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    • 制药工程专业英语(十四五高等教育课程思政改革系列教材)
      • 作者:编者:许瑞波//李姣姣|责编:高司洋
      • 出版社:南京大学
      • ISBN:9787305275722
      • 出版日期:2024/07/01
      • 页数:283
    • 售价:23.2
  • 内容大纲

        本书以药物研发、申报、生产、上市为脉络体系,内容涉及药物化学、药剂学、药物分析、药理学、药品申报审评、化学合成、天然产物提取、生物技术、生产设备等专业知识,以及专业英语翻译技巧、构词法和英文摘要写作等,共计七个章节。体裁包括科技文献、英文原版教材、专利、药品说明书、药典、政策法规及指导原则等。文章内容丰富,难度适中,保持了原版英文风格、习惯,反映了制药专业英语的文体特点与表达方式。书后附有词汇总表以便读者查询。本书可作为制药工程、药物制剂、药学、化学化工等专业本科生及研究生的专业英语教材,也可用作制药工程技术人员、科研院所、科研人员的专业参考资料。
  • 作者介绍

  • 目录

    Chapter 1  Drugs Development
      Unit 1  Exploration of Artemisinin Derivatives and Synthetic Peroxides in Antimalarial Drug Discovery Research
      Unit 2  β-Lactams Past and Present
      Unit 3  Chemotherapy: An Introduction (Ⅰ)
      Unit 4  Microgels and Nanogels for the Delivery of Poorly Water-Soluble Drugs
      Unit 5  Computer Aided Drug Design
      Unit 6  Cancer Drug Resistance Related microRNAs: Recent Advances in Detection Methods
      Unit 7  Progress Towards a Clinically-Successful ATR Inhibitor for Cancer Therapy
      Unit 8  New Anticancer Agents: Role of Clinical Pharmacy Services
      Unit 9  Methods for Isolation, Purification and Structural Elucidation of Bioactive Secondary Metabolites from Marine Invertebrates
      Unit 10  Growth Years and Post-Harvest Processing Methods Have Critical Roles on the Contents of Medicinal Active Ingredients of Scutellaria Baicalensis
    Chapter 2  Drugs Declaration
      Unit 1  Impurities in New Drug Substances
      Unit 2  Guideline on the Need for Carcinogenieity Studies of Pharmaceuticals
      Unit 3  Process Validation: General Principles
      Unit 4  The Recommended Stages of Process Qualification
      Unit 5  Rare Pediatric Disease Priority Review Vouchers, Questions and Answers
    Chapter 3  Drugs Production
      Unit 1  Production of Drugs
      Unit 2  Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
      Unit 3  Isolation of Caffeine from Tea
      Unit 4  Reactor Technology
      Unit 5  European Pharmacopoeia: Imatinib Mesilate
    Chapter 4  Drugs Approval Applications and Others
      Unit 1  Determining the Extent of Safety Data Collection Needed in Late Stage Premarket and Postapproval Clinical Investigations
      Unit 2  Points to Consider on the Clinical Requirements of Modified Release Products Submitted as a Line Extension of an Existing Marketing Authorisation
      Unit 3  USP Reference Standards
      Unit 4  Highlights of Prescribing Information for Gleevec--Imatinib Mesylate Tablet
    Chapter 5  Translation Techniques for EST
      Unit 1  Introduction of EST
      Unit 2  Introduction of Translation
      Unit 3  Translation Techniques
    Chapter 6  Specialized English Word-Building Method
      Unit 1  Conversion for Part of Speech
      Unit 2  Derivation
      Unit 3  Composition
      Unit 4  Shortening
      Unit 5  Blending
      Unit 6  Signs
      Unit 7  Letters Symbolizing
    Chapter 7  Writing on the Abstract of a Professional Paper
      Unit 1  A Short Guide to Writing Abstracts
      Unit 2  Characteristics and Writing of Abstracts of Scientific and Technical Papers
      Unit 3  Examples of English Abstracts of Scientific and Technical Papers
    Vocabulary
    References

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