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基于血液衍生物的产品中乙肝表面抗原(HBsAg)存在情况的控制调查。

Survey on controls for the presence of HBsAg in products based on hemoderivatives.

作者信息

Costantini A, Jori D, Maroccia E, Lostia O

出版信息

Boll Ist Sieroter Milan. 1977 Mar 31;56(2):108-14.

PMID:871341
Abstract

In Italy, Health Ministry provisions prohibit the marketing of products based on hemoderivatives unless they have first been controlled for the presence of HBsAg by means of radioimmunoassay. The present survey considers certificates submitted by Pharmaceutical Companies to the Health Department for permission to market their hemoderivative-based products. The results of the survey are discussed, and compared with the data obtained by the AA. in official control analyses, so as to arrive at some conclusion as to the applicability of currently employed RIA methods to HBsAg detection in hemoderivatives.

摘要

在意大利,卫生部规定禁止销售基于血液衍生物的产品,除非这些产品首先通过放射免疫测定法检测过乙肝表面抗原(HBsAg)的存在情况。本次调查研究了制药公司提交给卫生部的、用于申请销售其血液衍生物产品许可的证书。对调查结果进行了讨论,并与研究团队在官方对照分析中获得的数据进行了比较,以便就当前使用的放射免疫测定法在检测血液衍生物中乙肝表面抗原的适用性得出一些结论。

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