苹果手机怎么删除联系人71 STERILITY TESTS 无菌检查法
风度The following procedures are applicable for determining whether a Pharmacopeial article purporting to be sterile complies with the requirements t forth in the individual monograph with respect to the test for sterility. Pharmacopeial articles are to be tested by the Membrane Filtration method under Test for Sterility of the Product to be Examined where the nature of the product permits. If the membrane filtration technique is unsuitable, u the Direct Inoculation of the Culture Medium method under Test for Sterility of the Product to be Examined. All devices, with the exception of Devices with Pathways Labeled Sterile, are tested using the Direct Inoculation of the Culture Medium method. Provisions for retesting are included under Obrvation and Interpretation of Results.
下面这些步骤适用于测定是否某个用于无菌用途的药品是否符合其具体的各论中关于无菌检查的要求。只要其性质许可，这些药品将使用供试产品无菌检查法项下的膜过滤法来检测。如果膜过滤技术是不适合的，则使用在供试产品无菌检查法项下的培养基直接接种法。除了具有标记为无菌通道的设备之外，所有的设备均须使用培养基直接接种法进行检测。在结果的观测与理解项下包含了复验的规定。
Becau sterility testing is a very exacting procedure, where apsis of the procedure must be ensured for a correct interpretation of results, it is important that personnel be properly trained and qualified. The test for sterility is carried out under aptic conditions. In order to achieve such conditions, the test environment has to be adapted to the way in which the sterility test is performed. The precautions taken to avoid contamination are such that they do not affect any microorganisms that are to be revealed in the test. The working conditions in which the tests are performed are monitored regularly by appropriate sampling of the working area and by carrying out appropriate controls.花木兰影评
由于无菌检查法是一个非常精确的程序，在此过程中程序的无菌状态必须得到确保以实现对结果的正确理解，因此人员经过适当的培训并取得资质是非常重要的。无菌检查在无菌条件下进行。为了实现这样的条件，试验环境必须调整到适合进行无菌检查的方式。为避免污染而采取的特定预防措施应不会对任何试图在检查中发现的微生物产生影响。通过在工作区域作适当取样并进行适当控制，来定期监测进行此试验的工作条件。
The Pharmacopeial procedures are not by themlves designed to ensure that a batch of product is sterile or has been sterilized. This is accomplished primarily by validation of the sterilization process or of the aptic processing procedures.
这些药典规定程序自身的设计不能确保一批产品无菌或已经灭菌。这主要是通过灭菌工艺或者无菌操作程序的验证来完成。
When evidence of microbial contamination in the article is obtained by the appropriate Pharmacopeial method, the result so obtained is conclusive evidence of failure of the article to meet the requirements of the test for sterility, even if a different result is obtained by an alternative procedure. For additional information on sterility testing, e Sterilization and Sterility Assurance of Compendial Articles 1211 .
当通过适当的药典方法获得了某物品中微生物污染的证据，这样获得的结果是该物品未能
达到无菌检验要求的结论性证据，即便使用替代程序得到了不同的结果也无法否定此结果。 如要获得关于无菌检验的其他信息，见药品的灭菌和无菌保证<1211>
MEDIA 培养基
Prepare media for the tests as described below, or dehydrated formulations may be ud provided that, when reconstituted as directed by the manufacturer or distributor, they meet the requirements of the Growth Promotion Test of Aerobes, Anaerobes, and Fungi. Media are sterilized using a validated process.
按照下面描述的方法配制实验用培养基；或者使用脱水培养基，只要根据其制造商或者分销商说明进行恢复之后，其能够符合好氧菌、厌氧菌、霉菌生长促进试验的要求即可。使用经过验证的工艺对培养基进行灭菌操作。
The following culture media have been found to be suitable for the test for sterility. Fluid T
hioglycollate Medium is primarily intended for the culture of anaerobic bacteria. However, it will also detect aerobic bacteria. Soybean–Cain Digest Medium is suitable for the culture of both fungi and aerobic bacteria.
下面的培养基已经被证实适合进行无菌检查。巯基醋酸盐液体培养基主要用于厌氧菌的培养。但其也用于检测好氧菌。大豆酪蛋白消化物培养基适合于培养霉菌和好氧菌。
门卫制度
Fluid Thioglycollate Medium 巯基醋酸盐液体培养基
L-Cystine L-胱氨酸 | 0.5 g |
Sodium Chloride氯化钠 | 2.5 g |
Dextro (C6H12O6·H2O) 葡萄糖 | 5.5/5.0 g |
Agar, granulated (moisture content not
exceeding 15%) 琼脂，呈颗粒状(水分含量不超过15%) | 0.75 g |
Yeast Extract (water-soluble) 酵母提取物(水溶性) | 5.0 g |
Pancreatic Digest of Cain银行职业规划 酪蛋白胰酶消化物 | 15.0 g |
Sodium Thioglycollate巯基乙酸钠 | 0.5 g |
青年红色筑梦之旅or Thioglycolic Acid或者巯基乙酸 | 0.3 mL |
| 世界十大禁区 Resazurin Sodium Solution (1 in 1000),
freshly prepared 刃天青钠溶液(1比1000)，新配制 射手座和天蝎座 | 1.0 mL |
Purified Water 纯净水 | 1000 mL |
| |
Mix the L-cystine, sodium chloride, dextro, yeast extract, and pancreatic digest of cain with the purified water, and heat until solution is effected. Dissolve the sodium thioglycollate or thioglycolic acid in the solution and, if necessary, add 1 N sodium hydroxide so that, after sterilization, the solution will have a pH of 7.1 ± 0.2. If filtration is necessary, heat the solution again without boiling, and filter while hot through moistened filter paper. Add the resazurin sodium solution, mix, and place the medium in suitable vesls that provide a ratio of surface to depth of medium such that not more than the upper half of the medium has undergone a color change indicative of oxygen uptake at the end of the incubation period. Sterilize using a validated process. If the medium is stored, store at a temperature between 2 and 25 in a sterile, airtight container. If more than the upper one-third of the medium has acquired a pink color, the medium may be restored once by heating the containers in a water-bath or in free-flowing steam until the pink color disappears and by cooling quickly, taking care to prevent the introduction of nonsterile air into the container.
