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蛋氨酸羟基类似物锰螯合物用于所有动物物种的授权续展申请评估。

Assessment of the application for renewal of authorisation of manganese chelate of hydroxy analogue of methionine for all animal species.

作者信息

Bampidis Vasileios, Azimonti Giovanna, Bastos Maria de Lourdes, Christensen Henrik, Dusemund Birgit, Fašmon Durjava Mojca, Kouba Maryline, López-Alonso Marta, López Puente Secundino, Marcon Francesca, Mayo Baltasar, Pechová Alena, Petkova Mariana, Ramos Fernando, Sanz Yolanda, Villa Roberto Edoardo, Woutersen Ruud, Brozzi Rosella, Galobart Jaume, Gregoretti Lucilla, Innocenti Matteo L, Sofianidis Konstantinos, Vettori Maria Vittoria, López-Gálvez Gloria

出版信息

EFSA J. 2020 Nov 12;18(11):e06281. doi: 10.2903/j.efsa.2020.6281. eCollection 2020 Nov.

Abstract

The Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the application for renewal of authorisation of manganese chelate of hydroxy analogue of methionine (MintrexMn) for all animal species. The FEEDAP Panel has delivered three opinions (in 2008, 2009 and 2010) on the safety and efficacy of the additive. The additive was authorised in 2010 as 'Manganese chelate of hydroxy analogue of methionine' containing 15.5-17 % manganese, 77-78 % (2-hydroxy-4-methylthio)butanoic acid (dl-Methionine Hydroxy Analogue, HMTBa) and maximum 1% mineral oil. Following some modifications in the manufacturing process the additive does not contain mineral oil and the applicant proposes the following specifications: ≥ 14 % manganese and ≥ 76 % HMTBa. The data provided indicate that the additive complies with the new specifications. No new evidence was found that would make the FEEDAP Panel reconsidering its previous conclusions on the safety for target species, consumers and environment. The applicant provided new studies on the effects of the additive on the respiratory tract and on skin and eyes. Data on the characterisation of the additive and the new studies on skin/eyes led the Panel to reconsider the safety for the user. Owing to the manganese and nickel content of MintrexMn, the handling of the additive poses a risk to users by inhalation; the additive is not a skin or eye irritant but is considered as a skin sensitiser. The present application did not include a proposal for amending or supplementing the conditions of the original authorisation that would have an impact on the efficacy of the additive; therefore, there was no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.

摘要

动物饲料添加剂及产品或物质专家委员会(FEEDAP)被要求就蛋氨酸羟基类似物锰螯合物(MintrexMn)在所有动物物种中的授权续展申请发表科学意见。FEEDAP专家委员会已就该添加剂的安全性和有效性发表了三份意见(分别在2008年、2009年和2010年)。该添加剂于2010年被批准为“蛋氨酸羟基类似物锰螯合物”,含锰15.5 - 17%、77 - 78%(2 - 羟基 - 4 - 甲硫基)丁酸(dl - 蛋氨酸羟基类似物,HMTBa),且矿物油含量最高为1%。在制造工艺进行一些改进后,该添加剂不再含有矿物油,申请人提出以下规格:锰含量≥14%,HMTBa含量≥76%。所提供的数据表明该添加剂符合新规格。未发现新的证据使FEEDAP专家委员会重新考虑其先前关于目标物种、消费者和环境安全性的结论。申请人提供了关于该添加剂对呼吸道以及皮肤和眼睛影响的新研究。添加剂特性数据以及关于皮肤/眼睛的新研究使专家委员会重新考虑对使用者的安全性。由于MintrexMn的锰和镍含量,添加剂的处理对使用者存在吸入风险;该添加剂不是皮肤或眼睛刺激物,但被视为皮肤致敏剂。本次申请未包括对原授权条件进行修改或补充的提议,这些修改或补充会对添加剂的有效性产生影响;因此,在授权续展的背景下无需评估添加剂的有效性。

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