Ethotoin

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Overview of the anticonvulsant drug Ethotoin


Engineered Monoclonal Antibodies[edit source]

Diagram of engineered monoclonal antibodies

Engineered monoclonal antibodies are a class of biological therapies that are designed to target specific antigens on the surface of cells. These antibodies are produced using recombinant DNA technologies and are used in the treatment of various diseases, including cancer, autoimmune disorders, and infectious diseases.

Structure and Function[edit source]

Monoclonal antibodies are composed of two identical heavy chains and two identical light chains, forming a Y-shaped molecule. The tips of the "Y" contain the antigen-binding sites, which are highly specific to the target antigen. This specificity allows monoclonal antibodies to bind to their target with high affinity, blocking or modulating the function of the antigen.

Types of Engineered Monoclonal Antibodies[edit source]

There are several types of engineered monoclonal antibodies, each designed for specific therapeutic purposes:

  • Chimeric antibodies: These antibodies are composed of murine (mouse) variable regions and human constant regions. They are less immunogenic than fully murine antibodies.
  • Humanized antibodies: These antibodies are mostly human, with only the antigen-binding sites derived from murine sources. This reduces the risk of immune reactions.
  • Fully human antibodies: These are entirely human in origin, produced using transgenic mice or phage display technologies.
  • Bispecific antibodies: These antibodies are engineered to bind two different antigens simultaneously, offering unique therapeutic mechanisms.

Applications in Medicine[edit source]

Engineered monoclonal antibodies have revolutionized the treatment of many diseases:

  • Cancer therapy: Monoclonal antibodies can target specific tumor antigens, leading to direct tumor cell killing or recruitment of immune cells to attack the tumor.
  • Autoimmune diseases: By targeting specific components of the immune system, monoclonal antibodies can reduce inflammation and tissue damage in diseases such as rheumatoid arthritis and multiple sclerosis.
  • Infectious diseases: Monoclonal antibodies can neutralize pathogens or their toxins, providing passive immunity or enhancing the host's immune response.

Production[edit source]

The production of engineered monoclonal antibodies involves several steps:

1. Antigen identification: The target antigen is identified and characterized. 2. Hybridoma technology: B cells from immunized animals are fused with myeloma cells to create hybridomas that produce the desired antibody. 3. Recombinant DNA technology: Genes encoding the antibody are cloned and expressed in suitable host cells, such as Chinese hamster ovary cells. 4. Purification and formulation: The antibodies are purified and formulated for clinical use.

Challenges and Future Directions[edit source]

While engineered monoclonal antibodies have shown great promise, there are challenges such as high production costs, potential for immune reactions, and the development of resistance. Ongoing research aims to improve antibody design, reduce immunogenicity, and enhance therapeutic efficacy.

Related Pages[edit source]

Ethotoin is an anticonvulsant medication used primarily in the treatment of epilepsy. It is a member of the hydantoin class of drugs, which are known for their ability to stabilize neuronal membranes and reduce seizure activity.

Pharmacology[edit | edit source]

Ethotoin works by modulating the activity of sodium channels in the brain, which helps to prevent the excessive electrical activity that leads to seizures. Unlike some other anticonvulsants, Ethotoin is less likely to cause gingival hyperplasia or hirsutism.

Medical uses[edit | edit source]

Ethotoin is indicated for the management of tonic-clonic seizures and complex partial seizures. It is often used when other anticonvulsants, such as phenytoin, are not well tolerated by the patient.

Side effects[edit | edit source]

Common side effects of Ethotoin include drowsiness, dizziness, and ataxia. In some cases, patients may experience nausea, vomiting, or skin rash. Long-term use can lead to osteoporosis and folate deficiency.

Synthesis[edit | edit source]

Synthesis of Ethotoin

The synthesis of Ethotoin involves the reaction of ethyl acetoacetate with urea in the presence of a base to form the hydantoin ring. This process is a classic example of the Bucherer–Bergs reaction, which is commonly used in the synthesis of hydantoin derivatives.

History[edit | edit source]

Ethotoin was first introduced in the 1950s as an alternative to other anticonvulsants. It was developed to provide a treatment option with fewer side effects compared to phenobarbital and phenytoin.

Related pages[edit | edit source]

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Contributors: Prab R. Tumpati, MD