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Drug Products: Biologics, Biosimilars and Interchangeables01:28

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Body:Biologics, derived from living sources such as humans, animals, or microorganisms, represent a significant category of pharmaceuticals. These complex molecules, developed through advanced biotechnological methods or purified from natural sources, include essential medical treatments like insulin and growth hormones. The complexity of biologics arises from their large molecular structures and the intricate processes required for their production, making them distinct from conventional...
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Synthetic biology is an interdisciplinary science that involves using principles from disciplines such as engineering, molecular biology, cell biology, and systems biology. It involves remodeling existing organisms from nature or constructing completely new synthetic organisms for applications such as protein or enzyme production, bioremediation, value-added macromolecule production, and the addition of desirable traits to crops, to name a few.
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Bioequivalence studies: Biowaivers01:13

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Body:In certain scenarios, in vitro dissolution tests can replace in vivo bioequivalence studies. This is particularly true when a drug product, though available in varying strengths, maintains proportional similarity in its active and inactive ingredients. In such cases, the need for in vivo bioequivalence studies for lower strength variants may be waived, provided dissolution tests and in vivo studies on the highest strength yield satisfactory results.Bioequivalence can be indicated through...
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Bioequivalence: Overview01:16

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Pharmaceutical equivalents, by definition, are drug products with the same active ingredient in the same quantities, encapsulated in identical dosage forms, and intended for the same administration routes. These pharmaceutical equivalents are deemed bioequivalent if the bioavailability of the active entity in the drug preparations is similar. Moreover, pharmaceutical equivalents demonstrating bioequivalence are also regarded as therapeutically equivalent. This means that when used as directed,...
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Pharmaceutical substances known as xenobiotics are predominantly lipophilic and nonionized. This enables them to permeate lipid bilayers, such as cell membranes, and interact with intracellular target receptors. Lipophilic drugs have an advantage in crossing biological barriers and reaching their intended sites of action. However, lipophilic drugs often have a restricted capacity for renal expulsion or elimination from the body. When these drugs enter the kidneys and undergo glomerular...
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Biotransformation, also known as drug metabolism, is a vital physiological process that chemically alters drugs, facilitating their elimination from the body and terminating their action. This process involves two main phases: phase I and phase II reactions. Phase I reactions, including oxidation, reduction, and hydrolysis, introduce or unmask polar functional groups on the drug molecule, thereby increasing its water solubility. By enhancing water solubility, the drug becomes more hydrophilic...
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Related Experiment Video

Updated: Dec 13, 2025

Efficient Sampling of Genetically Encoded Biosensor Design Space Enabled with a Design of Experiments and Automation Workflow
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Explaining biosimilars and how reverse engineering plays a critical role in their development.

Salvatore Bellinvia1, Christopher J Edwards1

  • 1Department of Rheumatology and NIHR Clinical Research Facility, University Hospital Southampton NHS Foundation Trust , Southampton, UK.

Expert Opinion on Drug Discovery
|July 28, 2020
PubMed
Summary

Developing biosimilar products requires extensive reverse engineering of originator biologics due to complex manufacturing. This analytical approach is crucial for regulatory approval and ensuring biosimilarity.

Keywords:
Biosimilarsbiologicalsbiosimilarityreverse engineering

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Area of Science:

  • Biopharmaceuticals
  • Drug Development
  • Analytical Chemistry

Background:

  • Biological therapeutics are complex protein-based drugs.
  • Biosimilars offer alternatives as originator patents expire.
  • Biosimilar development is more complex and costly than generic small molecules.

Purpose of the Study:

  • To review the biosimilar development process, focusing on reverse engineering.
  • To examine the regulatory pathway for biosimilar approval.
  • To highlight critical analytical steps in biosimilar manufacturing.

Main Methods:

  • Extensive analysis and reverse engineering of originator biologics.
  • Comparative structural and functional assessments.
  • Review of regulatory requirements for biosimilarity.

Main Results:

  • Reverse engineering is fundamental for understanding originator manufacturing processes.
  • The biosimilar approval pathway emphasizes preclinical assessments.
  • Demonstrating biosimilarity requires rigorous structural and functional analysis.

Conclusions:

  • Well-designed reverse engineering is essential for successful biosimilar development.
  • The abbreviated biosimilar approval roadmap requires rigorous scientific standards.
  • Focusing on structural and functional biosimilarity reduces clinical trial costs and time.