Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Whei-Mei Wu"'
Publikováno v:
Journal of pharmaceutical sciences. 105(9)
Atopic dermatitis of sensitive areas such as the face, particularly in children, is a difficult disease to treat as the standard therapeutic, topical steroids, is contraindicated for this application in children. Hydrocortisone (HC) can be used in th
Publikováno v:
Pharmaceutical Research. 20:1681-1689
Purpose. To design and evaluate a new class of soft anticholinergics with subtype selectivity.
Publikováno v:
Journal of Drug Targeting. 10:63-71
Brain-targeted delivery of various drugs can be successfully achieved by chemical delivery systems (CDS) that contain a 1,4-dihydropyridine-based redox targetor moiety and undergo a sequential metabolism. However, the susceptibility of this moiety to
Publikováno v:
Bioorganic & Medicinal Chemistry. 8:1059-1063
A chemical targeting system for [Leu 2 , Pip 3 ]-TRH (Gln,Leu,Pip) was synthesized in order to allow its specific delivery to the central nervous system (CNS). Sequential metabolism of the obtained ‘packaged’ chemical delivery system, (CDS), DHT-
Publikováno v:
Journal of Medicinal Chemistry. 41:3773-3781
The design, synthesis, and pharmacological evaluation of brain-targeted chemical delivery systems (CDS) for a kyotorphin analogue (Tyr-Lys) are described. The brain-targeted compound contains the active peptide in a packaged, disguised form, flanked
Publikováno v:
Drug Development Research. 43:117-127
The design and evaluation of two new soft anticholinergic agents, ethoxycarbonylphenylcyclopentylacetyl-N,N-dimethyltropinium methyl sulfate (PCMS-1) and methoxycarbonylphenylcyclopentylacetyl-N,N-dimethyltropinium methyl sulfate (PCMS-2) are present
Autor:
Gábor Somogyi, Laszlo Prokai, Nicholas Bodor, M. Dulce C. Barros, Hassan H. Farag, Whei-Mei Wu
Publikováno v:
Journal of Ocular Pharmacology and Therapeutics. 13:389-403
S-(-)- Timolol maleate was oxidized, using the modified Pfitzner-Mofatt method, to the corresponding keto analog, which was then coupled with either hydroxylamine or methoxyamine in the same reaction medium. The products separated, timolone oxime (TO
Publikováno v:
Journal of Pharmaceutical Sciences. 85:496-504
We espouse the application of a novel chemical delivery system (CDS) approach to a delivery mechanism for drug targeting to lung tissue using the 1,2-dithiolane-3-pentyl moiety of lipoic acid as the “targetor moiety”. The synthesis and the physic
Publikováno v:
Pharmaceutical Research. 12:329-336
A new type of ultra-short acting β-blocker which might prove advantageous in treating acute arrhythmias was designed, synthesized and investigated. Based on the soft drug “inactive metabolite approach,” the inactive phenylacetic acid metabolite
Publikováno v:
Pharmaceutical Research. 12:869-874
Purpose. As a safe anti-inflammatory corticosteroid, the utility of loteprednol etabonate (LE) for the treatment of gastrointestinal inflammation, via oral and rectal administration, was investigated in rats.