Foreword
Research & Development
Nanotechnology Promise

Aala Santhosh Reddy
Editor,
Pharma Focus Asia
Persistent changes in the healthcare landscape in Asia are driving the demand for increased information to patients to empower them as consumers. Better access to information, more patient responsibility and a greater focus on prevention of disease should be the basis for modern healthcare in Asia.
Chris Lee,
Regional Head,
Bayer Schering Pharma,
Asia Pacific
Cross-border collaboration in biotech industry has been emphasised by both the public and private sectors of many Asian countries. Although there are still many obstacles to overcome, such efforts have started to bear fruits.
Ying Luo,
Chief Executive Officer,
GNI Ltd.,
Japan and Shanghai
Genomics, Inc.,
China
Though Arab drug industry is increasingly contributing to the production of biotechnology products, particularly vaccines and herbal medicines, the main challenge is to achieve the regional objective of self-sufficiency in the production of essential drugs and vaccines.
Abdel Aziz Saleh,
Ex-Special Adviser
to the Regional
Director for Medicines,
WHO / EMRO, Egypt
The concept of open source model which is a huge success in the software industry holds great promise for the pharma industry as it strives to lower the cost of drug discovery and improve the bottom lines.
Jagadeesh Napa,
Assistant Editor,
Pharma Focus Asia
Every single protein in the human body is a potential target for diagnosis and treatment of diseases. This article presents a brief description of biotechnology methods applied in proteomics that may help discovering new drugs.
Afif Abdel Nour,
Research Scientist
in Molecular Biotechnology
Thierry Aussenac,
Scientific Director
Institut Polytechnique
LaSalle Beauvais,
France
Breast, prostate and lung cancer most frequently metastasise to the skeleton Adoptive immunotherapy with antigen-specific T-lymphocytes may represent an alternative to standard treatment modalities such as chemotherapy and radiation, which can only provide palliation.
Dominik Rüttinger,
Surgical Oncologist,
Laboratory of Clinical
and Experimental Tumor
Immunology,
Department of Surgery,
Grosshadern
Medical Center,
Ludwig-Maximilians-
University, Germany
Bernard A Fox,
NIH-funded Researcher
Hong-Ming Hu,
NIH-funded Immunologist
Robert W Franz
Cancer Research
Center,
Earle A Chiles Research
Institute,
Providence Cancer Center,
Oregon Health and
Science University,
USA
In times of reduced productivity coupled with increasing costs within the pharmaceutical industry, “reductionistic” target-based drug discovery has come under pressure and phenotype-based discovery has gained momentum. Target deconvolution is an important aspect for efficient progression of compounds towards development.
Georg C Terstappen,
Chief Scientific Officer,
Siena Biotech S.p.A., Italy
Application of Lean Sigma to pharmaceutical research and development is a scientific process and requires high level of engagement from all key stakeholders.
Keith Russell,
Director,
Enhancing Product Delivery,
AstraZeneca, USA
Nanoencapsulation of low soluble cancer drugs has been elaborated through powerful ultrasonication of the drug powder and simultaneous sequential polyelectrolyte deposition. This is a novel approach that allows change in capsule wall thickness to adjust drug release rate, and to attach an antibody at the outer shell layer for targeted delivery.
Yuri Lvov,
Chemistry Professor,
Tolbert Pipes Eminent
Endowed Chair on
Micro and Nanosystems,
Institute for
Micromanufacturing
Anshul Agarwal,
Doctoral Candidate
in Biomedical Engineering
Department of Biomedical
Engineering,
Louisiana Tech University,
USA
Vladimir Torchilin,
Distinguished Professor
of Pharmaceutical Sciences
Chair
Department of
Pharmaceutical Sciences
and
Director,
Center for Pharmaceutical
Biotechnology
and Nanomedicine
Rishikesh Sawant,
Doctoral Candidate
in Pharmaceutics and
Drug Delivery Systems,
Department of
Pharmaceutical Sciences,
Northeastern University,
USA
Nanobiomechanics research carried out on human diseases provides new and important insights into their pathophysiology and may suggest new methods for early detection and diagnosis.
Chwee Teck LIM,
Deputy Director,
NUS Life Sciences
Institute,
Associate Professor,
Division of Bioengineering
& Department of
Mechanical Engineering,
National University
of Singapore, Singapore
Biological tools and assays developed through unconventional nanofabrication techniques are proving to be inexpensive.
George M Whitesides,
Woodford L
and Ann A Flowers
University Professor
Michael D Dickey,
Post Doctoral Fellow,
Whitesides Group,
Department of Chemistry,
Harvard University, USA
The means of measuring the biological activity of a new drug is of critical importance to its release. The process through which a manufacturer can achieve this measure should be clearly defined before pre-clinical studies are initiated. The quality and validation requirements of these studies are defined in a number of regulations but experience of interpretation of these guidelines is essential in establishing a regulatory-compliant assay.
Daniel N Galbraith,
Head,
Operations
Andrew Upsall,
Head, In vitro Services
BioOutsource Ltd., UK
Extensive adoption of single-use products in manufacturing has shown considerable cost reductions by limiting initial capital costs, utilities required and cleaning validation etc. Do they promise the same benefits in the Asian manufacturing scenario, where overall cost of production and labour are significantly lower than in the West?
Swapnil Ballal,
Head,
Biopharmaceutical Bulk
Manufacturing,
Intas
Biopharmaceuticals Ltd.,
India
Many new approaches have been considered for large-scale chromatography including membrane adsorbers. The benefits and drawbacks of these devices and their potential impact on the biopharmaceutical industry are discussed.
Uwe Gottschalk,
Vice-President,
Purification Technologies,
Sartorius-Stedim Biotech,
Germany
Modern process analytical technology systems generate continuous quality monitoring and provide plant process controllers with highly useful process information to increase the productivity and adhere to higher quality standards.
Frank E Sistare,
Principal PAT Scientist,
CAMO Technologies Inc.,
USA
Processes of today are often equipped with sensors and measurement systems collecting large amount of data. Chemometrics is developed to handle large amount of data for overview (monitoring) and relations between raw materials, process parameters, instruments and Critical Quality Attributes.
Petter Moree,
Director,
Online Products,
Umetrics AB, Sweden
The pharma industry can add value, reduce costs and improve the overall quality of its products by improving packaging and labelling processes, enabled by integrated Product Lifecycle Management solutions.
Marc Sluijs
EMEA Business
Development Director
Life Sciences,
Oracle Healthcare &
Life Sciences,
Europe,
Middle East & Africa
Although the factors that lead to the loss of subjects in clinical trials are poorly understood, lost to follow-up” is still too frequently recorded as an outcome. This article explores the issues involved in the planning and conduct of clinical trials, and suggests a number of practical and relatively simple steps that may be taken to enhance the retention of clinical trial subjects.
J Findlay Walker,
Vice President,
Administration,
Daiichi Sankyo
Development Ltd., UK
The discovery of a disease biomarker using mass spectrometry involves careful planning and strategy. The article describes how a rheumatoid arthritis biomarker was identified and explains various steps in biomarker discovery.
Leticia Cano
IRTA Postdoctoral Fellow,
Laboratory of Applied
Mass Spectrometry,
National Heart,
Lung and Blood Institute,
National Institutes of Health,
USA
R S Gaud
Dean,
School of Pharmacy &
Technology Management,
SVKM's Nursee
Monji Institute of
Management Studies
University, India
Mark Engel
Chairman,
Excel PharmaStudies,
China