eprintid: 7554 rev_number: 4 userid: 6 dir: disk0/00/00/75/54 datestamp: 2011-11-10 19:41:41 lastmod: 2016-11-15 13:42:08 status_changed: 2011-11-10 19:41:41 type: thesis_degree metadata_visibility: show contact_email: zhc3@pitt.edu item_issues_count: 0 eprint_status: archive creators_name: Chen, Zhi creators_email: zhc3@pitt.edu creators_id: ZHC3 title: High-Throughput Methods to Determine Intermolecular Association and Lipophilicity ispublished: unpub divisions: sch_as_chemistry full_text_status: public keywords: Binding Constant; Chirl Selector; Cyclodextrin; Lipophilicity; Intermolecular Association; Solid Phase Microextraction; High-Throughput; Phase Distribution abstract: Noncovalent intermolecular associations are omnipresent in chemical and biochemical systems. Binding constants provide a fundamental measure of the affinity of a solute to a ligand; hence their determination has been an important step in describing and understanding molecular interactions. A high-throughput method based on the concept of phase distribution has been developed to determine binding constants. The solute distribution coefficients between a polymer phase and an aqueous phase are measured in a 96-well format, in the presence and absence of the ligand in one of the two phases. Binding constants are then calculated through linear or nonlinear fitting analyses. The polymer is plasticized poly(vinyl chloride). This high-throughput approach has been employed in several applications. In the first one, the partition ratios (no ligand in either phase) of neutral solutes have been correlated with their lipophilicities (octanol-water partition coefficients). The established linear correlation between their logarithmic values can be used as a calibration curve to predict the lipophilicity of compounds with unknown lipophilicity values. The pKa value of a charged compound and the distribution coefficient of the ionic form can also be determined by this approach. In the second application, binding constants in the film phase have been determined for the fast evaluation of enantioselectivity of potential chiral selectors. The technique identified one chiral selector for the target econazole from a small library of twelve cyclopropyl dipeptide isosteres. Compared to other screening approaches, this protocol does not require the covalent attachment of either the target of the selector candidate hence decreases the time and labor required for screening. In addition, the amount of the potential chiral selector (~100 µg) needed is significantly reduced. Similarly, intermolecular association can be determined in the aqueous phase. In the last application, binding constants of drug-cyclodextrin complex formation have been measured at various cyclodextrin concentration and pH conditions with various cyclodextrins. Again, high throughput and low mass requirement are advantages of the method. date: 2007-06-29 date_type: completed institution: University of Pittsburgh refereed: TRUE etdcommittee_type: committee_chair etdcommittee_type: committee_member etdcommittee_type: committee_member etdcommittee_type: committee_member etdcommittee_name: Weber, Stephen G etdcommittee_name: Day, Billy etdcommittee_name: Amemiya, Shigeru etdcommittee_name: Petoud, Stephane etdcommittee_email: sweber@pitt.edu etdcommittee_email: bday@pitt.edu etdcommittee_email: amemiya@pitt.edu etdcommittee_email: spetoud@pitt.edu etdcommittee_id: SWEBER etdcommittee_id: BDAY etdcommittee_id: AMEMIYA etdcommittee_id: SPETOUD etd_defense_date: 2007-04-23 etd_approval_date: 2007-06-29 etd_submission_date: 2007-04-23 etd_access_restriction: immediate etd_patent_pending: FALSE assigned_doi: doi:10.5195/pitt.etd.2011.7554 thesis_type: dissertation degree: PhD committee: Stephen G. Weber (sweber@pitt.edu) - Committee Chair committee: Billy Day (bday@pitt.edu) - Committee Member committee: Shigeru Amemiya (amemiya@pitt.edu) - Committee Member committee: Stephane Petoud (spetoud@pitt.edu) - Committee Member etdurn: etd-04232007-180716 other_id: http://etd.library.pitt.edu/ETD/available/etd-04232007-180716/ other_id: etd-04232007-180716 citation: Chen, Zhi (2007) High-Throughput Methods to Determine Intermolecular Association and Lipophilicity. Doctoral Dissertation, University of Pittsburgh. (Unpublished) document_url: http://d-scholarship-dev.library.pitt.edu/7554/1/Zhi_Chen_Dissertation_2007.pdf