کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
8994282 1114277 2005 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Structures from lysine-based dendrons and dendrimers: monolayers, dendriplexes, dendrisomes, nanoparticles and micellar aggregates
موضوعات مرتبط
علوم پزشکی و سلامت داروسازی، سم شناسی و علوم دارویی اکتشاف دارویی
پیش نمایش صفحه اول مقاله
Structures from lysine-based dendrons and dendrimers: monolayers, dendriplexes, dendrisomes, nanoparticles and micellar aggregates
چکیده انگلیسی
In a series of dendrons (partial dendrimers) and dendrimers synthesised in our laboratories we have found and review here a wide range of solution and suspension behaviour, which depends on the ionic, hydrophobic or amphipathic nature of the compounds. The primary building blocks of the dendrimers comprise a glycine core from which emanate multiple branched lysine head groups, terminating either in free amino groups (up to 64) or, when these terminal groups are derivatised, with alkyl chains of varying chain lengths up to C18. The most hydrophobic members of this dendrimer series are insoluble in water and in several cases these 4-10 nm diameter dendrimers self-aggregate to form nanoparticles with a maximum diameter of 200-300 nm. The cationic members of the series can associate with polyanionic molecules such as DNA and heparin to form “dendriplexes”. Dendrons are asymmetric and have a branched lysine head group (with and without alkyl chains) and a tail which is modified to possess 1,2 or 3 alkyl groups of varying chain length. Cationic dendrons also can associate with, and hence condense, DNA. Some dendrons are clearly amphiphilic with a propensity to form micelle-like structures. Some, either in the presence or absence of cholesterol, form vesicular structures which we have termed “dendrisomes”. This array of supramolecular structures can be utilised in the development of drug, vaccine and gene delivery systems as well as potentially providing new molecular excipients.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Drug Delivery Science and Technology - Volume 15, Issue 1, 2005, Pages 11-18
نویسندگان
, , , ,