Technical Note | Open | Published:
Long-term stability of recombinant tissue plasminogen activator at -80 C
BMC Research Notesvolume 2, Article number: 117 (2009)
Recombinant tissue plasminogen activator (tPA) is a thrombolytic widely used clinically in the treatment of acute thrombotic disease such as ischemic stroke, myocardial infarction, and deep venous thrombosis. This has led to much interest in tPA based lytic therapies leading to laboratory based in-vitro and in-vivo investigations using this drug. However, tPA reconstituted in solution exhibits full activity for only 6–8 hours, according to the manufacturer. Therefore, methods to store reconstituted tPA for long durations while maintaining activity would be of assistance to laboratories using this enzyme.
In this work, the enzymatic activity of tPA stored at -80 C over time was measured, using an ELISA technique that measured the amount of active tPA bound to plasminogen activator inhibitor 1 (PAI-1) in a given sample. Sample of tPA solution mixed to a concentration of 1 (mg/ml) were stored in cryogenic vials at -80 C for up to 7 years. For a given sample, aliquots were assayed for tPA activity, and compared with a tPA standard to determine relative enzymatic activity. Results are reported as means with standard errors, and 12 measurements were performed for each sample age.
There was no decrease in tPA activity for samples stored up to 7 years. Such cryogenic storage is a viable method for the preservation of tPA solution for laboratory investigations of tPA-based lytic therapies.
Recombinant tissue plasminogen activator (tPA) is widely to treat thrombotic disorders such as acute ischemic stroke, deep venous thrombosis . As a result, there is much interest in optimizing lytic therapy using tPA in the treatment of such disease . Such optimization requires substantial in-vitro and in-vivo  work. Therefore the preservation of tPA for laboratory use in such studies is of substantial interest to laboratories engaged in such research.
Currently, tPA is available as a lyophilized powder from the manufacturer (Genentech, San Francisco, CA). According to the manufacturer, tPA can be used for 8 hours after reconstitution in sterile water at room temperature; this is a short period of time for laboratory use. Therefore, methods to store reconstituted tPA for long durations while maintaining activity would be of assistance to laboratories using this medication. In this work, the enzymatic activity of tPA stored at -80 C over time was measured.
The tPA was obtained as a lyophilized powder and mixed with sterile water to a concentration of 1 mg/mL (580,000 IU/ml), as per the manufacturer's instructions. Solution samples were then stored at -80 C as 0.5–2 mL aliquots for 0.5 to 7.2 years in cryogenic vials. For activity measurements, samples were thawed at room temperature and diluted with 3% bovine serum albumin in tris buffered saline to achieve a tPA concentration of 0.36, 0.73, 1.45, 2.9 or 3.6 (IU/ml). Three measurements at a given concentration were performed for each sample. The samples were assayed for tPA activity using an ELISA technique that measures active tPA using plasminogen activator inhibitor 1 (PAI-1) (Human tPA Activity Assay, #IHTPAKT, Innovative Research, Novi, MI, USA). In this assay, a biotinylated human PAI-1 antibody binds to the active tPA in a given sample. Inactive tPA or tPA complexed with another protein will not be detected.
Samples of the tPA solution were added to wells on the microtiter plate after preparation with the PAI-1 antibody. In addition, a tPA standard (provided with the kit) was used to prepare a series of standard solutions of 0.345, 0.69, 1.38, 2.76, and 4.14 IU/ml. After incubation, anti-human tPA antibody was added to the PAI-1 bound tPA. Finally, anti-rabbit horseradish peroxidase (HRP) was added, and 450 nm absorbance was determined (SpectraMax M5 dual-monochromator microplate reader, Molecular Devices Corporation, Sunnyvale, CA) as a measure of enzymatic activity. The intra-assay precision was 9.8%, as stated by the manufacturer.
The absorbance values for the tPA standard solutions were used to construct a calibration curve of absorbance vs tPA concentration; fits to the data were performed using Softmax Pro software (Molecular Devices Corporation, Sunnyvale, CA). This calibration curve was used to determine tPA activity in the various sample solutions from the absorbance values. tPA activity is reported (in percent) as the measured activity referenced by the standard activity at the same tPA concentration; an activity of 100% means that the sample tPA activity was equal to that of the standard. Twelve measurements were done for each sample age.
Figure 1 shows tPA activity versus sample age. The closed circles with error bars are mean activity with 95% confidence limits for all measurements at that sample age. The individual data points are the mean activity at a given sample age for a given concentration of tPA, as explicated in the legend. There is no decrease of tPA activity with sample age, and there is no definite trend in tPA activity as a function of tPA concentration. These results are similar to work by others [4, 5] for shorter durations. Overall, long-term low temperature storage of tPA preserves enzymatic activity and may be useful in preserving tPA solution for experimental use.
Adams HP, Brott TG, Furlan AJ, Gomez CR, Grotta J, Helgason CM, Kwiatkowski T, Lyden PD, Marler JR, Torner J, et al: Guidelines for Thrombolytic Therapy for Acute Stroke: a Supplement to the Guidelines for the Management of Patients with Acute Ischemic Stroke. A statement for healthcare professionals from a Special Writing Group of the Stroke Council, American Heart Association. Stroke. 1996, 27 (9): 1711-1718.
Pancioli AM, Brott TG: Therapeutic potential of platelet glycoprotein IIb/IIIa receptor antagonists in acute ischaemic stroke: scientific rationale and available evidence. CNS drugs. 2004, 18 (14): 981-988. 10.2165/00023210-200418140-00003.
Loren M, Fade-Garcia LJ, Toorado MC, Navarro JL: Thrombus age and tissue plasminogen activator mediated thrombolysis in rats. Thrombosis Research. 1989, 56: 67-76. 10.1016/0049-3848(89)90009-1.
Jaffe GJ, Green GD, Abrams GH: Stability of recombinant tissue plasminogen activator. American Journal of Ophthalmology. 1989, 108 (1): 90-91.
Wiernikowski JT, Crowther M, Clase CM, Ingram A, Andrew M, Chan AK: Stability and sterility of recombinant tissue plasminogen activator at -30 degrees C. Lancet. 2000, 355 (9222): 2221-2222. 10.1016/S0140-6736(00)02411-9.
The authors are grateful for the support of NIH/NINDS through grant K02-NS056253.
The authors declare that they have no competing interests.
GJS and JMM devised and planned the study, and GJS obtained the funding for the work. MS performed the tPA assays, and all authors assisted with data interpretation. GJS drafted the manuscript, and all authors assisted with revising the final paper, and approved the final document.