Abstract: Methods of inhibiting Barrett's esophagus and/or adenocarcinoma in a subject are provided. In a particular embodiment, the method comprises administering at least one composition comprising at least one zinc compound and at least one pharmaceutically acceptable carrier to the esophagus of the subject. The zinc may be a pharmaceutically acceptable salt of zinc, such as zinc gluconate. The zinc may be administered, for example, orally, topically, or by an implantable medical device. In a particular embodiment, the methods further comprise administering at least one analgesic, anesthetic, or other therapeutic agent or therapy for the treatment of Barrett's esophagus. The method may further comprise monitoring the progression of Barrett's esophagus in the subject.
Type:
Grant
Filed:
May 7, 2012
Date of Patent:
May 17, 2016
Assignees:
Lankenau Institute for Medical Research, Monk Street Partners LLC
Abstract: Methods of inhibiting Barrett's esophagus and/or adenocarcinoma in a subject are provided. In a particular embodiment, the method comprises administering at least one composition comprising at least one zinc compound and at least one pharmaceutically acceptable carrier to the esophagus of the subject. The zinc may be a pharmaceutically acceptable salt of zinc, such as zinc gluconate. The zinc may be administered, for example, orally, topically, or by an implantable medical device. In a particular embodiment, the methods further comprise administering at least one analgesic, anesthetic, or other therapeutic agent or therapy for the treatment of Barrett's esophagus. The method may further comprise monitoring the progression of Barrett's esophagus in the subject.
Type:
Application
Filed:
May 7, 2012
Publication date:
April 24, 2014
Applicants:
Monk Street Partners LLC, Lankenau Institute for Medical Research
Abstract: A method for determining the percentage of live cells or viability of cells in a sample is disclosed. In this method, a cell-containing sample is contacted with hydroxyethyldisulfide and the amount of mercaptoethanol produced is measured. The amount of mercaptoethanol is then compared to reference standard curves to determine the percentage of live cells in the sample or the viability of the cells.
Abstract: This disclosure demonstrates a novel therapy immunological approach using polyamine-based therapy (PBT) for relieving tumor-induced suppression of the patient's immune system. The demonstration of the pharmacological release from the naturally occurring polyamine-mediated immune suppression offers profound impact on the immunotherapy of cancer together with a variety of diseases caused by the disease-causing vector's ability to evade an immune reaction. This therapeutic approach is equally applicable to disease states whereby immune system suppression by polyamines has been demonstrated including; bacterial infections, parasitic infections including malaria and typanosomiasis, viral infections, peptic ulcers and gastric cancer due to H. Pylori infection together with prevention of pregnancy. With a small molecule drug, used in combination with DFMO, the pharmacological manipulation of polyamine levels for therapeutic benefit in various disease states is possible.
Type:
Application
Filed:
February 20, 2013
Publication date:
June 27, 2013
Applicants:
Lankenau Institute For Medical Research, Aminex Therapeutics
Inventors:
Aminex Therapeutics, Lankenau Institute For Medical Research
Abstract: Aspects of the invention relate to nucleic acids molecules that are useful for specifically destroying selected cells, tissues, or organs. Aspects of the invention are useful for treating diseases (e.g., cancer) that affect specific cells, tissues, or organs.
Type:
Application
Filed:
March 4, 2005
Publication date:
September 29, 2005
Applicants:
Massachusetts Institute of Technology, Lankenau Institute for Medical Research
Inventors:
Daniel Anderson, Robert Langer, Janet Sawicki, Weidan Peng
Abstract: The present invention involves the early diagnosis of cancerous or precancerous conditions in the gastrointestinal tract by detection of a backleak of signature proteins or carbohydrates in a biological sample obtained from the gastrointestinal tract.