Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Zhenping Wei"'
Autor:
Qiyue Zhang, Mengbin Qin, Zhihai Liang, Huali Huang, Yongfeng Tang, Lingyan Qin, Zhenping Wei, Mengtao Xu, Guodu Tang
Publikováno v:
Lipids in Health and Disease, Vol 18, Iss 1, Pp 1-9 (2019)
Abstract Objectives The aim of the current study was to evaluate influence of serum triglyceride levels on the course of acute pancreatitis (AP). Methods Rats models of hypertriglyceridemic were used in animal experiments. Following induction of acut
Externí odkaz:
https://doaj.org/article/d241d7d972c84de9a3cce67f37945614
Autor:
Wenli Liu, Xiaona Wang, Ruilian Chen, Kaixuan Zhang, Yao Li, Yi Li, Duanyun Si, Junbo Gong, Dianshu Yin, Yongli Wang, Zhenping Wei, Mingshi Yang
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 6, Iss 5, Pp 468-474 (2016)
The previous investigation has proved that their existed pharmacokinetic difference between the different crystal forms of the polymorphic drugs after oral administration. However, no systemic investigations have been made on the change of this pharm
Externí odkaz:
https://doaj.org/article/af29d33a0d104297822bf23d5ab18d18
Publikováno v:
Tobacco Regulatory Science. 7:4244-4253
Sericin nanomicelles (Sericin-PBLG) have the properties of efficiently and stably encapsulating hydrophobic chemotherapeutics in aqueous solution. The vitamin B12 (VB12) modified amphiphilic chitosan derivative can improve the delivery effect of oral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::121f3d1f8b2877198c66f5e38c08db0a
https://doi.org/10.18001/trs.7.5.1.201
https://doi.org/10.18001/trs.7.5.1.201
Publikováno v:
AAPS PharmSciTech. 23
Drugs are referred to as drug nanocrystals when they exist as nanoscale crystal structures. This kind of nanocarrier has been widely utilized to increase the solubility and absorption for poorly aqueous soluble drugs after oral administration, or pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec9c6f770baf45e9cc369691943bd77c
https://doi.org/10.1208/s12249-021-02200-w
https://doi.org/10.1208/s12249-021-02200-w
Publikováno v:
AAPS PharmSciTech. 23(1)
In the advancement of tumor therapy, in addition to the search for new antitumor compounds, the development of nano-drug delivery systems has opened up new pathways for tumor treatment by addressing some of the limitations of traditional drugs. Lipos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::660972d59d9d5c0c0b60a32e3a08231c
https://pubmed.ncbi.nlm.nih.gov/34907483
https://pubmed.ncbi.nlm.nih.gov/34907483
Publikováno v:
RSC Advances. 9:34472-34480
Two-photon polymerization (TPP) microfabrication technology can freely prepare micro/nano structures with different morphologies and high accuracy for micro/nanophotonics, micro-electromechanical systems, microfluidics, tissue engineering and drug de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4cbeb526767c5a6366661372b149a60
https://doi.org/10.1039/c9ra05645a
https://doi.org/10.1039/c9ra05645a
Publikováno v:
AAPS PharmSciTech. 22
Objective of the study was to design an injectable microsphere preparation with high drug loading of bupivacaine for prolonged release and local anesthetic. PLA or PLGA was used as the biodegradable matrix material to fabricate microspheres with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9c29bd80cdc2caeabdbf9f9c14a24b1
https://doi.org/10.1208/s12249-020-01878-8
https://doi.org/10.1208/s12249-020-01878-8
Autor:
Shichao Du, Shijie Xu, Zhenping Wei, Panpan Sun, Ergang Liu, Mingyang Chen, Junbo Gong, Yaping Wang, Sohrab Rohani
Publikováno v:
Crystal Growth & Design. 17:5790-5800
Vinpocetine was a BCS II drug, whose clinical applications had suffered from low oral bioavailability because of its inefficient dissolution in the GI tract. As the dissolution rate depended on the surface area of the drug crystals, we herein explore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a91bddd6801cafed184005ef9a16f70e
https://doi.org/10.1021/acs.cgd.7b00806
https://doi.org/10.1021/acs.cgd.7b00806
Publikováno v:
AAPS PharmSciTech. 18:224-230
The aim of this study was to prepare APAP crystals by cooling, anti-solvent, and solvent evaporation crystallization to enhance its dissolution rate and to make comparisons of the three methods. Agitating speeds and types were regarded as factors aff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87e926e535e2fa0cc66783d7e5d89498
https://doi.org/10.1208/s12249-016-0510-6
https://doi.org/10.1208/s12249-016-0510-6
Autor:
Mingshi Yang, Yongli Wang, Wenli Liu, Kaixuan Zhang, Dianshu Yin, Yi Li, Xiaona Wang, Junbo Gong, Ruilian Chen, Yao Li, Duanyun Si, Zhenping Wei
Publikováno v:
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica B, Vol 6, Iss 5, Pp 468-474 (2016)
Acta Pharmaceutica Sinica B, Vol 6, Iss 5, Pp 468-474 (2016)
The previous investigation has proved that their existed pharmacokinetic difference between the different crystal forms of the polymorphic drugs after oral administration. However, no systemic investigations have been made on the change of this pharm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60caf0c3a364bff12eb600d572445a5c
https://pubmed.ncbi.nlm.nih.gov/27709016
https://pubmed.ncbi.nlm.nih.gov/27709016