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Related Concept Videos

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence

Changes in polymorphic forms can significantly influence the bioavailability of poorly soluble drugs. Although the FDA defines pharmaceutical equivalence based on having the same active ingredient, dosage form, and route of administration, it does not automatically disqualify products with different polymorphic forms. This means two products with different polymorphs can still be deemed pharmaceutically equivalent. However, polymorphic differences can affect properties like wettability,...
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism01:21

Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism

Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
Disubstituted Cyclohexanes: cis-trans Isomerism02:37

Disubstituted Cyclohexanes: cis-trans Isomerism

Depending upon the different spatial orientation of the substituents, the disubstituted cycloalkanes exhibit two types of stereoisomers. The cis isomers have the substituents on the same side of the ring, whereas the trans isomers have the substituents on the opposite sides. These stereoisomers exhibit different physical properties and cannot be interconverted without breaking the carbon-carbon bonds.
In cyclohexane, the substituents can occupy different positions generating distinct isomers.
Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...

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Related Experiment Video

Updated: Jun 3, 2026

Enhanced Photoluminescence of Curcuma longa Extracts via Chitosan-Mediated Energy Transfer for Textile Authentication Applications
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Enhanced Photoluminescence of Curcuma longa Extracts via Chitosan-Mediated Energy Transfer for Textile Authentication Applications

Published on: December 22, 2023

New polymorphs of curcumin.

Palash Sanphui1, N Rajesh Goud, U B Rao Khandavilli

  • 1School of Chemistry, University of Hyderabad, Prof. C. R. Rao Road, Central University P.O., Hyderabad 500046, India.

Chemical Communications (Cambridge, England)
|March 25, 2011
PubMed
Summary
This summary is machine-generated.

Turmeric

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Area of Science:

  • Pharmaceutical Sciences
  • Materials Science

Background:

  • Curcumin, the active ingredient in turmeric, is a known compound with therapeutic potential.
  • Understanding curcumin's solid-state forms (polymorphs) is crucial for its pharmaceutical applications.
  • Existing research has identified certain crystalline forms of curcumin.

Purpose of the Study:

  • To report the discovery and characterization of new crystalline polymorphs and an amorphous phase of curcumin.
  • To compare the physicochemical properties of these newly identified forms with known curcumin polymorphs.

Main Methods:

  • Crystallization techniques were employed to obtain new solid-state forms of curcumin.
  • Analytical methods such as X-ray diffraction and spectroscopy were used for characterization.
  • Dissolution and solubility studies were performed to assess the performance of different curcumin forms.

Main Results:

  • Two novel crystalline polymorphs (curcumin polymorph 2 and another) and an amorphous phase of curcumin were successfully synthesized and identified.
  • Curcumin polymorph 2 demonstrated a significantly higher dissolution rate compared to the previously known polymorph 1.
  • Enhanced solubility was also observed for curcumin polymorph 2.

Conclusions:

  • The discovery of new curcumin polymorphs and an amorphous phase expands the understanding of its solid-state chemistry.
  • Curcumin polymorph 2 exhibits superior dissolution and solubility profiles, suggesting potential advantages for pharmaceutical formulation.
  • Further research into these new forms could lead to improved curcumin-based drug delivery systems.