Semin Thromb Hemost 2014; 40(02): 205-213
DOI: 10.1055/s-0033-1364188
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Biological Standards for Potency Assignment to Fibrinolytic Agents Used in Thrombolytic Therapy

Craig Thelwell
1   Biotherapeutics, Haemostasis Section, National Institute for Biological Standards and Control, South Mimms, United Kingdom
› Author Affiliations
Further Information

Publication History

Publication Date:
30 January 2014 (online)

Abstract

Thrombolytic drugs are used for the treatment of thrombotic disorders such as acute myocardial infarction, acute ischemic stroke, and pulmonary embolism. Biological standards are used for potency assignment to the range of fibrinolytic proteins used in thrombolytic therapy. The World Health Organization (WHO) International Standards are primary reference materials, calibrated in arbitrary units (international unit), assigned by collaborative study using the range of assay methods available at the time. Provided the standard and test material are equivalent, adhering to the principle of measuring like versus like, the exact nature of the assay method is unimportant. This approach has been applied successfully for several decades since the advent of fibrinolytic treatment, ensuring consistency for potency labeling and the correct dosing of patients. The emergence of generic biosimilar products and new recombinant variants poses a challenge to this system, where functional differences impact on the relative biological activity in different assay systems. A more demanding system of standardization may therefore be required on the basis of international reference materials with associated reference methods. WHO recognizes this, and where possible and practical is seeking to incorporate concepts of traceability, uncertainty, and commutability to International Standards. However, some caution is needed because limitations on the characterization of many complex biologicals remain real, and a flexible approach is required on the basis of real-world needs.

 
  • References

  • 1 Global status report on noncommunicable diseases 2010. World Health Organisation; 2011
  • 2 Kunadian V, Gibson CM. Thrombolytics and myocardial infarction. Cardiovasc Ther 2012; 30 (2) e81-e88
  • 3 Medcalf RL, Davis SM. Plasminogen activation and thrombolysis for ischemic stroke. Int J Stroke 2012; 7 (5) 419-425
  • 4 Tapson VF. Thrombolytic therapy in acute pulmonary embolism. Curr Opin Cardiol 2012; 27 (6) 585-591
  • 5 Flemmig M, Melzig MF. Serine-proteases as plasminogen activators in terms of fibrinolysis. J Pharm Pharmacol 2012; 64 (8) 1025-1039
  • 6 Wicky S, Pinto EG, Oklu R. Catheter-directed thrombolysis of arterial thrombosis. Semin Thromb Hemost 2013; 39 (4) 441-445
  • 7 Oklu R, Wicky S. Catheter-directed thrombolysis of deep venous thrombosis. Semin Thromb Hemost 2013; 39 (4) 446-451
  • 8 Lippi G, Mattiuzzi C, Favaloro EJ. Novel and emerging therapies: thrombus-targeted fibrinolysis. Semin Thromb Hemost 2013; 39 (1) 48-58
  • 9 Cannon CP. Exploring the issues of appropriate dosing in the treatment of acute myocardial infarction: potential benefits of bolus fibrinolytic agents. Am Heart J 2000; 140 (6, Suppl): S154-S160
  • 10 Mehta RH, Alexander JH, Van de Werf F , et al. Relationship of incorrect dosing of fibrinolytic therapy and clinical outcomes. JAMA 2005; 293 (14) 1746-1750
  • 11 Bristow AF, Barrowcliffe T, Bangham DR. Standardization of biological medicines: the first hundred years, 1900-2000. Notes Rec R Soc Lond 2006; 60 (3) 271-289
  • 12 World Health Organization. Recommendations for the Preparation, Characterization and Establishment of International and Other Biological Reference Standards (revised 2004). WHO Technical Report Series, No. 932. 2006
  • 13 Marder VJ, Novokhatny V. Direct fibrinolytic agents: biochemical attributes, preclinical foundation and clinical potential. J Thromb Haemost 2010; 8 (3) 433-444
  • 14 Sikri N, Bardia A. A history of streptokinase use in acute myocardial infarction. Tex Heart Inst J 2007; 34 (3) 318-327
  • 15 Bangham DR, Walton PL. The international standard for streptokinase-streptodornase. Bull World Health Organ 1965; 33 (2) 235-242
  • 16 Heath AB, Gaffney PJ. A collaborative study to establish the second international standard for streptokinase. Thromb Haemost 1990; 64 (2) 267-269
  • 17 Sands D, Whitton CM, Longstaff C. International collaborative study to establish the 3rd International Standard for Streptokinase. J Thromb Haemost 2004; 2 (8) 1411-1415
  • 18 Longstaff C, Thelwell C, Whitton C. The poor quality of streptokinase products in use in developing countries. J Thromb Haemost 2005; 3 (5) 1092-1093
  • 19 Hermentin P, Cuesta-Linker T, Weisse J , et al. Comparative analysis of the activity and content of different streptokinase preparations. Eur Heart J 2005; 26 (9) 933-940
  • 20 Couto LT, Donato JL, de Nucci G. Analysis of five streptokinase formulations using the euglobulin lysis test and the plasminogen activation assay. Braz J Med Biol Res 2004; 37 (12) 1889-1894
  • 21 Longstaff C, Whitton CM, Stebbings R, Gray E. How do we assure the quality of biological medicines?. Drug Discov Today 2009; 14 (1-2) 50-55
  • 22 Mahboubi A, Sadjady SK, Mirzaei Saleh Abadi M, Azadi S, Solaimanian R. Biological activity analysis of native and recombinant streptokinase using clot lysis and chromogenic substrate assay. Iran J Pharm Res 2012; 11 (4) 1087-1093
  • 23 Husain SS, Gurewich V, Lipinski B. Purification and partial characterization of a single-chain high-molecular-weight form of urokinase from human urine. Arch Biochem Biophys 1983; 220 (1) 31-38
  • 24 World Health Organisation. Twenty-first Meeting. Expert Committee on Biological Standardisation. WHO Technical Report Series No. 413. 1968
  • 25 White WF, Barlow GH, Mozen MM. The isolation and characterization of plasminogen activators (urokinase) from human urine. Biochemistry 1966; 5 (7) 2160-2169
  • 26 Philo RD, Gaffney PJ. Assay methodology for urokinase: its use in assessing the composition of mixtures of high- and low-molecular weight urokinase. Thromb Res 1981; 21 (1–2) 81-88
  • 27 Gaffney PJ, Heath AB. A collaborative study to establish a standard for high molecular weight urinary-type plasminogen activator (HMW/u-PA). Thromb Haemost 1990; 64 (3) 398-401
  • 28 Gaffney PJ, Curtis AD. A collaborative study of a proposed international standard for tissue plasminogen activator (t-PA). Thromb Haemost 1985; 53 (1) 134-136
  • 29 Gaffney PJ, Curtis AD. A collaborative study to establish the 2nd international standard for tissue plasminogen activator (t-PA). Thromb Haemost 1987; 58 (4) 1085-1087
  • 30 Gates J, Hartnell GG. When urokinase was gone: commentary on another year of thrombolysis without urokinase. J Vasc Interv Radiol 2004; 15 (1, Pt 1): 1-5
  • 31 Sands D, Whitton CM, Merton RE, Longstaff C. A collaborative study to establish the 3rd International Standard for tissue plasminogen activator. Thromb Haemost 2002; 88 (2) 294-297
  • 32 PRIMI Trial Study Group. Randomised double-blind trial of recombinant pro-urokinase against streptokinase in acute myocardial infarction. Lancet 1989; 1 (8643) 863-868
  • 33 Kasai S, Arimura H, Nishida M, Suyama T. Proteolytic cleavage of single-chain pro-urokinase induces conformational change which follows activation of the zymogen and reduction of its high affinity for fibrin. J Biol Chem 1985; 260 (22) 12377-12381
  • 34 Hanbücken FW, Schneider J, Günzler WA, Friderichs E, Giertz H, Flohé L. Selective fibrinolytic activity of recombinant non-glycosylated human pro-urokinase (single-chain urokinase-type plasminogen activator) from bacteria. Arzneimittelforschung 1987; 37 (8) 993-997
  • 35 Nolli ML, Sarubbi E, Corti A , et al. Production and characterization of human recombinant single chain urokinase-type plasminogen-activator from mouse cells. Fibrinolysis 1989; 3: 101-106
  • 36 Lenich C, Pannell R, Henkin J, Gurewich V. The influence of glycosylation on the catalytic and fibrinolytic properties of prourokinase. Thromb Haemost 1992; 68 (5) 539-544
  • 37 Munger MA, Forrence EA. Anistreplase: a new thrombolytic for the treatment of acute myocardial infarction. Clin Pharm 1990; 9 (7) 530-540
  • 38 Verstraete M. Third-generation thrombolytic drugs. Am J Med 2000; 109 (1) 52-58
  • 39 Gaffney PJ. Standards in fibrinolysis—current status and future challenges. Thromb Haemost 1995; 74 (6) 1389-1397
  • 40 Dunn CJ, Goa KL. Tenecteplase: a review of its pharmacology and therapeutic efficacy in patients with acute myocardial infarction. Am J Cardiovasc Drugs 2001; 1 (1) 51-66
  • 41 Armstrong PW, Burton JR, Palisaitis D , et al. Collaborative angiographic patency trial of recombinant staphylokinase (CAPTORS). Am Heart J 2000; 139 (5) 820-823
  • 42 Armstrong PW, Burton J, Pakola S , et al; CAPTORS II Investigators. Collaborative angiographic patency trial of recombinant staphylokinase (CAPTORS II). Am Heart J 2003; 146 (3) 484-488
  • 43 Laroche Y, Heymans S, Capaert S, De Cock F, Demarsin E, Collen D. Recombinant staphylokinase variants with reduced antigenicity due to elimination of B-lymphocyte epitopes. Blood 2000; 96 (4) 1425-1432
  • 44 Verhamme P, Goossens G, Maleux G, Collen D, Stas M. A dose-finding clinical trial of staphylokinase SY162 in patients with long-term venous access catheter thrombotic occlusion. J Thromb Thrombolysis 2007; 24 (1) 1-5
  • 45 Marder VJ, Landskroner K, Novokhatny V , et al. Plasmin induces local thrombolysis without causing hemorrhage: a comparison with tissue plasminogen activator in the rabbit. Thromb Haemost 2001; 86 (3) 739-745
  • 46 Sottrup-Jensen L, Claeys H, Zajdel M, Petersen T, Magnusson S. The primary structure of human plasminogen: isolation of two lysine-binding fragments and one “mini” plasminogen (MW 38000) by elastase-catalyzed specific limited proteolysis. In: Progress in Chemical Fibrinolysis and Thrombolysis. New York, NY: Raven Press; 1978: 191-209
  • 47 Wu HL, Shi GY, Wohl RC, Bender ML. Structure and formation of microplasmin. Proc Natl Acad Sci U S A 1987; 84 (24) 8793-8795
  • 48 Marder VJ, Manyak S, Gruber T , et al. Haemostatic safety of a unique recombinant plasmin molecule lacking kringles 2-5. Thromb Haemost 2010; 104 (4) 780-787
  • 49 Deitcher SR, Funk WD, Buchanan J, Liu SC, Levy MD, Toombs CF. Alfimeprase: a novel recombinant direct-acting fibrinolytic. Expert Opin Biol Ther 2006; 6 (12) 1361-1369
  • 50 Tsui I, Pan CK, Rahimy E, Schwartz SD. Ocriplasmin for vitreoretinal diseases. J Biomed Biotechnol 2012; ; doi: 10.1155/2012/354979
  • 51 Kirkwood TBL, Campbell PJ, Gaffney PJ. A standard for human plasmin. Thromb Diath Haemorrh 1975; 34 (1) 20-30
  • 52 Johnson AJ, Kline DL, Alkjaersig N. Assay methods and standard preparations for plasmin, plasminogen and urokinase in purified systems, 1967-1968. Thromb Diath Haemorrh 1969; 21 (2) 259-272
  • 53 Gaffney PJ, Mussett MV. International collaborative study for the establishment of the second International Reference Preparation of plasmin. Thromb Haemost 1983; 50 (3) 645-649
  • 54 Chase Jr T, Shaw E. p-Nitrophenyl-p'-guanidinobenzoate HCl: a new active site titrant for trypsin. Biochem Biophys Res Commun 1967; 29 (4) 508-514
  • 55 Panteghini M, Forest JC. Standardization in laboratory medicine: new challenges. Clin Chim Acta 2005; 355 (1–2) 1-12
  • 56 Jackson CM, White II GC, Barrowcliffe T , et al; Joint Committee of the IFCC Scientific Division and the ISTH Scientific and Standardization Committee. A reference system approach to future standardization of laboratory tests for hemostasis. A position paper of the Joint Committee of the IFCC Scientific Division and the ISTH Scientific and Standardization Committee. Thromb Haemost 2002; 87 (1) 165-169
  • 57 Longstaff C, Whitton CM. A proposed reference method for plasminogen activators that enables calculation of enzyme activities in SI units. J Thromb Haemost 2004; 2 (8) 1416-1421
  • 58 Longstaff C, Whitton C, Thelwell C, Belgrave D ; Fibrinolysis Subcommittee of the SSC of the ISTH. An international collaborative study to investigate a proposed reference method for the determination of potency measurements of fibrinolytics in absolute units. J Thromb Haemost 2007; 5 (2) 412-414
  • 59 Urano T, Urano S, Castellino FJ. Reaction of tissue-type plasminogen activator with 4-methylumbelliferyl-p-guanidinobenzoate hydrochloride. Biochem Biophys Res Commun 1988; 150 (1) 45-51
  • 60 Thelwell C, Longstaff C. The regulation by fibrinogen and fibrin of tissue plasminogen activator kinetics and inhibition by plasminogen activator inhibitor 1. J Thromb Haemost 2007; 5 (4) 804-811
  • 61 Hubbard AR, Dodt J, Lee T , et al; Factor VI I I and Factor IX Subcommittee of The Scientific and Standardisation Committee of The International Society on Thrombosis and Haemostasis. Recommendations on the potency labelling of factor VIII and factor IX concentrates. J Thromb Haemost 2013; 11 (5) 988-989