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1.
Phys Rev Lett ; 87(17): 177401, 2001 Oct 22.
Article in English | MEDLINE | ID: mdl-11690310

ABSTRACT

Spectra of the third-order nonlinear susceptibility chi((3)) have been investigated for one-dimensional Mott insulators, Sr(2)CuO(3) and Ca(2)CuO(3), by applying the third-harmonic generation (THG) spectroscopy on their single-crystalline thin films. The three-photon resonance to the lowest charge-transfer (CT) state with odd parity strongly enhances chi((3)), which is of the order of 10(-9) esu. The two-photon resonant structure unravels the even-CT state, located close to the odd-CT state. Two types of chi((3)) spectra obtained from THG and the electroreflectance measurements are explained based on the concept of spin-charge separation.

6.
8.
Phys Rev B Condens Matter ; 49(17): 12307-12310, 1994 May 01.
Article in English | MEDLINE | ID: mdl-10010116
9.
J Pharm Pharmacol ; 44(12): 1033-5, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1361553

ABSTRACT

Prostaglandin E1 (PGE1) and its inclusion complexes with beta-cyclodextrin (beta-CyD) and O-carboxymethyl-O-ethyl-beta-cyclodextrin (CME-beta-CyD) were made as topical preparations. The PGE1 preparations, when applied with a penetration enhancer, 1-[2-(decylthio)ethyl]azacyclopentane-2-one (HPE-101), markedly increased the regional blood flow in the ear of rabbits and were longer acting than when administered by the intravenous route. Topical application of the PGE1 preparations significantly protected rabbits against laurate-induced peripheral vascular occlusive sequelae; the protective potency increased in the order of PGE1 alone = beta-CyD complex < CME-beta-CyD complex preparation. The PGE1 preparations elicited skin reactions such as erythema and oedema depending on their vasodilating actions. These reactions disappeared gradually after removal of the preparations, and hence may not be serious obstacles for their safe use. These results suggest that combinations of CME-beta-CyD and HPE-101 work synergistically to facilitate the entry of PGE1 into the skin, and consequently enhance the therapeutic potential of PGE1 in the topical preparation tested.


Subject(s)
Alprostadil/therapeutic use , Cyclodextrins/pharmacology , Ear/blood supply , Peripheral Vascular Diseases/drug therapy , Pyrroles/pharmacology , Administration, Topical , Alprostadil/administration & dosage , Animals , Drug Carriers , Drug Combinations , Lauric Acids/toxicity , Male , Ointments , Peripheral Vascular Diseases/chemically induced , Rabbits
14.
Phys Rev B Condens Matter ; 40(16): 11400-11402, 1989 Dec 01.
Article in English | MEDLINE | ID: mdl-9991728
15.
Phys Rev B Condens Matter ; 40(13): 9286-9287, 1989 Nov 01.
Article in English | MEDLINE | ID: mdl-9991419
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