Bioanalysis of Pharmaceuticals

Sample Preparation, Separation Techniques and Mass Spectrometry

Steen Honoré Hansen, Stig Pedersen-Bjergaard, Steen Honoré Hansen, Stig Pedersen-Bjergaard

• Verlag: Wiley
• Jahr: 2015
• ISBN:
  9781118716861
• Auflage: 1
• Thema: Naturwissenschaften
• Thema: Analytische Chemie

Bioanalysis of Pharmaceuticals: Sample Preparation, Separation Techniques and Mass Spectrometry is the first student textbook on the separation science and mass spectrometry of pharmaceuticals present in biological fluids with an educational presentation of the principles, concepts and applications. It discusses the chemical structures and properties of low- and high-molecular drug substances; the different types of biological samples and fluids that are used; how to prepare the samples by extraction, and how to perform the appropriate analytical measurements by chromatographic and mass spectrometric methods.

Bioanalysis of Pharmaceuticals: Sample Preparation, Separation Techniques and Mass Spectrometry:

• Is an introductory student textbook discussing the different principles and concepts clearly and comprehensively, with many relevant and educational examples
• Focuses on substances that are administered as human drugs, including low-molecular drug substances, peptides, and proteins
• Presents both the basic principles that are regularly taught in universities, along with the practical use of bioanalysis as carried out by researchers in the pharmaceutical industry and in hospital laboratories
• Is aimed at undergraduate students, scientists, technicians and researchers in industry working in the areas of pharmaceutical analyses, biopharmaceutical analyses, biological and life sciences

The book includes multiple examples to illustrate the theory and application, with many practical aspects including calculations, thus helping the student to learn how to convert the data recorded by instruments into the real concentration of the drug substances within the biological sample.

Chapter 1
Introduction

Stig Pedersen-Bjergaard

School of Pharmacy, University of Oslo, Norway School of Pharmaceutical Sciences, University of Copenhagen, Denmark

Welcome to the field of bioanalysis! Through reading of this textbook, we hope you get fascinated by the world of bioanalysis, and also we hope that you learn to understand that bioanalysis is a highly important scientific discipline. In this chapter, five fundamental questions are raised and briefly discussed as an introduction to the textbook: (i) What is bioanalysis? (ii) What is the purpose of bioanalysis? (iii) Where is bioanalysis conducted? (iv) Why do you need theoretical understanding and skills in bioanalysis? And (v) how do you gain the understanding and the skills from reading this textbook?

1.1 What Is Bioanalysis?

In this textbook, we define bioanalysis as the chemical analysis of pharmaceutical substances in biological samples. The purpose of the chemical analysis is normally both to identify (identification) and to quantify (quantification) the pharmaceutical substance of interest in a given biological sample. This is performed by a bioanalytical chemist (scientist) using a bioanalytical method. The pharmaceutical substance of interest is often termed the analyte, and this term will be used throughout the textbook. Identification of the analyte implies that the exact chemical identity of the analyte is established unequivocally. Quantification of the analyte implies that the concentration of the analyte in the biological sample is measured. It is important to emphasize that quantification is associated with small inaccuracies, and the result is prone to errors. Thus, the quantitative data should be considered as an estimate of the true concentration. Based on theoretical and practical skills, and based on careful optimization and testing of the bioanalytical methods, the bioanalytical chemist tries to reduce the error level, providing concentration estimates that are very close to the true values.

Bioanalytical data are highly important in many aspects. As an example, a patient serum sample is analyzed for the antibiotic drug substance gentamicin, and gentamicin is measured in the sample at a concentration of 5 µg/ml. First, the identification of gentamicin in the blood serum sample confirms that the patient has taken the drug. This is important information because not all patients actually comply with the prescribed medication. Second, the exact concentration of gentamicin measured in the blood serum sample confirms that the amount of gentamicin taken is appropriate, as the recommended concentration level should be in the range of 4–10 µg/ml. For aminoglycoside antibiotics such as gentamicin, it is recommended to monitor the concentration in blood if the treatment is expected to continue for more than 72 hours as these antibiotics have the potential to cause severe adverse reactions, such as nephrotoxicity and ototoxicity.

As will be discussed in much more detail in this book, not only blood serum samples are used for bioanalysis. Bioanalysis can be performed on raw blood samples (whole blood) or on blood samples from which the blood cells have been removed (serum or plasma). Alternatively, bioanalysis can be performed from urine or saliva as examples, depending on the purpose of the bioanalysis. Bioanalysis is performed both on human samples and on samples from animal experiments.

1.2 What Is the Purpose of Bioanalysis, and Where Is It Conducted?

Bioanalysis is conducted in the pharmaceutical industry, in contract laboratories associated with the pharmaceutical industry, in hospital laboratories, in forensic toxicology laboratories, and in doping control laboratories. In the pharmaceutical industry and in the associated contract laboratories, bioanalysis is basically conducted to support the development of new drugs and new drug formulations. In hospital laboratories, bioanalysis is used to monitor existing drugs in patient samples, to check that individual patients take their drugs correctly. In forensic toxicology laboratories and doping laboratories, bioanalysis is used to check for abuse of drugs and drug-related substances.

1.2.1 Bioanalysis in the Pharmaceutical Industry

Bioanalytical laboratories are highly important in the development of new drugs and new drug formulations in the pharmaceutical industry. Thus, identification and quantification of drug substances and metabolites in biological samples like blood plasma, urine, and tissue play a very important role during drug development. Drug development begins with the identification of a medical need and hypotheses on how therapy can be improved. Drug discovery is the identification of new drug candidates based on combinatorial chemistry, high-throughput screening, genomics, and ADME (absorption, distribution, metabolism, and elimination). By combinatorial chemistry, a great number of new drug candidates are synthesized, and these are tested for pharmacological activity and potency in high-throughput screening (HTS) systems. The HTS systems simulate the interaction of the drug candidates with a specific biological receptor or target. Once a lead compound is found, a narrow range of similar drug candidates is synthesized and screened to improve the activity toward the specific target. Other studies investigate the ADME profile of drug candidates by analyzing samples collected at different time points from dosed laboratory animals (in vivo testing) and tissue cultures (in vitro testing).

Drug candidates passing the discovery phase are subjected to toxicity testing and further metabolism and pharmacological studies in the preclinical development phase. Both in vivo and in vitro tests are conducted, and various animal species are used to prove the pharmacokinetic profile of the candidate. The detailed information about the candidate forms the basis for further pharmaceutical research on the synthesis of raw materials, the development of dosage forms, quality control, and stability testing.

The clinical development phase can begin when a regulatory body has judged a drug candidate to be effective and to appear safe in healthy volunteers. In phase I, the goal is to establish a safe and efficient dosage regimen and to assess pharmacokinetics. Blood samples are collected and analyzed from a small group of healthy volunteers (20–80 persons). The data obtained form the basis for developing controlled phase II studies. The goal of phase II studies is to demonstrate a positive benefit–risk balance in a larger group of patients (200–800) and to further study pharmacokinetics. Monitoring of efficacy and monitoring of possible side effects are essential. Phase II studies can take up to two years to fulfill. At the end of phase II, a report is submitted to the regulatory body, and conditions for phase III studies are discussed. Additional information supporting the claims for a new drug is provided. Phase III begins when evidence for the efficacy of the drug candidate and supporting data have demonstrated a favorable outcome to the regulatory body. The phase III studies are large-scale efficacy studies with focus on the effectiveness and safety of the drug candidate in a large group of patients. In most cases, the drug candidate is compared with another drug already in use for treatment of the same condition. Phase III studies can last two to three years or more, and 3000–5000 patients can be involved. Carcinogenetic tests, toxicology tests, and metabolic studies in laboratory animals are conducted in parallel. The cumulative data form the basis for filing a new drug application to the regulatory body and for future plans for manufacturing and marketing. The regulatory body thoroughly evaluates the documentation that is provided before a market approval can be authorized and the drug product can be legally marketed. The time required from drug discovery to product launch is up t...