Capsules encapsulating solid particles of signal-generating organic substances and their use in vitro bioassays for detection of target molecules in a sample

• US 20040014073A1
• Filed: 07/29/2003
• Published: 01/22/2004
• Est. Priority Date: 08/08/2000
• Status: Abandoned Application

• Current Assignee: 8sens Biognostic AG
• Original Assignee: 8sens Biognostic AG
• Inventors: Caruso, Frank, Trau, Dieter, Renneberg, Reinhard, Lehmann, Matthias
• Application Number:
  US10/344,016
• Publication Number:
  US 20040014073A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: G01N 33/587 Nanoparticles

Abstract

The present invention refers to capsules encapsulating solid particles of signal-generating organic substances and carrying on the outer surface affinity molecules for specific recognition of and binding to target molecules in a sample. The invention is directed to the use of these capsules for signal production in the optical, electrochemical or chemical detection of target molecules. To obtain a signal the signal-generating organic substances are released and dissolved. A detection method and a kit are provided.

Claims

1. Capsules encapsulating solid particles of signal-generating organic substances and carrying on the outer surface affinity molecules for specific recognition of and binding to target molecules.

2. Capsules according to claim 1, characterized in that the affinity molecules are selected from the group of peptides or proteins, nucleic acids, carbohydrates, ligands with low molecular weight and molecular imprinted polymers (MIPs) or mixtures thereof.

3. Capsules according to claim 2, characterized in that the peptides or proteins are selected from the group of antibodies, receptors, antigens, lectins, avidins, oligopeptides, lipopoteins, glycoproteins, peptide hormones and allergenes or parts thereof.

4. Capsules according to claim 2, characterized in that the nucleic acids are selected from the group of single or double stranded DNA, RNAs, oligonucleotides, ribozymes, aptamers and parts thereof.

5. Capsules according to claim 2, characterized in that the carbohydrates are selected from the group of mono, oligo and polysaccharides, glycolipids, proteo-polysaccharides and parts thereof.

6. Capsules according to claim 2, characterized in that the low molecular weight ligands are biotin or biotin derivatives, steroids or hormones, a cofactor or coenzyme, activator, inhibitor, pseudosubstrate or prosthetic group of an enzyme, a drug, a pesticide, an allergen or digoxine or a hapten.

7. Capsules according to claim 2, characterized in that the affinity molecules are conjugated or bound directly or via linker molecules to the outer surface of the capsules.

8. Capsules according to claim 6, characterized in that the linker molecule is a biomolecule, preferably avidine, streptavidine, neutravidine, protein A, protein G, lectine or a low molecular crosslinker.

9. Capsules according to claim 1, characterized in that the encapsulated solid particles of signal-generating organic substances are crystals, amorphous or lyophilised particles, spray dried particles, milled particles or mixtures thereof.

10. Capsules according to claim 1, characterized in that the encapsulated solid particles have a particle size from 10 nm to 10 μ

m, preferably smaller than 1 μ

m.

11. Capsules according to claim 1 characterized in that the encapsulated solid particles of signal-generating organic substances are low molecular substances selected from the group of fluorophores, luminophores, chromophores, enzyme substrates, prosthetic groups, or redox active substances selected from redox mediators, electrodeactive substances.

12. Capsules according to claim 1, characterized in that the encapsulated solid particles of signal-generating organic substances are high-molecular substances selected from the group of enzymes and their precursors, bioluminogenic and fluorogenic proteins, nucleic acids, ribozymes and aptamers.

13. Capsules according to claim 1, characterized in that the capsule walls consist of one or multiple polyelectrolyte layers.

14. Capsules according to claim 1 characterized in that the capsul walls consist of one or multiple layers of substances bearing functional groups and being adsorbed or covalently linked.

15. Capsules according to claim 14 characterized in that the substances with functional groups are substances bearing —

COOR, —

NRR¹, —

SR, —

OR, —

SSR, —

C(O)R, —

OC(OH)RR¹ or —

SC(O)R goups, wherein R and R¹ are independently from one another hydrogen or a linear or branched alkyl group.

16. Capsules according to claim 13, characterized in that the polyelectrolytes in one layer and/or between the layers are cross-linked.

17. Capsules according to claim 13 or 14, characterized in that the polyelectrolytes or substances bearing functional groups are selected from organic polymers, biopolymers and mixtures thereof.

18. Capsules according to claim 17, characterized in that the organic polymer is a polymer selected from polyamin (PAH), polysulfonic acid (PSS), polyglycolic acid (PGA), polylactic acid (PLA), polyamides, poly-2-hydroxy butyrate (PHB), polycaprolactone (PCL), fluorescent labelled polymers and their copolymers and/or mixtures thereof.

19. Capsules according to claim 17, characterized in that the biopolymer is selected from polyaminoacids, especially peptides, polylysine, from polycarbohydrates, especially dextrin, pectin, alginate, glycogen, amylose, chitin, chondroitin, hyaluronic acid, from polynucleotides, especially DNA, RNA, oligonucleotides, and from modified biopolymers, especially carboxymethyl cellulose, carboxymethyl dextran, lignin sulfonates.

28. Use of capsules of claims 1 to 19 in in-vitro bioassays for optical, electrochemical or chemical detection of target molecules.

29. Use according to claim 28 together with a dipstick.

20. A method for optical, electrochemical or chemical detection of one or more target molecules in a sample using affinity-based interactions between the target molecule and an affinity molecule for specific recognition of the target molecule comprising the steps

i) incubating the target molecules with capsules encapsulating solid particles of signal-generating organic substances and carrying on their outer surface the corresponding affinity molecules,

ii) separating the resulting target-affinity molecule complex from the capsules with unreacted affinity molecules on their surface,

iii) releasing and dissolving the encapsulated solid particles of the signal-generating organic substances by treating the obtained target-affinity complex with physical or chemical means,

iv) detecting or quantifying the signal which is generated by the released and dissolved signal-generating substances and which is directly or indirectly related to the amount of the target molecules.

21. Method according to claim 20 characterized in that the release of the signal-generating substances from the capsules is achieved by chemical means, preferably by treating with an organic solvent or with an enzyme, ribozyme or aptamer or by changing the pH or ionic strength value.

22. Method according to claim 21, characterized in that the organic solvent is selected from the group of alcohols, especially ethanol and methanol, ketones, especially acetone, esters, especially ethylester, aromates, especially toluene, sulfoxides, especially DMSO and ethers, especially dimethylether, chloroform or from mixtures of organic solvents with one another or with water.

23. Method according to claim 20 characterized in that the release of the signal-generating substances from the capsules is achieved by physical means, preferably by ultrasonic disintegration, electric impulse or osmotic shock.

24. Kit for optical, electrochemical or chemical detection of target molecules in a sample comprising capsules encapsulating solid particles of signal-generating organic substances and carrying on the outer surface affinity molecules for specific recognition and binding to a target molecule.

25. Kit according to claim 24 comprising a dipstick.

26. Kit for optical, electrochemical or chemical detection of target molecules in a sample comprising

a) capsules encapsulating solid particles of signal-generating organic substances being designated to bind affinity molecules

b) agents for the modification of affinity molecules to make them suitable to bind to the surface of the capsules

c) agents for performing the binding reaction between the capsules and the affinity molecules.

27. Kit according to claim 26 comprising a dipstick.