@article { ISI:000268726500015,
	title = {Simple and efficient enzymatic transglycosylation of stevioside by beta-cyclodextrin glucanotransferase from Bacillus firmus},
	journal = {Biotechnology Letters},
	volume = {31},
	number = {9},
	year = {2009},
	note = {13th International Biotechnology Symposium and Exhibition (IBS-2008), Dalian, PEOPLES R CHINA, OCT 12-17, 2008},
	month = {SEP},
	pages = {1415-1420},
	publisher = {SPRINGER},
	address = {VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS},
	abstract = {<p>Stevioside was subjected to 1,4-intermolecular transglycosylation using beta-cyclodextrin glucanotransferase (beta-CGtase) produced from an alkalophilic strain of Bacillus firmus. The reaction was carried out by traditional, ultrasound-assisted and microwave-assisted techniques. Reaction under microwave conditions was faster and was completed in 1 min yielding two 1,4 transglycosylated products, 4{\textquoteright}-O-alpha-d-glycosyl stevioside (I) and 4{\textquoteright}{\textquoteright}-O-alpha-d-maltosyl stevioside (II) in 66\% and 24\%, respectively. The optimum transglycosylation occurred by using stevioside (1.24 mmol), beta-CD (1.76 mmol) and beta-CGtase (2 U/g) under microwave assisted reaction (MAR) in 5 ml sodium phosphate buffer (pH 7) at 50A degrees C and 80 W power. MAR is therefore potentially a useful and economical method for faster transglycosylation of stevioside.</p>},
	keywords = {beta-cyclodextrin, beta-Cyclodextrin glucanotransferase, Microwave-assisted reaction, Stevia rebaudiana, Stevioside, Transglycosylation},
	issn = {0141-5492},
	doi = {10.1007/s10529-009-0020-7},
	author = {Jaitak, V. and Kaul, V. Kumar and Bandna and Kumar, N. and Singh, B. and Savergave, L. S. and Jogdand, Vitthal V. and Nene, S.}
}
@article { ISI:000324679400001,
	title = {Structure elucidation of beta-cyclodextrin-xylazine complex by a combination of quantitative H-1-H-1 ROESY and molecular dynamics studies},
	journal = {Beilstein Journal of Organic Chemistry},
	volume = {9},
	year = {2013},
	month = {SEP},
	pages = {1917-1924},
	publisher = {BEILSTEIN-INSTITUT},
	address = {TRAKEHNER STRASSE 7-9, FRANKFURT AM MAIN, 60487, GERMANY},
	abstract = {<p>The complexation of xylazine with beta-cyclodextrin was studied in aqueous medium. H-1 NMR titrations confirmed the formation of a 1:1 inclusion complex. A ROESY spectrum was recorded with long mixing time which contained TOCSY artifacts. It only confirmed the presence of xylazine aromatic ring in the beta-cyclodextrin cavity. No information regarding the mode of penetration, from the wide or narrow side, could be obtained. We calculated the peak intensity ratio from the inter-proton distances for the most stable conformations obtained by molecular dynamics studies in vacuum. The results show that highly accurate structural information can be deduced efficiently by the combined use of quantitative ROESY and molecular dynamics analysis. On the other hand, a ROESY spectrum with no spin diffusion can only compliment an averaged ensemble conformation obtained by molecular dynamics which is generally considered ambiguous.</p>},
	keywords = {beta-cyclodextrin, inclusion complex, ROESY, simulation studies, xylazine},
	issn = {1860-5397},
	doi = {10.3762/bjoc.9.226},
	author = {Ali, Syed Mashhood and Fatma, Kehkeshan and Dhokale, Snehal A.}
}
@article {47572,
	title = {Construction of beta-cyclodextrin linked glycidyl methacrylate polymers for stereoselective separation of chiral drug},
	journal = {Journal of Polymer Research},
	volume = {28},
	year = {2021},
	month = {AUG},
	pages = {287},
	type = {Article},
	abstract = {In this present study, a series of cross-linked porous polymers based on Glycidyl Methacrylate (GMA) were synthesized by suspension polymerization using cyclohexanol and hexanol as pore generating solvents. beta-cyclodextrin (beta-CD) was covalently bonded to the polymers by using Hexamethylene Diisocyanate (HMDI) and Sebacoyl Chloride (SC) as spacer arms. The effects of matrix properties such as pore volume, type of crosslinker, and spacer on the loading of beta-cyclodextrin were investigated. The stereoselective binding of enantiomers of the anti-depressant drug citalopram was studied using beta-cyclodextrin loaded polymers under batch adsorption mode. The capacity factor and selectivity of isomers were investigated also. This study reveals that these beta-cyclodextrin bonded Glycidyl Methacrylate (GMA) polymers are potentially suitable for chromatographic separation of citalopram.},
	keywords = {beta-cyclodextrin, Citalopram, Glycidyl Methacrylate (GMA) beads, HPLC etc, Stereoslelctivity},
	issn = {1022-9760},
	doi = {10.1007/s10965-021-02634-7},
	author = {Wale, Apparav and Mulani, Khudbudin and Deshpande, Supriya and Rajan, C. R. and Ponrathnam, Surendra}
}
