Alcon, A Novartis Company
Director, New Products Ideation, Dry Eye, Global Vision Care Franchise
Novartis Feb 2016 - Jun 2018
Associate Technical Project Leader
Novartis Apr 2015 - Jan 2016
Fellow
Alcon, A Novartis Company Sep 1, 2008 - Mar 2015
Senior Scientist Ii and Principal Scientist
University of Connecticut May 2007 - Aug 2008
Post Doctoral Researcher
Education:
Stanford University 2014 - 2015
University of Connecticut 2000 - 2007
Doctorates, Doctor of Philosophy, Biochemistry
University of Madras 1998 - 2000
Master of Science, Masters, Biochemistry
University of Madras 1995 - 1998
Bachelors, Bachelor of Science, Zoology
Skills:
Protein Chemistry Biochemistry Molecular Biology Nutrition Nutraceuticals Cell Culture Pcr Rt Pcr Protein Engineering Protein Expression Protein Purification Elisa Bioassay Microsoft Office Blotting Cell Viability Assays Microplate Reader Hplc Glp Pharmaceutical Industry Chemistry Clinical Development
Robert R. Birge - Coventry CT, US Rekha Rangarajan - Fort Worth TX, US Kristina Nicole McCleary - Cheshire CT, US
Assignee:
University of Connecticut - Farmington CT
International Classification:
G11C 13/04 C07K 14/195
US Classification:
365151, 530350
Abstract:
Bacteriorhodopsin protein variants and methods using the bacteriorhodopsin variants for performance in holographic and three-dimensional (3D) memory storage devices are described. The amino acid and chemical modifications of bacteriorhodopsin provided herein achieve greatly enhanced protein performance. The memory storage devices write, read and erase data proficiently. The bacteriorhodopsin protein variants are useful in optical memory storage and associative processor systems. Irradiation of the light-sensitive protein with light of known wavelength causes the protein to switch between different states. The variants enter the branched photocycle via a single or a two photon process and form the permanent ‘Q’ state more efficiently than the wild-type bacteriorhodopsin protein. This branching photocycle of the variants is exploited in the fabrication of 3D memory storage devices.
Ophthalmic Compositions With Improved Dessication Protection And Retention
Howard Allen Ketelson - Dallas TX, US Elaine E. Campbell - Shelton CT, US David L. Meadows - Colleyville TX, US Rekha Rangarajan - Fort Worth TX, US
Assignee:
ALCON RESEARCH, LTD. - Fort Worth TX
International Classification:
A61K 31/736 A61K 31/728
US Classification:
514 54
Abstract:
The present invention relates to artificial tear compositions and ophthalmic compositions suitable for drug delivery. In one embodiment of the present invention, the compositions comprise a galactomannan polymer such as guar or hydroxypropyl guar, hyaluronic acid, and a cis-diol such as sorbitol. In a preferred embodiment, the compositions also comprise a borate compound.
Robert R. Birge - Coventry CT, US Rekha Rangarajan - Fort Worth TX, US
Assignee:
University of Connecticut - Farmington CT
International Classification:
H01L 31/04 H01L 31/18 C07K 14/195
US Classification:
136263, 438 1, 530408
Abstract:
Protein-based photovoltaic cells and the manufacture and use of protein-based photovoltaic cells are described. In one embodiment, bacteriorhodopsin from , which undergoes structural transitions when irradiated with a given wavelength of light, is used as the protein in the protein-based photovoltaic cells. In another embodiment, mutant bacteriorhodopsin from is used. Exposure of the protein to sunlight causes proton transfer across a membrane resulting in the generation of an electrical charge. The protein can be oriented and/or layered on a substrate and modified by mutation to enhance transmembrane proton transfer, covalent binding to a substrate and layering. The protein-based photovoltaic cells sequentially or simultaneously generate hydrogen gas from water or salt, which also can be harnessed to produce electricity.
Dissolvable Polymeric Eye Inserts With A Biodegradable Polymer And Method Of Using The Same
Polymeric eye inserts are provided that may be dissolvable when placed in the cul-de-sac of the eye. These inserts may contain one or more mucoadhesive polymers polymers, a biodegradable polymer as well as softener/plasticizer so that, when inserted into the eye, they may absorb tears, and dissolve and slowly release lubricant into the tear film to lubricate and protect the ocular surface for an extended duration of time. The biodegradable polymer containing eye insert may increase dissolution time on the ocular surface for longer lasting relief, may reduce dosing frequency and patient burden typically associated with topical drop usage. These polymeric eye inserts also may include one or more pharmaceutically active agents.
Ophthalmic Compositions With Improved Dessication Protection And Retention
- Fribourg, CH Howard Allen Ketelson - Dallas TX, US Elaine E. Campbell - Shelton CT, US David L. Meadows - Colleyville TX, US Rekha Rangarajan - Fort Worth TX, US
The present invention relates to artificial tear compositions and ophthalmic compositions suitable for drug delivery. In one embodiment of the present invention, the compositions comprise a galactomannan polymer such as guar or hydroxypropyl guar, hyaluronic acid, and a cis-diol such as sorbitol. In a preferred embodiment, the compositions also comprise a borate compound.
The present invention is directed to a lipid-based ophthalmic emulsion. The emulsion has an increased amount of a mucoadhesive galactomannan polymer that promotes a long-lasting protection against desiccation and moisture retention.
Ophthalmic Compositions With Improved Dessication Protection And Retention
- Fribourg, CH Howard Allen Ketelson - Dallas TX, US Elaine E. Campbell - Shelton CT, US David L. Meadows - Colleyville TX, US Rekha Rangarajan - Fort Worth TX, US
The present invention relates to artificial tear compositions and ophthalmic compositions suitable for drug delivery. In one embodiment of the present invention, the compositions comprise a galactomannan polymer such as guar or hydroxypropyl guar, hyaluronic acid, and a cis-diol such as sorbitol. In a preferred embodiment, the to compositions also comprise a borate compound.
Dissolvable Polymeric Eye Inserts And Method Of Using Same
Polymeric eye inserts are provided that may be dissolvable when placed in the cul-de-sac of the eye. These inserts may contain one or more polymers as well as a softener/plasticizer so that, when inserted into the eye, they may absorb tears, and dissolve and slowly release lubricant into the tear film to lubricate and protect the ocular surface for an extended duration of time. Increased retention time on the ocular surface for longer lasting relief may reduce dosing frequency and patient burden typically associated with topical drop usage. These polymeric eye inserts also may include one or more pharmaceutically active agents.