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9780470843277

Biopharmaceuticals Biochemistry and Biotechnology

by
  • ISBN13:

    9780470843277

  • ISBN10:

    0470843276

  • Edition: 2nd
  • Format: Paperback
  • Copyright: 2003-08-29
  • Publisher: Wiley-Blackwell

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Summary

The latest edition of this highly acclaimed textbook, provides a comprehensive and up-to-date overview of the science and medical applications of biopharmaceutical products. Biopharmaceuticals refers to pharmaceutical substances derived from biological sources, and increasingly, it is synonymous with 'newer' pharmaceutical substances derived from genetic engineering or hybridoma technology. This superbly written review of the important areas of investigation in the field, covers drug production, plus the biochemical and molecular mechanisms of action together with the biotechnology of major biopharmaceutical types on the market or currently under development. There is also additional material reflecting both the technical advances in the area and detailed information on key topics such as the influence of genomics on drug discovery.

Author Biography

Gary Walsh is a senior lecturer in industrial biochemistry at the University of Limerick, Ireland. He combines industrial experience within the pharmaceutical industry with an extensive teaching and academic research background in pharmaceutical biotechnology. He has published half a dozen highly acclaimed books on various aspects of protein biotechnology. He is on the editorial board of several biopharmaceutical journals and is closely affiliated with the European Association of Pharma Biotechnology, serving as its scientific secretary.

Table of Contents

Preface xvii
Chapter 1 Pharmaceuticals, biologics and biopharmaceuticals 1(42)
Introduction to pharmaceutical products
1(1)
Biopharmaceuticals and pharmaceutical biotechnology
1(2)
History of the pharmaceutical industry
3(2)
The age of biopharmaceuticals
5(3)
Biopharmaceuticals: current status and future prospects
8(4)
Traditional pharmaceuticals of biological origin
12(27)
Pharmaceuticals of animal origin
13(14)
The sex hormones
14(5)
The androgens
14(1)
Oestrogens
15(2)
Progesterone and progestogens
17(2)
Corticosteroids
19(2)
Catecholamines
21(2)
Prostaglandins
23(4)
Pharmaceutical substances of plant origin
27(6)
Alkaloids
28(2)
Atropine and scopalamine
28(1)
Morphine and cocaine
29(1)
Additional plant alkaloids
30(1)
Ergot alkaloids
30(1)
Flavonoids, xanthines and terpenoids
30(3)
Cardiac glycosides and coumarins
33(1)
Aspirin
33(1)
Pharmaceutical substances of microbial origin
33(11)
The macrolides and ansamycins
38(1)
Peptide and other antibiotics
39(1)
Conclusion
39(1)
Further reading
40(3)
Chapter 2 The drug development process 43(50)
Drug discovery
44(13)
The impact of genomics and related technologies upon drug discovery
45(7)
Gene chips
47(2)
Proteomics
49(1)
Structural genomics
50(1)
Pharmacogenetics
51(1)
Plants as a source of drugs
52(1)
Microbial drugs
53(1)
Rational drug design
54(2)
Combinatorial approaches to drug discovery
56(1)
Initial product characterization
57(1)
Patenting
57(9)
What is a patent and what is patentable?
57(5)
Patent types
62(1)
The patent application
63(1)
Patenting in biotechnology
64(2)
Delivery of biopharmaceuticals
66(3)
Oral delivery systems
66(1)
Pulmonary delivery
67(1)
Nasal, transmucosal and transdermal delivery systems
68(1)
Pre-clinical trials
69(4)
Pharmacokinetics and pharmacodynamics
69(2)
Toxicity studies
71(1)
Reproductive toxicity and teratogenicity
71(1)
Mutagenicity, carcinogenicity and other tests
72(1)
Clinical trials
73(5)
Clinical trial design
75(1)
Trial size and study population
75(1)
Randomized control studies
76(1)
Additional trial designs
76(2)
The role and remit of regulatory authorities
78(11)
The Food and Drug Administration
78(6)
The investigational new drug application
80(2)
The new drug application
82(2)
European regulations
84(4)
National regulatory authorities
84(1)
The EMEA and the new EU drug approval systems
85(1)
The centralized procedure
86(2)
Mutual recognition
88(1)
Drug registration in Japan
88(1)
World harmonization of drug approvals
89(1)
Conclusion
89(1)
Further reading
89(4)
Chapter 3 The drug manufacturing process 93(96)
International pharmacopoeia
93(1)
Martindale, the Extra Pharmacopoeia
94(1)
Guides to good manufacturing practice
94(3)
The manufacturing facility
97(15)
Clean rooms
98(3)
Cleaning, decontamination and sanitation (CDS)
101(1)
CDS of the general manufacturing area
102(1)
CDS of process equipment
102(2)
Water for biopharmaceutical processing
104(1)
Generation of purified water and water for injections (WFI)
105(2)
Distribution system for WFI
107(2)
Documentation
109(1)
Specifications
110(1)
Manufacturing formulae, processing and packaging instructions
110(1)
Records
111(1)
Generation of manufacturing records
111(1)
Sources of biopharmaceuticals
112(12)
E. coli as a source of recombinant, therapeutic proteins
112(4)
Expression of recombinant proteins in animal cell culture systems
116(1)
Additional production systems: yeasts
116(1)
Fungal production systems
117(1)
Transgenic animals
118(4)
Transgenic plants
122(1)
Insect cell-based systems
123(1)
Production of final product
124(35)
Cell banking systems
127(1)
Upstream processing
128(1)
Microbial cell fermentation
129(4)
Mammalian cell culture systems
133(1)
Downstream processing
134(6)
Final product formulation
140(2)
Some influences that can alter the biological activity of proteins
142(1)
Proteolytic degradation
143(1)
Protein deamidation
144(1)
Oxidation and disulphide exchange
145(2)
Alteration of glycoprotein glycosylation patterns
147(3)
Stabilizing excipients used in final product formulations
150(3)
Final product fill
153(2)
Freeze-drying
155(3)
Labelling and packing
158(1)
Analysis of the final product
159(26)
Protein-based contaminants
159(1)
Removal of altered forms of the protein of interest from the product stream
160(1)
Product potency
161(2)
Determination of protein concentration
163(1)
Detection of protein-based product impurities
164(2)
Capillary electrophoresis
166(1)
High-pressure liquid chromatography (HPLC)
167(1)
Mass spectrometry
168(1)
Immunological approaches to detection of contaminants
168(1)
Amino acid analysis
169(1)
Peptide mapping
170(1)
N-terminal sequencing
171(2)
Analysis of secondary and tertiary structure
173(1)
Endotoxin and other pyrogenic contaminants
173(1)
Endotoxin, the molecule
174(2)
Pyrogen detection
176(3)
DNA
179(1)
Microbial and viral contaminants
180(1)
Viral assays
181(1)
Miscellaneous contaminants
182(1)
Validation studies
183(2)
Further reading
185(4)
Chapter 4 The cytokines - the interferon family 189(34)
Cytokines
189(7)
Cytokine receptors
194(1)
Cytokines as biopharmaceuticals
195(1)
The interferons
196(23)
The biochemistry of interferon-α
197(1)
Interferon-β
198(1)
Interferon-γ
198(1)
Interferon signal transduction
198(1)
The interferon receptors
199(1)
The JAK-STAT pathway
199(3)
The interferon JAK-STAT pathway
202(1)
The biological effects of interferons
203(4)
The eIF-2α protein kinase system
207
Interferon biotechnology
201(9)
Production and medical uses of IFN-α
210(3)
Medical uses of IFN-α
213(1)
Medical applications of IFN-γ
214(2)
Interferon toxicity
216(2)
Additional interferons
218(1)
Conclusion
219(1)
Further reading
219(4)
Chapter 5 Cytokines: interleukins and tumour necrosis factor 223(32)
Interleukin-2 (IL-2)
225(7)
IL-2 production
228(1)
IL-2 and cancer treatment
228(2)
IL-2 and infectious diseases
230(1)
Safety issues
231(1)
Inhibition of IL-2 activity
231(1)
Interleukin-1 (IL-1)
232(3)
The biological activities of IL-1
233(1)
IL-1 biotechnology
234(1)
Interleukin-3: biochemistry and biotechnology
235(1)
Interleukin-4
236(2)
Interleukin-6
238(2)
Interleukin-11
240(1)
Interleukin-5
241(3)
Interleukin-12
244(2)
Tumour necrosis factors (TNFs)
246(6)
TNF biochemistry
246(1)
Biological activities of TNF-α
247(1)
Immunity and inflammation
248(1)
TNF receptors
249(1)
TNF: therapeutic aspects
250(2)
Further reading
252(3)
Chapter 6 Haemopoietic growth factors 255(22)
The interleukins as haemopoietic growth factors
257(1)
Granulocyte colony stimulating factor (G-CSF)
258(1)
Macrophage colony-stimulating factor (M-CSF)
259(1)
Granulocyte-macrophage colony stimulating factor (GM-CSF)
259(2)
Clinical application of CSFs
261(2)
Leukaemia inhibitory factor (LIF)
263(1)
Erythropoietin (EPO)
264(9)
The EPO receptor and signal transduction
261(6)
Regulation of EPO production
267(1)
Therapeutic applications of EPO
268(11)
Chronic disease and cancer chemotherapy
271(1)
Additional non-renal applications
272(1)
Tolerability
273(1)
Thrombopoietin
273(2)
Further reading
275(2)
Chapter 7 Growth factors 277(26)
Growth factors and wound healing
277(2)
Insulin-like growth factors (IGFs)
279(6)
IGF biochemistry
280(1)
IGF receptors
280(2)
IGF-binding proteins
282(1)
Biological effects
282(1)
IGF and fetal development
283(1)
IGFs and growth
283(1)
Renal and reproductive effects
284(1)
Neuronal and other effects
285(1)
Epidermal growth factor (EGF)
285(2)
The EGF receptor
286(1)
Platelet-derived growth factor (PDGF)
287(2)
The PDGF receptor and signal transduction
288(1)
PDGF and wound healing
289(1)
Fibroblast growth factors (FGFs)
289(1)
Transforming growth factors (TGFs)
290(3)
TGF-α
290(2)
TGF-β
292(1)
Neurotrophic factors
293(7)
The neurotrophies
294(2)
Neurotrophin receptors
296(1)
The neurotrophin low-affinity receptor
297(1)
Ciliary neurotrophic factor and glial cell line-derived neurotrophic factor
297(1)
Neurotrophic factors and neurodegenerative disease
298(1)
Amyotrophic lateral sclerosis (ALS) and peripheral neuropathy
298(1)
Neurotrophic factors and neurodegenerative diseases of the brain
298(2)
Further reading
300(3)
Chapter 8 Hormones of therapeutic interest 303(48)
Insulin
303(18)
Diabetes mellitus
304(1)
The insulin molecule
304(3)
The insulin receptor and signal transduction
307(1)
Insulin production
307(4)
Enzymatic conversion of porcine insulin
311(1)
Production of human insulin by recombinant DNA technology
312(2)
Formulation of insulin products
314(3)
Engineered insulins
317(3)
Additional means of insulin administration
320(1)
Treating diabetics with insulin-producing cells
321(1)
Glucagon
321(3)
Human growth hormone (hGH)
324(7)
Growth hormone releasing factor (GHRF) and inhibitory factor (GHRIF)
325(1)
The GH receptor
325(2)
Biological effects of GH
327(1)
Therapeutic uses of GH
328(1)
Recombinant hGH (rhGH) and pituitary dwarfism
328(2)
Idiopathic short stature and Turner's syndrome
330(1)
Metabolic effects of hGH
330(1)
GH, lactation and ovulation
331(1)
The gonadotrophins
331(17)
Follicle stimulating hormone (FSH), luteinizing hormone (LH) and human chorionic gonadotrophin (hCG)
331(4)
Pregnant mare serum gonadotrophin (PMSG)
335(2)
The inhibins and activins
337(1)
LHRH and regulation of gonadotrophin production
338(1)
Medical and veterinary applications of gonadotrophins
339(1)
Sources and medical uses of FSH, LH and hCG
340(2)
Recombinant gonadotrophins
342(2)
Veterinary uses of gonadotrophins
344(1)
Gonadotrophin releasing hormone (GnRH)
345(1)
Additional recombinant hormones now approved
345(3)
Conclusions
348(1)
Further reading
348(3)
Chapter 9 Blood products and therapeutic enzymes 351(52)
Disease transmission
351(2)
Whole blood
353(1)
Platelets and red blood cells
353(1)
Blood substitutes
353(5)
Dextrans
354(1)
Albumin
355(2)
Gelatin
357(1)
Oxygen-carrying blood substitutes
357(1)
Haemostasis
358(42)
The coagulation pathway
358(3)
Terminal steps of coagulation pathway
361(4)
Clotting disorders
365(1)
Factor VIII and haemophilia
366(5)
Production of factor VIII
368(3)
Factors IX, Vila and XIII
371(1)
Anticoagulants
372(7)
Heparin
372(3)
Vitamin K antimetabolites
375(1)
Hirudin
375(4)
Antithrombin
379(1)
Thrombolytic agents
380(9)
Tissue plasminogen activator (tPA)
381(4)
First-generation tPA
383(1)
Engineered tPA
383(2)
Streptokinase
385(1)
Urokinase
386(1)
Staphylokinase
386(2)
α1-Antitrypsin
388(1)
Enzymes of therapeutic value
389(14)
Asparaginase
390(2)
DNase
392(1)
Glucocerebrosidase
393(2)
α Galactosidase and urate oxidase
395(2)
Superoxide dismutase
397(1)
Debriding agents
397(1)
Digestive aids
398(2)
Lactase
400(1)
Further reading
400(3)
Chapter 10 Antibodies, vaccines and adjuvants 403(60)
Polyclonal antibody preparations
403(6)
Anti-D immunoglobulin
406(1)
Normal immunoglobulins
407(1)
Hepatitis B and tetanus immunoglobulin
407(1)
Snake and spider antivenins
408(1)
Monoclonal antibodies
409(26)
Production of monoclonals via hybridoma technology
411(1)
Antibody screening: phage display technology
412(2)
Therapeutic application of monoclonal antibodies
414(1)
Tumour immunology
415(13)
Antibody-based strategies for tumour detection/destruction
417(7)
Drug-based tumour immunotherapy
424(2)
First-generation anti-tumour antibodies: clinical disappointment
426(1)
Tumour-associated antigens
426(2)
Antigenicity of murine monoclonals
428(1)
Chimaeric and humanized antibodies
429(3)
Antibody fragments
432(1)
Additional therapeutic applications of monoclonal antibodies
433(2)
Cardiovascular and related disease
433(1)
Infectious diseases
433(1)
Autoimmune disease
434(1)
Transplantation
434(1)
Vaccine technology
435(25)
Traditional vaccine preparations
436(5)
Attenuated, dead or inactivated bacteria
438(1)
Attenuated and inactivated viral vaccines
439(1)
Toxoids, antigen-based and other vaccine preparations
440(1)
The impact of genetic engineering on vaccine technology
441(6)
Peptide vaccines
444(1)
Vaccine vectors
445(2)
Development of an AIDS vaccine
447(3)
Difficulties associated with vaccine development
450(1)
AIDS vaccines in clinical trials
450(2)
Cancer vaccines
452(1)
Recombinant veterinary vaccines
452(1)
Adjuvant technology
453(2)
Adjuvant mode of action
455(8)
Mineral-based adjuvants
455(1)
Oil-based emulsion adjuvants
455(2)
Bacteria/bacterial products as adjuvants
457(1)
Additional adjuvants
458(2)
Further reading
460(3)
Chapter 11 Nucleic acid therapeutics 463(36)
Gene therapy
463(25)
Basic approach to gene therapy
464(3)
Some additional questions
467(1)
Vectors used in gene therapy
468(12)
Retroviral vectors
468(4)
Additional viral-based vectors
472(2)
Manufacture of viral vectors
474(2)
Non-viral vectors
476(4)
Manufacture of plasmid DNA
480(2)
Gene therapy and genetic disease
482(3)
Gene therapy and cancer
485(1)
Gene therapy and AIDS
486(2)
Gene-based vaccines
488(1)
Gene therapy: some additional considerations
488(1)
Anti-sense technology
488(7)
Anti-sense oligonucleotides
490(1)
Uses, advantages and disadvantages of 'oligos'
491(2)
Delivery and cellular uptake of oligonucleotides
493(1)
Manufacture of oligonucleotides
493(1)
Vitravene, an approved antisense agent
494(1)
Antigene sequences and ribozymes
494(1)
Conclusion
495(1)
Further reading
496(3)
Appendix 1 Biopharmaceuticals thus far approved in the USA or European Union 499(10)
Appendix 2 Some Internet addresses relevant to the biopharmaceutical sector 509(6)
Appendix 3 Two selected monographs reproduced from the European Pharmacopoeia with permission from the European Commission:
I. Products of recombinant DNA technology
515(5)
II. Interferon α-2 concentrated solution
520(7)
Appendix 4 Manufacture of biological medicinal products for human use. (Annex 2 from The Rules Governing Medicinal Products in the European Community, Vol. 4, Good Manufacturing Practice for Medicinal Products) 527(6)
Index 533

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