Hemoglobin-haptoglobin complexes

a technology of haptoglobin and complexes, which is applied in the field of haptoglobin complexes, can solve problems such as difficulty in identifying and treating metastases

Inactive Publication Date: 2003-01-16
HEMOSOL
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0015] Further, the construct-complexes of the present invention may exert beneficial effects on neighboring cells, if the hepatocyte modifying substance is, for example, a drug which is active towards neighboring cells even if they are not hepatocytes. They may also modulate or initiate the activity of other therapeutic or diagnostic agents delivered by other methods for hepatocyte modification, such as prodrugs, enzymes or genes coding for enzymes and requiring activation to cause an effect. Agents effecting such action resulting in hepatocyte modification or effect on other agents or cells are hepatocyte modifying agents according to this invention.

Problems solved by technology

It is normally difficult to identify and treat metastases because of the systemic distribution and small size of such cancers.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

Conjugation of TTDS Cross-Linked Hemoglobin (THb) to Poly(L-lysine)

[0058] Poly(L-lysine) conjugates of TTDS cross-linked hemoglobin (THb-K.sub.n) were synthesized by adding poly(L-lysine) to THb-DBS (TTDS cross-linked hemoglobin with one unhydrolyzed 3,5-dibromosalicylate functionality) at 1:1 molar ratio to promote formation of conjugates in which only one molecule of hemoglobin is attached to a single poly(L-lysine) chain. The poly(L-lysine) used in this experiment is a linear polymer with an amide linkage between the carboxyl group and the .alpha.-amino group of lysine. Polymers with an average molecular weight of 4 kDa (K.sub.4kDa), 7.5 kDa (K.sub.7.5kDa), 26 kDa (K.sub.26kDa) and 37 kDa (K.sub.37kDa) were conjugated to THb.

[0059] TTDS (13.9 mg) in ethanol (100 .mu.L) was added to deoxyhemoglobin (5 mL, 8.5 g / dL) in 50 mM borate pH 9.0. The reaction mixture was stirred at 30.degree. C. under nitrogen for 45 min. The hemoglobin was then charged with CO (the solution was kept on i...

example 2

Complex Formation Between THb-K.sub.n and Haptoglobin 1-1

[0064] The following stock solutions were used for the preparation of the complexes: 1.74 mg / mL haptoglobin 1-1 (Hp) in water and 1.0 mg / mL solutions of the THb-K.sub.n (all THb-K.sub.n concentrations represent hemoglobin concentrations) in 50 mM sodium borate pH 9.0. Haptoglobin (14 .mu.L) was added to THb-K.sub.n in potassium phosphate pH 7.0 to give the following final concentrations: 0.12 mg / mL (1.22 .mu.M) haptoglobin and 0.19 mg / mL (2.9 .mu.M) THb-K.sub.n in 25 mM potassium phosphate pH 7.0 (200 .mu.L final volume). After incubation for 180 min. at room temperature, the samples were analyzed using SEC.

[0065] THb-K.sub.n complexes with haptoglobin 1-1: The formation of THb-K.sub.n complexes with haptoglobin can be followed using size exclusion chromatography (SEC). FIG. 2A shows the composition of the THb-K.sub.4kDa mixture with Hp after incubation at room temperature for 180 min. A new, high molecular weight peak appears...

example 3

DNA Binding to THb-K.sub.n and THb-K.sub.n-Hp. Gel Mobility Shift Assay

[0067] Gel mobility shift assays were conducted to evaluate the stoichiometry of binding of plasmid DNA (pCMVbeta) to the THb-K.sub.n conjugates. This gel electrophoretic method is based on the observation that the migratory properties of the DNA are altered upon binding protein. Neither proteins nor DNA-protein complexes in which protein constitutes a significant part of their mass enter 1% agarose gels. If mixtures with an increasing THb-K.sub.n to DNA ratio are analyzed, it is observed that the DNA band disappears at and above the ratio that corresponds to the stoichiometry of the complex. For each of the four conjugates and for the THb-K.sub.26kDa-Hp complex, solutions containing from 0.4 to 6400 ng of the conjugate (this weight based on the hemoglobin component) in 32 .mu.L of 20 mM HEPES pH 7.3 containing 150 mM NaCl were prepared. The plasmid DNA (560 ng in 28 .mu.L of 20 mM HEPES pH 7.3 containing 150 mM ...

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Abstract

Construct-complexes of a hemoglobin, a hepatocyte modifying substance bound to the hemoglobin, and a haptoglobin bound to the hemoglobin, are provided, for administration to mammalian patients. The construct-complex may be formed ex vivo, or a hemoglobin-hepatocyte modifying substance combination may be administered to the patient so that haptoglobin in the mammalian body bonds thereto to form the construct-complex in vivo. Disorders of the liver may be diagnosed and treated using construct-complexes described herein.

Description

[0001] This invention relates to protein complexes and use thereof in medical applications. More specifically, it relates to complexes of hemoglobin compounds with therapeutic substances such as drugs, genes etc. which have a therapeutic action on specific parts and / or organs of the body, and means for targeting such complexes to specific body parts and body organs. Also within the scope of the invention are complexes of hemoglobin with diagnostic substances, such as imaging agents.BACKGROUND OF THE INVENTION AND PRIOR ART[0002] The use of hemoglobin and modified hemoglobin as a drug delivery means has been proposed previously. Hemoglobin, as a natural component of red blood cells, present and circulating throughout the body in relatively large quantities, has well-established bioacceptability and the potential to deliver drugs throughout the body.[0003] Thus, Kluaer et al., U.S. Pat. No. 5,399,671 describe a hemoglobin compound which has been cross-linked to effect intramolecular s...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K38/16A61K49/00A61K47/66A61P1/16A61P43/00C07K14/805
CPCA61K47/48238A61K47/48307A61K47/62A61K47/6445A61P1/16A61P43/00
Inventor ADAMSON, J. GORDONWODZINSKA, JOLANTA M.MOORE, M.S. CELINE
Owner HEMOSOL
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