Method and device for collecting and stabilizing a biological sample

Abstract

A collection container and method for collecting a predetermined volume of a biological sample, and particularly a whole blood sample, includes an effective amount of at least one stabilizing agent. The stabilizing agent is able to stabilize nucleic acids in the biological sample at the point of collection to prevent enzymatic degradation of the nucleic acids. The stabilizing agents include cationic compounds, detergents, particularly cationic detergents, chaotropic salts, ribonuclease inhibitors, chelating agents, and mixtures thereof.

What is claimed is:  
     
         1 . An apparatus for collecting a biological sample, said apparatus comprising: 
 a container defining an internal chamber, and a closure closing said open end, and    at least one stabilizing component contained within said container in an amount effective to stabilize and preserve said biological sample.    
     
     
         2 . The apparatus of  claim 1 , wherein said biological sample is whole blood.  
     
     
         3 . The apparaus of  claim 1 , wherein said stabilizing component is an aqueous solution of a stabilizing agent selected from the group consisting of cationic compounds, detergents, chaotropic salts, ribonuclease inhibitors, chelating agents, and mixtures thereof, and wherein said aqueous solution of said stabilizing agent has a pH of about pH 2 to about pH 12.  
     
     
         4 . The apparatus of  claim 3 , wherein said aqueous solution has a pH of about pH 2 to about pH 10.  
     
     
         5 . The apparatus of  claim 3 , wherein said aqueous solution has a pH of about pH 3 to about pH 8.  
     
     
         6 . The apparatus of  claim 1 , wherein said stabilizing agent has the general formula  
       YR 1 R 2 R 3 R 4 X  
       wherein Y is nitrogen or phosphorous; 
 R 1 , R 2 , R 3 , and R 4  are independently selected from the group consisting of branched alkyl, non-branched alkyl, C 6 -C 20  aryl, and C 6 -C 26  aralkyl; and  
 X is an anion.  
 
     
     
         7 . The apparatus of  claim 6 , wherein X is an anion selected from the group consisting of phosphate, sulfate, formate, acetate, propionate, oxalate, malonate, succinate, citrate, bromide and chloride.  
     
     
         8 . The apparatus of  claim 6 , wherein Y is nitrogen and said stabilizing agent is a quaternary amine.  
     
     
         9 . The apparatus of  claim 6 , wherein said R 1  is an alkyl having 12, 14, or 16 carbon atoms and R 2 , R 3 , and R 4  are methyl.  
     
     
         10 . The apparatus of  claim 1 , wherein said container has an internal pressure less than atmospheric pressure, for drawing a predetermined volume of said biological sample into said container.  
     
     
         11 . The apparatus of  claim 3 , wherein said stabilizing agent is included in an amount to lyse cells in said biological sample.  
     
     
         12 . The apparatus of  claim 3 , wherein said stabilizing agent lyses reticulocytes, bacteria, red blood cells, white blood cells, and viruses.  
     
     
         13 . The apparatus of  claim 3 , wherein said stabilizing agent is included in an amount to preserve and stabilize nucleic acids in said biological sample.  
     
     
         14 . The apparatus of  claim 3 , wherein said stabilizing agent is included in an amount effective to prevent gene induction in said biological sample.  
     
     
         15 . The apparatus of  claim 3 , wherein said chaotropic salt is selected from the group consisting of guanidinium isocyanate and guanidinium hydrochloride.  
     
     
         16 . The apparatus of  claim 3 , wherein said detergent is selected from the group consisting of sodium dodecylsulfate and polyoxyethylene sorbitan monolaurate.  
     
     
         17 . The apparatus of  claim 3 , wherein said ribonuclease inhibitor is placental RNAse inhibitor protein.  
     
     
         18 . The apparatus of  claim 6 , further comprising at least one proton donor in an effective amount to stabilize nucleic acids in said sample.  
     
     
         19 . The apparatus of  claim 18 , wherein said portion donor is selected from the group consisting of alkenyl carboxylic acids, C 2 -C 6  aliphatic mono- and dicarboxylic acids, aliphatic ketodicarboxylic acids, amino acids, mineral acids and mixtures thereof.  
     
     
         20 . A method of stabilizing a biological sample comprising the steps of: 
 providing a sample collection container having a side wall, and a bottom defining an internal chamber, said container containing at least one stabilizing agent in an amount sufficient to stabilize and preserve a biological sample; and    obtaining a biological sample and immediately thereafter introducing said biological sample into said container and mixing said biological sample with said stabilizing agent to form a stabilized biological sample.    
     
     
         21 . The method of  claim 20 , wherein said stabilizing agent is in an aqueous medium containing a component selected from the group consisting of cationic compounds, detergents, chaotropic salts, ribonuclease inhibitors, chelating agents, and mixtures thereof.  
     
     
         22 . The method of  claim 20 , wherein said container has an internal pressure less than atmospheric pressure, said method comprising drawing a predetermined volume of said biological sample directly into said container and mixing with a stabilizing amount of said stabilizing agent.  
     
     
         23 . The method of  claim 22 , wherein said biological sample is whole blood and said method comprises withdrawing said whole blood sample from a patient and introducing said whole blood sample directly into contact with said stabilizing agent in said sample collection container to lyse cells and stabilize nucleic acids in said whole blood sample.  
     
     
         24 . The method of  claim 20 , wherein said biological sample is selected from the group consisting of red blood cell concentrates, platelet concentrates, leukocyte concentrates, plasma, serum, urine, bone marrow aspirates, tissue, and cerebral spinal fluid.  
     
     
         25 . The method of  claim 20 , wherein said stabilizing agent is included in an amount to inhibit gene induction in said biological sample.  
     
     
         26 . The method of  claim 21 , wherein said stabilizing agent is a cationic compound having the formula the general formula  
       YR 1 R 2 R 3 R 4 X  
       wherein Y is nitrogen or phosphorous; 
 R 1 , R 2 , R 3 , and R 4  are independently selected from the group consisting of branched alkyl, non-branched alkyl, C 6 -C 20  aryl, and C 6 -C 26  aralkyl; and  
 X is an anion.  
 
     
     
         27 . The method of  claim 26 , wherein X is selected from the group consisting of phosphate, sulfate, formate, acetate, propionate, oxalate, malonate, succinate, citrate, bromide and chloride.  
     
     
         28 . The method of  claim 26 , wherein said R 1  is an alkyl having 12, 14, or 16 carbon atoms and R 2 , R 3 , and R 4  are methyl.  
     
     
         29 . The method of  claim 26 , wherein Y is nitrogen.  
     
     
         30 . The method of  claim 21 , wherein said aqueous medium has a pH of about pH 3 to about pH 8.  
     
     
         31 . The method of  claim 21 , wherein said chaotropic salt is selected from the group consisting of guanidinium isothiocyanate and guanidinium hydrochloride.  
     
     
         32 . The method of  claim 21 , wherein said detergent is selected from the group consisting of sodium dodecylsulfate and polyoxyethylene sorbitan monolaurate.  
     
     
         33 . The method of  claim 21 , wherein said ribonuclease inhibitor is placental RNAse inhibitor protein.  
     
     
         34 . The container of  claim 26 , further comprising at least one proton donor in an effective amount to stabilize nucleic acids in said sample.  
     
     
         35 . The container of  claim 34 , wherein said proton donor is selected from the group consisting of alkenyl carboxylic acids, C 2 -C 6  aliphatic mono- and dicarboxylic acids, aliphatic ketodicarboxylic acids, amino acids, mineral acids and mixtures thereof.  
     
     
         36 . A method of collecting and stabilizing a whole blood sample, said method comprising: 
 providing a sample collection container having a side wall, a bottom wall and a closure member forming an internal chamber, said container enclosing an effective amount of an aqueous solution or dispersion of a nucleic acid stabilizing agent to stabilize and preserve nucleic acids in a whole blood sample, said internal chamber having pressure less than atmospheric pressure; and    collecting a whole blood sample directly from a patient in said collection container and mixing said blood sample with said stabilizing agent to form a stable whole blood sample.    
     
     
         37 . The method of  claim 36 , wherein said closure is a septum and said method comprises piercing said septum with a cannula and introducing said whole blood sample through said cannula into said collection container.  
     
     
         38 . The method of  claim 36 , wherein said stabilizing agent is selected from the group consisting of cationic compounds, detergents, chaotropic salts, ribonuclease inhibitors, chelating agents, and mixtures thereof, and wherein said aqueous solution or dispersion has a pH of about pH 2 to about pH 12.  
     
     
         39 . The method of  claim 36 , wherein said aqueous solution or dispersion has a pH of about pH 2 to about pH 5.  
     
     
         40 . The method of  claim 36 , wherein said aqueous solution or dispersion has a pH of about 3.6 to about pH 3.8.  
     
     
         41 . The method of  claim 36 , wherein said stabilizing agent is selected from the group consisting of guanidinium isothiocyanate, guanidinium hydrochloride, sodium dodecylsulfate, polyoxyethylene sorbitan monolaurate, placental RNAse inhibitor protein, and mixtures thereof.  
     
     
         42 . The method of  claim 38 , wherein said stabilizing agent has the general formula  
       YR 1 R 2 R 3 R 4 X  
       wherein Y is nitrogen or phosphorous R 1 , R 2 , R 3 , and R 4  are independently selected from the group consisting of branched alkyl, non-branched alkyl, C 6 -C 20  aryl, and C 6 -C 26  aralkyl; and 
 X is an anion.  
 
     
     
         43 . The container of  claim 18 , wherein said portion donor is selected from the group consisting of alkenyl carboxylic acids, C 2 -C 6  aliphatic mono- and dicarboxylic acids, aliphatic ketodicarboxylic acids, amino acids, mineral acids and mixtures thereof.