Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Xuyu Chai"'
Fused Deposition Modeling (FDM) 3D Printed Tablets for Intragastric Floating Delivery of Domperidone
Autor:
Xuyu Chai, Hongyu Chai, Xiaoyu Wang, Jingjing Yang, Jin Li, Yan Zhao, Weimin Cai, Tao Tao, Xiaoqiang Xiang
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Abstract The aim of this study was to explore the feasibility of fused deposition modeling (FDM) 3D printing to prepare intragastric floating sustained release (FSR) tablets. Domperidone (DOM), an insoluble weak base, was chosen as a model drug to in
Externí odkaz:
https://doaj.org/article/8f2c9fd73d224105875b2061744c0aba
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0160260 (2016)
Amoxicillin is a commonly used antibiotic which has a short half-life in human. The frequent administration of amoxicillin is often required to keep the plasma drug level in an effective range. The short dosing interval of amoxicillin could also caus
Externí odkaz:
https://doaj.org/article/141738f9ac414d0f8d3faf957a203d96
Publikováno v:
Oncology Letters
The autophagy involved in the occurrence, development and prognosis of human epidermal growth factor receptor 2 (HER2) gene-amplified cancer also controls the resistance of this type of cancer to the monoclonal antibody, trastuzumab (Tzb). In the pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5767cd6502607b253f561002d06901d6
http://europepmc.org/articles/PMC5835962
http://europepmc.org/articles/PMC5835962
Fused Deposition Modeling (FDM) 3D Printed Tablets for Intragastric Floating Delivery of Domperidone
Autor:
Chai Hongyu, Xiaoqiang Xiang, Tao Tao, Yan Zhao, Weimin Cai, Xiaoyu Wang, Jin Li, Xuyu Chai, Jingjing Yang
Publikováno v:
Scientific Reports
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
The aim of this study was to explore the feasibility of fused deposition modeling (FDM) 3D printing to prepare intragastric floating sustained release (FSR) tablets. Domperidone (DOM), an insoluble weak base, was chosen as a model drug to investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a49cec79bc7b48c07bbdd3eee377b562
http://europepmc.org/articles/PMC5460192
http://europepmc.org/articles/PMC5460192
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 8, p e0160260 (2016)
PLoS ONE, Vol 11, Iss 8, p e0160260 (2016)
Background Amoxicillin is a commonly used antibiotic which has a short half-life in human. The frequent administration of amoxicillin is often required to keep the plasma drug level in an effective range. The short dosing interval of amoxicillin coul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282f775a12f2327cc8582084b1d555f7
http://europepmc.org/articles/PMC4968835
http://europepmc.org/articles/PMC4968835
Publikováno v:
International Journal of Pharmaceutics. 337:127-132
This paper presents to investigate the levels of Huperzine A in plasma and CSF of rats after three different kinds of administrations and to find out whether intranasal administration is the best route to transfer the drug into the CNS. The drugs of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b5c9eb8a3efdee6b35e2db3f8190434
https://doi.org/10.1016/j.ijpharm.2006.12.029
https://doi.org/10.1016/j.ijpharm.2006.12.029
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 44:309-312
A simple reversed-phase high-performance liquid chromatography (HPLC)-fluorescence method for the determination of Huperzine A in rat plasma was developed and validated. Separation was achieved on Kromasil C(8) column (5 microm, 150 mm x 4.6mm i.d.).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::918ec8480fb5431008709e44732f2615
https://doi.org/10.1016/j.jpba.2007.02.019
https://doi.org/10.1016/j.jpba.2007.02.019
Publikováno v:
The Journal of pharmacy and pharmacology. 60(9)
We have evaluated the potential of intranasal administration of tramadol. The pharmacokinetic behaviour of tramadol in rat plasma and cerebrospinal fluid (CSF) after intranasal administration was determined and compared with those after intravenous a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a85db574b0ff076f0766e0947849ea2
https://pubmed.ncbi.nlm.nih.gov/18718117
https://pubmed.ncbi.nlm.nih.gov/18718117
Publikováno v:
Journal of Pharmacy & Pharmacology; Aug2008, Vol. 60 Issue 9, p1149-1154, 6p