@article{lee_whang_2011, title={Poly(vinyl alcohol) Blend Film with m-Aramid as an N-halamine Precursor for Antimicrobial Activity}, volume={122}, ISSN={["1097-4628"]}, DOI={10.1002/app.34055}, abstractNote={Abstract}, number={4}, journal={JOURNAL OF APPLIED POLYMER SCIENCE}, author={Lee, Jaewoong and Whang, Hyun Suk}, year={2011}, month={Nov}, pages={2345–2350} }
 @article{agrawal_kim_tonelli_whang_2010, title={Cyclodextrin Inclusion Complex Formation with Butylated Hydroxytoluene and Its Application in Polyethylene Film}, volume={118}, ISSN={["1097-4628"]}, DOI={10.1002/app.32543}, abstractNote={Abstract}, number={2}, journal={JOURNAL OF APPLIED POLYMER SCIENCE}, author={Agrawal, Manisha and Kim, Young Teck and Tonelli, Alan and Whang, Hyun Suk}, year={2010}, month={Oct}, pages={1184–1190} }
 @article{kim_kim_huang_whang_lee_2009, title={Antimicrobial Polyethylene Terephthalate (PET) Treated with an Aromatic N-Halamine Precursor, m-Aramid}, volume={114}, ISSN={["1097-4628"]}, DOI={10.1002/app.31016}, abstractNote={Abstract}, number={6}, journal={JOURNAL OF APPLIED POLYMER SCIENCE}, author={Kim, Sam Soo and Kim, Jiyoung and Huang, T. S. and Whang, Hyun Suk and Lee, Jaewoong}, year={2009}, month={Dec}, pages={3835–3840} }
 @article{whang_vendeix_gracz_gadsby_tonelli_2008, title={NMR studies of the inclusion complex of cloprostenol sodium salt with beta-cyclodextrin in aqueous solution}, volume={25}, ISSN={["1573-904X"]}, DOI={10.1007/s11095-007-9493-z}, abstractNote={{"Label"=>"PURPOSE", "NlmCategory"=>"OBJECTIVE"} Cloprostenol sodium salt (referred as cloprostenol) may be used for the synchronization of estrous cycles in farm animal species. Cyclodextrins (CDs) have potential as drug delivery systems through the formation of inclusion complexes between CDs and drugs. This is the first study of the inclusion complex of cloprostenol with beta-cyclodextrin (beta-CD) in aqueous solution using NMR and 3D molecular dynamics simulations. {"Label"=>"METHODS", "NlmCategory"=>"METHODS"} 1D proton NMR spectra of beta-CD, a complex of cloprostenol with beta-CD, and cloprostenol in D(2)O were assigned and confirmed. The cross relaxation interactions from ROESY were used as constraints for 3D molecular modeling studies. {"Label"=>"RESULTS", "NlmCategory"=>"RESULTS"} In the 2D ROESY of the complex, cross-peaks were observed between the aromatic protons of cloprostenol and protons of the beta-CD as well as between aliphatic protons and protons of the beta-CD. The stoichiometry of the complex was found that beta-CD forms a 1:1 inclusion complex with cloprostenol. The association constant K was 968 +/- 120 M(-1) at 298 K. {"Label"=>"CONCLUSIONS", "NlmCategory"=>"CONCLUSIONS"} Aromatic side and/or aliphatic side chains of the cloprostenol is included in the beta-CD while aliphatic side and/or aromatic side chains wraps around beta-CD, respectively. The molecular modeling also confirms that beta-CD forms a 1:1 inclusion complex with cloprostenol.}, number={5}, journal={PHARMACEUTICAL RESEARCH}, author={Whang, Hyun Suk and Vendeix, Franck A. P. and Gracz, Hanna S. and Gadsby, John and Tonelli, Alan}, year={2008}, month={May}, pages={1142–1149} }
 @article{whang_tonelli_2008, title={Release characteristics of the non-toxic insect repellant 2-undecanone from its crystalline inclusion compound with alpha-cyclodextrin}, volume={62}, ISSN={["1573-1111"]}, DOI={10.1007/s10847-008-9447-z}, number={1-2}, journal={JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY}, author={Whang, Hyun Suk and Tonelli, Alan}, year={2008}, month={Oct}, pages={127–134} }
 @article{whang_hunt_wrench_hockney_farin_tonelli_2007, title={Nonoxynol-9-alpha-cyclodextrin inclusion compound and its application for the controlled release of nonoxynol-9 spermicide}, volume={106}, ISSN={["1097-4628"]}, DOI={10.1002/app.26956}, abstractNote={Abstract}, number={6}, journal={JOURNAL OF APPLIED POLYMER SCIENCE}, author={Whang, Hyun Suk and Hunt, Marcus A. and Wrench, Nicola and Hockney, Jessica E. and Farin, Charlotte E. and Tonelli, Alan E.}, year={2007}, month={Dec}, pages={4104–4109} }
 @misc{whang_kirsch_zhu_yang_hudson_2005, title={Hemostatic agents derived from chitin and chitosan}, volume={C45}, ISSN={["1532-1797"]}, DOI={10.1080/15321790500304122}, abstractNote={A recent review detailing the role of new hemostatic agents for battlefield hemorrhage control describes the interest in and necessary specifications for such materials. As a consequence, the Defense Department authorized the development and use of three deployable and FDA approved hemostatic agents: Zeolite “Quikclot” and chitosanic “Hemcon” and the American Red Cross Fibrin Dressing. Although chitosan has a number of advantages over the other hemostatic agents, it is the least understood of the three agents noted above. The use of chitosan and chitin in different physical forms as a hemostatic agent is described. The chemical properties of chitosan related to hemostatis possibly include: molecular weight, extent of ionization, counter ion, degree of deacetylation, and degree of crystallinity. Also, its ability to bind with tissues are a function of these parameters. Chitosan can be used in medical and surgical procedures by its direct application to a bleeding surface using the various physical forms such as powder, solution, coating, film, hydrogel, and filament composite.}, number={4}, journal={JOURNAL OF MACROMOLECULAR SCIENCE-POLYMER REVIEWS}, author={Whang, HS and Kirsch, W and Zhu, YH and Yang, CZ and Hudson, SM}, year={2005}, pages={309–323} }