Biodegradable gelatin-aminodextran particle coatings of and processes for making same

• US 5,707,877 A
• Filed: 06/23/1995
• Issued: 01/13/1998
• Est. Priority Date: 10/31/1990
• Status: Expired due to Fees

• Current Assignee: Coulter International Corp. (Danaher Corporation)
• Original Assignee: Coulter Corporation (Danaher Corporation)
• Inventors: Gupta, Ravinder K., Burshteyn, Alexander, Siiman, Olavi
• Primary Examiner(s): Chin, Christopher L.
• Application Number:
  US08/493,973
• Time in Patent Office: 935 Days
• Field of Search: 536/112, 536/51, 436/518, 436/528, 436/529
• US Class Current: 436/518
• CPC Class Codes: B03C 1/01 by addition of magnetic adjuvants
• CPC Class Codes: G01N 2446/20 the magnetic material being present in the particle core
• CPC Class Codes: G01N 2446/30 the magnetic material being dispersed in the polymer composition before their conversion into particulate form
• CPC Class Codes: G01N 2446/84 Polymer coating, e.g. gelatin
• CPC Class Codes: G01N 2446/86 the coating being pre-functionalised for attaching immunoreagents, e.g. aminodextran
• CPC Class Codes: G01N 2446/90 characterised by small molecule linker used to couple immunoreagents to magnetic particles
• CPC Class Codes: G01N 33/531 Production of immunochemical test materials
• CPC Class Codes: G01N 33/54313 the carrier being characterised by its particulate form
• CPC Class Codes: G01N 33/5434 using magnetic particle immunoreagent carriers which constitute new materials per se
• CPC Class Codes: G01N 33/54393 Improving reaction conditions or stability, e.g. by coating or irradiation of surface, by reduction of non-specific binding, by promotion of specific binding
• CPC Class Codes: Y10S 530/81 Carrier - bound or immobilized peptides or proteins and the preparation thereof, e.g. biological cell or cell fragment as carrier
• CPC Class Codes: Y10S 530/812 Peptides or proteins is immobilized on, or in, an organic carrier
• CPC Class Codes: Y10S 530/813 Carrier is a saccharide
• CPC Class Codes: Y10T 428/2991 Coated

Abstract

The invention relates generally to colloidal particle having a core material and a gelatin/aminodextran coating with pendent functional groups attached thereto. Biological substances or molecules, especially monoclonal antibodies, may be attached to said particles. The monoclonal antibody containing particles are useful in a variety of positive and negative biological assays.

Claims

1. A method of preparing aminodextran compounds in aqueous solution comprising:

(a) partially oxidizing a dextran compound to dextran aldehyde using a chemical oxidizing agent such as sodium periodate at ambient room temperature;

(b) desalting the dextran-aldehyde solution of step (a);

(c) reacting the dextran-aldehyde of step (b) with a diamine at a temperature of about 5-10°

C. to form a plurality of Schiff'"'"'s base linkages between the dextran-aldehyde and amino groups of the diamine; and

(d) reducing the Schiff'"'"'s base linkages of step (c) to obtain an amino-dextran through the use of a chemical reducing agent.

2. The method of claim 1 wherein said dextran has a molecular weight in the range of 10,000 to two million daltons.

3. The method of claim 1 wherein said diamine is 1,3-diaminopropane.

4. The method of claim 1 wherein the diamine to periodate used has a molar ratio of greater than 2.2:

1.

5. The method of claim 1 wherein the diamine to chemical oxidizing agent used has a molar ratio of about 2.2:

1.

6. The aminodextran compounds produced by the method of claim 1.

7. The aminodextran compounds produced by the method of claim 1 wherein said compounds have a degree of sugar substitution in the range of about 3.3% to about 16.5%.

8. A method of preparing aminodextran compounds having about 3.3% to about 16.5% of sugar residues doubly-substituted by diamine groups, said method comprising:

(a) adding an aqueous periodate solution to an aqueous dextran solution over about a ten minute time period with vigorous stirring during the addition and stemming the resulting reaction mixture at room temperature for about 1.5 to about 3 hours to obtain a mixture wherein the dextran is partially oxidized to dextran aldehyde;

(b) desalting and washing the mixture of step (a) to obtain a solution of the polymer dextran-aldehyde;

(c) cooling the solution of polymer of step (b) to a temperature of about 5-10°

C., adding a diamine to the cooled solution over about a ten minute time period and reacting the resulting mixture for a sufficient time to form Schiff'"'"'s base, the duration of the reaction being determined by spectroscopic monitoring of the Schiff'"'"'s base formation and the molar amount of diamine added to the reaction mixture being greater than 2.2 times the molar amount of periodate used in step (a);

(d) reducing the Schiff'"'"'s base by reaction with borohydride anion in aqueous hydroxide at room temperature, the duration of said reaction being determined by spectroscopically monitoring the disappearance of the Schiff'"'"'s base to yield a reduced aminodextran; and

(e) purifying and drying the polymeric product of step (d) to obtain said aminodextran.

9. The method of claim 8 wherein said dextran has a molecular weight in the range of about 10,000 to two million Daltons.

10. The method of claim 8 wherein the diamine and periodate are used in a molar ratio of about 2.2:

1.

11. The method of claim 8 wherein said diamine is 1,3-diaminopropane.

12. The method of claim 8 wherein said temperature is in the range of 5-10°

C.

13. The method of claim 8 wherein the product of step (d) is purified by dialysis or hollow fiber membrane filtration to optimize yield.