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製藥工程專業英語(十四五高等教育課程思政改革系列教材)

  • 作者:編者:許瑞波//李姣姣|責編:高司洋
  • 出版社:南京大學
  • ISBN:9787305275722
  • 出版日期:2024/07/01
  • 裝幀:平裝
  • 頁數:283
人民幣:RMB 58 元      售價:
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內容大鋼
    本書以藥物研發、申報、生產、上市為脈絡體系,內容涉及藥物化學、藥劑學、藥物分析、藥理學、藥品申報審評、化學合成、天然產物提取、生物技術、生產設備等專業知識,以及專業英語翻譯技巧、構詞法和英文摘要寫作等,共計七個章節。體裁包括科技文獻、英文原版教材、專利、藥品說明書、藥典、政策法規及指導原則等。文章內容豐富,難度適中,保持了原版英文風格、習慣,反映了製藥專業英語的文體特點與表達方式。書後附有辭彙總表以便讀者查詢。本書可作為製藥工程、藥物製劑、藥學、化學化工等專業本科生及研究生的專業英語教材,也可用作製藥工程技術人員、科研院所、科研人員的專業參考資料。

作者介紹
編者:許瑞波//李姣姣|責編:高司洋

目錄
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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