ISO 167A/PD标准对BS 16782的脱水物理性质进行了描述 Mueller-Hinton肉汤（dMHB）和Mueller-Hinton琼脂（dMHA）以及性能标准 制造商可以评估其生产批次的dMHA和dMHB的性能特征。 所有用户都可以使用大量的肉汤或琼脂，包括体外药敏试验 设备制造商，作为抗菌药物敏感性测试性能的测试介质。本技术规范不涉及以下情况的补充剂（如血液或血液制品） 添加到培养基中以支持挑剔细菌的生长[3][4][5][6]。提供这些添加剂 在脱水培养基以液态制备为最终产品并落在培养基外后 本技术规范的范围。尽管dMHA可用于使用 琼脂稀释法[4][6]或梯度扩散法，本技术规范仅包括 按照临床和临床研究小组的描述，使用椎间盘扩散法对dMHA进行性能测试 实验室标准研究所（CLSI）[5]和欧洲抗生素敏感性委员会 测试（EUCAST）[3]。交叉引用:ISO 20776-1:2006CLSI M100NCCLS M32-P:2001CLSI M6-A2:2006CLSI M02-A12:2015CLSI M07-A10:2015CLSI M100S:2016购买本文件时可提供的所有当前修订均包含在购买本文件中。

BS PD ISO/TS 16782:2016 provides a standard description of the physical properties of dehydrated Mueller-Hinton broth (dMHB) and Mueller-Hinton agar (dMHA) and performance criteria by which manufacturers can assess the performance characteristics of their production lots of dMHA and dMHB. Production lots of broth or agar can then be utilized by all users, including in vitro susceptibility testing device manufacturers, as the test medium for performance of antimicrobial susceptibility testing.This Technical Specification does not address supplements (e.g. blood or blood products) that are added to the medium to support growth of fastidious bacteria[3][4][5][6]. Those additives are provided after the dehydrated medium is prepared in its liquid state as a final product and fall outside of the scope of this Technical Specification. Although dMHA can be used for determination of MICs using the agar dilution method[4][6] or the gradient diffusion method, this Technical Specification only includes performance testing of dMHA using disc diffusion methodology as described by the Clinical and Laboratory Standards Institute (CLSI)[5] and European Committee on Antimicrobial Susceptibility Testing (EUCAST)[3].Cross References:ISO 20776-1:2006CLSI M100NCCLS M32-P:2001CLSI M6-A2:2006CLSI M02-A12:2015CLSI M07-A10:2015CLSI M100S:2016All current amendments available at time of purchase are included with the purchase of this document.