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1.
Bioconjug Chem ; 21(5): 807-10, 2010 May 19.
Artículo en Inglés | MEDLINE | ID: mdl-20481501

RESUMEN

A versatile methodology for efficient synthesis of PEGylated lipopeptides via CuAAC "Click" conjugation between alkyne-bearing solid-supported lipopeptides and azido-functionalized PEGs is described. This new and very robust method offers a unique platform for synthesizing PEGylated lipopeptides with a high level of complexity. These molecules, obtained in a single purification step, are ideally suited for functionalization of solid-supported lipid bilayers and liposomal drug delivery systems and are particularly valuable in enzyme activation strategies.


Asunto(s)
Técnicas Químicas Combinatorias/métodos , Lipopéptidos/síntesis química , Polietilenglicoles/síntesis química , Secuencia de Aminoácidos , Técnicas Químicas Combinatorias/economía , Lipopéptidos/química , Polietilenglicoles/química
3.
J Pept Sci ; 11(8): 499-505, 2005 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-15747322

RESUMEN

Ten N(epsilon)-glycylornithineamide derivatives have been synthesized containing various N(alpha)-linked pyrimidine-1-ylacetyl groups which can undergo (2pi + 2pi) photodimerization on irradiation with UV light at 254 nm. The dimerization efficiency of the free and bound pyrimidine groups was compared in aqueous solution: it was dependent on the substitution of the pyrimidine ring. N(alpha),N(alpha')-bis-(uracil-1-ylacetyl)-(N(epsilon)-glycylornithineamide) and N(alpha),N(alpha')-bis-(5-bromouracil-1-ylacetyl)-(N(epsilon)-glycylornithineamide) were identified as possible candidates for optical data storage.


Asunto(s)
Dipéptidos/química , Pirimidinas/química , Acetatos/química , Dimerización , Fotoquímica , Espectrofotometría Ultravioleta
4.
J Am Chem Soc ; 125(44): 13366-7, 2003 Nov 05.
Artículo en Inglés | MEDLINE | ID: mdl-14583026

RESUMEN

A new method for quantitative etching of the poly(dimethylsiloxane) block in polystyrene-poly(dimethylsiloxane) (PS-PDMS) block copolymers is reported. Reacting the block copolymer with anhydrous hydrogen fluoride renders a nanoporous material (NPM) with the remaining glassy PS maintaining the original bulk morphology. 1H NMR, mass difference, size exclusion chromatography, and X-ray photoelectron spectroscopy were used to characterize the materials before and after etching. NPMs containing spherical and gyroid cavities were prepared, as ascertained by small-angle X-ray scattering. This is the first report on block copolymer-based NPM films of millimeter thickness containing secluded spherical holes. Surface images by AFM and SEM are consistent with the SAXS findings.

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