Method of and compounds for treatment for cystic fibrosis

Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form – Liposomes

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424 45, 424436, 424449, 424451, 424464, 436829, 514937, 514962, 514963, A61K 3722, A61K 970, A61F 902, A61L 904

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053841280

ABSTRACT:
This invention provides a method and compositions for increasing the permeability of epithelial cells to a chloride ion in a subject comprising administering a permeability enhancing amount of a composition comprising a nontoxic, nonionic surfactant having (1) a critical micelle concentration of less than about 10 mM and a hydrophile-lipophile balance number of from about 10 to 20 and (2) a suitable hydrophobic organic group joined by a linkage to a suitable hydrophilic polyol.

REFERENCES:
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Eduardo F. Tizzano et al., "Cystic Fibrosis: Beyond the Gene to Therapy," The Journal of Pediatrics, 120(3):337-349 (Mar. 1992).
Richard C. Boucher, "Drug Therapy in the 1990s: What Can We Expect for Cystic Fibrosis?" Drugs, 43(4):431-439 (1992).
Michael R. Knowles et al.,"A Pilot Study of Aerosolized Amiloride for the Treatment of Lung Disease in Cystic Fibrosis," N. Eng. J. Med., 322:1189-1194 (1990).
Igor M. Gladstone et al., "Effect of Artificial Surfactant on Pulmonary Function in Preterm and Full-Term Lambs," J. Appl. Physiol., 69:465-472 (1990).
Nikolaus Weber et al., "Metabolism of Orally Administered Alky .beta.-Glycosides in the Mouse," J. Nutr., 114:247-254 (1984).

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