The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Apr. 14, 1998

Filed:

Jun. 28, 1996
Applicant:
Inventors:

Joseph Edward Walton, Westerville, OH (US);

Terrence Bruce Mazer, Reynoldsburg, OH (US);

Ronita Kay Geckle, Columbus, OH (US);

Carl Joseph Piontek, Powell, OH (US);

Susan Beth Duel, Laurinburg, NC (US);

Andre Daab-Krzykowski, Columbus, OH (US);

Mark Anthony McCamish, Worthington, OH (US);

Robert Louis Joseph, Columbus, OH (US);

William Guy Pierson, Canal Winchester, OH (US);

Assignee:

Abbott Laboratories, Abbott Park, IL (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61M / ;
U.S. Cl.
CPC ...
604 83 ; 604 84 ; 604 85 ; 604-8 ; 6048901 ; 6048921 ;
Abstract

An apparatus is disclosed for modifying a liquid enteral nutritional product during delivery thereof from a supply thereof, such as a hangable container, to a feeding tube delivering the liquid enteral nutritional product to the gastrointestinal tract of a patient. The apparatus has at least one formulation chamber, such as a drip chamber, with at least one controlled release dosage form unit in the form of a coated tablet, osmotically driven device, coated capsule, microencapsulated microspheres, agglomerated molecular sieving type material, or a quantity of fine hollow permeable fibers located therein. The controlled release dosage form unit or units contain at least one beneficial agent selected from nutrients, medicaments, probiotics, or diagnostic agents or mixtures thereof, to any of which a physiologically acceptable marker dye in controlled release dosage form and/or the same or different beneficial agent not in controlled release dosage form may be added. A liquid nutritional product flows through the formulation chamber during enteral tube feeding of a patient.


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