免疫球蛋白G抗白喉血清被胃蛋白酶破坏的分因子分析

Fuad Pribadi, C. Riani, H. Setiadji
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引用次数: 0

摘要

。在过去5年中,观察到白喉暴发的次数相当高。在白喉爆发时治疗白喉的一种方法是使用抗白喉血清。多年来,由于一些国家的生产商已停止生产,世界范围内抗白喉血清产品的供应已减少。停止生产的部分原因是需求减少、生产失败以及从血液中生产日益严格的生物制品的监管要求。此外,随着2014年关于清真产品保证的第34号法律的颁布,使用某些类型的胃蛋白酶作为生产的组成部分成为问题。本研究旨在分析胃蛋白酶A替代胃蛋白酶B的使用情况,采用分数析因设计获得对IgG片段化有显著影响的参数,获得IgG片段化的最佳参数值(最高滴度、最短Kf时间和SDS PAGE中IgG条带缺失),提高抗白喉血清产物抗体滴度。采用鱼骨法和FMEA法进行风险分析,找出影响胃蛋白酶A对IgG抗白喉血清产品裂解过程的几个因素。可接受和不可接受分类的因素为纯化方法(RPN 60值)、破碎过程的pH终止值(RPN 100值)、破碎温度(RPN 60值)、胃蛋白酶数量(RPN 125值)和破碎时间(RPN 125值)。将硫酸铵分馏法改为初始血浆上使用100kDa滤膜进行滤滤的方法变化结果不显著。对4个因素进行分数因子分析,分别为:pH;温度;胃蛋白酶的量和时间。通过帕累托分析和主效应分析,以抗体滴度为主要反应时,这4个因素对胃蛋白酶a裂解IgG过程的影响非常显著(p值<0.05)。使用BCA测试和SDS PAGE对碎片化结果进行表征。本研究的结论是,胃蛋白酶A可以替代胃蛋白酶B,其中影响显著的因素是胃蛋白酶的用量、时间、温度和孵育终止时的pH值;胃蛋白酶A裂解IgG的最佳值(滴度最高、Kf时间最短、无IgG条带)为:胃蛋白酶用量1163mg / L、温度37℃、时间135 min、pH 5.95;和增加抗体效价在免疫球蛋白分裂阶段2.67倍比之前的方法使用胃蛋白酶B。本研究旨在分析使用胃蛋白酶代替胃蛋白酶B,获取参数对分化有重要影响的免疫球蛋白g利用分式析因设计,获得最优参数免疫球蛋白碎片(效价最高价值,Kf最短时间和缺乏免疫球蛋白的乐队在SDS PAGE)和增加抗白喉血清抗体效价的产品。酶解过程的优化参数为胃蛋白酶A用量、酶解温度、酶解终止pH、酶解时间。用于评估显著性因子(p值<0.05)的应答是IgG片段化过程的定量参数,即抗体滴度值。IgG片段化鉴定结果采用双双环酸(BCA)试验测定产生的总蛋白含量,SDS-PAGE分析观察IgG片段化成抗体片段F (ab) 2的特征。可接受(得分13-36);不能接受(37-64分);难以忍受(65-125)。在不可接受和不可容忍矩阵中的RPN分数使用析因分数设计进行分析,以确定这些因素的影响以及它们之间的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fractional Factorial Analysis Of Immunoglobulin G Anti-Diphtheria Serum Fragmentation By Pepsin
. The number of diphtheria outbreaks was observed to be quite high in the last 5 years. One way to treat diphtheria at the time of an outbreak is to use an anti-diphtheria serum. The availability of anti-diphtheria serum products worldwide has been reduced for years because manufacturers in several countries have stopped producing. The cessation of production is partly due to a decrease in demand, production failures and regulatory requirements in the manufacture of increasingly stringent biological products from the blood. In addition, the use of certain types of pepsin as a component of production becomes problematic with the issuance of Law No. 34 of 2014 concerning Guarantees of Halal Products. This study aims to analyze the use of pepsin A as a substitute for pepsin B, get parameters that have a significant effect on IgG fragmentation using fractional factorial design, get the optimum parameter value of IgG fragmentation (highest titer value, shortest Kf time and absence of IgG bands in SDS PAGE ) and increase anti-diphtheria serum product antibody titers. Risk analysis was carried out to find out several factors that influence the process of pepsin A fragmentation against IgG anti-diphtheria serum products using fishbone and FMEA methods. Factors belonging to the unacceptable and intolerable classification are purification methods (RPN 60 value), pH termination of the fragmentation process (RPN 100 value), fragmentation temperature (RPN 60 value), number of pepsin (RPN 125 value), and fragmentation time (RPN 125 value ) Changes in the method carried out by replacing the ammonium sulfate fractionation process to diafiltration using a 100kDa filter membrane on the initial plasma showed insignificant results. Fractional factorial analysis was carried out on 4 factors, namely: pH; temperature; amount of pepsin and time. Based on pareto analysis and main effect, the four factors showed a very significant effect on the IgG fragmentation process by pepsin A (p-value <0.05) by using antibody titers as the main response. Characterization of the results of fragmentation is done using the BCA test and SDS PAGE. The conclusion of this study is that pepsin A can replace pepsin B, a factor that has a significant effect is the amount of pepsin, time, temperature, and pH of the incubation termination; optimum value (highest titer, shortest Kf time and no IgG band) IgG fragmentation process by pepsin A is the amount of pepsin 1163mg / L, temperature 37ºC, time 135 minutes, and pH 5.95; and increasing antibody titer at IgG fragmentation stage to 2.67 times than the previous method using pepsin B. This study aims to analyze the use of pepsin A as a substitute for pepsin B, obtain parameters that have a significant effect on fragmentation of IgG by using fractional factorial design, obtain optimum parameters for IgG fragmentation (highest titer value, shortest Kf time and absence of IgG bands in SDS PAGE ) and increase the antibody titer of anti diphtheria serum products. Optimized parameters in the digestion process are the amount of pepsin A, incubation temperature, pH of digestion process termination, and digestion time. The response used in assessing a significant factor (P-value <0.05) is a quantitative parameter of the IgG fragmentation process, which is the antibody titer value. Characterization of IgG fragmentation results used bichinconic acid (BCA) test to determine the total protein content produced and SDS-PAGE profile to see the character of IgG fragmentation into antibody fragment F (ab) 2. acceptable (score 13-36); unacceptable (score 37-64); and intolerable (score 65-125). RPN scores that are in the unacceptable and intolerable matrices are analyzed using factorial fractional designs to determine the influence of these factors and the interactions between them.
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