supported by National Natural Science Foundation of China(Nos.82273867,82030107);Shanghai Science and Technology Project of Little Giant(No.1902HX76600);Shanghai Qingpu District Industry-University-Research Cooperative Development Funding Project(No.2022-7);High-level Talents of Fujian University of Chinese Medicine(No.X2019006-Talents).
Paclitaxel(PTX)is widely applied for the treatment of unresectable and metastasis breast carcinoma as well as other cancers,whereas its efficacy is always impeded by poor solubility.Liposomes are one kind of the most ...
supported by National Natural Science Foundation of China(Nos.21702153 and 21801194);Wuhan Science and Technology Bureau(No.whkxjsj009);the support of the Core Facility of Wuhan University and the Large-scale Instrument and Equipment Sharing Foundation of Wuhan University.
Chemotherapy combined with photodynamic therapy has emerged as a promising strategy for cancer treatment.However,simultaneously delivering chemotherapeutic drugs and photosensitizers and precisely adjusting the ratio ...
This work was supported by the National Natural Science Foundation of China(No.51773098);the Natural Science Foundation of Tianjin of China(No.18JCYBJC28300);the Fundamental Research Funds for Central Universities(China).
Although the antitumor drug cabazitaxel shows great therapeutic potential,its high toxicity and poor water solubility limit its utility.However,the use of stimuli-responsive prodrugs is a promising strategy for overco...
the financial supports from the National Natural Science Foundation of China(No.21374066);the Major Program of the Natural Science Project of Jiangsu Higher Education Institutions(No.15KJA150007);Natural Science Foundation of Jiangsu Province(No.BK20171212);the Project Funded by the Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions;Soochow-Waterloo University Joint Project for Nanotechnology from Suzhou Industrial Park
PEGylated prodrug,covalent attaching polyethylene glycol(PEG) polymer chains to therapeutic drugs,is one of the most promising techniques to improve the water-solubility,stability,and therapeutic effect of drugs.In th...
financially supported by grants from the National Natural Science Foundation of China(No.31671022);the Key Program for International S&T Cooperation Projects of China(No.2015DFA50310);the National Science and Technology Major Project(No.2014ZX09303301)
Molecular self-assembly is very ordinary phenomenon in the biological process such as protein folding,DNA encoding and etc.Inspired by this inherent biological process,nanostructure such as nanofibers,nanosphere,and s...
National Science and Technology Major Project for the support to this research;supported by Key New Drug Creation and Manufacturing Program, China(No.2009ZX09301-001)
To improve the aqueous solubility of an itraconazole analogue, compound 1 (YL-24), a series of novel prodrugs were synthesized. Among these prodrugs, the phosphate disodium salt compound 7 exhibited excellent aqueou...
supported by the Ph.D.Programs Foundation of Ministry of Education of China(No.20110181130011);the National Natural Science Foundation of China(No.81072532)
Received 4 November 2012 Received in revised form 17 December 2012 Accepted 31 December 2012 Available online 4 February 2013
supported by the grants from the National Natural Science Foundation of China(No.20962004);the Provincial Social Development Foundation of Guizhou,China(No.QKHSYZ[2009]3081);Provincial Special Assistant Foundation for High-level Talents of Guizhou,China(No.TZJF-2009-36);Science and Technology Foundation of Guizhou Province,China(No.QKHJZ[2008]2140)
A series of novel mono(2,2,2-trifluoroethyl) esters,mono L-amino acid ester prodrugs of acyclic nucleoside phosphonates was synthesized and their in vitro anti-HBVactivity was evaluated in HepG 2 2.2.15 cells.Compou...
16 ADT carboxylate esters were prepared by means of esterification and these compounds were expected to increase the bioavailability of 4-hydroxyanehole trithione.In vivo studies showed that ADT concentration of 3a in...
A series of novel L-amino acid esters prodrugs of acyclic nucleoside phosphonates was synthesized and their anti-HBV activity was evaluated in HepG2 2.2.15 cells. Compound 1d exhibited more potent anti-HBV activity an...