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科研机构
上海药物研究所 [18]
山东大学 [7]
复旦大学上海医学院 [3]
厦门大学 [2]
大连化学物理研究所 [2]
过程工程研究所 [2]
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期刊论文 [42]
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2022 [1]
2021 [1]
2019 [2]
2018 [3]
2017 [1]
2016 [4]
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浏览/检索结果:
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PEG-Bottlebrush Stabilizer-Based Worm-like Nanocrystal Micelles with Long-Circulating and Controlled Release for Delivery of a BCR-ABL Inhibitor against Chronic Myeloid Leukemia (CML)
期刊论文
PHARMACEUTICS, 2022, 卷号: 14
作者:
Liang, Huamin
;
Zou, Fengming
;
Fu, Liyi
;
Liu, Qingwang
;
Wang, Beilei
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2022/12/23
drug nanocrystal
stabilizer
micelle
BCR-ABL
chronic myeloid leukemia (CML)
Nanocrystal-loaded liposome for targeted delivery of poorly water-soluble antitumor drugs with high drug loading and stability towards efficient cancer therapy
期刊论文
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2021, 卷号: 599
作者:
Liang, Huamin
;
Zou, Fengming
;
Liu, Qingwang
;
Wang, Beilei
;
Fu, Liyi
收藏
  |  
浏览/下载:66/0
  |  
提交时间:2021/05/17
Liposome
Drug nanocrystal
Core-shell
Drug delivery
Tumor therapy
BCR-ABL
Supersaturated polymeric micelles for oral silybin delivery: the role of the Soluplus-PVPVA complex
期刊论文
ACTA PHARMACEUTICA SINICA B, 2019, 卷号: 9, 期号: 1, 页码: 107-117
作者:
Zhu, Chunliu
;
Gong, Shuang
;
Ding, Jinsong
;
Yu, Miaorong
;
Ahmad, Ejaj
收藏
  |  
浏览/下载:130/0
  |  
提交时间:2020/07/01
Silybin
Soluplus
PVPVA
Complex
Supersaturated drug delivery system
Oral bioavailability
supersaturatedpolymericmicellesfororalsilybindeliverytheroleofthesolupluspvpvacomplex
期刊论文
actapharmaceuticasinicab, 2019, 卷号: 9, 期号: 1, 页码: 107
作者:
Zhu Chunliu
;
Gong Shuang
;
Ding Jinsong
;
Yu Miaorong
;
Ahmad Ejaj
收藏
  |  
浏览/下载:64/0
  |  
提交时间:2020/07/01
SOLUBILITY-PERMEABILITY INTERPLAY
WATER-SOLUBLE DRUGS
MEMBRANE-TRANSPORT
FORMULATION DESIGN
IN-VITRO
SYSTEM
BIOAVAILABILITY
ABSORPTION
IMPACT
DISSOLUTION
Silybin
Soluplus
PVPVA
Complex
Supersaturated drug delivery system
Oral bioavailability
Enhanced digestion inhibition and mucus penetration of F127-modified self-nanoemulsions for improved oral delivery
期刊论文
ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 卷号: 13, 期号: 4, 页码: 326-335
作者:
Song, Wenyi
;
Yang, Yuting
;
Yu, Miaorong
;
Zhu, Quanlei
;
Damaneh, Mohammadali Soleimani
收藏
  |  
浏览/下载:34/0
  |  
提交时间:2019/01/08
Self-nanoemulsifying system (SNEs)
Oral absorption
Enzymatic degradation
Mucus penetration
Pluronic (R) F127
Transport mechanism of lipid covered saquinavir pure drug nanoparticles in intestinal epithelium
期刊论文
JOURNAL OF CONTROLLED RELEASE, 2018, 卷号: 269, 页码: 159-170
作者:
Xia, Dengning
;
He, Yuan
;
Li, Qiuxia
;
Hu, Cunde
;
Huang, Wei
收藏
  |  
浏览/下载:40/0
  |  
提交时间:2019/01/08
Surface modification
Phospholipid bilayer
Nanodrug
Endocytosis
Transcytosis
P-type glycoprotein substrate
Mesoporous silica nanoparticles for drug and gene delivery
期刊论文
Acta Pharmaceutica Sinica B, 2018, 卷号: 8, 期号: 2, 页码: 165
作者:
Zhou Yixian
;
Quan Guilan
;
Wu Qiaoli
;
Zhang Xiaoxu
;
Niu Boyi
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2020/12/24
Therapeutics. Pharmacology
RM1-950
Study on orally delivered paclitaxel nanocrystals:modification,characterization and activity in the gastrointestinal tract
期刊论文
ROYAL SOCIETY OPEN SCIENCE, 2017, 卷号: 4, 期号: 11, 页码: 170753
作者:
Xing GM(刑更妹)
;
Li M(李敏)
;
Zhao YL(赵宇亮)
;
Runcong Liu, Ya-Nan Chang, Gengmei Xing, Min Li and Yuliang Zhao
;
Chang YN(常亚男)
收藏
  |  
浏览/下载:22/0
  |  
提交时间:2019/08/27
oral delivery
paclitaxel nanocrystal
gastrointestinal tract
New Tanshinone IIA Delivery System Using Chitosan Nanomicelles of Small Size
期刊论文
CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 2016, 卷号: 37, 期号: 7, 页码: 1229-1231
作者:
Li Hong
;
Du Libo
;
Zhang Han
;
Zhao Yuming
;
Liu Yang
收藏
  |  
浏览/下载:26/0
  |  
提交时间:2016/12/29
Chitosan nanomicelles of small size
Tanshinone IIA
Neuroprotectant
Delivery for poorly soluble drugs
Interfacial Cohesion and Assembly of Bioadhesive Molecules for Design of Long Term Stable Hydrophobic Nanodrugs toward Effective Anticancer Therapy
期刊论文
ACS NANO, 2016, 卷号: 10, 期号: 6, 页码: 5720-5729
作者:
Shen, Guizhi
;
Xing, Ruirui
;
Zhang, Ning
;
Chen, Chengjun
;
Ma, Guanghui
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2016/08/22
hydrophobic drugs
nanoengineering
interfacial assembly
Ostwald ripening suppression
drug delivery
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