ASTM F895-2011
细胞培养及毒素屏蔽的标准试验方法

Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity


ASTM F895-2011 中,可能用到以下仪器设备

 

Luminex 200 液相芯片仪

Luminex 200 液相芯片仪

默克生命科学

 

N30E 纳米流式检测仪(Flow NanoAnalyzer)

N30E 纳米流式检测仪(Flow NanoAnalyzer)

北京欧波同光学仪器有限公司/欧波同/OPTON

 

C1单细胞自动制备系统

C1单细胞自动制备系统

富鲁达 Fluidigm

 

Vectra™全自动定量病理学工作站(6片连载型)

Vectra™全自动定量病理学工作站(6片连载型)

珀金埃尔默企业管理(上海)有限公司PerkinElmer

 

Vectra™全自动定量病理学工作站200片连载型

Vectra™全自动定量病理学工作站200片连载型

珀金埃尔默企业管理(上海)有限公司PerkinElmer

 

ClonePix 2细胞克隆筛选系统

ClonePix 2细胞克隆筛选系统

美谷分子仪器(上海)有限公司

 

Guava easyCyte 12系统

Guava easyCyte 12系统

默克生命科学

 

Guava easyCyte 6系统

Guava easyCyte 6系统

默克生命科学

 

Guava easyCyte 6HT系统

Guava easyCyte 6HT系统

默克生命科学

 

guava easyCyte 5系统

guava easyCyte 5系统

默克生命科学

 

Guava easyCyte 5HT系统

Guava easyCyte 5HT系统

默克生命科学

 

默克Millicell ERS-2 电阻仪

默克Millicell ERS-2 电阻仪

默克生命科学

 

赛默飞Attune NxT声波聚焦流式细胞仪

赛默飞Attune NxT声波聚焦流式细胞仪

赛默飞 AppliedBiosystems

 

赛默飞Attune CytPix成像型流式细胞仪

赛默飞Attune CytPix成像型流式细胞仪

赛默飞 AppliedBiosystems

 

皮升泵LPP01-100(细胞注射器)-LongerPump

皮升泵LPP01-100(细胞注射器)-LongerPump

保定兰格恒流泵有限公司

 

CyTOF XT 质谱流式细胞仪

CyTOF XT 质谱流式细胞仪

富鲁达 Fluidigm

 

Polaris单细胞实验系统

Polaris单细胞实验系统

富鲁达 Fluidigm

 

 

 

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标准号
ASTM F895-2011
发布日期
2011年
实施日期
废止日期
中国标准分类号
C05
国际标准分类号
07.100.10 (Medical microbiology)
发布单位
美国材料与试验协会
适用范围

This test method is useful for assessing the cytotoxic potential of new materials and formulations and as part of a quality control program for established medical devices and components.

This test method assumes that assessment of cytotoxicity provides useful information to aid in predicting the potential clinical applications in humans. Cell culture methods have shown good correlation with animal assays and are frequently more sensitive to cytotoxic agents.

This cell culture test method is suitable for incorporation into specifications and standards for materials to be used in the construction of medical devices that are to be implanted into the human body or placed in contact with tissue fluids or blood on a long-term basis.

Some biomaterials with a history of safe clinical use in medical devices are cytotoxic. This test method does not imply that all biomaterials must pass this assay to be considered safe for clinical use (Practice F748).

1.1 This test method is appropriate for materials in a variety of shapes and for materials that are not necessarily sterile. This test method would be appropriate in situations in which the amount of material is limited. For example, small devices or powders could be placed on the agar and the presence of a zone of inhibition of cell growth could be examined.

1.1.1 This test method is not appropriate for leachables that do not diffuse through agar or agarose.

1.1.2 While the agar layer can act as a cushion to protect the cells from the specimen, there may be materials that are sufficiently heavy to compress the agar and prevent diffusion or to cause mechanical damage to the cells. This test method would not be appropriate for these materials.

1.2 The L-929 cell line was chosen because it has a significant history of use in assays of this type. This is not intended to imply that its use is preferred, only that the L-929 is an established cell line, well characterized and readily available, that has demonstrated reproducible results in several laboratories.

1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.


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ASTM F895-2011 中可能用到的仪器设备





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