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Hydrotropic solubilization of poorly water-soluble drugs
Kim, Ji Young,Kim, Sungwon,Papp, Michelle,Park, Kinam,Pinal, Rodolfo Wiley Subscription Services, Inc., A Wiley Company 2010 journal of pharmaceutical sciences Vol.99 No.9
<P>The solubilizing ability of two aromatic hydrotropes, N,N-diethylnicotinamide (DENA) and N,N-dimethylbenzamide (DMBA), was investigated using a set of 13 poorly soluble, structurally diverse drugs. The number of aromatic rings in the solute molecule has a very strong effect on the solubility enhancement produced by either hydrotrope. However, although solubility enhancements in the order of 1000- to 10,000-fold were obtained with each of the hydrotropic agents, important differences were found between the two. DMBA is more hydrophobic and undergoes more extensive self-association than DENA, as determined by vapor osmometry. As a result, DMBA is generally a more powerful solubilizer of hydrophobic drugs. DENA, on the other hand, is more polar and its self-association is essentially limited to dimer formation. However, despite being less hydrophobic, DENA is an extremely powerful solubilizer of paclitaxel, a highly hydrophobic compound. Such a result is attributed to the higher hydrogen bonding ability of DENA over DMBA and the very high hydrogen bonding ability of paclitaxel. These observations in turn illustrate the strong interplay between specific and hydrophobic interactions on the observed solubilization by hydrotropic agents. © 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:3953–3965, 2010</P>
Stoichiometric Layered Potassium Transition Metal Oxide for Rechargeable Potassium Batteries
Kim, Haegyeom,Seo, Dong-Hwa,Urban, Alexander,Lee, Jinhyuk,Kwon, Deok-Hwang,Bo, Shou-Hang,Shi, Tan,Papp, Joseph K.,McCloskey, Bryan D.,Ceder, Gerbrand American Chemical Society 2018 Chemistry of materials Vol.30 No.18
<P>K-ion batteries are promising alternative energy storage systems for large-scale applications because of the globally abundant K reserves. K-ion batteries benefit from the lower standard redox potential of K/K<SUP>+</SUP> than that of Na/Na<SUP>+</SUP> and even Li/Li<SUP>+</SUP>, which can translate into a higher working voltage. Stable KC<SUB>8</SUB> can also be formed via K intercalation into a graphite anode, which contrasts with the thermodynamically unfavorable Na intercalation into graphite, making graphite a readily available anode for K-ion battery technology. However, to construct practical rocking-chair K-ion batteries, an appropriate cathode material that can accommodate reversible K release and storage is still needed. We show that stoichiometric KCrO<SUB>2</SUB> with a layered O3-type structure can function as a cathode for K-ion batteries and demonstrate a practical rocking-chair K-ion battery. In situ X-ray diffraction and electrochemical titration demonstrate that K<SUB><I>x</I></SUB>CrO<SUB>2</SUB> is stable for a wide K content, allowing for topotactic K extraction and reinsertion. We further explain why stoichiometric KCrO<SUB>2</SUB> is unique in forming the layered structure unlike other stoichiometric K-transition metal oxide compounds, which form nonlayered structures; this fundamental understanding provides insight for the future design of other layered cathodes for K-ion batteries.</P> [FIG OMISSION]</BR>