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用于糖尿病足溃疡的快速生物动力血凝凝胶(一种富含自体血小板和白细胞的血浆凝胶)的制造与初步表征

Manufacture and Initial Characterisation of RAPID Biodynamic Haematogel, an Autologous Platelet and Leukocyte-Rich Plasma Gel for Diabetic Foot Ulcers.

作者信息

Olszewska Aleksandra, Duan Jiajing, Javorovic Jana, Chan K L Andrew, Rickard James, Pitchford Simon, Forbes Ben

机构信息

Institute of Pharmaceutical Science, King's College London, Franklin-Wilkins Building, Stamford Street, London SE1 9NH, UK.

Biotherapy Services Ltd., The Clarence Centre for Enterprise & Innovation, 6 St George's Circus, London SE1 6FE, UK.

出版信息

Gels. 2024 Sep 2;10(9):572. doi: 10.3390/gels10090572.

Abstract

This observational study reports the process for the manufacture of RAPID Biodynamic Haematogel and explores the properties of the platelet and leukocyte-rich plasma gels formed. Gels were manufactured from 60 mL of human blood using the protocol of Biotherapy Services. Platelet and leukocyte content, time-to-gel, gel weight and the temporal profile of liquid exudation from the gels were measured, along with the content of growth factors VEGF and PDGF in the releasate. The effect of the releasate on human keratinocyte (HaCat) cell proliferation was also determined. The platelet and leukocyte concentrations in donor blood were 1.60-8.10 × 10 and 1.00 × 10-2.00 × 10 cells/mL, which were concentrated 2.67- and 1.12-fold, respectively, during processing. Structurally weak gels were formed which exuded a clear liquid releasate (77.4% / of gel weight over 60 min) that contained 278 pg/mL VEGF and 1319 pg/mL PDGF. The releasate produced concentration-dependent proliferation of HaCat cells: 5-15% releasate produced a 2.7-8.9-fold increase in growth over 48 h. In conclusion, we have described the point-of-care manufacturing protocol and characterised the gel properties of RAPID Biodynamic Haematogel. This is an essential first step towards identifying, understanding and controlling critical processing parameters that impact on this medicinal product's quality.

摘要

这项观察性研究报告了快速生物动力血凝凝胶的制造过程,并探讨了所形成的富含血小板和白细胞的血浆凝胶的特性。使用生物治疗服务协议,从60毫升人体血液中制备凝胶。测量了血小板和白细胞含量、凝胶形成时间、凝胶重量以及凝胶液体渗出的时间曲线,同时还测量了释放液中生长因子VEGF和PDGF的含量。还确定了释放液对人角质形成细胞(HaCat)增殖的影响。供体血液中的血小板和白细胞浓度分别为1.60 - 8.10×10和1.00×10 - 2.00×10细胞/毫升,在处理过程中分别浓缩了2.67倍和1.12倍。形成了结构较弱的凝胶,其渗出清澈的液体释放液(60分钟内占凝胶重量的77.4%),其中含有278 pg/mL的VEGF和1319 pg/mL的PDGF。释放液对HaCat细胞产生浓度依赖性增殖:5 - 15%的释放液在48小时内使生长增加了2.7 - 8.9倍。总之,我们描述了即时护理制造方案,并对快速生物动力血凝凝胶的凝胶特性进行了表征。这是朝着识别、理解和控制影响该药品质量的关键加工参数迈出的重要第一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/283d/11431608/1afdda0f73f2/gels-10-00572-g001.jpg

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