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市場調查報告書

生物製程相關課題的因應對策

Confronting the Bioprocessing Challenge

出版商 Decision Resources, Inc.
出版日期 2007年03月 商品編碼 50588
內容資訊 英文 25 Pages
價格
本報告書已不再販售

本報告已在2011年12月21日停止出版。

簡介

進入2000年之後,因為製造方法和技術有畫時代的進歩,蛋白質生長能力不足的問題得以解決。2006年的規模成長到680億美元的生物製程市場在蛋白質治療領域中,將被期望能發展出更具成本效益的有效製造方法。

專門於醫療產業相關廣泛調查的美國市調公司 Decision Resources Inc. (總公司:Massachusetts State),針對生物製程相關課題的因應對策進行調查分析,並系統整理調查結果後出版報告書  "Confronting the Bioprocessing Challenge" 。

本報告書內容包括:基因重組蛋白質與單細胞繁殖抗體相關製造上的課題、認可及銷售動向、精鍊過程、哺乳類細胞培養的技術趨勢、加醣作用化、生物製程的未來發展前景等。共計25頁的內容綱要摘記如下:

實施概要

序章

生物製程概要

  • 生產流程
  • 法規限制考量事項

產能充裕

  • 製造能力提昇
  • 低於期望的認可
  • 技術改良:改善成本效益

上游製程:哺乳類細胞培養

  • 哺乳類細胞腺體
  • 生物反應器技術
    • 生物反應器硬體設備
    • 微載體
    • 拋棄式
  • 培養基培養
  • 加醣作用

下游製程:蛋白質精鍊

  • 淨化與過濾
  • 親和性配體
  • 氫氧磷灰精鍊
  • 拋棄式精製設備

生物製造的未來發展預測

  • 製造方法
  • 排除生產瓶頸
  • 替代的發現系統
  • 可拋棄的重要性

  • 治療用蛋白質製造能力的增加
  • 基因重組蛋白質及單細胞繁殖抗體的委外生產
  • 已上市的治療用單細胞繁殖抗體
  • 蛋白質發現平台

  • 全球治療用基因重組蛋白質及單細胞繁殖抗體的銷售金額
  • 生物製程的整體架構
  • 美國單細胞繁殖抗體的認可:1997年∼2006年

目錄

Abstract

Introduction

In the early 2000s, an anticipated shortfall in protein production capacity was averted thanks to breakthroughs in manufacturing approaches and technologies. Today, new challenges and bottlenecks threaten the costeffective and adequate manufacture of protein therapeutics-which constituted a roughly $68 billion market in 2006. Again, new manufacturing approaches and a host of technological developments promise to address these issues.

Get the Answers You Need to Shape Your Strategy

Growing demand for protein-based therapeutics, particularly MAbs, has encouraged manufacturers of these drugs to rapidly expand their production capacity. Which companies have built or are planning to build additional biopharmaceutical manufacturing capacity? What factors influence the decision to expand or add new facilities? The need for increased bioprocessing capacity has spawned a market for contract manufacturing organizations. How large is this new industry? How can it serve the biopharma industry? What are the leading CMOs? Manufacturers have several strategic options for sidestepping bottlenecks and rising costs. How can they influence upstream and downstream production processes? What new technologies (e.g., non-mammalian cell lines, disposable purification devices) will make a difference in throughput?

Scope

  • Recombinant proteins and monoclonal antibodies: processes and challenges for their manufacture, trends in approvals and sales.
  • Mammalian cell culture: Mammalian cell lines and non-mammalian alternatives, bioreactor technology, media formulation, glycosylation.
  • Protein purification: Clarification and filtration, affinity ligands, hydroxyapatite purification, disposable purification devices.

Companies Mentioned in This Spectrum Report

  • Abbott Bioresearch Center
  • A-Bio
  • Affinity Life Sciences
  • Amersham Bioscience
  • Amgen
  • Avecia
  • Avid Bioservices
  • Baxter Biopharma
  • Solutions
  • Biocon
  • Biogen Idec
  • BioInvent International
  • Biolex Therapeutics
  • Bio-Rad
  • BioReliance
  • Boehringer Ingelheim
  • Bristol-Myers Squibb
  • Cangene
  • Cardinal Health
  • Cellectis
  • Celliance
  • Celltrion
  • Centocor
  • Chromos Molecular
  • Systems
  • Chugai
  • CMC Biopharmaceuticals
  • Cobra Biologics
  • Cook Pharmica
  • Corixa
  • Crucell
  • Daiichi Asubio Pharma
  • Dainippon Sumitomo
  • Diosynth Biotechnology
  • Dowpharma
  • DSM Biologics
  • Elan Pharma
  • Eli Lilly
  • Eurogentec
  • Florida Biologix
  • Fluorometrix
  • Gala Biotech
  • GE Healthcare
  • Genentech
  • Genzyme Flanders
  • GlaxoSmithKline
  • Glycart
  • GlycoFi
  • Glycotope
  • Goodwin Biotechnology
  • HyClone
  • IBA Biologics
  • Imclone Systems
  • Invitrogen Bioservices
  • Johnson & Johnson
  • Laureate Pharma
  • Lonza Biologics
  • MedImmune
  • Merck
  • Merck-Serono
  • MetaBios
  • Millipore
  • Molecular Medicine
  • BioServices
  • Nalgene
  • Neose Technologies
  • New Brunswick Scientific
  • Novartis
  • Novo Nordisk
  • Nunc
  • Organon
  • Orpegen Pharma
  • Pall
  • PDL BioPharma
  • Percell Biolytica
  • QSV Biologics
  • Rentschler Biotechnologie
  • Roche
  • Sandoz
  • Sanquin Pharmaceutical
  • Services
  • Sartorius
  • Schering AG
  • Schering-Plough
  • Selexis
  • Siegfried
  • SoloHill
  • SynCo Partners
  • Tanabe
  • Viral Antigens
  • Vista Biologicals
  • Vivalis
  • Wave Biotech
  • Wyeth
  • Wyeth-Ayerst Laboratories
  • Xcellerex
  • Xoma

Table of Contents

  • Executive Summary
    • Strategic Considerations
    • Stakeholder Implications
  • Introduction
  • Biomanufacturing Overview
    • The Production Process
    • Regulatory Considerations
  • No Shortfall in Production Capacity
    • Expansion of Manufacturing Capacity
    • Fewer Approvals Than Expected
    • Improved Technologies, Higher Yields
  • Upstream Processes: Mammalian Cell Culture Production
    • Mammalian Cell Lines
    • Bioreactor Technology
      • Bioreactor Hardware
      • Microcarriers
      • Disposables
    • Media Formulation
    • Glycosylation
  • Downstream Processes: Protein Purifi cation
    • Clarifi cation and Filtration
    • Affi nity Ligands
    • Hydroxyapatite Purifi cation
    • Disposable Purifi cation Devices
  • Outlook for Biomanufacturing
    • Manufacturing Options
    • Pushing the Limits of Production
    • Alternative Expression Systems
    • Importance of Disposables

Tables

  • 1. Increases in Therapeutic Protein Manufacturing Capacity
  • 2. Contract Manufacturers of Recombinant Proteins and Monoclonal Antibodies
  • 3. Marketed Therapeutic Monoclonal Antibodies
  • 4. Protein Expression Platforms

Figures

  • 1. Worldwide Sales of Recombinant Therapeutic Proteins and Therapeutic Monoclonal Antibodies
  • 2. General Bioprocessing Scheme
  • 3. U.S. Monoclonal Antibody Approvals, 1997-2006
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