J
James C. McRea
Researcher at University of Utah
Publications - 39
Citations - 1461
James C. McRea is an academic researcher from University of Utah. The author has contributed to research in topics: Controlled release & Insulin. The author has an hindex of 16, co-authored 39 publications receiving 1431 citations. Previous affiliations of James C. McRea include Myriad Genetics & Baxter International.
Papers
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Journal ArticleDOI
Biodegradable block copolymers for delivery of proteins and water-insoluble drugs
Gaylen M. Zentner,Ramesh Rathi,Chung Shih,James C. McRea,Min Hyo Seo,Hunseung Oh,B. G. Rhee,Jiri Mestecky,Zina Moldoveanu,Michael H. Morgan,Steven D. Weitman +10 more
TL;DR: ReGel's inherent ability to solubilize (400 to >2000-fold) and stabilize poorly soluble and sensitive drugs, including proteins is a substantial benefit and the gel provided excellent control of the release of paclitaxel for approximately 50 days.
Patent
Salvage of autologous blood via selective membrane/sorption technologies
TL;DR: In this article, a combination device for salvaging blood comprises a closed plasma chamber containing a plasma chamber solution, a hollow fiber plasma-separating membrane for receiving blood and permitting plasma to be transported therethrough into the plasma chamber solutions and for refiltering the treated plasma back into the blood circuit, and an ultrafiltration membrane for removing water, fluids, and low molecular weight components from the plasma.
Patent
Plasma filter sorbent system for removal of components from blood
Udipi Shettigar,James C. McRea +1 more
TL;DR: In this paper, a system and method of achieving both convective and diffusive transport of plasma across a membrane accompanied by the selective removal of plasma components using sorbents followed by reinfusion of the purified plasma in a blood circulation system is achieved by pumping blood through a filter comprising a bundle of "U" shaped hollow fibers immersed in a closed plasma chamber.
Journal ArticleDOI
Heparinized polyurethanes: in vitro and in vivo studies.
TL;DR: Immobilized heparin-polyurethane catheters implanted in canine femoral and jugular veins for 1 h periods exhibited significant reduction in thrombus formation compared with untreated PU contralateral controls and provided even greater improvement in antithrombogenicity.
Journal ArticleDOI
Self-regulating insulin delivery systems: III. In vivo studies
TL;DR: In vitro characterization of the complementary and competitive binding behavior of the Con A-G-insulin complexes has shown that, when challenged with varying concentrations of glucose, corresponding levels of G- Insulin are released and it has been shown that G-ins insulin exhibits enhanced stability against aggregation.