冻干检查指南(中英文对照)

更新时间:2023-07-18 07:43:14 阅读: 评论:0

GUIDE TO INSPECTIONS OF 加拿大留学机构
LYOPHILIZATION OF PARENTERALS
viper是什么意思Note: This document is reference material for investigators and other FDA personnel. The document does not bind FDA, and does no confer any rights, privileges, benefits, or immunities for or on any person(s).
INTRODUCTION
Lyophilization or freeze drying is a process in which water is removed from a product after it is frozen and placed under a vacuum, allowing the ice to change directly from solid to vapor without passing through a liquid pha. The process consists of three parate, unique, and interdependent process; freezing, primary drying (sublimation), and condary drying (desorption).
冻干是将产品置于冷冻和真空的状态下,除去水分的过程。在这个过程中冰有固态直接变为水蒸汽,而不经过液态。这个过程由三个独立的分开的又相互影响的过程组成。冷冻、主干
燥(生化)和二次干燥(解吸附)。
The advantages of lyophilization include:
冻干的优点:
考雅思多少钱Ea of processing a liquid, which simplifies aptic handling
简单的液体过程,无菌处理简单。
Enhanced stability of a dry powder
提高干粉的稳定性。
Removal of water without excessive heating of the product
不需要过多的加热产品就可以除去水分。
Enhanced product stability in a dry state
在干燥的情况下提高产品的稳定性。
Rapid and easy dissolution of reconstituted product
快速简单的产品复溶
Disadvantages of lyophilization include:
冻干的缺点
Incread handling and processing time
增加操作和处理时间
Need for sterile diluent upon reconstitution
还原时需要无菌液体
Cost and complexity of equipment
理事长英文
负责、昂贵的设备
The lyophilization process generally includes the following steps:
冻干过程包括下列步骤:
Dissolving the drug and excipients in a suitable solvent, generally water for injection (WFI).
把产品和赋形剂溶解于适当的溶媒中,通常是注射用水。
Sterilizing the bulk solution by passing it through a 0.22 micron bacteria-retentive filter.
使用0.22微米的除菌滤摸过滤原液,进行灭菌。
Filling into individual sterile containers and partially stoppering the containers under aptic conditions.
在无菌条件下分倒装单个的无菌容器中,半加塞。
Transporting the partially stoppered containers to the lyophilizer and loading into the chamber under aptic conditions.
在无菌条件下转移半加塞的容器到冻干机中,放置在前箱中。
get back
Freezing the solution by placing the partially stoppered containers on cooled shelves in a freeze-drying chamber or pre-freezing in another chamber.
在冻干机的前箱板层或其他的预冷冻箱体内将半加塞容器内的液体冷冻。
Applying a vacuum to the chamber and heating the shelves in order to evaporate the water from the frozen state.理由英语
使用真空泵并加热板层,使水分由冷冻状态下蒸。发
Complete stoppering of the vials usually by hydraulic or screw rod stoppering mechanisms installed in the lyophilizers.
使用安装在冻干机内的液压装置或螺杆全加塞。
There are many new parenteral products, including anti-infectives, biotechnology derived products, and in-vitro diagnostics which are manufactured as lyophilized products. Additionally, inspections have disclod potency, sterility and stability problems associate
d with the manufacture and control of lyophilized products. In order to provide guidance and information to investigators, some industry procedures and deficiencies associated with lyophilized products are identified in this Inspection Guide.
一些新的非肠道给药产品,包括抗感染药物、生物技术起源的药物、诊断药物采用冻干的方法生产。在检查中发现,无菌和稳定性问题与冻干产品的制造和控制密切联系。
It is recognized that there is complex technology associated with the manufacture and control of a lyophilized pharmaceutical dosage form. Some of the important aspects of the operations include: the formulation of solutions; filling of vials and validation of the filling operation; sterilization and engineering aspects of the lyophilizer; scale-up and validation of the lyophilization cycle; and testing of the end product. This discussion will address some of the problems associated with the manufacture and control of a lyophilized dosage form.britishchamber
现在公认复杂的技术与冻干制剂的制造和控制相互关联。关键的步骤包括:溶液的处方、瓶子灌装和灌装操作的验证、冻干机的灭菌和动力因素、按比例扩大和冻干周期的验证、宝贝英文
最终产品的测试。这个讨论是关于与冻干制剂制造和控制相关的问题。
PRODUCT TYPE/FORMULATIONcereal
产品类型和处方
smartdrv
Products are manufactured in the lyophilized form due to their instability when in solution. Many of the antibiotics, such as some of the mi-synthetic penicillins, cephalosporins, and also some of the salts of erythromycin, doxycycline and chloramphenicol are made by the lyophilization process. Becau they are antibiotics, low bioburden of the formulations would be expected at the time of batching. However, some of the other dosage forms that are lyophilized, such as hydrocortisone sodium succinate, methylprednisolone sodium succinate and many of the biotechnology derived products, have no antibacterial effect when in solution.
使用冻干方法进行制造产品是由于它在溶液中不稳定。一些抗生素如半合成的青霉素、一些含盐的红霉素、强力霉素、氯霉素使用冻干方法制造。因为它们是抗生素,所以在定量
的时候处方里有较低的微生物污染水平。然而有些其他的剂形采用冻干方法,如一些激素类的产品和生物技术来源的产品,当它们是溶液时没有抗菌能力。
For the types of products, bioburden should be minimal and the bioburden should be determined prior to sterilization of the bulk solutions prior to filling. Obviously, the batching or compounding of the bulk solutions should be controlled in order to prevent any potential increa in microbiological levels that may occur up to the time that the bulk solutions are filtered (sterilized). The concern with any microbiological level is the possible increa in endotoxins that may develop. Good practice for the compounding of lyophilized products would also include batching in a controlled environment and in aled tanks, particularly if the solution is to be held for any length of time prior to sterilization.

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