نتایج جستجو برای: cyclodextrin

تعداد نتایج: 7063  

1997
R. P. Patel M. M. Patel Rakesh P. Patel

Several attempts have been made to improve the solubility of water insoluble drugs. Over the years, inclusion complexation of drugs with β-cyclodextrin has emerged as a viable attempt to improve the dissolution of water insoluble drugs. The aim of the present work was to improve the dissolution rate of lovastatin, a water insoluble drug, by inclusion complexation with β-cyclodextrin. The stoich...

2010
M. A. Saleem Sumanji Bala Liyakat A. Aeajaz

The ability of β-cyclodextrin, hydroxypropyl-β-cyclodextrin, polyvinyl pyrrolidone and urea to influence the percutaneous absorption of meloxicam through isolated rat skin was evaluated. Carrier complex were prepared by kneading method in 1:1 and 1:2 in molar ratios for β-cyclodextrin and hydroxypropyl-β-cyclodextrin and in 1:1, 1:3 and 1:5 in weight ratios for polyvinyl pyrrolidone and urea. T...

1994
RICHÈLE D. WIND WOLFGANG LIEBL REINETTA M. BUITELAAR DIRK PENNINGA ANDREAS SPREINAT LUBBERT DIJKHUIZEN

glycosyltransferase. the enzyme as a cyclodextrin thermosulfurigenes EM1 and reclassification of alpha-amylase of Thermoanaerobacterium Cyclodextrin formation by the thermostable

Journal: :Organic & biomolecular chemistry 2005
Manickam C Durai Manickam Subramanian Annalakshmi Kasi Pitchumani Chockalingam Srinivasan

Multiple recognition by cyclodextrin in a bimolecular reaction, namely bromination of styrene, methyl cinnamate, phenylacetylene and allylbenzene, has been studied. Bromohydrin is obtained as a major product along with dibromide in the bromination of styrene and methyl cinnamate. The percentage of bromohydrin decreases as the cavity size increases. With phenylacetylene, bromophenylacetylene and...

2009
Rafael L. Bowen Gary E. Schumacher Anthony A. Giuseppetti Charles M. Guttman Clifton M. Carey

The objective of this work was to determine bonding characteristics of a hydrophilic monomer formulation containing polymerizable cyclodextrin derivatives. The hypothesis was that a formulation containing hydrophilic cross-linking diluent comonomers and cyclodextrins with functional groups attached by hydrolytically stable ether linkages could form strong adhesive bonds to dentin. The previousl...

Journal: :Journal of molecular modeling 2013
L Barrientos E Lang G Zapata-Torres C Celis-Barros C Orellana P Jara N Yutronic

The structural elucidation of 2α-cyclodextrin/1-octanethiol, 2α-cyclodextrin/1-octylamine and 2α-cyclodextrin/1-nonanoic acid inclusion complexes by nuclear magnetic resonance (NMR) spectroscopy and molecular modeling has been achieved. The detailed spatial configurations are proposed for the three inclusion complexes based on 2D NMR method. ROESY experiments confirm the inclusion of guest mole...

2014
Toshiaki Kudo Kazuaki Sakamoto Masashi Akinaga Ayumi Kawauchi Tomomi Nakahara Xiaochi Zhang Akinori Yamada Kenshiro Oshima Wataru Suda Hirokazu Kuwahara Nobuyuki Nakamura Yuichi Nogi Keiko Kitamura Masahiro Yuki Toshiya Iida Shigeharu Moriya Tetsushi Inoue Yuichi Hongoh Masahira Hattori Moriya Ohkuma

Bacillus strains JCM 19045, JCM 19046, and JCM 19047 are alkaliphiles that produce β-cyclodextrin from starch. They are related to Bacillus xiaoxiensis and Bacillus lehensis. The genome information for these three strains will be useful for studies of the physiological role of cyclodextrin and cyclodextrin production.

Journal: :International journal of pharmaceutics 2005
Stéphane Gibaud Siham Ben Zirar Pierre Mutzenhardt Isabelle Fries Alain Astier

Melarsoprol, a water-insoluble drug, is mainly used in the treatment of trypanosomiasis and has demonstrated an in vitro activity on myeloid and lymphoid leukemia derived cell lines. It is marketed as a very poorly tolerated non-aqueous solution (Arsobal). The aim of our work was to develop melarsoprol-cyclodextrin complexes in order to improve the tolerability and the bioavailability of melars...

Journal: :Investigative ophthalmology & visual science 1991
W W Li R Casey E M Gonzalez J Folkman

It is known that hydrocortisone can be converted to a potent angiogenesis inhibitor by coadministration with heparin or with a sulfated cyclodextrin. The activity of tetrahydrocortisol-S, a purely angiostatic corticosteroid, can be potentiated by beta-cyclodextrin tetradecasulfate as shown in this study. This drug "pair" and other pairs of corticosteroids and beta-cyclodextrin tetradecasulfate ...

2008
B. D. Shewale N. P. Sapkal N. A. Raut N. J. Gaikwad R. A. Fursule

The present study was undertaken to examine the effect of pH and concentration of hydroxypropyl-beta-cyclodextrin on the solubility of carvedilol as it shows pH-dependent solubility. The equilibrium solubility of carvedilol in a series of solutions of varying pH (from 1.2 to 11) was determined and compared with the equilibrium solubility of carvedilol in the presence of 20% hydroxypropyl-beta-c...

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