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GB/T 41309-2022: Nanotechnologies - Endotoxin test on nanomaterial samples for in vitrosystems - Limulus amebocyte lysate (LAL) test
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Nanotechnologies - Endotoxin test on nanomaterial samples for in vitrosystems - Limulus amebocyte lysate (LAL) test
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GB/T 41309-2022
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Basic data | Standard ID | GB/T 41309-2022 (GB/T41309-2022) | | Description (Translated English) | Nanotechnologies - Endotoxin test on nanomaterial samples for in vitrosystems - Limulus amebocyte lysate (LAL) test | | Sector / Industry | National Standard (Recommended) | | Classification of Chinese Standard | C04 | | Word Count Estimation | 20,216 | | Issuing agency(ies) | State Administration for Market Regulation, China National Standardization Administration | GB/T 41309-2022: Nanotechnologies - Endotoxin test on nanomaterial samples for in vitrosystems - Limulus amebocyte lysate (LAL) test
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Nanotechnologies - Endotoxin test on nanomaterial samples for in vitrosystems - Limulus amebocyte lysate (LAL) test
ICS 07.030
CCSC04
National Standards of People's Republic of China
Endotoxin in nanotechnology nanomaterials
In vitro test Limulus reagent method
(ISO 29701.2010, IDT)
Published on 2022-03-09
2022-10-01 Implementation
State Administration for Market Regulation
Released by the National Standardization Administration
foreword
This document is in accordance with the provisions of GB/T 1.1-2020 "Guidelines for Standardization Work Part 1.Structure and Drafting Rules of Standardization Documents"
drafted.
This document is equivalent to ISO 29701.2010 "Limulus Reagent Method for In Vitro Endotoxin Testing of Nanomaterials in Nanotechnology".
This document adds a chapter "Normative References".
Please note that some content of this document may be patented. The issuing agency of this document assumes no responsibility for identifying patents.
This document is proposed by the Chinese Academy of Sciences.
This document is under the jurisdiction of the National Nanotechnology Standardization Technical Committee (SAC/TC279).
This document is drafted by. Institute of Basic Medicine, Chinese Academy of Medical Sciences, Peking University, Capital Medical University, China Food and Drug Control Research Institute
Graduate School, Suzhou University.
The main drafters of this document. Meng Jie, Wen Tao, Xu Haiyan, Jia Guang, Sun Zhiwei, Xu Liming, Chen Dandan, Wang Yangyun.
Introduction
Endotoxins (lipopolysaccharide LPS) are gram-negative bacteria such as Escherichia coli, Salmonella, Shigella, Pseudomonas, Neisseria and
Part of the outer membrane of cell walls such as Haemophilus. Endotoxins can cause various systemic reactions in mammals, including humans, such as fever,
Disseminated intravascular coagulation, hypotension, shock, and death. These responses are mediated by a variety of cytokines, complement system and coagulation cascade activation, etc.
guide. Endotoxins are also present in the everyday environment. In the in vitro and in vivo testing systems of nanomaterials, most of the tests have to go through a variety of preparations.
process; special care needs to be taken during preparation, otherwise endotoxins are likely to contaminate the nanomaterials.
For toxicity screening of nanomaterials, biocompatibility testing, and study of toxicity mechanisms caused by nanomaterials, a variety of substrates have been developed and used.
In vitro test systems and animal models for cells. Among them, macrophages and other related mammalian cells are the main surveillance cells in vivo.
cells, often used as test cells, these cells are highly reactive to endotoxin and it is difficult to distinguish whether the response is caused by endotoxin or nanomaterials
of. Therefore, endotoxin contamination can interfere with the results of in vitro tests.
Following proper precautions when preparing samples to be tested can reduce endotoxin contamination. To minimize endotoxin contamination or to determine
If there is no significant endotoxin in the test sample, preliminary detection of endotoxin is required. In order to fully interpret the data obtained in the in vitro biological test system
It is also important to quantify endotoxin levels.
Endotoxins may also contaminate medical devices and drugs applied by parenteral routes, so quantitative and semi-quantitative assays have been developed,
Detection of endotoxins in vivo and in vitro for regulation and standardization of laboratory procedures related to nanomaterials (see References
[6]). Detection of bacterial endotoxin using Limulus Reagent (LAL) has been developed as an in vitro assay to test for the presence of endotoxin contamination;
As an alternative method for the detection of rabbit pyrogens, the Limulus reagent method has been described in the pharmacopoeia of many countries.
This document provides considerations for the detection of nanomaterial samples using Limulus Reagent (LAL) for in vitro bioassays.
Endotoxin in nanotechnology nanomaterials
In vitro test Limulus reagent method
1 Scope
This document describes the application of the Limulus assay (LAL) to evaluate the endotoxin levels of nanomaterials for in vitro biosystem applications. The test party
The method is suitable for the detection of nanomaterials dispersed in aqueous solutions such as water, serum or reaction solution, and these media can be incubated with nanomaterials at 37 °C
a certain time.
This document is applicable to the detection of in vitro samples, and these methods are also applicable to the application of nanomaterials to animals by parenteral routes.
Material.
2 Normative references
There are no normative references in this document.
3 Terms and Definitions
The following terms and definitions apply to this document.
3.1
coagulogen
The coagulable protein in the LAL reagent plays a primary role in gel formation caused by endotoxin.
3.2
coagulin
Coagulation protein is digested by coagulation protease in LAL reagent.
47-Phenylalanine 175) (see reference [7]).
3.3
endotoxin
Part of the outer component of the cell wall of Gram-negative bacteria.
NOTE. The main active ingredient is lipopolysaccharide (LPS).
3.4
endotoxinunit
EU
Standard unit of endotoxin activity.
Note 1.According to the definition of endotoxin unit formulated by the World Health Organization (WHO) Expert Committee on Biological Standardization (ECBS) in.1996, 0.1ng of Escherichia coli
The 0113.HK10.K(-)-derived WHO Reference Standard for Endotoxin (RSE) has an activity of 10 EU/ng (see reference [8]).
Note 2.EU is equivalent to the International Unit (IU) of endotoxin.
3.5
lambda
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