Drug-nutrient cocrystallization-driven strategy towards self-assembly of milrinone and ferulic acid provides an exemplification in perfecting in vitro/vivo characteristics of anti-heart failure drugs. (17th May 2022)
- Record Type:
- Journal Article
- Title:
- Drug-nutrient cocrystallization-driven strategy towards self-assembly of milrinone and ferulic acid provides an exemplification in perfecting in vitro/vivo characteristics of anti-heart failure drugs. (17th May 2022)
- Main Title:
- Drug-nutrient cocrystallization-driven strategy towards self-assembly of milrinone and ferulic acid provides an exemplification in perfecting in vitro/vivo characteristics of anti-heart failure drugs
- Authors:
- Liu, Lu
Yu, Yue-Ming
Yu, Yu
Bu, Fan-Zhi
Wu, Zhi-Yong
Yan, Cui-Wei
Li, Yan-Tuan - Abstract:
- Abstract : The in vitro / vivo properties of the anti-heart failure drug milrinone were optimized by cocrystallizing with a nutraceutical, ferulic acid. Abstract : A drug-nutrient cocrystallization-driven strategy has been established to highlight the superiority of nutraceutical ferulic acid (FEA) in perfecting the biopharmaceutical peculiarities of anti-heart failure drug milrinone (MLN). Taking the strategy as guidance, a novel cocrystal of MLN with FEA, namely MLN–FEA, is assembled and characterized, which reveals that the obtained solid form is a cocrystal of MLN molecule and FEA with the ratio of 1 : 1. There are milrinone–ferulic acid hydrogen-bonding couples, which are assembled into hydrogen-bonding chains in the crystal, and these chains connect the bilayer structure of MLN molecules gathering with π⋯π interactions of CO/CN groups with the pyridine rings to the whole three-dimensional framework. The combination of theoretical and experimental approaches proves that the aggregation motifs and structural features constituted by the introduction of ferulic acid in the crystal lattice have a significant effect on improving the solubility and permeability of the cocrystal. Interestingly, compared with the parent drug MLN, the ameliorated properties in vitro can be effectively transformed into a pharmacokinetic trait in vivo, revealing the extended half-life and raised bioavailability. Thereby, the current research not only supplies a novel solid form of MLN withAbstract : The in vitro / vivo properties of the anti-heart failure drug milrinone were optimized by cocrystallizing with a nutraceutical, ferulic acid. Abstract : A drug-nutrient cocrystallization-driven strategy has been established to highlight the superiority of nutraceutical ferulic acid (FEA) in perfecting the biopharmaceutical peculiarities of anti-heart failure drug milrinone (MLN). Taking the strategy as guidance, a novel cocrystal of MLN with FEA, namely MLN–FEA, is assembled and characterized, which reveals that the obtained solid form is a cocrystal of MLN molecule and FEA with the ratio of 1 : 1. There are milrinone–ferulic acid hydrogen-bonding couples, which are assembled into hydrogen-bonding chains in the crystal, and these chains connect the bilayer structure of MLN molecules gathering with π⋯π interactions of CO/CN groups with the pyridine rings to the whole three-dimensional framework. The combination of theoretical and experimental approaches proves that the aggregation motifs and structural features constituted by the introduction of ferulic acid in the crystal lattice have a significant effect on improving the solubility and permeability of the cocrystal. Interestingly, compared with the parent drug MLN, the ameliorated properties in vitro can be effectively transformed into a pharmacokinetic trait in vivo, revealing the extended half-life and raised bioavailability. Thereby, the current research not only supplies a novel solid form of MLN with potential commercial value, but provides some new opinions for the applications of nutritients in cardiotonic pharmaceutical cocrystals. … (more)
- Is Part Of:
- New journal of chemistry. Volume 46:Number 21(2022)
- Journal:
- New journal of chemistry
- Issue:
- Volume 46:Number 21(2022)
- Issue Display:
- Volume 46, Issue 21 (2022)
- Year:
- 2022
- Volume:
- 46
- Issue:
- 21
- Issue Sort Value:
- 2022-0046-0021-0000
- Page Start:
- 10357
- Page End:
- 10367
- Publication Date:
- 2022-05-17
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d2nj01509a ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21777.xml