May 2010 to 2000 Formulations Manager, FMC Professional SolutionsPhiladelphia University
2001 to 2000 Adjunct Professor, ChemistryPfizer Animal Health
1997 to 2003 Senior Research ChemistCarter-Wallace Inc Cranbury, NJ 1987 to 1997 Director, Product DevelopmentSmithKline Animal Health Chester, PA 1985 to 1987 Pharmaceutical ChemistRohm and Haas Philadelphia, PA 1979 to 1985 ChemistAmchem Inc Ambler, PA 1976 to 1979 Technician
Education:
University of the Sciences in Philadelphia 1992 to 1996 PhD (ABD) in PharmaceuticsTemple University 1985 to 1988 M.S. in PharmaceuticsPhiladelphia College of Textiles and Science 1984 B.S. in Chemistry
Medicine Doctors
Dr. Robert C Albright, Farmington MN - DO (Doctor of Osteopathic Medicine)
103 15Th Ave Se, Lonsdale, MN 55046 (507)7443245 (Phone)
Certifications:
Critical Care Medicine, 2009 Internal Medicine, 2005 Nephrology, 2008
Awards:
Healthgrades Honor Roll
Languages:
English
Hospitals:
4645 Knutsen Dr, Farmington, MN 55024
103 15Th Ave Se, Lonsdale, MN 55046
Park Nicollet Methodist Hospital 6500 Excelsior Boulevard, Saint Louis Park, MN 55426
Saint Mary's Hospital at Amsterdam 427 Guy Parks Avenue, Amsterdam, NY 12010
Northfield Hospital 2000 North Avenue, Northfield, MN 55057
Education:
Medical School Philadelphia College Of Osteopathic Medicine Graduated: 1991 Medical School Comm Hospital Graduated: 1992 Medical School Mayo Clin Grad School Med Graduated: 1995
Dr. Albright graduated from the Pennsylvania State University College of Medicine in 1979. He works in Edgewood, KY and specializes in Medical Oncology. Dr. Albright is affiliated with Christ Hospital, Good Samaritan Hospital and St Elizabeth Healthcare Edgewood.
Size-selective hemocompatible porous polymeric adsorbents are provided with a pore structure capable of excluding molecules larger than 50,000 Daltons, but with a pore system that allows good ingress and egress of molecules smaller than 35,000 Daltons. The pore system in these porous polymeric adsorbents is controlled by the method of synthesis so that 98% of the total pore volume is located in pores smaller than 300 Angstroms (Å) in diameter with a working pore size range within 100 to 300 Å in diameter. The porous polymeric adsorbents of this invention are very selective for extracting midsize proteins, such as cytokines and β-microglobulin, from blood and other physiologic fluids while keeping the components required for good health such as cells, platelets, albumin, hemoglobin, fibrinogen, and other serum proteins intact.
The present invention provides a stable composition which comprises a non-hydroxyl-group-containing solvent mixture comprising N,N-diethyl-m-toluamide and γ-hexalactone, optionally with dimethyl sulfoxide, eucalyptol and 1-methoxy-2-propyl acetate; and an effective amount of each of amitraz and at least one additional parasiticidal compound, such as R-28153. Said composition allows for high concentrations of a mixture of parasiticidal agents in a single application and is useful for treating and controlling parasiticidal infection and infestation in a homeothermic animal.
Wei-Tai Young - Hillsborough NJ, US Robert L. Albright - Southampton PA, US Thomas D. Golobish - Princeton NJ, US Vincent Capponi - Monmouth Junction NJ, US Philip Chan - Cherry Hill NJ, US
A size-selective hemocompatible porous polymeric adsorbent system is provided, the polymer system comprises at least one polymer with a plurality of pores, and the polymer has at least one transport pore with a diameter from about 250 Angstroms to about 2000 Angstroms, and the polymer has a transport pore volume greater than about 1. 8% to about 78% of a capacity pore of volume of the polymer.
Jacob Allen Zupan - Yardley PA, US Robert Bruce Albright - Chalfont PA, US Douglas Rugg - Lebanon NJ, US Izabela Galeska - Pennington NJ, US
Assignee:
Wyeth - Madison NJ
International Classification:
A01N 43/02 A01N 37/52 A01P 7/02
US Classification:
514450, 514637
Abstract:
The present invention relates to a stable, antiparasitic, non-aqueous pour-on parasiticidal composition which comprises an effective amount of amitraz, optionally a macrocyclic lactone, a stabilizer and a carrier system having no active hydroxyl group.
Wei-Tai Young - Hillsborough NJ, US Robert L. Albright - Southampton PA, US Thomas D. Golobish - Princeton NJ, US Vincent Capponi - Monmouth Junction NJ, US Philip Chan - Cherry Hill NJ, US
International Classification:
B01J 20/28 B01J 20/32
US Classification:
502 7
Abstract:
A size-selective hemocompatible porous polymeric adsorbent system is provided, the polymer system comprises at least one crosslinking agent and at least one dispersing agent, and the polymer has a plurality of pores with diameters in the range from about 17 to about 40,000 Angstroms
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