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Reliable Assays for Pentosan Polysulfate Sodium

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R43HL118788-01A1
Agency Tracking Number: R43HL118788
Amount: $335,702.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: NHLBI
Solicitation Number: PA13-088
Timeline
Solicitation Year: 2014
Award Year: 2014
Award Start Date (Proposal Award Date): 2014-02-15
Award End Date (Contract End Date): 2016-07-31
Small Business Information
108 EAGLE TRACE DRIVE, Half Moon Bay, CA, 94019-2286
DUNS: 961937666
HUBZone Owned: N
Woman Owned: N
Socially and Economically Disadvantaged: N
Principal Investigator
 STEPHEN EMBURY
 (415) 203-0436
 sembury@itsa.ucsf.edu
Business Contact
 STEPHEN EMBURY
Phone: (415) 203-0436
Email: shembury@gmail.com
Research Institution
N/A
Abstract
DESCRIPTION provided by applicant Sickle cell disease SCD remains a poorly treated disease Based on evidence that endothelial P selectin is central to the abnormal microvascular blood flow in SCD we are targeting this molecule with our therapy Our in vitro and preliminary clinical data show that pentosan polysulfate sodium PPS improves microvascular blood flow in SCD However commercially available PPS is not a viable therapy because of its marginal oral bioavailability and limited duration of action Our plan to develop an improved second generation PPS that will overcome these limitations is precluded at this time by the lack of useful PPS assays Creation of reliable assays will enable development and commercialization of PPS SCD is an inherited disorder that afflicts millions of patients worldwide in the US Most SCD morbidity is due to abnormal blood flow conspicuously the acute pain crises that are caused by stoppage of microvascular flow Our overarching goal is to improve the quality of life of patients with SCD by bringing to market PPS as an oral P selectin blocking drug for long term administration to prevent sickle red blood cell sticking to the lining of blood vessels improve blood flow and avert acute painful episodes In this application we propose to create reliable assays for quantifying PPS candidate compounds in plasma and determining its activity in blood The assays will be necessary for preclinical and clinical testing and useful for clinical monitoring The inadequacy of standard assays relates to extensive molecular heterogeneity of PPS lack of specific PPS antibodies and plasma substances that interfere with assays First we will exploit the greater homogeneity of a lower molecular weight fraction of PPS as a target for a physical quantification assay method We will adapt hydrophilic interaction chromatography HILIC MS for assaying our PPS fraction We will test the reliability of this assay in plasma samples from experimental animals administered PPS fraction Next we will utilize the exquisite specificity provided by human combinatorial PPS MAb which overcomes challenges that interfering plasma substances posed for hybridoma generated MAb and polyclonal antibodies We will obtain from AbD Serotec a recombinant PPS MAb pair generated using phage display selection for use in a sandwich ELISA We will test the assay for quantification of high and lower molecular weight PPS candidates in plasma samples from experimental animals administered the PPS test items Lastly Klaus Ley of the La Jolla Institute of Allergy and Immunology will devise a microfluidics device for point of care functional assessment of P selectin blocking activity in a drop of blood Determining biological activity rather than physical concentration overcomes challenges with biological variation of PPS and allows monitoring functional activity in patients The device will be validated by assessing P selectin blocking activity in whole blood spiked with PPS or PPS fraction and in blood samples from mice dosed with each This Phase I SBIR will provide the reliable quantitative and functional assays for PPS and PPS fraction necessary for PPS development PUBLIC HEALTH RELEVANCE Sickle cell disease SCD a condition that affects millions worldwide and approximately individuals in the United States remains a poorly treated disease because current therapies are limited A drug called pentosan polysulfate sodium PPS has been shown to improve blood flow in SCD and could prevent painful debilitating symptoms of the disease Vanguard Therapeutics is proposing to create accurate tests that would allow reliable measurement of PPS in blood in order to conduct crucial clinical trials of PPS a version of PPS that should be better absorbed as a pill

* Information listed above is at the time of submission. *

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