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New long-term action insulin formulations obtained using polycations for heparin neutralization

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Języki publikacji
EN
Abstrakty
EN
Phenomena that occur between an insulin and four different positively charged polymers (protamine, cationic dextran, chitosan, and poliallylamine derivatives) were studied by dynamic light scattering and fluorescence measurements (using fluorescein-labeled polymers). These processes were compared to the reaction of polycations with heparin that is responsible for the neutralization of anticoagulant activity in blood stream.The nature of polycations interaction with heparin is electrostatic, while the interaction with insulin is more complicated.We observed that the presence of zinc atoms (and its complexing by nitrogen from macromolecules) is critical for insulin suspensions formation and stability. The differences between the nature of these two reactions were revealed. The highly immunogenic action of protamine present in long-acting insulin products makes it reasonable to develop similar systems based on the nonprotein polycations.
Słowa kluczowe
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art. no. 20190029
Opis fizyczny
Bibliogr. 29 poz., rys.
Twórcy
  • Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland
  • Chair of Medical Biochemistry, Jagiellonian University, Collegium Medicum, Kopernika 7C, 31-034, Krakow, Poland
  • Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland
  • Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland
  • Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland
  • Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland
Bibliografia
  • [1] Urwin N, Whiting D, Guariguata L, Ghyoot G, Gan D, editors. International Diabetes Federation’s 5th ed. of the Diabetes Atlas, Brussels, 14 November -World Diabetes Day, 2011.
  • [2] Rother KI. Diabetes treatment - bridging the divide. N Engl J Med 2007;356:1499-501.
  • [3] Hirsch IB. Treatment of patients with severe insulin deficiency: what we have learned over the past 2 years. Am J Med 2004;116:17-22.
  • [4] Lindholm A. New insulins in the treatment of diabetes mellitus. Best Pract Res Clin Gastroenterol 2002;16:475-92.
  • [5] Baganz HM, Carfagno SC, Cowan BY, Dillon ES. NPH insulin; its comparison with previous insulin regimens. Am Med Sci 1951;2:22.
  • [6] Burnham DK. Insulin and insulin mixtures; NPH insulin. Calif Med 1951;75:412-5.
  • [7] Byun Y, Singh VK, Yang VC. Low molecular weight protamine: a potential nontoxic heparin antagonist. Thrombosis Res 1999;94:53-61.
  • [8] Ando T, Yamsaki M, Suzuki K. Protamines. Isolation, characterisation, structure and function. Mol Biol Biochem Biophys 1973;12:1-109.
  • [9] Chu YQ, Cai LJ, Jiang DC, Jia D, Yan SY, Wang YQ. Allergic shock and death associated with protamine administration in a diabetic patient. Clin Therapeut 2010;32:1729-32.
  • [10] Nell LJ and Thomas JW. Frequency and specificity of protamine antibodies in diabetic and control subjects. Diabetes 1988;37:172-6.
  • [11] Baur X, Bossert J, Koops F. IgE-mediated allergy to recombinant human insulin in a diabetic. Allergy 2003;58:676-8.
  • [12] Aris A, Solanes H, Bonnin JO, Garin R, Caralps JM. Intraaortic administration of protamine: method for heparin neutralization after cardiopulmonary bypass. Cardiovasc Dis 1981;8:23-8.
  • [13] Panos A, Orrit X, Chevalley C, Kalangos A. Dramatic post-cardiotomy outcome, due to severe anaphylactic reaction to protamine. Eur Cardio-thoracic Surg 2003;24:325-7.
  • [14] Mclaughlin KE, Dunning J. In patients post cardiac surgery do high doses of protamine cause increased bleeding? Interactive Cardiovascular Thoracic Surg 2003:2:424-6.
  • [15] Gale AJ, Elias DJ, Averell PM, Teirstein PS, Buck M, Brown SD, et al. Engineered virus-like nanoparticles reverse heparin anticoagulation more consistently than protamine in plasma from heparin-treated patients. Thrombosis Res 2011;128:9-13.
  • [16] Kamiński K, Szczubiałka K, Zazakowny K, Lach R, Nowakowska M. Chitosan derivatives as novel potential heparin reversal agents. J Med Chem 2010;53:4141-7.
  • [17] Kamiński K, Płonka M, Ciejka J, Szczubiałka K, Nowakowska M, Lorkowska B, et al. Cationic derivatives of dextran and hydroxypropylcellulose as novel potential heparin antagonists. J Med Chem 2011;54:6586-96.
  • [18] Kim JJ and Park K. Modulated insulin delivery from glucose-sensitive hydrogel dosage forms. J Controlled Release 2001;77:39-47.
  • [19] Merisko-Liversidge E, McGurk SL, Liversidge GG. Insulin nanoparticles: anovel formulation approach for poorly water soluble Zn-insulin. Pharmaceut Res 2004;21:1545-53.
  • [20] Sarmento B, Ferreira D, Veiga F, Ribeiro A. Characterization of insulin-loaded alginate nanoparticles produced by ionotropic pre-gelation through DSC and FTIR studies. Carbohydr Polym 2006;66:1-7.
  • [21] Samal SK, Dash M, Van Vlierberghe S, Kaplan DL, Chiellini E, van Blitterswijk C, et al. Cationic polymers and their therapeutic potential. Chem Soc Rev 2012;41:7147-94.
  • [22] Kalaska B, Kaminski K, Sokolowska E, Czaplicki D, Kujdowicz M, Stalinska K, et al. Nonclinical evaluation of vovel cationically modified polysaccharide antidotes for unfractionated heparin. PLoS One 2015;10:e0119486.
  • [23] Kalaska B, Kaminski K, Miklosz J, Yusa SI, Sokolowska E, Blazejczyk A, et al. Heparin-binding copolymer (HBC) reverses effects of unfractionated heparin, enoxaparin and fondaparinux in rats and mice. Transl Res 2016;177:98-112.
  • [24] Kamiński K, Kałaska B, Koczurkiewicz P, Michalik M, Szczubiałka K, Mogielnicki A, et al. New arginine substituted derivative of poly(allylamine hydrochloride) for heparin reversal. Med Chem Commun 2014;5:489-95.
  • [25] Gok E, Olgaz S. Binding of fluorescein isothiocyanate to insulin: afluorimetric labeling study. Fluorescence 2004;14:2.
  • [26] He1 H, David AE, Zhang J, Park YS, Wang J, Huang Y, et al. Low molecular weight protamine/insulin formulation with potential to attenuate protamine-masqueraded insulin allergy. Macromol Res 2011;19:1224-6.
  • [27] Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970;227:680-5.
  • [28] Graham PA, Nash AS, McKellar QA. Pharmacokinetics of a porcine insulin zinc suspension in diabetic dogs. J Small Animal Practice 1997;38:434-8.
  • [29] Norrmana M, Hubaleka F, Schluckebier G. Structural characterization of insulin NPH formulations. Eur J Pharmaceut Sci 2007;30:414-23.
Uwagi
Opracowanie rekordu ze środków MNiSW, umowa Nr 461252 w ramach programu "Społeczna odpowiedzialność nauki" - moduł: Popularyzacja nauki i promocja sportu (2020).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-b1fb4926-3a46-4cf8-a416-065a65e15164
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