scholarly journals Natural channel protein inserts and functions in a completely artificial, solid-supported bilayer membrane

2013 ◽  
Vol 3 (1) ◽  
Author(s):  
Xiaoyan Zhang ◽  
Wangyang Fu ◽  
Cornelia G. Palivan ◽  
Wolfgang Meier
Langmuir ◽  
2000 ◽  
Vol 16 (7) ◽  
pp. 2991-2994 ◽  
Author(s):  
C. Tordeux ◽  
J.-B. Fournier

2010 ◽  
Vol 132 (27) ◽  
pp. 9320-9327 ◽  
Author(s):  
Andreia M. Smith ◽  
Madhuri Vinchurkar ◽  
Niels Gronbech-Jensen ◽  
Atul N. Parikh

Author(s):  
J M Shah ◽  
N.H Shah ◽  
Hadiya P D

Pharmaceutical technology has developed various newer modes of novel drug delivery aspects. Modifications in the previously existing drug delivery methods have led to various newly innovated technologies serving as a safe and effective means of improvement over the existing ones. Novasome technology is one of the new innovations of liposomes which have solved many of the problems related to liposomal drug delivery system. It offers a seven bilayer membrane which has the ability to incorporate both water soluble and insoluble drugs. It has an excellent entrapment efficiency which provides better medication. Formulation of novasomes is achieved in a high shear device. Due to its numerous advantages, novasomes have been used extensively in various fields like cosmetics, chemical, personal care, foods, pharmaceuticals and agrochemicals.


1969 ◽  
Vol 9 (2) ◽  
pp. 49-66
Author(s):  
Masayuki TAKAGI
Keyword(s):  

2021 ◽  
Author(s):  
Istvan Kocsis ◽  
Yudi Ding ◽  
Nicholas H. Williams ◽  
Christopher A. Hunter

Synthetic transducers transport externally added metal ion cofactors across the lipid bilayer membrane of vesicles to trigger catalysis of ester hydrolysis in the inner compartment. Signal transduction activity is modulated by hydrazone formation.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Koshi Nishida ◽  
Toshifumi Tojo ◽  
Takeshi Kondo ◽  
Makoto Yuasa

AbstractPorphyrin derivatives accumulate selectively in cancer cells and are can be used as carriers of drugs. Until now, the substituents that bind to porphyrins (mainly at the meso-position) have been actively investigated, but the effect of the functional porphyrin positions (β-, meso-position) on tumor accumulation has not been investigated. Therefore, we investigated the correlation between the functional position of substituents and the accumulation of porphyrins in cancer cells using cancer cells. We found that the meso-derivative showed higher accumulation in cancer cells than the β-derivative, and porphyrins with less bulky substituent actively accumulate in cancer cells. When evaluating the intracellular distribution of porphyrin, we found that porphyrin was internalized by endocytosis and direct membrane permeation. As factors involved in these two permeation mechanisms, we evaluated the affinity between porphyrin-protein (endocytosis) and the permeability to the phospholipid bilayer membrane (direct membrane permeation). We found that the binding position of porphyrin affects the factors involved in the transmembrane permeation mechanisms and impacts the accumulation in cancer cells.


1990 ◽  
Vol 265 (33) ◽  
pp. 20094-20097
Author(s):  
V E Scott ◽  
D N Parcej ◽  
J N Keen ◽  
J B Findlay ◽  
J O Dolly

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