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Quantification of BSA in Tissue Engineered Medical Products by ELSA - Problems and Solutions

机译:ELSA对组织工程医疗产品中BSA的定量分析-问题与解决方案

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Aim In this study, the adaptability of an ELISA kit for quantification the residual BSA in TEMPs, the influence of rinsing protocol on reducing the residual BSA in TEMPs and the effectiveness of ultra-filtration on reducing the matrix effects of TEMPs immersion on BSA quantitative by ELISA were discussed. Methods Three kinds of TEMPs used in this study were: tissue engineered skin (TES), recombination human acellular dermal matrix (rhADM) and combination chitosan tissue engineered skin (cC-TES). The devices were rinsed according to the Directions for Use firstly. To investigating the influence of rinsing protocol on reducing the residual BSA in TEMPs, TES were rinsed by two different protocols separately. Then TEMPs immersions were prepared according to ISO10993.12, physiological saline (NS) was used as immersion medium. BSA concentration in immersions and filtrate were determined by using the "Quantitative measure of residual BSA ELISA kit" (detection range was 12.5-200ng/mL, manufactured by WUXI BOSHENG MEDICAL BIO-TEC DEVELOPMENT CO., LTD. As suspected to have some matrix effect on BSA quantification by ELISA kit, rhADM immersion was ultra-filtrated before detection. Results The results showed good correlation between dilution factors and the A450nm of TES and cC-TES immersions, correlation coefficient (r) was 0.9943 + 0.0007 and -0.9835 + 0.0037, respectively. No significant effect on BSA detection was found when NS was used as immersion medium. Comparing the results of protocol 1 and 2, the A450nm of TES immersion was significantly decreased after rising by protocol 2. After ultra-filtration, the correlations between absorption and dilution factors of rhADM immersion were improved significantly; the correlation coefficient (r) was raised from -0.7264±0.0089 to -0.9606±0.0039. Conclusions The quantitative ELISA kit was considered to be adaptability for detect the BSA in TEMPs. Different rinsing protocol may obviously affect on reducing the residual BSA in TEMPs. The matrix effects of rhADM immersion can be reduced obviously by using ultrafiltration.
机译:目的在这项研究中,ELISA试剂盒用于定量TEMP中残留BSA的适应性,漂洗方案对减少TEMP中残留BSA的影响以及超滤对降低TEMP浸入基质对BSA定量的基质效应的有效性讨论了ELISA。方法本研究使用的三种TEMPs是:组织工程皮肤(TES),重组人脱细胞真皮基质(rhADM)和组合壳聚糖组织工程皮肤(cC-TES)。首先根据使用说明冲洗设备。为了研究漂洗规程对减少TEMP中残留BSA的影响,分别通过两种不同的规程漂洗了TES。然后根据ISO10993.12制备TEMPs浸入液,将生理盐水(NS)用作浸入介质。使用“无定形残留BSA ELISA试剂盒的定量方法”(检测范围为12.5-200ng / mL,由无锡博盛医药生物技术开发有限公司生产)测定沉浸液和滤液中的BSA浓度。结果表明,稀释因子与TES和cC-TES浸泡液的A450nm之间存在良好的相关性,相关系数(r)分别为0.9943 + 0.0007和-0.9835 +当NS用作浸没介质时,对BSA的检测没有显着影响,比较方案1和2的结果,通过方案2上升后,TES浸没的A450nm明显降低了。 rhADM浸没的吸收因子和稀释因子之间的关系得到了显着改善;相关系数(r)从-0.7264±0.0089提高到-0.9606±0.0039。 ELISA试剂盒被认为对检测TEMP中的BSA具有适应性。不同的冲洗方案可能会明显减少TEMP中残留的BSA。通过超滤可以显着降低rhADM浸入的基质效应。

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