 college of pharm...
6 篇 national recogni...
5 篇 school of pharma...
5 篇 department of ph...
4 篇 national key lab...
4 篇 苏州大学
4 篇 中山大学
3 篇 兰州大学第一医院
3 篇 华中科技大学
3 篇 四川省中医药科学...
3 篇 school of pharma...
3 篇 河南省南阳纺织集...
3 篇 北大药学院
3 篇 department of ma...
3 篇 四川大学
3 篇 college of pharm...
3 篇 中国药学会
3 篇 浙江大学
3 篇 中科院生物物理研...
3 篇 pharmaceutics fa...

作者

11 篇 李范珠
8 篇 zhirong zhang
7 篇 jianping zhou
7 篇 zhenzhong zhang
6 篇 yan ma
6 篇 qiang zheng
6 篇 xiao ke
5 篇 xun sun
5 篇 hong yuan
5 篇 wei wu
5 篇 徐汉友
5 篇 weiyue lu
4 篇 tao gong
4 篇 fu-qiang hu
4 篇 yong-zhong du
4 篇 jinjin shi
4 篇 jian-qing gao
4 篇 wanhui liu
4 篇 郭哲宁
4 篇 honghong wang

语言

533 篇 英文
58 篇 中文
1 篇 法文

检索条件"任意字段=2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会"

共 592 条记录，以下是511-520 订阅

全选清除本页清除全部题录导出标记到"检索档案"

详细简洁

排序：

Study on hyaluronic acid/PEI-dexamethasone/DNA ternary complexes for targeting gene delivery

Study on hyaluronic acid/PEI-dexamethasone/DNA ternary compl...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Ying Fan~(1,a),Jing Yao~(1,2,a),Jianping Zhou~(1,2*),Yun Lu~1 1 Department of pharmaceutics,China Pharmaceutical University,24 Tongjiaxiang,Nanjing 210009,China 2State Key Laboratory of Natural Medicines,China Pharmaceutical University,24 Tongjiaxiang,Nanjing 210009,China

Aims:Hyaluronic acid（HA）/polyethyleneimine-dexamethasone（PEI-Dex）/DNA ternary complexes were developed for targeted gene delivery to improve the transfection efficiency and decrease the cytotoxicity of polycation non-viral gene carriers. Methods:The formation of ternary complex was evaluated by gel retardation *** particle size,zeta potential and morphology of ternary complexes were *** transfection effciency,cytotoxicity,in vitro cellular uptake were evaluated systemically. Cytotoxicity was analyzed by MTT assay. Results:Molecular weight of PEI-Dex might impact the formation of complexes and the ability of condensation changed as follows PEI-Dex>PEI-Dex>*** particle sizes and zeta potentials of the ternary complexes at optical charge ratio were 100-200nm and less than-30mv,*** transfection efficiency of optimized ternary complexes was superior to that of complexes formed with PEI 25kDa and *** MTT assay showed that no significant cytotoxicity was found among the PEI-Dex at all concentrations tested. Conclusions:HA/PEI-Dex/DNA ternary complexes might be a promising targeted gene delivery system.

关键词： Hyaluronic acid Ternary complexes Gene carrier targeting delivery

来源：评论

学校读者我要写书评

暂无评论

Surface Charge of PLA Nanoparticles Regulate Antigen Loading,Phagocytosis and Activation of Macrophage and Immunity Effect in vivo

Surface Charge of PLA Nanoparticles Regulate Antigen Loading...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Lianvan Wang.Xiaoming Chen,Yuying Liu and Guanghui Ma National Key Laboratory of Biochemical Engineering,Institute of Process Engineering,Chinese Academy of Sciences,Beijing, 100190,PR China

Aim:Surface properties of nanoparticles(including size,surface chemistry,hydrophilicity,surface charge and so on)have significant influence on antigen loading,phagocytosis and activation of macrophage,which further affect the immune effect in vivo. However,we still don't know how these properties affect the immunity *** this study,Polylactic acid nanoparticles(PLA)with different surface charge were prepared,and the effects of surface charge on antigen loading efficiency and immune response were systematically investigated,which was favorable for designation of particulate vaccine adjuvents. Methods:PLA nanoparticles were firstly prepared by premix membrane emulsification ***,the nanoparticles were modified by Chitosan,Chitosan Chloride and Polyethyleneimine,*** nanoparticles with different charge were formed, which were further employed to adsorb model antigen of *** nanoparticles loaded with antigen were used for evaluation of phagocytosis and activation of Macrophage and immunity response in vivo. Results & Conclusion:Uniform-sized PLA nanoparticles with different surface charge were succeffuly obtained by premix membrane emulsification technique combination with physical *** antigen adsorption effeciency increased with increase of surface charge as shown in *** nanoparticles with higher surface charge also improved the phagocytosis and activation of microphage,which elevate immune response of antibody and cytokine secretion in vivo as shown in ***,the nanoparticles with higher surface charge owned excellent adjuvant effect especially for improvement of cellular immunity.

关键词： Nanoparticle surface charge macrophage activation immune response

来源：评论

学校读者我要写书评

暂无评论

The influence of particle size on the taste of fast-dissolving drug delivery system

The influence of particle size on the taste of fast-dissolvi...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Wan Wang,Lanjin Deng,Qiyu Zhang,Yan Ma,Xiao Ke,Qiang Zheng National recognized enterprise center,Chengdu Kanghong Pharmaceutical Co.Ltd.

Objective:To investigate the influence of particle size on the taste of fast-dissolving drug delivery systems(FDDS),develop a applicable method for improving patient compliance. Method:Aripiprazole and agomelatine were used as model *** direct compressed aripiprazole orally disintegrating tablets (ODTs)were prepared by using Avicel PH 101 and Avicel PH 102 as main *** direct compressed agomelatine sublingual tablets(SUBT)were prepared by carefully controlling the API particle size in three different ranges(<300mesh,300-100 mesh,>100mesh).Before tab letting,profiles of blend powder were ***,two types of fast-dissolving tablets(FDTs)were tasted and scored by 6 healthy volunteers. Results:The particle size of FDTs affects taste *** smaller the particle size of the filler is,the less grittiness the aripiprazole ODTs *** PH 101 is appropriate for the direct compressed aripiprazole ***,the particle size of agomelatine drug substance affects sublingual tablets taste in different direction,lager than 100 mesh leads grittiness and low dissolution,but smaller than 300 mesh leads severe *** appropriate range of agomelatine drug substance particle size is between 100 and 300 mesh. Conclusion:By carefully choosing excipients or adjusting the particle size within a specific range,the taste of FDTs was improved. This novel and convenient method can improve patient compliance effectively and can be easily applied in FDDS industry.

关键词： FDDS particle size taste

来源：评论

学校读者我要写书评

暂无评论

Biocompatibility of Theophylline/Carboxymethyl Chitosan/β-cyclodextrin Microspheres

Biocompatibility of Theophylline/Carboxymethyl Chitosan/β-c...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Weifen Zhang~*,Juanjuan Cui,Zhanqin Feng,Juan Chen,Guiyu Zhao,Yanjie Zhang,Ziqi Ding, Department of Pharmacy and Biological Science,Weifang Medical University,Weifang,P.R.China,261053

OBJECTIVE:The main aim of this study was to evaluate the biocompatibility of the theophylline/ carboxymethyl chitosan/β-cyclodextrin microspheres,which was made by spray drying method intended for pulmonary delivery. METHODS:Theophylline/carboxymethyl chitosan/β-cyclodextrin microspheres obtained were prepared by spray drying.A series experiments have been carried *** hemolysis test was carried out to estimate blood toxicity;Blood was obtained from male rabbit after death by cardiac *** cytotoxicity was determined using Fibroblasts by the MTT method which was used to evaluate in vitro cytotoxicity,The in vivo tissue biocompatibility of theophylline/carboxymethyl chitosan/p-cyclodextrin microspheres was examined by implanting the microspheres in the skeletal muscle of SD rats. RESULTS:Microspheres obtained after spray drying were found to be spherical shaped with smooth or wrinkled *** results of cell culture showed that the cytotoxicity was depended on the concentration and had no cytoxicity at low concentration;in addition,the cell cytotoxicity had no significant increase with time *** results of the hemolysis test indicated that the microspheres had no hemolysis activity;the test of muscle implantation test also indicates that the wounds were free from suppuration and necrosis after muscle implantation in all periods even did not cause any adverse effect such as hepatotoxicity,renal toxicity and hemoglobin synthesis *** time prolonged,the inflammatory reaction is gradually lighted and disappeared in the *** inflammations of muscle tissue were not significantly different from that of the operative suture. CONCLUSIONS:Theophylline/carboxymethyl chitosan/β-cyclodextrin microspheres successfully produced by spray drying *** results suggest that the microspheres possess good biocompability.

关键词： Carboxymethyl Chitosan Theophylline Microspheres Biocompatibility

来源：评论

学校读者我要写书评

暂无评论

Synthesis and in vitro evaluation of a novel vitamin C conjugated prodrug of ibuprofen

Synthesis and in vitro evaluation of a novel vitamin C conju...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Li Ling,Tuo Jue,Hu Haiyan~* School of Pharmaceutical Sciences,Sun Yat-sen University.

NSAID are widely used *** recent years,plenty of evidence suggests that NSAID can act as neuroprotective agents,and has curative effect of *** their distribution in the brain are very ***,we choose ibuprofen as a model drug,nutritional substance Vitamin C as the *** plan to synthesis a new prodrug,then study its ability for brain targeting. The prodrug was synthesis by three-steps *** consideration of 6 and 5 hydroxyls on Vitamin C were involved with the mechanism of the ***,we previous protected hydroxyl functions with benzyl *** on AA was carried out by a general procedure,in the presence of N,N-dicyclohexylcarbodimide（DCC）.After purification,the 6-O-ascorbates were then deprotected by hydrogenolysis treatment with Pd/*** final compound were confirmed by UV、RI、HNMR and mass spectroscopy （MS）. We determined the aqueous solubility and water partition coefficient of the prodrug and *** of prodrug was study in different pH PBS and plasma and brain homogenates（33%）for 24 *** prodrug showed higher aqueous solubility compare to *** show good stability in PBS except in alkaline *** hydrolysis in plasma make sure that the prodrug will not lose brain-targeted function until its reach to *** the obvious hydrolysis in the brain is good for efficacy. The UPLC-MSMS methods was set up to determine the concentrations of ibuprofen in the tissues including heat,liver,spleen, lung,kidney,brain and plasma of the *** recovery and precision could satisfy the determination requirements about the *** tissue distribution and pharmacokinetics were determined after *** of prodrug and ibuprofen into mice,*** TE、TI、RTE were used to evaluate the brain targeting *** results indicated that compared with direct injection of ibuprofen,the prodrug show markedly targeting efficiency and different biodistribution and pharmacokinetics. The Mad

关键词： Brain-targeting Prodrug VitaminC Ibuprof

来源：评论

学校读者我要写书评

暂无评论

Effects of Xiaozhiping Tablets on Serum Lipid in Rats With Experimental Hyperlipemia

Effects of Xiaozhiping Tablets on Serum Lipid in Rats With E...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Ren Hai-xiang,Su Hua,Zhou Xiao-dong~* Department of Preparation Division,Nanjing General Hospital of Nanjing Military Command,PLA,Nanjing 210002,Jiangsu, China

Objective:To investigate the effects of xiaozhiping tablets on serum lipid of experimental hyperlipemia in ***:The rats were offered high fat diet to create a hyperlipemia(HL)*** tablets and xuezhikang capsules were given intragastrically for treated drugs,the course was nine *** the variability for the body weight of the *** total cholesterol(TC),serum triglyceride(TG),low-density lipoprotein cholesterol(LDL-C),high-density lipoprotein cholesterol (HDL-C),apolipoprotein A-l(ApoA-1),apolipoprotein B(Apo-B),superoxide dismutase(SOD),malondialdehyde(MDA), glutathione peroxidase(GSH-PX),nitric oxide(NO)and the activity of PHPA,hepatic lipase(HL)and lipoprotein lipase(LPL)were ***:Body weight of the rats offered high fat diet decreased much less in xiaozhiping tablets group than that in the *** serum TC,TG,LDL-C and Apo-B in xiaozhiping tablets group were lower than that in the control,while the serum HDL-C,ApoA-1 and the ApoA-1/Apo-B ratio ***,atherosclerotic index(TC/ HDL-C)and the serum MDA in xiaozhiping tablets group degraded,while the activity of SOD,GSH-PX,NO,LPL,HL and PHPA ***:Xiaozhiping tablets are effective in reducing the blood-lipoprotein level in the experimental rats,which may be closely related with the raised activity of LPL and *** tablets might play an antioxidant effect by inhibiting lipid peroxidation to improve free radical metabolism,so that the function of blood vessel endothelium can be improved which had suffered from oxidative damage causing by hyperlipemia.

关键词： Effects of Xiaozhiping Tablets on Serum Lipid in Rats With Experimental Hyperlipemia

来源：评论

学校读者我要写书评

暂无评论

N-octyl-N-Arginine chitosan Micelles for insulin oral administration

N-octyl-N-Arginine chitosan Micelles for insulin oral admini...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Sarra Abbad Department of Pharmaceutics China Pharmaceutical University

Aim:To synthesis a novel chitosan derivative,N-octyl-N-arginine chitosan（OACS）,with a mimetic structure of Arginine rich *** micelles loaded Insulin（Ins-OACS）was prepared,characterized and ***:Octyl groups were introduced onto chitosan by nucleophilic addition and the subsequent *** the formed products were conjugated with arginine under the catalysis of EDC and NHS to form *** structure of OACS was evaluated by elemental analysis, spectrophotometry,FT-IR,H NMR *** self-assembled micelles of insulin were prepared by the conventional stirring technique,which were characterized by Dynamic light scattering,transmission electron microscopy and differential scanning *** docking by Discovery studio software was used to confirm the interactions between OACS and *** vitro,the protective effect for insulin by trapped into OACS micelles were determined by methods of the degradation experiment of enzyme;and the uptake test in Caco-2 cell was used to evaluate the enhancing internalization effect of OACS for *** vivo,the pharmacological activity PA%was determined to investigate the hypoglycemic effect of ***:Octyl and arginine groups were successfully introduced to *** product OACS can self-assemble in water to form a micelle solution with light blue *** micelles successfully loaded insulin with encapsulation efficiency of 75%and drug loading of 13%.The mean size of INS-OACS micelles was 327nm with polydisperse index of 0.148;theζpotential was +6.31 *** results showed that insulin exists in the micelle structure in an amorphous form or as a *** images confirmed Ins-OACS micelle has a regular sphere form with clear core-shell structure and a uniform particle *** docking by Discovery studio software confirmed that the interactions between OACS and insulin were mostly electrostatic in *** result of the degradation experiment by enzyme showed that

关键词： Chitosan N-octyl-N-Arginine chitosan Cell penetration peptides insulin Arginine-rich polymeric micelles Oral administration

来源：评论

学校读者我要写书评

暂无评论

Low molecular weight polyethylenimine-graft-Tween 85 for effective gene delivery:synthesis and in vitro characteristics

Low molecular weight polyethylenimine-graft-Tween 85 for eff...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Jisheng Xiao,Xiaopin Duan,Qi Yin,Haijun Yu,Yaping Li Center of Pharmaceutics,Shanghai Institute of Materia Medica,Chinese Academy of Sciences,Shanghai 201203,China

Objective:To develop a safe and efficient non-viral gene delivery vector. Methods:A new polymer,Tween 85-polyethylenimine conjugate（TP）,was synthesized by modifying low molecular weight polyethylenimine（PEI 2K）with Tween 85,and characterized by H NMR and *** ability of TP to condense DNA,the cytotoxicity and stability against salt-induced aggregation and enzymatic degradation of TP/DNA complexes（TPCs）were evaluated. In addition,the cellular uptake,transfection efficiency and intracellular location of TPCs were also ***,the effect of Tween 85 on the cellular uptake,transfection efficiency and intracellular location of TPCs ware evaluated in the presence of free Tween 85. Results:TP could condense DNA efficiently and did not exhibit obvious *** showed high resistance to salt-induced aggregation and enzymatic *** addition,the introduction of Tween 85 led to significant increase in the cellular uptake of TPCs with high transfection efficiency,which was strongly inhibited with the addition of free Tween 85 in MCF-7/ADR cells,but not in MCF-7 cells,indicating that the complexes might be taken up mainly by Tween 85-mediated endocytosis in MCF-7/ADR cells. Conclusion:TP could be a potential safe and effective vector for gene delivery.

关键词： Gene Polyethylenimine Tween 85 DNA Gene vector

来源：评论

学校读者我要写书评

暂无评论

Fe3O4/DNA/PEI/HA magnetic nanoparticles by lay-by-lay assembled in gene delivery

Fe3O4/DNA/PEI/HA magnetic nanoparticles by lay-by-lay assemb...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Ge JIANG Yu-jiao YUAN Shool of Life science and Biotechnology,Dalian University.Dalian 116622. Shool of Life science and Biotechnology Dalian UniversityDalian 116622

Objective:To develop a novel vector for gene delivery with FeO,Polyethylenimine（PEI）and hyaluronic acid（HA）.The magnetic nanoparticles of FeO/DNA/PEI/HA complex was successfully developed using a layer-by-layer method for target-specific intracellular delivery of DNA by HA receptor mediated endocytosis. Methods:The properties of FeO/DNA/PEI/HA magnetic nanoparticles complex were characterized by Atomic force microscopic and zeta potential *** DNA binding ability of FeO was erected by gel electrophoresis retardation *** cytotoxicity of FeO/DNA/PEI/HA magnetic nanoparticles complex was evaluated by MTT *** FeO/DNA/PEI/HA magnetic nanoparticles complex in vitro PGL3 gene expressing efficiency was evaluated by plasmid / liposome transfection method. Results:The particle size of FeO/DNA/PEI/HA magnetic nanoparticles complex was about 40 *** a negligible cytotoxicity, FeO/DNA/PEI/HA magnetic nanoparticles complex showed an excellent target-specific gene silencing efficiency in the presence of 50 vol%serum,which was statistically much higher than that of DNA/Lipofectamine 2000 *** the competitive binding tests with free HA,MRI confirmed the target-specific intracellular delivery of FeO/DNA/PEI/HA complex to MCF-7 cells with HA receptors. Conclusion:FeO/DNA/PEI/HA magnetic nanoparticles complex as a specific target cells gene carrier is promising.

关键词： Fe3O4 polyethyleneimine hyaluronic acid targeted delivery

来源：评论

学校读者我要写书评

暂无评论

Induction of Acute Cell Necrosis by Cationic Liposomesin a Charge-Dependent Way

Induction of Acute Cell Necrosis by Cationic Liposomesin a C...

引用

2012年中国药物制剂大会——中国药学会药剂专业委员会年会、亚洲阿登制药技术研讨会暨国际控释协会中国分会年会

作者： Xiawei Wei~*,Zhirong Zhang Key Laboratory of Drug Targeting of Ministry of Education,West China School of Pharmacy,Sichuan University,No.17,Block 3, Southern Renmin Road,Chengdu 610041,PR China.

One of the important characteristics of a nanoparticle is the charge on the *** understand the potential interactions between the charge of the nanocarriers and cells is of great importance for developing better and safer *** use a variety of charged liposomes as a nanoparticle model,as well as other cationic materials as controls to observe biological behavior of the treated cells. We found that cationic liposomes as well as cationic carriers induced cell necrosis in vitro and in animal *** increased cell membrane permeability to propidium iodide was found after 2 minutes' incubation of cells with cationic *** the morphological changes of the cells were in accordance with general description for cell necrosis,and diffuse cytoplasmic cathepsin-B immunofluorescence was observed without the caspase activation of apoptosis(Figure B).Furthermore,the cell membrane depolarization was detected in less than 60 seconds of *** was a good correlation between the zeta-potential of cationic liposomes and the percentages of induced necrotic cell *** cell necrosis can be attenuated by neutralization of cationic charge of *** addition,the necrotic cell death cannot be blocked by specific necrosis inhibitor Necrostatin-1,whereas,has apparent changes in intracellular calcium concentration and reactive oxygen *** genes closely related to programmed cell death did not show significant change in expression level in the necrotic cells induced by cationic ***,our findings suggested that the cationic liposomes as well as other cationic carriers could induce cell necrosis in a rapid and charge-dependent way,and may be of importance in the design of nanocarriers in drug delivery systems.

关键词： Induction of Acute Cell Necrosis by Cationic Liposomesin a Charge-Dependent Way

来源：评论

学校读者我要写书评

暂无评论

没有更多数据了...

全选清除本页清除全部题录导出标记到“检索档案”

共60页 << < 48 49 50 51 52 53 54 55 56 57 > >>

检索报告对象比较合并检索0

隐藏清空

合并搜索

回到顶部

执行限定条件

内容：

评分：

请选择保存的检索档案：

请选择收藏分类：

订阅名称：

通借通还

温馨提示：

图书名称：

借书校区：

取书校区：

手机号码：

邮箱地址：

一卡通帐号：

电话和邮箱必须正确填写，我们会与您联系确认。

联系人：

所在院系：

联系邮箱：

联系电话：

内蒙古自治区呼和浩特市赛罕区大学西街235号邮编: 010021

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：