Preservation of fetal nucleic acids in maternal plasma
AssigneeStreck, Inc.
InventorsM. Rohan Fernando, Kate Chao-Wei Chen
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Abstract
A method for preserving and processing fetal nucleic acids located within maternal plasma is disclosed, wherein a sample of maternal blood containing fetal nucleic acids is treated to reduce both cell lysis of the maternal blood cells and deoxyribonuclease (DNase) and ribonuclease (RNase) activity within the fetal nucleic acids. The treatment of the sample aids in increasing the amount of fetal nucleic acids that can be identified and tested while maintaining the structure and integrity of the fetal nucleic acids.
Claims20
A method for stabilizing, storing, isolating and analyzing cell-free fetal nucleic acid comprising:
- drawing a blood sample including a plasma containing donor cellular nucleic acid and cell-free nucleic acid including cell-free fetal nucleic acid directly into an evacuated blood collection tube containing about 0.05 ml to 1.0 ml of a protective agent wherein the protective agent is a solution formed from ingredients including:
- a) 0.1 to 3 g/ml of imidazolidinyl urea;
- b) glycine;
- and
- c) EDTA;
- wherein an amount of imidazolidinyl urea relative to an amount of glycine is 10 parts by weight of imidazolidinyl urea to 1 part by weight glycine;
- storing the blood sample including the plasma for 1 to 14 days,
- separating the plasma from the blood sample;
- isolating the cell-free nucleic acid-from the plasma of the stabilized blood sample;
- and analyzing at least the cell-free fetal nucleic acid isolated from the plasma of the stabilized blood sample;
- wherein the blood sample and the plasma is not frozen prior to the step of isolating.
A method for stabilizing, storing and isolating cell-free fetal nucleic acid comprising:
- contacting a drawn blood sample containing donor cellular nucleic acid and cell-free nucleic acid including the cell-free fetal nucleic acid with a protective agent that is a solution formed from ingredients including:
- (i) about 300 g/l to about 700 g/l imidazolidinyl urea;
- (ii) about 20 g/l to about 60 g/l glycine;
- and
- (iii) about 60 g/l to about 100 g/l of EDTA;
- wherein the solution includes a solvent;
- allowing a period of time to lapse;
- and
- after the period of time has elapsed, separating a plasma from the drawn blood sample and isolating the cell-free nucleic acid from the plasma, wherein the cell-free nucleic acid is free of cell-free nucleic acid attributable to apoptosis, cell death and lysis of nucleated maternal blood cells post blood draw.
A method for stabilizing, storing, isolating and analyzing cell-free fetal nucleic acid comprising:
- drawing about a 10 ml blood sample containing donor cellular nucleic acid and a plasma comprising cell-free nucleic acid, including a cell-free fetal nucleic acid, directly into an evacuated blood collection tube containing about 0.1 ml to about 0.3 ml protective agent that is formed from a solvent, and ingredients consisting of:
- (i) about 300 g/l to about 700 g/l imidazolidinyl urea;
- (ii) about 20 g/l to about 60 g/l glycine;
- and
- (iii) about 60 g/l to about 100 g/l EDTA;
- wherein the protective agent contacts and stabilizes storing the blood sample including the plasma for 1 to 14 days;
- separating the plasma from the stored blood sample;
- isolating the cell-free nucleic acid, including the cell-free fetal nucleic acid, from the plasma;
- and
- amplifying the isolated fetal cell-free nucleic acid by at least 80-fold using whole genome amplification (WGA);
- wherein the blood sample and the plasma is not frozen prior to the step of isolating.
Dependencies are inferred from the claim text.