<?xml version="1.1" encoding="utf-8"?>
<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">JMDS</journal-id><journal-title-group><journal-title>Journal of Medicines Development Sciences</journal-title></journal-title-group><issn>2382-6363</issn><eissn>2382-6371</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18063/JMDS.v10i4.1206</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Performance Evaluation of Autologous Thrombin Produced from Platelet‑rich Plasma (PRP) Tubes</title><url>https://artdesignp.com/journal/JMDS/10/4/10.18063/JMDS.v10i4.1206</url><author>LiuQiang,WangMeng</author><pub-date pub-type="publication-year"><year>2025</year></pub-date><volume>10</volume><issue>4</issue><history><date date-type="pub"><published-time>2025-12-26</published-time></date></history><abstract>Thrombin derived from bovine sources is commonly&amp;nbsp;used to arrest bleeding during surgical procedures. However, there are risks associated with the use of bovine-derived thrombin, such as postoperative bleeding and the risk of infection in patients. Therefore, it is essential to develop a technology to generate autologous thrombin. In this study, autologous thrombin was produced from platelet-poor plasma (PPP) obtained using PRP tubes, mixed with 10% calcium gluconate, and halloysite nanotubes (HNTs), and evaluated the stability of prepared&amp;nbsp;thrombin when stored at room temperature. The experiment demonstrated that the combination of 3 ml of platelet-poor plasma (PPP), 2.3 ml of 10% calcium gluconate, and a minimum of 1.5 mg of HNTs produces autologous thrombin with enhanced activity and stability, providing&amp;nbsp;experimental evidence for its potential clinical application.</abstract><keywords>autologous thrombin, stability, 10% calcium gluconate, platelet-poor  plasma, halloysite nanotubes</keywords></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>[1] Al Dieri R, De Laat B, Hemker HC, 2012, Thrombin Generation: What Have We Learned?&amp;nbsp;Blood Reviews, 26(5): 197-203.
[2] Jasani B, Donaldson LJ, Baxter-Smith DC, et al., 1977, Topical Thrombin and Control of Wound Haematoma.&amp;nbsp;Lancet, 310(8033): 332-333.
[3] Ofodile FA, Sadana MK, 1991, The Role of Topical Thrombin in Skin Grafting.&amp;nbsp;Journal of the National Medical Association, 83(5): 416-418.
[4] Codispoti M, Mankad PS, 2002, Significant Merits of a Fibrin Sealant in the Presence of Coagulopathy Following Paediatric Cardiac Surgery: Randomised Controlled Trial.&amp;nbsp;European Journal of Cardio-Thoracic Surgery, 22(2): 200-205.
[5] Kajitani M, Ozdemir A, Aguinaga M, et al., 2000, Severe Hemorrhagic Complication Due to Acquired Factor V Inhibitor After Single Exposure to Bovine Thrombin Product.&amp;nbsp;Journal of Cardiac Surgery, 15(6): 378-382.
[6] Beghi E, Gandolfo C, Ferrarese C, et al., 2004, Bovine Spongiform Encephalopathy and Creutzfeldt-Jakob Disease: Facts and Uncertainties Underlying the Causal Link Between Animal and Human Diseases.&amp;nbsp;Neurological Sciences, 25(3): 122-129.
[7] Kumar V, Madsen T, Zhu H, et al., 2006, Stability of Human Thrombin Produced From 11 ml of Plasma Using the Thrombin Processing Device.&amp;nbsp;The Journal of Extra-Corporeal Technology, 37(4): 390-395.
[8] Rawtani D, 2012, Multifarious Applications of Halloysite Nanotubes: A Review.&amp;nbsp;Reviews on Advanced Materials Science, 30(3): 282-295.
[9] Satish S, Tharmavaram M, Rawtani D, 2019, Halloysite Nanotubes as a Nature's Boon for Biomedical Applications.&amp;nbsp;Nanobiomedicine,&amp;nbsp;6(11):&amp;nbsp;1849.
[10] Trapaidze A, 2015, Integration of Thrombin-Binding Aptamers in Point-of-Care Devices for Continuous Monitoring of Thrombin in Plasma.
[11] Feng Y, Luo X, Wu F, et al., 2022, Systematic Studies on Blood Coagulation Mechanisms of Halloysite Nanotubes-Coated PET Dressing as Superior Topical Hemostatic Agent.&amp;nbsp;Chemical Engineering Journal, 428: 132049.
[12] Clauss A, 1957, Gerinnungsphysiologische Schnellmethode zur Bestimmung des Fibrinogens.&amp;nbsp;Acta Haematologica, 17(4): 237-246.</p><pub-id pub-id-type="doi"/></element-citation></ref></ref-list></back></article>
