期刊文献+

ELISA法检测组织工程产品中残留牛血清蛋白含量 被引量:4

Quantitative Measure of Residual BSA in TEMPs-ELISA Method
下载PDF
导出
摘要 目的探讨定量检测牛血清白蛋白(Bull serum albumin,BSA)酶联免疫试剂盒用于组织工程医疗产品(Medical products of tissue engineering,TEMPs)残留BSA检测的适用性,以及清洗程序对产品BSA残留量的影响。材料和方法检测了三种组织工程医疗产品(组织工程骨、组织工程肌腱以及组织工程角膜贴片)中BSA的残留量,并比较了经不同清洗程序清洗后角膜贴片中残留BSA含量。结果(1)组织工程骨、组织工程肌腱以及组织工程角膜贴片中BSA残留量分别为31.8ng/ml,4.9ng/ml和低于2.5ng/ml,且测定值与其稀释倍数呈正相关;(2)生理盐水及无血清的MEM培养基平均OD值与试剂盒中零浓度标准品接近,表明生理盐水或无血清MEM作为样品浸提介质对最终的实验结果无明显影响;(3)样品复孔比均小于1.24,符合试剂盒有效性要求。经清洗程序2处理后,角膜贴片中残留BSA较清洗程序1明显减少。结论(1)该试剂盒适用于组织工程医疗产品中BSA残留量的检测。(2)对于组织工程医疗产品而言,不同的清洗程序对BSA的残留量有非常明显的影响。生产商应根据其预期用途制定有效的清洗程序,并在说明书中给予足够的阐述。 Aim This paper was aimed to study the suitability of a Quantitative measure of residual BSA ELISA kit in detecting residual BSA in TEMPs, and to investigate the effects of rinsing protocol on reducing residual BSA in TEMPs. Materials and methods Three kinds of TEMPs used in this study were: tissue engineered bone, tissue engineered tendon and tissue engineered corneal stroma. The immersion of each product was prepared after the rinsing procedure according to the Direction For Use. Physiological saline and MEM was used as immersion medium. Using a Quantitative measure of residual BSA ELISA kit for BSA, and the results of engineered corneal stroma were compared after different rinsing protocol. Results and conclusion (1)The concentration of BSA residual in the immersions of tissue engineered bone, tissue engineered tendon and tissue engineered corneal stroma was 31.8 ng/ml, 4.9 ng/ml and 〈 2.5 ng/ml, respectively. It also showed some relativity between OD and the sample dilution. The mean value of the OD of physiological saline and MEM were similar to that of 0 ng/ml standard. It indicated that there were no obvious effects on the results when physiological saline or MEM was used as immersion medium. The kit was suitable for detect the residual BSA in TEMPs . (2)The mean value of the OD of the corneal rinsing by protocoll was 2.067, that was upper the reading of the highest standard (40 ng/ml) for 3.3 times, while the OD of that by rinsing protocol 2 was below the reading of the lowest standard (2.5 ng/ml). The results showed significant different of BSA residual may caused by different rinsing protocol for a TEMPs.
出处 《组织工程与重建外科杂志》 2008年第1期12-14,共3页 Journal of Tissue Engineering and Reconstructive Surgery
关键词 组织工程医疗产品 牛血清白蛋白 残留量 酶联免疫法 清洗程序 Medical products of tissue engineering (TEMPs) Bull serum albumin (BSA) Residual ELISA Rinsing protocol
  • 相关文献

参考文献5

二级参考文献28

  • 1孙皎,丁婷婷,章平.生物材料和医疗器械的免疫学评价[J].中国医疗器械杂志,2005,29(5):313-315. 被引量:6
  • 2Dutaud D, Aubry L, Henry L, et al. Development and evaluation of a sandwich ELISA for quantification of the 20S proteasome in human plasma. J Immunol Methods,2002,260:183-193. 被引量:1
  • 3Sasaki D, Mitchell R A. How to obtain reproducible quantitative ELISA results. Oxford Biomed Res, Oxford MI 48371. 被引量:1
  • 4Wentworth P Jr,McDunn JE,Wentworth AD,et al.Evidence for antibody catalyzed ozoneformation in bacterial killing and inflammation.Science,2002; 298(13):2195 被引量:1
  • 5Marques AP,Reis RL,Hunt JA,et al.The biocompatibility of novel starch-based polymers and composites:in vitro studies.Biomaterials,2002;23(6):1471 被引量:1
  • 6Kalltorp M,Obiogina S,Jacobsson S,et al.In vivo cell recruitment,cytokine release and chemiluminescence response at gold,and thiol functionalized surfaces.Biomaterials,1999;20(22):2123 被引量:1
  • 7Kao WJ.Evaluation of leukocyte adhesion on polyurethanes:the effects of shear stress and blood proteins.Biomaterials,2000;21(22):2295 被引量:1
  • 8Luqiu C,Madoka K,Kenji F,et al.Continuous exposure of mice to superantigenic toxins induces a high-level protracted expansion and an immunological memory in the toxin-reactive CD4+ T cells,The Journal of Immunology,2002; 168:3817 被引量:1
  • 9Kao WJ.Evaluation of protein-modulated macrophage behavior on biomaterials:designing biomimetic materials for cellular engineering.Biomaterials,1999;20(23-24):2213 被引量:1
  • 10Jeanway CA.Immunlbiology.Fourth edition,Elsevier Science Led.USA,1999 被引量:1

共引文献16

同被引文献33

引证文献4

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部