Further extensions of the cosinor approach to problems of the pharmaceutical industry

F Knappen1, C Bingham, F Halberg

  • 1Boehringer GmbH, Ingelheim, FRG.

Progress in Clinical and Biological Research
|January 1, 1990
PubMed

Related Concept Videos

Biopharmaceutics and Pharmacokinetics: Overview01:28

Biopharmaceutics and Pharmacokinetics: Overview

Understanding drugs, drug products, and their performance in pharmaceutical science is pivotal. Drugs, whether simple molecules or complex compounds, are designed to interact with the body's biological systems to diagnose, treat, or prevent diseases. Drug products include various delivery systems such as tablets, capsules, injections, and inhalers. The performance of these drug products is gauged by their ability to deliver the active ingredient to the desired site of action at the appropriate...
Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems01:22

Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems

Bioavailability is a critical pharmacological concept that measures the extent and rate at which an active drug ingredient or therapeutic moiety enters the systemic circulation, remaining unchanged. It's a pivotal factor in determining a drug's efficacy and safety.The Biopharmaceutics Classification System (BCS) plays an essential role in drug development by categorizing drugs into four classes based on their solubility and permeability. This classification aids in understanding drug absorption...
Biopharmaceutical Factors Influencing Drug Product Design: Overview01:22

Biopharmaceutical Factors Influencing Drug Product Design: Overview

Rational drug product design integrates knowledge of the drug’s physicochemical properties, formulation components, manufacturing techniques, and intended route of administration. Each factor influences the drug’s performance, including how it is released, absorbed, and eliminated in the body.The physicochemical properties of a drug—such as solubility, stability, and particle size—affect its compatibility with excipients and the choice of dosage form. Excipients, though pharmacologically...
Pharmaceutical Equivalents01:26

Pharmaceutical Equivalents

As defined by regulatory standards, pharmaceutical equivalents require generic drug products to have identical dosage forms and chemically identical active pharmaceutical ingredients (APIs). They must adhere to compendial or applicable standards for potency, content uniformity, disintegration times, and dissolution rates. In the case of modified-release dosage forms, variations in drug content are permissible as long as the delivered amount remains consistent with the innovator drug product.
Integrals of Powers of Sine and Cosine01:29

Integrals of Powers of Sine and Cosine

Trigonometric integrals involve the integration of expressions containing powers of sine, cosine, and related functions. They are common in calculus problems and have applications in physics and engineering. The method for integrating expressions of the form sinm(x)cosn(x) depends on whether the exponents are odd or even.If the power of sine is odd, one sine factor is separated from the integrand, leaving an even power of sine. The remaining sine terms are rewritten in terms of cosine using the...
The Law of Cosines01:15

The Law of Cosines

The Law of Cosines is a fundamental result in trigonometry that relates the lengths of the sides of a triangle to the cosine of one of its angles. It serves as a generalization of the Pythagorean Theorem, enabling calculations in non-right triangles where the simple relationships of right-angled geometry no longer apply. The formula is especially useful in scenarios where direct measurement of one side or angle is not feasible, such as in surveying, navigation, and engineering applications.For...