Wdowiak_2023_Molecules_28_

Reference

Title : Hot-Melt Extrusion as an Effective Technique for Obtaining an Amorphous System of Curcumin and Piperine with Improved Properties Essential for Their Better Biological Activities - Wdowiak_2023_Molecules_28_
Author(s) : Wdowiak K , Pietrzak R , Tykarska E , Cielecka-Piontek J
Ref : Molecules , 28 : , 2023
Abstract :

Poor bioavailability hampers the use of curcumin and piperine as biologically active agents. It can be improved by enhancing the solubility as well as by using bioenhancers to inhibit metabolic transformation processes. Obtaining an amorphous system of curcumin and piperine can lead to the overcoming of these limitations. Hot-melt extrusion successfully produced their amorphous systems, as shown by XRPD and DSC analyses. Additionally, the presence of intermolecular interactions between the components of the systems was investigated using the FT-IR/ATR technique. The systems were able to produce a supersaturation state as well as improve the apparent solubilities of curcumin and piperine by 9496- and 161-fold, respectively. The permeabilities of curcumin in the GIT and BBB PAMPA models increased by 12578- and 3069-fold, respectively, whereas piperine's were raised by 343- and 164-fold, respectively. Improved solubility had a positive effect on both antioxidant and anti-butyrylcholinesterase activities. The best system suppressed 96.97 +/- 1.32% of DPPH radicals, and butyrylcholinesterase activity was inhibited by 98.52 +/- 0.87%. In conclusion, amorphization remarkably increased the dissolution rate, apparent solubility, permeability, and biological activities of curcumin and piperine.

PubMedSearch : Wdowiak_2023_Molecules_28_
PubMedID: 37175257

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Citations formats

Wdowiak K, Pietrzak R, Tykarska E, Cielecka-Piontek J (2023)
Hot-Melt Extrusion as an Effective Technique for Obtaining an Amorphous System of Curcumin and Piperine with Improved Properties Essential for Their Better Biological Activities
Molecules 28 :

Wdowiak K, Pietrzak R, Tykarska E, Cielecka-Piontek J (2023)
Molecules 28 :